Anticoagulation for Patients with Atrial Fibrillation Receiving Dialysis: A Pilot Randomized Controlled Trial.

IF 10.3 1区 医学 Q1 UROLOGY & NEPHROLOGY
Ziv Harel, Brendan Smyth, Sunil V Badve, Daniel Blum, William Beaubien-Souligny, Samuel A Silver, Edward Clark, Rita Suri, Thomas A Mavrakanas, Joanna Sasal, Bhanu Prasad, John Eikelboom, Karthik Tennankore, Claudio Rigatto, Ivana Prce, Francois Madore, Fabrice Mac-Way, Andrew Steele, Yangmin Zeng, Michelle Sholzberg, Paul Dorian, Andrew T Yan, Manish M Sood, David J Gladstone, Eric Tseng, Abhijat Kitchlu, Michael Walsh, Danny Sapir, Matthew J Oliver, Murali Krishnan, Mercedeh Kiaii, Nikki Wong, Sradha Kotwal, Marissa Batisstella, Rey Acedillo, Charmaine Lok, Matthew Weir, Ron Wald
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引用次数: 0

Abstract

Background: Atrial fibrillation is common in individuals receiving dialysis. The role of oral anticoagulation in this population is uncertain given its exclusion from previous seminal clinical trials. Our objective was to determine the feasibility of performing a large definitive trial to establish the optimal anticoagulation strategy in individuals with atrial fibrillation receiving dialysis.

Methods: The SAFE-D trial was a parallel-group, open-label, allocation-concealed, pilot randomized control trial that took place at 28 centres in Canada and Australia. The trial included adults (≥18 y) undergoing dialysis with a history of non-valvular atrial fibrillation who met the CHADS-65 criteria. Participants were randomized 1:1:1 to receive dose-adjusted warfarin, apixaban 5 mg twice daily, or no oral anticoagulation and followed for 26 weeks. The primary outcomes evaluated the following measures of feasibility: a) recruitment of the target population within 2 years from the start of the trial; and b) adherence of >80% of randomized patients to the allocated treatment strategy at the conclusion of follow-up. Secondary outcomes included stroke and bleeding.

Results: From December 2019 through June 2022, 151 patients were enrolled and randomized to apixaban (n =51), warfarin (n=52) or no oral anticoagulation (n=48). Allowing for pauses related to the COVID pandemic, recruitment was completed in 30 months, and 123 (83%) of participants completed follow-up in their allocated treatment arm. There was one adjudicated stroke event. Eight participants had a major bleeding event (4 warfarin, 2 apixaban, 2 no oral anticoagulation). Death occurred in 15 participants (9 warfarin, 2 apixaban, 4 no oral anticoagulation). Time in the therapeutic range for warfarin recipients was 58% (IQR 47%-70%).

Conclusions: We have demonstrated the feasibility of recruitment and adherence in a trial that compared different anticoagulation strategies in patients with atrial fibrillation receiving dialysis.

接受透析的心房颤动患者的抗凝治疗:一项试点随机对照试验。
背景:心房颤动是透析患者的常见病。由于口服抗凝药被排除在之前的开创性临床试验之外,因此口服抗凝药在这一人群中的作用尚不确定。我们的目标是确定进行一项大型确定性试验的可行性,以确定接受透析的心房颤动患者的最佳抗凝策略:SAFE-D试验是一项平行分组、开放标签、分配隐藏的试验性随机对照试验,在加拿大和澳大利亚的28个中心进行。试验对象包括符合 CHADS-65 标准、正在接受透析且有非瓣膜性心房颤动病史的成年人(≥18 岁)。参与者按1:1:1的比例随机接受剂量调整后的华法林、阿哌沙班(5 毫克,每天两次)或无口服抗凝药治疗,并随访26 周。主要结果对以下可行性措施进行了评估:a) 自试验开始后 2 年内招募到目标人群;b) 随访结束时,大于 80% 的随机患者坚持所分配的治疗策略。次要结果包括中风和出血:从2019年12月到2022年6月,151名患者入组并随机接受阿哌沙班(n =51)、华法林(n =52)或无口服抗凝药(n =48)治疗。由于 COVID 大流行而暂停,招募工作在 30 个月内完成,123 名参与者(83%)在分配的治疗组完成了随访。经判定发生了一起中风事件。8名参与者发生了大出血事件(4名华法林、2名阿哌沙班、2名未进行口服抗凝治疗)。15名参与者死亡(9名华法林,2名阿哌沙班,4名未进行口服抗凝治疗)。华法林接受者在治疗范围内的时间为 58%(IQR 47%-70%):我们证明了在一项比较接受透析的心房颤动患者不同抗凝策略的试验中招募和坚持治疗的可行性。
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来源期刊
Journal of The American Society of Nephrology
Journal of The American Society of Nephrology 医学-泌尿学与肾脏学
CiteScore
22.40
自引率
2.90%
发文量
492
审稿时长
3-8 weeks
期刊介绍: The Journal of the American Society of Nephrology (JASN) stands as the preeminent kidney journal globally, offering an exceptional synthesis of cutting-edge basic research, clinical epidemiology, meta-analysis, and relevant editorial content. Representing a comprehensive resource, JASN encompasses clinical research, editorials distilling key findings, perspectives, and timely reviews. Editorials are skillfully crafted to elucidate the essential insights of the parent article, while JASN actively encourages the submission of Letters to the Editor discussing recently published articles. The reviews featured in JASN are consistently erudite and comprehensive, providing thorough coverage of respective fields. Since its inception in July 1990, JASN has been a monthly publication. JASN publishes original research reports and editorial content across a spectrum of basic and clinical science relevant to the broad discipline of nephrology. Topics covered include renal cell biology, developmental biology of the kidney, genetics of kidney disease, cell and transport physiology, hemodynamics and vascular regulation, mechanisms of blood pressure regulation, renal immunology, kidney pathology, pathophysiology of kidney diseases, nephrolithiasis, clinical nephrology (including dialysis and transplantation), and hypertension. Furthermore, articles addressing healthcare policy and care delivery issues relevant to nephrology are warmly welcomed.
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