Evidence map›Paper›PMID 41868114›Full record

ArticleFrontiers in pharmacology2026

Analysis of the clinical characteristics of direct oral anticoagulants-associated atraumatic splenic rupture.

Can Shi, Xia Wang, Siyi Zhang, Ren Guo, Tian Wu

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Can ShiThird Xiangya Hospital, Central South University, Changsha, China.
Xia WangThird Xiangya Hospital, Central South University, Changsha, China.
Siyi ZhangThird Xiangya Hospital, Central South University, Changsha, China.
Ren GuoThird Xiangya Hospital, Central South University, Changsha, China.
Tian WuThird Xiangya Hospital, Central South University, Changsha, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Atraumatic splenic rupture (ASR), though rare, is an adverse event linked to direct oral anticoagulants (DOACs). Given their widespread use and potentially fatal consequences if undiagnosed, heightened clinical awareness of DOAC-associated ASR is crucial. Our aim was to analyze the occurrence and clinical characteristics of ASR induced by DOACs. Methods: We conducted a retrospective analysis of all reported DOAC-associated ASR cases through 15 April 2025, without language restrictions. Results: A total of 27 patients (11 males and 16 females) were included with a median age of 64 years. Among them, apixaban (n = 17) was the most common DOAC, followed by rivaroxaban (n = 8) and dabigatran (n = 2), with atrial fibrillation (81.5%, n = 22) being the primary indication. The comorbidities observed among patients with DOAC-associated ASR risk included hypertension (25.9%), coronary heart disease (18.5%), malignancy (18.5%), and infections (18.5%). Among 27 patients, 11 (40.7%) received concomitant medications that may potentiate DOAC effects, with 5 patients taking four interacting drugs simultaneously. Only 4 of the 11 patients had documented anticoagulant dosages, half of which were full-dose regimens. Management included immediate DOAC cessation (100.0%), transfusion (77.8%), splenic artery embolization (44.4%), and splenectomy (70.4%) - with 31.6% of splenectomies representing salvage procedures following failed embolization. All patients were successfully discharged with no mortality. Conclusion: ASR is a potentially life-threatening but preventable DOAC complication. Early recognition-particularly in elderly patients with comorbidities and polypharmacy-and urgent imaging for abdominal pain are crucial for improving clinical outcomes.

Indexed as

abdominal painatraumatic splenic rupture (ASR)direct oral anticoagulants (DOACs)pharmacovigilancepolypharmacy

Identifiers

PMID41868114
PMCPMC13002362

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