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Published on: February 26, 2013
Gastrointestinal Bleeding and Direct Oral Anticoagulants among Patients with Atrial Fibrillation: Risk, Prevention,
Paolo Zappulla1, Valeria Calvi1
1Division of Cardiology, Centro alte specialità e trapianti (C.A.S.T.), Azienda Ospedaliero-Universitaria Policlinico "G. Rodolico - San Marco," University of Catania, Catania, Italy.
Insights
Direct oral anticoagulants (DOACs) increase gastrointestinal bleeding (GIB) risk, with rivaroxaban, dabigatran, and edoxaban showing higher risks. Apixaban did not increase GIB risk compared to warfarin.
Area of Science:
- Pharmacology
- Gastroenterology
- Clinical Medicine
Background:
- Gastrointestinal bleeding (GIB) is a significant complication for patients on oral anticoagulation therapy.
- The introduction of direct oral anticoagulants (DOACs) has heightened concerns regarding GIB.
- Patient quality of life (QOL) is impacted by long-term anticoagulation, necessitating lifestyle changes and increasing bleeding risk without clear symptomatic benefit.
Purpose of the Study:
- To examine current evidence on GIB associated with oral anticoagulants, focusing on DOACs.
- To compare the GIB risk profiles of different DOACs and warfarin.
- To summarize GIB risk factors, prevention strategies, and management of DOAC therapy post-GIB.
Main Methods:
- Review of randomized controlled trials.
- Analysis of meta-analyses.
- Evaluation of postmarketing observational studies.
Main Results:
- Rivaroxaban and dabigatran (150-mg dose) were associated with an increased risk of GIB.
- Edoxaban use also showed a dose-dependent increase in GIB risk.
- Apixaban demonstrated no higher GIB risk compared to warfarin.
Conclusions:
- Different DOACs exhibit varying GIB risk profiles.
- Understanding individual anticoagulant risks is crucial for patient safety.
- Strategies for GIB prevention and post-episode management are essential for optimizing anticoagulation therapy.
Abstract:
A significant problem for patients undergoing oral anticoagulation therapy is gastrointestinal bleeding (GIB), a problem that has become increasingly urgent following the introduction of direct oral anticoagulants (DOACs). Furthermore, in recent years a greater focus has been placed on the quality of life (QOL) of patients on long-term oral anticoagulant therapy, which necessitates changes in lifestyle, as well as posing an increased risk of bleeding without producing objective symptomatic relief. Here, we examine current evidence linked to GIB associated with oral anticoagulants, with a focus on randomized control trials, meta-analyses, and postmarketing observational studies. Rivaroxaban and dabigatran (especially the 150-mg bis-in-die dose) appeared to be linked to an increased risk of GIB. The risk of GIB was also greater when edoxaban was used, although this was dependent on the dose. Apixaban did not pose a higher risk of GIB in comparison with warfarin. We provided a summary of current knowledge regarding GIB risk factors for individual anticoagulants, prevention strategies that lower the risk of GIB and management of DOAC therapy after a GIB episode.
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