<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns="http://purl.org/rss/1.0/"
 xmlns:dc="http://purl.org/dc/elements/1.1/"
 xmlns:dcterms="http://purl.org/dc/terms/"
 xmlns:cc="http://web.resource.org/cc/"
 xmlns:prism="http://prismstandard.org/namespaces/basic/2.0/"
 xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
 xmlns:admin="http://webns.net/mvcb/"
 xmlns:content="http://purl.org/rss/1.0/modules/content/">
    <channel rdf:about="https://www.mdpi.com/rss/journal/cardiovascmed">
		<title>Cardiovascular Medicine</title>
		<description>Latest open access articles published in Cardiovasc. Med. at https://www.mdpi.com/journal/cardiovascmed</description>
		<link>https://www.mdpi.com/journal/cardiovascmed</link>
		<admin:generatorAgent rdf:resource="https://www.mdpi.com/journal/cardiovascmed"/>
		<admin:errorReportsTo rdf:resource="mailto:support@mdpi.com"/>
		<dc:publisher>MDPI</dc:publisher>
		<dc:language>en</dc:language>
		<dc:rights>Creative Commons Attribution (CC-BY)</dc:rights>
						<prism:copyright>MDPI</prism:copyright>
		<prism:rightsAgent>support@mdpi.com</prism:rightsAgent>
		<image rdf:resource="https://pub.mdpi-res.com/img/design/mdpi-pub-logo.png?13cf3b5bd783e021?1777446772"/>
				<items>
			<rdf:Seq>
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/29/2/16" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/29/2/15" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/29/2/14" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/29/2/13" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/29/1/12" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/29/1/11" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/29/1/10" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/29/1/9" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/29/1/8" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/29/1/7" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/29/1/6" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/29/1/5" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/29/1/4" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/29/1/3" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/29/1/2" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/29/1/1" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/28/1/6" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/28/1/5" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/28/1/4" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/28/1/3" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/28/1/2" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/28/1/1" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/5/139" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/4/99" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/4/108" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/4/122" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/4/127" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/4/125" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/4/120" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/4/114" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/4/117" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/4/129" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/4/97" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/3/71" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/3/65" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/3/80" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/3/85" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/3/68" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/3/94" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/3/90" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/3/77" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/2/41" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/2/58" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/2/33" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/2/52" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/2/55" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/2/47" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/2/63" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/1/18" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/1/25" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/1/28" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/1/31" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/1/8" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/1/6" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/27/1/1" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/6/206" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/6/194" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/6/190" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/6/202" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/6/199" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/6/182" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/6/179" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/5/20" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/5/2223" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/5/144" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/5/698" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/5/176" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/5/174" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/5/1" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/5/160" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/4/116" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/4/119" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/4/130" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/4/133" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/4/136" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/4/127" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/4/138" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/4/111" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/4/122" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/4/107" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/3/74" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/3/80" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/3/96" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/3/88" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/3/100" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/3/70" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/3/67" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/2/64" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/2/50" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/2/43" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/2/38" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/2/60" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/2/46" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/2/35" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/1/6" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/1/18" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/1/34" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/1/10" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/26/1/3" />
            				<rdf:li rdf:resource="https://www.mdpi.com/1664-204X/24/1/w10047" />
                    	</rdf:Seq>
		</items>
				<cc:license rdf:resource="https://creativecommons.org/licenses/by/4.0/" />
	</channel>

        <item rdf:about="https://www.mdpi.com/1664-204X/29/2/16">

	<title>Cardiovascular Medicine, Vol. 29, Pages 16: Device-Related Thrombosis After Left Atrial Appendage Occlusion: Updated Management and Contemporary Challenges</title>
	<link>https://www.mdpi.com/1664-204X/29/2/16</link>
	<description>Percutaneous left atrial appendage occlusion (LAAO) has become an established alternative to long-term oral anticoagulation for stroke prevention in patients with atrial fibrillation, with expanding indications beyond those with absolute contraindications to anticoagulation. Alongside its broader adoption, device-related thrombus (DRT) has emerged as a clinically relevant complication that directly compromises the protective intent of LAAO. This comprehensive narrative review synthesizes contemporary evidence on the incidence, mechanisms, predictors, clinical impact, and management of DRT. DRT is a multifactorial phenomenon that carries an annual incidence ranging from 1.75% to almost 5%, resulting from the interplay between post-implant flow dynamics, device engineering, endothelialization processes, procedural factors, and patient-specific prothrombotic features. Accumulating data from observational registries links DRT to increased risks of ischemic stroke, systemic embolism, major adverse cardiovascular events (MACE), and mortality. Although evidence is growing, optimal management regimens for both the prevention and treatment of DRT remain undefined. Moreover, a lack of standardization also affects diagnosis and imaging surveillance, mainly performed by transesophageal echocardiography or cardiac computed tomography. By integrating mechanistic insights, clinical predictors, device-specific considerations, and therapeutic evidence, this review highlights current knowledge gaps and proposes practical considerations to inform individualized risk stratification, surveillance, and management of DRT in contemporary LAAO practice.</description>
	<pubDate>2026-04-16</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 29, Pages 16: Device-Related Thrombosis After Left Atrial Appendage Occlusion: Updated Management and Contemporary Challenges</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/29/2/16">doi: 10.3390/cardiovascmed29020016</a></p>
	<p>Authors:
		Vincenzo Paragliola
		Emanuele Chiarazzo
		Andrea Giovanni Parato
		Marcello Marchetta
		Stefano Sasso
		Giuseppe Massimo Sangiorgi
		Andrea Natale
		Mario Iannaccone
		</p>
	<p>Percutaneous left atrial appendage occlusion (LAAO) has become an established alternative to long-term oral anticoagulation for stroke prevention in patients with atrial fibrillation, with expanding indications beyond those with absolute contraindications to anticoagulation. Alongside its broader adoption, device-related thrombus (DRT) has emerged as a clinically relevant complication that directly compromises the protective intent of LAAO. This comprehensive narrative review synthesizes contemporary evidence on the incidence, mechanisms, predictors, clinical impact, and management of DRT. DRT is a multifactorial phenomenon that carries an annual incidence ranging from 1.75% to almost 5%, resulting from the interplay between post-implant flow dynamics, device engineering, endothelialization processes, procedural factors, and patient-specific prothrombotic features. Accumulating data from observational registries links DRT to increased risks of ischemic stroke, systemic embolism, major adverse cardiovascular events (MACE), and mortality. Although evidence is growing, optimal management regimens for both the prevention and treatment of DRT remain undefined. Moreover, a lack of standardization also affects diagnosis and imaging surveillance, mainly performed by transesophageal echocardiography or cardiac computed tomography. By integrating mechanistic insights, clinical predictors, device-specific considerations, and therapeutic evidence, this review highlights current knowledge gaps and proposes practical considerations to inform individualized risk stratification, surveillance, and management of DRT in contemporary LAAO practice.</p>
	]]></content:encoded>

	<dc:title>Device-Related Thrombosis After Left Atrial Appendage Occlusion: Updated Management and Contemporary Challenges</dc:title>
			<dc:creator>Vincenzo Paragliola</dc:creator>
			<dc:creator>Emanuele Chiarazzo</dc:creator>
			<dc:creator>Andrea Giovanni Parato</dc:creator>
			<dc:creator>Marcello Marchetta</dc:creator>
			<dc:creator>Stefano Sasso</dc:creator>
			<dc:creator>Giuseppe Massimo Sangiorgi</dc:creator>
			<dc:creator>Andrea Natale</dc:creator>
			<dc:creator>Mario Iannaccone</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed29020016</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2026-04-16</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2026-04-16</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>16</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed29020016</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/29/2/16</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/29/2/15">

	<title>Cardiovascular Medicine, Vol. 29, Pages 15: Kv11.1 Channels in Cardiac Health and Disease: Molecular Insights and Clinical Relevance</title>
	<link>https://www.mdpi.com/1664-204X/29/2/15</link>
	<description>Kv11.1 (hERG1) channels, encoded by KCNH2, mediate the rapid delayed rectifier potassium current (IKr) crucial for cardiac repolarization. Disruptions, via mutations or antiarrhythmic drugs like dofetilide cause severe arrhythmogenic disorders, including Long QT Syndrome Type 2 (LQT2), Brugada Syndrome (BrS), and Torsades de Pointes (TdP). While Kv11.1&amp;amp;rsquo;s role in channelopathies and drug-induced arrhythmias is established, understanding its complex regulation and therapeutic targeting remains a challenge. This review synthesizes the structural, functional, and regulatory aspects of Kv11.1 channels and their clinical implications. Recent studies using iPSC-derived cardiomyocytes highlight regulation by PI3K/Akt, PKC, and PKA signaling via phosphorylation (Ser283, Ser890) and interactions with proteins like 14-3-3. Beyond electrophysiology, Kv11.1 influences pathological hypertrophy and non-cardiac functions including insulin secretion. Pharmacological efforts focus on activators to shorten action potential duration and suppress TdP, and blockers with overdose risks. Mutation heterogeneity, exemplified by trafficking impairment (G785D) in LQT2 and gain-of-function (R397C) in BrS, complicates precision therapy. Clinically, systematic risk stratification using electrocardiographic parameters and genotype-specific approaches enables personalized management. Beta-blockers remain first-line therapy for LQTS2, while rigorous avoidance of QT-prolonging medications and electrolyte monitoring form the cornerstones of preventive care. Advancing Kv11.1-targeted therapies with approaches like CRISPR-Cas9 and pharmacological chaperones (e.g., lumacaftor) holds promise for personalized treatments, ultimately reducing arrhythmic events and sudden cardiac death.</description>
	<pubDate>2026-04-07</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 29, Pages 15: Kv11.1 Channels in Cardiac Health and Disease: Molecular Insights and Clinical Relevance</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/29/2/15">doi: 10.3390/cardiovascmed29020015</a></p>
	<p>Authors:
		Mitko Mladenov
		Vadim Mitrokhin
		Stanislav Schileyko
		Anastasija Rodina
		Alexandra Zolotareva
		Valentin Zolotarev
		Natalia Bocharnikova
		Dmitry Kaminer
		Emilija Antova
		Radoslav Stojchevski
		Slavica Josifovska
		Dimiter Avtanski
		Andre Kamkin
		Nikola Hadzi-Petrushev
		</p>
	<p>Kv11.1 (hERG1) channels, encoded by KCNH2, mediate the rapid delayed rectifier potassium current (IKr) crucial for cardiac repolarization. Disruptions, via mutations or antiarrhythmic drugs like dofetilide cause severe arrhythmogenic disorders, including Long QT Syndrome Type 2 (LQT2), Brugada Syndrome (BrS), and Torsades de Pointes (TdP). While Kv11.1&amp;amp;rsquo;s role in channelopathies and drug-induced arrhythmias is established, understanding its complex regulation and therapeutic targeting remains a challenge. This review synthesizes the structural, functional, and regulatory aspects of Kv11.1 channels and their clinical implications. Recent studies using iPSC-derived cardiomyocytes highlight regulation by PI3K/Akt, PKC, and PKA signaling via phosphorylation (Ser283, Ser890) and interactions with proteins like 14-3-3. Beyond electrophysiology, Kv11.1 influences pathological hypertrophy and non-cardiac functions including insulin secretion. Pharmacological efforts focus on activators to shorten action potential duration and suppress TdP, and blockers with overdose risks. Mutation heterogeneity, exemplified by trafficking impairment (G785D) in LQT2 and gain-of-function (R397C) in BrS, complicates precision therapy. Clinically, systematic risk stratification using electrocardiographic parameters and genotype-specific approaches enables personalized management. Beta-blockers remain first-line therapy for LQTS2, while rigorous avoidance of QT-prolonging medications and electrolyte monitoring form the cornerstones of preventive care. Advancing Kv11.1-targeted therapies with approaches like CRISPR-Cas9 and pharmacological chaperones (e.g., lumacaftor) holds promise for personalized treatments, ultimately reducing arrhythmic events and sudden cardiac death.</p>
	]]></content:encoded>

	<dc:title>Kv11.1 Channels in Cardiac Health and Disease: Molecular Insights and Clinical Relevance</dc:title>
			<dc:creator>Mitko Mladenov</dc:creator>
			<dc:creator>Vadim Mitrokhin</dc:creator>
			<dc:creator>Stanislav Schileyko</dc:creator>
			<dc:creator>Anastasija Rodina</dc:creator>
			<dc:creator>Alexandra Zolotareva</dc:creator>
			<dc:creator>Valentin Zolotarev</dc:creator>
			<dc:creator>Natalia Bocharnikova</dc:creator>
			<dc:creator>Dmitry Kaminer</dc:creator>
			<dc:creator>Emilija Antova</dc:creator>
			<dc:creator>Radoslav Stojchevski</dc:creator>
			<dc:creator>Slavica Josifovska</dc:creator>
			<dc:creator>Dimiter Avtanski</dc:creator>
			<dc:creator>Andre Kamkin</dc:creator>
			<dc:creator>Nikola Hadzi-Petrushev</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed29020015</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2026-04-07</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2026-04-07</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>15</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed29020015</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/29/2/15</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/29/2/14">

	<title>Cardiovascular Medicine, Vol. 29, Pages 14: Excimer Laser Atherectomy: Mechanisms and Applications in Coronary and Peripheral Arteries</title>
	<link>https://www.mdpi.com/1664-204X/29/2/14</link>
	<description>The use of excimer laser atherectomy (ELA) has significantly evolved from the mid-1990s to the present, showing substantial improvements in both coronary and peripheral artery interventions. Initially associated with suboptimal outcomes due to low-energy settings and limited techniques, advancements such as high-energy delivery, improved catheter designs, contrast injection protocols, and refined procedural approaches have greatly enhanced clinical efficacy. In coronary applications, ELA has become an established technique for treating intracoronary thrombus, under-expanded stents, in-stent restenosis, and heavily calcified lesions, offering favorable procedural and clinical outcomes with low complication rates. The excimer laser operates through photochemical, photothermal, and photomechanical mechanisms, enabling precise plaque ablation with minimal collateral damage. In peripheral interventions, especially in critical limb ischemia (CLI), ELA has emerged as a viable option for complex, non-crossable lesions and in-stent restenosis, demonstrating high technical success, improved patency, and promising limb salvage rates. Multiple clinical trials and registries support the safety and effectiveness of ELA, particularly in high-risk patient populations. This narrative review summarizes current evidence and practical considerations on the use of excimer laser atherectomy in coronary and peripheral interventions.</description>
	<pubDate>2026-04-01</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 29, Pages 14: Excimer Laser Atherectomy: Mechanisms and Applications in Coronary and Peripheral Arteries</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/29/2/14">doi: 10.3390/cardiovascmed29020014</a></p>
	<p>Authors:
		Ferrazzo Giuseppe
		Giulia Laterra
		Giampiero Avruscio
		Carmen Tirrito
		Sonia Ragazzo
		Orazio Strazzieri
		Lorenzo Scalia
		Giampiero Vizzari
		Antonio Micari
		Paolo Mazzone
		Giovanni Ruscica
		Giorgio Sacchetta
		Marco Contarini
		Marco Barbanti
		</p>
	<p>The use of excimer laser atherectomy (ELA) has significantly evolved from the mid-1990s to the present, showing substantial improvements in both coronary and peripheral artery interventions. Initially associated with suboptimal outcomes due to low-energy settings and limited techniques, advancements such as high-energy delivery, improved catheter designs, contrast injection protocols, and refined procedural approaches have greatly enhanced clinical efficacy. In coronary applications, ELA has become an established technique for treating intracoronary thrombus, under-expanded stents, in-stent restenosis, and heavily calcified lesions, offering favorable procedural and clinical outcomes with low complication rates. The excimer laser operates through photochemical, photothermal, and photomechanical mechanisms, enabling precise plaque ablation with minimal collateral damage. In peripheral interventions, especially in critical limb ischemia (CLI), ELA has emerged as a viable option for complex, non-crossable lesions and in-stent restenosis, demonstrating high technical success, improved patency, and promising limb salvage rates. Multiple clinical trials and registries support the safety and effectiveness of ELA, particularly in high-risk patient populations. This narrative review summarizes current evidence and practical considerations on the use of excimer laser atherectomy in coronary and peripheral interventions.</p>
	]]></content:encoded>

	<dc:title>Excimer Laser Atherectomy: Mechanisms and Applications in Coronary and Peripheral Arteries</dc:title>
			<dc:creator>Ferrazzo Giuseppe</dc:creator>
			<dc:creator>Giulia Laterra</dc:creator>
			<dc:creator>Giampiero Avruscio</dc:creator>
			<dc:creator>Carmen Tirrito</dc:creator>
			<dc:creator>Sonia Ragazzo</dc:creator>
			<dc:creator>Orazio Strazzieri</dc:creator>
			<dc:creator>Lorenzo Scalia</dc:creator>
			<dc:creator>Giampiero Vizzari</dc:creator>
			<dc:creator>Antonio Micari</dc:creator>
			<dc:creator>Paolo Mazzone</dc:creator>
			<dc:creator>Giovanni Ruscica</dc:creator>
			<dc:creator>Giorgio Sacchetta</dc:creator>
			<dc:creator>Marco Contarini</dc:creator>
			<dc:creator>Marco Barbanti</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed29020014</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2026-04-01</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2026-04-01</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>14</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed29020014</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/29/2/14</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/29/2/13">

	<title>Cardiovascular Medicine, Vol. 29, Pages 13: Anatomy-Specific Association of Circulating Sortilin with Proximal Left Anterior Descending Artery Obstruction</title>
	<link>https://www.mdpi.com/1664-204X/29/2/13</link>
	<description>Background: Sortilin (SORT1), linked to the 1p13.3 coronary risk locus, is implicated in lipid trafficking and atherogenesis; however, clinical studies of circulating SORT1 have produced inconsistent results. We evaluated whether circulating SORT1 is associated with angiographic burden and lesion localization in patients with premature or early clinical debut coronary atherosclerosis. Methods: This single-center, cross-sectional study analyzed a dataset collected from January to May 2023. Participants were classified as coronary atherosclerosis cases if the dataset contained an age of clinical debut of clinically significant atherosclerosis (n = 101). Controls had no recorded debut age and 0% stenosis in all assessed coronary segments (n = 27). Blood was collected in clot activator tubes; serum was stored at &amp;amp;minus;40 &amp;amp;deg;C until analysis. SORT1 (ng/mL) was measured using an Aviscera Bioscience ELISA. Coronary stenoses were recorded as percent diameter stenosis for left main (LM), proximal/mid/distal LAD, proximal/mid/distal LCx, and proximal/mid/distal RCA. Burden metrics included the number of segments with any stenosis (&amp;amp;gt;0%), the number of obstructive segments (&amp;amp;ge;50%), the number of diseased vessels, and maximum stenosis. The prespecified primary endpoint was obstructive proximal LAD stenosis (&amp;amp;ge;50%). Nonparametric tests and Spearman correlations were used. Logistic regression evaluated the association between log2-transformed SORT1 and proximal LAD obstruction, adjusted for age, sex, LDL-C, statin use, and smoking/diabetes/hypertension durations. Results: SORT1 was higher in cases than controls (8.60 [2.60&amp;amp;ndash;17.10] vs. 2.30 [1.25&amp;amp;ndash;10.65] ng/mL; p = 0.0058). Within cases, SORT1 did not correlate with global angiographic burden (any-stenosis segments: &amp;amp;rho; = &amp;amp;minus;0.066, p = 0.513; obstructive segments: &amp;amp;rho; = &amp;amp;minus;0.060, p = 0.552; diseased vessels: &amp;amp;rho; = &amp;amp;minus;0.045, p = 0.652; maximum stenosis: &amp;amp;rho; = &amp;amp;minus;0.084, p = 0.403). Obstructive proximal LAD stenosis occurred in 44/101 (43.6%) and was associated with higher SORT1 (12.25 [4.18&amp;amp;ndash;17.45] vs. 4.10 [2.20&amp;amp;ndash;11.60] ng/mL; p = 0.0093). Each doubling of SORT1 was independently associated with proximal LAD obstruction (adjusted OR 1.48, 95% CI 1.12&amp;amp;ndash;1.95; p = 0.005). Conclusions: In this cross-sectional cohort, circulating SORT1 was associated with obstructive proximal LAD stenosis but not with global angiographic burden metrics. These findings are hypothesis-generating and warrant validation in independent cohorts with standardized preanalytics and prospective designs to assess temporal relationships and clinical utility.</description>
	<pubDate>2026-03-25</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 29, Pages 13: Anatomy-Specific Association of Circulating Sortilin with Proximal Left Anterior Descending Artery Obstruction</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/29/2/13">doi: 10.3390/cardiovascmed29020013</a></p>
	<p>Authors:
		Alim Namitokov
		Irina Gilevich
		Olga Malyarevskaya
		Natalia Iraklionova
		Karina Karabakhtsieva
		Dana Namitokova
		</p>
	<p>Background: Sortilin (SORT1), linked to the 1p13.3 coronary risk locus, is implicated in lipid trafficking and atherogenesis; however, clinical studies of circulating SORT1 have produced inconsistent results. We evaluated whether circulating SORT1 is associated with angiographic burden and lesion localization in patients with premature or early clinical debut coronary atherosclerosis. Methods: This single-center, cross-sectional study analyzed a dataset collected from January to May 2023. Participants were classified as coronary atherosclerosis cases if the dataset contained an age of clinical debut of clinically significant atherosclerosis (n = 101). Controls had no recorded debut age and 0% stenosis in all assessed coronary segments (n = 27). Blood was collected in clot activator tubes; serum was stored at &amp;amp;minus;40 &amp;amp;deg;C until analysis. SORT1 (ng/mL) was measured using an Aviscera Bioscience ELISA. Coronary stenoses were recorded as percent diameter stenosis for left main (LM), proximal/mid/distal LAD, proximal/mid/distal LCx, and proximal/mid/distal RCA. Burden metrics included the number of segments with any stenosis (&amp;amp;gt;0%), the number of obstructive segments (&amp;amp;ge;50%), the number of diseased vessels, and maximum stenosis. The prespecified primary endpoint was obstructive proximal LAD stenosis (&amp;amp;ge;50%). Nonparametric tests and Spearman correlations were used. Logistic regression evaluated the association between log2-transformed SORT1 and proximal LAD obstruction, adjusted for age, sex, LDL-C, statin use, and smoking/diabetes/hypertension durations. Results: SORT1 was higher in cases than controls (8.60 [2.60&amp;amp;ndash;17.10] vs. 2.30 [1.25&amp;amp;ndash;10.65] ng/mL; p = 0.0058). Within cases, SORT1 did not correlate with global angiographic burden (any-stenosis segments: &amp;amp;rho; = &amp;amp;minus;0.066, p = 0.513; obstructive segments: &amp;amp;rho; = &amp;amp;minus;0.060, p = 0.552; diseased vessels: &amp;amp;rho; = &amp;amp;minus;0.045, p = 0.652; maximum stenosis: &amp;amp;rho; = &amp;amp;minus;0.084, p = 0.403). Obstructive proximal LAD stenosis occurred in 44/101 (43.6%) and was associated with higher SORT1 (12.25 [4.18&amp;amp;ndash;17.45] vs. 4.10 [2.20&amp;amp;ndash;11.60] ng/mL; p = 0.0093). Each doubling of SORT1 was independently associated with proximal LAD obstruction (adjusted OR 1.48, 95% CI 1.12&amp;amp;ndash;1.95; p = 0.005). Conclusions: In this cross-sectional cohort, circulating SORT1 was associated with obstructive proximal LAD stenosis but not with global angiographic burden metrics. These findings are hypothesis-generating and warrant validation in independent cohorts with standardized preanalytics and prospective designs to assess temporal relationships and clinical utility.</p>
	]]></content:encoded>

	<dc:title>Anatomy-Specific Association of Circulating Sortilin with Proximal Left Anterior Descending Artery Obstruction</dc:title>
			<dc:creator>Alim Namitokov</dc:creator>
			<dc:creator>Irina Gilevich</dc:creator>
			<dc:creator>Olga Malyarevskaya</dc:creator>
			<dc:creator>Natalia Iraklionova</dc:creator>
			<dc:creator>Karina Karabakhtsieva</dc:creator>
			<dc:creator>Dana Namitokova</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed29020013</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2026-03-25</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2026-03-25</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>13</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed29020013</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/29/2/13</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/29/1/12">

	<title>Cardiovascular Medicine, Vol. 29, Pages 12: Atrial Fibrillation as a Marker of High-Risk Phenotype in Acute Coronary Syndrome</title>
	<link>https://www.mdpi.com/1664-204X/29/1/12</link>
	<description>Background: Atrial fibrillation (AF) is frequently encountered in patients presenting with acute coronary syndrome (ACS); however, its clinical significance beyond being a simple rhythm disturbance remains debated. We hypothesized that AF at presentation may be associated with a high-risk clinical profile characterized by hemodynamic instability and increased inflammatory and ischemic activity. Methods: This single-center, retrospective observational study included consecutive adult patients with acute coronary syndrome admitted to a tertiary cardiology center between January 2022 and December 2024. Patients were classified into two groups according to cardiac rhythm at presentation: AF and sinus rhythm. Baseline demographic characteristics, hemodynamic parameters, laboratory biomarkers, validated risk scores, and revascularization strategies were compared between groups. Multivariable logistic regression analysis was performed to evaluate whether AF was independently associated with a high-risk presentation, primarily defined by elevated GRACE risk score, reduced left ventricular ejection fraction, and increased inflammatory markers. Results: A total of 158 patients were included, of whom 50 (31.6%) presented with atrial fibrillation (mean age 71.2 &amp;amp;plusmn; 11.4 years, 46% female). Compared with patients in sinus rhythm, those with AF had significantly higher GRACE risk scores, lower left ventricular ejection fraction, faster heart rate, and higher white blood cell counts and peak high-sensitivity troponin levels. These associations remained significant after multivariable adjustment. Patients with AF also showed a numerically higher prevalence of severe angina at presentation. Conclusions: In patients presenting with ACS, atrial fibrillation is associated with a high-risk hemodynamic profile accompanied by increased inflammatory and ischemic activity. Rather than being an incidental finding, AF may represent a clinically relevant marker of acute cardiovascular stress and may contribute to early risk stratification in this setting.</description>
	<pubDate>2026-03-09</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 29, Pages 12: Atrial Fibrillation as a Marker of High-Risk Phenotype in Acute Coronary Syndrome</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/29/1/12">doi: 10.3390/cardiovascmed29010012</a></p>
	<p>Authors:
		Gamze Yeter Arslan
		Erkan Baysal
		</p>
	<p>Background: Atrial fibrillation (AF) is frequently encountered in patients presenting with acute coronary syndrome (ACS); however, its clinical significance beyond being a simple rhythm disturbance remains debated. We hypothesized that AF at presentation may be associated with a high-risk clinical profile characterized by hemodynamic instability and increased inflammatory and ischemic activity. Methods: This single-center, retrospective observational study included consecutive adult patients with acute coronary syndrome admitted to a tertiary cardiology center between January 2022 and December 2024. Patients were classified into two groups according to cardiac rhythm at presentation: AF and sinus rhythm. Baseline demographic characteristics, hemodynamic parameters, laboratory biomarkers, validated risk scores, and revascularization strategies were compared between groups. Multivariable logistic regression analysis was performed to evaluate whether AF was independently associated with a high-risk presentation, primarily defined by elevated GRACE risk score, reduced left ventricular ejection fraction, and increased inflammatory markers. Results: A total of 158 patients were included, of whom 50 (31.6%) presented with atrial fibrillation (mean age 71.2 &amp;amp;plusmn; 11.4 years, 46% female). Compared with patients in sinus rhythm, those with AF had significantly higher GRACE risk scores, lower left ventricular ejection fraction, faster heart rate, and higher white blood cell counts and peak high-sensitivity troponin levels. These associations remained significant after multivariable adjustment. Patients with AF also showed a numerically higher prevalence of severe angina at presentation. Conclusions: In patients presenting with ACS, atrial fibrillation is associated with a high-risk hemodynamic profile accompanied by increased inflammatory and ischemic activity. Rather than being an incidental finding, AF may represent a clinically relevant marker of acute cardiovascular stress and may contribute to early risk stratification in this setting.</p>
	]]></content:encoded>

	<dc:title>Atrial Fibrillation as a Marker of High-Risk Phenotype in Acute Coronary Syndrome</dc:title>
			<dc:creator>Gamze Yeter Arslan</dc:creator>
			<dc:creator>Erkan Baysal</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed29010012</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2026-03-09</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2026-03-09</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>12</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed29010012</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/29/1/12</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/29/1/11">

	<title>Cardiovascular Medicine, Vol. 29, Pages 11: OCT Findings from a Spontaneously Recanalized Coronary Thrombus Treated with a Drug-Coated Balloon</title>
	<link>https://www.mdpi.com/1664-204X/29/1/11</link>
	<description>Background: Spontaneous recanalized coronary thrombus (SRCT) is an uncommon and often underrecognized coronary pathology that may be angiographically subtle despite having functional significance. Optical coherence tomography (OCT) enables accurate diagnosis and treatment planning. However, optimal treatment strategies remain incompletely defined. Materials and Methods: A 55-year-old man presenting with severe exertional dyspnea, atypical chest pain episodes, and abnormal stress echocardiography underwent invasive coronary assessment with angiography, fractional flow reserve (FFR), and OCT. An SRCT of the left anterior descending artery (LAD) was identified and treated using OCT-guided lesion preparation followed by sirolimus-coated drug-coated-balloon (DCB) angioplasty. Results: Although there was only moderate angiographic disease, a functional assessment confirmed significant ischemia. OCT revealed a characteristic honeycomb morphology. Post-procedural OCT demonstrated satisfactory lumen gain, with preserved vessel integrity. Follow-up imaging showed vessel-healing and late lumen enlargement, and the patient remained asymptomatic. Conclusion: OCT-guided drug-coated-balloon angioplasty may be an effective &amp;amp;ldquo;leave-nothing-behind&amp;amp;rdquo; strategy for selected SRCT lesions, highlighting the importance of intracoronary imaging beyond angiography.</description>
	<pubDate>2026-03-02</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 29, Pages 11: OCT Findings from a Spontaneously Recanalized Coronary Thrombus Treated with a Drug-Coated Balloon</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/29/1/11">doi: 10.3390/cardiovascmed29010011</a></p>
	<p>Authors:
		Firat Erdogan
		Luca Vercelli
		Mehdi Madanchi
		Nicola von Rotz
		Florim Cuculi
		Matthias Bossard
		</p>
	<p>Background: Spontaneous recanalized coronary thrombus (SRCT) is an uncommon and often underrecognized coronary pathology that may be angiographically subtle despite having functional significance. Optical coherence tomography (OCT) enables accurate diagnosis and treatment planning. However, optimal treatment strategies remain incompletely defined. Materials and Methods: A 55-year-old man presenting with severe exertional dyspnea, atypical chest pain episodes, and abnormal stress echocardiography underwent invasive coronary assessment with angiography, fractional flow reserve (FFR), and OCT. An SRCT of the left anterior descending artery (LAD) was identified and treated using OCT-guided lesion preparation followed by sirolimus-coated drug-coated-balloon (DCB) angioplasty. Results: Although there was only moderate angiographic disease, a functional assessment confirmed significant ischemia. OCT revealed a characteristic honeycomb morphology. Post-procedural OCT demonstrated satisfactory lumen gain, with preserved vessel integrity. Follow-up imaging showed vessel-healing and late lumen enlargement, and the patient remained asymptomatic. Conclusion: OCT-guided drug-coated-balloon angioplasty may be an effective &amp;amp;ldquo;leave-nothing-behind&amp;amp;rdquo; strategy for selected SRCT lesions, highlighting the importance of intracoronary imaging beyond angiography.</p>
	]]></content:encoded>

