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Published on: February 26, 2013
Outcomes Associated With Resuming Direct Oral Anticoagulant Therapy Following Admission for a Gastrointestinal Bleed
Sara M Valanejad1, Kyle A Davis1, Sarah A Nisly2
1Wake Forest Baptist Medical Center, Winston-Salem, NC, USA.
Insights
Direct oral anticoagulants (DOACs) are associated with gastrointestinal bleeds (GIB). Resuming DOAC therapy within 7 days of a GIB hospitalization did not increase the risk of recurrent GIB within 90 days.
Area of Science:
- Cardiology
- Gastroenterology
- Pharmacology
Background:
- Direct oral anticoagulants (DOACs) are increasingly used for anticoagulation.
- Gastrointestinal bleeds (GIB) are a known complication of DOAC therapy.
- Limited data exist on outcomes after resuming DOACs following a GIB.
Purpose of the Study:
- To evaluate practice patterns and clinical outcomes of patients hospitalized with GIB while on DOAC therapy.
- To assess the safety of resuming DOAC therapy after a GIB.
Main Methods:
- Retrospective, single-system study of adult patients on DOACs admitted with GIB.
- Analysis of 57 patients from January 2013 to October 2018.
- Comparison of outcomes between patients with DOAC therapy held >7 days versus resumed within 7 days.
Main Results:
- Most patients received rivaroxaban for atrial fibrillation and presented with major GIB requiring transfusion.
- Rates of recurrent GIB within 90 days were similar for patients holding or resuming DOACs (2.5% vs. 5.6%, P=0.83).
- 12-month mortality rates were not significantly different between groups (10.8% vs. 22.2%, P=0.28).
Conclusions:
- Resuming anticoagulation within 7 days of GIB admission was not associated with recurrent GIB.
- These findings suggest that early resumption of DOAC therapy may be safe following a GIB.
Background:
Although direct oral anticoagulants (DOACs) carry a lower bleeding risk compared with warfarin, gastrointestinal bleeds (GIB) are a known complication. There are limited data observing outcomes associated with resuming DOACs following a GIB.
Objective:
The purpose of this study was to evaluate practice patterns and clinical outcomes of patients admitted with an index GIB while receiving DOAC therapy.
Methods:
This retrospective, single-system study included adult patients receiving DOAC therapy prior to admission and hospitalized with an index GIB between January 1, 2013, and October 31, 2018. Patient exclusion criteria were a history of immune thrombocytopenia purpura or inflammatory bowel disease; discharge to hospice; leaving against medical advice; or death during hospitalization. The primary objective was 90-day readmission for a recurrent GIB.
Results:
There were 57 patients included for analysis; 37 patients had DOAC therapy held >7 days, 18 patients resumed DOAC therapy within 7 days, and 2 patients switched to warfarin. The majority of patients received rivaroxaban (59.6%) prior to admission for atrial fibrillation (71.9%), were admitted with a major GIB (66.7%), and required a blood transfusion (61.4%). The rates of recurrent GIB were 2.5% (n = 1) and 5.6% (n = 1) for those who had their DOAC held and resumed, respectively (P = 0.83). Mortality within 12 months of discharge occurred in 4 patients (10.8%) who had their DOAC held and 4 patients (22.2%) who resumed DOAC therapy (P = 0.28).
Conclusion And Relevance:
Resuming anticoagulation within 7 days of admission for an index GIB was not associated with a recurrent GIB within 90 days of discharge.
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