Role of Transcatheter Treatment in Intermediate-to High-risk Pulmonary Embolism.

IF 0.2 0 PHILOSOPHY
Interventional Cardiology Review Pub Date : 2025-05-23 eCollection Date: 2025-01-01 DOI:10.15420/icr.2024.47
Federica Fumarola, Francesco Colombo, Claudio Corsaro, Lucia Savi, Riccardo Mangione, Daniele Savio, Giacomo Boccuzzi, Mario Iannaccone
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引用次数: 0

Abstract

Pulmonary embolism (PE) is the third major cause of cardiovascular death in western countries. High-risk PE, defined by haemodynamic instability, necessitates immediate reperfusion therapy. Intermediate-high-risk patients, although stable, are vulnerable to rapid deterioration and therefore require intensive monitoring. To accurately stratify these patients, predict mortality and identify those who may benefit from more aggressive therapies, it is essential to consider various clinical and imaging parameters. Catheter-directed therapy (CDT) has been shown to reduce clot burden and right ventricle overload with fewer bleeding complications than systemic thrombolysis. CDT's clinical utility in the management of PE continues to expand, guided by the expertise of pulmonary embolism response teams, ensuring a multidisciplinary approach tailored to each patient's risk and clinical profile. As PE management advances, ongoing research and large-scale trials are essential for validating CDT's role in reducing morbidity and mortality in intermediate-high-risk PE cases. This review aims to provide a more in-depth perspective on intermediate-high-risk PE.

经导管治疗在中高危肺栓塞中的作用。
肺栓塞(PE)是西方国家心血管死亡的第三大原因。高危PE,由血流动力学不稳定定义,需要立即再灌注治疗。中高危患者虽然病情稳定,但容易迅速恶化,因此需要密切监测。为了准确地对这些患者进行分类,预测死亡率,并确定那些可能从更积极的治疗中受益的患者,必须考虑各种临床和影像学参数。导管定向治疗(CDT)已被证明可以减少凝块负担和右心室负荷,与全身溶栓相比,出血并发症更少。在肺栓塞反应小组的专业知识指导下,CDT在PE管理方面的临床应用不断扩大,确保针对每个患者的风险和临床情况量身定制多学科方法。随着PE管理的进步,正在进行的研究和大规模试验对于验证CDT在降低中高危PE病例发病率和死亡率方面的作用至关重要。本综述旨在为中高危PE提供更深入的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Interventional Cardiology Review
Interventional Cardiology Review Medicine-Cardiology and Cardiovascular Medicine
CiteScore
0.30
自引率
0.00%
发文量
18
审稿时长
12 weeks
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