	<dc:title>OCT Findings from a Spontaneously Recanalized Coronary Thrombus Treated with a Drug-Coated Balloon</dc:title>
			<dc:creator>Firat Erdogan</dc:creator>
			<dc:creator>Luca Vercelli</dc:creator>
			<dc:creator>Mehdi Madanchi</dc:creator>
			<dc:creator>Nicola von Rotz</dc:creator>
			<dc:creator>Florim Cuculi</dc:creator>
			<dc:creator>Matthias Bossard</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed29010011</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2026-03-02</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2026-03-02</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>11</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed29010011</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/29/1/11</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/29/1/10">

	<title>Cardiovascular Medicine, Vol. 29, Pages 10: External Validation and Performance of an Artificial Intelligence-Based Quantitative Coronary Angiography Software in a European Cohort</title>
	<link>https://www.mdpi.com/1664-204X/29/1/10</link>
	<description>Artificial intelligence-based quantitative coronary angiography (AI-QCA) has recently emerged as a promising tool for real-time lesion assessment in cardiology. We aimed to validate a novel AI-QCA software, trained on a Korean dataset, in a European cohort. We analyzed 556 lesions from 252 subjects in two European datasets. The AI-QCA system performed automated vessel segmentation and measurements of minimum lumen diameter, proximal and distal reference diameters, percent diameter stenosis (%DS) and lesion length. The performance of AI-QCA was assessed using both automated and manual frame selection methods, with all measurements validated against expert manual QCA. AI-QCA achieved a lesion detection rate of 86.2% in automated frame selection. AI-QCA and manual QCA showed strong agreement (Pearson&amp;amp;rsquo;s r &amp;amp;gt; 0.90, R2 &amp;amp;gt; 0.8 for all QCA measurements). For %DS categorization (&amp;amp;lt;50%, 50% to &amp;amp;lt;70%, and &amp;amp;ge;70%), 433 lesions were classified into the same category by both methods, with a weighted &amp;amp;kappa; of 0.832 (95% CI, 0.743&amp;amp;ndash;0.922). Vessel segmentation achieved a mean DSC of 0.953. This study validated the performance of AI-QCA using a European dataset and demonstrated high lesion detection rate and its strong agreement with manual QCA, which supports its applicability for real-time clinical decision-making during percutaneous coronary intervention.</description>
	<pubDate>2026-02-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 29, Pages 10: External Validation and Performance of an Artificial Intelligence-Based Quantitative Coronary Angiography Software in a European Cohort</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/29/1/10">doi: 10.3390/cardiovascmed29010010</a></p>
	<p>Authors:
		Sangmin Lee
		Bora Kim
		Soyeon Kim
		Soohyun Kim
		Rahel Kesterke
		Barbara E. Stähli
		Alessandro Candreva
		</p>
	<p>Artificial intelligence-based quantitative coronary angiography (AI-QCA) has recently emerged as a promising tool for real-time lesion assessment in cardiology. We aimed to validate a novel AI-QCA software, trained on a Korean dataset, in a European cohort. We analyzed 556 lesions from 252 subjects in two European datasets. The AI-QCA system performed automated vessel segmentation and measurements of minimum lumen diameter, proximal and distal reference diameters, percent diameter stenosis (%DS) and lesion length. The performance of AI-QCA was assessed using both automated and manual frame selection methods, with all measurements validated against expert manual QCA. AI-QCA achieved a lesion detection rate of 86.2% in automated frame selection. AI-QCA and manual QCA showed strong agreement (Pearson&amp;amp;rsquo;s r &amp;amp;gt; 0.90, R2 &amp;amp;gt; 0.8 for all QCA measurements). For %DS categorization (&amp;amp;lt;50%, 50% to &amp;amp;lt;70%, and &amp;amp;ge;70%), 433 lesions were classified into the same category by both methods, with a weighted &amp;amp;kappa; of 0.832 (95% CI, 0.743&amp;amp;ndash;0.922). Vessel segmentation achieved a mean DSC of 0.953. This study validated the performance of AI-QCA using a European dataset and demonstrated high lesion detection rate and its strong agreement with manual QCA, which supports its applicability for real-time clinical decision-making during percutaneous coronary intervention.</p>
	]]></content:encoded>

	<dc:title>External Validation and Performance of an Artificial Intelligence-Based Quantitative Coronary Angiography Software in a European Cohort</dc:title>
			<dc:creator>Sangmin Lee</dc:creator>
			<dc:creator>Bora Kim</dc:creator>
			<dc:creator>Soyeon Kim</dc:creator>
			<dc:creator>Soohyun Kim</dc:creator>
			<dc:creator>Rahel Kesterke</dc:creator>
			<dc:creator>Barbara E. Stähli</dc:creator>
			<dc:creator>Alessandro Candreva</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed29010010</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2026-02-20</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2026-02-20</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>10</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed29010010</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/29/1/10</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/29/1/9">

	<title>Cardiovascular Medicine, Vol. 29, Pages 9: Factors Associated with Developing Cancer Therapy-Related Cardiac Dysfunction Differ by Cancer Diagnosis</title>
	<link>https://www.mdpi.com/1664-204X/29/1/9</link>
	<description>Background: Cancer and cardiovascular disease are the two leading causes of death in Canada. Although treatments have improved tremendously across the years, interventions such as radiotherapy and chemotherapies are known to have negative impacts on cardiovascular health and can lead to death if not treated in time. Using a retrospective approach, we determined factors associated with cancer therapy-related cardiac dysfunction (CTRCD). Methods: Patients followed through a dedicated Cardio-Oncology clinic with comprehensive screening for CTRCD were identified. CTRCD was defined as a drop in left ventricular ejection fraction of at least 10% to a value lower than 53%. We performed multivariable logistic regression to determine factors associated with CTRCD. Results: In total, 2460 patients with cancer were identified from clinical records&amp;amp;mdash;919 had breast cancer, 758 had hematologic malignancies, and 783 had other cancer types. Patients with breast cancer and hematologic malignancies were more likely to experience CTRCD, with odds ratios (ORs) of 2.10 (p = 0.059) and 1.96 (p = 0.047), respectively. Anthracycline and trastuzumab use were independently associated with CTRCD, with ORs of 1.98 (p = 0.002) and 3.19 (p &amp;amp;lt; 0.001), respectively. In hematologic malignancy patients, hypertension (OR = 2.18, p = 0.047) and diabetes (OR = 2.31, p = 0.036) were also significant predictors of CTRCD. Conclusions: We confirmed the importance of anthracycline, trastuzumab, and radiation in the development of CTRCD. However, among patients with hematologic malignancies, traditional cardiovascular risk factors are also associated with CTRCD. This information could help physicians personalize CTRCD surveillance strategies.</description>
	<pubDate>2026-02-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 29, Pages 9: Factors Associated with Developing Cancer Therapy-Related Cardiac Dysfunction Differ by Cancer Diagnosis</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/29/1/9">doi: 10.3390/cardiovascmed29010009</a></p>
	<p>Authors:
		Ella Dunsmore
		Alda Aleksi
		Debra Bosley
		Jeffrey Cao
		Andrew Daly
		Jonathan Howlett
		Louis Kolman
		Lyndsay Litwin
		Sasha Lupichuk
		Sudhir Nishtala
		Roger Y. Tsang
		Robert J. H. Miller
		</p>
	<p>Background: Cancer and cardiovascular disease are the two leading causes of death in Canada. Although treatments have improved tremendously across the years, interventions such as radiotherapy and chemotherapies are known to have negative impacts on cardiovascular health and can lead to death if not treated in time. Using a retrospective approach, we determined factors associated with cancer therapy-related cardiac dysfunction (CTRCD). Methods: Patients followed through a dedicated Cardio-Oncology clinic with comprehensive screening for CTRCD were identified. CTRCD was defined as a drop in left ventricular ejection fraction of at least 10% to a value lower than 53%. We performed multivariable logistic regression to determine factors associated with CTRCD. Results: In total, 2460 patients with cancer were identified from clinical records&amp;amp;mdash;919 had breast cancer, 758 had hematologic malignancies, and 783 had other cancer types. Patients with breast cancer and hematologic malignancies were more likely to experience CTRCD, with odds ratios (ORs) of 2.10 (p = 0.059) and 1.96 (p = 0.047), respectively. Anthracycline and trastuzumab use were independently associated with CTRCD, with ORs of 1.98 (p = 0.002) and 3.19 (p &amp;amp;lt; 0.001), respectively. In hematologic malignancy patients, hypertension (OR = 2.18, p = 0.047) and diabetes (OR = 2.31, p = 0.036) were also significant predictors of CTRCD. Conclusions: We confirmed the importance of anthracycline, trastuzumab, and radiation in the development of CTRCD. However, among patients with hematologic malignancies, traditional cardiovascular risk factors are also associated with CTRCD. This information could help physicians personalize CTRCD surveillance strategies.</p>
	]]></content:encoded>

	<dc:title>Factors Associated with Developing Cancer Therapy-Related Cardiac Dysfunction Differ by Cancer Diagnosis</dc:title>
			<dc:creator>Ella Dunsmore</dc:creator>
			<dc:creator>Alda Aleksi</dc:creator>
			<dc:creator>Debra Bosley</dc:creator>
			<dc:creator>Jeffrey Cao</dc:creator>
			<dc:creator>Andrew Daly</dc:creator>
			<dc:creator>Jonathan Howlett</dc:creator>
			<dc:creator>Louis Kolman</dc:creator>
			<dc:creator>Lyndsay Litwin</dc:creator>
			<dc:creator>Sasha Lupichuk</dc:creator>
			<dc:creator>Sudhir Nishtala</dc:creator>
			<dc:creator>Roger Y. Tsang</dc:creator>
			<dc:creator>Robert J. H. Miller</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed29010009</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2026-02-20</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2026-02-20</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>9</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed29010009</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/29/1/9</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/29/1/8">

	<title>Cardiovascular Medicine, Vol. 29, Pages 8: Impact of New-Onset Atrial Fibrillation in Critically Ill Patients&amp;mdash;A Retrospective Study</title>
	<link>https://www.mdpi.com/1664-204X/29/1/8</link>
	<description>Background and Aim: New-onset atrial fibrillation (NOAF) is a common condition in critically ill patients, yet the evidence on optimal NOAF management and outcomes is limited. This study evaluates the impact of management strategies on short- and long-term outcomes in patients who develop NOAF during their intensive care unit (ICU) stay. Methods: A retrospective, single-centre study was conducted of all patients with NOAF admitted in a multidisciplinary ICU between 2020 and 2023. The clinical characteristics and outcomes of the patients were collected. The endpoints included the characterisation of management strategies, short-term outcomes during ICU stays (including atrial fibrillation [AF] recurrence), and long-term outcomes after discharge (including AF recurrence and a composite of death or cardiovascular hospitalisation). Results: A total of 160 patients developed NOAF (mean age 69.5 &amp;amp;plusmn; 11.8 years; 63% male). Most had cardiovascular comorbidities and high illness severity, with frequent mechanical ventilation (87%) and vasopressor (89%) use. Rhythm-control strategies&amp;amp;mdash;predominantly amiodarone&amp;amp;mdash;were associated with lower in-hospital AF recurrence (OR 0.28, p = 0.044) and a numerical reduction in post-discharge recurrence. Anticoagulation was initiated in 45% of patients and continued at discharge in 44%, without major bleeding. ICU and in-hospital mortality were 33% and 43%, respectively. During a median follow-up of 10 (range 0&amp;amp;ndash;56) months, post-ICU discharge AF recurrence occurred in 34% of patients initially discharged in sinus rhythm. Anticoagulation at discharge was not associated with recurrence, while rhythm control in the ICU and absence of in-hospital recurrence strongly predicted reduced post-discharge recurrence (p &amp;amp;lt; 0.001). Nine patients required readmission, mainly for heart failure or ischaemic stroke. The composite long-term outcome occurred in 24 patients (27%). Conclusions: Post-ICU discharge AF recurrence after NOAF was common. Early rhythm-control strategies were associated with lower in-hospital and post-discharge AF recurrence, and individualised anticoagulation appeared safe in this observational cohort. These findings support proactive post-ICU monitoring and risk-adapted management strategies.</description>
	<pubDate>2026-02-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 29, Pages 8: Impact of New-Onset Atrial Fibrillation in Critically Ill Patients&amp;mdash;A Retrospective Study</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/29/1/8">doi: 10.3390/cardiovascmed29010008</a></p>
	<p>Authors:
		Catarina Gregório
		Ana Rita Figueiredo
		Inês Pinto
		João Ribeiro
		Susana M. Fernandes
		Doroteia Silva
		</p>
	<p>Background and Aim: New-onset atrial fibrillation (NOAF) is a common condition in critically ill patients, yet the evidence on optimal NOAF management and outcomes is limited. This study evaluates the impact of management strategies on short- and long-term outcomes in patients who develop NOAF during their intensive care unit (ICU) stay. Methods: A retrospective, single-centre study was conducted of all patients with NOAF admitted in a multidisciplinary ICU between 2020 and 2023. The clinical characteristics and outcomes of the patients were collected. The endpoints included the characterisation of management strategies, short-term outcomes during ICU stays (including atrial fibrillation [AF] recurrence), and long-term outcomes after discharge (including AF recurrence and a composite of death or cardiovascular hospitalisation). Results: A total of 160 patients developed NOAF (mean age 69.5 &amp;amp;plusmn; 11.8 years; 63% male). Most had cardiovascular comorbidities and high illness severity, with frequent mechanical ventilation (87%) and vasopressor (89%) use. Rhythm-control strategies&amp;amp;mdash;predominantly amiodarone&amp;amp;mdash;were associated with lower in-hospital AF recurrence (OR 0.28, p = 0.044) and a numerical reduction in post-discharge recurrence. Anticoagulation was initiated in 45% of patients and continued at discharge in 44%, without major bleeding. ICU and in-hospital mortality were 33% and 43%, respectively. During a median follow-up of 10 (range 0&amp;amp;ndash;56) months, post-ICU discharge AF recurrence occurred in 34% of patients initially discharged in sinus rhythm. Anticoagulation at discharge was not associated with recurrence, while rhythm control in the ICU and absence of in-hospital recurrence strongly predicted reduced post-discharge recurrence (p &amp;amp;lt; 0.001). Nine patients required readmission, mainly for heart failure or ischaemic stroke. The composite long-term outcome occurred in 24 patients (27%). Conclusions: Post-ICU discharge AF recurrence after NOAF was common. Early rhythm-control strategies were associated with lower in-hospital and post-discharge AF recurrence, and individualised anticoagulation appeared safe in this observational cohort. These findings support proactive post-ICU monitoring and risk-adapted management strategies.</p>
	]]></content:encoded>

	<dc:title>Impact of New-Onset Atrial Fibrillation in Critically Ill Patients&amp;amp;mdash;A Retrospective Study</dc:title>
			<dc:creator>Catarina Gregório</dc:creator>
			<dc:creator>Ana Rita Figueiredo</dc:creator>
			<dc:creator>Inês Pinto</dc:creator>
			<dc:creator>João Ribeiro</dc:creator>
			<dc:creator>Susana M. Fernandes</dc:creator>
			<dc:creator>Doroteia Silva</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed29010008</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2026-02-20</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2026-02-20</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>8</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed29010008</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/29/1/8</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/29/1/7">

	<title>Cardiovascular Medicine, Vol. 29, Pages 7: Short-Term Outcomes in Influenza Virus-Related Myocarditis: A Single-Centre Real-Life Experience</title>
	<link>https://www.mdpi.com/1664-204X/29/1/7</link>
	<description>Background: Myocarditis is a potentially life-threatening inflammation of the myocardium that can be triggered by viral infections, including influenza. While corticosteroids have historically been used with caution in viral myocarditis due to concerns over impaired viral clearance, recent insights&amp;amp;mdash;particularly those emerging from the COVID-19 pandemic&amp;amp;mdash;suggest that early, moderate-dose corticosteroid therapy may offer clinical benefits in selected inflammatory cardiac syndromes. This study aimed to assess the incidence and clinical features, as well as short-term outcomes of influenza-related myocarditis and/or pericarditis. Methods: A retrospective, observational study was conducted, including all consecutive patients diagnosed with acute myocarditis and/or pericarditis between December 2024 and March 2025 who presented with chest pain or dyspnea and had a confirmed Influenza A (H1N1) infection. The diagnostic evaluation included cardiac biomarkers, ECG, TTE, and cardiovascular magnetic resonance (CMR). All patients were monitored during a three-month follow-up period. Results: Of 281 patients with laboratory-confirmed H1N1 infection, six (2%) were diagnosed with myocarditis and/or pericarditis. All patients diagnosed with myocarditis received corticosteroid therapy and an antiviral drug (oseltamivir). CMR confirmed the diagnosis in all cases of inflammatory cardiomyopathy. At 30 days, median LVEF improved from 49% to 58%. No deaths or rehospitalizations were reported. Conclusions: Influenza-related myocarditis and/or pericarditis are relatively uncommon, occurring in approximately 2% of cases. When they occur, they are primarily associated with an uncomplicated clinical course and with favourable short-term outcomes, including a rapid recovery of left ventricular function and the absence of adverse events at three-month follow-up.</description>
	<pubDate>2026-02-12</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 29, Pages 7: Short-Term Outcomes in Influenza Virus-Related Myocarditis: A Single-Centre Real-Life Experience</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/29/1/7">doi: 10.3390/cardiovascmed29010007</a></p>
	<p>Authors:
		Lucia Ilaria Birtolo
		Antonio Lattanzio
		Vincenzo Myftari
		Gianluca Di Pietro
		Giovanna Manzi
		Bartolomeo Fabrizio Lovero
		Margherita Pugliese
		Annalisa Caputo
		Gianmarco Scoccia
		Maria Antonella Zingaropoli
		Nicola Galea
		Cristina Chimenti
		Paolo Severino
		Viviana Maestrini
		Massimo Mancone
		Roberto Badagliacca
		Guido Antonelli
		Carmine Dario Vizza
		</p>
	<p>Background: Myocarditis is a potentially life-threatening inflammation of the myocardium that can be triggered by viral infections, including influenza. While corticosteroids have historically been used with caution in viral myocarditis due to concerns over impaired viral clearance, recent insights&amp;amp;mdash;particularly those emerging from the COVID-19 pandemic&amp;amp;mdash;suggest that early, moderate-dose corticosteroid therapy may offer clinical benefits in selected inflammatory cardiac syndromes. This study aimed to assess the incidence and clinical features, as well as short-term outcomes of influenza-related myocarditis and/or pericarditis. Methods: A retrospective, observational study was conducted, including all consecutive patients diagnosed with acute myocarditis and/or pericarditis between December 2024 and March 2025 who presented with chest pain or dyspnea and had a confirmed Influenza A (H1N1) infection. The diagnostic evaluation included cardiac biomarkers, ECG, TTE, and cardiovascular magnetic resonance (CMR). All patients were monitored during a three-month follow-up period. Results: Of 281 patients with laboratory-confirmed H1N1 infection, six (2%) were diagnosed with myocarditis and/or pericarditis. All patients diagnosed with myocarditis received corticosteroid therapy and an antiviral drug (oseltamivir). CMR confirmed the diagnosis in all cases of inflammatory cardiomyopathy. At 30 days, median LVEF improved from 49% to 58%. No deaths or rehospitalizations were reported. Conclusions: Influenza-related myocarditis and/or pericarditis are relatively uncommon, occurring in approximately 2% of cases. When they occur, they are primarily associated with an uncomplicated clinical course and with favourable short-term outcomes, including a rapid recovery of left ventricular function and the absence of adverse events at three-month follow-up.</p>
	]]></content:encoded>

	<dc:title>Short-Term Outcomes in Influenza Virus-Related Myocarditis: A Single-Centre Real-Life Experience</dc:title>
			<dc:creator>Lucia Ilaria Birtolo</dc:creator>
			<dc:creator>Antonio Lattanzio</dc:creator>
			<dc:creator>Vincenzo Myftari</dc:creator>
			<dc:creator>Gianluca Di Pietro</dc:creator>
			<dc:creator>Giovanna Manzi</dc:creator>
			<dc:creator>Bartolomeo Fabrizio Lovero</dc:creator>
			<dc:creator>Margherita Pugliese</dc:creator>
			<dc:creator>Annalisa Caputo</dc:creator>
			<dc:creator>Gianmarco Scoccia</dc:creator>
			<dc:creator>Maria Antonella Zingaropoli</dc:creator>
			<dc:creator>Nicola Galea</dc:creator>
			<dc:creator>Cristina Chimenti</dc:creator>
			<dc:creator>Paolo Severino</dc:creator>
			<dc:creator>Viviana Maestrini</dc:creator>
			<dc:creator>Massimo Mancone</dc:creator>
			<dc:creator>Roberto Badagliacca</dc:creator>
			<dc:creator>Guido Antonelli</dc:creator>
			<dc:creator>Carmine Dario Vizza</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed29010007</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2026-02-12</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2026-02-12</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>7</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed29010007</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/29/1/7</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/29/1/6">

	<title>Cardiovascular Medicine, Vol. 29, Pages 6: Prolonged Sinus Arrest Following Traumatic Brain Injury: A Case of Reversible Autonomic Cardiac Dysfunction</title>
	<link>https://www.mdpi.com/1664-204X/29/1/6</link>
	<description>Cardiac disturbances are well-recognized in traumatic brain injury (TBI), but most involve supraventricular arrhythmias or repolarization abnormalities, while sinus arrest is rarely reported. We present a case of a 37-year-old man who developed recurrent, prolonged sinus arrest following severe TBI. He arrived intubated for airway protection after an assault, and imaging demonstrated an acute, depressed, comminuted right temporoparietal skull fracture scattered subarachnoid hemorrhage, and bilateral humeral head fractures with posterior shoulder subluxation. After craniotomy and placement of an external ventricular drain (EVD) for intracranial pressure (ICP) monitoring, the patient experienced multiple spontaneous sinus arrest episodes lasting up to 15 s despite normal metabolic, electrolyte, and toxicology evaluations. A transvenous pacemaker (TVP) was inserted to maintain adequate cardiac output and cerebral perfusion. As ICP improved, the sinus arrests resolved and the TVP was removed. This case highlights a rare neurocardiac manifestation of TBI, demonstrating that elevated ICP can precipitate profound conduction disturbances that may require temporary pacing to manage hemodynamics and prevent secondary brain injury.</description>
	<pubDate>2026-02-10</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 29, Pages 6: Prolonged Sinus Arrest Following Traumatic Brain Injury: A Case of Reversible Autonomic Cardiac Dysfunction</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/29/1/6">doi: 10.3390/cardiovascmed29010006</a></p>
	<p>Authors:
		Krishna Patel
		Chris Sani
		Asher Gorantla
		Varshitha T. Panduranga
		Usaid Raqeeb
		Adam Budzikowski
		</p>
	<p>Cardiac disturbances are well-recognized in traumatic brain injury (TBI), but most involve supraventricular arrhythmias or repolarization abnormalities, while sinus arrest is rarely reported. We present a case of a 37-year-old man who developed recurrent, prolonged sinus arrest following severe TBI. He arrived intubated for airway protection after an assault, and imaging demonstrated an acute, depressed, comminuted right temporoparietal skull fracture scattered subarachnoid hemorrhage, and bilateral humeral head fractures with posterior shoulder subluxation. After craniotomy and placement of an external ventricular drain (EVD) for intracranial pressure (ICP) monitoring, the patient experienced multiple spontaneous sinus arrest episodes lasting up to 15 s despite normal metabolic, electrolyte, and toxicology evaluations. A transvenous pacemaker (TVP) was inserted to maintain adequate cardiac output and cerebral perfusion. As ICP improved, the sinus arrests resolved and the TVP was removed. This case highlights a rare neurocardiac manifestation of TBI, demonstrating that elevated ICP can precipitate profound conduction disturbances that may require temporary pacing to manage hemodynamics and prevent secondary brain injury.</p>
	]]></content:encoded>

	<dc:title>Prolonged Sinus Arrest Following Traumatic Brain Injury: A Case of Reversible Autonomic Cardiac Dysfunction</dc:title>
			<dc:creator>Krishna Patel</dc:creator>
			<dc:creator>Chris Sani</dc:creator>
			<dc:creator>Asher Gorantla</dc:creator>
			<dc:creator>Varshitha T. Panduranga</dc:creator>
			<dc:creator>Usaid Raqeeb</dc:creator>
			<dc:creator>Adam Budzikowski</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed29010006</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2026-02-10</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2026-02-10</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>6</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed29010006</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/29/1/6</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/29/1/5">

	<title>Cardiovascular Medicine, Vol. 29, Pages 5: The Prevalence of Cardiovascular&amp;ndash;Kidney&amp;ndash;Metabolic Syndrome: A Review of Published Estimates and New Findings from BRFSS Surveys</title>
	<link>https://www.mdpi.com/1664-204X/29/1/5</link>
	<description>Because CKMS was only proposed by the American Heart Association in 2023, there has been a paucity of information about the distribution and determinants of the syndrome across population groups. We reviewed published studies of the prevalence of CKMS in the U.S. and other countries and obtained new estimates of the prevalence of this syndrome among U.S. adults by birth decade and sociodemographic attributes using 2019, 2021, and 2023 Behavioral Risk Factor Surveillance System (BRFSS) data. The results of this study indicate that CKMS is widespread in the general U.S. population, especially among older cohorts born before 1940 and during the 1940s, 1950s, and 1960s. Except for the three younger cohorts, born in the 1980s, 1990s, and 2000 or later, the prevalence of CKMS stage 4 was significantly higher among males than in females. Among those born between the 1950s and 1990s, the prevalence was significantly higher among non-Hispanic Blacks compared to their non-Hispanic white counterparts. Across all birth decades, prevalence of CKMS stage 4 was generally higher among those without a college degree, from a low-income household, and residing in rural areas. These prevalence rate estimates will further our understanding of the burden and unique needs of different population groups in improving cardiovascular&amp;amp;ndash;kidney&amp;amp;ndash;metabolic health across the life course.</description>
	<pubDate>2026-02-03</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 29, Pages 5: The Prevalence of Cardiovascular&amp;ndash;Kidney&amp;ndash;Metabolic Syndrome: A Review of Published Estimates and New Findings from BRFSS Surveys</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/29/1/5">doi: 10.3390/cardiovascmed29010005</a></p>
	<p>Authors:
		Steven S. Coughlin
		Nikul Parikh
		Ashley Oh
		Biplab Datta
		Marlo Vernon
		Jennifer Sullivan
		</p>
	<p>Because CKMS was only proposed by the American Heart Association in 2023, there has been a paucity of information about the distribution and determinants of the syndrome across population groups. We reviewed published studies of the prevalence of CKMS in the U.S. and other countries and obtained new estimates of the prevalence of this syndrome among U.S. adults by birth decade and sociodemographic attributes using 2019, 2021, and 2023 Behavioral Risk Factor Surveillance System (BRFSS) data. The results of this study indicate that CKMS is widespread in the general U.S. population, especially among older cohorts born before 1940 and during the 1940s, 1950s, and 1960s. Except for the three younger cohorts, born in the 1980s, 1990s, and 2000 or later, the prevalence of CKMS stage 4 was significantly higher among males than in females. Among those born between the 1950s and 1990s, the prevalence was significantly higher among non-Hispanic Blacks compared to their non-Hispanic white counterparts. Across all birth decades, prevalence of CKMS stage 4 was generally higher among those without a college degree, from a low-income household, and residing in rural areas. These prevalence rate estimates will further our understanding of the burden and unique needs of different population groups in improving cardiovascular&amp;amp;ndash;kidney&amp;amp;ndash;metabolic health across the life course.</p>
	]]></content:encoded>

	<dc:title>The Prevalence of Cardiovascular&amp;amp;ndash;Kidney&amp;amp;ndash;Metabolic Syndrome: A Review of Published Estimates and New Findings from BRFSS Surveys</dc:title>
			<dc:creator>Steven S. Coughlin</dc:creator>
			<dc:creator>Nikul Parikh</dc:creator>
			<dc:creator>Ashley Oh</dc:creator>
			<dc:creator>Biplab Datta</dc:creator>
			<dc:creator>Marlo Vernon</dc:creator>
			<dc:creator>Jennifer Sullivan</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed29010005</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2026-02-03</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2026-02-03</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>5</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed29010005</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/29/1/5</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/29/1/4">

