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Gastrointestinal bleeding during anticoagulation with direct oral anticoagulants compared to vitamin K antagonists
Kanchan Dongre1, Yasmin Schmid2, Luana Nussbaum2
1Department of Patient Safety, Medical Directorate, University Hospital Basel, Switzerland.
Insights
Patients on vitamin K antagonists (VKAs) have more gastrointestinal bleeding (GIB) risk factors than those on direct oral anticoagulants (DOACs). DOACs are linked to early GIB, requiring vigilance in the initial months of treatment.
Area of Science:
- Gastroenterology
- Pharmacology
- Internal Medicine
Background:
- Oral anticoagulants, including vitamin K antagonists (VKAs) and direct oral anticoagulants (DOACs), increase the risk of gastrointestinal bleeding (GIB).
- Understanding the comparative risk profiles of VKAs and DOACs in GIB is crucial for patient safety.
Purpose of the Study:
- To compare gastrointestinal bleeding (GIB) cases associated with VKAs and DOACs.
- To analyze differences in risk factors, timing, severity, and outcomes of GIB between VKA and DOAC users.
Main Methods:
- Retrospective analysis of 248 patients with GIB treated at a Swiss university hospital between 2012 and 2018.
- Comparison of patient demographics, comorbidities, medication use, bleeding risk scores (HAS-BLED), INR levels, and GIB characteristics between VKA and DOAC groups.
Main Results:
- VKA patients exhibited a higher propensity for risk factors like comorbidities and interacting medications (higher HAS-BLED scores).
- Gastrointestinal bleeding occurred earlier in the DOAC group (median 3 months) compared to the VKA group (median 23.5 months).
- Amiodarone co-medication was significantly associated with GIB in the DOAC group.
Conclusions:
- While VKA users have more pre-existing risk factors for GIB, DOACs are associated with earlier onset GIB.
- Increased vigilance is recommended during the initial months of DOAC therapy due to the risk of early GIB.
- Amiodarone co-administration may represent a specific risk factor for GIB in patients taking DOACs.
Abstract:
Aim: Patients receiving oral anticoagulants with vitamin K antagonists (VKAs) and direct oral anticoagulants (DOACs) have an increased risk of gastrointestinal bleeding (GIB). We compared cases of GIB associated with VKAs and DOACs in terms of risk factors, scores, timing, location, severity, and outcome. Methods: Data from patients treated at a university hospital in Switzerland for GIB under VKA and DOACs between 2012 and 2018 were analyzed in this investigator-driven, retrospective, single-center study. Results: A total of 248 patients (110 males; median age, 80 years; 134 VKA, 114 DOAC) were included. No significant differences in age, weight or sex were observed. The propensity of the VKA group for risk factors such as comorbidities, interacting medications, or a high risk for bleeding (HAS-BLED score) was higher than that of the DOAC group. 56% of the VKA-treated patients had a supratherapeutic INR, and 25% in the DOAC group received an unlicensed dose. Significantly more patients in the DOAC group were not formally overdosed with OAC whilst receiving amiodarone compared to the VKA group (57% vs. 18%, respectively, p = 0.03). Latency between the documented start of oral anticoagulation and GIB was shorter in the DOAC group (median 3 months) than in the VKA group (median 23.5 months, p¡0.001). There were no differences in terms of location and severity of the GIB, length of hospitalization, or mortality. Conclusion: Patients taking VKAs displayed more risk factors for GIB than those taking DOACs. Treatment with DOACs was associated with early GIB and calls for increased vigilance during the first months after commencement. Co-medication with amiodarone appeared to be a risk factor for GIB in patients taking DOACs.
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