{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,20]],"date-time":"2026-10-20T11:51:25Z","timestamp":1792497085849,"version":"4.5.0"},"reference-count":59,"publisher":"American Medical Association (AMA)","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi240142-4\">\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>Selective serotonin reuptake inhibitors (SSRIs) are commonly prescribed antidepressants associated with a small increased risk of major bleeding. However, the risk of bleeding associated with the concomitant use of SSRIs and oral anticoagulants (OACs) has not been well characterized.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi240142-5\">\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>To assess whether concomitant use of SSRIs with OACs is associated with an increased risk of major bleeding compared with OAC use alone, describe how the risk varies with duration of use, and identify key clinical characteristics modifying this risk.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi240142-6\">\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>A population-based, nested case-control study was conducted among patients with atrial fibrillation initiating OACs between January 2, 1998, and March 29, 2021. Patients were from approximately 2000 general practices in the UK contributing to the Clinical Practice Research Datalink. With the use of risk-set sampling, for each case of major bleeding during follow-up, up to 30 controls were selected from risk sets defined by the case and matched on age, sex, cohort entry date, and follow-up duration.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi240142-7\">\n                    <jats:title>Exposures<\/jats:title>\n                    <jats:p>Concomitant use of SSRIs and OACs (direct OACs and vitamin K antagonists [VKAs]) compared with OAC use alone.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi240142-8\">\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>The main outcome was incidence rate ratios (IRRs) of hospitalization for bleeding or death due to bleeding.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi240142-9\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>There were 42\u202f190 patients with major bleeding (mean [SD] age, 74.2 [9.3] years; 59.8% men) matched to 1\u202f156\u202f641 controls (mean [SD] age, 74.2 [9.3] years; 59.8% men). Concomitant use of SSRIs and OACs was associated with an increased risk of major bleeding compared with OACs alone (IRR, 1.33; 95% CI, 1.24-1.42). The risk peaked during the initial months of treatment (first 30 days of use: IRR, 1.74; 95% CI, 1.37-2.22) and persisted for up to 6 months. The risk did not vary with age, sex, history of bleeding, chronic kidney disease, and potency of SSRIs. An association was present both with concomitant use of SSRIs and direct OACs compared with direct OAC use alone (IRR, 1.25; 95% CI, 1.12-1.40) and concomitant use of SSRIs and VKAs compared with VKA use alone (IRR, 1.36; 95% CI, 1.25-1.47).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi240142-10\">\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>This study suggests that among patients with atrial fibrillation, concomitant use of SSRIs and OACs was associated with an increased risk of major bleeding compared with OAC use alone, requiring close monitoring and management of risk factors for bleeding, particularly in the first few months of use.<\/jats:p>\n                  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