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Review

From Fluid Responsiveness to Prognosis: The Emerging Role of Point-of-Care Echocardiography in Sepsis

by
Andrea Piccioni
1,*,
Gloria Rozzi
2,*,
Giacomo Spaziani
2,
Michela Novelli
2,
Mariella Fuorlo
1,
Marcello Candelli
1,
Giulia Pignataro
1,
Luca Santarelli
1,
Marcello Covino
1,2,
Antonio Gasbarrini
3 and
Francesco Franceschi
1,2
1
Department of Emergency Medicine, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, 00168 Rome, Italy
2
Department of Emergency Medicine, Università Cattolica del Sacro Cuore of Rome, 00168 Rome, Italy
3
Department of Translational Medicine and Surgery, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Università Cattolica del Sacro Cuore di Roma, 00168 Roma, Italy
*
Authors to whom correspondence should be addressed.
Diagnostics 2025, 15(20), 2612; https://doi.org/10.3390/diagnostics15202612
Submission received: 10 September 2025 / Revised: 29 September 2025 / Accepted: 9 October 2025 / Published: 16 October 2025
(This article belongs to the Section Point-of-Care Diagnostics and Devices)

Abstract

Sepsis is a life-threatening condition that requires early recognition and intervention to improve patient outcomes. Optimizing hemodynamic management is crucial, and clinicians must utilize all available tools to guide therapy effectively. Echocardiography is a rapid, non-invasive, and repeatable method that has emerged as a valuable tool in the management of septic patients. Studying its role can provide insights into both therapeutic guidance and prognostic assessment. The primary aim of this review is to highlight the importance of echocardiography in the hemodynamic management of patients with sepsis. The secondary objective is to assess its prognostic value, as echocardiography can inform both the immediate management of critically ill patients and their overall prognosis. A narrative review of the literature published in the last 15 years was conducted using PubMed, and references were managed with Mendeley. Articles focusing on adult and pediatric patients, as well as relevant animal studies, which evaluated echocardiographic assessment of cardiac function, fluid responsiveness, or hemodynamic management were included. Multiple studies demonstrate that echocardiography is a reliable, non-invasive, and easily repeatable tool for assessing fluid responsiveness in septic patients. It allows for dynamic monitoring of stroke volume, VTI, and other hemodynamic parameters, supporting tailored fluid and vasoactive therapy. Additionally, echocardiography provides prognostic insights, with right ventricular dysfunction emerging as a strong predictor of increased mortality. Other parameters, including global longitudinal strain and left ventricular diastolic function, further contribute to risk stratification. Echocardiography is an indispensable tool in the management of sepsis, offering both real-time guidance for hemodynamic optimization and valuable prognostic information. Its routine use can enhance personalized care and improve clinical outcomes in critically ill septic patients.

1. Introduction

Sepsis is a life-threatening organ dysfunction resulting from a dysregulated host response to infection [1,2]. Its incidence and severity are higher in the elderly, males, and certain racial and ethnic groups, and are further amplified by socioeconomic disadvantage, geographic factors, and comorbidities [3].
Early recognition remains challenging, making sepsis a leading cause of death in emergency departments [4,5].
Diagnosis is complex. Clinicians rely on scores, such as qSOFA, SIRS, or EWS [6], alongside biomarkers like procalcitonin [7] and presepsin [8,9].
Clinical presentations vary as some patients show classic infection signs, while others—particularly the elderly or immunocompromised—display subtle neurological or systemic symptoms [10]. Septic shock represents the extreme manifestation.
Sepsis triggers a dysregulated inflammatory response, disrupting endothelial, hormonal, metabolic, and immune pathways. These changes drive multi-organ dysfunction, affecting cardiovascular, hematologic, neurological, pulmonary, hepatic, and renal systems [11].
Cardiovascular compromise arises primarily from vasoplegia, relative or absolute hypovolemia, and septic myocardial dysfunction [12].
Endothelial dysfunction mediates inflammation and coagulation via nitric oxide, prostacyclins, and cytokines (e.g., TNF-α, IL-1, IL-6), impairing alpha-adrenergic-receptor sensitivity and vasoconstrictive responses [13].
Vasoplegia promotes relative hypovolemia through peripheral vasodilation, increased capillary permeability, and plasma redistribution, reducing effective intravascular volume and necessitating aggressive fluid therapy [14,15,16].
Myocardial dysfunction, characterized by impaired contractility and often associated with ischemia, contributes significantly to multi-organ failure, driven by cytokine excess, oxidative stress, acidosis, and altered cardiac metabolism [17].
Clinically, it manifests as reduced ejection fraction, elevated ventricular filling pressures, and diminished responsiveness to inotropes.
In this context, point-of-care echocardiography (POC-Echo) has emerged as a rapid bedside tool for real-time assessment of cardiac function. It enables tailored hemodynamic management by guiding fluid resuscitation, vasopressor, and inotropic therapy. Furthermore, echocardiographic parameters provide prognostic insights, helping clinicians identify patients at higher risk of adverse outcomes [18,19].
Given the complexity of sepsis-induced cardiovascular dysfunction and the need for timely intervention, this review explores the role of POC-Echo in guiding treatment decisions and supporting prognostic evaluation in critically ill patients.

2. Materials and Methods

This narrative review was conducted by searching PubMed for articles published in the last 15 years using keywords such as “echocardiography and sepsis,” “sepsis and fluid responsiveness,” “stroke volume and sepsis,” “GLS and sepsis,” “echocardiography, prognosis, and sepsis,” and “septic cardiomyopathy.” Studies were initially screened based on titles and abstracts, and full texts were reviewed when relevant. Articles focusing on adult and pediatric patients, as well as animal studies evaluating echocardiographic assessment of cardiac function, fluid responsiveness, or hemodynamic management, were included. Studies published before 2010 were excluded. References were organized using Mendeley, and key data extracted included echocardiographic parameters, fluid management strategies, hemodynamic outcomes, and clinical endpoints such as mortality and vasopressor use.