	<title>Cardiovascular Medicine, Vol. 29, Pages 4: Pharmacovigilance-Based Safety Profile of Bortezomib: A Disproportionality Analysis Using FAERS Data</title>
	<link>https://www.mdpi.com/1664-204X/29/1/4</link>
	<description>Bortezomib is a 26S proteasome inhibitor used to treat multiple myeloma and systemic amyloidosis. While effective in prolonging survival, bortezomib has been increasingly associated with cardiovascular adverse events (CVAEs), including cardiac failure and arrhythmias, yet a comprehensive post-marketing cardiac safety profile remains incompletely defined. We analyzed cardiovascular adverse events reported between May 2003 and May 2025 using the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) via the OpenVigil 2.1 platform. Disproportionality analysis was performed using reporting odds ratios (RORs) with 95% confidence intervals (CIs). Among over 9 million drug-related adverse events in FAERS, 552 cardiac events were linked to bortezomib. Several cardiac outcomes, including atrial flutter, left ventricular dysfunction, cardiac failure, cardiomyopathy, atrial fibrillation, right ventricular failure, myocarditis, and supraventricular tachycardia, demonstrated elevated disproportionality signals. Separately, cardiac amyloidosis exhibited the highest disproportionality signal (ROR: 35.58; 95% CI: 28.16&amp;amp;ndash;44.95), a finding that reflects underlying disease severity rather than treatment-emergent cardiotoxicity. Cardiac failure accounted for the greatest number of hospitalizations (301) and deaths (208), followed by atrial fibrillation and cardiac amyloidosis. Older adults (&amp;amp;ge;65 years) and patients with amyloidosis or multiple myeloma were the most vulnerable populations. Overall, bortezomib was associated with serious cardiac adverse events, particularly cardiac failure and atrial arrhythmias, underscoring the need for routine cardiovascular risk assessment and proactive monitoring in high-risk patients.</description>
	<pubDate>2026-01-31</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 29, Pages 4: Pharmacovigilance-Based Safety Profile of Bortezomib: A Disproportionality Analysis Using FAERS Data</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/29/1/4">doi: 10.3390/cardiovascmed29010004</a></p>
	<p>Authors:
		Matthew Nho
		Ayushi Mittal
		Ahmed Abdel-Latif
		Anand Prakash Singh
		</p>
	<p>Bortezomib is a 26S proteasome inhibitor used to treat multiple myeloma and systemic amyloidosis. While effective in prolonging survival, bortezomib has been increasingly associated with cardiovascular adverse events (CVAEs), including cardiac failure and arrhythmias, yet a comprehensive post-marketing cardiac safety profile remains incompletely defined. We analyzed cardiovascular adverse events reported between May 2003 and May 2025 using the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) via the OpenVigil 2.1 platform. Disproportionality analysis was performed using reporting odds ratios (RORs) with 95% confidence intervals (CIs). Among over 9 million drug-related adverse events in FAERS, 552 cardiac events were linked to bortezomib. Several cardiac outcomes, including atrial flutter, left ventricular dysfunction, cardiac failure, cardiomyopathy, atrial fibrillation, right ventricular failure, myocarditis, and supraventricular tachycardia, demonstrated elevated disproportionality signals. Separately, cardiac amyloidosis exhibited the highest disproportionality signal (ROR: 35.58; 95% CI: 28.16&amp;amp;ndash;44.95), a finding that reflects underlying disease severity rather than treatment-emergent cardiotoxicity. Cardiac failure accounted for the greatest number of hospitalizations (301) and deaths (208), followed by atrial fibrillation and cardiac amyloidosis. Older adults (&amp;amp;ge;65 years) and patients with amyloidosis or multiple myeloma were the most vulnerable populations. Overall, bortezomib was associated with serious cardiac adverse events, particularly cardiac failure and atrial arrhythmias, underscoring the need for routine cardiovascular risk assessment and proactive monitoring in high-risk patients.</p>
	]]></content:encoded>

	<dc:title>Pharmacovigilance-Based Safety Profile of Bortezomib: A Disproportionality Analysis Using FAERS Data</dc:title>
			<dc:creator>Matthew Nho</dc:creator>
			<dc:creator>Ayushi Mittal</dc:creator>
			<dc:creator>Ahmed Abdel-Latif</dc:creator>
			<dc:creator>Anand Prakash Singh</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed29010004</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2026-01-31</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2026-01-31</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>4</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed29010004</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/29/1/4</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/29/1/3">

	<title>Cardiovascular Medicine, Vol. 29, Pages 3: The 2023 Senning Lecture—Developments in Heart Surgery and Shaping the Future of Younger Surgeons</title>
	<link>https://www.mdpi.com/1664-204X/29/1/3</link>
	<description>This is the summary of the 2023 SGHC Senning Lecture, in which surgical developments and the components of education and training in cardiovascular surgery are discussed. Special emphasis is placed on the problems, challenges, education models, and the dynamics of education and training for the benefit of the trainees and, ultimately, the patients.</description>
	<pubDate>2026-01-30</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 29, Pages 3: The 2023 Senning Lecture—Developments in Heart Surgery and Shaping the Future of Younger Surgeons</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/29/1/3">doi: 10.3390/cardiovascmed29010003</a></p>
	<p>Authors:
		Carlos Mestres
		</p>
	<p>This is the summary of the 2023 SGHC Senning Lecture, in which surgical developments and the components of education and training in cardiovascular surgery are discussed. Special emphasis is placed on the problems, challenges, education models, and the dynamics of education and training for the benefit of the trainees and, ultimately, the patients.</p>
	]]></content:encoded>

	<dc:title>The 2023 Senning Lecture—Developments in Heart Surgery and Shaping the Future of Younger Surgeons</dc:title>
			<dc:creator>Carlos Mestres</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed29010003</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2026-01-30</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2026-01-30</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Conference Report</prism:section>
	<prism:startingPage>3</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed29010003</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/29/1/3</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/29/1/2">

	<title>Cardiovascular Medicine, Vol. 29, Pages 2: A Promising New Beginning for Cardiovascular Medicine&amp;mdash;The Journal for the Interdisciplinary Heart Team</title>
	<link>https://www.mdpi.com/1664-204X/29/1/2</link>
	<description>What a remarkable first three months it has been for Cardiovascular Medicine! [...]</description>
	<pubDate>2026-01-16</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 29, Pages 2: A Promising New Beginning for Cardiovascular Medicine&amp;mdash;The Journal for the Interdisciplinary Heart Team</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/29/1/2">doi: 10.3390/cardiovascmed29010002</a></p>
	<p>Authors:
		Peter Matt
		</p>
	<p>What a remarkable first three months it has been for Cardiovascular Medicine! [...]</p>
	]]></content:encoded>

	<dc:title>A Promising New Beginning for Cardiovascular Medicine&amp;amp;mdash;The Journal for the Interdisciplinary Heart Team</dc:title>
			<dc:creator>Peter Matt</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed29010002</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2026-01-16</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2026-01-16</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>2</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed29010002</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/29/1/2</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/29/1/1">

	<title>Cardiovascular Medicine, Vol. 29, Pages 1: The Heart Under Pressure: Transient ST-Segment Elevation Due to Severe Intestinal Distension</title>
	<link>https://www.mdpi.com/1664-204X/29/1/1</link>
	<description>Acute extracardiac conditions can occasionally produce electrocardiographic abnormalities that closely mimic acute coronary occlusion, posing a diagnostic challenge and increasing the risk of unnecessary activation of invasive cardiac pathways. Severe gastrointestinal distension, although uncommon, is a recognized cause of transient ST-segment elevation due to mechanical displacement of the heart, autonomic imbalance, and abrupt changes in ventricular loading conditions. These alterations may be particularly misleading in patients with chronic regional wall motion abnormalities, in whom new ECG changes risk being misinterpreted as recurrent ischemia. We report the case of a 68-year-old man with a history of inferior myocardial infarction who presented with marked abdominal distension secondary to a closed-loop small bowel obstruction. Despite the absence of chest pain, his ECG showed significant anterolateral ST-segment elevation. High-sensitivity troponin I remained negative, and transthoracic echocardiography demonstrated preserved anterior and apical motion, chronic inferior akinesia, and unchanged global longitudinal strain. Following nasogastric decompression, the ST-segment normalized completely within fifteen minutes. Subsequent imaging confirmed a closed-loop volvulus requiring urgent surgical intervention, with full bowel viability preserved. This case underscores the importance of integrating clinical context, biomarkers, and rapid echocardiographic assessment when evaluating ST-segment elevation, helping avoid unnecessary coronary angiography in the presence of extracardiac causes.</description>
	<pubDate>2025-12-24</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 29, Pages 1: The Heart Under Pressure: Transient ST-Segment Elevation Due to Severe Intestinal Distension</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/29/1/1">doi: 10.3390/cardiovascmed29010001</a></p>
	<p>Authors:
		Fulvio Cacciapuoti
		Angela Iannuzzi
		Ferdinando Fusco
		Alessandro De Masi
		Flavia Casolaro
		Angelo Sasso
		</p>
	<p>Acute extracardiac conditions can occasionally produce electrocardiographic abnormalities that closely mimic acute coronary occlusion, posing a diagnostic challenge and increasing the risk of unnecessary activation of invasive cardiac pathways. Severe gastrointestinal distension, although uncommon, is a recognized cause of transient ST-segment elevation due to mechanical displacement of the heart, autonomic imbalance, and abrupt changes in ventricular loading conditions. These alterations may be particularly misleading in patients with chronic regional wall motion abnormalities, in whom new ECG changes risk being misinterpreted as recurrent ischemia. We report the case of a 68-year-old man with a history of inferior myocardial infarction who presented with marked abdominal distension secondary to a closed-loop small bowel obstruction. Despite the absence of chest pain, his ECG showed significant anterolateral ST-segment elevation. High-sensitivity troponin I remained negative, and transthoracic echocardiography demonstrated preserved anterior and apical motion, chronic inferior akinesia, and unchanged global longitudinal strain. Following nasogastric decompression, the ST-segment normalized completely within fifteen minutes. Subsequent imaging confirmed a closed-loop volvulus requiring urgent surgical intervention, with full bowel viability preserved. This case underscores the importance of integrating clinical context, biomarkers, and rapid echocardiographic assessment when evaluating ST-segment elevation, helping avoid unnecessary coronary angiography in the presence of extracardiac causes.</p>
	]]></content:encoded>

	<dc:title>The Heart Under Pressure: Transient ST-Segment Elevation Due to Severe Intestinal Distension</dc:title>
			<dc:creator>Fulvio Cacciapuoti</dc:creator>
			<dc:creator>Angela Iannuzzi</dc:creator>
			<dc:creator>Ferdinando Fusco</dc:creator>
			<dc:creator>Alessandro De Masi</dc:creator>
			<dc:creator>Flavia Casolaro</dc:creator>
			<dc:creator>Angelo Sasso</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed29010001</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2025-12-24</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2025-12-24</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>1</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed29010001</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/29/1/1</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/28/1/6">

	<title>Cardiovascular Medicine, Vol. 28, Pages 6: A Didactic Case of Long QT Associated with Pheochromocytoma</title>
	<link>https://www.mdpi.com/1664-204X/28/1/6</link>
	<description>Long QT associated with pheochromocytoma is rare but clinically significant. A 43-year-old woman presented with palpitations, chest pain, and recurrent syncope. ECG showed ST-segment elevation, while coronary angiography revealed normal arteries but Takotsubo-like left ventricular dysfunction. Hypertension and tachycardia raised suspicion for pheochromocytoma, later confirmed by imaging and biochemical tests. The patient exhibited QT prolongation (QTc 570 ms) in parallel with Takotsubo episodes. Following adrenalectomy, both QT duration and ventricular function normalized. The European Society of Cardiology now classifies pheochromocytoma-induced cardiomyopathy within the Takotsubo spectrum. Early recognition is crucial due to the risk of sudden cardiac death.</description>
	<pubDate>2025-12-11</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 28, Pages 6: A Didactic Case of Long QT Associated with Pheochromocytoma</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/28/1/6">doi: 10.3390/cardiovascmed28010006</a></p>
	<p>Authors:
		Selma T. Cook
		Malica Cook
		</p>
	<p>Long QT associated with pheochromocytoma is rare but clinically significant. A 43-year-old woman presented with palpitations, chest pain, and recurrent syncope. ECG showed ST-segment elevation, while coronary angiography revealed normal arteries but Takotsubo-like left ventricular dysfunction. Hypertension and tachycardia raised suspicion for pheochromocytoma, later confirmed by imaging and biochemical tests. The patient exhibited QT prolongation (QTc 570 ms) in parallel with Takotsubo episodes. Following adrenalectomy, both QT duration and ventricular function normalized. The European Society of Cardiology now classifies pheochromocytoma-induced cardiomyopathy within the Takotsubo spectrum. Early recognition is crucial due to the risk of sudden cardiac death.</p>
	]]></content:encoded>

	<dc:title>A Didactic Case of Long QT Associated with Pheochromocytoma</dc:title>
			<dc:creator>Selma T. Cook</dc:creator>
			<dc:creator>Malica Cook</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed28010006</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2025-12-11</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2025-12-11</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>6</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed28010006</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/28/1/6</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/28/1/5">

	<title>Cardiovascular Medicine, Vol. 28, Pages 5: Mechanisms Involved in the Adverse Cardiovascular Effects of Selective Cyclooxygenase-2 Inhibitors</title>
	<link>https://www.mdpi.com/1664-204X/28/1/5</link>
	<description>Nonsteroidal anti-inflammatory drugs (NSAIDs) are widely used for managing inflammation, but they are associated with gastrointestinal and renal toxicity upon long-term use. Selective cyclooxygenase-2 (COX-2) inhibitors, or coxibs, were developed to avoid these adverse effects while maintaining anti-inflammatory efficacy. However, accumulating evidence indicates that coxibs may increase the risk of cardiovascular complications. This review explores the pathophysiological mechanisms underlying adverse cardiovascular effects in patients treated with COX-2 inhibitors. These mechanisms include an imbalance between prothrombotic and antithrombotic factors, an altered endocannabinoid metabolism, and downregulation of PPAR&amp;amp;delta;, contributing to thrombosis. Additionally, COX-2 inhibition disrupts renal prostaglandin synthesis, particularly PGE2 and prostacyclins, reduces EP4 receptor expression in macrophages, promotes chemotaxis, and elevates arterial pressure via increased iNOS, ADMA, and L-NMMA activity. At the molecular level, genetic polymorphisms, matrix metalloproteinases, signaling cross-talk, and direct cardiomyocyte injury are implicated. Collectively, these alterations promote a prothrombotic state, fluid retention, enhanced vasoconstriction, impaired vasodilation, myocardial injury, cell death, and cardiac fibrosis. Despite these risks, coxibs are often prescribed without adequate cardiovascular assessment, particularly in patients with pre-existing cardiovascular risk factors. Greater awareness of these mechanisms is essential to optimize the benefit&amp;amp;ndash;risk ratio in clinical decision-making involving selective COX-2 inhibitors.</description>
	<pubDate>2025-11-28</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 28, Pages 5: Mechanisms Involved in the Adverse Cardiovascular Effects of Selective Cyclooxygenase-2 Inhibitors</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/28/1/5">doi: 10.3390/cardiovascmed28010005</a></p>
	<p>Authors:
		Oscar Jesus Leal-Ramos
		Luis Felipe Arias-Ruiz
		José Miguel Huerta-Velázquez
		José Pablo Lamoreaux-Aguayo
		Dalton Butcher
		Asela Berenice López-Cuellar
		Karina Iveth Orozco-Jiménez
		Olivia Torres-Bugarín
		</p>
	<p>Nonsteroidal anti-inflammatory drugs (NSAIDs) are widely used for managing inflammation, but they are associated with gastrointestinal and renal toxicity upon long-term use. Selective cyclooxygenase-2 (COX-2) inhibitors, or coxibs, were developed to avoid these adverse effects while maintaining anti-inflammatory efficacy. However, accumulating evidence indicates that coxibs may increase the risk of cardiovascular complications. This review explores the pathophysiological mechanisms underlying adverse cardiovascular effects in patients treated with COX-2 inhibitors. These mechanisms include an imbalance between prothrombotic and antithrombotic factors, an altered endocannabinoid metabolism, and downregulation of PPAR&amp;amp;delta;, contributing to thrombosis. Additionally, COX-2 inhibition disrupts renal prostaglandin synthesis, particularly PGE2 and prostacyclins, reduces EP4 receptor expression in macrophages, promotes chemotaxis, and elevates arterial pressure via increased iNOS, ADMA, and L-NMMA activity. At the molecular level, genetic polymorphisms, matrix metalloproteinases, signaling cross-talk, and direct cardiomyocyte injury are implicated. Collectively, these alterations promote a prothrombotic state, fluid retention, enhanced vasoconstriction, impaired vasodilation, myocardial injury, cell death, and cardiac fibrosis. Despite these risks, coxibs are often prescribed without adequate cardiovascular assessment, particularly in patients with pre-existing cardiovascular risk factors. Greater awareness of these mechanisms is essential to optimize the benefit&amp;amp;ndash;risk ratio in clinical decision-making involving selective COX-2 inhibitors.</p>
	]]></content:encoded>

	<dc:title>Mechanisms Involved in the Adverse Cardiovascular Effects of Selective Cyclooxygenase-2 Inhibitors</dc:title>
			<dc:creator>Oscar Jesus Leal-Ramos</dc:creator>
			<dc:creator>Luis Felipe Arias-Ruiz</dc:creator>
			<dc:creator>José Miguel Huerta-Velázquez</dc:creator>
			<dc:creator>José Pablo Lamoreaux-Aguayo</dc:creator>
			<dc:creator>Dalton Butcher</dc:creator>
			<dc:creator>Asela Berenice López-Cuellar</dc:creator>
			<dc:creator>Karina Iveth Orozco-Jiménez</dc:creator>
			<dc:creator>Olivia Torres-Bugarín</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed28010005</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2025-11-28</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2025-11-28</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>5</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed28010005</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/28/1/5</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/28/1/4">

	<title>Cardiovascular Medicine, Vol. 28, Pages 4: Double TAVI: What&amp;rsquo;s Next?</title>
	<link>https://www.mdpi.com/1664-204X/28/1/4</link>
	<description>Transcatheter aortic valve implantation is rapidly emerging as the leading treatment for severe aortic valve stenosis, especially in elderly and high-risk or inoperable patients. Prosthetic embolism is a rare but serious complication of transcatheter aortic valve replacement. Patients who develop prosthetic embolism are at increased risk of mortality and morbidity. These include stroke and aortic dissection associated with manipulation of the prosthesis in the ascending aorta. Treatment of valve embolisms into the aorta may differ depending on the type of valve; however, it traditionally relies on repositioning the valve to an appropriate position. To date, there are no established pharmaceutical guidelines for the management of patients with valve prosthesis embolization. We present a case report of the implantation of a second aortic valve prosthesis after periprocedural embolization of the first transcatheter valve, resulting in residual floating in the ascending aorta and following treatment with oral anticoagulation as well as single antiplatelet therapy due to the increased risk of thrombogenesis. This case report provides an example of the management of a transcatheter valve embolization with residual floating and highlights the need for further studies to address this issue.</description>
	<pubDate>2025-11-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 28, Pages 4: Double TAVI: What&amp;rsquo;s Next?</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/28/1/4">doi: 10.3390/cardiovascmed28010004</a></p>
	<p>Authors:
		Ruta Ratyte
		Mirjam Löffel
		Christoph Ado Kaiser
		</p>
	<p>Transcatheter aortic valve implantation is rapidly emerging as the leading treatment for severe aortic valve stenosis, especially in elderly and high-risk or inoperable patients. Prosthetic embolism is a rare but serious complication of transcatheter aortic valve replacement. Patients who develop prosthetic embolism are at increased risk of mortality and morbidity. These include stroke and aortic dissection associated with manipulation of the prosthesis in the ascending aorta. Treatment of valve embolisms into the aorta may differ depending on the type of valve; however, it traditionally relies on repositioning the valve to an appropriate position. To date, there are no established pharmaceutical guidelines for the management of patients with valve prosthesis embolization. We present a case report of the implantation of a second aortic valve prosthesis after periprocedural embolization of the first transcatheter valve, resulting in residual floating in the ascending aorta and following treatment with oral anticoagulation as well as single antiplatelet therapy due to the increased risk of thrombogenesis. This case report provides an example of the management of a transcatheter valve embolization with residual floating and highlights the need for further studies to address this issue.</p>
	]]></content:encoded>

	<dc:title>Double TAVI: What&amp;amp;rsquo;s Next?</dc:title>
			<dc:creator>Ruta Ratyte</dc:creator>
			<dc:creator>Mirjam Löffel</dc:creator>
			<dc:creator>Christoph Ado Kaiser</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed28010004</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2025-11-20</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2025-11-20</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>4</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed28010004</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/28/1/4</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/28/1/3">

	<title>Cardiovascular Medicine, Vol. 28, Pages 3: Global Prevalence of Isolated Systolic, Isolated Diastolic, and Systodiastolic Hypertension: A Systematic Review and Meta-Analysis</title>
	<link>https://www.mdpi.com/1664-204X/28/1/3</link>
	<description>Arterial hypertension (HTN) is a global public health problem with three distinct subtypes: isolated systolic hypertension (ISH), isolated diastolic hypertension (IDH), and systodiastolic hypertension (SDH), each with unique clinical implications. This systematic review and meta-analysis aimed to determine the global prevalence of ISH, IDH, and SDH and their variability. Following PRISMA guidelines, a search was conducted in SCOPUS, Web of Science, PubMed, and EMBASE. A random-effects model with the Freeman-Tukey transformation was used for the meta-analysis, and a meta-regression was performed to assess temporal trends. Twenty-seven studies from five continents were included, revealing pooled global prevalence rates of 10.72% for ISH, 5.07% for IDH, and 11.71% for SDH. Extreme heterogeneity was observed (I2 = 100%), reflecting substantial methodological diversity. The meta-regression suggested an increasing trend for ISH over time, while non-significant decreasing trends were observed for IDH and SDH. In conclusion, all three HTN subtypes show clinically relevant prevalences, with ISH and SDH being nearly twice as common as IDH. The high heterogeneity underscores the urgent need for research standardization, and these findings highlight the importance of differentiating subtypes for more effective population-level screening and public health planning.</description>
	<pubDate>2025-11-17</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 28, Pages 3: Global Prevalence of Isolated Systolic, Isolated Diastolic, and Systodiastolic Hypertension: A Systematic Review and Meta-Analysis</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/28/1/3">doi: 10.3390/cardiovascmed28010003</a></p>
	<p>Authors:
		Víctor Juan Vera-Ponce
		Lupita Ana Maria Valladolid-Sandoval
		Jhosmer Ballena-Caicedo
		Fiorella E. Zuzunaga-Montoya
		</p>
	<p>Arterial hypertension (HTN) is a global public health problem with three distinct subtypes: isolated systolic hypertension (ISH), isolated diastolic hypertension (IDH), and systodiastolic hypertension (SDH), each with unique clinical implications. This systematic review and meta-analysis aimed to determine the global prevalence of ISH, IDH, and SDH and their variability. Following PRISMA guidelines, a search was conducted in SCOPUS, Web of Science, PubMed, and EMBASE. A random-effects model with the Freeman-Tukey transformation was used for the meta-analysis, and a meta-regression was performed to assess temporal trends. Twenty-seven studies from five continents were included, revealing pooled global prevalence rates of 10.72% for ISH, 5.07% for IDH, and 11.71% for SDH. Extreme heterogeneity was observed (I2 = 100%), reflecting substantial methodological diversity. The meta-regression suggested an increasing trend for ISH over time, while non-significant decreasing trends were observed for IDH and SDH. In conclusion, all three HTN subtypes show clinically relevant prevalences, with ISH and SDH being nearly twice as common as IDH. The high heterogeneity underscores the urgent need for research standardization, and these findings highlight the importance of differentiating subtypes for more effective population-level screening and public health planning.</p>
	]]></content:encoded>

	<dc:title>Global Prevalence of Isolated Systolic, Isolated Diastolic, and Systodiastolic Hypertension: A Systematic Review and Meta-Analysis</dc:title>
			<dc:creator>Víctor Juan Vera-Ponce</dc:creator>
			<dc:creator>Lupita Ana Maria Valladolid-Sandoval</dc:creator>
			<dc:creator>Jhosmer Ballena-Caicedo</dc:creator>
			<dc:creator>Fiorella E. Zuzunaga-Montoya</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed28010003</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2025-11-17</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2025-11-17</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Systematic Review</prism:section>
	<prism:startingPage>3</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed28010003</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/28/1/3</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/28/1/2">

	<title>Cardiovascular Medicine, Vol. 28, Pages 2: Editor-in-Chief&amp;rsquo;s Editorial: A New Chapter for Cardiovascular Medicine</title>
	<link>https://www.mdpi.com/1664-204X/28/1/2</link>
	<description>It is with great pride and enthusiasm that we announce the relaunch of Cardiovascular Medicine, a journal with a longstanding tradition in the Swiss and international cardiology community [...]</description>
	<pubDate>2025-10-10</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 28, Pages 2: Editor-in-Chief&amp;rsquo;s Editorial: A New Chapter for Cardiovascular Medicine</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/28/1/2">doi: 10.3390/cardiovascmed28010002</a></p>
	<p>Authors:
		Peter Matt
		</p>
	<p>It is with great pride and enthusiasm that we announce the relaunch of Cardiovascular Medicine, a journal with a longstanding tradition in the Swiss and international cardiology community [...]</p>
	]]></content:encoded>

	<dc:title>Editor-in-Chief&amp;amp;rsquo;s Editorial: A New Chapter for Cardiovascular Medicine</dc:title>
			<dc:creator>Peter Matt</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed28010002</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2025-10-10</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2025-10-10</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>2</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed28010002</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/28/1/2</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/28/1/1">

	<title>Cardiovascular Medicine, Vol. 28, Pages 1: Publisher&amp;rsquo;s Note: Welcome to the New Home of Cardiovascular Medicine</title>
	<link>https://www.mdpi.com/1664-204X/28/1/1</link>
	<description>Cardiovascular Medicine was launched in 1998 under the title Kardiovaskul&amp;amp;auml;re Medizin, publishing articles in German, French, and English [...]</description>
	<pubDate>2025-09-17</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 28, Pages 1: Publisher&amp;rsquo;s Note: Welcome to the New Home of Cardiovascular Medicine</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/28/1/1">doi: 10.3390/cardiovascmed28010001</a></p>
	<p>Authors:
		Carla Aloè
		</p>
	<p>Cardiovascular Medicine was launched in 1998 under the title Kardiovaskul&amp;amp;auml;re Medizin, publishing articles in German, French, and English [...]</p>
	]]></content:encoded>

	<dc:title>Publisher&amp;amp;rsquo;s Note: Welcome to the New Home of Cardiovascular Medicine</dc:title>
			<dc:creator>Carla Aloè</dc:creator>
		<dc:identifier>doi: 10.3390/cardiovascmed28010001</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2025-09-17</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2025-09-17</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>1</prism:startingPage>
		<prism:doi>10.3390/cardiovascmed28010001</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/28/1/1</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/5/139">

	<title>Cardiovascular Medicine, Vol. 26, Pages 139: A Paradox or a Different Perspective?</title>
	<link>https://www.mdpi.com/1664-204X/26/5/139</link>
	<description>The latest issue of Cardiovascular Medicine deals with various topics on cardiovascular diseases, again with a focus on sex-specific subjects [...]</description>
	<pubDate>2024-08-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 139: A Paradox or a Different Perspective?</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/5/139">doi: 10.4414/cvm.2023.1239215883</a></p>
	<p>Authors:
		Peter Matt
		</p>
	<p>The latest issue of Cardiovascular Medicine deals with various topics on cardiovascular diseases, again with a focus on sex-specific subjects [...]</p>
	]]></content:encoded>

	<dc:title>A Paradox or a Different Perspective?</dc:title>
			<dc:creator>Peter Matt</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.1239215883</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-08-14</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-08-14</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>139</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.1239215883</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/5/139</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/4/99">

	<title>Cardiovascular Medicine, Vol. 27, Pages 99: Plaque Characterization Using Intracoronary Imaging: Effects of Lipid-Lowering Therapies</title>
	<link>https://www.mdpi.com/1664-204X/27/4/99</link>
	<description>Over the past few years, large observational trials have confirmed the consistent association between vulnerable plaques identified by intracoronary imaging and major cardiovascular events in patients with coronary artery disease. Lipid-lowering therapies have reduced the occurrence of cardiovascular events in these patients; however, the exact pathophysiological mechanisms behind their clinical benefits have remained underexplored. Intracoronary imaging modalities, including intravascular ultrasonography, near-infrared spectroscopy, and optical coherence tomography have provided fundamental insight into the biological plausibility of these clinical results. Imaging trials employing serial intravascular ultrasonography have suggested that lipid-lowering therapies can either slow disease progression or promote plaque regression, depending on the degree of lipid lowering achieved. More recently, new randomized trials have added significant insights on the additional beneficial effects of achieving very low low-density lipoprotein cholesterol levels on high-risk plaque features, including fibrous cap thickness, lipid accumulation, and inflammatory cell accumulations. This literature review aimed to summarize current evidence on the clinical usefulness of plaque characterization using contemporary intracoronary imaging and the effects of high-intensity lipid-lowering therapies on vulnerable plaque features.</description>
	<pubDate>2024-08-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 99: Plaque Characterization Using Intracoronary Imaging: Effects of Lipid-Lowering Therapies</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/4/99">doi: 10.4414/cvm.2024.1379478206</a></p>
	<p>Authors:
		Flavio Giuseppe Biccirè
		Lorenz Räber
		</p>
	<p>Over the past few years, large observational trials have confirmed the consistent association between vulnerable plaques identified by intracoronary imaging and major cardiovascular events in patients with coronary artery disease. Lipid-lowering therapies have reduced the occurrence of cardiovascular events in these patients; however, the exact pathophysiological mechanisms behind their clinical benefits have remained underexplored. Intracoronary imaging modalities, including intravascular ultrasonography, near-infrared spectroscopy, and optical coherence tomography have provided fundamental insight into the biological plausibility of these clinical results. Imaging trials employing serial intravascular ultrasonography have suggested that lipid-lowering therapies can either slow disease progression or promote plaque regression, depending on the degree of lipid lowering achieved. More recently, new randomized trials have added significant insights on the additional beneficial effects of achieving very low low-density lipoprotein cholesterol levels on high-risk plaque features, including fibrous cap thickness, lipid accumulation, and inflammatory cell accumulations. This literature review aimed to summarize current evidence on the clinical usefulness of plaque characterization using contemporary intracoronary imaging and the effects of high-intensity lipid-lowering therapies on vulnerable plaque features.</p>
	]]></content:encoded>

