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Hirschsprung’s disease in children: a five year experience at a University teaching hospital in northwestern Tanzania

BACKGROUND: Hirschsprung’s disease (HD) is the commonest cause of functional intestinal obstruction in children and poses challenges to pediatricians and pediatric surgeons practicing in resource-limited countries. This study describes the clinical characteristics and outcome of management of this d...

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Autores principales: Mabula, Joseph B, Kayange, Neema M, Manyama, Mange, Chandika, Alphonce B, Rambau, Peter F, Chalya, Phillipo L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4083133/
https://www.ncbi.nlm.nih.gov/pubmed/24973940
http://dx.doi.org/10.1186/1756-0500-7-410
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author Mabula, Joseph B
Kayange, Neema M
Manyama, Mange
Chandika, Alphonce B
Rambau, Peter F
Chalya, Phillipo L
author_facet Mabula, Joseph B
Kayange, Neema M
Manyama, Mange
Chandika, Alphonce B
Rambau, Peter F
Chalya, Phillipo L
author_sort Mabula, Joseph B
collection PubMed
description BACKGROUND: Hirschsprung’s disease (HD) is the commonest cause of functional intestinal obstruction in children and poses challenges to pediatricians and pediatric surgeons practicing in resource-limited countries. This study describes the clinical characteristics and outcome of management of this disease in our setting and highlights challenges associated with the care of these patients and proffer solutions for improved outcome. METHODS: This was a descriptive prospective study of children aged ≤ 10 years who were histologically diagnosed and treated for HD at our centre between July 2008 and June 2013. RESULTS: A total of 110 patients (M: F ratio= 3.6:1) with a median age of 24 months were studied. Six (5.5%) patients were in the neonatal period. Sixty-four (58.2%) patients had complete intestinal obstruction whereas 42 (38.2%) and 4 (3.6%) patients had chronic intestinal obstruction and intestinal perforation respectively. No patient had enterocolitis. Constipation (94.5%) was the most common complaints. 109 (99.1%) patients had colostomy prior to the definitive pull-through. The median duration of colostomy before definitive pull-through was 4 months. The majority of patients (67.3%) had short segment of aganglionosis localized to the recto-sigmoid region. The definitive pull-through was performed in 94 (85.5%) patients (Swenson’s pull-through 76 (80.9%), Duhamel’s pull-through (12.8%) and Soave’s pull-through 4 (4.3%) patients). Postoperative complication rate was 47.3%. The median length of hospital stay was 26 days. Patients who developed complications stayed longer in the hospital and this was statistically significant (p <0.001). Mortality rate was 21.8%. The age < 4 weeks, delayed presentation and surgical site infection were the main predictors of mortality (p < 0.001). During the follow-up period, the results of Swenson’s and Duhamel’s pull through procedures were generally good in 87.8% and 42.9% of patients respectively. The result of Soave’s procedures was generally poor in this study. CONCLUSION: HD remains the commonest cause of functional intestinal obstruction in children and contributes significantly to high morbidity and mortality in our setting. The majority of patients present late when the disease becomes complicated. Early diagnosis and timely definitive pull through procedure are essential in order to decrease the morbidity and mortality associated with this disease.
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spelling pubmed-40831332014-07-08 Hirschsprung’s disease in children: a five year experience at a University teaching hospital in northwestern Tanzania Mabula, Joseph B Kayange, Neema M Manyama, Mange Chandika, Alphonce B Rambau, Peter F Chalya, Phillipo L BMC Res Notes Research Article BACKGROUND: Hirschsprung’s disease (HD) is the commonest cause of functional intestinal obstruction in children and poses challenges to pediatricians and pediatric surgeons practicing in resource-limited countries. This study describes the clinical characteristics and outcome of management of this disease in our setting and highlights challenges associated with the care of these patients and proffer solutions for improved outcome. METHODS: This was a descriptive prospective study of children aged ≤ 10 years who were histologically diagnosed and treated for HD at our centre between July 2008 and June 2013. RESULTS: A total of 110 patients (M: F ratio= 3.6:1) with a median age of 24 months were studied. Six (5.5%) patients were in the neonatal period. Sixty-four (58.2%) patients had complete intestinal obstruction whereas 42 (38.2%) and 4 (3.6%) patients had chronic intestinal obstruction and intestinal perforation respectively. No patient had enterocolitis. Constipation (94.5%) was the most common complaints. 109 (99.1%) patients had colostomy prior to the definitive pull-through. The median duration of colostomy before definitive pull-through was 4 months. The majority of patients (67.3%) had short segment of aganglionosis localized to the recto-sigmoid region. The definitive pull-through was performed in 94 (85.5%) patients (Swenson’s pull-through 76 (80.9%), Duhamel’s pull-through (12.8%) and Soave’s pull-through 4 (4.3%) patients). Postoperative complication rate was 47.3%. The median length of hospital stay was 26 days. Patients who developed complications stayed longer in the hospital and this was statistically significant (p <0.001). Mortality rate was 21.8%. The age < 4 weeks, delayed presentation and surgical site infection were the main predictors of mortality (p < 0.001). During the follow-up period, the results of Swenson’s and Duhamel’s pull through procedures were generally good in 87.8% and 42.9% of patients respectively. The result of Soave’s procedures was generally poor in this study. CONCLUSION: HD remains the commonest cause of functional intestinal obstruction in children and contributes significantly to high morbidity and mortality in our setting. The majority of patients present late when the disease becomes complicated. Early diagnosis and timely definitive pull through procedure are essential in order to decrease the morbidity and mortality associated with this disease. BioMed Central 2014-06-28 /pmc/articles/PMC4083133/ /pubmed/24973940 http://dx.doi.org/10.1186/1756-0500-7-410 Text en Copyright © 2014 Mabula et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Mabula, Joseph B
Kayange, Neema M
Manyama, Mange
Chandika, Alphonce B
Rambau, Peter F
Chalya, Phillipo L
Hirschsprung’s disease in children: a five year experience at a University teaching hospital in northwestern Tanzania
title Hirschsprung’s disease in children: a five year experience at a University teaching hospital in northwestern Tanzania
title_full Hirschsprung’s disease in children: a five year experience at a University teaching hospital in northwestern Tanzania
title_fullStr Hirschsprung’s disease in children: a five year experience at a University teaching hospital in northwestern Tanzania
title_full_unstemmed Hirschsprung’s disease in children: a five year experience at a University teaching hospital in northwestern Tanzania
title_short Hirschsprung’s disease in children: a five year experience at a University teaching hospital in northwestern Tanzania
title_sort hirschsprung’s disease in children: a five year experience at a university teaching hospital in northwestern tanzania
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4083133/
https://www.ncbi.nlm.nih.gov/pubmed/24973940
http://dx.doi.org/10.1186/1756-0500-7-410
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