Burden of major gastrointestinal bleeding among oral anticoagulant-treated non-valvular atrial fibrillation patients

Author:

Deitelzweig Steven1,Keshishian Allison23ORCID,Kang Amiee4,Dhamane Amol D.4,Luo Xuemei5,Balachander Neeraja4,Rosenblatt Lisa4,Mardekian Jack6,Jiang Jenny4,Yuce Huseyin3,Lip Gregory Y. H.7

Affiliation:

1. Department of Hospital Medicine, Ochsner Clinic Foundation, New Orleans, LA, USA and The University of Queensland School of Medicine, Ochsner Clinical School, 1514 Jefferson Highway, 11th Floor – Hospital Medicine Ochsner Health System, New Orleans, LA 70121, USA

2. STATinMED Research, Health Economics and Outcomes Research, Ann Arbor, MI, USA

3. New York City College of Technology, City University of New York, New York, NY, USA

4. Bristol-Myers Squibb Company, Lawrenceville, NJ, USA

5. Pfizer, Inc., Groton, CT, USA

6. Pfizer, Inc., New York, NY, USA

7. Liverpool Centre for Cardiovascular Science, University of Liverpool and Liverpool Heart & Chest Hospital, Liverpool, UK; and Aalborg Thrombosis Research Unit, Department of Clinical Medicine, Aalborg University, Aalborg, Denmark

Abstract

Background: Gastrointestinal (GI) bleeding is the most common type of major bleeding associated with oral anticoagulant (OAC) treatment. Patients with major bleeding are at an increased risk of a stroke if an OAC is not reinitiated. Methods: Non-valvular atrial fibrillation (NVAF) patients initiating OACs were identified from the Centers for Medicare and Medicaid Services ( CMS) Medicare data and four US commercial claims databases. Patients who had a major GI bleeding event (hospitalization with primary diagnosis of GI bleeding) while on an OAC were selected. A control cohort of patients without a major GI bleed during OAC treatment was matched to major GI bleeding patients using propensity scores. Stroke/systemic embolism (SE), major bleeding, and mortality (in the CMS population) were examined using Cox proportional hazards models with robust sandwich estimates. Results: A total of 15,888 patients with major GI bleeding and 833,052 patients without major GI bleeding were included in the study. Within 90 days of the major GI bleed, 58% of patients discontinued the initial OAC treatment. Patients with a major GI bleed had a higher risk of stroke/SE [hazard ratio (HR): 1.57, 95% confidence interval (CI): 1.42–1.74], major bleeding (HR: 2.79, 95% CI: 2.64–2.95), and all-cause mortality (HR: 1.29, 95% CI: 1.23–1.36) than patients without a major GI bleed. Conclusion: Patients with a major GI bleed on OAC had a high rate of OAC discontinuation and significantly higher risk of stroke/SE, major bleeding, and mortality after hospital discharge than those without. Effective management strategies are needed for patients with risk factors for major GI bleeding.

Funder

Pfizer

Bristol-Myers Squibb

Publisher

SAGE Publications

Subject

Gastroenterology

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