	<dc:title>Plaque Characterization Using Intracoronary Imaging: Effects of Lipid-Lowering Therapies</dc:title>
			<dc:creator>Flavio Giuseppe Biccirè</dc:creator>
			<dc:creator>Lorenz Räber</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1379478206</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-08-14</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-08-14</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>99</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1379478206</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/4/99</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/4/108">

	<title>Cardiovascular Medicine, Vol. 27, Pages 108: Contemporary Antithrombotic Drug Removal via Hemoadsorption in Cardiac Surgery</title>
	<link>https://www.mdpi.com/1664-204X/27/4/108</link>
	<description>The incidence of severe bleeding in patients treated with dual antiplatelet therapy, including the new P2Y12 inhibitors or new direct oral anticoagulants, who are undergoing urgent cardiac surgery is very high. Novel strategies, including the removal of antithrombotics via intraoperative hemoadsorption, have shown promising results, which are summarized in this holistic review. Overall, current evidence supports antithrombotic removal via hemoadsorption as a potential new therapy in the management of perioperative bleeding risk in patients on antithrombotic medications undergoing cardiopulmonary bypass-assisted cardiac surgery.</description>
	<pubDate>2024-08-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 108: Contemporary Antithrombotic Drug Removal via Hemoadsorption in Cardiac Surgery</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/4/108">doi: 10.4414/cvm.2024.1387770349</a></p>
	<p>Authors:
		Daniel Wendt
		Efthymios Deliargyris
		Stephan Geidel
		</p>
	<p>The incidence of severe bleeding in patients treated with dual antiplatelet therapy, including the new P2Y12 inhibitors or new direct oral anticoagulants, who are undergoing urgent cardiac surgery is very high. Novel strategies, including the removal of antithrombotics via intraoperative hemoadsorption, have shown promising results, which are summarized in this holistic review. Overall, current evidence supports antithrombotic removal via hemoadsorption as a potential new therapy in the management of perioperative bleeding risk in patients on antithrombotic medications undergoing cardiopulmonary bypass-assisted cardiac surgery.</p>
	]]></content:encoded>

	<dc:title>Contemporary Antithrombotic Drug Removal via Hemoadsorption in Cardiac Surgery</dc:title>
			<dc:creator>Daniel Wendt</dc:creator>
			<dc:creator>Efthymios Deliargyris</dc:creator>
			<dc:creator>Stephan Geidel</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1387770349</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-08-14</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-08-14</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>108</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1387770349</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/4/108</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/4/122">

	<title>Cardiovascular Medicine, Vol. 27, Pages 122: Atrial Tachycardia Coexisting with Atrioventricular Nodal Reentrant Tachycardia</title>
	<link>https://www.mdpi.com/1664-204X/27/4/122</link>
	<description>The interpretation of the surface electrocardiogram and intracardiac recordings is key for the appropriate diagnosis and interventional treatment of cardiac arrhythmias. This report describes a patient with both a focal atrial tachycardia (AT) and an atypical atrioventricular-nodal reentrant tachycardia that were repeatedly induced and terminated by atrial ectopic beats. Radiofrequency ablation of the slow pathway, as well as targeted ablation of the specific AT focus effectively eliminated both tachycardias.</description>
	<pubDate>2024-08-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 122: Atrial Tachycardia Coexisting with Atrioventricular Nodal Reentrant Tachycardia</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/4/122">doi: 10.4414/cvm.2024.1416403729</a></p>
	<p>Authors:
		Fu Guan
		Firat Duru
		Urs Eriksson
		</p>
	<p>The interpretation of the surface electrocardiogram and intracardiac recordings is key for the appropriate diagnosis and interventional treatment of cardiac arrhythmias. This report describes a patient with both a focal atrial tachycardia (AT) and an atypical atrioventricular-nodal reentrant tachycardia that were repeatedly induced and terminated by atrial ectopic beats. Radiofrequency ablation of the slow pathway, as well as targeted ablation of the specific AT focus effectively eliminated both tachycardias.</p>
	]]></content:encoded>

	<dc:title>Atrial Tachycardia Coexisting with Atrioventricular Nodal Reentrant Tachycardia</dc:title>
			<dc:creator>Fu Guan</dc:creator>
			<dc:creator>Firat Duru</dc:creator>
			<dc:creator>Urs Eriksson</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1416403729</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-08-14</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-08-14</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Introduction</prism:section>
	<prism:startingPage>122</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1416403729</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/4/122</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/4/127">

	<title>Cardiovascular Medicine, Vol. 27, Pages 127: Perspectives on the Longevity of Cardiac Rhythm Management Devices</title>
	<link>https://www.mdpi.com/1664-204X/27/4/127</link>
	<description>Cardiac arrhythmias are a major cause of morbidity and mortality. Cardiac rhythm management devices (CRMDs) are used to diagnose and treat heart rhythm abnormalities. Many prospective randomized trials over the past decade have established the efficacy of CRMD therapy in reducing all-cause mortality and improving the quality of life. The manufacturer of every device provides its longevity in its technical characteristics, which are, as studies show, shorter in practice. Patients are concerned about the replacement procedure due to the risk of the procedure and other socioeconomic reasons. The longer the longevity of the devices, the better for the patients, the payers, the doctors and the health care systems. Given the recently redefined term of health technology assessment on a European level, a new regulatory framework has been proposed. Its intention is that, across different healthcare systems, the upfront costs and the reimbursement costs of these devices should be proportional to their longevity.</description>
	<pubDate>2024-08-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 127: Perspectives on the Longevity of Cardiac Rhythm Management Devices</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/4/127">doi: 10.4414/cvm.2024.1443408577</a></p>
	<p>Authors:
		John Fanourgiakis
		</p>
	<p>Cardiac arrhythmias are a major cause of morbidity and mortality. Cardiac rhythm management devices (CRMDs) are used to diagnose and treat heart rhythm abnormalities. Many prospective randomized trials over the past decade have established the efficacy of CRMD therapy in reducing all-cause mortality and improving the quality of life. The manufacturer of every device provides its longevity in its technical characteristics, which are, as studies show, shorter in practice. Patients are concerned about the replacement procedure due to the risk of the procedure and other socioeconomic reasons. The longer the longevity of the devices, the better for the patients, the payers, the doctors and the health care systems. Given the recently redefined term of health technology assessment on a European level, a new regulatory framework has been proposed. Its intention is that, across different healthcare systems, the upfront costs and the reimbursement costs of these devices should be proportional to their longevity.</p>
	]]></content:encoded>

	<dc:title>Perspectives on the Longevity of Cardiac Rhythm Management Devices</dc:title>
			<dc:creator>John Fanourgiakis</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1443408577</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-08-14</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-08-14</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Commentary</prism:section>
	<prism:startingPage>127</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1443408577</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/4/127</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/4/125">

	<title>Cardiovascular Medicine, Vol. 27, Pages 125: A Patient with Chest Pain and Precordial ST-Segment Elevation</title>
	<link>https://www.mdpi.com/1664-204X/27/4/125</link>
	<description>We present a challenging case of a patient with an isolated right ventricular myocardial infarction (iRVMI) caused by the spontaneous occlusion of a right ventricular branch mimicking an anterior myocardial infarction on the electrocardiogram. A high index of suspicion is required to diagnose an iRVMI because the electrocardiogram may be misleading.</description>
	<pubDate>2024-08-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 125: A Patient with Chest Pain and Precordial ST-Segment Elevation</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/4/125">doi: 10.4414/cvm.2024.1486643913</a></p>
	<p>Authors:
		Andreas Y. Andreou
		Elena Leonidou
		Andreas Tryfonos
		</p>
	<p>We present a challenging case of a patient with an isolated right ventricular myocardial infarction (iRVMI) caused by the spontaneous occlusion of a right ventricular branch mimicking an anterior myocardial infarction on the electrocardiogram. A high index of suspicion is required to diagnose an iRVMI because the electrocardiogram may be misleading.</p>
	]]></content:encoded>

	<dc:title>A Patient with Chest Pain and Precordial ST-Segment Elevation</dc:title>
			<dc:creator>Andreas Y. Andreou</dc:creator>
			<dc:creator>Elena Leonidou</dc:creator>
			<dc:creator>Andreas Tryfonos</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1486643913</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-08-14</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-08-14</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Interesting Images</prism:section>
	<prism:startingPage>125</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1486643913</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/4/125</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/4/120">

	<title>Cardiovascular Medicine, Vol. 27, Pages 120: Recurrent Takotsubo Syndrome with Contemporary Brady- and Tachyarrhythmic Presentation</title>
	<link>https://www.mdpi.com/1664-204X/27/4/120</link>
	<description>We present a case of recurrent takotsubo syndrome with contemporary brady- and tachyarrhythmic presentation, a rare clinical pattern for which the correct treatment is still a matter of debate.</description>
	<pubDate>2024-08-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 120: Recurrent Takotsubo Syndrome with Contemporary Brady- and Tachyarrhythmic Presentation</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/4/120">doi: 10.4414/cvm.2024.1514199273</a></p>
	<p>Authors:
		Andrea Demarchi
		Lorenzo Greco
		Francois Regoli
		Marcello Di Valentino
		Marco Amoruso
		Alessandro Felice Chiesa
		Silvia Pirroni
		Mauro Foletti
		Angelo Di Simone
		Simone Sarzilla
		Andrea Menafoglio
		</p>
	<p>We present a case of recurrent takotsubo syndrome with contemporary brady- and tachyarrhythmic presentation, a rare clinical pattern for which the correct treatment is still a matter of debate.</p>
	]]></content:encoded>

	<dc:title>Recurrent Takotsubo Syndrome with Contemporary Brady- and Tachyarrhythmic Presentation</dc:title>
			<dc:creator>Andrea Demarchi</dc:creator>
			<dc:creator>Lorenzo Greco</dc:creator>
			<dc:creator>Francois Regoli</dc:creator>
			<dc:creator>Marcello Di Valentino</dc:creator>
			<dc:creator>Marco Amoruso</dc:creator>
			<dc:creator>Alessandro Felice Chiesa</dc:creator>
			<dc:creator>Silvia Pirroni</dc:creator>
			<dc:creator>Mauro Foletti</dc:creator>
			<dc:creator>Angelo Di Simone</dc:creator>
			<dc:creator>Simone Sarzilla</dc:creator>
			<dc:creator>Andrea Menafoglio</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1514199273</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-08-14</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-08-14</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>120</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1514199273</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/4/120</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/4/114">

	<title>Cardiovascular Medicine, Vol. 27, Pages 114: Delayed Intervention’s Impact on Transcatheter Mitral Valve Implantation Strategy</title>
	<link>https://www.mdpi.com/1664-204X/27/4/114</link>
	<description>Transcatheter mitral valve implantation (TMVI) is used for treating severe mitral valve regurgitation in patients deemed unsuitable for open-heart surgery. However, delays between preoperative workup and therapy can lead to changes in the clinical condition and structural valve findings, necessitating a meticulous reevaluation of diagnostic and therapeutic options. Case Presentation: A 77-year-old woman with severe mitral valve regurgitation and severe comorbidities was referred to our Heart Team and was deemed suitable for TMVI based on the initial evaluation. The echocardiographic finding showed a severe degenerative mitral valve regurgitation with prolapse of the A3 and P3 segments and an eccentric jet directed posteriorly to the atrial roof but without the complete picture of Barlow’s disease. Due to delayed approval by the patient, the therapeutic procedure was postponed. Subsequent echocardiographic reevaluation six months later revealed a hypermobile anterior mitral leaflet resulting from chordal elongation in conjunction with a septal bulge, raising the risk for postoperative left ventricular outflow tract (LVOT) obstruction. To mitigate this risk, TMVI combined with the Laceration of the Anterior Mitral Leaflet to Prevent Outflow Obstruction (LAMPOON) was performed. Post-implantation echocardiography revealed a well-functioning mitral valve prosthesis without para- and transvalvular leak, a mean gradient of 3 mm Hg, and no LVOT obstruction. Conclusions: The diagnostic and therapeutic evaluation of TMVI remains intricate and time-consuming, necessitating thorough planning. Prompt performance of the procedure is crucial to prevent unforeseen structural changes that could jeopardize the patient’s outcome. The combination of TMVI with the LAMPOON technique for preventing LVOT obstruction appears feasible and suitable for selected patients.</description>
	<pubDate>2024-08-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 114: Delayed Intervention’s Impact on Transcatheter Mitral Valve Implantation Strategy</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/4/114">doi: 10.4414/cvm.2024.1514206641</a></p>
	<p>Authors:
		Ion Vasiloi
		Thomas Nestelberger
		Beat A. Kaufmann
		Fabien Praz
		Oliver T. Reuthebuch
		</p>
	<p>Transcatheter mitral valve implantation (TMVI) is used for treating severe mitral valve regurgitation in patients deemed unsuitable for open-heart surgery. However, delays between preoperative workup and therapy can lead to changes in the clinical condition and structural valve findings, necessitating a meticulous reevaluation of diagnostic and therapeutic options. Case Presentation: A 77-year-old woman with severe mitral valve regurgitation and severe comorbidities was referred to our Heart Team and was deemed suitable for TMVI based on the initial evaluation. The echocardiographic finding showed a severe degenerative mitral valve regurgitation with prolapse of the A3 and P3 segments and an eccentric jet directed posteriorly to the atrial roof but without the complete picture of Barlow’s disease. Due to delayed approval by the patient, the therapeutic procedure was postponed. Subsequent echocardiographic reevaluation six months later revealed a hypermobile anterior mitral leaflet resulting from chordal elongation in conjunction with a septal bulge, raising the risk for postoperative left ventricular outflow tract (LVOT) obstruction. To mitigate this risk, TMVI combined with the Laceration of the Anterior Mitral Leaflet to Prevent Outflow Obstruction (LAMPOON) was performed. Post-implantation echocardiography revealed a well-functioning mitral valve prosthesis without para- and transvalvular leak, a mean gradient of 3 mm Hg, and no LVOT obstruction. Conclusions: The diagnostic and therapeutic evaluation of TMVI remains intricate and time-consuming, necessitating thorough planning. Prompt performance of the procedure is crucial to prevent unforeseen structural changes that could jeopardize the patient’s outcome. The combination of TMVI with the LAMPOON technique for preventing LVOT obstruction appears feasible and suitable for selected patients.</p>
	]]></content:encoded>

	<dc:title>Delayed Intervention’s Impact on Transcatheter Mitral Valve Implantation Strategy</dc:title>
			<dc:creator>Ion Vasiloi</dc:creator>
			<dc:creator>Thomas Nestelberger</dc:creator>
			<dc:creator>Beat A. Kaufmann</dc:creator>
			<dc:creator>Fabien Praz</dc:creator>
			<dc:creator>Oliver T. Reuthebuch</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1514206641</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-08-14</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-08-14</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>114</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1514206641</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/4/114</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/4/117">

	<title>Cardiovascular Medicine, Vol. 27, Pages 117: Early Onset Filamin C Cardiomyopathy</title>
	<link>https://www.mdpi.com/1664-204X/27/4/117</link>
	<description>We present the case of a 27-year-old man who was admitted with new-onset acute heart failure. The echocardiogram revealed biventricular dilatation with a severely reduced systolic function. A genetic study identified a truncated variant of the filamin-C (FLNC) gene. Since the systolic function did not improve under heart failure guideline-directed medical therapy, an implantable cardioverter-defibrillator was placed. After two years, the patient is currently being considered for epicardial ventricular tachycardia (VT) ablation due to the failure of appropriate therapies for monomorphic VT despite recovery of the left ventricular (LV) systolic function. Filamin C truncating variants have been recognized as one cause of an overlapping phenotype in dilated and arrhythmogenic cardiomyopathies. These patients typically present with a mildly reduced LV ejection fraction (LVEF), with or without dilatation, and extensive myocardial fibrosis, which heightens the risk of complex ventricular arrhythmias (VAs). Our patient presented a combined phenotype with biventricular dilated cardiomyopathy with a severely reduced LVEF at an unusual young age, as well as an increased incidence of VAs. With this clinical case, we aim to highlight the importance of genetic evaluation in dilated cardiomyopathy, as it can be decisive in its orientation and, consequently, in its prognosis.</description>
	<pubDate>2024-08-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 117: Early Onset Filamin C Cardiomyopathy</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/4/117">doi: 10.4414/cvm.2024.1514905178</a></p>
	<p>Authors:
		Catarina Ribeiro Carvalho
		Marta Catarina Bernardo
		Ana Baptista
		Ilídio Moreira
		</p>
	<p>We present the case of a 27-year-old man who was admitted with new-onset acute heart failure. The echocardiogram revealed biventricular dilatation with a severely reduced systolic function. A genetic study identified a truncated variant of the filamin-C (FLNC) gene. Since the systolic function did not improve under heart failure guideline-directed medical therapy, an implantable cardioverter-defibrillator was placed. After two years, the patient is currently being considered for epicardial ventricular tachycardia (VT) ablation due to the failure of appropriate therapies for monomorphic VT despite recovery of the left ventricular (LV) systolic function. Filamin C truncating variants have been recognized as one cause of an overlapping phenotype in dilated and arrhythmogenic cardiomyopathies. These patients typically present with a mildly reduced LV ejection fraction (LVEF), with or without dilatation, and extensive myocardial fibrosis, which heightens the risk of complex ventricular arrhythmias (VAs). Our patient presented a combined phenotype with biventricular dilated cardiomyopathy with a severely reduced LVEF at an unusual young age, as well as an increased incidence of VAs. With this clinical case, we aim to highlight the importance of genetic evaluation in dilated cardiomyopathy, as it can be decisive in its orientation and, consequently, in its prognosis.</p>
	]]></content:encoded>

	<dc:title>Early Onset Filamin C Cardiomyopathy</dc:title>
			<dc:creator>Catarina Ribeiro Carvalho</dc:creator>
			<dc:creator>Marta Catarina Bernardo</dc:creator>
			<dc:creator>Ana Baptista</dc:creator>
			<dc:creator>Ilídio Moreira</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1514905178</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-08-14</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-08-14</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>117</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1514905178</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/4/117</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/4/129">

	<title>Cardiovascular Medicine, Vol. 27, Pages 129: Strike Early and Strike Strong After MI: Lowering LDL-C to Target and Below</title>
	<link>https://www.mdpi.com/1664-204X/27/4/129</link>
	<description>Based on the growing clinical evidence on the benefit of very low LDL-C levels in combination with the availability of highly effective lipid-lowering therapy (LLT) options [...]</description>
	<pubDate>2024-08-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 129: Strike Early and Strike Strong After MI: Lowering LDL-C to Target and Below</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/4/129">doi: 10.4414/cvm.2024.1547920225</a></p>
	<p>Authors:
		Baris Gencer
		</p>
	<p>Based on the growing clinical evidence on the benefit of very low LDL-C levels in combination with the availability of highly effective lipid-lowering therapy (LLT) options [...]</p>
	]]></content:encoded>

	<dc:title>Strike Early and Strike Strong After MI: Lowering LDL-C to Target and Below</dc:title>
			<dc:creator>Baris Gencer</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1547920225</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-08-14</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-08-14</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>129</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1547920225</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/4/129</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/4/97">

	<title>Cardiovascular Medicine, Vol. 27, Pages 97: Evolving Concepts in Plaque Characterization</title>
	<link>https://www.mdpi.com/1664-204X/27/4/97</link>
	<description>Dear Readers, Once again, a new issue of the journal has been printed. Every time I read the articles in the CVM journal, I am proud of how diverse, contemporary, and fascinating the field of cardiovascular medicine is [...]</description>
	<pubDate>2024-08-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 97: Evolving Concepts in Plaque Characterization</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/4/97">doi: 10.4414/cvm.2024.1566105391</a></p>
	<p>Authors:
		Andreas Flammer
		</p>
	<p>Dear Readers, Once again, a new issue of the journal has been printed. Every time I read the articles in the CVM journal, I am proud of how diverse, contemporary, and fascinating the field of cardiovascular medicine is [...]</p>
	]]></content:encoded>

	<dc:title>Evolving Concepts in Plaque Characterization</dc:title>
			<dc:creator>Andreas Flammer</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1566105391</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-08-14</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-08-14</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>97</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1566105391</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/4/97</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/3/71">

	<title>Cardiovascular Medicine, Vol. 27, Pages 71: Challenges in the Lifetime Management of Patients with Aortic Stenosis</title>
	<link>https://www.mdpi.com/1664-204X/27/3/71</link>
	<description>Despite an extensive body of literature, there are still many gaps in the evidence surrounding the lifetime management of aortic stenosis (AS) and upstream interventions to prevent or slow down the progression of the disease are yet to be developed. The contemporary shift from simple grading to a more outcome-related staging of AS has ren dered the traditional belief that aortic valve intervention is only indicated in severe symptomatic AS obsolete and opened the debate on the optimal timing for intervention. Transcatheter aortic valve implantation (TAVI) has stood the test of time as a convenient, safe and effective treatment of AS across all risk categories. However, with the expansion of TAVI to younger patients with a longer life expectancy, there has been a gradual shift in focus from periprocedural outcomes to lifetime management, especially in patients who are likely to outlive their first valve prosthesis. In a standard scenario, when choosing the first valve, many actors come to the stage, including out comes and challenges of repeated valve implantations.</description>
	<pubDate>2024-05-29</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 71: Challenges in the Lifetime Management of Patients with Aortic Stenosis</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/3/71">doi: 10.4414/cvm.2024.1317114789</a></p>
	<p>Authors:
		Bashir Alaour
		Thomas Pilgrim
		</p>
	<p>Despite an extensive body of literature, there are still many gaps in the evidence surrounding the lifetime management of aortic stenosis (AS) and upstream interventions to prevent or slow down the progression of the disease are yet to be developed. The contemporary shift from simple grading to a more outcome-related staging of AS has ren dered the traditional belief that aortic valve intervention is only indicated in severe symptomatic AS obsolete and opened the debate on the optimal timing for intervention. Transcatheter aortic valve implantation (TAVI) has stood the test of time as a convenient, safe and effective treatment of AS across all risk categories. However, with the expansion of TAVI to younger patients with a longer life expectancy, there has been a gradual shift in focus from periprocedural outcomes to lifetime management, especially in patients who are likely to outlive their first valve prosthesis. In a standard scenario, when choosing the first valve, many actors come to the stage, including out comes and challenges of repeated valve implantations.</p>
	]]></content:encoded>

	<dc:title>Challenges in the Lifetime Management of Patients with Aortic Stenosis</dc:title>
			<dc:creator>Bashir Alaour</dc:creator>
			<dc:creator>Thomas Pilgrim</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1317114789</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-05-29</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-05-29</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>71</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1317114789</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/3/71</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/3/65">

	<title>Cardiovascular Medicine, Vol. 27, Pages 65: New Responsibilities for the HEART-Team</title>
	<link>https://www.mdpi.com/1664-204X/27/3/65</link>
	<description>Dear Readers, In this issue of Cardiovascular Medicine, Bashir Alaour and Thomas Pilgrim take on the demanding task of summarizing the challenges involved in the management of patients with [...]</description>
	<pubDate>2024-05-29</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 65: New Responsibilities for the HEART-Team</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/3/65">doi: 10.4414/cvm.2024.1324051349</a></p>
	<p>Authors:
		Luca Koechlin
		</p>
	<p>Dear Readers, In this issue of Cardiovascular Medicine, Bashir Alaour and Thomas Pilgrim take on the demanding task of summarizing the challenges involved in the management of patients with [...]</p>
	]]></content:encoded>

	<dc:title>New Responsibilities for the HEART-Team</dc:title>
			<dc:creator>Luca Koechlin</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1324051349</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-05-29</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-05-29</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>65</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1324051349</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/3/65</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/3/80">

	<title>Cardiovascular Medicine, Vol. 27, Pages 80: Bempedoic Acid: Results of the CLEAR Program</title>
	<link>https://www.mdpi.com/1664-204X/27/3/80</link>
	<description>Bempedoic acid is a fairly small molecule acting as a prodrug which is converted into the active compound bempedoyl-CoA in the liver. This active metabolite of bempedoic acid inhibits the enzyme ATP citrate lyase leading to low-density lipoprotein (LDL) reduction. The CLEAR (Cholesterol Lowering via Bempedoic Acid, an ACL-Inhibiting Regimen) Harmony trial showed that bempedoic acid reduced LDL cholesterol (LDL-C) by 12.6–16.5% and the CLEAR Tranquility and Serenity showed a reduction of LDL-C in statin-intolerant patients by a mean of 21% in monotherapy and 38% in combination with ezetimibe. Similar to statins but in contrast to ezetimibe or PCSK9 inhibitors, there was a consistent reduction of high-sensitive C-reactive protein in patients treated with bempedoic acid throughout all those studies. The CLEAR Outcomes trial included patients with established atherosclerotic cardiovascular disease (ASCVD) or a high risk of developing it, a documented intolerance to statin and a LDL ≥2.6 mmol/l despite maximal tolerated lipid-lowering therapy. The study showed that bempedoic acid lowered LDL by 21% and reduced the risk of cardiovascular death, nonfatal myocardial infarction, nonfatal stroke or coronary revascularization (primary composite endpoint) over a median of 3.4 years in statin-intolerant patients. The safety profile showed a slight increase in uric acid, gout and cholelithiasis. Bempedoic acid, used alone or with ezetimibe, is an effective LDL-lowering therapy for patients who do not attain adequate LDL-C control with maximal tolerated statin therapy and in statin-intolerant patients at risk for ASCVD.</description>
	<pubDate>2024-05-29</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 80: Bempedoic Acid: Results of the CLEAR Program</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/3/80">doi: 10.4414/cvm.2024.1379434015</a></p>
	<p>Authors:
		Isabella Sudano
		</p>
	<p>Bempedoic acid is a fairly small molecule acting as a prodrug which is converted into the active compound bempedoyl-CoA in the liver. This active metabolite of bempedoic acid inhibits the enzyme ATP citrate lyase leading to low-density lipoprotein (LDL) reduction. The CLEAR (Cholesterol Lowering via Bempedoic Acid, an ACL-Inhibiting Regimen) Harmony trial showed that bempedoic acid reduced LDL cholesterol (LDL-C) by 12.6–16.5% and the CLEAR Tranquility and Serenity showed a reduction of LDL-C in statin-intolerant patients by a mean of 21% in monotherapy and 38% in combination with ezetimibe. Similar to statins but in contrast to ezetimibe or PCSK9 inhibitors, there was a consistent reduction of high-sensitive C-reactive protein in patients treated with bempedoic acid throughout all those studies. The CLEAR Outcomes trial included patients with established atherosclerotic cardiovascular disease (ASCVD) or a high risk of developing it, a documented intolerance to statin and a LDL ≥2.6 mmol/l despite maximal tolerated lipid-lowering therapy. The study showed that bempedoic acid lowered LDL by 21% and reduced the risk of cardiovascular death, nonfatal myocardial infarction, nonfatal stroke or coronary revascularization (primary composite endpoint) over a median of 3.4 years in statin-intolerant patients. The safety profile showed a slight increase in uric acid, gout and cholelithiasis. Bempedoic acid, used alone or with ezetimibe, is an effective LDL-lowering therapy for patients who do not attain adequate LDL-C control with maximal tolerated statin therapy and in statin-intolerant patients at risk for ASCVD.</p>
	]]></content:encoded>

	<dc:title>Bempedoic Acid: Results of the CLEAR Program</dc:title>
			<dc:creator>Isabella Sudano</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1379434015</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-05-29</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-05-29</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>80</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1379434015</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/3/80</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/3/85">

	<title>Cardiovascular Medicine, Vol. 27, Pages 85: Should We Pace the His Bundle or the Left Bundle Branch Area?</title>
	<link>https://www.mdpi.com/1664-204X/27/3/85</link>
	<description>His bundle pacing is the most physiological form of pacing as it replicates the patient’s natural ventricular activation. Its adoption has significantly grown over the last years. However, the technique has several limitations, including suboptimal thresholds. Left bundle branch area pacing has been introduced more recently and has gained much interest as it also delivers physiological pacing but with more favorable electrical parameters. However, there are also several unresolved issues with this technique. This article compares these strategies and highlights their advantages and disadvantages to provide guidance on which technique to select for a specific patient.</description>
	<pubDate>2024-05-29</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 85: Should We Pace the His Bundle or the Left Bundle Branch Area?</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/3/85">doi: 10.4414/cvm.2024.1379472814</a></p>
	<p>Authors:
		Myriam Kaddour
		Haran Burri
		</p>
	<p>His bundle pacing is the most physiological form of pacing as it replicates the patient’s natural ventricular activation. Its adoption has significantly grown over the last years. However, the technique has several limitations, including suboptimal thresholds. Left bundle branch area pacing has been introduced more recently and has gained much interest as it also delivers physiological pacing but with more favorable electrical parameters. However, there are also several unresolved issues with this technique. This article compares these strategies and highlights their advantages and disadvantages to provide guidance on which technique to select for a specific patient.</p>
	]]></content:encoded>

	<dc:title>Should We Pace the His Bundle or the Left Bundle Branch Area?</dc:title>
			<dc:creator>Myriam Kaddour</dc:creator>
			<dc:creator>Haran Burri</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1379472814</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-05-29</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-05-29</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>85</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1379472814</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/3/85</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/3/68">

	<title>Cardiovascular Medicine, Vol. 27, Pages 68: «Sie müssen das System entfetten!»</title>
	<link>https://www.mdpi.com/1664-204X/27/3/68</link>
	<description>Vor einigen Jahren wurde meine damalige Klinik am Inselspital von einer deutschen Beratungs Unternehmung durchleuchtet [...]</description>
	<pubDate>2024-05-29</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 68: «Sie müssen das System entfetten!»</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/3/68">doi: 10.4414/cvm.2024.1379572570</a></p>
	<p>Authors:
		Thierry Carrel
		</p>
	<p>Vor einigen Jahren wurde meine damalige Klinik am Inselspital von einer deutschen Beratungs Unternehmung durchleuchtet [...]</p>
	]]></content:encoded>

	<dc:title>«Sie müssen das System entfetten!»</dc:title>
			<dc:creator>Thierry Carrel</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1379572570</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-05-29</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-05-29</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Commentary</prism:section>
	<prism:startingPage>68</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1379572570</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/3/68</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/3/94">

