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心外膜左心耳夹闭术与直接口服抗凝剂降低非阵发性心房颤动患者卒中风险的比较(LAA-CLIP):一项多中心随机对照试验的原理、设计和研究方案。

Epicardial left atrial appendage clipping versus direct oral anticoagulant to reduce stroke risk in non-paroxysmal atrial fibrillation (LAA-CLIP): rationale, design and study protocol for a multicentre randomised controlled trial.

机构信息

State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.

Department of Cardiovascular Surgery, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.

出版信息

BMJ Open. 2024 Mar 5;14(3):e083153. doi: 10.1136/bmjopen-2023-083153.

Abstract

INTRODUCTION

The prevalence of atrial fibrillation (AF) is increasing globally, and stroke prevention is the key to reduce the morbidity and mortality related to AF. Currently, direct oral anticoagulants (DOACs) are the primary options for stroke prevention, while it increases risk of bleeding. Left atrial appendage (LAA) is suspected as a vital source of cerebral emboli and may lead to ischaemic stroke, and thoracoscopic LAA clipping procedure provides an alternative option for stroke prevention in high-risk patients. However, high-quality evidence comparing LAA clipping to DOACs in terms of stroke prevention is lacking. This trial is designed to assess whether the efficacy of thoracoscopic LAA clipping is superior to DOACs for stroke prevention in AF patients at high risk of thrombosis (CHADS-VASc≥2 in men and ≥3 in women)[CHA2DS2-VASc stands for "congestive heart failure, hypertension, age ≥75 (doubled), diabetes, stroke (doubled), vascular disease, age 65 to 74 and sex category (female)"].

METHODS AND ANALYSIS

This is a prospective, multicentre, open-labelled, randomised controlled study. This trial will randomly assign 290 patients with non-paroxysmal AF to thoracoscopic LAA clipping group or DOAC therapy group in a 1:1 randomisation. The primary endpoint is defined as a composite endpoint event consisting of stroke, systemic embolism, all-cause mortality, major bleeding events and clinically relevant non-major bleeding events at 24 months after randomisation. The secondary endpoints consist of the components of the primary composite endpoint, surgery-related adverse events and minor bleeding events.

ETHICS AND DISSEMINATION

The central ethics committee at Fuwai Hospital approved the trial entitled "Epicardial left atrial appendage clipping versus direct oral anticoagulant to reduce stroke risk in non-paroxysmal atrial fibrillation (LAA-CLIP trial)". The results of this study will be disseminated through publications in peer-reviewed journals and conference presentations.

TRIAL REGISTRATION NUMBER

NCT06021808.

摘要

简介

心房颤动(AF)的患病率在全球范围内不断增加,预防中风是降低与 AF 相关发病率和死亡率的关键。目前,直接口服抗凝剂(DOACs)是预防中风的主要选择,但会增加出血风险。左心耳(LAA)被怀疑是脑栓塞的重要来源,可能导致缺血性中风,胸腔镜 LAA 夹闭术为高风险患者预防中风提供了另一种选择。然而,缺乏高质量的证据比较 LAA 夹闭与 DOACs 在预防中风方面的效果。本试验旨在评估胸腔镜 LAA 夹闭术在 CHADS-VASc 评分男性≥2 分和女性≥3 分(CHA2DS2-VASc 代表“充血性心力衰竭、高血压、年龄≥75 岁(加倍)、糖尿病、中风(加倍)、血管疾病、年龄 65 岁至 74 岁和性别类别(女性)”)的 AF 高危患者中预防中风的疗效是否优于 DOACs。

方法和分析

这是一项前瞻性、多中心、开放标签、随机对照研究。本试验将 290 例非阵发性 AF 患者随机分为胸腔镜 LAA 夹闭组或 DOAC 治疗组,比例为 1:1。主要终点定义为随机分组后 24 个月时发生的中风、全身性栓塞、全因死亡率、主要出血事件和临床相关非大出血事件的复合终点事件。次要终点包括主要复合终点的组成部分、与手术相关的不良事件和轻微出血事件。

伦理和传播

阜外医院中心伦理委员会批准了这项名为“心外膜左心耳夹闭术与直接口服抗凝剂降低非阵发性心房颤动中风风险(LAA-CLIP 试验)”的试验。本研究的结果将通过发表在同行评议期刊和会议报告中进行传播。

试验注册编号

NCT06021808。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d67/10916171/c002ecb372d0/bmjopen-2023-083153f01.jpg

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