左心室血栓患者的口服抗凝药--系统回顾和荟萃分析。

IF 5.3 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS European Heart Journal - Cardiovascular Pharmacotherapy Pub Date : 2024-08-14 DOI:10.1093/ehjcvp/pvae042
Paul M Haller, Niema Kazem, Stefan Agewall, Claudio Borghi, Claudio Ceconi, Dobromir Dobrev, Elisabetta Cerbai, Erik Lerkevang Grove, Juan Carlos Kaski, Basil S Lewis, Alexander Niessner, Bianca Rocca, Giuseppe Rosano, Gianluigi Savarese, Renate B Schnabel, Anne Grete Semb, Samuel Sossalla, Sven Wassmann, Patrick Sulzgruber
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引用次数: 0

摘要

目的:直接口服抗凝剂(DOAC)越来越多地被用于治疗左心室血栓(LVT)患者。我们分析了现有的荟萃数据,比较了 DOAC 和维生素 K 拮抗剂(VKAs)的疗效和安全性:我们对 LVT 患者中 DOAC 与 VKAs 比较的观察性和随机数据进行了系统检索和荟萃分析。研究终点为中风或全身性栓塞、血栓溶解、全因死亡和综合出血终点。使用随机效应模型荟萃分析对估计值进行汇总,并使用敏感性分析和影响分析对其稳健性进行研究:我们确定了 22 篇文章(18 项观察性研究、4 项小型随机临床试验),共报告了 3,587 名患者(2,489 名患者接受 VKA 治疗,1,098 名患者接受 DOAC 治疗)。中风或全身性栓塞(OR 0.81;95% CI [0.57,1.15])和血栓溶解(OR 1.12;95% CI [0.86,1.46])的汇总估计值相当,纳入研究的总体异质性较低。使用 DOAC 可降低全因死亡几率(OR 0.65;95%CI [0.46;0.92])和复合出血终点(OR 0.67;95%CI [0.47;0.97])。特别是观察性报告存在明显的偏倚风险,漏斗图显示了一些发表偏倚:在这项以观察性数据为主的综合分析中,与 VKA 治疗相比,使用 DOACs 与中风、全身性栓塞或血栓溶解的显著差异无关。使用 DOACs 与较低的全因死亡率和较少的出血事件有关。需要进行足够规模的随机临床试验来证实这些研究结果,这样才能在 LVT 患者中更广泛地采用 DOACs。
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Oral anticoagulation in patients with left ventricular thrombus: a systematic review and meta-analysis.

Aims: Direct oral anticoagulants (DOACs) are increasingly used off-label to treat patients with left ventricular thrombus (LVT). We analysed available meta-data comparing DOACs and vitamin K antagonists (VKAs) for efficacy and safety.

Methods: We conducted a systematic search and meta-analysis of observational and randomized data comparing DOACs vs. VKAs in patients with LVT. Endpoints of interest were stroke or systemic embolism, thrombus resolution, all-cause death, and a composite bleeding endpoint. Estimates were pooled using a random-effects model meta-analysis, and their robustness was investigated using sensitivity and influential analyses.

Results: We identified 22 articles (18 observational studies, 4 small randomized clinical trials) reporting on a total of 3587 patients (2489 VKA vs. 1098 DOAC therapy). The pooled estimates for stroke or systemic embolism [odds ratio (OR): 0.81; 95% confidence interval (CI): 0.57, 1.15] and thrombus resolution (OR: 1.12; 95% CI: 0.86, 1.46) were comparable, and there was low heterogeneity overall across the included studies. The use of DOACs was associated with lower odds of all-cause death (OR: 0.65; 95% CI: 0.46, 0.92) and a composite bleeding endpoint (OR: 0.67; 95% CI: 0.47, 0.97). A risk of bias was evident particularly for observational reports, with some publication bias suggested in funnel plots.

Conclusion: In this comprehensive analysis of mainly observational data, the use of DOACs was not associated with a significant difference in stroke or systemic embolism, or thrombus resolution, compared with VKA therapy. The use of DOACs was associated with a lower rate of all-cause death and fewer bleeding events. Adequately sized randomized clinical trials are needed to confirm these findings, which could allow a wider adoption of DOACs in patients with LVT.

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来源期刊
European Heart Journal - Cardiovascular Pharmacotherapy
European Heart Journal - Cardiovascular Pharmacotherapy Medicine-Cardiology and Cardiovascular Medicine
CiteScore
10.10
自引率
14.10%
发文量
65
期刊介绍: The European Heart Journal - Cardiovascular Pharmacotherapy (EHJ-CVP) is an international, peer-reviewed journal published in English, specifically dedicated to clinical cardiovascular pharmacology. EHJ-CVP publishes original articles focusing on clinical research involving both new and established drugs and methods, along with meta-analyses and topical reviews. The journal's primary aim is to enhance the pharmacological treatment of patients with cardiovascular disease by interpreting and integrating new scientific developments in this field. While the emphasis is on clinical topics, EHJ-CVP also considers basic research articles from fields such as physiology and molecular biology that contribute to the understanding of cardiovascular drug therapy. These may include articles related to new drug development and evaluation, the physiological and pharmacological basis of drug action, metabolism, drug interactions, and side effects.
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