3. Results

3.1. Echocardiography-Guided Hemodynamic Management in Sepsis

Echocardiography is a fast, non-invasive, and versatile tool for managing hemodynamics in cases of sepsis and septic shock. It enables continuous monitoring of cardiac function and volume status, helping to identify specific patterns such as sepsis-induced myocardial dysfunction, hypovolemia, or right ventricular alterations—conditions that may not be immediately evident using traditional clinical parameters. The use of echocardiography has been linked to a significant reduction in mortality at 28 days [20], a decrease in the volume of fluids administered, and a quicker discontinuation of vasopressors [21]. Additionally, in patients with sepsis due to trauma, echocardiography-guided monitoring demonstrated a reduction in mortality, with a hazard ratio of approximately 0.83 (95% CI 0.73–0.95) [20].
  • Preload and fluid responsiveness
    • Inferior vena cava (IVC): Measurement of diameter and respiratory variations is useful for estimating intravascular volume and the probability of response to fluids.
      Ultrasound-driven fluid resuscitation strategies, particularly those that involve measuring the inferior vena cava (IVC) and conducting passive leg lift tests, have shown effectiveness in reducing the volume of fluids infused, shortening hospital stays, and decreasing the number of days spent in intensive care [22]. However, not all studies indicate a clear benefit concerning mortality rates. For example, a randomized controlled trial (RCT) found that respiratory variation in the diameter of the IVC did not improve survival at 30 days, although it did lead to a decrease in the volume of fluids administered [23,24]. The collapse index of the cava vein is actually a good indicator of the end-diastolic volume index during fluid resuscitation [25]. Nonetheless, ultrasound-guided fluid resuscitation is a useful and practical approach for patients with septic shock during the first seven days after admission. This method is associated with reduced early mortality, lower fluid administration, and a decreased incidence of pulmonary oedema compared to early goal-directed therapy [26].
      In summary, echocardiography is a crucial tool for personalized hemodynamic management, helping refine the administration of fluids and vasoactive support by using IVC parameters.
    • Stroke volume variation (SVV): Change in systolic volume indicates relative hypovolemia and predicts response to fluid therapy. The fluid challenge involves rapidly administering 250–500 mL of fluid in less than 30 min. A 15% increase in stroke volume indicates fluid responsiveness [27].
      During sepsis and septic shock, stroke volume (SV) plays a crucial role in evaluating dynamic hemodynamics and fluid responsiveness, surpassing the limitations of static indices such as central pressure [28].
      SV is a reliable dynamic parameter that allows for the assessment of fluid responsiveness over time. A French observational study revealed that 51.3% of patients who initially respond to fluid therapy maintain this response 30 min after the start of fluid infusion, while only 41.3% exhibit a transient response. This insight is crucial for enabling effective therapy that lasts over time, ultimately enhancing patient outcomes [29].
      A narrative review highlights that, according to the Frank–Starling principle, increasing preload raises SV until optimum volume is reached. Beyond this point, additional fluid infusion may be harmful, leading to fluid overload, tissue oedema, and strain on already impaired cardiac function [30].
      Clinical studies demonstrate that dynamic measures, such as SVV, more accurately predict hemodynamic responses compared to static indices, achieving notable performance in assessing fluid responsiveness, even in ventilated patients. In cases where a septic patient requires mechanical ventilation, these parameters can be utilized to better manage the patient’s hemodynamic and enhance their fluid responsiveness to therapy [31].
      A meta-analysis involving ventilated patients with low tidal volumes (≤8 mL/kg) confirms that SVV has an area under the curve (AUC) of approximately 0.90 for predicting fluid responsiveness. This is further supported by dynamic tests such as the end-expiratory occlusion test and tidal volume challenge, both of which have an AUC of around 0.92 [32].
      An observational study indicated that septic patients who showed an improvement in SV during treatment received, on average, about 350 mL more fluids than those who did not show improvement (1241 mL vs. 893 mL; p = 0.018). This suggests that adequate volume expansion may be essential for increasing SV and, consequently, enhancing organ perfusion. Therefore, monitoring SV may serve as an excellent parameter for determining the appropriate volume of fluids to be administered to a patient for achieving genuine improvement [33].
  • Cardiac output and perfusion
    • LVOT VTI (Velocity Time Integral of the left ventricular outflow pathway) is a valuable tool for calculating cardiac output and evaluating tissue perfusion.
    • The Velocity Time Integral (VTI), measured at the left ventricular outflow tract (LVOT), is increasingly recognized in the hemodynamic evaluation of patients with sepsis and septic shock due to its ability to noninvasively estimate systolic output and cardiac output. Studies conducted in emergency rooms and intensive care units have demonstrated its feasibility, reproducibility, and clinical usefulness [34].
    • VTI has proven to be a reliable predictor of fluid responsiveness [35].
    • This is evident through its response to an ultrasound-guided fluid challenge lasting 10 s [36], and by assessing the percentage change in VTI-LVOT after volume loading in patients with septic shock who are on mechanical ventilation [37,38].
    • Innovative applications, such as the VTI-VeXUS index, integrate output measurement with the assessment of venous congestion for a more complete hemodynamic evaluation and as a predictor of mortality [39].
    • Other studies have illustrated a moderate concordance between VTI-LVOT and alternative measures of cardiac output, such as those obtained from the carotid artery. Nonetheless, VTI is considered superior to these alternative methods, increasing its relevance in emergency contexts [40]. Furthermore, point-of-care ultrasound has shown a significant clinical impact of VTI in assessing volume responsiveness and circulatory function in patients with septic shock, especially when compared to variations in the inferior vena cava diameter [41]. Overall, VTI is emerging as a dynamic and versatile parameter, supported by growing evidence that underscores its importance for personalizing fluid therapy [42], and optimizing tissue perfusion in sepsis, as well as for critically ill patients in general [38,43].
  • Serial Monitoring
    • Serial monitoring entails performing repeated echocardiographic assessments over time [44]. This approach allows us to track changes in cardiac function, highlighting potential prognostic implications [45], the effectiveness of fluid therapy, and the response to vasoactive drugs. It enables a personalized management strategy for sepsis.
    • As demonstrated by the observational analysis conducted by Geri et al. (2019) [46], integrating echocardiographic parameters with clinical data can help identify different cardiovascular phenotypes in septic shock, thereby enhancing the personalization of therapeutic strategies. Specifically, echocardiography can distinguish patients for whom preload is the primary determinant of cardiac output from those in which myocardial dysfunction is dominant. This differentiation aids in deciding between volume expansion and inotropic support [46].
    • In this context, Vignon (2020) underscores the importance of serial assessment over simple continuous monitoring of cardiac output, as echocardiography incorporates qualitative elements concerning ventricular function and cardiac filling [47].
    • Recent literature indicates that echocardiography provides more comprehensive and contextualized information compared to cardiac flow monitors. This added detail is not only beneficial for predicting the response to fluids but also for guiding the timing and indications for utilizing inotropes [48].
    • Overall, echocardiography stands out as a central and multimodal tool, capable of addressing the limitations of standard monitoring and supporting a tailored strategy in managing septic shock (Table 1).

3.2. Pathophysiology of Septic Cardiomyopathy

Sepsis-induced cardiomyopathy (SIC) is a transient but clinically significant syndrome characterized by impaired left ventricular (LV) systolic and diastolic function, right ventricular (RV) dysfunction, and reduced myocardial strain. The underlying pathophysiology is multifactorial. Inflammatory mediators, including TNF-α, IL-1β, and IL-6, play a central role, leading to nitric oxide overproduction, mitochondrial dysfunction, impaired calcium handling, and autonomic dysregulation, all of which contribute to reversible myocardial depression [49,50,51].
Microvascular dysfunction and altered ventricular loading conditions further impair cardiac output and oxygen delivery, amplifying tissue hypoperfusion [52]. Experimental studies in animal models have confirmed these mechanisms and have demonstrated echocardiographic correlates that mimic human disease, providing a translational basis for clinical observations [53,54,55].
The clinical presentation of SIC is highly heterogeneous. Patients with multiple comorbidities, particularly elderly individuals or those with cardiovascular risk factors, are more likely to develop diastolic dysfunction of the left ventricle and typically have elevated troponin levels. In contrast, patients experiencing right ventricular dysfunction tend to show higher values of the SOFA score and NT-proBNP [56,57]. LV ejection fraction (LVEF) may remain preserved despite significant myocardial impairment, particularly in patients with concurrent RV dysfunction or diastolic abnormalities [58]. Furthermore, pre-existing cardiac dysfunction has been shown to predispose patients to worse outcomes during sepsis, highlighting the importance of baseline cardiac assessment [59].

3.3. Prognostic Role of Echocardiography

Echocardiography is a cornerstone in the prognostic evaluation of septic patients. Early identification of myocardial dysfunction allows risk stratification and guides hemodynamic management [52,60,61]. The global longitudinal strain (GLS), measured using speckle-tracking echocardiography, is a sensitive indicator of left ventricular systolic function. In cases of sepsis, GLS has been found to be both earlier and more accurate than ejection fraction (EF) in detecting subclinical myocardial dysfunction. Reduced GLS values are associated with greater clinical severity, a higher need for vasopressor support, and increased mortality rates [62,63,64,65]. Therefore, GLS is an effective tool for prognostic assessment and risk stratification in septic patients [66].
Although LV systolic dysfunction has shown variable associations with mortality, LV diastolic dysfunction consistently predicts adverse outcomes, including prolonged ICU stay and increased mortality [67,68].
RV dysfunction has emerged as one of the strongest echocardiographic predictors of short- and long-term mortality, independent of LV function [56,57,69,70,71,72,73,74]. It is associated with 30 days mortality even in mechanically ventilated patients [75]. In a meta-analysis including 1373 patients, RV dysfunction was present in about one-third of cases and was associated with increased need for renal replacement therapy and with both higher short- and long-term mortality [76].
Key RV parameters, including tricuspid annular plane systolic excursion (TAPSE) and RV strain, provide robust prognostic information and have been validated across multiple cohorts and systematic reviews [77,78,79].
In a cohort of 104 patients, right ventricular dysfunction—defined as TAPSE <16 mm and RV FAC < 35%—was found to be a predictor of 28-day in-hospital mortality, and was further associated with elevated lactate levels and prolonged ICU length of stay [70].
Numerous studies indicate that echocardiograms are more reliable predictors of mortality in sepsis patients compared to troponin levels alone. While troponin primarily indicates acute myocardial damage and can be elevated due to non-ischemic factors, echocardiography directly assesses ventricular function and the hemodynamic changes caused by the systemic inflammatory response [80,81,82]. This makes echocardiograms more closely associated with prognosis and risk stratification in septic patients.
Serial echocardiography is recommended over a single assessment, as SIC is dynamic and reversible. Repeated measurements allow monitoring of cardiac recovery and response to therapeutic interventions and it can identify patients with persistent RV or biventricular dysfunction, who are at particularly high risk for mortality [83,84,85,86]. Integrating echocardiography into routine management of sepsis therefore offers both mechanistic insights and prognostic guidance (Table 2), reinforcing its role as an essential tool in critical care [86,87,88].

