Key result
NOAC therapy carries a ~2% annual risk of gastrointestinal bleeding, largely driven by upper tract events.
Why the study?
Clinical characteristics of gastrointestinal bleeding during NOAC therapy have not been fully elucidated.
What are the clinical characteristics and risk factors for upper versus lower gastrointestinal bleeding in patients taking nonvitamin K oral anticoagulants?
Cohort (n=658)
What are the clinical characteristics and risk factors for upper versus lower gastrointestinal bleeding in patients taking nonvitamin K oral anticoagulants?
Answers are grounded in this paper and cite their sources.
In patients taking NOACs, upper gastrointestinal bleeding is associated with past digestive ulcers and lack of PPI use, whereas lower GIB is associated with NSAIDs, dual antiplatelet therapy, and prior GIB.
Nonvitamin K oral anticoagulants (NOACs) sometimes cause hemorrhage, and the gastrointestinal tract is a common site of involvement. However, clinical characteristics of gastrointestinal bleeding (GIB) during NOAC therapy have not been fully elucidated. We studied 658 patients who were prescribed dabigatran, rivaroxaban, or apixaban between April 2011 and November 2015. Medical charts were reviewed to examine whether clinically relevant bleeding (Bleeding Academic Research Consortium criteria type 2 or greater) developed. The incidence of GIB was 2.0%/year, and one-third was from the upper GI. Among all hemorrhagic events, GIB was the most common cause. The extent of bleeding from the GI tract, particularly the upper GI tract, was more serious than bleeding from the other site. Multiple regression analysis showed that both past digestive ulcer and absence of concomitant proton pump inhibitors were significantly associated with the incidence of upper GIB, while concomitant nonsteroidal anti-inflammatory drugs, dual antiplatelets, and past GIB were significant factors regarding lower GIB. GIB was common and serious in patients taking NOACs. Upper GIB tended to become more serious than lower GIB. Proton pump inhibitors seem to be key drugs for preventing upper GIB during NOAC therapy.
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Maruyama et al. (2018) conducted a cohort in Patients taking Nonvitamin K Oral Anticoagulants (n=658). Nonvitamin K oral anticoagulants (dabigatran, rivaroxaban, or apixaban) was evaluated on Clinically relevant bleeding (Bleeding Academic Research Consortium criteria type 2 or greater). In patients taking NOACs, the incidence of gastrointestinal bleeding was 2.0%/year, with upper GIB being more serious and associated with past ulcers and absence of proton pump inhibitors.
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