Evidence map›Paper›PMID 42056366›Full record

ArticleJournal of general internal medicine2026

Severity of Gastrointestinal Bleeding in Anticoagulant Therapy with Vitamin K Antagonist or Direct Oral Anticoagulant Therapy.

Christine Benn Christiansen, Nadia A Henriksen, Jakob Burcharth, Morten Lamberts, Emil Fosbøl, Jawad Haider Butt, Gunnar Gislason, Christian Torp-Pedersen

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Article in Journal of general internal medicine, 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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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Christine Benn ChristiansenDepartment of Cardiology, Nordsjaellands Hospital, Hillerød, Denmark. christinebenn@hotmail.com.ORCID http://orcid.org/0000-0002-0330-8997
Nadia A HenriksenDigestive Disease Center, Bispebjerg Hospital, Copenhagen, Denmark.
Jakob BurcharthDepartment of Gastrointestinal and Hepatic Diseases, Herlev and Gentofte Hospital, Herlev, Denmark.
Morten LambertsDepartment of Cardiology, Herlev and Gentofte Hospital, Herlev, Denmark.
Emil FosbølDepartment of Cardiology, Rigshospitalet, Copenhagen, Denmark.
Jawad Haider ButtDepartment of Cardiology, Rigshospitalet, Copenhagen, Denmark.
Gunnar GislasonDepartment of Cardiology, Herlev and Gentofte Hospital, Herlev, Denmark.
Christian Torp-PedersenDepartment of Public Health, University of Copenhagen, Copenhagen, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIt remains undetermined whether gastrointestinal bleeding (GIB) associated with direct oral anticoagulant (DOAC) or vitamin K antagonists (VKA) is more severe.

methodsIn Danish nationwide registries, we identified patients with atrial fibrillation (AF) treated with anticoagulation with gastrointestinal bleeding (GIB). Logistic regression models were used to compare GIB severity between DOAC and VKA users, defined by 1. red blood cell transfusion or in-hospital death and 2. endoscopies.

resultsFrom 2012-2018, 6,784 anticoagulated AF patients with GIB were identified; 3,724 patients VKA users and 3,060 DOAC (apixaban, dabigatran or rivaroxaban) users. The proportion of upper GIB was 49% in VKA users and 40.1% in DOAC users. Blood transfusions were administered to 58.2% and 43.8-48.9% of patients with VKA and DOAC, respectively. Odds ratios (OR, adjusted for age, sex, and comorbidities) for severe GIB were significantly reduced for all DOACs compared to VKA (apixaban 0.71 (95% confidence interval (CI) 0.59-0.85), dabigatran 0.64 (95% CI 0.55-0.75) and rivaroxaban 0.69 (95% CI 0.59-0.81)). Odds for endoscopy was significantly reduced in apixaban (OR 0.77 (95% CI 0.65-0.90) and dabigatran (OR 0.81 (95% CI 0.71-0.93) compared to VKA, and borderline reduced for rivaroxaban (OR 0.88 (95% CI 0.77-1.02)). In patients with upper GIB, compared to VKA the use of gastroscopy was significantly reduced for apixaban (0.68 (95% CI 0.53-0.87)) but not for dabigatran or rivaroxaban.

conclusionVKA use was associated with more severe GIB and more frequent endoscopies compared to DOAC. Future studies should identify subgroups at particular risk of severe GIB.

Indexed as

atrial fibrillationdirect oral anticoagulationgastrointestinal bleedingvitamin K antagonist

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.