ArticleProceedings (Baylor University. Medical Center)2026
Does aspirin worsen Crohn's disease outcomes? A multicenter propensity-matched cohort study.
Article in Proceedings (Baylor University. Medical Center), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Authors and funding
7 authors.
Funding
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Abstract
Background: Aspirin is widely used for cardiovascular prevention, but its safety in Crohn's disease (CD) is unclear. Because CD involves chronic epithelial disruption and impaired mucosal repair, patients may be especially susceptible to aspirin-related injury. This study evaluated the association between aspirin use and major clinical outcomes in a large CD cohort. Methods: Using the TriNetX Network, we identified adults with CD and matched aspirin users 1:1 with nonusers using propensity scores incorporating demographics, comorbidities, and CD severity indicators. The primary outcome was all-cause mortality. Secondary outcomes included CD exacerbations, bowel obstruction, fistula, intestinal abscess, toxic megacolon, colorectal cancer, and colectomy. Risk ratios (RRs) with 95% confidence intervals (CIs) were calculated. Results: Among 376,833 adults with CD, 41,752 aspirin users were matched to 41,752 nonusers. Aspirin use was associated with higher all-cause mortality (RR 1.23) and increased CD exacerbations (RR 1.93). Rates of intestinal abscess (RR 1.32) and toxic megacolon (RR 1.87) were also elevated. No significant differences were observed for colorectal cancer or colectomy. Conclusion: Aspirin use in CD was associated with increased mortality and intestinal morbidity, underscoring the need for individualized prescribing.
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