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胸腔穿刺术缓解急性心力衰竭胸腔积液:多中心、开放标签、随机对照 TAP-IT 试验研究方案。

Thoracentesis to alleviate pleural effusion in acute heart failure: study protocol for the multicentre, open-label, randomised controlled TAP-IT trial.

机构信息

Department of Cardiology, Copenhagen University Hospital-Bispebjerg and Frederiksberg, Copenhagen, Denmark

Department of Cardiology, Copenhagen University Hospital-Bispebjerg and Frederiksberg, Copenhagen, Denmark.

出版信息

BMJ Open. 2024 Jan 19;14(1):e078155. doi: 10.1136/bmjopen-2023-078155.

Abstract

INTRODUCTION

Pleural effusion is present in half of the patients hospitalised with acute heart failure. The condition is treated with diuretics and/or therapeutic thoracentesis for larger effusions. No evidence from randomised trials or guidelines supports thoracentesis to alleviate pleural effusion due to acute heart failure. The Thoracentesis to Alleviate cardiac Pleural effusion Interventional Trial (TAP-IT) will investigate if a strategy of referring patients with acute heart failure and pleural effusion to up-front thoracentesis by pleural pigtail catheter insertion in addition to pharmacological therapy compared with pharmacological therapy alone can increase the number of days the participants are alive and not hospitalised during the 90 days following randomisation.

METHODS AND ANALYSIS

TAP-IT is a pragmatic, multicentre, open-label, randomised controlled trial aiming to include 126 adult patients with left ventricular ejection fraction ≤45% and a non-negligible pleural effusion due to heart failure. Participants will be randomised 1:1, stratified according to site and anticoagulant treatment, and assigned to referral to up-front ultrasound-guided pleural pigtail catheter thoracentesis in addition to standard pharmacological therapy or to standard pharmacological therapy only. Thoracentesis is performed according to local guidelines and can be performed in participants in the pharmacological treatment arm if their condition deteriorates or if no significant improvement is observed within 5 days. The primary endpoint is how many days participants are alive and not hospitalised within 90 days from randomisation and will be analysed in the intention-to-treat population. Key secondary outcomes include 90-day mortality, complications, readmissions, and quality of life.

ETHICS AND DISSEMINATION

The study has been approved by the Capital Region of Denmark Scientific Ethical Committee (H-20060817) and Knowledge Center for Data Reviews (P-2021-149). All participants will sign an informed consent form. Enrolment began in August 2021. Regardless of the nature, results will be published in a peer-reviewed medical journal.

TRIAL REGISTRATION NUMBER

NCT05017753.

摘要

简介

胸腔积液存在于一半因急性心力衰竭住院的患者中。对于较大的胸腔积液,该病症通过利尿剂和/或治疗性胸腔穿刺进行治疗。随机试验或指南均无证据支持胸腔穿刺术可缓解因急性心力衰竭导致的胸腔积液。胸腔穿刺术以缓解急性心力衰竭相关胸腔积液的干预试验(TAP-IT)将研究对于胸腔积液因心力衰竭而存在的急性心力衰竭患者,除药物治疗外,通过胸膜猪尾导管插入术立即进行胸腔穿刺术的策略是否与单独药物治疗相比,可以增加参与者在随机分组后 90 天内存活且未住院的天数。

方法和分析

TAP-IT 是一项实用的、多中心、开放标签、随机对照试验,旨在纳入 126 名左心室射血分数≤45%且因心力衰竭而有大量胸腔积液的成年患者。参与者将按 1:1 随机分组,按地点和抗凝治疗分层,并分配到除标准药物治疗外,还进行超声引导下胸膜猪尾导管胸腔穿刺术的转介或仅进行标准药物治疗。根据当地指南进行胸腔穿刺术,如果药物治疗组的病情恶化或在 5 天内无明显改善,也可对该组的参与者进行胸腔穿刺术。主要终点是从随机分组后 90 天内参与者存活且未住院的天数,将在意向治疗人群中进行分析。关键次要结局包括 90 天死亡率、并发症、再入院和生活质量。

伦理和传播

该研究已获得丹麦首都地区科学伦理委员会(H-20060817)和知识数据审查中心(P-2021-149)的批准。所有参与者都将签署知情同意书。招募于 2021 年 8 月开始。无论结果性质如何,结果都将发表在同行评议的医学期刊上。

试验注册号

NCT05017753。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b808/10806591/536d28696e47/bmjopen-2023-078155f01.jpg

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