Management of Gastrointestinal Bleeding Under Direct Oral Anticoagulants

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital, Strasbourg, France

About this trial

Gastrointestinal bleeding (GIB) is a common emergency in hepatology and gastroenterology, with an overall mortality rate ranging from 5% to 10% depending on the study. GIB is classified into two categories: upper GIB (80% of cases) and lower GIB (20% of cases). There are many risk factors for GIB, including anticoagulants. In cases of GD under anticoagulants, there are specific management recommendations. In particular, in cases of severe bleeding under direct oral anticoagulants (DOACs), it is recommended to stop treatment and correct coagulation parameters according to the severity of the bleeding and the associated thrombotic risk. Various treatments can be used for this purpose, including specific antidotes, fresh frozen plasma, and prothrombin complex concentrate (PCC). However, the role of PCC in this indication is uncertain, as is the efficacy and safety data for this drug, due to significant methodological limitations in the few studies conducted on the subject.

Eligibility criteria

Qualifiers

Adult patient (≥ 18 years)

Male or female

Patient admitted to the emergency department for gastrointestinal bleeding (hematemesis, melena, rectal bleeding, or hematochezia)

Taking a direct oral anticoagulant (dabigatran, apixaban, or rivaroxaban)

Disqualifiers

Subject who has expressed their objection to the reuse of their data for scientific research purposes.

Subject under guardianship, curatorship, or legal protection.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed