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The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
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Mortality after major bleeding in Asian atrial fibrillation patients receiving different direct oral anticoagulants:
Jiun-Hao Yu1,2, Pei-Ru Li3, Dong-Yi Chen4,5
1Department of Emergency Medicine, China Medical University Hsinchu Hospital, China Medical University, Hsinchu, Taiwan.
Scientific Reports
|February 27, 2024
Summary
Direct oral anticoagulants (DOACs) are used for atrial fibrillation (AF). This study found factor Xa inhibitors increased 7-day mortality after major bleeding compared to dabigatran in AF patients.
Area of Science:
- Cardiology
- Pharmacology
- Public Health
Background:
- Atrial fibrillation (AF) management often involves anticoagulation.
- Direct oral anticoagulants (DOACs) are widely prescribed for AF.
- Major bleeding events are a significant complication in patients on anticoagulation therapy.
Purpose of the Study:
- To assess and compare 7-day and 30-day mortality rates following major bleeding events in atrial fibrillation patients treated with different DOACs.
- To identify potential differences in mortality risk among various DOACs after major bleeding episodes.
Main Methods:
- Retrospective cohort study using the Taiwan National Health Insurance Research Database (2016-2019).
- Inclusion of atrial fibrillation patients experiencing major bleeding while on dabigatran, rivaroxaban, apixaban, or edoxaban.
- Application of propensity score stabilized weighting to create comparable pseudo-DOAC groups for analysis.
Main Results:
- A total of 2770 patients were analyzed, with 85.3% on low-dose regimens.
- The 7-day mortality rate was 9.0%, increasing to 16.0% by day 30.
- Factor Xa inhibitors (rivaroxaban, apixaban, edoxaban) showed significantly higher 7-day mortality risk compared to dabigatran (p=0.012).
Conclusions:
- Factor Xa inhibitors are associated with a higher risk of 7-day mortality post-major bleeding compared to dabigatran in AF patients.
- This finding was consistent even in the subgroup receiving lower-dose DOACs.
- Clinical vigilance and further research are warranted regarding DOAC selection post-bleeding events.
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