3.4. Comparison Between POC-Echo and Invasive Hemodynamic Monitoring in Sepsis

Recent evidence also highlights the potential role of invasive hemodynamic monitoring in selected septic patients. In particular, the early use of pulmonary artery catheterization in cases complicated by sepsis-associated cardiogenic shock has been associated with lower in-hospital mortality and increased utilization of advanced circulatory support strategies [89]. In this context, echocardiography can be used as a screening tool to identify septic patients with a potential cardiogenic component. In such cases, a pulmonary artery catheter (PAC) may be useful for continuous invasive monitoring [90]. However, invasive hemodynamic monitoring in septic patients requires an intensive care environment, is a delicate procedure, and is impractical to perform in the emergency department or in the emergency room setting. Moreover, it demands highly advanced technical skills, which not all clinicians possess.
Echocardiography remains an extremely valuable and effective tool in the emergency management of sepsis, particularly for the rapid assessment of hemodynamic status. However, in selected clinical scenarios, invasive monitoring using a PAC may also be warranted. Importantly, these two approaches are not mutually exclusive; one does not replace the other. Rather, they can be complementary, with echocardiography providing an initial, noninvasive assessment of the patient’s hemodynamic condition, while invasive monitoring may be reserved for more severe or complex cases where detailed, continuous data are clinically necessary. Although current evidence remains largely observational, these findings suggest that combining noninvasive and invasive modalities can enhance clinical decision-making and potentially improve patient outcomes.

3.5. Clinical Relevance of Echocardiography in Early Sepsis Management vs. Accuracy of Cardiac Magnetic Resonance (CMR)

Cardiac Magnetic Resonance Imaging (MRI) has emerged as a crucial tool in the investigation of sepsis and septic shock with associated cardiomyopathy, given its ability to provide detailed structural and functional information. In large animal models, septic animals compared to controls developed significant impairment of left ventricular function, including reduced ejection fraction, strain, and ventricular–arterial coupling, changes that were not explained by differences in preload, afterload, or heart rate. CMR has also documented myocardial alterations that closely resemble those seen in humans, showing that ventricular dysfunction may occur independently of microvascular ischemia or catecholamine surges [91].
In both human and animal septic shock, reductions in ejection fraction and progressive increases in end-diastolic volumes have been observed, with normalization within 10 days in survivors. Cardiac dysfunction appears to be primarily linked to edema, wall thinning, and loss of ventricular mass, rather than hemodynamic loading conditions. In non-survivors, by contrast, the absence of an increase in end-diastolic volume and the presence of more severe early diastolic dysfunction correlate with poor outcome [92].
In clinical studies of critically ill patients, CMR has revealed a heterogeneous septic cardiomyopathy phenotype, with reduced systolic function, abnormal strain, and ventricular remodeling, offering superior characterization compared with echocardiography [93]
Collectively, these findings support the role of CMR as a key non-invasive modality to elucidate the pathophysiology of septic cardiomyopathy, validate experimental models, and inform prognosis and therapeutic strategies. However, echocardiography remains the superior tool in the early management of sepsis, given its widespread availability, lower cost, and immediate applicability at the bedside. CMR, in contrast, is limited by restricted access in emergency settings, high cost, the need for specialized expertise, long waiting lists, and the additional delays caused by infection-control protocols in potentially contagious patients. Thus, while CMR provides unparalleled insights into cardiac structure and function, echocardiography continues to be the most useful non-invasive modality for guiding hemodynamic assessment and therapeutic management in septic patients. Future studies should aim to clarify the true clinical contribution of CMR in sepsis.

4. Discussion

This review highlights the pivotal role of POC-Echo in both hemodynamic management and prognostic evaluation of septic patients. Dynamic echocardiographic parameters, including SV, SVV, and LVOT VTI, reliably predict fluid responsiveness, enabling tailored fluid resuscitation and vasoactive therapy [33,94].
Our findings align with prior observational studies and meta-analyses demonstrating that echocardiographic evaluation of RV function is a powerful prognostic tool in sepsis. RV dysfunction has consistently been associated with both short- and long-term mortality, independent of left ventricular performance [71,73,80]. Unlike static measures such as central venous pressure (CVP), which provide only a snapshot of intravascular volume and have shown limited predictive accuracy, echocardiography allows dynamic, real-time assessment of ventricular function and hemodynamic responsiveness. Similarly, conventional biomarkers like troponin primarily reflect myocardial injury but do not capture functional impairment or the complex hemodynamic derangements characteristic of sepsis [80,82].
By directly visualizing RV performance—including parameters such as TAPSE, RV FAC, and RV strain—echocardiography provides a more sensitive and specific evaluation of cardiac compromise [77,78]. This dynamic insight not only enables earlier identification of high-risk patients but also guides clinical decision-making regarding fluid resuscitation and vasoactive therapy. For example, detecting RV dysfunction can inform individualized fluid management strategies, preventing both under- and over-resuscitation, and help tailor vasopressor support to optimize cardiac output and tissue perfusion. In this way, echocardiography bridges prognostic assessment with therapeutic guidance, reinforcing its superior value over static measures or biomarker-based evaluations and highlighting its role as a key tool in improving patient-centered outcomes in sepsis.
The strength of this review lies in the wide range of clinical studies considered, including adult, paediatric, mechanically ventilated patients, those with comorbidities such as diabetes, and even animal models, providing robust scientific support for the findings. Furthermore, a substantial proportion of the evidence derives from high-impact meta-analyses and systematic reviews, most of which have been published within the last five years, underscoring both the robustness and contemporary relevance of the available data.
Importantly, the clinical utility of echocardiography is underscored: an experienced clinician can integrate echocardiographic assessment with laboratory and instrumental tests during bedside evaluation, enabling the development of standardized protocols in which POC-Echo plays a central role in sepsis therapy.
Given the life-threatening nature of sepsis, every available tool that aids in management and improves outcomes is invaluable.
However, several limitations must be acknowledged. Echocardiography remains operator-dependent, introducing potential biases. This emphasizes the need for emergency physicians—the first responders in sepsis—to acquire comprehensive skills in echocardiography, ensuring accurate interpretation and optimal patient care.
Moreover, not all hospitals have the resources to equip their emergency departments with echocardiography devices, which restricts access to this valuable diagnostic tool. In addition, structured training programs and certification courses can be expensive, creating further barriers for institutions and practitioners. Even when training is available, achieving proficiency requires years of consistent practice, making the learning curve particularly steep. Finally, echocardiography is inherently subject to personal interpretation; as a result, evaluations may vary between operators and occasional errors in clinical judgment remain inevitable. These constraints highlight the importance of both systematic training and cautious integration of echocardiography into routine sepsis management.
Anyway, the clinical implications are significant. Integration of POC-Echo into sepsis management protocols facilitates individualized hemodynamic optimization, reduces the risk of fluid overload, and enables earlier recognition of myocardial dysfunction. By providing real-time, bedside assessment, echocardiography can improve decision-making regarding fluid therapy, inotropic support, and vasopressor titration, ultimately contributing to improved patient outcomes and resource utilization.
Future research should focus on standardizing POC-Echo protocols and conducting multicentre trials to evaluate its impact on patient-centered outcomes, including mortality, organ failure, and ICU length of stay. Such studies will help define optimal strategies for echocardiography-guided management and strengthen its role in early sepsis care.
In conclusion, POC-Echo represents an indispensable tool in the management of septic patients. By guiding fluid and vasoactive therapy, detecting cardiac dysfunction, and providing prognostic information—particularly through RV assessment and GLS measurement—it enhances individualized care and supports timely, evidence-based clinical decisions.

5. Conclusions

Echocardiography is a powerful, non-invasive tool that should become a standard component of sepsis management. By guiding fluid therapy, detecting cardiac dysfunction, and providing prognostic insights—especially through right ventricular assessment—it enables more precise and timely interventions. Integrating echocardiography into emergency and critical care protocols has the potential to improve outcomes and save lives, making it an indispensable tool in modern sepsis care. Future studies should assess standardized point-of-care echocardiography protocols for managing sepsis.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The original contributions presented in this study are included in the article. Further inquiries can be directed to the corresponding authors.

