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A Modified Rectal Mucosal Biopsy for the Diagnosis of Hirschsprung’s Disease: Zaria Experience

BACKGROUND: Full-thickness rectal biopsy is often used for the diagnosis of Hirschsprung’s disease (where a suction biopsy kit is not available). This is associated with some challenges such as limited theatre space and the need for general anaesthesia. We aim to highlight the usefulness and sensiti...

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Autores principales: Sholadoye, Tunde Talib, Aliyu, Halima Oziohu, Mshelbwala, Philip Mari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010578/
https://www.ncbi.nlm.nih.gov/pubmed/36923812
http://dx.doi.org/10.4103/jwas.jwas_241_22
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author Sholadoye, Tunde Talib
Aliyu, Halima Oziohu
Mshelbwala, Philip Mari
author_facet Sholadoye, Tunde Talib
Aliyu, Halima Oziohu
Mshelbwala, Philip Mari
author_sort Sholadoye, Tunde Talib
collection PubMed
description BACKGROUND: Full-thickness rectal biopsy is often used for the diagnosis of Hirschsprung’s disease (where a suction biopsy kit is not available). This is associated with some challenges such as limited theatre space and the need for general anaesthesia. We aim to highlight the usefulness and sensitivity of a modification of the rectal mucosal biopsy without general anaesthesia in the diagnosis of Hirschsprung’s disease. MATERIALS AND METHODS: This is a retrospective analysis of children with Hirschsprung’s disease who had rectal mucosal biopsy over a 16-year period (January 2004–December 2019). Research was approved with institutional number ABUTHZ/HREC/H22/2022. The patients had the biopsy with small, curved artery forceps, surgical blade, and dissecting scissors. Histological analyses of tissue were done. Clinical data and results were recorded on a structured pro forma, and the data were analysed. RESULTS: There were 263 boys and 97 girls with a median age of 10.5 months. Only 37 (10.3%) of the rectal biopsies were done by consultants. Hirschsprung’s disease was confirmed in 279 (75.5%) of the partial-thickness biopsies, whereas 52 (14.4%) biopsies were inadequate specimens. Resident doctors were responsible for 92.2% (47) of inadequate biopsies (P = 0.63), although they did 89.7% of all biopsies. In one (0.3%) patient, the procedure ended as a full-thickness biopsy leading to a significant haemorrhage that required blood transfusion. CONCLUSIONS: The modified rectal mucosal biopsy is a simple, safe, and effective method for making the diagnosis of Hirschsprung’s disease. This is performed without general anaesthesia and is useful where a suction biopsy kit is unavailable.
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spelling pubmed-100105782023-03-14 A Modified Rectal Mucosal Biopsy for the Diagnosis of Hirschsprung’s Disease: Zaria Experience Sholadoye, Tunde Talib Aliyu, Halima Oziohu Mshelbwala, Philip Mari J West Afr Coll Surg Original Article BACKGROUND: Full-thickness rectal biopsy is often used for the diagnosis of Hirschsprung’s disease (where a suction biopsy kit is not available). This is associated with some challenges such as limited theatre space and the need for general anaesthesia. We aim to highlight the usefulness and sensitivity of a modification of the rectal mucosal biopsy without general anaesthesia in the diagnosis of Hirschsprung’s disease. MATERIALS AND METHODS: This is a retrospective analysis of children with Hirschsprung’s disease who had rectal mucosal biopsy over a 16-year period (January 2004–December 2019). Research was approved with institutional number ABUTHZ/HREC/H22/2022. The patients had the biopsy with small, curved artery forceps, surgical blade, and dissecting scissors. Histological analyses of tissue were done. Clinical data and results were recorded on a structured pro forma, and the data were analysed. RESULTS: There were 263 boys and 97 girls with a median age of 10.5 months. Only 37 (10.3%) of the rectal biopsies were done by consultants. Hirschsprung’s disease was confirmed in 279 (75.5%) of the partial-thickness biopsies, whereas 52 (14.4%) biopsies were inadequate specimens. Resident doctors were responsible for 92.2% (47) of inadequate biopsies (P = 0.63), although they did 89.7% of all biopsies. In one (0.3%) patient, the procedure ended as a full-thickness biopsy leading to a significant haemorrhage that required blood transfusion. CONCLUSIONS: The modified rectal mucosal biopsy is a simple, safe, and effective method for making the diagnosis of Hirschsprung’s disease. This is performed without general anaesthesia and is useful where a suction biopsy kit is unavailable. Wolters Kluwer - Medknow 2023 2023-01-18 /pmc/articles/PMC10010578/ /pubmed/36923812 http://dx.doi.org/10.4103/jwas.jwas_241_22 Text en Copyright: © 2023 Journal of West African College of Surgeons https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Sholadoye, Tunde Talib
Aliyu, Halima Oziohu
Mshelbwala, Philip Mari
A Modified Rectal Mucosal Biopsy for the Diagnosis of Hirschsprung’s Disease: Zaria Experience
title A Modified Rectal Mucosal Biopsy for the Diagnosis of Hirschsprung’s Disease: Zaria Experience
title_full A Modified Rectal Mucosal Biopsy for the Diagnosis of Hirschsprung’s Disease: Zaria Experience
title_fullStr A Modified Rectal Mucosal Biopsy for the Diagnosis of Hirschsprung’s Disease: Zaria Experience
title_full_unstemmed A Modified Rectal Mucosal Biopsy for the Diagnosis of Hirschsprung’s Disease: Zaria Experience
title_short A Modified Rectal Mucosal Biopsy for the Diagnosis of Hirschsprung’s Disease: Zaria Experience
title_sort modified rectal mucosal biopsy for the diagnosis of hirschsprung’s disease: zaria experience
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010578/
https://www.ncbi.nlm.nih.gov/pubmed/36923812
http://dx.doi.org/10.4103/jwas.jwas_241_22
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