作者
Ziv Harel,Brendan Smyth,Sunil V. Badve,Daniel Blum,William Beaubien‐Souligny,Samuel A. Silver,Edward G. Clark,Rita S. Suri,Thomas A. Mavrakanas,Joanna Sasal,Bhanu Prasad,John W. Eikelboom,Karthik Tennankore,Claudio Rigatto,Ivana Prce,François Madore,Fabrice Mac‐Way,Andrew Steele,Yangmin Zeng,Michelle Sholzberg,Paul Dorian,Andrew T. Yan,Manish M. Sood,David J. Gladstone,Chia‐Lin Tseng,Abhijat Kitchlu,Michael Walsh,Danny Sapir,Matthew J. Oliver,Murali Krishnan,Mercedeh Kiaii,Nikki Wong,Sradha Kotwal,Marissa Batisstella,Rey Acedillo,Charmaine E. Lok,M. Lynn Weir,Ron Wald
摘要
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.