AI Article Synopsis

  • A study was conducted to evaluate how prednisolone affects clinical outcomes and safety in ulcerative colitis patients treated with infliximab, with a focus on corticosteroid-free clinical remission (CFCR).
  • Among the 147 patients reviewed, there was no overall association between prednisolone use and CFCR at weeks 14 or 52, but standard tapering of prednisolone showed better results compared to faster tapering regimens.
  • Despite no impact on infliximab levels, higher infection rates were noted in patients taking prednisolone, especially in those with greater disease severity, suggesting that corticosteroid therapy may benefit certain patients.

Article Abstract

Background And Objective: The influence of concomitant prednisolone on clinical outcomes and safety in infliximab-treated ulcerative colitis (UC) patients is unknown.

Design, Setting, Participants And Outcome Measures: A retrospective cohort study was performed, including 147 UC patients treated with infliximab at a tertiary inflammatory bowel disease (IBD) centre. Primary outcome was corticosteroid-free clinical remission (CFCR) at week 14 and week 52. Patients were grouped according to prednisolone tapering regimens: standard (≤5 mg/week), fast (>5 mg/week), direct discontinuation or no prednisolone. Patients intolerant to corticosteroids and patients stopping corticosteroids in preparation for surgery including colectomy during their initial admission were excluded.

Results: There was no overall association between prednisolone exposure or no exposure and CFCR at weeks 14 or 52 of infliximab. The proportion of patients with C reactive protein ≤5 mg/L was higher in the standard tapering at week 14 as compared with faster regimens or no prednisolone. In subgroup analyses, the standard tapering was associated with a higher rate of CFCR at week 14 compared with the fast-tapering regimen in patients receiving ≥40 mg prednisolone at initiation of infliximab (64.3% vs 26.3%, p=0.04) and among patients admitted with acute severe UC (66.6% vs 23.5%, p<0.05). Similar data were seen at week 52. Prednisolone did not affect infliximab trough levels but increased infection rates (10/77 vs 2/70, p=0.03), in particular infection.

Conclusion: In UC patients with limited disease burden, prednisolone did not affect effectiveness of infliximab. However, patients with increased disease burden seem to benefit from corticosteroid combination therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11085681PMC
http://dx.doi.org/10.1136/bmjgast-2024-001343DOI Listing

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