	<title>Cardiovascular Medicine, Vol. 27, Pages 94: A Wide Complex Tachycardia in a 31-Year-Old Male</title>
	<link>https://www.mdpi.com/1664-204X/27/3/94</link>
	<description>We present the case of a young male presenting with a wide complex tachycardia. The diagnostic approach based on the electrocardiogram findings is discussed. The final diagnosis could be made following an adenosine challenge at baseline, underlying the use of this drug for diagnostic purposes even in the absence of ongoing tachycardia.</description>
	<pubDate>2024-05-29</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 94: A Wide Complex Tachycardia in a 31-Year-Old Male</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/3/94">doi: 10.4414/cvm.2024.1412183678</a></p>
	<p>Authors:
		Hari Vivekanantham
		Guy Amit
		</p>
	<p>We present the case of a young male presenting with a wide complex tachycardia. The diagnostic approach based on the electrocardiogram findings is discussed. The final diagnosis could be made following an adenosine challenge at baseline, underlying the use of this drug for diagnostic purposes even in the absence of ongoing tachycardia.</p>
	]]></content:encoded>

	<dc:title>A Wide Complex Tachycardia in a 31-Year-Old Male</dc:title>
			<dc:creator>Hari Vivekanantham</dc:creator>
			<dc:creator>Guy Amit</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1412183678</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-05-29</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-05-29</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Interesting Images</prism:section>
	<prism:startingPage>94</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1412183678</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/3/94</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/3/90">

	<title>Cardiovascular Medicine, Vol. 27, Pages 90: Post-Operative Takotsubo Cardiomyopathy in Elective Mitral Valve Replacement</title>
	<link>https://www.mdpi.com/1664-204X/27/3/90</link>
	<description>Takotsubo cardiomyopathy is a type of stress cardiomyopathy that is usually seen in postmenopausal patients and can be triggered by emotional stress, hypoglycemia, hypothyroidism, and surgery. A patient post cardiac surgery can present with multiple complications causing hemodynamic compromise. Hence, takotsubo cardiomyopathy remains a diagnostic dilemma. Here, we present an interesting electrocardiogram (ECG) of the same condition in a patient after mitral valve replacement with normal patent coronaries but presenting with anterolateral massive infarction with shark fin pattern in the ECG.</description>
	<pubDate>2024-05-29</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 90: Post-Operative Takotsubo Cardiomyopathy in Elective Mitral Valve Replacement</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/3/90">doi: 10.4414/cvm.2024.1412187259</a></p>
	<p>Authors:
		Abhishek Potnis
		Sushrut Potwar
		Uday Jadhav
		</p>
	<p>Takotsubo cardiomyopathy is a type of stress cardiomyopathy that is usually seen in postmenopausal patients and can be triggered by emotional stress, hypoglycemia, hypothyroidism, and surgery. A patient post cardiac surgery can present with multiple complications causing hemodynamic compromise. Hence, takotsubo cardiomyopathy remains a diagnostic dilemma. Here, we present an interesting electrocardiogram (ECG) of the same condition in a patient after mitral valve replacement with normal patent coronaries but presenting with anterolateral massive infarction with shark fin pattern in the ECG.</p>
	]]></content:encoded>

	<dc:title>Post-Operative Takotsubo Cardiomyopathy in Elective Mitral Valve Replacement</dc:title>
			<dc:creator>Abhishek Potnis</dc:creator>
			<dc:creator>Sushrut Potwar</dc:creator>
			<dc:creator>Uday Jadhav</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1412187259</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-05-29</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-05-29</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Interesting Images</prism:section>
	<prism:startingPage>90</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1412187259</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/3/90</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/3/77">

	<title>Cardiovascular Medicine, Vol. 27, Pages 77: 70-jähriger Mann mit Polyneuropathie und kardialer Transthyretin-Amyloidose (ATTR-CM)</title>
	<link>https://www.mdpi.com/1664-204X/27/3/77</link>
	<description>Fall Der 70-jährige Patient stellte sich 2020 bei uns infolge Pensionierung des behandelnden Kar diologen vor. Er klagte über eine kardiale Leistungseinbusse und ausserdem über Prob- leme mit dem Bewegungsapparat [...]</description>
	<pubDate>2024-05-29</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 77: 70-jähriger Mann mit Polyneuropathie und kardialer Transthyretin-Amyloidose (ATTR-CM)</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/3/77">doi: 10.4414/cvm.2024.1455989891</a></p>
	<p>Authors:
		Otmar Pfister
		</p>
	<p>Fall Der 70-jährige Patient stellte sich 2020 bei uns infolge Pensionierung des behandelnden Kar diologen vor. Er klagte über eine kardiale Leistungseinbusse und ausserdem über Prob- leme mit dem Bewegungsapparat [...]</p>
	]]></content:encoded>

	<dc:title>70-jähriger Mann mit Polyneuropathie und kardialer Transthyretin-Amyloidose (ATTR-CM)</dc:title>
			<dc:creator>Otmar Pfister</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1455989891</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-05-29</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-05-29</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>77</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1455989891</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/3/77</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/2/41">

	<title>Cardiovascular Medicine, Vol. 27, Pages 41: Pulsed Field Ablation for the Treatment of Atrial Fibrillation</title>
	<link>https://www.mdpi.com/1664-204X/27/2/41</link>
	<description>Atrial fibrillation (AF) has become the most common arrhythmia worldwide and its incidence is increasing. Treatment strategies for symptomatic patients include stroke prevention, management of cardiovascular comorbidities, and direct treatment of AF itself. With regard to interventional AF treatment, a novel technique called pulsed field ablation has emerged. Large registry data in more than 15,000 patients have demonstrated a high efficacy in reducing the burden of AF with a very high safety. This review provides an overview of the technical aspects of pulsed field ablation and the published clinical data.</description>
	<pubDate>2024-03-27</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 41: Pulsed Field Ablation for the Treatment of Atrial Fibrillation</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/2/41">doi: 10.4414/cvm.2024.1297020794</a></p>
	<p>Authors:
		Alexander Breitenstein
		Laurent Roten
		Tobias Reichlin
		</p>
	<p>Atrial fibrillation (AF) has become the most common arrhythmia worldwide and its incidence is increasing. Treatment strategies for symptomatic patients include stroke prevention, management of cardiovascular comorbidities, and direct treatment of AF itself. With regard to interventional AF treatment, a novel technique called pulsed field ablation has emerged. Large registry data in more than 15,000 patients have demonstrated a high efficacy in reducing the burden of AF with a very high safety. This review provides an overview of the technical aspects of pulsed field ablation and the published clinical data.</p>
	]]></content:encoded>

	<dc:title>Pulsed Field Ablation for the Treatment of Atrial Fibrillation</dc:title>
			<dc:creator>Alexander Breitenstein</dc:creator>
			<dc:creator>Laurent Roten</dc:creator>
			<dc:creator>Tobias Reichlin</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1297020794</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-03-27</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-03-27</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>41</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1297020794</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/2/41</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/2/58">

	<title>Cardiovascular Medicine, Vol. 27, Pages 58: Palpitations in the Young during Stress Episodes</title>
	<link>https://www.mdpi.com/1664-204X/27/2/58</link>
	<description>Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a fatal rare inherited cardiac channelopathy. Affected patients are susceptible to develop deadly ventricular arrythmias after physical or emotional stress. The typical arrhythmia presents as bidirectional and/or polymorphic ventricular tachycardias. To illustrate the clinical challenges in properly diagnosing this disease, we report two cases of CPVT together with a brief literature review.</description>
	<pubDate>2024-03-27</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 58: Palpitations in the Young during Stress Episodes</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/2/58">doi: 10.4414/cvm.2024.1297024900</a></p>
	<p>Authors:
		Linn Ryberg
		Norma Balderrábano-Saucedo
		Argelia Medeiros-Domingo
		</p>
	<p>Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a fatal rare inherited cardiac channelopathy. Affected patients are susceptible to develop deadly ventricular arrythmias after physical or emotional stress. The typical arrhythmia presents as bidirectional and/or polymorphic ventricular tachycardias. To illustrate the clinical challenges in properly diagnosing this disease, we report two cases of CPVT together with a brief literature review.</p>
	]]></content:encoded>

	<dc:title>Palpitations in the Young during Stress Episodes</dc:title>
			<dc:creator>Linn Ryberg</dc:creator>
			<dc:creator>Norma Balderrábano-Saucedo</dc:creator>
			<dc:creator>Argelia Medeiros-Domingo</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1297024900</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-03-27</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-03-27</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>58</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1297024900</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/2/58</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/2/33">

	<title>Cardiovascular Medicine, Vol. 27, Pages 33: A New Surgical Section and More</title>
	<link>https://www.mdpi.com/1664-204X/27/2/33</link>
	<description>Are you interested in a new section in Cardio vascular Medicine focusing on cardiac surgery [...]</description>
	<pubDate>2024-03-27</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 33: A New Surgical Section and More</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/2/33">doi: 10.4414/cvm.2024.1324052009</a></p>
	<p>Authors:
		Peter Matt
		</p>
	<p>Are you interested in a new section in Cardio vascular Medicine focusing on cardiac surgery [...]</p>
	]]></content:encoded>

	<dc:title>A New Surgical Section and More</dc:title>
			<dc:creator>Peter Matt</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1324052009</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-03-27</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-03-27</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>33</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1324052009</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/2/33</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/2/52">

	<title>Cardiovascular Medicine, Vol. 27, Pages 52: Not All Statins Are Equal–Environmental and Genetic Myotoxicity Risk Factors</title>
	<link>https://www.mdpi.com/1664-204X/27/2/52</link>
	<description>Dose-dependent statin-related myotoxicity (SRM) is a rare adverse effect of statin treatment. Differences in the pharmacokinetics and interactions with environmental and genetic factors constitute important risk factors for the development of SRM. We present the case of an 82-year-old female patient with severe simvastatin-related myotoxicity and several risk factors of SRM, namely a pharmacokinetic interaction with verapamil, a pharmacogenetic interaction with a SLCO1B1*1/*5 variant, high age, female gender and impaired renal function. A comprehensive evaluation of distinct pharmacokinetic and pharmacogenetic properties of different statins and a pharmacogenetic panel test guided the diagnosis and options for further clinical management. Inspired by this and other similar cases, we developed a pocket card as practical companion for statin prescribing in clinical practice and provide it as an addition to this report.</description>
	<pubDate>2024-03-27</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 52: Not All Statins Are Equal–Environmental and Genetic Myotoxicity Risk Factors</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/2/52">doi: 10.4414/cvm.2024.1327305240</a></p>
	<p>Authors:
		Anna Katharina Schmid
		Victor Voicu
		Sarah Parejo
		Franziska M. Jakobs
		David F. Niedrig
		Sandro Baumgartner
		Markus Béchir
		Stefan Russmann
		</p>
	<p>Dose-dependent statin-related myotoxicity (SRM) is a rare adverse effect of statin treatment. Differences in the pharmacokinetics and interactions with environmental and genetic factors constitute important risk factors for the development of SRM. We present the case of an 82-year-old female patient with severe simvastatin-related myotoxicity and several risk factors of SRM, namely a pharmacokinetic interaction with verapamil, a pharmacogenetic interaction with a SLCO1B1*1/*5 variant, high age, female gender and impaired renal function. A comprehensive evaluation of distinct pharmacokinetic and pharmacogenetic properties of different statins and a pharmacogenetic panel test guided the diagnosis and options for further clinical management. Inspired by this and other similar cases, we developed a pocket card as practical companion for statin prescribing in clinical practice and provide it as an addition to this report.</p>
	]]></content:encoded>

	<dc:title>Not All Statins Are Equal–Environmental and Genetic Myotoxicity Risk Factors</dc:title>
			<dc:creator>Anna Katharina Schmid</dc:creator>
			<dc:creator>Victor Voicu</dc:creator>
			<dc:creator>Sarah Parejo</dc:creator>
			<dc:creator>Franziska M. Jakobs</dc:creator>
			<dc:creator>David F. Niedrig</dc:creator>
			<dc:creator>Sandro Baumgartner</dc:creator>
			<dc:creator>Markus Béchir</dc:creator>
			<dc:creator>Stefan Russmann</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1327305240</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-03-27</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-03-27</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>52</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1327305240</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/2/52</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/2/55">

	<title>Cardiovascular Medicine, Vol. 27, Pages 55: Complete Heart Block without Ventricular Escape Rhythm during Left Ventriculography</title>
	<link>https://www.mdpi.com/1664-204X/27/2/55</link>
	<description>Complete heart block (CHB) is a rare complication during left ventriculography. We present a case of transient CHB without ventricular escape rhythm in a patient with an incomplete trifascicular block.</description>
	<pubDate>2024-03-27</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 55: Complete Heart Block without Ventricular Escape Rhythm during Left Ventriculography</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/2/55">doi: 10.4414/cvm.2024.1338832878</a></p>
	<p>Authors:
		Peter Laurenz Dietrich
		Silvan Meier
		Raban Jeger
		</p>
	<p>Complete heart block (CHB) is a rare complication during left ventriculography. We present a case of transient CHB without ventricular escape rhythm in a patient with an incomplete trifascicular block.</p>
	]]></content:encoded>

	<dc:title>Complete Heart Block without Ventricular Escape Rhythm during Left Ventriculography</dc:title>
			<dc:creator>Peter Laurenz Dietrich</dc:creator>
			<dc:creator>Silvan Meier</dc:creator>
			<dc:creator>Raban Jeger</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1338832878</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-03-27</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-03-27</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>55</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1338832878</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/2/55</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/2/47">

	<title>Cardiovascular Medicine, Vol. 27, Pages 47: Is Dental Clearance before Cardiac Surgery Necessary?</title>
	<link>https://www.mdpi.com/1664-204X/27/2/47</link>
	<description>Background: Dental clearance is routinely performed before cardiac surgery, as it is thought to be essential in reducing postoperative bacteremia and endocarditis. However, there is a lack of evidence supporting this routine. Objectives: This study aimed to investigate the impact of dental clearance on postoperative outcomes after cardiac surgery. Methods: This is a comprehensive review and analysis of relevant studies published between 1 January 1990 and 1 January 2023 in two electronic databases (PubMed and EMBASE). Pooled estimates in terms of relative risk (RR) or standardized mean difference were calculated according to outcome measures. Risk of bias and quality of studies were evaluated. A total of 7040 articles were found through the MEDLINE, EMBASE and Cochrane databases. Five articles were found to be eligible for inclusion in this review. Results: There is no statistically significant benefit of preoperative dental clearance in terms of postoperative outcomes, including all-cause mortality (RR 0.92, 95% Confidence Interval [CI] 0.43–1.97), prosthetic valve endocarditis (RR 1.32, 95% CI 0.51–3.43), postsurgical infection (RR 1.02, 95% CI 0.77–1.36), and length of hospital stay (weighted mean difference 4.00, 95% CI −2.70–10.70). Conclusions: Although the literature emphasizes the importance of preoperative dental clearance, no significant effect was seen with respect to all-cause mortality, infection, endocarditis, and length of hospital stay.</description>
	<pubDate>2024-03-27</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 47: Is Dental Clearance before Cardiac Surgery Necessary?</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/2/47">doi: 10.4414/cvm.2024.1356564558</a></p>
	<p>Authors:
		Mevlüt Çelik
		Maria Nucera
		Fabio Pregaldini
		Clarence Pingpoh
		Thomas Pilgrim
		Matthias Siepe
		David Reineke
		</p>
	<p>Background: Dental clearance is routinely performed before cardiac surgery, as it is thought to be essential in reducing postoperative bacteremia and endocarditis. However, there is a lack of evidence supporting this routine. Objectives: This study aimed to investigate the impact of dental clearance on postoperative outcomes after cardiac surgery. Methods: This is a comprehensive review and analysis of relevant studies published between 1 January 1990 and 1 January 2023 in two electronic databases (PubMed and EMBASE). Pooled estimates in terms of relative risk (RR) or standardized mean difference were calculated according to outcome measures. Risk of bias and quality of studies were evaluated. A total of 7040 articles were found through the MEDLINE, EMBASE and Cochrane databases. Five articles were found to be eligible for inclusion in this review. Results: There is no statistically significant benefit of preoperative dental clearance in terms of postoperative outcomes, including all-cause mortality (RR 0.92, 95% Confidence Interval [CI] 0.43–1.97), prosthetic valve endocarditis (RR 1.32, 95% CI 0.51–3.43), postsurgical infection (RR 1.02, 95% CI 0.77–1.36), and length of hospital stay (weighted mean difference 4.00, 95% CI −2.70–10.70). Conclusions: Although the literature emphasizes the importance of preoperative dental clearance, no significant effect was seen with respect to all-cause mortality, infection, endocarditis, and length of hospital stay.</p>
	]]></content:encoded>

	<dc:title>Is Dental Clearance before Cardiac Surgery Necessary?</dc:title>
			<dc:creator>Mevlüt Çelik</dc:creator>
			<dc:creator>Maria Nucera</dc:creator>
			<dc:creator>Fabio Pregaldini</dc:creator>
			<dc:creator>Clarence Pingpoh</dc:creator>
			<dc:creator>Thomas Pilgrim</dc:creator>
			<dc:creator>Matthias Siepe</dc:creator>
			<dc:creator>David Reineke</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1356564558</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-03-27</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-03-27</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>47</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1356564558</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/2/47</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/2/63">

	<title>Cardiovascular Medicine, Vol. 27, Pages 63: A Forgotten Prosthesis in a Forgotten Valve: A Surprising Case Report</title>
	<link>https://www.mdpi.com/1664-204X/27/2/63</link>
	<description>The development of prosthetic heart valves has allowed to drastically improve the quality of life and the life expectancy in patients who would otherwise have succumbed to the inevitable course of the disease. While prosthetic heart valves are invaluable resources in therapy, they are not devoid of possible complications, some inherent to the prosthesis itself (structural damage, thrombosis, etc.), others related to the patient (e.g., thrombophilia, non-adherence to medication). The case of a patient is presented whose findings are surprising and show that there is always an exception to the rule.</description>
	<pubDate>2024-03-27</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 63: A Forgotten Prosthesis in a Forgotten Valve: A Surprising Case Report</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/2/63">doi: 10.4414/cvm.2024.1373944239</a></p>
	<p>Authors:
		Jessy Steve Masso-Bueso
		David Jacobo Sánchez-Amaya
		Oscar Andrés Pérez-Orpinel
		</p>
	<p>The development of prosthetic heart valves has allowed to drastically improve the quality of life and the life expectancy in patients who would otherwise have succumbed to the inevitable course of the disease. While prosthetic heart valves are invaluable resources in therapy, they are not devoid of possible complications, some inherent to the prosthesis itself (structural damage, thrombosis, etc.), others related to the patient (e.g., thrombophilia, non-adherence to medication). The case of a patient is presented whose findings are surprising and show that there is always an exception to the rule.</p>
	]]></content:encoded>

	<dc:title>A Forgotten Prosthesis in a Forgotten Valve: A Surprising Case Report</dc:title>
			<dc:creator>Jessy Steve Masso-Bueso</dc:creator>
			<dc:creator>David Jacobo Sánchez-Amaya</dc:creator>
			<dc:creator>Oscar Andrés Pérez-Orpinel</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1373944239</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-03-27</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-03-27</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Interesting Images</prism:section>
	<prism:startingPage>63</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1373944239</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/2/63</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/1/18">

	<title>Cardiovascular Medicine, Vol. 27, Pages 18: Specialized Clinical Care Pathway for Non-ST-Elevation Myocardial Infarction</title>
	<link>https://www.mdpi.com/1664-204X/27/1/18</link>
	<description>Background: The mortality reduction associated with immediate coronary reperfusion in patients with ST-elevation myocardial infarction is extensively documented. The gap between available knowledge and care delivery is primarily due to lacking coordination between the patient contact points. We postulate that the same applies to non-ST-elevation myocardial infarction (NSTEMI) and that a more consistent care delivery could improve outcomes. Methods: We conducted a single-center retrospective observational study in NSTEMI patients who presented to the emergency department (ED) at our institution between October 2017 and September 2019, covering the last twelve months before implementing our new NSTEMI care pathway (pre-intervention) and the first twelve months thereafter (post-intervention). Primary endpoint was the door-to-cardiology time, i.e., time between ED admission and admission to the cardiology department. Co-primary endpoint was the door-to-needle time, i.e., time between ED admission and initiation of coronary angiography. Secondary endpoints included total hospital stay (time between ED admission and discharge), in-hospital mortality (%), and retrospective misdiagnoses with the coronary angiography showing no or non-relevant coronary lesions (%). Results: 271 consecutive NSTEMI patients were treated during the study period. 112 (41.3%) in the year before and 159 (58.7%) in the year after the NSTEMI care pathway implementation. NSTEMI care pathway led to a significant reduction in median door-to-cardiology time from twelve hours (interquartile range [IQR] 6–24 h) pre-intervention to six hours (IQR 4–9 h) post-intervention (p &amp;amp;lt; 0.0001); a significant reduction in median length of hospital stay from five days (IQR 3–10 days) pre-intervention to three days (IQR 2–7 days) post-intervention (p &amp;amp;lt;0.0001); and a significant reduction of misdiagnoses from 16.96% pre-intervention to 8.81% post-intervention (p = 0.0341). There was no significant change in median door-to-needle time (28 h pre-intervention to 24 h post-intervention, p = 0.0736) nor in in-hospital mortality (0.89% pre-intervention versus 2.52% post-intervention, p = 0.6519). Conclusions: The NSTEMI care pathway significantly reduced door-to-cardiology time, length of hospital stay and number of misdiagnoses. It proved feasible in routine clinical practice and could be implemented on a larger scale.</description>
	<pubDate>2024-01-24</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 18: Specialized Clinical Care Pathway for Non-ST-Elevation Myocardial Infarction</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/1/18">doi: 10.4414/cvm.2024.1220454347</a></p>
	<p>Authors:
		Jérôme Dällenbach
		Grégoire Girod
		Pierre Monney
		Wongsakorn Luangphiphat
		Eric Eeckhout
		</p>
	<p>Background: The mortality reduction associated with immediate coronary reperfusion in patients with ST-elevation myocardial infarction is extensively documented. The gap between available knowledge and care delivery is primarily due to lacking coordination between the patient contact points. We postulate that the same applies to non-ST-elevation myocardial infarction (NSTEMI) and that a more consistent care delivery could improve outcomes. Methods: We conducted a single-center retrospective observational study in NSTEMI patients who presented to the emergency department (ED) at our institution between October 2017 and September 2019, covering the last twelve months before implementing our new NSTEMI care pathway (pre-intervention) and the first twelve months thereafter (post-intervention). Primary endpoint was the door-to-cardiology time, i.e., time between ED admission and admission to the cardiology department. Co-primary endpoint was the door-to-needle time, i.e., time between ED admission and initiation of coronary angiography. Secondary endpoints included total hospital stay (time between ED admission and discharge), in-hospital mortality (%), and retrospective misdiagnoses with the coronary angiography showing no or non-relevant coronary lesions (%). Results: 271 consecutive NSTEMI patients were treated during the study period. 112 (41.3%) in the year before and 159 (58.7%) in the year after the NSTEMI care pathway implementation. NSTEMI care pathway led to a significant reduction in median door-to-cardiology time from twelve hours (interquartile range [IQR] 6–24 h) pre-intervention to six hours (IQR 4–9 h) post-intervention (p &amp;amp;lt; 0.0001); a significant reduction in median length of hospital stay from five days (IQR 3–10 days) pre-intervention to three days (IQR 2–7 days) post-intervention (p &amp;amp;lt;0.0001); and a significant reduction of misdiagnoses from 16.96% pre-intervention to 8.81% post-intervention (p = 0.0341). There was no significant change in median door-to-needle time (28 h pre-intervention to 24 h post-intervention, p = 0.0736) nor in in-hospital mortality (0.89% pre-intervention versus 2.52% post-intervention, p = 0.6519). Conclusions: The NSTEMI care pathway significantly reduced door-to-cardiology time, length of hospital stay and number of misdiagnoses. It proved feasible in routine clinical practice and could be implemented on a larger scale.</p>
	]]></content:encoded>

	<dc:title>Specialized Clinical Care Pathway for Non-ST-Elevation Myocardial Infarction</dc:title>
			<dc:creator>Jérôme Dällenbach</dc:creator>
			<dc:creator>Grégoire Girod</dc:creator>
			<dc:creator>Pierre Monney</dc:creator>
			<dc:creator>Wongsakorn Luangphiphat</dc:creator>
			<dc:creator>Eric Eeckhout</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1220454347</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-01-24</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-01-24</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>18</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1220454347</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/1/18</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/1/25">

	<title>Cardiovascular Medicine, Vol. 27, Pages 25: Conservative Treatment of Permanent Junctional Reciprocating Tachycardia</title>
	<link>https://www.mdpi.com/1664-204X/27/1/25</link>
	<description>Permanent junctional reciprocating tachycardia (PJRT) is a rare form of atrioventricular reentrant tachycardia due to an accessory pathway characterized by slow and decremental retrograde con duction. The arrhythmia typically presents before adulthood with incessant tachycardia leading to cardiomyopathy and heart failure. We report the case of a woman with tachycardia induced cardiomyopathy due to PJRT detected at the age of 54 years. The patient refused to undergo catheter ablation and was successfully treated with a beta blocker.</description>
	<pubDate>2024-01-24</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 25: Conservative Treatment of Permanent Junctional Reciprocating Tachycardia</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/1/25">doi: 10.4414/cvm.2024.1243919841</a></p>
	<p>Authors:
		Tatiana Peer
		Andreas Müller-Burri
		</p>
	<p>Permanent junctional reciprocating tachycardia (PJRT) is a rare form of atrioventricular reentrant tachycardia due to an accessory pathway characterized by slow and decremental retrograde con duction. The arrhythmia typically presents before adulthood with incessant tachycardia leading to cardiomyopathy and heart failure. We report the case of a woman with tachycardia induced cardiomyopathy due to PJRT detected at the age of 54 years. The patient refused to undergo catheter ablation and was successfully treated with a beta blocker.</p>
	]]></content:encoded>

	<dc:title>Conservative Treatment of Permanent Junctional Reciprocating Tachycardia</dc:title>
			<dc:creator>Tatiana Peer</dc:creator>
			<dc:creator>Andreas Müller-Burri</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1243919841</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-01-24</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-01-24</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>25</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1243919841</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/1/25</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/1/28">

	<title>Cardiovascular Medicine, Vol. 27, Pages 28: Personalized Management of Coronary Atherosclerosis</title>
	<link>https://www.mdpi.com/1664-204X/27/1/28</link>
	<description>We present the diagnostic pathway and management of an asymptomatic patient with a solitary, potentially high-risk coronary plaque, utilizing modern and advanced non-invasive and invasive pathophysiological, morphological, and functional assessment. By using coronary computed to mography angiography, computer-based solutions were employed enabling non-invasive under standing of the plaque characteristics and the local and global functional micro-environment. Invasive coronary angiography-based, computational, and wire-free hemodynamic lesion assess ment as well as intracoronary imaging with optical coherence tomography were further utilized, allowing for personalized management and guiding coronary revascularization.</description>
	<pubDate>2024-01-24</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 28: Personalized Management of Coronary Atherosclerosis</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/1/28">doi: 10.4414/cvm.2024.1246902814</a></p>
	<p>Authors:
		Apostolos Tsinaridis
		Marko Gajic
		Alessandro Candreva
		Philipp A. Kaufmann
		Ronny R. Buechel
		Barbara E. Stähli
		Andreas A. Giannopoulos
		</p>
	<p>We present the diagnostic pathway and management of an asymptomatic patient with a solitary, potentially high-risk coronary plaque, utilizing modern and advanced non-invasive and invasive pathophysiological, morphological, and functional assessment. By using coronary computed to mography angiography, computer-based solutions were employed enabling non-invasive under standing of the plaque characteristics and the local and global functional micro-environment. Invasive coronary angiography-based, computational, and wire-free hemodynamic lesion assess ment as well as intracoronary imaging with optical coherence tomography were further utilized, allowing for personalized management and guiding coronary revascularization.</p>
	]]></content:encoded>

	<dc:title>Personalized Management of Coronary Atherosclerosis</dc:title>
			<dc:creator>Apostolos Tsinaridis</dc:creator>
			<dc:creator>Marko Gajic</dc:creator>
			<dc:creator>Alessandro Candreva</dc:creator>
			<dc:creator>Philipp A. Kaufmann</dc:creator>
			<dc:creator>Ronny R. Buechel</dc:creator>
			<dc:creator>Barbara E. Stähli</dc:creator>
			<dc:creator>Andreas A. Giannopoulos</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1246902814</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-01-24</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-01-24</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>28</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1246902814</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/1/28</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/1/31">

	<title>Cardiovascular Medicine, Vol. 27, Pages 31: Of Nutty Professors and Pristine Coronary Arteries</title>
	<link>https://www.mdpi.com/1664-204X/27/1/31</link>
	<description>“Professor Meier is nuts!” [...]</description>
	<pubDate>2024-01-24</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 31: Of Nutty Professors and Pristine Coronary Arteries</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/1/31">doi: 10.4414/cvm.2024.1262905452</a></p>
	<p>Authors:
		Franz H. Messerli
		Manuel R. Blum
		Bernhard Meier
		</p>
	<p>“Professor Meier is nuts!” [...]</p>
	]]></content:encoded>

	<dc:title>Of Nutty Professors and Pristine Coronary Arteries</dc:title>
			<dc:creator>Franz H. Messerli</dc:creator>
			<dc:creator>Manuel R. Blum</dc:creator>
			<dc:creator>Bernhard Meier</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1262905452</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-01-24</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-01-24</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Commentary</prism:section>
	<prism:startingPage>31</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1262905452</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/1/31</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/1/8">

