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BACKGROUND aHR, 1.45; 95% CI, 1.30-1.61). This excess risk was observed in all IBD subtypes: Crohn's disease (aHR, 1.42; 95% CI, 1.16-1.73), ulcerative colitis (aHR, 1.44; 95% CI, 1.26-1.65), and IBD unclassified (aHR, 1.56; 95% CI, 1.01-2.41). Clinically active IBD was also associated with an increased 2-year all-cause mortality compared to quiescent IBD (mortality rate: 352.6 vs 106.3 per 10,000 person-years; aHR, 3.35; 95% CI, 3.21-3.49). Even in patients with clinically quiescent IBD, histologic inflammation was associated with an increased 2-year all-cause mortality (aHR, 1.42; 95% CI, 1.08-1.87). CONCLUSIONS: Both histologic inflammation and clinical activity of IBD were associated with increased all-cause mortality, suggesting that improved disease control may reduce mortality risk in IBD.
Sun et al. (Sun,) studied this question.