TY - JOUR
T1 - Mortality after major bleeding in Asian atrial fibrillation patients receiving different direct oral anticoagulants
T2 - a nationwide, propensity score study
AU - Yu, Jiun Hao
AU - Li, Pei Ru
AU - Chen, Dong Yi
AU - Huang, Wen Kuan
AU - See, Lai Chu
N1 - © 2024. The Author(s).
PY - 2024/2/27
Y1 - 2024/2/27
N2 - 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.
AB - 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.
KW - Humans
KW - Atrial Fibrillation/complications
KW - Rivaroxaban
KW - Dabigatran/adverse effects
KW - Anticoagulants/adverse effects
KW - Warfarin
KW - Factor Xa Inhibitors/adverse effects
KW - Stroke/complications
KW - Propensity Score
KW - Retrospective Studies
KW - Hemorrhage/drug therapy
KW - Administration, Oral
KW - Pyridines
KW - Thiazoles
UR - http://www.scopus.com/inward/record.url?scp=85186179758&partnerID=8YFLogxK
U2 - 10.1038/s41598-024-55500-z
DO - 10.1038/s41598-024-55500-z
M3 - 文章
C2 - 38413742
AN - SCOPUS:85186179758
SN - 2045-2322
VL - 14
SP - 4771
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 4771
ER -