	<title>Cardiovascular Medicine, Vol. 27, Pages 8: A New Therapeutic Principle in Anticoagulation</title>
	<link>https://www.mdpi.com/1664-204X/27/1/8</link>
	<description>Thrombosis remains a significant clinical challenge with potential life-threatening consequences. Despite advancements in anticoagulants, concerns about bleeding and the delicate balance of thrombotic risks persist, especially in patients with specific comorbidities such as renal insufficiency, cirrhosis, and those with medical devices. The search for effective anticoagulant therapies that can prevent thrombotic events while minimizing bleeding risks, has led to the emergence of factor XI (FXI) inhibition as a promising approach. These inhibitors target FXI using different mechanisms of action, routes of administration and durations, offering flexibility for various clinical conditions. Early findings from phase II trials have shown a promising trend of reduced bleeding risks in both venous thrombosis and arterial thromboembolism. The results from these trials, particularly the ongoing phase III trials, will yield valuable insights into the efficacy of FXI inhibitors in preventing thrombosis. Specific patient populations, including individuals with end-stage renal disease and those with mechanical devices or blood exposed to artificial surfaces (commonly referred to as artificial contact surfaces associated thrombosis), alongside patients with conditions like thrombotic antiphospholipid syndrome or sickle cell disease, might experience distinct advantages from the application of FXI inhibitors. Dedicated clinical studies focusing on these patient groups are crucial to establish the effectiveness and safety of FXI inhibitors in their management. Moreover, it is imperative to address the development of effective strategies to reverse the anticoagulant effects of FXI inhibitors, ensuring comprehensive patient management, especially for agents with long half-lives. This review article provides a comprehensive overview of the current understanding and research progress in FXI inhibition for thrombosis prevention.</description>
	<pubDate>2024-01-24</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 8: A New Therapeutic Principle in Anticoagulation</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/1/8">doi: 10.4414/cvm.2024.1270682599</a></p>
	<p>Authors:
		Pratintip Lee
		Hans-Jürg Beer
		</p>
	<p>Thrombosis remains a significant clinical challenge with potential life-threatening consequences. Despite advancements in anticoagulants, concerns about bleeding and the delicate balance of thrombotic risks persist, especially in patients with specific comorbidities such as renal insufficiency, cirrhosis, and those with medical devices. The search for effective anticoagulant therapies that can prevent thrombotic events while minimizing bleeding risks, has led to the emergence of factor XI (FXI) inhibition as a promising approach. These inhibitors target FXI using different mechanisms of action, routes of administration and durations, offering flexibility for various clinical conditions. Early findings from phase II trials have shown a promising trend of reduced bleeding risks in both venous thrombosis and arterial thromboembolism. The results from these trials, particularly the ongoing phase III trials, will yield valuable insights into the efficacy of FXI inhibitors in preventing thrombosis. Specific patient populations, including individuals with end-stage renal disease and those with mechanical devices or blood exposed to artificial surfaces (commonly referred to as artificial contact surfaces associated thrombosis), alongside patients with conditions like thrombotic antiphospholipid syndrome or sickle cell disease, might experience distinct advantages from the application of FXI inhibitors. Dedicated clinical studies focusing on these patient groups are crucial to establish the effectiveness and safety of FXI inhibitors in their management. Moreover, it is imperative to address the development of effective strategies to reverse the anticoagulant effects of FXI inhibitors, ensuring comprehensive patient management, especially for agents with long half-lives. This review article provides a comprehensive overview of the current understanding and research progress in FXI inhibition for thrombosis prevention.</p>
	]]></content:encoded>

	<dc:title>A New Therapeutic Principle in Anticoagulation</dc:title>
			<dc:creator>Pratintip Lee</dc:creator>
			<dc:creator>Hans-Jürg Beer</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1270682599</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-01-24</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-01-24</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>8</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1270682599</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/1/8</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/1/6">

	<title>Cardiovascular Medicine, Vol. 27, Pages 6: A Tribute to Istvan Babotai, PhD</title>
	<link>https://www.mdpi.com/1664-204X/27/1/6</link>
	<description>In 1956, at the age of 17, Istvan Babotai fled Hungary, became an electrical engineer and ultimately a pioneering figure of cardi ac pacing in Switzerland [...]</description>
	<pubDate>2024-01-24</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 6: A Tribute to Istvan Babotai, PhD</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/1/6">doi: 10.4414/cvm.2024.1282909062</a></p>
	<p>Authors:
		Etienne Delacrétaz
		Christian Sticherling
		</p>
	<p>In 1956, at the age of 17, Istvan Babotai fled Hungary, became an electrical engineer and ultimately a pioneering figure of cardi ac pacing in Switzerland [...]</p>
	]]></content:encoded>

	<dc:title>A Tribute to Istvan Babotai, PhD</dc:title>
			<dc:creator>Etienne Delacrétaz</dc:creator>
			<dc:creator>Christian Sticherling</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1282909062</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-01-24</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-01-24</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>6</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1282909062</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/1/6</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/27/1/1">

	<title>Cardiovascular Medicine, Vol. 27, Pages 1: Cardiac Sarcoidosis—An Underrecognized Myocardial Disease</title>
	<link>https://www.mdpi.com/1664-204X/27/1/1</link>
	<description>Sarcoidosis is a multisystemic, chronic inflamma tory disorder involving lymph nodes and lungs characterized by a non-caseating [...]</description>
	<pubDate>2024-01-24</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 27, Pages 1: Cardiac Sarcoidosis—An Underrecognized Myocardial Disease</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/27/1/1">doi: 10.4414/cvm.2024.1324050930</a></p>
	<p>Authors:
		Thomas Lüscher
		Rakesh Sharma
		Kshama Wechalekar
		Vasileios Kouranos
		</p>
	<p>Sarcoidosis is a multisystemic, chronic inflamma tory disorder involving lymph nodes and lungs characterized by a non-caseating [...]</p>
	]]></content:encoded>

	<dc:title>Cardiac Sarcoidosis—An Underrecognized Myocardial Disease</dc:title>
			<dc:creator>Thomas Lüscher</dc:creator>
			<dc:creator>Rakesh Sharma</dc:creator>
			<dc:creator>Kshama Wechalekar</dc:creator>
			<dc:creator>Vasileios Kouranos</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2024.1324050930</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2024-01-24</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2024-01-24</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>1</prism:startingPage>
		<prism:doi>10.4414/cvm.2024.1324050930</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/27/1/1</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/6/206">

	<title>Cardiovascular Medicine, Vol. 26, Pages 206: Isolated Right Ventricular Myocardial Infarction</title>
	<link>https://www.mdpi.com/1664-204X/26/6/206</link>
	<description>A 67-year-old man with known coronary artery disease was rescued after an out-of-hospital cardiac arrest due to ventricular fibrillation (VF) and admitted to the catheterization laboratory with inferior ST-segment elevation, right bundle branch block and atrial fibrillation on the electrocardiogram. The patient had had an elective percutaneous coronary intervention (PCI) with implantation of a bare metal stent to the dominant mid left circumflex artery three years before and a second PCI with implantation of a drug-eluting stent to the proximal/mid left anterior descending artery at another local institution three months earlier. The prescribed dual antiplatelet therapy was interrupted by the patient right after discharge. Therefore, a stent thrombosis was initially deemed the most probable cause of his clinical presentation (the elephant in the room). Nevertheless, the coronary angiography showed patent stents and the left ventriculography revealed a normal left ventricular function. After excluding aortic dissection and pulmonary embolism, cardiac magnetic resonance imaging showed signs of acute isolated right ventricular myocardial infarction. Upon review of previous angiograms, a small occluded right ventricular branch appeared to be the lesion that triggered the VF.</description>
	<pubDate>2023-11-22</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 206: Isolated Right Ventricular Myocardial Infarction</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/6/206">doi: 10.4414/cvm.2023.1190638221</a></p>
	<p>Authors:
		Andrea Papa
		Edira Bekiri
		Marco Giacchi
		Gregor Leibundgut
		</p>
	<p>A 67-year-old man with known coronary artery disease was rescued after an out-of-hospital cardiac arrest due to ventricular fibrillation (VF) and admitted to the catheterization laboratory with inferior ST-segment elevation, right bundle branch block and atrial fibrillation on the electrocardiogram. The patient had had an elective percutaneous coronary intervention (PCI) with implantation of a bare metal stent to the dominant mid left circumflex artery three years before and a second PCI with implantation of a drug-eluting stent to the proximal/mid left anterior descending artery at another local institution three months earlier. The prescribed dual antiplatelet therapy was interrupted by the patient right after discharge. Therefore, a stent thrombosis was initially deemed the most probable cause of his clinical presentation (the elephant in the room). Nevertheless, the coronary angiography showed patent stents and the left ventriculography revealed a normal left ventricular function. After excluding aortic dissection and pulmonary embolism, cardiac magnetic resonance imaging showed signs of acute isolated right ventricular myocardial infarction. Upon review of previous angiograms, a small occluded right ventricular branch appeared to be the lesion that triggered the VF.</p>
	]]></content:encoded>

	<dc:title>Isolated Right Ventricular Myocardial Infarction</dc:title>
			<dc:creator>Andrea Papa</dc:creator>
			<dc:creator>Edira Bekiri</dc:creator>
			<dc:creator>Marco Giacchi</dc:creator>
			<dc:creator>Gregor Leibundgut</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.1190638221</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-11-22</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-11-22</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>206</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.1190638221</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/6/206</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/6/194">

	<title>Cardiovascular Medicine, Vol. 26, Pages 194: Leadless Pacemaker Implantation via the Internal Jugular Vein</title>
	<link>https://www.mdpi.com/1664-204X/26/6/194</link>
	<description>Background: Leadless pacemaker therapy was introduced in 2013 to overcome lead- and pocket- related complications in conventional transvenous pacemaker therapy. These leadless devices are self-contained, right ventricular, single-chamber pacemakers, implanted via a femoral percutaneous approach. However, the femoral route is not always possible due to various reasons. The aim of this analysis is to share our first experience using a jugular approach for the implantation procedure. Methods: The first ten patients who underwent leadless pacemaker implantation via the right internal jugular venous route at our center were analyzed prospectively. Follow-up period was three months. Interventional and electrical parameters of the jugular approach were compared with the data of the first 100 patients who underwent a femoral leadless pacemaker implantation at our center (implanted from 2015–2019). Results: Data from ten consecutive patients (mean age 83.3 ± 3.6 years, six males) were collected. All leadless pacemakers were implanted successfully via the internal right jugular vein. Mean procedure time was 31.9 ± 6.4 min with a mean fluoroscopy time of 3.4 ± 2.4 min. The device was positioned at the inferior septum in three patients and midseptal in seven patients. The mean pacing threshold was 0.47 ± 0.14 V at 0.24 ms pulse width with a sensed amplitude of 9.1 ± 3.8 mV. There were no complications during the procedure as well as during the three months follow-up. Pacing parameters remained stable in all patients. Conclusion: The jugular approach seems to be a safe and efficient alternative to the femoral implantation method for currently available leadless pacemakers.</description>
	<pubDate>2023-11-22</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 194: Leadless Pacemaker Implantation via the Internal Jugular Vein</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/6/194">doi: 10.4414/cvm.2023.1216876634</a></p>
	<p>Authors:
		Nadine Molitor
		Alexander Breitenstein
		</p>
	<p>Background: Leadless pacemaker therapy was introduced in 2013 to overcome lead- and pocket- related complications in conventional transvenous pacemaker therapy. These leadless devices are self-contained, right ventricular, single-chamber pacemakers, implanted via a femoral percutaneous approach. However, the femoral route is not always possible due to various reasons. The aim of this analysis is to share our first experience using a jugular approach for the implantation procedure. Methods: The first ten patients who underwent leadless pacemaker implantation via the right internal jugular venous route at our center were analyzed prospectively. Follow-up period was three months. Interventional and electrical parameters of the jugular approach were compared with the data of the first 100 patients who underwent a femoral leadless pacemaker implantation at our center (implanted from 2015–2019). Results: Data from ten consecutive patients (mean age 83.3 ± 3.6 years, six males) were collected. All leadless pacemakers were implanted successfully via the internal right jugular vein. Mean procedure time was 31.9 ± 6.4 min with a mean fluoroscopy time of 3.4 ± 2.4 min. The device was positioned at the inferior septum in three patients and midseptal in seven patients. The mean pacing threshold was 0.47 ± 0.14 V at 0.24 ms pulse width with a sensed amplitude of 9.1 ± 3.8 mV. There were no complications during the procedure as well as during the three months follow-up. Pacing parameters remained stable in all patients. Conclusion: The jugular approach seems to be a safe and efficient alternative to the femoral implantation method for currently available leadless pacemakers.</p>
	]]></content:encoded>

	<dc:title>Leadless Pacemaker Implantation via the Internal Jugular Vein</dc:title>
			<dc:creator>Nadine Molitor</dc:creator>
			<dc:creator>Alexander Breitenstein</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.1216876634</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-11-22</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-11-22</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>194</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.1216876634</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/6/194</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/6/190">

	<title>Cardiovascular Medicine, Vol. 26, Pages 190: Digitalization and Artificial Intelligence in (Heart-) Medicine</title>
	<link>https://www.mdpi.com/1664-204X/26/6/190</link>
	<description>Digitalization of the healthcare sector is changing its landscape. Artificial intelligence is bound to have a major impact on care providers and their interactions with their patients. As promising as new technologies may be, there will be side effects. New Technologies will place new and higher demands on its users and will require an extremely high level of expertise to check plausibility. Alongside increases in efficiency and effectiveness, the demands on the humans in healthcare will also rise.</description>
	<pubDate>2023-11-22</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 190: Digitalization and Artificial Intelligence in (Heart-) Medicine</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/6/190">doi: 10.4414/cvm.2023.1236103712</a></p>
	<p>Authors:
		Guido Schüpfer
		Peter Matt
		</p>
	<p>Digitalization of the healthcare sector is changing its landscape. Artificial intelligence is bound to have a major impact on care providers and their interactions with their patients. As promising as new technologies may be, there will be side effects. New Technologies will place new and higher demands on its users and will require an extremely high level of expertise to check plausibility. Alongside increases in efficiency and effectiveness, the demands on the humans in healthcare will also rise.</p>
	]]></content:encoded>

	<dc:title>Digitalization and Artificial Intelligence in (Heart-) Medicine</dc:title>
			<dc:creator>Guido Schüpfer</dc:creator>
			<dc:creator>Peter Matt</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.1236103712</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-11-22</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-11-22</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>190</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.1236103712</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/6/190</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/6/202">

	<title>Cardiovascular Medicine, Vol. 26, Pages 202: Treatment of Complex Atrial Arrhythmias in Lamin Heart Disease</title>
	<link>https://www.mdpi.com/1664-204X/26/6/202</link>
	<description>We report unusual manifestations of Lamin mutations (noncompaction, vertical pulmonary vein connection) associated with highly complex atrial arrhythmias, which were not mappable by contact mapping due to unstable reference and activation patterns. The advantages of a novel noncontact mapping technology allowing beat-to-beat analysis of electrical activation in the entire heart chamber simultaneously by localizing electrical charge density (Coulomb/area) are discussed.</description>
	<pubDate>2023-11-22</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 202: Treatment of Complex Atrial Arrhythmias in Lamin Heart Disease</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/6/202">doi: 10.4414/cvm.2023.1243927837</a></p>
	<p>Authors:
		Stefano Caselli
		Lam Dang
		Kurt Mayer
		Christine Attenhofer Jost
		Christoph Scharf
		</p>
	<p>We report unusual manifestations of Lamin mutations (noncompaction, vertical pulmonary vein connection) associated with highly complex atrial arrhythmias, which were not mappable by contact mapping due to unstable reference and activation patterns. The advantages of a novel noncontact mapping technology allowing beat-to-beat analysis of electrical activation in the entire heart chamber simultaneously by localizing electrical charge density (Coulomb/area) are discussed.</p>
	]]></content:encoded>

	<dc:title>Treatment of Complex Atrial Arrhythmias in Lamin Heart Disease</dc:title>
			<dc:creator>Stefano Caselli</dc:creator>
			<dc:creator>Lam Dang</dc:creator>
			<dc:creator>Kurt Mayer</dc:creator>
			<dc:creator>Christine Attenhofer Jost</dc:creator>
			<dc:creator>Christoph Scharf</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.1243927837</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-11-22</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-11-22</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>202</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.1243927837</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/6/202</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/6/199">

	<title>Cardiovascular Medicine, Vol. 26, Pages 199: Right-Sided Atrial Flutter Ablation After Tricuspid Valve-in-Valve Replacement</title>
	<link>https://www.mdpi.com/1664-204X/26/6/199</link>
	<description>A patient with previous transcatheter tricuspid valve-in-valve replacement underwent catheter ablation for symptomatic atrial flutter. An incisional and cavo-tricuspid isthmus (CTI) dependent right atrial flutter was confirmed. Ablation of the critical isthmus at the lateral right atrial wall and CTI ablation sustainably terminated the flutter. This case highlights the feasibility and safety of CTI-dependent atrial flutter ablation after tricuspid valve-in-valve replacement, which has not been reported so far.</description>
	<pubDate>2023-11-22</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 199: Right-Sided Atrial Flutter Ablation After Tricuspid Valve-in-Valve Replacement</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/6/199">doi: 10.4414/cvm.2023.1246902735</a></p>
	<p>Authors:
		Gonca Suna
		Fu Guan
		Jonathan Michel
		Ardan Saguner
		</p>
	<p>A patient with previous transcatheter tricuspid valve-in-valve replacement underwent catheter ablation for symptomatic atrial flutter. An incisional and cavo-tricuspid isthmus (CTI) dependent right atrial flutter was confirmed. Ablation of the critical isthmus at the lateral right atrial wall and CTI ablation sustainably terminated the flutter. This case highlights the feasibility and safety of CTI-dependent atrial flutter ablation after tricuspid valve-in-valve replacement, which has not been reported so far.</p>
	]]></content:encoded>

	<dc:title>Right-Sided Atrial Flutter Ablation After Tricuspid Valve-in-Valve Replacement</dc:title>
			<dc:creator>Gonca Suna</dc:creator>
			<dc:creator>Fu Guan</dc:creator>
			<dc:creator>Jonathan Michel</dc:creator>
			<dc:creator>Ardan Saguner</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.1246902735</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-11-22</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-11-22</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>199</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.1246902735</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/6/199</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/6/182">

	<title>Cardiovascular Medicine, Vol. 26, Pages 182: Strong German Hearts 2023</title>
	<link>https://www.mdpi.com/1664-204X/26/6/182</link>
	<description>What do the special task forces of the Federal Police and heart surgeons have in common [...]</description>
	<pubDate>2023-11-22</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 182: Strong German Hearts 2023</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/6/182">doi: 10.4414/cvm.2023.1249054251</a></p>
	<p>Authors:
		Laura Rings
		Luca Koechlin
		</p>
	<p>What do the special task forces of the Federal Police and heart surgeons have in common [...]</p>
	]]></content:encoded>

	<dc:title>Strong German Hearts 2023</dc:title>
			<dc:creator>Laura Rings</dc:creator>
			<dc:creator>Luca Koechlin</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.1249054251</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-11-22</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-11-22</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>182</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.1249054251</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/6/182</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/6/179">

	<title>Cardiovascular Medicine, Vol. 26, Pages 179: Diversity and Variety of Cardiovascular Medicine</title>
	<link>https://www.mdpi.com/1664-204X/26/6/179</link>
	<description>Dear readers [...]</description>
	<pubDate>2023-11-22</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 179: Diversity and Variety of Cardiovascular Medicine</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/6/179">doi: 10.4414/cvm.2023.1293793614</a></p>
	<p>Authors:
		Andreas Flammer
		</p>
	<p>Dear readers [...]</p>
	]]></content:encoded>

	<dc:title>Diversity and Variety of Cardiovascular Medicine</dc:title>
			<dc:creator>Andreas Flammer</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.1293793614</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-11-22</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-11-22</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>179</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.1293793614</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/6/179</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/5/20">

	<title>Cardiovascular Medicine, Vol. 26, Pages 20: Relapsing Terlipressin-Induced Acute Pulmonary Oedema in a Patient with Hepatorenal Syndrome</title>
	<link>https://www.mdpi.com/1664-204X/26/5/20</link>
	<description>Terlipressin is a synthetic analogue of vasopressin recommended as a vasoactive drug with relative specificity for the splanchnic circulation in patients with portal hypertension and bleeding oesophageal varices or hepatorenal syndrome. We report a relapsing terlipressin-induced acute pulmonary oedema in a 59 year-old man with Child B9 alcoholic liver cirrhosis.</description>
	<pubDate>2023-09-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 20: Relapsing Terlipressin-Induced Acute Pulmonary Oedema in a Patient with Hepatorenal Syndrome</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/5/20">doi: 10.4414/cvm.2022.02222</a></p>
	<p>Authors:
		Baudouin Bourlond
		Jean-Michel Dogné
		Luis Urbano
		Oscar Marchetti
		</p>
	<p>Terlipressin is a synthetic analogue of vasopressin recommended as a vasoactive drug with relative specificity for the splanchnic circulation in patients with portal hypertension and bleeding oesophageal varices or hepatorenal syndrome. We report a relapsing terlipressin-induced acute pulmonary oedema in a 59 year-old man with Child B9 alcoholic liver cirrhosis.</p>
	]]></content:encoded>

	<dc:title>Relapsing Terlipressin-Induced Acute Pulmonary Oedema in a Patient with Hepatorenal Syndrome</dc:title>
			<dc:creator>Baudouin Bourlond</dc:creator>
			<dc:creator>Jean-Michel Dogné</dc:creator>
			<dc:creator>Luis Urbano</dc:creator>
			<dc:creator>Oscar Marchetti</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2022.02222</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-09-20</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-09-20</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>20</prism:startingPage>
		<prism:doi>10.4414/cvm.2022.02222</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/5/20</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/5/2223">

	<title>Cardiovascular Medicine, Vol. 26, Pages 2223: Uncommon Cause for Hemorrhagic Tamponade in a 26-Year Old Male</title>
	<link>https://www.mdpi.com/1664-204X/26/5/2223</link>
	<description>By our case report, we want to bring to light the necessity of further workup in young patients with syncope, chest pain and dyspnea. A 26-year-old male was admitted due to syncope after complaining of chest pain and breathing difficulties. Transthoracic echocardiography showed cardiac tamponade and pericardiocentesis was performed with removal of hemorrhagic fluid. Cardiac magnetic resonance showed a heterogeneous, highly perfused mass located in the right atrium (RA) with necrotic areas. Histopathology during cardiac surgery determined a high grade angiosarcoma in the RA and R0 margins. Adjuvant chemotherapy was started but a local relapse occurred followed by multiple metastases and death. Haemorrhagic pericardial effusion is highly suspicious of cardiac malignancies and warrants further workup by a multidisciplinary team.</description>
	<pubDate>2023-09-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 2223: Uncommon Cause for Hemorrhagic Tamponade in a 26-Year Old Male</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/5/2223">doi: 10.4414/cvm.2022.02223</a></p>
	<p>Authors:
		Alexandra-Maria Neagoe
		David Reineke
		Attila Kollár
		Yara Banz
		Kerstin Wustmann
		</p>
	<p>By our case report, we want to bring to light the necessity of further workup in young patients with syncope, chest pain and dyspnea. A 26-year-old male was admitted due to syncope after complaining of chest pain and breathing difficulties. Transthoracic echocardiography showed cardiac tamponade and pericardiocentesis was performed with removal of hemorrhagic fluid. Cardiac magnetic resonance showed a heterogeneous, highly perfused mass located in the right atrium (RA) with necrotic areas. Histopathology during cardiac surgery determined a high grade angiosarcoma in the RA and R0 margins. Adjuvant chemotherapy was started but a local relapse occurred followed by multiple metastases and death. Haemorrhagic pericardial effusion is highly suspicious of cardiac malignancies and warrants further workup by a multidisciplinary team.</p>
	]]></content:encoded>

	<dc:title>Uncommon Cause for Hemorrhagic Tamponade in a 26-Year Old Male</dc:title>
			<dc:creator>Alexandra-Maria Neagoe</dc:creator>
			<dc:creator>David Reineke</dc:creator>
			<dc:creator>Attila Kollár</dc:creator>
			<dc:creator>Yara Banz</dc:creator>
			<dc:creator>Kerstin Wustmann</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2022.02223</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-09-20</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-09-20</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>2223</prism:startingPage>
		<prism:doi>10.4414/cvm.2022.02223</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/5/2223</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/5/144">

	<title>Cardiovascular Medicine, Vol. 26, Pages 144: Nachruf – Professor Paul J. E. Erne</title>
	<link>https://www.mdpi.com/1664-204X/26/5/144</link>
	<description>Am 22. Juli 2023 ist der bekannte Schweizer Kardiologe Paul J. E. Erne nach langer Krankheit verstorben […]</description>
	<pubDate>2023-09-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 144: Nachruf – Professor Paul J. E. Erne</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/5/144">doi: 10.4414/cvm.2023.1243787466</a></p>
	<p>Authors:
		Thomas Lüscher
		Hans Rickli
		Michel Zuber
		</p>
	<p>Am 22. Juli 2023 ist der bekannte Schweizer Kardiologe Paul J. E. Erne nach langer Krankheit verstorben […]</p>
	]]></content:encoded>

	<dc:title>Nachruf – Professor Paul J. E. Erne</dc:title>
			<dc:creator>Thomas Lüscher</dc:creator>
			<dc:creator>Hans Rickli</dc:creator>
			<dc:creator>Michel Zuber</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.1243787466</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-09-20</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-09-20</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>144</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.1243787466</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/5/144</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/5/698">

	<title>Cardiovascular Medicine, Vol. 26, Pages 698: Sex-Specific Aspects of Cardiac Electrophysiology and Arrhythmias</title>
	<link>https://www.mdpi.com/1664-204X/26/5/698</link>
	<description>This article provides a condensed but comprehensive summary of the latest knowledge of sex-specific aspects of arrhythmias. Starting with sex-based differences in electrophysiological properties of the heart, it further covers sex- and gender-differences in supraventricular tachycardia, atrial fibrillation, ventricular tachycardia and selected inherited cardiac arrhythmias.</description>
	<pubDate>2023-09-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 698: Sex-Specific Aspects of Cardiac Electrophysiology and Arrhythmias</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/5/698">doi: 10.4414/cvm.2023.1243790698</a></p>
	<p>Authors:
		Aline Mühl
		Babken Asatryan
		Hildegard Tanner
		</p>
	<p>This article provides a condensed but comprehensive summary of the latest knowledge of sex-specific aspects of arrhythmias. Starting with sex-based differences in electrophysiological properties of the heart, it further covers sex- and gender-differences in supraventricular tachycardia, atrial fibrillation, ventricular tachycardia and selected inherited cardiac arrhythmias.</p>
	]]></content:encoded>

	<dc:title>Sex-Specific Aspects of Cardiac Electrophysiology and Arrhythmias</dc:title>
			<dc:creator>Aline Mühl</dc:creator>
			<dc:creator>Babken Asatryan</dc:creator>
			<dc:creator>Hildegard Tanner</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.1243790698</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-09-20</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-09-20</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>698</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.1243790698</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/5/698</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/5/176">

	<title>Cardiovascular Medicine, Vol. 26, Pages 176: A Case of Acute Coronary Syndrome Featuring a Forgotten and Disguised Intruder</title>
	<link>https://www.mdpi.com/1664-204X/26/5/176</link>
	<description>An infrequently diagnosed case of atrial infarction which occurred in conjunction with left ventricular myocardial infarction is presented. Atrial infarction was recognised by the presence of PR segment depression in conjunction with premature atrial complexes. Spatial vector analysis of premature atrial complexes, is highlighted as a means to localise atrial infarction.</description>
	<pubDate>2023-09-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 176: A Case of Acute Coronary Syndrome Featuring a Forgotten and Disguised Intruder</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/5/176">doi: 10.4414/cvm.2023.1243822743</a></p>
	<p>Authors:
		Andreas Andreou
		</p>
	<p>An infrequently diagnosed case of atrial infarction which occurred in conjunction with left ventricular myocardial infarction is presented. Atrial infarction was recognised by the presence of PR segment depression in conjunction with premature atrial complexes. Spatial vector analysis of premature atrial complexes, is highlighted as a means to localise atrial infarction.</p>
	]]></content:encoded>

	<dc:title>A Case of Acute Coronary Syndrome Featuring a Forgotten and Disguised Intruder</dc:title>
			<dc:creator>Andreas Andreou</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.1243822743</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-09-20</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-09-20</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>176</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.1243822743</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/5/176</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/5/174">

	<title>Cardiovascular Medicine, Vol. 26, Pages 174: Intrapericardial Doppler Flow Signals in a Patient with Pericardial Effusion</title>
	<link>https://www.mdpi.com/1664-204X/26/5/174</link>
	<description>We present the case of a 50-year-old woman with a chemotherapeutically treated primary mediastinal lymphoma and circumferential pericardial effusion, whose echocardiogram revealed unusual intrapericardial colour and pulsed-wave Doppler flow signals. Insights on workup and hypotheses are discussed.</description>
	<pubDate>2023-09-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 174: Intrapericardial Doppler Flow Signals in a Patient with Pericardial Effusion</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/5/174">doi: 10.4414/cvm.2023.1243882557</a></p>
	<p>Authors:
		Samuel Stempfel
		Kerstin Wustmann
		Stéphane Cook
		Diego Arroyo
		</p>
	<p>We present the case of a 50-year-old woman with a chemotherapeutically treated primary mediastinal lymphoma and circumferential pericardial effusion, whose echocardiogram revealed unusual intrapericardial colour and pulsed-wave Doppler flow signals. Insights on workup and hypotheses are discussed.</p>
	]]></content:encoded>

	<dc:title>Intrapericardial Doppler Flow Signals in a Patient with Pericardial Effusion</dc:title>
			<dc:creator>Samuel Stempfel</dc:creator>
			<dc:creator>Kerstin Wustmann</dc:creator>
			<dc:creator>Stéphane Cook</dc:creator>
			<dc:creator>Diego Arroyo</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.1243882557</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-09-20</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-09-20</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>174</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.1243882557</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/5/174</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/5/1">

