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Gastrointestinal Bleeding on Oral Anticoagulation: What is Currently Known
Arnar B Ingason1, Johann P Hreinsson2, Einar S Björnsson3,4
1General Surgery Department, University of Vermont Medical Center, Burlington, VT, USA.
Insights
Direct oral anticoagulants (DOACs) show higher gastrointestinal bleeding (GIB) rates than warfarin in atrial fibrillation patients. However, bleeding risks vary among DOACs, with rivaroxaban potentially posing a higher GIB risk.
Area of Science:
- Cardiology
- Gastroenterology
- Pharmacology
Background:
- Gastrointestinal bleeding (GIB) is a significant concern for patients on oral anticoagulation therapy.
- Direct oral anticoagulants (DOACs) have been linked to increased GIB rates compared to warfarin in atrial fibrillation, but study heterogeneity exists.
Approach:
- Meta-analyses of randomized controlled trials (RCTs) and observational studies were reviewed to compare GIB rates.
- Direct comparisons between individual DOACs are limited, with observational studies providing the primary data.
Key Points:
- Rivaroxaban, high-dose dabigatran, and high-dose edoxaban showed higher GIB rates than warfarin in some analyses.
- Apixaban and low-dose dabigatran had similar GIB rates to warfarin.
- Observational studies suggest rivaroxaban may have a higher GIB risk compared to other DOACs.
Conclusions:
- While DOACs offer benefits, careful consideration of GIB risk, particularly with rivaroxaban, is crucial.
- Oral anticoagulation may aid colorectal cancer detection, and warfarin might reduce cancer incidence.
Abstract:
Gastrointestinal bleeding (GIB) is the most common type of bleeding occurring in patients on oral anticoagulation. A meta-analysis of the landmark randomized controlled trials (RCTs) for patients with atrial fibrillation demonstrated that direct oral anticoagulants (DOACs) were associated with higher GIB rates compared to warfarin. However, significant heterogeneity existed between studies. While rivaroxaban, high-dose dabigatran, and high-dose edoxaban were associated with higher GIB rates than warfarin, GIB rates were similar between warfarin users and both apixaban and low-dose dabigatran users. Additionally, previous observational studies have yielded conflicting reports on whether GIB rates differ between warfarin and DOACs. Meta-analyses of observational studies demonstrated that warfarin is associated with lower rates of GIB compared to rivaroxaban, similar or lower rates compared to dabigatran, and higher rates compared to apixaban. Importantly, no RCT has compared individual DOACs directly and due to the different selection criteria of the initial RCTs, indirect comparisons between DOACs using these studies are unreliable. The best available information of comparisons between individual DOACs is therefore limited to observational studies. There is mounting evidence that suggests that rivaroxaban is associated with a higher risk of GIB compared to other DOACs. Finally, GIB induced by oral anticoagulation may have some positive aspects. Interestingly, there are studies that indicate oral anticoagulation facilitates colorectal cancer detection. Furthermore, results from RCTs and observational studies suggest that warfarin may even decrease the incidence of cancer.
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