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

The following abbreviations are used in this manuscript:
POC-EchoPoint-of-Care Echocardiography
qSOFAquick Sequential Organ Failure Assessment
SIRSSystemic Inflammatory Response Syndrome
EWSEarly Warning Score
SVStroke Volume
SVVStroke Volume Variation
LVOTLeft Ventricular Outflow Tract
VTIVelocity Time Integral
VTI-LVOTVelocity Time Integral measured at the Left Ventricular Outflow Tract
VTI-VeXUSVTI-Venous Excess Ultrasound Score
IVCInferior Vena Cava
RCTRandomized Controlled Trial
LVLeft Ventricle
RVRight Ventricle
LVEFLeft Ventricular Ejection Fraction
TAPSETricuspid Annular plane systolic excursion
MRIMagnetic Resonance Imaging
CMRCardiac Magnetic Resonance

References

  1. Srzić, I.; Adam, V.N.; Pejak, D.T. Sepsis definition: What’s new in the Treatment Guidelines. Acta Clin. Croat. 2022, 61, 61–72. [Google Scholar] [CrossRef]
  2. Evans, L.; Rhodes, A.; Alhazzani, W.; Antonelli, M.; Coopersmith, C.M.; French, C.; Machado, F.R.; Mcintyre, L.; Ostermann, M.; Prescott, H.C.; et al. Surviving sepsis campaign: International guidelines for management of sepsis and septic shock 2021. Intensiv. Care Med. 2021, 47, 1181–1247. [Google Scholar] [CrossRef] [PubMed]
  3. Arina, P.; Hofmaenner, D.A.; Singer, M. Definition and Epidemiology of Sepsis. Semin. Respir. Crit. Care Med. 2024, 45, 461–468. [Google Scholar] [CrossRef] [PubMed]
  4. Kim, H.-J.; Ko, R.-E.; Lim, S.Y.; Park, S.; Suh, G.Y.; Lee, Y.J. Sepsis Alert Systems, Mortality, and Adherence in Emergency Departments. JAMA Netw. Open 2024, 7, e2422823. [Google Scholar] [CrossRef] [PubMed]
  5. Rudd, K.E.; Johnson, S.C.; Agesa, K.M.; Shackelford, K.A.; Tsoi, D.; Kievlan, D.R.; Colombara, D.V.; Ikuta, K.S.; Kissoon, N.; Finfer, S.; et al. Global, regional, and national sepsis incidence and mortality, 1990–2017: Analysis for the Global Burden of Disease Study. Lancet 2020, 395, 200–211. [Google Scholar] [CrossRef]
  6. Chua, W.L.; Rusli KDBin Aitken, L.M. Early warning scores for sepsis identification and prediction of in-hospital mortality in adults with sepsis: A systematic review and meta-analysis. J. Clin. Nurs. 2024, 33, 2005–2018. [Google Scholar] [CrossRef]
  7. Velissaris, D.; Zareifopoulos, N.; Lagadinou, M.; Platanaki, C.; Tsiotsios, K.; Stavridis, E.L.; Kasartzian, D.; Pierrakos, C.; Karamouzos, V. Procalcitonin and sepsis in the emergency department: An update. Eur. Rev. Med. Pharmacol. Sci. 2021, 25, 466–479. [Google Scholar] [CrossRef]
  8. Piccioni, A.; Baroni, S.; Rozzi, G.; Belvederi, F.; Leggeri, S.; Spagnuolo, F.; Novelli, M.; Pignataro, G.; Candelli, M.; Covino, M.; et al. Evaluation of Presepsin for Early Diagnosis of Sepsis in the Emergency Department. J. Clin. Med. 2025, 14, 2480. [Google Scholar] [CrossRef]
  9. Piccioni, A.; Santoro, M.C.; de Cunzo, T.; Tullo, G.; Cicchinelli, S.; Saviano, A.; Valletta, F.; Pascale, M.M.; Candelli, M.; Covino, M.; et al. Presepsin as early marker of sepsis in emergency department: A narrative review. Medicina 2021, 57, 770. [Google Scholar] [CrossRef]
  10. Kellum, J.A.; Formeck, C.L.; Kernan, K.F.; Gómez, H.; Carcillo, J.A. Subtypes and Mimics of Sepsis. Crit. Care Clin. 2022, 38, 195–211. [Google Scholar] [CrossRef]
  11. Lelubre, C.; Vincent, J.L. Mechanisms and treatment of organ failure in sepsis. Nat. Rev. Nephrol. 2018, 14, 417–427. [Google Scholar] [CrossRef] [PubMed]
  12. Ranjit, S.; Natraj, R. Hemodynamic Management Strategies in Pediatric Septic Shock: Ten Concepts for the Bedside Practitioner. Indian Pediatr. 2024, 61, 265–275. [Google Scholar] [CrossRef] [PubMed]
  13. Girardis, M.; David, S.; Ferrer, R.; Helms, J.; Juffermans, N.P.; Martin-Loeches, I.; Povoa, P.; Russell, L.; Shankar-Hari, M.; Iba, T.; et al. Understanding, assessing and treating immune, endothelial and haemostasis dysfunctions in bacterial sepsis. Intensiv. Care Med. 2024, 50, 1580–1592. [Google Scholar] [CrossRef] [PubMed]
  14. Burgdorff, A.M.; Bucher, M.; Schumann, J. Vasoplegia in patients with sepsis and septic shock: Pathways and mechanisms. J. Int. Med. Res. 2018, 46, 1303–1310. [Google Scholar] [CrossRef]
  15. Ratnani, I.; Ochani, R.K.; Shaikh, A.; Jatoi, H.N. Vasoplegia: A Review. Methodist Debakey Cardiovasc. J. 2023, 19, 38–47. [Google Scholar] [CrossRef]
  16. De Backer, D.; Ricottilli, F.; Ospina-Tascón, G.A. Septic shock: A microcirculation disease. Curr. Opin. Anaesthesiol. 2021, 34, 85–91. [Google Scholar] [CrossRef]
  17. Yang, C.; Xia, W.; Liu, X.; Lin, J.; Wu, A. Role of TXNIP/NLRP3 in sepsis-induced myocardial dysfunction. Int. J. Mol. Med. 2019, 44, 417–426. [Google Scholar] [CrossRef]
  18. Hestenes, S.M.; Halvorsen, P.S.; Skulstad, H.; Remme, E.W.; Espinoza, A.; Hyler, S.; Bugge, J.F.; Fosse, E.; Nielsen, E.W.; Edvardsen, T. Advantages of strain echocardiography in assessment of myocardial function in severe sepsis: An experimental study. Crit. Care Med. 2014, 42, e432–e440. [Google Scholar] [CrossRef]
  19. Santos, T.M.; Franci, D.; Schweller, M.; Ribeiro, D.L.; Gontijo-Coutinho, C.M.; Matos-Souza, J.R.; de Carvalho-Filho, M.A. Left ventricle tissue doppler imaging predicts disease severity in septic patients newly admitted in an emergency unit. J. Emerg. Med. 2015, 49, 907–915. [Google Scholar] [CrossRef]
  20. Lan, P.; Wang, T.-T.; Li, H.-Y.; Yan, R.-S.; Liao, W.-C.; Yu, B.-W.; Wang, Q.-Q.; Lin, L.; Pan, K.-H.; Yu, Y.-S.; et al. Utilization of echocardiography during septic shock was associated with a decreased 28-day mortality: A propensity score-matched analysis of the MIMIC-III database. Ann. Transl. Med. 2019, 7, 662. [Google Scholar] [CrossRef]
  21. Feng, M.; McSparron, J.I.; Kien, D.T.; Stone, D.J.; Roberts, D.H.; Schwartzstein, R.M.; Vieillard-Baron, A.; Celi, L.A. Transthoracic echocardiography and mortality in sepsis: Analysis of the MIMIC-III database. Intensiv. Care Med. 2018, 44, 884–892. [Google Scholar] [CrossRef] [PubMed]
  22. Chen, Z.; Han, X.; Liu, Y.; Wang, M.; Wang, B.; Wang, L.; Jin, H. Ultrasound-guided fluid resuscitation versus usual care guided fluid resuscitation in patients with septic shock: A systematic review and meta-analysis. Emerg. Crit. Care Med. 2024, 4, 82–89. [Google Scholar] [CrossRef]
  23. Musikatavorn, K.; Plitawanon, P.; Lumlertgul, S.; Narajeenron, K.; Rojanasarntikul, D.; Tarapan, T.; Saoraya, J. Randomized controlled trial of ultrasound-guided fluid resuscitation of sepsis-induced hypoperfusion and septic shock. West. J. Emerg. Med. 2021, 22, 369–378. [Google Scholar] [CrossRef] [PubMed]
  24. Yan, Z.; Dai, L.; Cheng, L.; Lu, J.; Pei, Y.; Wang, J. Inferior vena cava diameter combined with lung ultrasound B-line score to guide fluid resuscitation in patients with septic shock. Chin. Crit. Care Med. 2020, 32, 1356–1360. [Google Scholar] [CrossRef]
  25. Zhao, J.; Wang, G. Inferior vena cava collapsibility index is a valuable and non-invasive index for elevated general heart end-diastolic volume index estimation in septic shock patients. Med. Sci. Monit. 2016, 22, 3843–3848. [Google Scholar] [CrossRef]
  26. Yuan, J.; Yang, X.; Yuan, Q.; Li, M.; Chen, Y.; Dong, C. Systematic review of ultrasound-guided fluid resuscitation vs. early goal-directed therapy in patients with septic shock. Zhonghua Wei Zhong Bing Ji Jiu Yi Xue 2020, 32, 56–61. [Google Scholar] [CrossRef]
  27. Martin, G.S.; Kaufman, D.A.; Marik, P.E.; Shapiro, N.I.; Levett, D.Z.H.; Whittle, J.; MacLeod, D.B.; Chappell, D.; Lacey, J.; Woodcock, T.; et al. Perioperative Quality Initiative (POQI) consensus statement on fundamental concepts in perioperative fluid management: Fluid responsiveness and venous capacitance. Perioper. Med. 2020, 9, 12. [Google Scholar] [CrossRef]
  28. Kenny, J.É.S.; Prager, R.; Rola, P.; Haycock, K.; Gibbs, S.O.; Johnston, D.H.; Horner, C.; Eibl, J.K.; Lau, V.C.; Kemp, B.O. Simultaneous Venous-Arterial Doppler Ultrasound During Early Fluid Resuscitation to Characterize a Novel Doppler Starling Curve: A Prospective Observational Pilot Study. J. Intensiv. Care Med. 2024, 39, 628–635. [Google Scholar] [CrossRef]
  29. Roger, C.; Zieleskiewicz, L.; Demattei, C.; Lakhal, K.; Piton, G.; Louart, B.; Constantin, J.-M.; Chabanne, R.; Faure, J.-S.; Mahjoub, Y.; et al. Time course of fluid responsiveness in sepsis: The fluid challenge revisiting (FCREV) study. Crit. Care 2019, 23, 179. [Google Scholar] [CrossRef]
  30. Weigl, W.; Adamski, J.; Onichimowski, D.; Nowakowski, P.; Wagner, B. Methods of assessing fluid responsiveness in septic shock patients: A narrative review. Anaesthesiol. Intensiv. Ther. 2022, 54, 175–183. [Google Scholar] [CrossRef]
