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

Author:

Hohmann ChristopherORCID,Pfister Roman,Frerker Christian,Beckmann Andreas,Walther Thomas,Bleiziffer Sabine,Ensminger Stephan,Bekeredjian Raffi,Seiffert MoritzORCID,Sinning Jan-Malte,Möllmann Helge,Beyersdorf Friedhelm,Baldus Stephan,Böning Andreas,Herrmann Eva,Balaban Ümniye,Kuhn Elmar

Abstract

ObjectiveAfter 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.MethodsThe 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.ResultsOf 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.ConclusionsThis study supports evidence of the efficacy of DOAC use after TAVI in patients with an indication for oral anticoagulation.

Funder

Deutsche Herzstiftung

Deutsches Zentrum für Herz-Kreislaufforschung

Publisher

BMJ

Subject

Cardiology and Cardiovascular Medicine

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