Mortality after major bleeding in Asian atrial fibrillation patients receiving different direct oral anticoagulants: a nationwide, propensity score study

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作者
Jiun-Hao Yu
Pei-Ru Li
Dong-Yi Chen
Wen-Kuan Huang
Lai-Chu See
机构
[1] China Medical University,Department of Emergency Medicine, China Medical University Hsinchu Hospital
[2] Chang Gung University,Graduate Institute of Management
[3] Chang Gung University,Department of Public Health, College of Medicine
[4] Chang Gung Memorial Hospital at Linkou,Division of Cardiology, Department of Internal Medicine
[5] Chang Gung University,School of Medicine, College of Medicine
[6] Chang Gung Memorial Hospital at Linkou,Division of Hematology/Oncology, Department of Internal Medicine
[7] Chang Gung Memorial Hospital at Linkou,Division of Rheumatology, Allergy, and Immunology
[8] Chang Gung University,Biostatistics Core Laboratory, Molecular Medicine Research Center
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In this research, we assessed mortality after major bleeding events in atrial fibrillation (AF) patients taking four direct oral anticoagulants (DOACs). Drawing data from the Taiwan National Health Insurance Research Database between 2016 and 2019, we focused on AF patients on DOACs who had major bleeding episodes. Using propensity score stabilized weighting, we established four comparable pseudo-DOAC groups. Among 2770 patients (460 dabigatran, 1322 rivaroxaban, 548 apixaban, 440 edoxaban), 85.3% were prescribed low-dose regimens. The 7-day mortality rate was 9.0%, surging to 16.0% by the 30th day. Compared with dabigatran, there was a distinct divergence in 7-day mortality of factor Xa inhibitors (p = 0.012), with hazard ratios of 1.83 (95% CI 1.11–3.00, p = 0.017) for rivaroxaban, 2.13 (95% CI 1.23–3.66, p = 0.007) for apixaban, and 2.41 (95% CI 1.39–4.19, p = 0.002) for edoxaban. This pattern remained consistent when analyzing the subgroup that received lower dosages of DOACs. In conclusion, factor Xa inhibitors were associated with a significantly higher risk of 7-day mortality following major bleeding events than dabigatran among AF patients.
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