S1389 Clinical Outcomes of Gastrointestinal Bleeding in DOAC and Warfarin-Related Hospitalizations: A Population-Based Cohort Study

Introduction: Gastrointestinal (GI) bleeding is a frequent and serious adverse event associated with anticoagulant therapy. Although direct oral anticoagulants (DOACs) offer advantages such as fixed dosing and reduced monitoring needs, concerns remain regarding their bleeding risk, particularly in the gastrointestinal tract. Our study evaluates the relative risk of GI bleeding among hospitalized patients experiencing adverse effects from DOACs compared to warfarin, aiming to inform safer practices. Methods: We conducted a population-based cohort study using de-identified and publicly available of adults hospitalized in Texas to acute care hospitals (2016–2023) with a diagnosis of initial encounter for adverse effect of DOAC or Warfarin identified using ICD-10 codes T45.515A and T45.516A The primary outcome was a diagnosis of gastrointestinal tract bleeding using codes selected from Clinical Classification Software Refined category “DIG021: Gastrointestinal Hemorrhage”. Overlap propensity score weighting was applied to adjust for confounders. Results were reported as adjusted risk ratios (aRR) with 95% confidence intervals. Subgroup analyses were performed by age, sex, race/ethnicity, insurance type, and Deyo comorbidity index. Results: A total of 56,092 hospitalizations from 388 hospitals were analyzed, including 5,401 (9.6%) with adverse effects attributed to warfarin. Compared to DOAC-related hospitalizations, patients in the warfarin group were younger (35.9% vs 71.9% aged ≥65 years, P < 0.0001), had a lower comorbidity burden (mean Deyo index 2.22 ± 2.11 vs 2.53 ± 2.21, P < 0.0001), and shorter hospital stays (5.14 ± 5.04 vs 6.80 ± 6.97 days, P < 0.0001). Gastrointestinal bleeding occurred less frequently in the warfarin group (2.7% vs 21.1%), and this association persisted after adjustment (aRR 0.22; 95% CI: 0.18–0.26). Hospital mortality was higher with DOACs group (4.7% vs 1.2%). Subgroup analyses yielded consistent findings across all strata. Conclusion: In this large population-based cohort, warfarin use was associated with a significantly lower adjusted risk of gastrointestinal bleeding compared to DOACs. These findings highlight important safety considerations in anticoagulant selection and support the need for risk stratification in clinical decision-making.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001133016.01395.b9
Primary Topic
Gastrointestinal Bleeding Diagnosis and Treatment
Type
article
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article

S1389 Clinical Outcomes of Gastrointestinal Bleeding in DOAC and Warfarin-Related Hospitalizations: A Population-Based Cohort Study

Sachi Khemka, Avneet Kaur, John E. Garza, Anjul Verma et al.
The American Journal of Gastroenterology
Gastrointestinal Bleeding Diagnosis and Treatment
article

S1389 Clinical Outcomes of Gastrointestinal Bleeding in DOAC and Warfarin-Related Hospitalizations: A Population-Based Cohort Study

Sachi Khemka, Avneet Kaur, John E. Garza, Anjul Verma, Merry Mathew
article en

Abstract

Introduction: Gastrointestinal (GI) bleeding is a frequent and serious adverse event associated with anticoagulant therapy. Although direct oral anticoagulants (DOACs) offer advantages such as fixed dosing and reduced monitoring needs, concerns remain regarding their bleeding risk, particularly in the gastrointestinal tract. Our study evaluates the relative risk of GI bleeding among hospitalized patients experiencing adverse effects from DOACs compared to warfarin, aiming to inform safer practices. Methods: We conducted a population-based cohort study using de-identified and publicly available of adults hospitalized in Texas to acute care hospitals (2016–2023) with a diagnosis of initial encounter for adverse effect of DOAC or Warfarin identified using ICD-10 codes T45.515A and T45.516A The primary outcome was a diagnosis of gastrointestinal tract bleeding using codes selected from Clinical Classification Software Refined category “DIG021: Gastrointestinal Hemorrhage”. Overlap propensity score weighting was applied to adjust for confounders. Results were reported as adjusted risk ratios (aRR) with 95% confidence intervals. Subgroup analyses were performed by age, sex, race/ethnicity, insurance type, and Deyo comorbidity index. Results: A total of 56,092 hospitalizations from 388 hospitals were analyzed, including 5,401 (9.6%) with adverse effects attributed to warfarin. Compared to DOAC-related hospitalizations, patients in the warfarin group were younger (35.9% vs 71.9% aged ≥65 years, P < 0.0001), had a lower comorbidity burden (mean Deyo index 2.22 ± 2.11 vs 2.53 ± 2.21, P < 0.0001), and shorter hospital stays (5.14 ± 5.04 vs 6.80 ± 6.97 days, P < 0.0001). Gastrointestinal bleeding occurred less frequently in the warfarin group (2.7% vs 21.1%), and this association persisted after adjustment (aRR 0.22; 95% CI: 0.18–0.26). Hospital mortality was higher with DOACs group (4.7% vs 1.2%). Subgroup analyses yielded consistent findings across all strata. Conclusion: In this large population-based cohort, warfarin use was associated with a significantly lower adjusted risk of gastrointestinal bleeding compared to DOACs. These findings highlight important safety considerations in anticoagulant selection and support the need for risk stratification in clinical decision-making.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 45%
Gastrointestinal Bleeding Diagnosis and Treatment
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