All-cause mortality, stroke, and bleeding in patients with atrial fibrillation and valvular heart disease. Issue Volume 7:Issue FI1(2021) (17th February 2020)

• Record Type: Journal Article
• Authors: Strange, Jarl Emanuel; Sindet-Pedersen, Caroline; Staerk, Laila; Grove, Erik Lerkevang; Gerds, Thomas Alexander; Torp-Pedersen, Christian; Gislason, Gunnar H; Olesen, Jonas Bjerring
• Is Part Of: European heart journal. Volume 7:Issue FI1(2021)
• Page Start: f93
• Page End: f100
• Publication Date: 2020-02-17
• Subjects: Atrial fibrillation -- Anticoagulation -- Bleeding -- Mortality -- Stroke -- Valvular heart disease; Cardiovascular pharmacology -- Periodicals; 615.71
• DOI: 10.1093/ehjcvp/pvaa011
• Languages: English
• ISSNs: 2055-6837

Abstract

Abstract: Aims : To compare the risk of all-cause mortality, stroke, and bleeding in patients with atrial fibrillation (AF) and valvular heart disease (VHD) treated with vitamin K antagonist (VKA) or factor Xa-inhibitors (FXa-I; rivaroxaban and apixaban). Methods and results : We cross-linked data from Danish nationwide registries identifying patients with AF and VHD (aortic stenosis/insufficiency, mitral insufficiency, bioprosthetic heart valves, mitral-, and aortic valve repair) initiating VKA or FXa-I between January 2014 and June 2017. Outcomes were all-cause mortality, stroke, and bleeding. Using cause-specific Cox regression, we reported the standardized absolute 2-year risk of the outcomes and absolute risk differences (ARD). We identified 1115 (41.7%), 620 (23.1%), and 942 (35.2%) patients initiating treatment with VKA, rivaroxaban, and apixaban, respectively. The standardized absolute risk (95% confidence interval) of all-cause mortality associated with VKA treatment was 34.1% (30.4–37.8%) with corresponding ARD for FXa-I of −2.7% (−6.7% to 1.4%). The standardized absolute risk of stroke for VKA was 3.8% (2.2–5.4%) with corresponding ARD for FXa-I of –0.1% (−2.0% to 1.8%). The standardized risk of bleeding for VKA was 10.4% (7.2–12.9%) with corresponding ARD for FXa-I of –2.0% (−5.1% to 1.1%). The risk of bleeding was significantly reduced in subgroup analyses of apixaban compared with VKA [ARD: −3.9% (−7.0% to −0.9%)] and rivaroxaban [ARD: −5.6% (−9.5% to −1.7%)]. Conclusion : In this nationwide cohort study, there were no significant differences in the risks of all-cause mortality, stroke, and bleeding in patients with AF and VHD treated with VKA compared with FXa-I.