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

Jiun Hao Yu, Pei Ru Li, Dong Yi Chen, Wen Kuan Huang, Lai Chu See*

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

2 Scopus citations

Abstract

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.

Original languageEnglish
Article number4771
Pages (from-to)4771
JournalScientific Reports
Volume14
Issue number1
DOIs
StatePublished - 27 02 2024

Bibliographical note

© 2024. The Author(s).

Keywords

  • Humans
  • Atrial Fibrillation/complications
  • Rivaroxaban
  • Dabigatran/adverse effects
  • Anticoagulants/adverse effects
  • Warfarin
  • Factor Xa Inhibitors/adverse effects
  • Stroke/complications
  • Propensity Score
  • Retrospective Studies
  • Hemorrhage/drug therapy
  • Administration, Oral
  • Pyridines
  • Thiazoles

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