	<title>Cardiovascular Medicine, Vol. 26, Pages 1: Acute Coronary Syndromes in Women and Men</title>
	<link>https://www.mdpi.com/1664-204X/26/5/1</link>
	<description>Acute coronary syndrome (ACS) remains a major cause of morbidity and mortality worldwide. Emerging data indicates that there are relevant sex-specific differences in the pathobiology, clinical presentation, and management of ACS in women and men. Premenopausal women appear to be largely protected from typical ACS, with women presenting 5 to 10 years later than men. Females tend to experience chest pain or discomfort less frequently and more often present with other associated symptoms, which may contribute to longer prehospital delays and less frequently administered guideline-directed care. Indeed, females are less likely to undergo coronary angiography and percutaneous coronary interventions, and less likely to get a prescription for statins after the acute event. Over the past decades, we made remarkable progress in ACS treatment, reducing short-term mortality from far above 50% to below 10% in both women and men. Novel risk tools for clinical risk assessment such as the machine learning-based GRACE 3.0 risk score may help to further improve the management of female and male non-ST segment elevation ACS patients. In this review, we discuss the role of sex in the diagnosis, management, and outcomes of patients with ACS.</description>
	<pubDate>2023-09-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 1: Acute Coronary Syndromes in Women and Men</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/5/1">doi: 10.4414/cvm.2023.1246812107</a></p>
	<p>Authors:
		Florian Wenzl
		Simon Kraler
		Giovanni Camici
		Thomas Lüscher
		</p>
	<p>Acute coronary syndrome (ACS) remains a major cause of morbidity and mortality worldwide. Emerging data indicates that there are relevant sex-specific differences in the pathobiology, clinical presentation, and management of ACS in women and men. Premenopausal women appear to be largely protected from typical ACS, with women presenting 5 to 10 years later than men. Females tend to experience chest pain or discomfort less frequently and more often present with other associated symptoms, which may contribute to longer prehospital delays and less frequently administered guideline-directed care. Indeed, females are less likely to undergo coronary angiography and percutaneous coronary interventions, and less likely to get a prescription for statins after the acute event. Over the past decades, we made remarkable progress in ACS treatment, reducing short-term mortality from far above 50% to below 10% in both women and men. Novel risk tools for clinical risk assessment such as the machine learning-based GRACE 3.0 risk score may help to further improve the management of female and male non-ST segment elevation ACS patients. In this review, we discuss the role of sex in the diagnosis, management, and outcomes of patients with ACS.</p>
	]]></content:encoded>

	<dc:title>Acute Coronary Syndromes in Women and Men</dc:title>
			<dc:creator>Florian Wenzl</dc:creator>
			<dc:creator>Simon Kraler</dc:creator>
			<dc:creator>Giovanni Camici</dc:creator>
			<dc:creator>Thomas Lüscher</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.1246812107</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-09-20</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-09-20</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>1</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.1246812107</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/5/1</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/5/160">

	<title>Cardiovascular Medicine, Vol. 26, Pages 160: Takotsubo Syndrome and Spontaneous Coronary Artery Dissection</title>
	<link>https://www.mdpi.com/1664-204X/26/5/160</link>
	<description>Acute coronary syndrome (ACS) in women presents unique challenges in terms of pathophysiology, diagnosis and management. Rare forms of ACS, such as takotsubo syndrome (TTS) and spontaneous coronary artery dissection (SCAD), have gained increasing attention in recent years. TTS is characterized by transient left ventricular dysfunction in the absence of epicardial culprit lesions, while SCAD involves separation within layers of the arterial wall of the coronary arteries leading to blood flow disruption and potential myocardial infarction. Despite a different pathogenesis, TTS and SCAD share common features such as a significantly higher prevalence in women and a higher rate of recurrent events compared to traditional ACS. Additionally, both conditions are typically anticipated by emotional or physical stressors and have higher incidence in individuals with neuropsychiatric disorders. These similarities suggest that there could be shared risk factors and pathophysiological mechanisms underlying these conditions, which could inform future research and management strategies. The purpose of this review is to provide a comprehensive clinical overview of TTS and SCAD focusing on various aspects of these conditions including epidemiology, clinical profiles, diagnostic workup, prognosis, and management. By highlighting these key areas, this review aims to increase awareness and understanding of these rare forms of ACS among healthcare professionals leading to improved management and treatment.</description>
	<pubDate>2023-09-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 160: Takotsubo Syndrome and Spontaneous Coronary Artery Dissection</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/5/160">doi: 10.4414/cvm.2023.1246945772</a></p>
	<p>Authors:
		Davide Vece
		Christian Templin
		Jelena Rima Ghadri
		</p>
	<p>Acute coronary syndrome (ACS) in women presents unique challenges in terms of pathophysiology, diagnosis and management. Rare forms of ACS, such as takotsubo syndrome (TTS) and spontaneous coronary artery dissection (SCAD), have gained increasing attention in recent years. TTS is characterized by transient left ventricular dysfunction in the absence of epicardial culprit lesions, while SCAD involves separation within layers of the arterial wall of the coronary arteries leading to blood flow disruption and potential myocardial infarction. Despite a different pathogenesis, TTS and SCAD share common features such as a significantly higher prevalence in women and a higher rate of recurrent events compared to traditional ACS. Additionally, both conditions are typically anticipated by emotional or physical stressors and have higher incidence in individuals with neuropsychiatric disorders. These similarities suggest that there could be shared risk factors and pathophysiological mechanisms underlying these conditions, which could inform future research and management strategies. The purpose of this review is to provide a comprehensive clinical overview of TTS and SCAD focusing on various aspects of these conditions including epidemiology, clinical profiles, diagnostic workup, prognosis, and management. By highlighting these key areas, this review aims to increase awareness and understanding of these rare forms of ACS among healthcare professionals leading to improved management and treatment.</p>
	]]></content:encoded>

	<dc:title>Takotsubo Syndrome and Spontaneous Coronary Artery Dissection</dc:title>
			<dc:creator>Davide Vece</dc:creator>
			<dc:creator>Christian Templin</dc:creator>
			<dc:creator>Jelena Rima Ghadri</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.1246945772</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-09-20</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-09-20</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>160</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.1246945772</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/5/160</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/4/116">

	<title>Cardiovascular Medicine, Vol. 26, Pages 116: Arrhythmogenic Syncope</title>
	<link>https://www.mdpi.com/1664-204X/26/4/116</link>
	<description>Syncope is defined as a transient loss of consciousness due to transient cerebral hypoperfusion. It is a frequent cause of consulting in the emergency department, and cardiac arrhythmias play an important role in differential diagnosis. This review article outlines the different arrhythmic causes of syncope and their management, as well as the warning signs that should raise the sus picion of arrhythmia.</description>
	<pubDate>2023-08-02</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 116: Arrhythmogenic Syncope</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/4/116">doi: 10.4414/cvm.2023.02202</a></p>
	<p>Authors:
		Claudia Siklódy
		Patrizio Pascale
		</p>
	<p>Syncope is defined as a transient loss of consciousness due to transient cerebral hypoperfusion. It is a frequent cause of consulting in the emergency department, and cardiac arrhythmias play an important role in differential diagnosis. This review article outlines the different arrhythmic causes of syncope and their management, as well as the warning signs that should raise the sus picion of arrhythmia.</p>
	]]></content:encoded>

	<dc:title>Arrhythmogenic Syncope</dc:title>
			<dc:creator>Claudia Siklódy</dc:creator>
			<dc:creator>Patrizio Pascale</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02202</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-08-02</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-08-02</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>116</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02202</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/4/116</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/4/119">

	<title>Cardiovascular Medicine, Vol. 26, Pages 119: Stroke after Valve Intervention–How to Look For an Embolic Source</title>
	<link>https://www.mdpi.com/1664-204X/26/4/119</link>
	<description>Valve interventions in left sided valvular heart disease, mainly such as transcatheter aortic valve implantations (TAVI) and transcatheter edge-to-edge repairs (TEER) have emerged as alternative treatments in symptomatic severe aortic stenosis and severe mitral regurgitation. However, stroke remains a serious concern. The two main causes of embolisation after valve intervention are thrombosis and vegetations. This review summarises the role of all the different tools of cardiac imaging including transthoracic echocardiography (TTE), transoesophageal echocardiography (TOE), cardiac computed tomography (CT) and 18F-fluorodeoxyglucose-positron emission tomography (FDG-PET) in the diagnosis and work-up of potential cardiac or aortal sources of embolism associated with valve interventions. TTE provides a more comprehensive understanding of the implanted valve including its location and function. Contrast enhanced echocardiography offers additional value in order to detect left ventricular thrombus. Increased valve gradients can be attributed to patient-prosthesis mismatch, thrombus or pannus on the leaflets. Therefore, echocardiography performed immediately after the procedure, followed by follow-ups 4 weeks post-intervention and then annually is of major importance. In addition to echocardiography, cardiac CT can be highly beneficial for confirming or ruling out an abscess, pseudoaneurysm, fistulae and thrombosis. Nuclear molecular techniques, such as 18F-FDG-PET is another important advanced imaging technique, particularly in the management of infective endocarditis.</description>
	<pubDate>2023-08-02</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 119: Stroke after Valve Intervention–How to Look For an Embolic Source</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/4/119">doi: 10.4414/cvm.2023.02232</a></p>
	<p>Authors:
		H. Yakup Yakupoglu
		Tobias Fuchs
		</p>
	<p>Valve interventions in left sided valvular heart disease, mainly such as transcatheter aortic valve implantations (TAVI) and transcatheter edge-to-edge repairs (TEER) have emerged as alternative treatments in symptomatic severe aortic stenosis and severe mitral regurgitation. However, stroke remains a serious concern. The two main causes of embolisation after valve intervention are thrombosis and vegetations. This review summarises the role of all the different tools of cardiac imaging including transthoracic echocardiography (TTE), transoesophageal echocardiography (TOE), cardiac computed tomography (CT) and 18F-fluorodeoxyglucose-positron emission tomography (FDG-PET) in the diagnosis and work-up of potential cardiac or aortal sources of embolism associated with valve interventions. TTE provides a more comprehensive understanding of the implanted valve including its location and function. Contrast enhanced echocardiography offers additional value in order to detect left ventricular thrombus. Increased valve gradients can be attributed to patient-prosthesis mismatch, thrombus or pannus on the leaflets. Therefore, echocardiography performed immediately after the procedure, followed by follow-ups 4 weeks post-intervention and then annually is of major importance. In addition to echocardiography, cardiac CT can be highly beneficial for confirming or ruling out an abscess, pseudoaneurysm, fistulae and thrombosis. Nuclear molecular techniques, such as 18F-FDG-PET is another important advanced imaging technique, particularly in the management of infective endocarditis.</p>
	]]></content:encoded>

	<dc:title>Stroke after Valve Intervention–How to Look For an Embolic Source</dc:title>
			<dc:creator>H. Yakup Yakupoglu</dc:creator>
			<dc:creator>Tobias Fuchs</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02232</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-08-02</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-08-02</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>119</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02232</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/4/119</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/4/130">

	<title>Cardiovascular Medicine, Vol. 26, Pages 130: Atrioventricular Nodal Reentrant Tachycardia with Upper Common Pathway Block</title>
	<link>https://www.mdpi.com/1664-204X/26/4/130</link>
	<description>We present the case of a 34-year-old man with paroxysmal narrow complex tachycardias. An EP study revealed AVNRT with upper common pathway block. Our case shows a diagnostic ap proach and treatment for this rare scenario in the EP lab.</description>
	<pubDate>2023-08-02</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 130: Atrioventricular Nodal Reentrant Tachycardia with Upper Common Pathway Block</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/4/130">doi: 10.4414/cvm.2023.02233</a></p>
	<p>Authors:
		Jan Berg
		Daniel Hofer
		Feifan Ouyang
		Ardan Saguner
		</p>
	<p>We present the case of a 34-year-old man with paroxysmal narrow complex tachycardias. An EP study revealed AVNRT with upper common pathway block. Our case shows a diagnostic ap proach and treatment for this rare scenario in the EP lab.</p>
	]]></content:encoded>

	<dc:title>Atrioventricular Nodal Reentrant Tachycardia with Upper Common Pathway Block</dc:title>
			<dc:creator>Jan Berg</dc:creator>
			<dc:creator>Daniel Hofer</dc:creator>
			<dc:creator>Feifan Ouyang</dc:creator>
			<dc:creator>Ardan Saguner</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02233</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-08-02</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-08-02</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>130</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02233</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/4/130</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/4/133">

	<title>Cardiovascular Medicine, Vol. 26, Pages 133: The Turkish Sabre</title>
	<link>https://www.mdpi.com/1664-204X/26/4/133</link>
	<description>Scimitar syndrome manifesting in adulthood can easily be overlooked owing to mild symptoms. Once diagnosed, operative correction should not be delayed as it can cause severe right heart dysfunction. There are several surgical approaches to recreating normal flow conditions. To identify the best suitable method, one needs to take into account the individual patient’s anatomy.</description>
	<pubDate>2023-08-02</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 133: The Turkish Sabre</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/4/133">doi: 10.4414/cvm.2023.02235</a></p>
	<p>Authors:
		Teresa Podstatzky-Lichtenstein
		Pascal Berdat
		Lars Englberger
		</p>
	<p>Scimitar syndrome manifesting in adulthood can easily be overlooked owing to mild symptoms. Once diagnosed, operative correction should not be delayed as it can cause severe right heart dysfunction. There are several surgical approaches to recreating normal flow conditions. To identify the best suitable method, one needs to take into account the individual patient’s anatomy.</p>
	]]></content:encoded>

	<dc:title>The Turkish Sabre</dc:title>
			<dc:creator>Teresa Podstatzky-Lichtenstein</dc:creator>
			<dc:creator>Pascal Berdat</dc:creator>
			<dc:creator>Lars Englberger</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02235</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-08-02</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-08-02</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>133</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02235</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/4/133</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/4/136">

	<title>Cardiovascular Medicine, Vol. 26, Pages 136: Wide-Complex Tachycardia in a Patient with Previous Accessory Pathway Ablation</title>
	<link>https://www.mdpi.com/1664-204X/26/4/136</link>
	<description>Case Presentation. A 60-year-old man with a history of a right-sided accessory pathway ablated at age 50, presented to a smaller hospital with recurrent palpitations and a regular wide-complex tach ycardia (WCT) (fig. 1) [...]</description>
	<pubDate>2023-08-02</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 136: Wide-Complex Tachycardia in a Patient with Previous Accessory Pathway Ablation</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/4/136">doi: 10.4414/cvm.2023.02236</a></p>
	<p>Authors:
		Tolga Çimen
		Nadine Molitor
		Thomas Wolber
		Fırat Duru
		Ardan Saguner
		</p>
	<p>Case Presentation. A 60-year-old man with a history of a right-sided accessory pathway ablated at age 50, presented to a smaller hospital with recurrent palpitations and a regular wide-complex tach ycardia (WCT) (fig. 1) [...]</p>
	]]></content:encoded>

	<dc:title>Wide-Complex Tachycardia in a Patient with Previous Accessory Pathway Ablation</dc:title>
			<dc:creator>Tolga Çimen</dc:creator>
			<dc:creator>Nadine Molitor</dc:creator>
			<dc:creator>Thomas Wolber</dc:creator>
			<dc:creator>Fırat Duru</dc:creator>
			<dc:creator>Ardan Saguner</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02236</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-08-02</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-08-02</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Interesting Images</prism:section>
	<prism:startingPage>136</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02236</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/4/136</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/4/127">

	<title>Cardiovascular Medicine, Vol. 26, Pages 127: Intracardiac Echocardiography to Guide Biopsy of an Intracardiac Right-Sided Mass</title>
	<link>https://www.mdpi.com/1664-204X/26/4/127</link>
	<description>Introduction: The diagnosis and characterisation of intracardiac tumours is challenging. Transoesophageal echocardiographic guided biopsy is an established method to confirm the pathology. Intracardiac echography (ICE) may help to increase the diagnostic outcome of biopsies, particularly in right-sided cardiac masses. Case Report: We report on a 62-year-old patient who presented with recurrent pericardial effusions of unknown origin. Pericardial puncture did not reveal any significant findings. Positron emission tomography-computed tomography revealed a mass in the right atrium. Due to excellent nearfield imaging capacities for right-sided cardiac structures, ICE was used to guide the biopsy. Biopsy was performed safely and demonstrated a primary cardiac angiosarcoma. Conclusion: ICE-guided biopsy can be a reasonable approach, particularly for right-sided structures, allowing a safe, minimally invasive way of diagnosing intracardiac tumours.</description>
	<pubDate>2023-08-02</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 127: Intracardiac Echocardiography to Guide Biopsy of an Intracardiac Right-Sided Mass</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/4/127">doi: 10.4414/cvm.2023.02237</a></p>
	<p>Authors:
		Teodor Serban
		Diego Mannhart
		Otmar Pfister
		Michael Kühne
		Christian Sticherling
		Patrick Badertscher
		</p>
	<p>Introduction: The diagnosis and characterisation of intracardiac tumours is challenging. Transoesophageal echocardiographic guided biopsy is an established method to confirm the pathology. Intracardiac echography (ICE) may help to increase the diagnostic outcome of biopsies, particularly in right-sided cardiac masses. Case Report: We report on a 62-year-old patient who presented with recurrent pericardial effusions of unknown origin. Pericardial puncture did not reveal any significant findings. Positron emission tomography-computed tomography revealed a mass in the right atrium. Due to excellent nearfield imaging capacities for right-sided cardiac structures, ICE was used to guide the biopsy. Biopsy was performed safely and demonstrated a primary cardiac angiosarcoma. Conclusion: ICE-guided biopsy can be a reasonable approach, particularly for right-sided structures, allowing a safe, minimally invasive way of diagnosing intracardiac tumours.</p>
	]]></content:encoded>

	<dc:title>Intracardiac Echocardiography to Guide Biopsy of an Intracardiac Right-Sided Mass</dc:title>
			<dc:creator>Teodor Serban</dc:creator>
			<dc:creator>Diego Mannhart</dc:creator>
			<dc:creator>Otmar Pfister</dc:creator>
			<dc:creator>Michael Kühne</dc:creator>
			<dc:creator>Christian Sticherling</dc:creator>
			<dc:creator>Patrick Badertscher</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02237</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-08-02</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-08-02</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>127</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02237</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/4/127</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/4/138">

	<title>Cardiovascular Medicine, Vol. 26, Pages 138: Acute Chest Pain in the Era of Digital Watches</title>
	<link>https://www.mdpi.com/1664-204X/26/4/138</link>
	<description>A 38-year-old male smoker with serum LDL-cholesterol of 6.4 mmol/l and a family history of coronary artery disease (father with acute myocardial infarction at the age of 45)[...]</description>
	<pubDate>2023-08-02</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 138: Acute Chest Pain in the Era of Digital Watches</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/4/138">doi: 10.4414/cvm.2023.02238</a></p>
	<p>Authors:
		Marcello Di Valentino
		Tardu Özkartal
		Andrea Menafoglio
		François Regoli
		Stefano Cafarotti
		</p>
	<p>A 38-year-old male smoker with serum LDL-cholesterol of 6.4 mmol/l and a family history of coronary artery disease (father with acute myocardial infarction at the age of 45)[...]</p>
	]]></content:encoded>

	<dc:title>Acute Chest Pain in the Era of Digital Watches</dc:title>
			<dc:creator>Marcello Di Valentino</dc:creator>
			<dc:creator>Tardu Özkartal</dc:creator>
			<dc:creator>Andrea Menafoglio</dc:creator>
			<dc:creator>François Regoli</dc:creator>
			<dc:creator>Stefano Cafarotti</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02238</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-08-02</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-08-02</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Interesting Images</prism:section>
	<prism:startingPage>138</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02238</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/4/138</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/4/111">

	<title>Cardiovascular Medicine, Vol. 26, Pages 111: How to Assess Bleeding Risk in Patients Undergoing Percutaneous Coronary Interventions</title>
	<link>https://www.mdpi.com/1664-204X/26/4/111</link>
	<description>A relevant proportion of patients undergoing percutaneous coronary intervention (PCI) have a high risk of bleeding. The associated individual risk of ischaemia can be differentiated by an app-based approach and helps to determine the duration of intensified antithrombotic therapy.</description>
	<pubDate>2023-08-02</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 111: How to Assess Bleeding Risk in Patients Undergoing Percutaneous Coronary Interventions</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/4/111">doi: 10.4414/cvm.2023.02270</a></p>
	<p>Authors:
		Hans Rickli
		Micha Maeder
		</p>
	<p>A relevant proportion of patients undergoing percutaneous coronary intervention (PCI) have a high risk of bleeding. The associated individual risk of ischaemia can be differentiated by an app-based approach and helps to determine the duration of intensified antithrombotic therapy.</p>
	]]></content:encoded>

	<dc:title>How to Assess Bleeding Risk in Patients Undergoing Percutaneous Coronary Interventions</dc:title>
			<dc:creator>Hans Rickli</dc:creator>
			<dc:creator>Micha Maeder</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02270</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-08-02</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-08-02</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>111</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02270</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/4/111</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/4/122">

	<title>Cardiovascular Medicine, Vol. 26, Pages 122: Percutaneous Coronary Interventions During Automated Chest Compression for Arrest</title>
	<link>https://www.mdpi.com/1664-204X/26/4/122</link>
	<description>Background: The Lund University Cardiopulmonary Assist System-2/-3 was developed for auto-matic chest compressions during cardiopulmonary resuscitation (mechanical CPR or MCPR) and often allows a patient suffering from cardiac arrest to be taken to the cardiac catheterization room. We report the clinical outcomes of percutaneous coronary interventions (PCI) performed in cardiac arrest patients under automatic MCPR devices. Methods: We retrieved all patients with cardiac arrest who were referred to PCI under MCPR devices from the Cardio-FR database (003-REP-CER-FR) from January 2016 to December 2021. Patients who were hemodynamically stable at the time of coronary examination/intervention (even those who had been resuscitated immediately before) were excluded from the analysis. Baseline patient and procedure characteristics were collected. The primary outcome was the return of spontaneous circulation (ROSC). Results: Of all patients who were on MCPR at the cardiac catheterization room, eleven still required active CPR during coronary examination/intervention and were included in the analysis. Mean age was 67.9 ± 10 years, nine were male. The MCPR device was initiated on average after 8.5 ± 8.1 minutes. All patients had ventricular defibrillation and received an average of 3.4 ± 3.6 shocks and 82% adrenaline boluses. The MCPR was used for an average of 51.1 ± 34.4 minutes. Total resuscitation time was on average 59.6 ± 38.3 minutes. Of the eleven patients, nine underwent ad hoc PCI. ROSC was achieved in four patients after 36.5 ± 49.8 minutes. The survival was 36% (four patients) at 24 hours and 27% (three patients) at three months. Only one of the patients resuscitated for &amp;amp;gt;25 minutes survived. Patients with in-hospital cardiac arrest were associated with shorter ROSC (p &amp;amp;lt;0.01), shorter resuscitation time (p = 0.009) and better survival (p = 0.03) than patients with out-of-hospital cardiac arrest. Conclusions: MCPR allows patients in cardiac arrest to reach the cardiac catheterization room. However, the prognosis is grim with high mortality. Only one patient survived after &amp;amp;gt;25 minutes of mechanical resuscitation.</description>
	<pubDate>2023-08-02</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 122: Percutaneous Coronary Interventions During Automated Chest Compression for Arrest</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/4/122">doi: 10.4414/cvm.2023.02279</a></p>
	<p>Authors:
		Thomas Fishman
		Vincent Ribordy
		Serban Puricel
		Mario Togni
		Sébastien Doll
		Diego Arroyo
		Stéphane Cook
		</p>
	<p>Background: The Lund University Cardiopulmonary Assist System-2/-3 was developed for auto-matic chest compressions during cardiopulmonary resuscitation (mechanical CPR or MCPR) and often allows a patient suffering from cardiac arrest to be taken to the cardiac catheterization room. We report the clinical outcomes of percutaneous coronary interventions (PCI) performed in cardiac arrest patients under automatic MCPR devices. Methods: We retrieved all patients with cardiac arrest who were referred to PCI under MCPR devices from the Cardio-FR database (003-REP-CER-FR) from January 2016 to December 2021. Patients who were hemodynamically stable at the time of coronary examination/intervention (even those who had been resuscitated immediately before) were excluded from the analysis. Baseline patient and procedure characteristics were collected. The primary outcome was the return of spontaneous circulation (ROSC). Results: Of all patients who were on MCPR at the cardiac catheterization room, eleven still required active CPR during coronary examination/intervention and were included in the analysis. Mean age was 67.9 ± 10 years, nine were male. The MCPR device was initiated on average after 8.5 ± 8.1 minutes. All patients had ventricular defibrillation and received an average of 3.4 ± 3.6 shocks and 82% adrenaline boluses. The MCPR was used for an average of 51.1 ± 34.4 minutes. Total resuscitation time was on average 59.6 ± 38.3 minutes. Of the eleven patients, nine underwent ad hoc PCI. ROSC was achieved in four patients after 36.5 ± 49.8 minutes. The survival was 36% (four patients) at 24 hours and 27% (three patients) at three months. Only one of the patients resuscitated for &amp;amp;gt;25 minutes survived. Patients with in-hospital cardiac arrest were associated with shorter ROSC (p &amp;amp;lt;0.01), shorter resuscitation time (p = 0.009) and better survival (p = 0.03) than patients with out-of-hospital cardiac arrest. Conclusions: MCPR allows patients in cardiac arrest to reach the cardiac catheterization room. However, the prognosis is grim with high mortality. Only one patient survived after &amp;amp;gt;25 minutes of mechanical resuscitation.</p>
	]]></content:encoded>

	<dc:title>Percutaneous Coronary Interventions During Automated Chest Compression for Arrest</dc:title>
			<dc:creator>Thomas Fishman</dc:creator>
			<dc:creator>Vincent Ribordy</dc:creator>
			<dc:creator>Serban Puricel</dc:creator>
			<dc:creator>Mario Togni</dc:creator>
			<dc:creator>Sébastien Doll</dc:creator>
			<dc:creator>Diego Arroyo</dc:creator>
			<dc:creator>Stéphane Cook</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02279</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-08-02</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-08-02</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>122</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02279</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/4/122</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/4/107">

	<title>Cardiovascular Medicine, Vol. 26, Pages 107: Ein Paradoxon zum Nachdenken</title>
	<link>https://www.mdpi.com/1664-204X/26/4/107</link>
	<description>Damals, in tiefer Vergangenheit, ging es gelegentlich wild zu und her [...]</description>
	<pubDate>2023-08-02</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 107: Ein Paradoxon zum Nachdenken</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/4/107">doi: 10.4414/cvm.2023.02289</a></p>
	<p>Authors:
		Thomas Lüscher
		</p>
	<p>Damals, in tiefer Vergangenheit, ging es gelegentlich wild zu und her [...]</p>
	]]></content:encoded>

	<dc:title>Ein Paradoxon zum Nachdenken</dc:title>
			<dc:creator>Thomas Lüscher</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02289</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-08-02</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-08-02</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>107</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02289</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/4/107</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/3/74">

	<title>Cardiovascular Medicine, Vol. 26, Pages 74: Hypertension in Women: What Is Different?</title>
	<link>https://www.mdpi.com/1664-204X/26/3/74</link>
	<description>Hypertension is the number one killer for women, with a greater burden for women than men and it is an important risk factor for target organ damage. Women are less frequently affected by arterial hypertension than men during their reproductive life, but their risk catches up and exceeds men’s after menopause. There is a knowledge gap about the specificity of arterial hypertension in women due to an under inclusion of women in clinical trials. Hypertensive disorders during pregnancy are a recognised ulterior cardiovascular risk factor and obstetrical history must be part of the evaluation of hypertensive women. Furthermore, efficient cardiovascular prevention must be applied after pregnancies. Both endogenous and exogenous female sex hormones influence the blood pressure (BP) across life course, with specific characteristics relating to pregnancy, lactation, oral contraceptives, menopause, hormones substitution and elderly women. Altogether, effective treatment and control of hypertension ameliorates cardiovascular issues. Concerning medical treatment, due to the lack of data we propose to lower the doses of antihypertensive medications in women, due to increased efficiency and increased risk of secondary effects, most notably for thiazide diuretics and calcium channel blockers.</description>
	<pubDate>2023-05-17</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 74: Hypertension in Women: What Is Different?</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/3/74">doi: 10.4414/cvm.2023.02267</a></p>
	<p>Authors:
		Sophie Huegli
		Antoinette Pechère-Bertschi
		</p>
	<p>Hypertension is the number one killer for women, with a greater burden for women than men and it is an important risk factor for target organ damage. Women are less frequently affected by arterial hypertension than men during their reproductive life, but their risk catches up and exceeds men’s after menopause. There is a knowledge gap about the specificity of arterial hypertension in women due to an under inclusion of women in clinical trials. Hypertensive disorders during pregnancy are a recognised ulterior cardiovascular risk factor and obstetrical history must be part of the evaluation of hypertensive women. Furthermore, efficient cardiovascular prevention must be applied after pregnancies. Both endogenous and exogenous female sex hormones influence the blood pressure (BP) across life course, with specific characteristics relating to pregnancy, lactation, oral contraceptives, menopause, hormones substitution and elderly women. Altogether, effective treatment and control of hypertension ameliorates cardiovascular issues. Concerning medical treatment, due to the lack of data we propose to lower the doses of antihypertensive medications in women, due to increased efficiency and increased risk of secondary effects, most notably for thiazide diuretics and calcium channel blockers.</p>
	]]></content:encoded>

	<dc:title>Hypertension in Women: What Is Different?</dc:title>
			<dc:creator>Sophie Huegli</dc:creator>
			<dc:creator>Antoinette Pechère-Bertschi</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02267</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-05-17</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-05-17</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>74</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02267</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/3/74</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/3/80">

	<title>Cardiovascular Medicine, Vol. 26, Pages 80: Hypertension in Pregnancy</title>
	<link>https://www.mdpi.com/1664-204X/26/3/80</link>
	<description>Cardiovascular diseases in pregnancy are increasing, and account for the majority of pregnancy-induced maternal deaths. Among them, hypertensive disorders are the most frequent, affecting 6–8% of all pregnancies. More severe forms, like preeclampsia and HELLP syndrome, represent serious complications and are associated with far-reaching consequences for mother and child, such as stillbirth, peripartum cardiomyopathy, diastolic heart failure, eclampsia and a long-term increased risk for cardiovascular disease. While risk factors such as obesity, smoking, diabetes mellitus, twin pregnancy, multiparity, advanced age of the mother, in-vitro fertilisation (IVF) are well known, the exact pathophysiology of preeclampsia has still not been precisely clarified. Therefore, specific treatment options are limited, also in part due to the challenge of performing clinical trials in pregnant women. The present review provides an overview of the current state of knowledge and summarises treatment strategies and therapy options.</description>
	<pubDate>2023-05-17</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 80: Hypertension in Pregnancy</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/3/80">doi: 10.4414/cvm.2023.02272</a></p>
	<p>Authors:
		Viola Schaefer
		Denise Hilfiker-Kleiner
		Corinna Keil
		</p>
	<p>Cardiovascular diseases in pregnancy are increasing, and account for the majority of pregnancy-induced maternal deaths. Among them, hypertensive disorders are the most frequent, affecting 6–8% of all pregnancies. More severe forms, like preeclampsia and HELLP syndrome, represent serious complications and are associated with far-reaching consequences for mother and child, such as stillbirth, peripartum cardiomyopathy, diastolic heart failure, eclampsia and a long-term increased risk for cardiovascular disease. While risk factors such as obesity, smoking, diabetes mellitus, twin pregnancy, multiparity, advanced age of the mother, in-vitro fertilisation (IVF) are well known, the exact pathophysiology of preeclampsia has still not been precisely clarified. Therefore, specific treatment options are limited, also in part due to the challenge of performing clinical trials in pregnant women. The present review provides an overview of the current state of knowledge and summarises treatment strategies and therapy options.</p>
	]]></content:encoded>