  31. de Freitas Chaves, R.C.; Barbas, C.S.V.; Queiroz, V.N.F.; Serpa Neto, A.; Deliberato, R.O.; Pereira, A.J.; Timenetsky, K.T.; Júnior, J.M.S.; Takaoka, F.; de Backer, D.; et al. Assessment of fluid responsiveness using pulse pressure variation, stroke volume variation, plethysmographic variability index, central venous pressure, and inferior vena cava variation in patients undergoing mechanical ventilation: A systematic review and meta-analysis. Crit. Care 2024, 28, 289. [Google Scholar] [CrossRef]
  32. Alvarado Sánchez, J.I.; Caicedo Ruiz, J.D.; Diaztagle Fernández, J.J.; Amaya Zuñiga, W.F.; Ospina-Tascón, G.A.; Cruz Martínez, L.E. Predictors of fluid responsiveness in critically ill patients mechanically ventilated at low tidal volumes: Systematic review and meta-analysis. Ann. Intensiv. Care 2021, 11, 28. [Google Scholar] [CrossRef]
  33. Latham, H.; Harenski, K.; Javed, M.; Rickelman, J.; Sahatjian, J.; Boggerty, K.; Hansell, D. 158: Treatment Fluid Volume May Predict Stroke Volume Improvement. Crit. Care Med. 2023, 51, 62. [Google Scholar] [CrossRef]
  34. McGregor, D.; Sharma, S.; Gupta, S.; Ahmad, S.; Godec, T.; Harris, T. Emergency department non-invasive cardiac output study (EDNICO): A feasibility and repeatability study. Scand. J. Trauma, Resusc. Emerg. Med. 2019, 27, 30. [Google Scholar] [CrossRef] [PubMed]
  35. Parker, C.W.; Kolimas, A.M.; Kotini-Shah, P. Velocity-Time Integral: A Bedside Echocardiography Technique Finding a Place in the Emergency Department. J. Emerg. Med. 2022, 63, 382–388. [Google Scholar] [CrossRef] [PubMed]
  36. Wu, Y.; Zhou, S.; Zhou, Z.; Liu, B. A 10-second fluid challenge guided by transthoracic echocardiography can predict fluid responsiveness. Crit. Care 2014, 18, R108. [Google Scholar] [CrossRef]
  37. Wang, J.; Zhou, D.; Gao, Y.; Wu, Z.; Wang, X.; Lv, C. Effect of VTILVOTvariation rate on the assessment of fluid responsiveness in septic shock patients. Medicine 2020, 99, e22702. [Google Scholar] [CrossRef]
  38. Sasidharan, P.; Kaeley, N.; Sharma, P.; Jain, G.; Shankar, T.; Jayachandran, S.; Kumar, B.; Kumar, M.A.; Jose, J.R.; Lalotra, D.K. The Left Ventricular Outflow Tract Velocity Time Integral as a Predictor of Fluid Responsiveness in Patients with Sepsis-Related Acute Circulatory Failure. Cureus 2025, 17, e77353. [Google Scholar] [CrossRef]
  39. Prager, R.; Pupulin, S.; Chakera, H.; Saha, R.; Orozco, N.; Kenny, J.-E.; Rola, P.; Wong, M.Y.S.; Slessarev, M.; Lewis, K.; et al. The VTI-VeXUS Index in Septic Shock: An Exploratory Proof-of-Concept Observational Study of a Novel Hemodynamic Parameter. J. Clin. Med. 2025, 14, 5774. [Google Scholar] [CrossRef]
  40. Chanthawatthanarak, S.; Boonasa, K.; Apiratwarakul, K.; Cheung, L.W.; Tiamkao, S.; Ienghong, K. Agreement between carotid and LVOT non-invasive cardiac output measurements in ED septic shock patients: A prospective observational study. Sci. Rep. 2025, 15, 19911. [Google Scholar] [CrossRef]
  41. Dai, R.; Zhang, X.; Wang, H.; Zhang, F.; Qin, B. Clinical value of point of care ultrasound on cardiac output and volume responsiveness in patients with septic shock. Chin. Crit. Care Med. 2021, 33, 1479–1483. [Google Scholar] [CrossRef]
  42. Saji, S.Z.; Murga, O.; Khurana, S.; Hung Phan, B.; Khalil, B.; Nagra, A.M.; Aragon, S.F.; Kolagatla, D.; Arruarana, V.S.; Herrera, D.A.; et al. Utilization of left ventricular outflow tract velocity time integral in the assessment of fluid responsiveness in adult patients with sepsis or septic shock—A systematic review. J. Ultrasound 2025, 1–11. [Google Scholar] [CrossRef] [PubMed]
  43. Blanco, P. Rationale for using the velocity–time integral and the minute distance for assessing the stroke volume and cardiac output in point-of-care settings. Ultrasound J. 2020, 12, 21. [Google Scholar] [CrossRef] [PubMed]
  44. Soliman-Aboumarie, H.; Pastore, M.C.; Galiatsou, E.; Gargani, L.; Pugliese, N.R.; Mandoli, G.E.; Valente, S.; Hurtado-Doce, A.; Lees, N.; Cameli, M. Echocardiography in the intensive care unit: An essential tool for diagnosis, monitoring and guiding clinical decision-making. Imaging 2021, 1, 1–15. [Google Scholar] [CrossRef]
  45. de Braga Lima Carvalho Canesso, M.; Borges, I.N.; de Deus Queiroz Santos, T.A.; Ris, T.H.; de Barros, M.V.L.; Nobre, V.; Nunes, M.C.P. Value of speckle-tracking echocardiography changes in monitoring myocardial dysfunction during treatment of sepsis: Potential prognostic implications. Int. J. Cardiovasc. Imaging 2019, 35, 855–859. [Google Scholar] [CrossRef]
  46. Geri, G.; Vignon, P.; Aubry, A.; Fedou, A.L.; Charron, C.; Silva, S.; Repessé, X.; Vieillard-Baron, A. Cardiovascular clusters in septic shock combining clinical and echocardiographic parameters: A post hoc analysis. Intensiv. Care Med. 2019, 45, 657–667. [Google Scholar] [CrossRef]
  47. Vignon, P. Continuous cardiac output assessment or serial echocardiography during septic shock resuscitation? Ann. Transl. Med. 2020, 8, 797. [Google Scholar] [CrossRef]
  48. Suh, G.J.; Shin, T.G.; Kwon, W.Y.; Kim, K.; Jo, Y.H.; Choi, S.H.; Chung, S.P.; Kim, W.Y.; Korean Shock Society Investigators. Hemodynamic management of septic shock: Beyond the Surviving Sepsis Campaign guidelines. Clin. Exp. Emerg. Med. 2023, 10, 255–264. [Google Scholar] [CrossRef]
  49. Carbone, F.; Liberale, L.; Preda, A.; Schindler, T.H.; Montecucco, F. Septic Cardiomyopathy: From Pathophysiology to the Clinical Setting. Cells 2022, 11, 2833. [Google Scholar] [CrossRef]
  50. Wang, R.; Xu, Y.; Fang, Y.; Wang, C.; Xue, Y.; Wang, F.; Cheng, J.; Ren, H.; Wang, J.; Guo, W.; et al. Pathogenetic mechanisms of septic cardiomyopathy. J. Cell. Physiol. 2022, 237, 49–58. [Google Scholar] [CrossRef]
  51. Martin, L.; Derwall, M.; Thiemermann, C.; Schürholz, T. Herz in der Sepsis. Anaesthesist 2017, 66, 479–490. [Google Scholar] [CrossRef] [PubMed]
  52. Hasegawa, D.; Ishisaka, Y.; Maeda, T.; Prasitlumkum, N.; Nishida, K.; Dugar, S.; Sato, R. Prevalence and Prognosis of Sepsis-Induced Cardiomyopathy: A Systematic Review and Meta-Analysis. J. Intensiv. Care Med. 2023, 38, 797–808. [Google Scholar] [CrossRef] [PubMed]
  53. Ince, M.E.; Turgut, K.; Akar, A.; Naseri, A.; Sen, I.; Süleymanoglu, H.; Ertan, M.; Sagmanligil, V. Prognostic importance of tissue Doppler imaging of systolic and diastolic functions in dogs with severe sepsis and septic shock. Acta Vet. Hung. 2019, 67, 517–528. [Google Scholar] [CrossRef]
  54. Cao, Y.; Han, X.; Pan, H.; Jiang, Y.; Peng, X.; Xiao, W.; Rong, J.; Chen, F.; He, J.; Zou, L.; et al. Retraction Note: Emerging protective roles of shengmai injection in septic cardiomyopathy in mice by inducing myocardial mitochondrial autophagy via caspase-3/Beclin-1 axis. Inflamm. Res. 2023, 72, 745. [Google Scholar] [CrossRef]
  55. Naseri, A.; Akyuz, E.; Turgut, K.; Guzelbektes, H.; Sen, I. Sepsis-induced cardiomyopathy in animals: From experimental studies to echocardiography-based clinical research. Can. Vet. J. 2023, 64, 871–877. [Google Scholar]
  56. Lu, N.-F.; Niu, H.-X.; Liu, A.-Q.; Chen, Y.-L.; Liu, H.-N.; Zhao, P.-H.; Shao, J.; Xi, X.-M. Types of Septic Cardiomyopathy: Prognosis and Influencing Factors—A Clinical Study. Risk Manag. Healthc. Policy 2024, 17, 1015–1025. [Google Scholar] [CrossRef]
  57. Liu, C.; Wang, H.; Liu, C.; Cao, M. The predictive value of SOFA and APSIII scores for 28-day mortality risk in SIMI: A cohort study based on the MIMIC-IV database. Front. Cell. Infect. Microbiol. 2025, 15, 1574625. [Google Scholar] [CrossRef]
  58. Ravikumar, N.; Sayed, M.A.; Poonsuph, C.J.; Sehgal, R.; Shirke, M.M.; Harky, A. Septic Cardiomyopathy: From Basics to Management Choices. Curr. Probl. Cardiol. 2021, 46, 100767. [Google Scholar] [CrossRef]
  59. Stevens, D.L.; Bryant, A.E. Complexities of cardiomyopathy in septic shock. Curr. Opin. Infect. Dis. 2025, 38, 214–221. [Google Scholar] [CrossRef]
  60. El Mokadem, M.; El Maraghi, S.; El Hosseiny, R.; Moawad, A.; Yassin, A. The Usefulness of Strain Echocardiography as Diagnostic and Prognostic Index of Cardiac Dysfunction in Septic Patients in Correlation with Cardiac Biomarkers. J. Cardiovasc. Echogr. 2024, 34, 114–119. [Google Scholar] [CrossRef]
  61. Tucker, R.V.; Williams, K.; Theyyunni, N.; Fung, C.M. Sepsis-Induced Cardiomyopathy Detected with Focused Cardiac Ultrasound in the Emergency Department. J. Emerg. Med. 2022, 63, e91–e99. [Google Scholar] [CrossRef]
