Effect of colchicine on perioperative atrial fibrillation and myocardial injury after non-cardiac surgery in patients undergoing major thoracic surgery (COP-AF): an international randomised trial.

IF 98.4 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
The Lancet Pub Date : 2023-11-04 Epub Date: 2023-08-25 DOI:10.1016/S0140-6736(23)01689-6
David Conen, Michael Ke Wang, Ekaterine Popova, Matthew T V Chan, Giovanni Landoni, Juan P Cata, Cara Reimer, Sean R McLean, Sadeesh K Srinathan, Juan Carlos Trujillo Reyes, Ascension Martín Grande, Anna Gonzalez Tallada, Daniel I Sessler, Edith Fleischmann, Barbara Kabon, Luca Voltolini, Patrícia Cruz, Donna E Maziak, Laura Gutiérrez-Soriano, William F McIntyre, Vikas Tandon, Elisabeth Martínez-Téllez, Juan Jose Guerra-Londono, Deborah DuMerton, Randolph H L Wong, Anna L McGuire, Biniam Kidane, Diego Parise Roux, Yaron Shargall, Jennifer R Wells, Sandra N Ofori, Jessica Vincent, Lizhen Xu, Zhuoru Li, John W Eikelboom, Sanjit S Jolly, Jeff S Healey, P J Devereaux
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引用次数: 0

Abstract

Background: Higher levels of inflammatory biomarkers are associated with an increased risk of perioperative atrial fibrillation and myocardial injury after non-cardiac surgery (MINS). Colchicine is an anti-inflammatory drug that might reduce the incidence of these complications.

Methods: COP-AF was a randomised trial conducted at 45 sites in 11 countries. Patients aged 55 years or older and undergoing major non-cardiac thoracic surgery were randomly assigned (1:1) to receive oral colchicine 0·5 mg twice daily or matching placebo, starting within 4 h before surgery and continuing for 10 days. Randomisation was done with use of a computerised, web-based system, and was stratified by centre. Health-care providers, patients, data collectors, and adjudicators were masked to treatment assignment. The coprimary outcomes were clinically important perioperative atrial fibrillation and MINS during 14 days of follow-up. The main safety outcomes were a composite of sepsis or infection, and non-infectious diarrhoea. The intention-to-treat principle was used for all analyses. This trial is registered with ClinicalTrials.gov, NCT03310125.

Findings: Between Feb 14, 2018, and June 27, 2023, we enrolled 3209 patients (mean age 68 years [SD 7], 1656 [51·6%] male). Clinically important atrial fibrillation occurred in 103 (6·4%) of 1608 patients assigned to colchicine, and 120 (7·5%) of 1601 patients assigned to placebo (hazard ratio [HR] 0·85, 95% CI 0·65 to 1·10; absolute risk reduction [ARR] 1·1%, 95% CI -0·7 to 2·8; p=0·22). MINS occurred in 295 (18·3%) patients assigned to colchicine and 325 (20·3%) patients assigned to placebo (HR 0·89, 0·76 to 1·05; ARR 2·0%, -0·8 to 4·7; p=0·16). The composite outcome of sepsis or infection occurred in 103 (6·4%) patients in the colchicine group and 83 (5·2%) patients in the placebo group (HR 1·24, 0·93-1·66). Non-infectious diarrhoea was more common in the colchicine group (134 [8·3%] events) than the placebo group (38 [2·4%]; HR 3·64, 2·54-5·22).

Interpretation: In patients undergoing major non-cardiac thoracic surgery, administration of colchicine did not significantly reduce the incidence of clinically important atrial fibrillation or MINS but increased the risk of mostly benign non-infectious diarrhoea.

Funding: Canadian Institutes of Health Research, Accelerating Clinical Trials Consortium, Innovation Fund of the Alternative Funding Plan for the Academic Health Sciences Centres of Ontario, Population Health Research Institute, Hamilton Health Sciences, Division of Cardiology at McMaster University, Canada; Hanela Foundation, Switzerland; and General Research Fund, Research Grants Council, Hong Kong.

秋水仙碱对大胸外科手术(COP-AF)患者围术期心房颤动和非心脏手术后心肌损伤的影响:一项国际随机试验
背景:较高水平的炎症生物标志物与非心脏手术后围手术期心房颤动和心肌损伤的风险增加有关。秋水仙碱是一种抗炎药,可以降低这些并发症的发生率。方法:COP-AF是一项随机试验,在11个国家的45个地点进行。年龄在55岁或55岁以上并接受大型非心脏胸部手术的患者被随机分配(1:1)接受口服秋水仙碱0.5 mg,每日两次或匹配的安慰剂,在手术前4小时内开始,持续10天。使用计算机化、基于网络的系统进行随机分组,并按中心进行分层。医疗服务提供者、患者、数据采集者和裁决者都被掩盖在治疗任务之外。在14天的随访中,共同主要结果是具有临床意义的围手术期心房颤动和MINS。主要的安全性结果是败血症或感染以及非感染性腹泻的复合。所有分析均采用意向治疗原则。该试验在ClinicalTrials.gov,NCT03310125上注册。研究结果:在2018年2月14日至2023年6月27日期间,我们招募了3209名患者(平均年龄68岁[SD7],1656[51.6%]男性)。1608名服用秋水仙碱的患者中有103名(6.4%)发生了临床上重要的心房颤动,1601名服用安慰剂的患者中也有120名(7.5%)发生了心房颤动(危险比[HR]0.85,95%CI 0.65-1.10;绝对风险降低[ARR]1.1%,95%CI-0.7-2.8;p=0.22)。在295名(18.3%)服用秋水仙碱的患者和325名(20.3%)服用安慰剂的患者中发生了MINS(HR0.89,0.76至1.05;ARR2.0%,-0.8至4.7;p=0.16)。秋水仙碱组103例(6.4%)患者和安慰剂组83例(5.2%)患者出现败血症或感染的综合转归(HR 1.24,0.93-1.66)。非感染性腹泻在秋水仙碱组(134例[8.3%])比安慰剂组(38例[2.4%];HR 3.64,2.54-5.22)更常见,秋水仙碱的给药并没有显著降低临床上重要的心房颤动或MINS的发生率,但增加了大多数良性非感染性腹泻的风险。资助:加拿大卫生研究院、加速临床试验联盟、安大略省学术健康科学中心替代资助计划创新基金、人口健康研究所、汉密尔顿健康科学、加拿大麦克马斯特大学心脏病学系;哈内拉基金会,瑞士;香港研究资助局普通研究基金。
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
The Lancet
The Lancet 医学-医学:内科
CiteScore
148.10
自引率
0.70%
发文量
2220
审稿时长
3 months
期刊介绍: The Lancet is a world-leading source of clinical, public health, and global health knowledge. It was founded in 1823 by Thomas Wakley and has been an independent, international weekly general medical journal since then. The journal has an Impact Factor of 168.9, ranking first among 167 general and internal medicine journals globally. It also has a Scopus CiteScore of 133·2, ranking it second among 830 general medicine journals. The Lancet's mission is to make science widely available to serve and transform society, positively impacting people's lives. Throughout its history, The Lancet has been dedicated to addressing urgent topics, initiating debate, providing context for scientific research, and influencing decision makers worldwide.
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