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Medical Treatment for Microscopic Colitis: A Community Hospital’s Experience

BACKGROUND: Lymphocytic colitis (LC) is a chronic disorder characterized by watery diarrhea. This study sought to evaluate if LC recurs after therapy, and the time frame in which this occurs. Secondary objectives included length and type of therapy, drug-free intervals, and reasons for drug disconti...

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Autores principales: Haidar, Abdallah, Kaur, Savreet, Jackson, Nancy, Parungao, Jose Mari, Piper, Michael, Cutler, Alan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5755633/
https://www.ncbi.nlm.nih.gov/pubmed/29317939
http://dx.doi.org/10.14740/gr907w
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author Haidar, Abdallah
Kaur, Savreet
Jackson, Nancy
Parungao, Jose Mari
Piper, Michael
Cutler, Alan
author_facet Haidar, Abdallah
Kaur, Savreet
Jackson, Nancy
Parungao, Jose Mari
Piper, Michael
Cutler, Alan
author_sort Haidar, Abdallah
collection PubMed
description BACKGROUND: Lymphocytic colitis (LC) is a chronic disorder characterized by watery diarrhea. This study sought to evaluate if LC recurs after therapy, and the time frame in which this occurs. Secondary objectives included length and type of therapy, drug-free intervals, and reasons for drug discontinuation. METHODS: A retrospective chart review between January 1, 2008 and October 30, 2015 of patients with biopsy-confirmed lymphocytic, collagenous, or microscopic colitis was conducted. Patient-reported average bowel movements/day were reviewed. Demographic data, dates of colonoscopy, follow-up, type and dose of medications used, and therapy start/stop dates were reviewed. RESULTS: Patients presenting with colonoscopic documented LC (n = 114) were predominantly female (88%), Caucasian (97%), with mean bowel movements/day of five. A total of 58/114 (51%) patients were placed on a therapy. Patients taking budesonide saw bowel movements/day reduced from 4.7 to 2.4 compared to 5.8 to 2.8 for those given 5-aminosalicylic acid (5-ASA). First-line medications budesonide and 5-aminosalicylic acid failed in 12/58 (21%) of patients, other drugs also resulted in therapy changes. Thirty-five percent required their initial therapy changed and of those 40% required a second change. Symptom exacerbations were documented during therapy for 19% of patients; therapy changes resulted in good response. CONCLUSIONS: Almost half of all LC cases (56/114) gradually improved without requiring therapy. Seventy-six percent of our treated patients responded well to budesonide when used as the first-line therapy. Similarly, 61.5% responded to 5-ASA. Budesonide was the drug of choice for flares. Tailoring drug therapy to meet individual patient’s needs appears to be the best current approach to managing LC.
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spelling pubmed-57556332018-01-09 Medical Treatment for Microscopic Colitis: A Community Hospital’s Experience Haidar, Abdallah Kaur, Savreet Jackson, Nancy Parungao, Jose Mari Piper, Michael Cutler, Alan Gastroenterology Res Original Article BACKGROUND: Lymphocytic colitis (LC) is a chronic disorder characterized by watery diarrhea. This study sought to evaluate if LC recurs after therapy, and the time frame in which this occurs. Secondary objectives included length and type of therapy, drug-free intervals, and reasons for drug discontinuation. METHODS: A retrospective chart review between January 1, 2008 and October 30, 2015 of patients with biopsy-confirmed lymphocytic, collagenous, or microscopic colitis was conducted. Patient-reported average bowel movements/day were reviewed. Demographic data, dates of colonoscopy, follow-up, type and dose of medications used, and therapy start/stop dates were reviewed. RESULTS: Patients presenting with colonoscopic documented LC (n = 114) were predominantly female (88%), Caucasian (97%), with mean bowel movements/day of five. A total of 58/114 (51%) patients were placed on a therapy. Patients taking budesonide saw bowel movements/day reduced from 4.7 to 2.4 compared to 5.8 to 2.8 for those given 5-aminosalicylic acid (5-ASA). First-line medications budesonide and 5-aminosalicylic acid failed in 12/58 (21%) of patients, other drugs also resulted in therapy changes. Thirty-five percent required their initial therapy changed and of those 40% required a second change. Symptom exacerbations were documented during therapy for 19% of patients; therapy changes resulted in good response. CONCLUSIONS: Almost half of all LC cases (56/114) gradually improved without requiring therapy. Seventy-six percent of our treated patients responded well to budesonide when used as the first-line therapy. Similarly, 61.5% responded to 5-ASA. Budesonide was the drug of choice for flares. Tailoring drug therapy to meet individual patient’s needs appears to be the best current approach to managing LC. Elmer Press 2017-12 2018-01-03 /pmc/articles/PMC5755633/ /pubmed/29317939 http://dx.doi.org/10.14740/gr907w Text en Copyright 2017, Haidar et al. http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Haidar, Abdallah
Kaur, Savreet
Jackson, Nancy
Parungao, Jose Mari
Piper, Michael
Cutler, Alan
Medical Treatment for Microscopic Colitis: A Community Hospital’s Experience
title Medical Treatment for Microscopic Colitis: A Community Hospital’s Experience
title_full Medical Treatment for Microscopic Colitis: A Community Hospital’s Experience
title_fullStr Medical Treatment for Microscopic Colitis: A Community Hospital’s Experience
title_full_unstemmed Medical Treatment for Microscopic Colitis: A Community Hospital’s Experience
title_short Medical Treatment for Microscopic Colitis: A Community Hospital’s Experience
title_sort medical treatment for microscopic colitis: a community hospital’s experience
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5755633/
https://www.ncbi.nlm.nih.gov/pubmed/29317939
http://dx.doi.org/10.14740/gr907w
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