  62. Zakynthinos, G.E.; Giamouzis, G.; Xanthopoulos, A.; Oikonomou, E.; Kalogeras, K.; Karavidas, N.; Dimeas, I.E.; Gialamas, I.; Gounaridi, M.I.; Siasos, G.; et al. Septic Cardiomyopathy: Difficult Definition, Challenging Diagnosis, Unclear Treatment. J. Clin. Med. 2025, 14, 986. [Google Scholar] [CrossRef] [PubMed]
  63. Yu, J.; Zheng, R.; Yang, P.; Wang, D. Construction of a predictive model and prognosis of left ventricular systolic dysfunction in patients with sepsis based on the diagnosis using left ventricular global longitudinal strain. J. Intensiv. Care 2022, 10, 29. [Google Scholar] [CrossRef] [PubMed]
  64. Innocenti, F.; Palmieri, V.; Guzzo, A.; Stefanone, V.T.; Donnini, C.; Pini, R. SOFA score and left ventricular systolic function as predictors of short-term outcome in patients with sepsis. Intern. Emerg. Med. 2018, 13, 51–58. [Google Scholar] [CrossRef] [PubMed]
  65. Vallabhajosyula, S.; Rayes, H.A.; Sakhuja, A.; Murad, M.H.; Geske, J.B.; Jentzer, J.C. Global Longitudinal Strain Using Speckle-Tracking Echocardiography as a Mortality Predictor in Sepsis: A Systematic Review. J. Intensiv. Care Med. 2019, 34, 87–93. [Google Scholar] [CrossRef]
  66. Zhao, J.L.; Wang, R.; Dai, Q.C.; Dong, S.M. The value of right ventricular ultrasound assessment and cardiac biomarkers in the prognosis of sepsis. Eur. Rev. Med. Pharmacol. Sci. 2023, 27, 7891–7897. [Google Scholar] [CrossRef]
  67. Lima, M.R.; Silva, D. Septic cardiomyopathy: A narrative review. Rev. Port. Cardiol. 2023, 42, 471–481. [Google Scholar] [CrossRef]
  68. Thockchom, N.; Bairwa, M.; Kant, R.; Kumar, B.; Bahurupi, Y.; Goyal, B. Prognostic Significance of Diastolic Dysfunction in Type 2 Diabetes Mellitus Patients with Sepsis and Septic Shock: Insights from a Longitudinal Tertiary Care Study. Cureus 2023, 15, e45894. [Google Scholar] [CrossRef]
  69. Lin, Y.M.; Lee, M.C.; Toh, H.S.; Chang, W.T.; Chen, S.Y.; Kuo, F.H.; Tang, H.-J.; Hua, Y.-M.; Wei, D.; Melgarejo, J.; et al. Association of sepsis-induced cardiomyopathy and mortality: A systematic review and meta-analysis. Ann. Intensiv. Care 2022, 12, 112. [Google Scholar] [CrossRef]
  70. Koowattanatianchai, S.; Kochaiyapatana, P.; Eungsuwat, N.; Rangsrisaeneepitak, V.; Thammakumpee, K.; Kaladee, K. Significance of Right Ventricular Dysfunction in Predicting Short-Term Survival Among Patients with Sepsis and Septic Shock: A Prognostic Analysis. Crit. Care Res. Pract. 2025, 2025, 5511135. [Google Scholar] [CrossRef]
  71. Lanspa, M.J.; Cirulis, M.M.; Wiley, B.M.; Olsen, T.D.; Wilson, E.L.; Beesley, S.J.; Brown, S.M.; Hirshberg, E.L.; Grissom, C.K. Right Ventricular Dysfunction in Early Sepsis and Septic Shock. Chest 2021, 159, 1055–1063. [Google Scholar] [CrossRef]
  72. Innocenti, F.; Palmieri, V.; Stefanone, V.T.; Donnini, C.; D’Argenzio, F.; Cigana, M.; Tassinari, I.; Pini, R. Epidemiology of right ventricular systolic dysfunction in patients with sepsis and septic shock in the emergency department. Intern. Emerg. Med. 2020, 15, 1281–1289. [Google Scholar] [CrossRef] [PubMed]
  73. Kim, J.S.; Kim, Y.J.; Kim, M.; Ryoo, S.M.; Kim, W.Y. Association between right ventricle dysfunction and poor outcome in patients with septic shock. Heart 2020, 106, 1665–1671. [Google Scholar] [CrossRef] [PubMed]
  74. Vallabhajosyula, S.; Kumar, M.; Pandompatam, G.; Sakhuja, A.; Kashyap, R.; Kashani, K.; Gajic, O.; Geske, J.B.; Jentzer, J.C. Prognostic impact of isolated right ventricular dysfunction in sepsis and septic shock: An 8-year historical cohort study. Ann. Intensiv. Care 2017, 7, 94. [Google Scholar] [CrossRef] [PubMed]
  75. Zhang, H.; Huang, W.; Zhang, Q.; Chen, X.; Wang, X.; Liu, D. Prevalence and prognostic value of various types of right ventricular dysfunction in mechanically ventilated septic patients. Ann. Intensiv. Care 2021, 11, 108. [Google Scholar] [CrossRef]
  76. Vallabhajosyula, S.; Shankar, A.; Vojjini, R.; Cheungpasitporn, W.; Sundaragiri, P.R.; DuBrock, H.M.; Sekiguchi, H.; Frantz, R.P.; Cajigas, H.R.; Kane, G.C.; et al. Impact of Right Ventricular Dysfunction on Short-term and Long-term Mortality in Sepsis: A Meta-analysis of 1,373 Patients. Chest 2021, 159, 2254–2263. [Google Scholar] [CrossRef]
  77. Perencin, A.; Curreri, C.; Zanforlini, B.M.; Bertocco, A.; Ceolin, C.; Papa, M.V.; Sergi, G.; De Rui, M. Beyond APACHE II: The role of TAPSE in predicting mortality among septic patients and septic shock; a systematic review and metanalysis Right heart, right prognosis: TAPSE, a new tool for predicting mortality among septic patients and septic shock; a systematic review and metanalysis. Clin. Res. Cardiol. 2025, 1–12. [Google Scholar] [CrossRef]
  78. Liu, H.; He, H.; Lin, Z.; Lin, X.; Jiang, L.; Huang, L.; Shang, X.; Wang, X. Prognostic value of TAPSE in patients with septic cardiomyopathy: A retrospective observational cohort study. Front. Med. 2025, 12, 1632964. [Google Scholar] [CrossRef]
  79. Sanderson, T.; Samuels, T. A cohort study evaluating myocardial work and right ventricle strain in sepsis in critical care. Sci. Rep. 2025, 15, 16606. [Google Scholar] [CrossRef]
  80. Innocenti, F.; Palmieri, V.; Stefanone, V.T.; D’Argenzio, F.; Cigana, M.; Montuori, M.; Capretti, E.; De Paris, A.; Calcagno, S.; Tassinari, I.; et al. Comparison of Troponin I levels versus myocardial dysfunction on prognosis in sepsis. Intern. Emerg. Med. 2022, 17, 223–231. [Google Scholar] [CrossRef]
  81. Gajardo, A.I.J.; Ferrière-Steinert, S.; Valenzuela Jiménez, J.; Heskia Araya, S.; Kouyoumdjian Carvajal, T.; Ramos-Rojas, J.; Medel, J.N. Early high-sensitivity troponin elevation and short-term mortality in sepsis: A systematic review with meta-analysis. Crit. Care 2025, 29, 76. [Google Scholar] [CrossRef] [PubMed]
  82. Wang, T.T.; Jiang, L. Relationship between highly sensitive cardiac troponin T and sepsis and outcome in critically ill patients. Zhonghua Nei Ke Za Zhi 2017, 56, 738–742. [Google Scholar] [PubMed]
  83. Vallabhajosyula, S.; Pruthi, S.; Shah, S.; Wiley, B.M.; Mankad, S.V.; Jentzer, J.C. Basic and advanced echocardiographic evaluation of myocardial dysfunction in sepsis and septic shock. Anaesth. Intensiv. Care 2018, 46, 13–24. [Google Scholar] [CrossRef] [PubMed]
  84. Innocenti, F.; Palmieri, V.; Stefanone, V.T.; D’Argenzio, F.; Cigana, M.; Montuori, M.; Capretti, E.; De Paris, A.; Calcagno, S.; Tassinari, I.; et al. Prognostic stratification in septic patients with overt and cryptic shock by speckle tracking echocardiography. Intern. Emerg. Med. 2021, 16, 757–764. [Google Scholar] [CrossRef]
  85. Iyer, S.; Kennedy, J.N.; Jentzer, J.C.; Senussi, M.H.; Seymour, C.W. Cardiac Function Before Sepsis and Clinical Outcomes. JAMA 2024, 331, 1496. [Google Scholar] [CrossRef]
  86. Guérin, L.; Vieillard-Baron, A. The Use of Ultrasound in Caring for Patients with Sepsis. Clin. Chest Med. 2016, 37, 299–307. [Google Scholar] [CrossRef]
  87. Nemani, L.; Palmer, L.J.; Nabzdyk, C.G.S. Echocardiography in Sepsis: Can One Snapshot Tell the Whole Story? J. Cardiothorac. Vasc. Anesth. 2024, 38, 1620–1622. [Google Scholar] [CrossRef]
  88. Griffee, M.J.; Merkel, M.J.; Wei, K.S. The Role of Echocardiography in Hemodynamic Assessment of Septic Shock. Crit. Care Clin. 2010, 26, 365–382. [Google Scholar] [CrossRef]
  89. Sato, R.; Hasegawa, D.; Guo, S.C.; Nishida, K.; Dugar, S. Invasive hemodynamic monitoring with pulmonary artery catheter in sepsis-associated cardiogenic shock. Shock 2024, 61, 712–717. [Google Scholar] [CrossRef]
  90. Sato, R.; Hasegawa, D.; Guo, S.; Nuqali, A.E.; Moreno, J.E.P. Sepsis-induced cardiogenic shock: Controversies and evidence gaps in diagnosis and management. J. Intensiv. Care 2025, 13, 1. [Google Scholar] [CrossRef]
  91. Ford, V.J.; Applefeld, W.N.; Wang, J.; Sun, J.; Solomon, S.B.; Klein, H.G.; Feng, J.; Lertora, J.; Parizi-Torabi, P.; Danner, R.L.; et al. In a Canine Model of Septic Shock, Cardiomyopathy Occurs Independent of Catecholamine Surges and Cardiac Microvascular Ischemia. J. Am. Hear. Assoc. 2024, 13, e034027. [Google Scholar] [CrossRef]
  92. Ford, V.J.; Applefeld, W.N.; Wang, J.; Sun, J.; Solomon, S.B.; Sidenko, S.; Feng, J.; Sheffield, C.; Klein, H.G.; Yu, Z.; et al. Cardiac Magnetic Resonance Studies in a Large Animal Model that Simulates the Cardiac Abnormalities of Human Septic Shock. J. Am. Hear. Assoc. 2024, 13, e034026. [Google Scholar] [CrossRef]
  93. Muehlberg, F.; Blaszczyk, E.; Will, K.; Wilczek, S.; Brederlau, J.; Schulz-Menger, J. Characterization of critically ill patients with septic shock and sepsis-associated cardiomyopathy using cardiovascular MRI. ESC Heart Fail. 2022, 9, 2147–2156. [Google Scholar] [CrossRef]
