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Acellular dermal matrix allograft: An effective adjunct to oronasal fistula repair in patients with cleft palate

CONTEXT: Oronasal fistula (ONF) following cleft palate (CP) repair are a challenging problem associated with high recurrent rates. Acellular dermal matrix allograft is an available tissue substitute. AIMS: The aim of this study was to evaluate the effectiveness of acellular dermal matrix in the repa...

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Autores principales: El-Kassaby, Marwa AbdElWahhab, Khalifah, Mosaad Abd Al-Jawwad, Metwally, Salah Abdelfattah, Abd ElKader, Khaled Abd Elmonaem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4293835/
https://www.ncbi.nlm.nih.gov/pubmed/25593864
http://dx.doi.org/10.4103/2231-0746.147108
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author El-Kassaby, Marwa AbdElWahhab
Khalifah, Mosaad Abd Al-Jawwad
Metwally, Salah Abdelfattah
Abd ElKader, Khaled Abd Elmonaem
author_facet El-Kassaby, Marwa AbdElWahhab
Khalifah, Mosaad Abd Al-Jawwad
Metwally, Salah Abdelfattah
Abd ElKader, Khaled Abd Elmonaem
author_sort El-Kassaby, Marwa AbdElWahhab
collection PubMed
description CONTEXT: Oronasal fistula (ONF) following cleft palate (CP) repair are a challenging problem associated with high recurrent rates. Acellular dermal matrix allograft is an available tissue substitute. AIMS: The aim of this study was to evaluate the effectiveness of acellular dermal matrix in the repair of ONF associated with CP that is recurrent or larger than 15 mm in any dimension. SETTINGS AND DESIGN: This is a prospective study where 12 patients with repaired CP suffering from ONF of the hard palate >15 mm in diameter were included. MATERIALS AND METHODS: Age ranged from 12 to 25 years. Acellular dermal matrix was firmly secured between repaired oral and nasal mucosal layers. Patients were clinically followed-up for 6 months postoperatively to assess total time for complete healing, dehiscence and/or refistulaization. STATISTICAL ANALYSIS USED: Fisher's exact test. RESULTS: Acellular dermal matrix was integrated with successful fistula closure in all except 1 patient where failure of graft integration was noticed early postoperatively. In 6 patients, the oral mucosal layer showed dehiscence, through which the graft was exposed. Graft integration extended from 4 to 12 weeks postoperatively during which patients were instructed to follow a soft diet and meticulous oral hygiene measures. CONCLUSIONS: Acellular dermal matrix allografts are safe and effective adjuncts for use in closure of ONF in the hard palate that is recurrent or larger than 15 mm in any dimension.
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spelling pubmed-42938352015-01-15 Acellular dermal matrix allograft: An effective adjunct to oronasal fistula repair in patients with cleft palate El-Kassaby, Marwa AbdElWahhab Khalifah, Mosaad Abd Al-Jawwad Metwally, Salah Abdelfattah Abd ElKader, Khaled Abd Elmonaem Ann Maxillofac Surg Original Article - Evaluative Research CONTEXT: Oronasal fistula (ONF) following cleft palate (CP) repair are a challenging problem associated with high recurrent rates. Acellular dermal matrix allograft is an available tissue substitute. AIMS: The aim of this study was to evaluate the effectiveness of acellular dermal matrix in the repair of ONF associated with CP that is recurrent or larger than 15 mm in any dimension. SETTINGS AND DESIGN: This is a prospective study where 12 patients with repaired CP suffering from ONF of the hard palate >15 mm in diameter were included. MATERIALS AND METHODS: Age ranged from 12 to 25 years. Acellular dermal matrix was firmly secured between repaired oral and nasal mucosal layers. Patients were clinically followed-up for 6 months postoperatively to assess total time for complete healing, dehiscence and/or refistulaization. STATISTICAL ANALYSIS USED: Fisher's exact test. RESULTS: Acellular dermal matrix was integrated with successful fistula closure in all except 1 patient where failure of graft integration was noticed early postoperatively. In 6 patients, the oral mucosal layer showed dehiscence, through which the graft was exposed. Graft integration extended from 4 to 12 weeks postoperatively during which patients were instructed to follow a soft diet and meticulous oral hygiene measures. CONCLUSIONS: Acellular dermal matrix allografts are safe and effective adjuncts for use in closure of ONF in the hard palate that is recurrent or larger than 15 mm in any dimension. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4293835/ /pubmed/25593864 http://dx.doi.org/10.4103/2231-0746.147108 Text en Copyright: © Annals of Maxillofacial Surgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article - Evaluative Research
El-Kassaby, Marwa AbdElWahhab
Khalifah, Mosaad Abd Al-Jawwad
Metwally, Salah Abdelfattah
Abd ElKader, Khaled Abd Elmonaem
Acellular dermal matrix allograft: An effective adjunct to oronasal fistula repair in patients with cleft palate
title Acellular dermal matrix allograft: An effective adjunct to oronasal fistula repair in patients with cleft palate
title_full Acellular dermal matrix allograft: An effective adjunct to oronasal fistula repair in patients with cleft palate
title_fullStr Acellular dermal matrix allograft: An effective adjunct to oronasal fistula repair in patients with cleft palate
title_full_unstemmed Acellular dermal matrix allograft: An effective adjunct to oronasal fistula repair in patients with cleft palate
title_short Acellular dermal matrix allograft: An effective adjunct to oronasal fistula repair in patients with cleft palate
title_sort acellular dermal matrix allograft: an effective adjunct to oronasal fistula repair in patients with cleft palate
topic Original Article - Evaluative Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4293835/
https://www.ncbi.nlm.nih.gov/pubmed/25593864
http://dx.doi.org/10.4103/2231-0746.147108
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