Colon to Rectum

Am J Gastroenterol. 2022;117(8):1311–5

Tome J, Sehgal K, Kamboj AK, Comstock B, Harmsen WS, Khanna S, Pardi DS

Budesonide maintenance in microscopic colitis: Clinical outcomes and safety profile from a population-based study


Introduction: Outcomes and safety of budesonide maintenance therapy in microscopic colitis (MC) are not well known.
Methods: Adult residents of Olmsted County, MN, diagnosed with MC (2002–2019) and treated with budesonide were identified using the Rochester Epidemiology Project. Response was assessed at 12 ± 4 weeks after initiation of therapy and defined as complete (resolution of diarrhea), partial (≥ 50% improvement in the number of bowel movements), non-response (< 50% improvement), and intolerance (discontinued because of side effects). For safety outcomes, cases (budesonide maintenance) and MC controls (no budesonide therapy) were matched by sex and age at diagnosis (± 2 years).
Results: A total of 450 patients were identified, of whom 162 (36.0%) were treated with budesonide for induction of clinical remission (median age, 67 [23–91] years and 126 women [77.8%]). Clinical outcomes for induction were as follows: 130 (80.2%) complete response, 22 (13.6%) partial response, 8 (4.9%) no response, and 2 (1.2%) intolerance. After induction, 96 (63.2%) had recurrence after discontinuation, of whom 27 (28.1%) required further budesonide induction treatment without maintenance, 56 (58.3%) required long-term budesonide maintenance, and 13 (13.5%) were treated with other therapies. Of those receiving budesonide maintenance, all responded (55 [98.2%] complete and 1 [1.8%] partial). No patient stopped maintenance from adverse events. The median duration of follow-up was 5.6 (0.3–18.9) years. There was no significant difference between cases and controls in the incidence of osteopenia/osteoporosis, diabetes mellitus, hypertension, glaucoma, or cataracts.

Discussion: The long-term use of budesonide in microscopic colitis seems to be effective and generally well tolerated with limited adverse effects.

D.S. Pardi, M.D., Professor of Medicine, Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA,
E-Mail: pardi.darrell@mayo.edu

DOI: 10.14309/ajg.0000000000001774

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