American College of Gastroenterology-Canadian Association of Gastroenterology Clinical Practice Guideline: Management of Anticoagulants and Antiplatelets During Acute Gastrointestinal Bleeding and the Periendoscopic Period
- PMID: 35297395
- PMCID: PMC8966740
- DOI: 10.14309/ajg.0000000000001627
American College of Gastroenterology-Canadian Association of Gastroenterology Clinical Practice Guideline: Management of Anticoagulants and Antiplatelets During Acute Gastrointestinal Bleeding and the Periendoscopic Period
Abstract
We conducted systematic reviews of predefined clinical questions and used the Grading of Recommendations, Assessment, Development and Evaluations approach to develop recommendations for the periendoscopic management of anticoagulant and antiplatelet drugs during acute gastrointestinal (GI) bleeding and the elective endoscopic setting. The following recommendations target patients presenting with acute GI bleeding: For patients on warfarin, we suggest against giving fresh frozen plasma or vitamin K; if needed, we suggest prothrombin complex concentrate (PCC) compared with fresh frozen plasma administration; for patients on direct oral anticoagulants (DOACs), we suggest against PCC administration; if on dabigatran, we suggest against the administration of idarucizumab, and if on rivaroxaban or apixaban, we suggest against andexanet alfa administration; for patients on antiplatelet agents, we suggest against platelet transfusions; and for patients on cardiac acetylsalicylic acid (ASA) for secondary prevention, we suggest against holding it, but if the ASA has been interrupted, we suggest resumption on the day hemostasis is endoscopically confirmed. The following recommendations target patients in the elective (planned) endoscopy setting: For patients on warfarin, we suggest continuation as opposed to temporary interruption (1-7 days), but if it is held for procedures with high risk of GI bleeding, we suggest against bridging anticoagulation unless the patient has a mechanical heart valve; for patients on DOACs, we suggest temporarily interrupting rather than continuing these; for patients on dual antiplatelet therapy for secondary prevention, we suggest temporary interruption of the P2Y12 receptor inhibitor while continuing ASA; and if on cardiac ASA monotherapy for secondary prevention, we suggest against its interruption. Evidence was insufficient in the following settings to permit recommendations. With acute GI bleeding in patients on warfarin, we could not recommend for or against PCC administration when compared with placebo. In the elective periprocedural endoscopy setting, we could not recommend for or against temporary interruption of the P2Y12 receptor inhibitor for patients on a single P2Y12 inhibiting agent. We were also unable to make a recommendation regarding same-day resumption of the drug vs 1-7 days after the procedure among patients prescribed anticoagulants (warfarin or DOACs) or P2Y12 receptor inhibitor drugs because of insufficient evidence.
Copyright © 2022 The American College of Gastroenterology and the Canadian Association of Gastroenterology.
Conflict of interest statement
Guarantors of the article: Neena S. Abraham and Alan N. Barkun.
Specific author contributions: Neena S. Abraham and Alan N. Barkun contributed equally to this work. N.S.A. and A.N.B.: planning and execution; all authors: PICO development; G.I.L. and B.G.S.: assessment of evidence using GRADE method; G.I.L. and B.G.S.: preparation of evidence profiles; N.S.A., A.N.B., L.L., J.J.T., P.A.N., J.D., and G.I.L.: drafting of manuscript; all authors: critical review and approval of manuscript.
Financial support: No external support from an industry partner was obtained for this joint ACG/CAG guideline. The ACG and CAG equally shared the cost of producing this document.
Potential competing interests: N.S.A.: none declared. A.N.B.: Olympus Inc (Advisory Board Consulting); Pendopharm Inc (research presentation); Takeda (research presentation); none related to the topic of this guideline. B.G.S.: none declared. J.D.: Potential COI related to direct oral anticoagulants and low-molecular-weight heparin (Pfizer, Sanofi, Leo Pharma, Bristol-Myers Squibb, Portola, and Janssen). L.L.: none declared. P.A.N.: Medtronic (research), Optum (advisory panel), and AliveCor (equity/royalty relationship); none related to the topic of this guideline. J.J.T.: none declared. G.I.L.: none declared.
Comment in
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ACG-CAG provided suggestions for periendoscopic management of anticoagulants and antiplatelets.Ann Intern Med. 2022 Jul;175(7):JC74. doi: 10.7326/J22-0041. Epub 2022 Jul 5. Ann Intern Med. 2022. PMID: 35785542
References
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- Abraham NS, Noseworthy PA, Yao X, et al. . Gastrointestinal safety of direct oral anticoagulants: A large population-based study. Gastroenterology 2017;152(5):1014–21. e1011. - PubMed
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