	<dc:title>Hypertension in Pregnancy</dc:title>
			<dc:creator>Viola Schaefer</dc:creator>
			<dc:creator>Denise Hilfiker-Kleiner</dc:creator>
			<dc:creator>Corinna Keil</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02272</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-05-17</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-05-17</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>80</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02272</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/3/80</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/3/96">

	<title>Cardiovascular Medicine, Vol. 26, Pages 96: Sex Differences in Type 2 Diabetes</title>
	<link>https://www.mdpi.com/1664-204X/26/3/96</link>
	<description>The influence of sex–considered to be the biological differences between women and men– and gender–considered to be sociologically constructed differences based on membership in one of the two sex categories–appears to be particularly important for noncommunicable diseases such as type 2 diabetes (T2D) and obesity. Many T2D risk factors are behavioural and greatly, but not only, influenced by gender-related determinants, making them modifiable factors. In this review, we focus on sex-related biological differences in the prevalence of diabetes and its biological risk factors, such as obesity, fat distribution, metabolic syndrome and glucose homoeostasis, with a particular interest in the influence of menopause and pregnancy. Globally, men have had a higher prevalence of T2D than women with regional, socioeconomic and age-related variations. Overall, women tend to be more protected from cardiometabolic diseases before menopause than men. However, hormonal variation over the course of life, particularly during menopause, modifies these risks. Similarly to T2D, there are differences in the prevalence of obesity between women and men that change during the lifespan. The link between obesity and T2D seems to be stronger in women compared to men. Various hormones have an impact on glycaemic levels and on body fat and their concentrations and effect on metabolic parameters can differ by sex. Understanding and acknowledging sex-related differences in T2D and its risk factors is important to improve health research, lead to better clinical care, more suitable preventive policies and programs for both women and men.</description>
	<pubDate>2023-05-17</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 96: Sex Differences in Type 2 Diabetes</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/3/96">doi: 10.4414/cvm.2023.02273</a></p>
	<p>Authors:
		Paco Estoppey
		Carole Clair
		Diane Auderset
		Jardena Puder
		</p>
	<p>The influence of sex–considered to be the biological differences between women and men– and gender–considered to be sociologically constructed differences based on membership in one of the two sex categories–appears to be particularly important for noncommunicable diseases such as type 2 diabetes (T2D) and obesity. Many T2D risk factors are behavioural and greatly, but not only, influenced by gender-related determinants, making them modifiable factors. In this review, we focus on sex-related biological differences in the prevalence of diabetes and its biological risk factors, such as obesity, fat distribution, metabolic syndrome and glucose homoeostasis, with a particular interest in the influence of menopause and pregnancy. Globally, men have had a higher prevalence of T2D than women with regional, socioeconomic and age-related variations. Overall, women tend to be more protected from cardiometabolic diseases before menopause than men. However, hormonal variation over the course of life, particularly during menopause, modifies these risks. Similarly to T2D, there are differences in the prevalence of obesity between women and men that change during the lifespan. The link between obesity and T2D seems to be stronger in women compared to men. Various hormones have an impact on glycaemic levels and on body fat and their concentrations and effect on metabolic parameters can differ by sex. Understanding and acknowledging sex-related differences in T2D and its risk factors is important to improve health research, lead to better clinical care, more suitable preventive policies and programs for both women and men.</p>
	]]></content:encoded>

	<dc:title>Sex Differences in Type 2 Diabetes</dc:title>
			<dc:creator>Paco Estoppey</dc:creator>
			<dc:creator>Carole Clair</dc:creator>
			<dc:creator>Diane Auderset</dc:creator>
			<dc:creator>Jardena Puder</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02273</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-05-17</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-05-17</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>96</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02273</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/3/96</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/3/88">

	<title>Cardiovascular Medicine, Vol. 26, Pages 88: Impact of Sex and Gender on Heart Failure</title>
	<link>https://www.mdpi.com/1664-204X/26/3/88</link>
	<description>The prevalence of heart failure (HF) is increasing mainly due to population aging. There are important biological (sex) and sociocultural (gender) differences in epidemiology, pathophysiology, phenotype, prognosis and treatment of HF between women and men. While the overall lifetime risk of HF is similar between men and women, women with HF are older, have more comorbidities and a higher incidence of heart failure with preserved ejection fraction (HFpEF) than men. Men instead present a predisposition to the development of heart failure with reduced ejection fraction (HFrEF) due to their higher incidence of coronary artery disease. Sex differences are also notable in the penetrance of genetic cardiomyopathies, HF risk factors as well as in sex-specific conditions such as peripartum cardiomyopathy (PPCM), cancer treatment-induced cardiomyopathy and Takotsubo cardiomyopathy. Although women with HF have a better age-adjusted prognosis than men they experience a worse quality of life. Underpinning current sex disparities in HF, HF treatment is limited by a profound underrepresentation of women in clinical trials, which has resulted in a lesser understanding of disease behaviour in female patients and in treatment guidelines that are predominantly based on male-derived data. In addition, a full understanding of the impact of sociocultural gender on HF management and disease course is lacking. This review outlines the key sex differences with respect to clinical characteristics, pathophysiology and therapeutic responses to HF treatments. Finally, we address existing knowledge gaps in sex-specific mechanisms, optimal drug doses for women and sex-specific criteria for device therapy and heart transplantation.</description>
	<pubDate>2023-05-17</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 88: Impact of Sex and Gender on Heart Failure</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/3/88">doi: 10.4414/cvm.2023.02274</a></p>
	<p>Authors:
		Alessia Delco
		Angela Portmann
		Nidaa Mikail
		Alexia Rossi
		Ahmed Haider
		Susan Bengs
		Catherine Gebhard
		</p>
	<p>The prevalence of heart failure (HF) is increasing mainly due to population aging. There are important biological (sex) and sociocultural (gender) differences in epidemiology, pathophysiology, phenotype, prognosis and treatment of HF between women and men. While the overall lifetime risk of HF is similar between men and women, women with HF are older, have more comorbidities and a higher incidence of heart failure with preserved ejection fraction (HFpEF) than men. Men instead present a predisposition to the development of heart failure with reduced ejection fraction (HFrEF) due to their higher incidence of coronary artery disease. Sex differences are also notable in the penetrance of genetic cardiomyopathies, HF risk factors as well as in sex-specific conditions such as peripartum cardiomyopathy (PPCM), cancer treatment-induced cardiomyopathy and Takotsubo cardiomyopathy. Although women with HF have a better age-adjusted prognosis than men they experience a worse quality of life. Underpinning current sex disparities in HF, HF treatment is limited by a profound underrepresentation of women in clinical trials, which has resulted in a lesser understanding of disease behaviour in female patients and in treatment guidelines that are predominantly based on male-derived data. In addition, a full understanding of the impact of sociocultural gender on HF management and disease course is lacking. This review outlines the key sex differences with respect to clinical characteristics, pathophysiology and therapeutic responses to HF treatments. Finally, we address existing knowledge gaps in sex-specific mechanisms, optimal drug doses for women and sex-specific criteria for device therapy and heart transplantation.</p>
	]]></content:encoded>

	<dc:title>Impact of Sex and Gender on Heart Failure</dc:title>
			<dc:creator>Alessia Delco</dc:creator>
			<dc:creator>Angela Portmann</dc:creator>
			<dc:creator>Nidaa Mikail</dc:creator>
			<dc:creator>Alexia Rossi</dc:creator>
			<dc:creator>Ahmed Haider</dc:creator>
			<dc:creator>Susan Bengs</dc:creator>
			<dc:creator>Catherine Gebhard</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02274</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-05-17</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-05-17</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>88</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02274</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/3/88</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/3/100">

	<title>Cardiovascular Medicine, Vol. 26, Pages 100: Breast Cancer and Cardiovascular Rsk</title>
	<link>https://www.mdpi.com/1664-204X/26/3/100</link>
	<description>With the continuous improvement of therapies against breast cancer, the long-term onset of cardiovascular disease (CVD) is becoming increasingly relevant for both cardiologists and oncologists. Not only CVD arises from known cardiac side effects of several anti-cancer therapies, but cancer itself seems to promote CVD. On the other hand, there is increasing evidence that CVDs such as myocardial infarction and heart failure predispose to future development of cancer. The fast-developing field of cardio-oncology aims to characterise cancer patients in order to implement effective tools for surveillance and prevention of cardiovascular adverse events and to raise awareness for the increased cancer incidence in patients with CVD. The aim of this review is to highlight cardiovascular side effects and toxicities of some of the most important breast cancer therapies and to provide an overview of what is known on the complex interplay between CVD and breast cancer.</description>
	<pubDate>2023-05-17</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 100: Breast Cancer and Cardiovascular Rsk</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/3/100">doi: 10.4414/cvm.2023.02275</a></p>
	<p>Authors:
		Valentina Rossi
		Anton Oseledchyk
		Gabriela Kuster
		</p>
	<p>With the continuous improvement of therapies against breast cancer, the long-term onset of cardiovascular disease (CVD) is becoming increasingly relevant for both cardiologists and oncologists. Not only CVD arises from known cardiac side effects of several anti-cancer therapies, but cancer itself seems to promote CVD. On the other hand, there is increasing evidence that CVDs such as myocardial infarction and heart failure predispose to future development of cancer. The fast-developing field of cardio-oncology aims to characterise cancer patients in order to implement effective tools for surveillance and prevention of cardiovascular adverse events and to raise awareness for the increased cancer incidence in patients with CVD. The aim of this review is to highlight cardiovascular side effects and toxicities of some of the most important breast cancer therapies and to provide an overview of what is known on the complex interplay between CVD and breast cancer.</p>
	]]></content:encoded>

	<dc:title>Breast Cancer and Cardiovascular Rsk</dc:title>
			<dc:creator>Valentina Rossi</dc:creator>
			<dc:creator>Anton Oseledchyk</dc:creator>
			<dc:creator>Gabriela Kuster</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02275</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-05-17</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-05-17</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>100</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02275</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/3/100</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/3/70">

	<title>Cardiovascular Medicine, Vol. 26, Pages 70: Albrecht von Haller Awards of the Swiss Heart Foundation 2023</title>
	<link>https://www.mdpi.com/1664-204X/26/3/70</link>
	<description>Albrecht von Haller [...]</description>
	<pubDate>2023-05-17</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 70: Albrecht von Haller Awards of the Swiss Heart Foundation 2023</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/3/70">doi: 10.4414/cvm.2023.02276</a></p>
	<p>Authors:
		Thomas Lüscher
		Rolf Kaiser
		Stefan Osswald
		</p>
	<p>Albrecht von Haller [...]</p>
	]]></content:encoded>

	<dc:title>Albrecht von Haller Awards of the Swiss Heart Foundation 2023</dc:title>
			<dc:creator>Thomas Lüscher</dc:creator>
			<dc:creator>Rolf Kaiser</dc:creator>
			<dc:creator>Stefan Osswald</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02276</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-05-17</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-05-17</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>70</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02276</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/3/70</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/3/67">

	<title>Cardiovascular Medicine, Vol. 26, Pages 67: Sex and Cardiovascular Disease</title>
	<link>https://www.mdpi.com/1664-204X/26/3/67</link>
	<description>For many years, cardiovascular disease was considered a male disease.[...]</description>
	<pubDate>2023-05-17</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 67: Sex and Cardiovascular Disease</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/3/67">doi: 10.4414/cvm.2023.02284</a></p>
	<p>Authors:
		Thomas Lüscher
		Andreas Flammer
		Gabriela Kuster
		</p>
	<p>For many years, cardiovascular disease was considered a male disease.[...]</p>
	]]></content:encoded>

	<dc:title>Sex and Cardiovascular Disease</dc:title>
			<dc:creator>Thomas Lüscher</dc:creator>
			<dc:creator>Andreas Flammer</dc:creator>
			<dc:creator>Gabriela Kuster</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02284</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-05-17</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-05-17</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>67</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02284</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/3/67</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/2/64">

	<title>Cardiovascular Medicine, Vol. 26, Pages 64: Re-Entrant Atrial Tachycardia in a Patient with Arrhythmogenic Right Ventricular Cardiomyopathy</title>
	<link>https://www.mdpi.com/1664-204X/26/2/64</link>
	<description>Although typical atrial flutter and atrial fibrillation are not uncommon in patients with arrhythmogenic right ventricular cardiomyopathy (ARVC), there is limited information on atrial tachycardia in this population. A 59-year-old man with a diagnosis of definite ARVC according to the 2010 Task Force Criteria without overt left ventricular involvement presented with recurrent palpitations. The surface 12-lead electrocardiogram raised the suspicion of atrial tachycardia. The patient had no history of cardiac surgery or cardiac ablation. During tachycardia passive activation of the right atrium was visible through invasive electroanatomical mapping indicating a left atrial origin of the tachycardia. High-density mapping of the left atrium confirmed a re-entrant tachycardia with a figure-of-eight activation pattern originating from a small scar in the anterior left atrial wall. Radiofrequency catheter ablation targeting the area of slow conduction in this area terminated the tachycardia and rendered it non-inducible.</description>
	<pubDate>2023-03-22</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 64: Re-Entrant Atrial Tachycardia in a Patient with Arrhythmogenic Right Ventricular Cardiomyopathy</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/2/64">doi: 10.4414/cvm.2023.02207</a></p>
	<p>Authors:
		Fu Guan
		Firat Duru
		Ardan Saguner
		</p>
	<p>Although typical atrial flutter and atrial fibrillation are not uncommon in patients with arrhythmogenic right ventricular cardiomyopathy (ARVC), there is limited information on atrial tachycardia in this population. A 59-year-old man with a diagnosis of definite ARVC according to the 2010 Task Force Criteria without overt left ventricular involvement presented with recurrent palpitations. The surface 12-lead electrocardiogram raised the suspicion of atrial tachycardia. The patient had no history of cardiac surgery or cardiac ablation. During tachycardia passive activation of the right atrium was visible through invasive electroanatomical mapping indicating a left atrial origin of the tachycardia. High-density mapping of the left atrium confirmed a re-entrant tachycardia with a figure-of-eight activation pattern originating from a small scar in the anterior left atrial wall. Radiofrequency catheter ablation targeting the area of slow conduction in this area terminated the tachycardia and rendered it non-inducible.</p>
	]]></content:encoded>

	<dc:title>Re-Entrant Atrial Tachycardia in a Patient with Arrhythmogenic Right Ventricular Cardiomyopathy</dc:title>
			<dc:creator>Fu Guan</dc:creator>
			<dc:creator>Firat Duru</dc:creator>
			<dc:creator>Ardan Saguner</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02207</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-03-22</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-03-22</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>64</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02207</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/2/64</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/2/50">

	<title>Cardiovascular Medicine, Vol. 26, Pages 50: Paediatric Pulmonary Hypertension</title>
	<link>https://www.mdpi.com/1664-204X/26/2/50</link>
	<description>Introduction. Children can present at any age with pulmonary hypertension [...]</description>
	<pubDate>2023-03-22</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 50: Paediatric Pulmonary Hypertension</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/2/50">doi: 10.4414/cvm.2023.02212</a></p>
	<p>Authors:
		Julie Wacker
		Maurice Beghetti
		</p>
	<p>Introduction. Children can present at any age with pulmonary hypertension [...]</p>
	]]></content:encoded>

	<dc:title>Paediatric Pulmonary Hypertension</dc:title>
			<dc:creator>Julie Wacker</dc:creator>
			<dc:creator>Maurice Beghetti</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02212</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-03-22</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-03-22</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>50</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02212</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/2/50</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/2/43">

	<title>Cardiovascular Medicine, Vol. 26, Pages 43: Subclinical Atrial Fibrillation in Implantable and Wearable Devices—A Short Update</title>
	<link>https://www.mdpi.com/1664-204X/26/2/43</link>
	<description>Atrial fibrillation (AF) is electrically defined as an uncoordinated[...]</description>
	<pubDate>2023-03-22</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 43: Subclinical Atrial Fibrillation in Implantable and Wearable Devices—A Short Update</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/2/43">doi: 10.4414/cvm.2023.02219</a></p>
	<p>Authors:
		Alexander Breitenstein
		</p>
	<p>Atrial fibrillation (AF) is electrically defined as an uncoordinated[...]</p>
	]]></content:encoded>

	<dc:title>Subclinical Atrial Fibrillation in Implantable and Wearable Devices—A Short Update</dc:title>
			<dc:creator>Alexander Breitenstein</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02219</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-03-22</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-03-22</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>43</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02219</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/2/43</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/2/38">

	<title>Cardiovascular Medicine, Vol. 26, Pages 38: Impact of Diet on Disease Prevention and Progression in Heart Failure Patients: What&#039;s the Evidence?</title>
	<link>https://www.mdpi.com/1664-204X/26/2/38</link>
	<description>Similar to other developed countries...</description>
	<pubDate>2023-03-22</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 38: Impact of Diet on Disease Prevention and Progression in Heart Failure Patients: What&#039;s the Evidence?</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/2/38">doi: 10.4414/cvm.2023.02226</a></p>
	<p>Authors:
		David Faeh
		</p>
	<p>Similar to other developed countries...</p>
	]]></content:encoded>

	<dc:title>Impact of Diet on Disease Prevention and Progression in Heart Failure Patients: What&#039;s the Evidence?</dc:title>
			<dc:creator>David Faeh</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02226</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-03-22</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-03-22</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>38</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02226</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/2/38</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/2/60">

	<title>Cardiovascular Medicine, Vol. 26, Pages 60: Management of a Recurrent Pregnancy-Related Incessant Adenosine-Sensitive Atrial Tachycardia</title>
	<link>https://www.mdpi.com/1664-204X/26/2/60</link>
	<description>A 27-year-old pregnant woman (29th week) reported palpitations, dizziness and exertional dysp-noea. The heart rate was 130 bpm at rest, up to 180 bpm during mild exertion, without haemody-namic compromise. The electrocardiogram (ECG) showed atrial tachycardia. An adenosine inter-mittent interruption of the atrial tachycardia was observed. Metoprolol combined with flecainide controlled the ventricular rate to 80–85 bpm followed by conversion to sinus rhythm. The patient stayed asymptomatic until a second pregnancy, when the same atrial tachycardia recurred. Symptoms were controlled by combining metoprolol and flecainide at an earlier stage.</description>
	<pubDate>2023-03-22</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 60: Management of a Recurrent Pregnancy-Related Incessant Adenosine-Sensitive Atrial Tachycardia</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/2/60">doi: 10.4414/cvm.2023.02255</a></p>
	<p>Authors:
		Albana Thartori
		Francesca Usardi
		Andrea Menafoglio
		François Regoli
		</p>
	<p>A 27-year-old pregnant woman (29th week) reported palpitations, dizziness and exertional dysp-noea. The heart rate was 130 bpm at rest, up to 180 bpm during mild exertion, without haemody-namic compromise. The electrocardiogram (ECG) showed atrial tachycardia. An adenosine inter-mittent interruption of the atrial tachycardia was observed. Metoprolol combined with flecainide controlled the ventricular rate to 80–85 bpm followed by conversion to sinus rhythm. The patient stayed asymptomatic until a second pregnancy, when the same atrial tachycardia recurred. Symptoms were controlled by combining metoprolol and flecainide at an earlier stage.</p>
	]]></content:encoded>

	<dc:title>Management of a Recurrent Pregnancy-Related Incessant Adenosine-Sensitive Atrial Tachycardia</dc:title>
			<dc:creator>Albana Thartori</dc:creator>
			<dc:creator>Francesca Usardi</dc:creator>
			<dc:creator>Andrea Menafoglio</dc:creator>
			<dc:creator>François Regoli</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02255</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-03-22</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-03-22</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Case Report</prism:section>
	<prism:startingPage>60</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02255</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/2/60</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/2/46">

	<title>Cardiovascular Medicine, Vol. 26, Pages 46: Where and How to Pace in 2023?</title>
	<link>https://www.mdpi.com/1664-204X/26/2/46</link>
	<description>Introduction. In the past decade, cardiac pacing techniques evolved significantly – resulting in a large vari ety of available approaches that are used to tai lor stimulation individually to the patient’s needs [...]</description>
	<pubDate>2023-03-22</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 46: Where and How to Pace in 2023?</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/2/46">doi: 10.4414/cvm.2023.02256</a></p>
	<p>Authors:
		Fabian Noti
		Andreas Haeberlin
		</p>
	<p>Introduction. In the past decade, cardiac pacing techniques evolved significantly – resulting in a large vari ety of available approaches that are used to tai lor stimulation individually to the patient’s needs [...]</p>
	]]></content:encoded>

	<dc:title>Where and How to Pace in 2023?</dc:title>
			<dc:creator>Fabian Noti</dc:creator>
			<dc:creator>Andreas Haeberlin</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02256</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-03-22</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-03-22</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>46</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02256</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/2/46</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/2/35">

	<title>Cardiovascular Medicine, Vol. 26, Pages 35: From Diet to Pacing and Paedi­atric Pulmonary Hypertension</title>
	<link>https://www.mdpi.com/1664-204X/26/2/35</link>
	<description>We welcome you to this issue of Cardiovascular Medicine, which once again provides a broad overview of cardiovascular medicine with outstanding review articles in heart failure, electrophysiology, and paediatric cardiology [...]</description>
	<pubDate>2023-03-22</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 35: From Diet to Pacing and Paedi­atric Pulmonary Hypertension</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/2/35">doi: 10.4414/cvm.2023.02277</a></p>
	<p>Authors:
		Luca Koechlin
		Peter Matt
		</p>
	<p>We welcome you to this issue of Cardiovascular Medicine, which once again provides a broad overview of cardiovascular medicine with outstanding review articles in heart failure, electrophysiology, and paediatric cardiology [...]</p>
	]]></content:encoded>

	<dc:title>From Diet to Pacing and Paedi­atric Pulmonary Hypertension</dc:title>
			<dc:creator>Luca Koechlin</dc:creator>
			<dc:creator>Peter Matt</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02277</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-03-22</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-03-22</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>35</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02277</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/2/35</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/1/6">

	<title>Cardiovascular Medicine, Vol. 26, Pages 6: W. and L. Rutishauser Fund - Academic Career Advancement Travel Fellowship</title>
	<link>https://www.mdpi.com/1664-204X/26/1/6</link>
	<description>The Swiss Heart Foundation is pleased to announce the «W. und L. Rutishauser Fund» [...]</description>
	<pubDate>2023-01-25</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 6: W. and L. Rutishauser Fund - Academic Career Advancement Travel Fellowship</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/1/6">doi: 10.4414/cvm.2023.02168</a></p>
	<p>Authors:
		Franziska Hiltpold
		</p>
	<p>The Swiss Heart Foundation is pleased to announce the «W. und L. Rutishauser Fund» [...]</p>
	]]></content:encoded>

	<dc:title>W. and L. Rutishauser Fund - Academic Career Advancement Travel Fellowship</dc:title>
			<dc:creator>Franziska Hiltpold</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02168</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-01-25</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-01-25</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>6</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02168</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/1/6</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/1/18">

	<title>Cardiovascular Medicine, Vol. 26, Pages 18: Colchicine Revival?</title>
	<link>https://www.mdpi.com/1664-204X/26/1/18</link>
	<description>Colchicine is an alkaloid extracted from Colchicum plants (Colchicum autumnale, Herbstzeitlose)[...]</description>
	<pubDate>2023-01-25</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 18: Colchicine Revival?</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/1/18">doi: 10.4414/cvm.2023.02220</a></p>
	<p>Authors:
		Matthias Hermann
		</p>
	<p>Colchicine is an alkaloid extracted from Colchicum plants (Colchicum autumnale, Herbstzeitlose)[...]</p>
	]]></content:encoded>

	<dc:title>Colchicine Revival?</dc:title>
			<dc:creator>Matthias Hermann</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02220</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-01-25</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-01-25</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>18</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02220</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/1/18</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/1/34">

	<title>Cardiovascular Medicine, Vol. 26, Pages 34: Isolated Native Pulmonary Valve Endocarditis</title>
	<link>https://www.mdpi.com/1664-204X/26/1/34</link>
	<description>A 74-year-old male patient presented with malaise, fever, chills, and palpitations for the past five days[...]</description>
	<pubDate>2023-01-25</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 34: Isolated Native Pulmonary Valve Endocarditis</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/1/34">doi: 10.4414/cvm.2023.02229</a></p>
	<p>Authors:
		Oskar Galuszka
		Richard Kobza
		Simon Stämpfli
		</p>
	<p>A 74-year-old male patient presented with malaise, fever, chills, and palpitations for the past five days[...]</p>
	]]></content:encoded>

	<dc:title>Isolated Native Pulmonary Valve Endocarditis</dc:title>
			<dc:creator>Oskar Galuszka</dc:creator>
			<dc:creator>Richard Kobza</dc:creator>
			<dc:creator>Simon Stämpfli</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02229</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-01-25</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-01-25</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Interesting Images</prism:section>
	<prism:startingPage>34</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02229</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/1/34</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/1/10">

	<title>Cardiovascular Medicine, Vol. 26, Pages 10: Die Evaluation von Forschern und Universitäten: Möglichkeiten und Grenzen</title>
	<link>https://www.mdpi.com/1664-204X/26/1/10</link>
	<description>Jede Tätigkeit muss sich heute einer Überprüfung stellen, so auch die For schung [...]</description>
	<pubDate>2023-01-25</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 10: Die Evaluation von Forschern und Universitäten: Möglichkeiten und Grenzen</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/1/10">doi: 10.4414/cvm.2023.02266</a></p>
	<p>Authors:
		Thomas Lüscher
		</p>
	<p>Jede Tätigkeit muss sich heute einer Überprüfung stellen, so auch die For schung [...]</p>
	]]></content:encoded>

	<dc:title>Die Evaluation von Forschern und Universitäten: Möglichkeiten und Grenzen</dc:title>
			<dc:creator>Thomas Lüscher</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02266</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-01-25</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-01-25</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>10</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02266</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/1/10</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/26/1/3">

	<title>Cardiovascular Medicine, Vol. 26, Pages 3: Cardiovascular Medicine—Official Journal of the Swiss Society of Cardiac Surgery</title>
	<link>https://www.mdpi.com/1664-204X/26/1/3</link>
	<description>Cardiovascular Medicine is one of the most widely read medical journals in Switzerland [...]</description>
	<pubDate>2023-01-25</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 26, Pages 3: Cardiovascular Medicine—Official Journal of the Swiss Society of Cardiac Surgery</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/26/1/3">doi: 10.4414/cvm.2023.02268</a></p>
	<p>Authors:
		Peter Matt
		</p>
	<p>Cardiovascular Medicine is one of the most widely read medical journals in Switzerland [...]</p>
	]]></content:encoded>

	<dc:title>Cardiovascular Medicine—Official Journal of the Swiss Society of Cardiac Surgery</dc:title>
			<dc:creator>Peter Matt</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2023.02268</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2023-01-25</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2023-01-25</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>3</prism:startingPage>
		<prism:doi>10.4414/cvm.2023.02268</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/26/1/3</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/1664-204X/24/1/w10047">

	<title>Cardiovascular Medicine, Vol. 24, Pages w10047: ICD Insertion in Previously Undiagnosed Left Brachiocephalic Vein Obstruction</title>
	<link>https://www.mdpi.com/1664-204X/24/1/w10047</link>
	<description>A 43-year-old male underwent implantable cardioverter defibrillator (ICD) insertion, 8 months after an out-of-hospital cardiac arrest following acute ST segment-elevation myocardial infarction [...]</description>
	<pubDate>2022-11-23</pubDate>

	<content:encoded><![CDATA[
	<p><b>Cardiovascular Medicine, Vol. 24, Pages w10047: ICD Insertion in Previously Undiagnosed Left Brachiocephalic Vein Obstruction</b></p>
	<p>Cardiovascular Medicine <a href="https://www.mdpi.com/1664-204X/24/1/w10047">doi: 10.4414/cvm.2021.02139</a></p>
	<p>Authors:
		Lukas Padraig O Brien
		Anthony Buckley
		Joseph Galvin
		</p>
	<p>A 43-year-old male underwent implantable cardioverter defibrillator (ICD) insertion, 8 months after an out-of-hospital cardiac arrest following acute ST segment-elevation myocardial infarction [...]</p>
	]]></content:encoded>

	<dc:title>ICD Insertion in Previously Undiagnosed Left Brachiocephalic Vein Obstruction</dc:title>
			<dc:creator>Lukas Padraig O Brien</dc:creator>
			<dc:creator>Anthony Buckley</dc:creator>
			<dc:creator>Joseph Galvin</dc:creator>
		<dc:identifier>doi: 10.4414/cvm.2021.02139</dc:identifier>
	<dc:source>Cardiovascular Medicine</dc:source>
	<dc:date>2022-11-23</dc:date>

	<prism:publicationName>Cardiovascular Medicine</prism:publicationName>
	<prism:publicationDate>2022-11-23</prism:publicationDate>
	<prism:volume>24</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Interesting Images</prism:section>
	<prism:startingPage>w10047</prism:startingPage>
		<prism:doi>10.4414/cvm.2021.02139</prism:doi>
	<prism:url>https://www.mdpi.com/1664-204X/24/1/w10047</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
    
<cc:License rdf:about="https://creativecommons.org/licenses/by/4.0/">
	<cc:permits rdf:resource="https://creativecommons.org/ns#Reproduction" />
	<cc:permits rdf:resource="https://creativecommons.org/ns#Distribution" />
	<cc:permits rdf:resource="https://creativecommons.org/ns#DerivativeWorks" />
</cc:License>

</rdf:RDF>
