Publication

Association of Type of Antidepressant With Bleeding Risk in Atrial Fibrillation Patients Taking Oral Anticoagulants

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Last modified
  • 05/22/2025
Type of Material
Authors
    Iris Yuefan Shao, Emory UniversityJ’Neka S Claxton, Emory UniversityPamela L Lutsey, University of Minnesota, MinneapolisLin Yee Chen, University of Minnesota, MinneapolisRichard F MacLehose, University of Minnesota, MinneapolisAlvaro Alonso, Emory University
Language
  • English
Date
  • 2019-01-01
Publisher
  • LIPPINCOTT WILLIAMS & WILKINS
Publication Version
Copyright Statement
  • © The Author(s) 2021
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 139
Issue
  • 3
Start Page
  • 383
End Page
  • 391
Grant/Funding Information
  • This work was additionally supported by American Heart Association grant 16EIA26410001 (Alonso).
  • Research reported in this publication was supported by the National Institutes of Health under Award Numbers R01HL122200, R21AG058445, and K24HL14852. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Supplemental Material (URL)
Abstract
  • Background: Inconsistent evidence suggests that use of certain antidepressants, particularly selective serotonin reuptake inhibitors (SSRIs), in patients using oral anticoagulants (OACs) might be associated with an elevated risk of bleeding. Objective: This study aims to investigate the risk of bleeding associated with initiation of different types of antidepressants among atrial fibrillation (AF) patients on OAC therapy. Patients and methods: A total of 30,336 AF patients (mean age 72.2 years; 54% female) on OAC therapy that started antidepressant treatment were identified from the Truven Health Analytics MarketScan Commercial and Medicare Databases for the period 2007–2015. Exposure was defined as filling a prescription for antidepressant, and categorized as SSRI, serotonin/norepinephrine reuptake inhibitors (SNRIs), serotonin reuptake inhibitors (SRIs), tricyclic antidepressants (TCAs), or other antidepressants. The primary outcome was incident hospitalized bleeding. Associations of antidepressant type with bleeding were assessed calculating hazard ratios (HRs) and 95% confidence intervals (CIs) with adjusted Cox models in pairwise propensity score-matched cohorts. Results: During a mean follow-up of 21 months, we identified 1612 bleeding episodes. In pairwise comparisons, SSRI use was associated with an increased risk of bleeding when compared to most other antidepressants (HR 1.22, 95% CI 0.96–1.54 vs SNRI; HR 1.10, 95% CI 0.90–1.35 vs SRI; HR 1.03, 95% CI 0.82–1.30 vs TCA). SNRI use was associated with the lowest bleeding risk. Results did not differ by OAC type, age, and sex. Conclusions: Among AF patients on OAC initiating antidepressants, risk of bleeding varied across antidepressant type. This information can inform treatment choices among patients receiving OAC.
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Keywords
Research Categories
  • Health Sciences, Epidemiology

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