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Direct oral anticoagulants versus vitamin K antagonist after transcatheter aortic valve implantation

医学 维生素K拮抗剂 敌手 主动脉瓣 维生素k 内科学 心脏病学 心房颤动 华法林 受体
作者
Christopher Hohmann,Roman Pfister,Christian Frerker,Andreas Beckmann,Thomas Walther,Sabine Bleiziffer,Stephan Ensminger,Raffi Bekeredjian,Moritz Seiffert,Jan‐Malte Sinning,Helge Möllmann,Friedhelm Beyersdorf,Stephan Baldus,Andreas Böning,Eva Herrmann,Ümniye Balaban,Elmar Kuhn
出处
期刊:Heart [BMJ]
卷期号:109 (22): 1706-1713 被引量:4
标识
DOI:10.1136/heartjnl-2023-322548
摘要

Objective After transcatheter aortic valve implantation (TAVI), the optimal regimen of anticoagulant therapy in patients with an additional indication for oral anticoagulation remains a matter of debate. This study investigates the efficacy of direct oral anticoagulants (DOACs) versus vitamin K antagonists (VKAs) in patients after TAVI in a real-world population. Methods The German Aortic Valve RegistrY (GARY) is a prospective, multicentre registry enrolling patients undergoing invasive treatment for aortic valve disease. From January 2011 to December 2019, 1 41 790 patients from 92 hospitals in Germany were enrolled. Anticoagulatory treatment regimens were assessed at hospital discharge for patients after TAVI procedures. All-cause mortality and the combined endpoint ‘cardiac and cerebrovascular events’ containing myocardial infarction, stroke, transient ischaemic attack, aortic prosthesis reintervention and all-cause mortality in the first year after TAVI were examined by treatment regimen. Results Of 45 598 patients (mean age 80.7±5.7 years, 49.3% males) undergoing TAVI, 16 974 patients (37.2%) received an anticoagulant regimen that included VKA or DOAC. Hereof, the majority of patients were prescribed VKA (n=11 333, 66.8%) compared with DOAC (n=5641, 33.2%) with an increase of DOAC use from 9.4% in 2011 to 69.9% in 2019. During the 1-year follow-up, the absolute event rates per 100 person-years for all-cause mortality and the combined endpoint cardiac and cerebrovascular events were 1.9 and 1.3 for VKA-treated and 1.7 and 1.2 for DOAC-treated patients, respectively. After adjustment for baseline confounders, all-cause mortality (HR 0.95, 95% CI 0.88 to 1.01, p=0.114) and cardiac and cerebrovascular event-free survival (HR 0.93, 95% CI 0.86 to 1.01, p=0.071) did not differ significantly between VKA and DOAC groups. Conclusions This study supports evidence of the efficacy of DOAC use after TAVI in patients with an indication for oral anticoagulation.
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