  94. Myatra, S.N.; Prabu, N.R.; DIvatia, J.V.; Monnet, X.; Kulkarni, A.P.; Teboul, J.L. The Changes in Pulse Pressure Variation or Stroke Volume Variation after a “tidal Volume Challenge” Reliably Predict Fluid Responsiveness during Low Tidal Volume Ventilation. Crit. Care Med. 2017, 45, 415–421. [Google Scholar] [CrossRef]
Table 1. Comparative Table about the role of echocardiography in fluid management in sepsis. Symbol legend: ↓ denotes a decrease or reduction (for example, in mortality, incidence, or other measured outcomes).
Table 1. Comparative Table about the role of echocardiography in fluid management in sepsis. Symbol legend: ↓ denotes a decrease or reduction (for example, in mortality, incidence, or other measured outcomes).
ReferenceYearStudy TypePopulation/ModelEchocardiographic FocusPrognostic Implications
Chen Z et al. [22]2024Systematic review & meta-analysisPatients with septic shockUltrasound-guided fluid resuscitation (IVC, PLR)↓ mortality, ↓ infused fluids, ↓ hospital/ICU stay
Musikatavorn K et al. [23]2021Randomized Controlled Trial202 patients, sepsis/septic shockPoint-of-care ultrasound vs. clinical managementReduced infused fluids, no clear survival benefit
Yan Z et al. [24]2020Clinical study40 patients with septic shockIVC diameter + lung ultrasound B-linesBetter assessment of fluid responsiveness, ↓ risk of fluid overload
Zhao J & Wang G [25]2016Observational42 septic shock patientsIVC collapsibility index vs. GEDVI, CI, CVPIVCCI correlated with GEDVI; useful non-invasive index of intravascular volume
Yuan J et al. [26]2020Systematic reviewSeptic shock patientsUltrasound vs. Early Goal-Directed Therapy (EGDT)↓ early mortality (7 d), ↓ fluids, ↓ pulmonary edema; no benefit at 28 days mortality
Martin GS et al. [27]2020Consensus statement (POQI)Perioperative/critically ill patientsFluid responsiveness & venous capacitanceDefines concepts and recommends dynamic ultrasound assessment
Kenny JÉS et al. [28]2024Prospective observational pilotPatients in early resuscitationSimultaneous venous-arterial Doppler (Starling curve)Feasibility study; proposes a novel hemodynamic index
Roger C et al. [29]2019Observational (FCREV study)143 Septic patientsFluid challenge + echocardiographyFluid responsiveness is dynamic and changes over time
Latham H et al. [33]2023Observational (abstract, CCM)Sepsis/shock patientsInfused fluid volume vs. stroke volume changeEarly fluid volume may predict hemodynamic response
Parker CW et al. [35]2022Review/EducationalEmergency DepartmentVTI (Velocity-Time Integral)VTI useful for bedside stroke volume and CO assessment
Wu Y et al. [36]2014Clinical studySeptic patients10-second fluid challenge + TTE (VTI-LVOT)Change in VTI predicts fluid responsiveness
Wang J et al. [37]2020Clinical studySeptic shock patientsVTILVOT variation rateUseful for assessing fluid responsiveness
Sasidharan P et al. [38]2025Clinical studySepsis-related acute circulatory failureLVOT VTILVOT VTI predictive of fluid responsiveness
Prager R et al. [39]2025Exploratory observationalSeptic shock patientsVTI-VeXUS index (novel hemodynamic marker)Promising tool to stratify congestion and response
Chanthawatthanarak S et al. [40]2025Prospective studyED septic shock patientsCarotid vs. LVOT cardiac output (non-invasive)Good correlation; feasible alternative method, VTI better performance
Saji SZ et al. [42]2025Systematic reviewAdults with sepsis/septic shockLVOT VTILVOT VTI is accurate for fluid management
Blanco P [43]2020ReviewCritically ill patientsVTI & stroke volumeProvides rationale for using VTI as reliable bedside measure
Soliman-Aboumarie H et al. [44]2021ReviewICU patientsMultiparametric echocardiographyEssential ICU tool for diagnosis and decision-making
de Braga Lima Carvalho Canesso M et al. [45]2019Clinical study50 septic patientsSpeckle-tracking echocardiography (GLS)GLS changes correlated with dysfunction and prognosis
Suh GJ et al. [48]2023Narrative reviewSeptic shockHemodynamic management beyond SSC guidelinesEcho central to advanced hemodynamic strategies
Table 2. Comparative Table of Clinical Studies about prognostic role of echocardiography. Symbol legend: ↑ denotes an increase (for example, in mortality, incidence, or other measured outcomes).
Table 2. Comparative Table of Clinical Studies about prognostic role of echocardiography. Symbol legend: ↑ denotes an increase (for example, in mortality, incidence, or other measured outcomes).
ReferenceYearStudy TypePopulation/ModelEchocardiographic FocusPrognostic Implications
Carbone F, Liberale L, et al. [49]2022Narrative ReviewHuman/experimentalGeneral echo in SCMDescribes diagnostic & prognostic potential
Hasegawa D, Ishisaka Y, et al. [52]2023Systematic review/meta-analysis23 studies, >2000 patientsLV/RV dysfunctionSCM associated with ↑ mortality
Ince ME, Turgut K, et al. [53]2019ObservationalDogsTissue Doppler (systolic/diastolic)Abnormal indices predicted worse prognosis
Lu N-F, Niu H-X, et al. [56]2024Clinical studySeptic patients (~184)LV vs. RV vs. biventricularPhenotypes linked to different prognoses-RV dysfunction ↑ mortality
Ravikumar N, Sayed MA, et al. [58]2021ReviewHumanLV/RV dysfunctionPresence of SIC ↑ mortality
El Mokadem M, El Maraghi S, et al. [60]2024Clinical observational50 septic patients LV strain, biomarkersGLS predictor of in-hospital mortality
Tucker RV, Williams K, et al. [61]2022Observational110 ED septic patientsFocused cardiac USSIC is associated with increased 90-day mortality.
Yu J, Zheng R, et al. [63]2022Cohort study124 Septic patientsLV-GLSLV-GLS predicted LV systolic dysfunction & death
Innocenti F, Palmieri V, et al. [64]2018ObservationalSeptic patients (~200)LV systolic-GLSGLS predicts short-term outcomes, independent of SOFA
Vallabhajosyula S, Rayes HA, et al. [65]2019Systematic reviewSeptic patients (120 studies)Speckle-tracking echocardiography (STE)STE strong predictor of mortality
Zhao JL, Wang R, et al. [66]2023Observational58 Septic patientsRV echo + GLS + biomarkersGLS + biomarkers predicted mortality
Thockchom N, Bairwa M, et al. [68]2023Longitudinal study132 patients Sepsis + diabetesLV diastolicDiastolic dysfunction predicted worse outcome
Lin YM, Lee MC, et al. [69]2022Meta-analysis>20 studiesLV/RVSICM linked with increased mortality
Koowattanatianchai S, Kochaiyapatana P, et al. [70]2025Prognostic analysis104 Septic patientsRV systolicRV dysfunction predicted short-term survival
Lanspa MJ, Cirulis MM, et al. [71]2021Cohort study393 Septic shock patientsRV parametersRV dysfunction associated with worse outcomes
Innocenti F, Palmieri V, et al. [72]2020Observational252 ED septic patientsRV systolicRV dysfunction frequent, prognostic role
Kim JS, Kim YJ, et al. [73]2020Observational778 Septic shock patientsRV functionRV dysfunction linked with mortality
Vallabhajosyula S, Kumar M, et al. [74]2017Historical cohort (8 years)388 ICU septic patientsRV dysfunctionRV dysfunction independently predicted mortality
Zhang H, Huang W, et al. [75]2021Observational215 Ventilated septic ptsVarious RV dysfunction typesRV failure and RV dysfunction are associated with 30 days mortality
Vallabhajosyula S, Shankar A, et al. [76]2021Meta-analysis1373 patientsRV dysfunctionRV dysfunction ↑ short- & long-term mortality
Perencin A, Curreri C, et al. [77]2025Systematic review/meta-analysis1812 Septic/septic shock patientsTAPSETAPSE predictive of mortality
Liu H, He H, et al. [78]2025Retrospective cohort93 SCM patientsTAPSELow TAPSE predicted poor outcome
Sanderson T, Samuels T. et al. [79]2025Cohort studyICU septic patientsRV strain, myocardial workBoth associated with mortality
Sukrisd Koowattanatianchai et al. [70]2025prospective cohort study104 adult septic patients RV dysfunctionRV dysfunction ↑ mortality
Innocenti F, Palmieri V, et al. [80]2022ObservationalSeptic patientsEcho vs. troponinEcho predicts the short- and medium-term mortality rate
Gajardo AIJ, Ferrière-Steinert S, et al. [81]2025Systematic review/meta-analysis6242 patients from 17 studiesBiomarkers (not echo)Elevated troponin not predicted higher mortality in sepsis
Wang TT, Jiang L. [82]2017Observational125 Critically ill septic patientsBiomarker studyhs-cTnT not associated with severity of sepsis
Innocenti F, Palmieri V, et al. [85]2021ObservationalSeptic shock ptsSpeckle trackingLV and RV dysfunction
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MDPI and ACS Style

