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Probiotic for irritable bowel syndrome in pediatric patients: a randomized controlled clinical trial
BACKGROUND: Irritable bowel syndrome (IBS) is a common gastrointestinal disorder in children. Recently, probiotics have been suggested as a treatment option for gastrointestinal disorders. The most effective species and the most appropriate doses are still unknown. OBJECTIVE: The aim of this study w...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Electronic physician
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4590561/ https://www.ncbi.nlm.nih.gov/pubmed/26435825 http://dx.doi.org/10.14661/1255 |
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author | Kianifar, Hamidreza Jafari, Seyed Ali Kiani, Mohammadali Ahanchian, Hamid Ghasemi, Seyed Vahid Grover, Zubin Mahmoodi, Leili Zarif Bagherian, Rita Khalesi, Maryam |
author_facet | Kianifar, Hamidreza Jafari, Seyed Ali Kiani, Mohammadali Ahanchian, Hamid Ghasemi, Seyed Vahid Grover, Zubin Mahmoodi, Leili Zarif Bagherian, Rita Khalesi, Maryam |
author_sort | Kianifar, Hamidreza |
collection | PubMed |
description | BACKGROUND: Irritable bowel syndrome (IBS) is a common gastrointestinal disorder in children. Recently, probiotics have been suggested as a treatment option for gastrointestinal disorders. The most effective species and the most appropriate doses are still unknown. OBJECTIVE: The aim of this study was to assess the effects of Lactobacillus GG (LGG) for treating IBS in pediatric patients. METHODS: In a controlled, double blind, randomized trial, patients with IBS diagnosed by Rome III criteria from August 2012 to September 2012 at Dr. Sheikh Hospital, Mashhad University of Medical Sciences, Iran, were assigned to one of two groups, i.e., intervention and control groups. For four weeks, the intervention group received a probiotic in capsule form that contained LGG at a concentration of 1×10(10) cfu/ml bacteria. For the same period, the control group received a placebo capsule that had the same shape and color but only contained inulin, which also was present in the LGG capsules. The primary outcome was any change in the severity of the patients’ pain, and we used a five-point Likert scale to evaluate the severity of their pain. Secondary outcomes were ghanges of the functional scale, stool patterns, and associated problems. RESULTS: Fifty-two patients participated in the study, and 26 patients were assigned randomly to each of the two groups. The severity of the patients’ pain decreased significantly in the intervention group after one, two, three, and four weeks of treatment, as indicated by P-values of 0.01, 0.00, 0.00, and 0.00, respectively. Also, there was significant improvement in the functional scale after two weeks of treatment (P-value ≤ 0.00). CONCLUSION: Lactobacillus GG at a concentration of 1×10(10) cfu/ml for a period of four weeks can lessen the severity of the patients’ pain and improve the functional scale in patients with irritable bowel syndrome. Probiotics can have therapeutic effects for IBS patients. |
format | Online Article Text |
id | pubmed-4590561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Electronic physician |
record_format | MEDLINE/PubMed |
spelling | pubmed-45905612015-10-02 Probiotic for irritable bowel syndrome in pediatric patients: a randomized controlled clinical trial Kianifar, Hamidreza Jafari, Seyed Ali Kiani, Mohammadali Ahanchian, Hamid Ghasemi, Seyed Vahid Grover, Zubin Mahmoodi, Leili Zarif Bagherian, Rita Khalesi, Maryam Electron Physician Original Article BACKGROUND: Irritable bowel syndrome (IBS) is a common gastrointestinal disorder in children. Recently, probiotics have been suggested as a treatment option for gastrointestinal disorders. The most effective species and the most appropriate doses are still unknown. OBJECTIVE: The aim of this study was to assess the effects of Lactobacillus GG (LGG) for treating IBS in pediatric patients. METHODS: In a controlled, double blind, randomized trial, patients with IBS diagnosed by Rome III criteria from August 2012 to September 2012 at Dr. Sheikh Hospital, Mashhad University of Medical Sciences, Iran, were assigned to one of two groups, i.e., intervention and control groups. For four weeks, the intervention group received a probiotic in capsule form that contained LGG at a concentration of 1×10(10) cfu/ml bacteria. For the same period, the control group received a placebo capsule that had the same shape and color but only contained inulin, which also was present in the LGG capsules. The primary outcome was any change in the severity of the patients’ pain, and we used a five-point Likert scale to evaluate the severity of their pain. Secondary outcomes were ghanges of the functional scale, stool patterns, and associated problems. RESULTS: Fifty-two patients participated in the study, and 26 patients were assigned randomly to each of the two groups. The severity of the patients’ pain decreased significantly in the intervention group after one, two, three, and four weeks of treatment, as indicated by P-values of 0.01, 0.00, 0.00, and 0.00, respectively. Also, there was significant improvement in the functional scale after two weeks of treatment (P-value ≤ 0.00). CONCLUSION: Lactobacillus GG at a concentration of 1×10(10) cfu/ml for a period of four weeks can lessen the severity of the patients’ pain and improve the functional scale in patients with irritable bowel syndrome. Probiotics can have therapeutic effects for IBS patients. Electronic physician 2015-09-16 /pmc/articles/PMC4590561/ /pubmed/26435825 http://dx.doi.org/10.14661/1255 Text en © 2015 The Authors This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (http://creativecommons.org/licenses/by-nc-nd/3.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Original Article Kianifar, Hamidreza Jafari, Seyed Ali Kiani, Mohammadali Ahanchian, Hamid Ghasemi, Seyed Vahid Grover, Zubin Mahmoodi, Leili Zarif Bagherian, Rita Khalesi, Maryam Probiotic for irritable bowel syndrome in pediatric patients: a randomized controlled clinical trial |
title | Probiotic for irritable bowel syndrome in pediatric patients: a randomized controlled clinical trial |
title_full | Probiotic for irritable bowel syndrome in pediatric patients: a randomized controlled clinical trial |
title_fullStr | Probiotic for irritable bowel syndrome in pediatric patients: a randomized controlled clinical trial |
title_full_unstemmed | Probiotic for irritable bowel syndrome in pediatric patients: a randomized controlled clinical trial |
title_short | Probiotic for irritable bowel syndrome in pediatric patients: a randomized controlled clinical trial |
title_sort | probiotic for irritable bowel syndrome in pediatric patients: a randomized controlled clinical trial |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4590561/ https://www.ncbi.nlm.nih.gov/pubmed/26435825 http://dx.doi.org/10.14661/1255 |
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