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Case report: Pentoxifylline treatment in microscopic colitis

RATIONALE: Microscopic colitis is a common cause of diarrhea. Pentoxifylline, a xanthine derivative with anti-tumor necrosis factor-alpha properties, is prescribed for intermittent claudication and other disorders. Our goal was to evaluate the outcomes of patients with microscopic colitis treated wi...

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Autores principales: Cotter, Thomas G., Kamboj, Amrit K., Hicks, Stephen Bradley, Tremaine, William J., Loftus, Edward V., Pardi, Darrell S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704791/
https://www.ncbi.nlm.nih.gov/pubmed/29145246
http://dx.doi.org/10.1097/MD.0000000000008355
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author Cotter, Thomas G.
Kamboj, Amrit K.
Hicks, Stephen Bradley
Tremaine, William J.
Loftus, Edward V.
Pardi, Darrell S.
author_facet Cotter, Thomas G.
Kamboj, Amrit K.
Hicks, Stephen Bradley
Tremaine, William J.
Loftus, Edward V.
Pardi, Darrell S.
author_sort Cotter, Thomas G.
collection PubMed
description RATIONALE: Microscopic colitis is a common cause of diarrhea. Pentoxifylline, a xanthine derivative with anti-tumor necrosis factor-alpha properties, is prescribed for intermittent claudication and other disorders. Our goal was to evaluate the outcomes of patients with microscopic colitis treated with pentoxifylline. PATIENT CONCERNS: Nine patients with microscopic colitis (8 collagenous colitis and 1 lymphocytic colitis) seen at Mayo Clinic, Rochester, between January 1, 1997 and November 30, 2016, were included. The median age was 56.9 years (range 51.6–60.2), 8 were female (89%), and the median disease duration was 64.8 months (range 60–109). The indications for treatment were budesonide refractoriness in 7 patients, budesonide dependence in 1 patient, and budesonide intolerance in 1 patient. DIAGNOSES: A histological diagnosis of microscopic colitis was confirmed in all patients. INTERVENTIONS: Pentoxifylline 400 mg three times a day was used for a median of 3 months (range 2.5–8.3). OUTCOMES: Complete response occurred in 1 patient (11%) and partial response in 3 patients (33%). The patient who achieved complete response was treated with pentoxifylline due to budesonide intolerance, and completed 43 months of successful maintenance therapy. There were no adverse effects reported. LESSONS: The majority of budesonide-experienced patients with active microscopic colitis did not respond to pentoxifylline. However, it was well-tolerated, with 1 patient achieving long-term remission and one-third of the cohort having a partial response. Larger controlled studies are required to evaluate the efficacy of pentoxifylline and predictors of response in microscopic colitis. In particular, patients who are not budesonide-refractory may be more likely to respond.
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spelling pubmed-57047912017-12-07 Case report: Pentoxifylline treatment in microscopic colitis Cotter, Thomas G. Kamboj, Amrit K. Hicks, Stephen Bradley Tremaine, William J. Loftus, Edward V. Pardi, Darrell S. Medicine (Baltimore) 4500 RATIONALE: Microscopic colitis is a common cause of diarrhea. Pentoxifylline, a xanthine derivative with anti-tumor necrosis factor-alpha properties, is prescribed for intermittent claudication and other disorders. Our goal was to evaluate the outcomes of patients with microscopic colitis treated with pentoxifylline. PATIENT CONCERNS: Nine patients with microscopic colitis (8 collagenous colitis and 1 lymphocytic colitis) seen at Mayo Clinic, Rochester, between January 1, 1997 and November 30, 2016, were included. The median age was 56.9 years (range 51.6–60.2), 8 were female (89%), and the median disease duration was 64.8 months (range 60–109). The indications for treatment were budesonide refractoriness in 7 patients, budesonide dependence in 1 patient, and budesonide intolerance in 1 patient. DIAGNOSES: A histological diagnosis of microscopic colitis was confirmed in all patients. INTERVENTIONS: Pentoxifylline 400 mg three times a day was used for a median of 3 months (range 2.5–8.3). OUTCOMES: Complete response occurred in 1 patient (11%) and partial response in 3 patients (33%). The patient who achieved complete response was treated with pentoxifylline due to budesonide intolerance, and completed 43 months of successful maintenance therapy. There were no adverse effects reported. LESSONS: The majority of budesonide-experienced patients with active microscopic colitis did not respond to pentoxifylline. However, it was well-tolerated, with 1 patient achieving long-term remission and one-third of the cohort having a partial response. Larger controlled studies are required to evaluate the efficacy of pentoxifylline and predictors of response in microscopic colitis. In particular, patients who are not budesonide-refractory may be more likely to respond. Wolters Kluwer Health 2017-11-17 /pmc/articles/PMC5704791/ /pubmed/29145246 http://dx.doi.org/10.1097/MD.0000000000008355 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0
spellingShingle 4500
Cotter, Thomas G.
Kamboj, Amrit K.
Hicks, Stephen Bradley
Tremaine, William J.
Loftus, Edward V.
Pardi, Darrell S.
Case report: Pentoxifylline treatment in microscopic colitis
title Case report: Pentoxifylline treatment in microscopic colitis
title_full Case report: Pentoxifylline treatment in microscopic colitis
title_fullStr Case report: Pentoxifylline treatment in microscopic colitis
title_full_unstemmed Case report: Pentoxifylline treatment in microscopic colitis
title_short Case report: Pentoxifylline treatment in microscopic colitis
title_sort case report: pentoxifylline treatment in microscopic colitis
topic 4500
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704791/
https://www.ncbi.nlm.nih.gov/pubmed/29145246
http://dx.doi.org/10.1097/MD.0000000000008355
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