Management of Acute Pulmonary Embolism

A special issue of Medicina (ISSN 1648-9144). This special issue belongs to the section "Pulmonology".

Deadline for manuscript submissions: closed (31 July 2023) | Viewed by 2661

Special Issue Editor


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Guest Editor
Clinic of Cardiology and Emergency Internal Medicine, Military Medical Academy, University of Defense, Belgrade, Serbia
Interests: lung embolism; embolectomy; blood clot lysis; atrial myxoma; acute coronary syndrome

Special Issue Information

Dear Colleagues,

Acute pulmonary embolism is the third cardio-vascular disease for mortality after myocardial infarction and stroke. Pulmonary embolism is a part of venous-thromboembolic disease, with many other diseases and conditions behind the thrombotic process that can strongly influence the management of patients. Anticoagulant therapy is a cornerstone of treating acute PE; however, the intensity and duration of therapy need a personal approach with huge gaps in knowledge. Regarding acute PE management, the classical European Society of Cardiology model for the assessment of mortality risk is far from clinical needs, and there is room for many fine tunings here. For instance, should we have sex adjustment of the many cut-off parameters used for risk stratification, for instance, even for arterial systolic blood pressure cut-off for the high-risk determination? In clinical praxis, we feel that many patients with intermediate-high risk acute PE who have some high-risk features or do not improve on anticoagulation therapy alone could benefit from reperfusion therapy before hemodynamic deterioration. However, what is the best reperfusion therapy? Lower-dose systemic thrombolysis, lower-dose catheter-directed thrombolysis, catheter mechanical therapy, or surgical embolectomy. Additionally, how can we estimate the risk for bleeding in thrombolysis, which is the main obstacle to this treatment, and does the use of local thrombolysis with a low dose of thrombolytic drugs or mechanical reperfusion can prevent serious bleeding? The important questions are also how to prevent the late complications of acute PE, such as chronic thromboembolic pulmonary hypertension and post-thrombotic syndrome. Are direct oral anticoagulant drugs better for this purpose? Do we need percutaneous intervention for patients with large thrombus burden, trying to reduce it in the subacute phase of PE? Oncology patients with acute PE need special consideration. Do we need special thromboembolic treatment for various malignant diseases since the pathophysiology of thrombosis in oncology patients might differ?

Prof. Dr. Slobodan Obradović
Guest Editor

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Keywords

  • pulmonary embolism
  • risk stratification
  • pathophysiology
  • anticoagulant therapy
  • reperfusion therapy

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Published Papers (1 paper)

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Research

17 pages, 3073 KiB  
Article
ACE2 and a Traditional Chinese Medicine Formula NRICM101 Could Alleviate the Inflammation and Pathogenic Process of Acute Lung Injury
by Cheng-Han Lin, Yi-Ju Chen, Meng-Wei Lin, Ho-Ju Chang, Xin-Rui Yang and Chih-Sheng Lin
Medicina 2023, 59(9), 1554; https://doi.org/10.3390/medicina59091554 - 26 Aug 2023
Cited by 5 | Viewed by 2203
Abstract
COVID-19 is a highly transmittable respiratory illness caused by SARS-CoV-2, and acute lung injury (ALI) is the major complication of COVID-19. The challenge in studying SARS-CoV-2 pathogenicity is the limited availability of animal models. Therefore, it is necessary to establish animal models that [...] Read more.
COVID-19 is a highly transmittable respiratory illness caused by SARS-CoV-2, and acute lung injury (ALI) is the major complication of COVID-19. The challenge in studying SARS-CoV-2 pathogenicity is the limited availability of animal models. Therefore, it is necessary to establish animal models that can reproduce multiple characteristics of ALI to study therapeutic applications. The present study established a mouse model that has features of ALI that are similar to COVID-19 syndrome to investigate the role of ACE2 and the administration of the Chinese herbal prescription NRICM101 in ALI. Mice with genetic modifications, including overexpression of human ACE2 (K18-hACE2 TG) and absence of ACE2 (mACE2 KO), were intratracheally instillated with hydrochloric acid. The acid intratracheal instillation induced severe immune cell infiltration, cytokine storms, and pulmonary disease in mice. Compared with K18-hACE2 TG mice, mACE2 KO mice exhibited dramatically increased levels of multiple inflammatory cytokines (IL-6 and TNF-α) in bronchoalveolar lavage fluid, histological evidence of lung injury, and dysregulation of MAPK and MMP activation. In mACE2 KO mice, NRICM101 could ameliorate the disease progression of acid-induced ALI. In conclusion, the established mouse model provided an effective platform for researchers to investigate pathological mechanisms and develop therapeutic strategies for ALI, including COVID-19-related ALI. Full article
(This article belongs to the Special Issue Management of Acute Pulmonary Embolism)
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