Key result
Oral anticoagulant initiation is linked to ~81% higher odds of abnormal uterine bleeding vs nonuse.
Why the study?
The real-world incidence of abnormal uterine bleeding after oral anticoagulant initiation stratified by agent and age group was not well established.
Does the initiation of oral anticoagulants increase the risk of abnormal uterine bleeding in women treated for DVT, PE, or atrial fibrillation/flutter?
Case-Control (n=1,661,466)
Does the initiation of oral anticoagulants increase the risk of abnormal uterine bleeding in women treated for DVT, PE, or atrial fibrillation/flutter?
Odds Ratio: 1.81 (95% CI 1.69–1.93)
Absolute Event Rate: 6.1% vs 3%
Initiation of oral anticoagulants significantly increases the real-world risk of abnormal uterine bleeding, with the highest risk observed among women under 50 years of age and those taking rivaroxaban.
Anticoagulant users may warrant closer AUB monitoring; this case-control association leaves open causality and agent-specific risks.
OBJECTIVE: To estimate the real-world incidence of abnormal uterine bleeding after oral anticoagulant initiation with a large national claims database, stratified by agent and age group. METHODS: We conducted a nested matched case-control study using the MarketScan Research Databases (2008-2022). Women 18 years of age or older initiating oral anticoagulants (warfarin, apixaban, rivaroxaban, dabigatran, and edoxaban) for deep venous thrombosis, pulmonary embolism, or atrial fibrillation or flutter were matched 1:5 to anticoagulant nonusers. The primary outcome was abnormal uterine bleeding (AUB) within 1 year. Secondary outcomes included the risk of hospitalizations, emergency department visits, and outpatient encounters related to AUB. All estimates were derived from conditional logistic regression models adjusted for matching factors and baseline clinical covariates. RESULTS: Among 276,911 anticoagulant users and 1,384,555 matched controls, the incidence of AUB was significantly higher in anticoagulant users (6.1% vs 3.0%, adjusted odds ratio [AOR] 1.81, 95% CI, 1.69-1.93). Anticoagulant users had higher odds of AUB-related hospitalization (0.8% vs 0.01%, AOR 62.32, 95% CI, 30.94-125.53), emergency department visits (0.9% vs 0.2%, AOR 5.78, 95% CI, 4.02-8.31), and outpatient encounters (4.6% vs 2.8%, AOR 1.42, 95% CI, 1.32-1.52). Women younger than 50 years of age had a greater relative increase in AUB (19.7% vs 9.2%, AOR 1.96, 95% CI, 1.79-2.14) compared with women 50 years of age or older (3.8% vs 2.0%, AOR 1.63, 95% CI, 1.50-1.78). Among all agents, rivaroxaban was associated with the highest risk of AUB. CONCLUSION: Oral anticoagulant therapy is associated with significantly increased odds of AUB, particularly among younger women. Rivaroxaban conferred the highest AUB risk.
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Yellin et al. (2026) conducted a case-control in Deep venous thrombosis, pulmonary embolism, or atrial fibrillation or flutter (n=1,661,466). Oral anticoagulants (warfarin, apixaban, rivaroxaban, dabigatran, edoxaban) vs. Anticoagulant nonusers was evaluated on Abnormal uterine bleeding (AUB) within 1 year (AOR 1.81, 95% CI 1.69-1.93). Oral anticoagulant initiation was associated with significantly increased odds of abnormal uterine bleeding compared to nonusers (6.1% vs 3.0%; AOR 1.81, 95% CI 1.69-1.93).
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