Piccioni, A.; Rozzi, G.; Spaziani, G.; Novelli, M.; Fuorlo, M.; Candelli, M.; Pignataro, G.; Santarelli, L.; Covino, M.; Gasbarrini, A.; et al. From Fluid Responsiveness to Prognosis: The Emerging Role of Point-of-Care Echocardiography in Sepsis. Diagnostics 2025, 15, 2612. https://doi.org/10.3390/diagnostics15202612

AMA Style

Piccioni A, Rozzi G, Spaziani G, Novelli M, Fuorlo M, Candelli M, Pignataro G, Santarelli L, Covino M, Gasbarrini A, et al. From Fluid Responsiveness to Prognosis: The Emerging Role of Point-of-Care Echocardiography in Sepsis. Diagnostics. 2025; 15(20):2612. https://doi.org/10.3390/diagnostics15202612

Chicago/Turabian Style

Piccioni, Andrea, Gloria Rozzi, Giacomo Spaziani, Michela Novelli, Mariella Fuorlo, Marcello Candelli, Giulia Pignataro, Luca Santarelli, Marcello Covino, Antonio Gasbarrini, and et al. 2025. "From Fluid Responsiveness to Prognosis: The Emerging Role of Point-of-Care Echocardiography in Sepsis" Diagnostics 15, no. 20: 2612. https://doi.org/10.3390/diagnostics15202612

APA Style

Piccioni, A., Rozzi, G., Spaziani, G., Novelli, M., Fuorlo, M., Candelli, M., Pignataro, G., Santarelli, L., Covino, M., Gasbarrini, A., & Franceschi, F. (2025). From Fluid Responsiveness to Prognosis: The Emerging Role of Point-of-Care Echocardiography in Sepsis. Diagnostics, 15(20), 2612. https://doi.org/10.3390/diagnostics15202612

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