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Multicenter Study
. 2012 Sep;107(9):1409-22.
doi: 10.1038/ajg.2012.218. Epub 2012 Aug 14.

Serious infection and mortality in patients with Crohn's disease: more than 5 years of follow-up in the TREAT™ registry

Affiliations
Free PMC article
Multicenter Study

Serious infection and mortality in patients with Crohn's disease: more than 5 years of follow-up in the TREAT™ registry

Gary R Lichtenstein et al. Am J Gastroenterol. 2012 Sep.
Free PMC article

Abstract

Objectives: The objective of this study was to contribute long-term safety data for infliximab and other therapies in Crohn's disease (CD).

Methods: We prospectively evaluated CD patients enrolled in the large, observational Crohn's Therapy, Resource, Evaluation, and Assessment Tool registry, established to compare infliximab safety with conventional nonbiological medications in CD.

Results: A total of 6,273 patients were enrolled and evaluated on or before 23 February 2010; 3,420 received infliximab (17,712 patient-years; 89.9% received ≥ 2 infusions) and 2,853 received other-treatments-only (13,251 patient-years). Mean length of patient follow-up was 5.2 years. More infliximab- than other-treatments-only-treated patients had moderate-to-severe (30.6% vs. 10.7%) or severe-to-fulminant (2.5% vs. 0.6%) disease severity (P < 0.001). In the year before enrollment, more infliximab- than other-treatments-only-treated patients required surgical intervention (17.4% vs. 13.6%), medical hospitalization (14.2% vs. 8.8%), prednisone (47.8% vs. 31.4%), immunomodulators (52.0% vs. 32.1%), and narcotic analgesics (17.3% vs. 9.1%). Patient mortality was similar for infliximab- and other-treatments-only-treated patients (0.58 vs. 0.59/100 patient-years). In multivariate logistic regression analyses, treatment with prednisone (hazard ratio (HR) = 2.14, 95% confidence interval (CI) = 1.55, 2.95; P < 0.001) or narcotic analgesics (HR = 1.79, 95% CI = 1.29, 2.48; P < 0.001) and age (HR = 1.08, 95% CI = 1.07, 1.09; P < 0.001) were associated with increased mortality risk. Neither infliximab nor immunomodulator treatment was associated with increased mortality risk. Factors independently associated with serious infections included moderate-to-severe disease activity (HR = 2.24, 95% CI = 1.57, 3.19; P < 0.001), narcotic analgesic treatment (HR = 1.98, 95% CI = 1.44, 2.73; P < 0.001), prednisone therapy (HR = 1.57, 95% CI = 1.17, 2.10; P = 0.002), and infliximab treatment (HR = 1.43, 95% CI = 1.11, 1.84; P = 0.006).

Conclusions: Mortality was similar between infliximab- and other-treatments-only-treated CD patients. An increased risk of serious infection with infliximab was observed, although CD severity and use of prednisone or narcotic analgesics carried higher risks.

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Figures

Figure 1
Figure 1
Flow of participation in the Therapy, Resource, Evaluation, and Assessment Tool registry. Infliximab-treated patients are those patients who received infliximab within 12 weeks before registration, who were scheduled to receive infliximab within 30 days of registration, or who received infliximab at some other point in the registry (i.e., exposed while participating in the registry). Note that one patient who died after 23 February 2010 is included.

Comment in

References

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