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Interposition grafting of collagen-gelatin sponge impregnated with basic fibroblast growth factor in primary palatoplasty
INTRODUCTION: An oronasal fistula is a challenging post-operative complication of palatoplasty due to impaired velopharyngeal function or its high recurrence rate. Muscle repositioning, a key procedure in palatoplasty, causes dead space at the junction between the hard and soft palates. Consequently...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japanese Society for Regenerative Medicine
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406600/ https://www.ncbi.nlm.nih.gov/pubmed/37559871 http://dx.doi.org/10.1016/j.reth.2023.07.010 |
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author | Katsube, Motoki Utsunomiya, Natsuko Katayama, Yasuhiro Yamanaka, Hiroki Tsuge, Itaru Sowa, Yoshihiro Sakamoto, Michiharu Morimoto, Naoki |
author_facet | Katsube, Motoki Utsunomiya, Natsuko Katayama, Yasuhiro Yamanaka, Hiroki Tsuge, Itaru Sowa, Yoshihiro Sakamoto, Michiharu Morimoto, Naoki |
author_sort | Katsube, Motoki |
collection | PubMed |
description | INTRODUCTION: An oronasal fistula is a challenging post-operative complication of palatoplasty due to impaired velopharyngeal function or its high recurrence rate. Muscle repositioning, a key procedure in palatoplasty, causes dead space at the junction between the hard and soft palates. Consequently, thin oral and nasal mucosae are prone to break down and form fistulas. In this study, we used basic fibroblast growth factor-impregnated collagen gelatin sponge (bFGF-CGS) in primary palatoplasty to reduce fistula formation. METHODS: This retrospective study assessed the complications and efficacy of bFGF-CGS to reduce fistula formation. Patients who underwent primary palatoplasty with bFGF-CGS were included. The same number of patients who underwent primary palatoplasty without bFGF-CGS was included as a control group. The outcomes included post-operative oronasal fistula formation, delayed healing, bleeding, and infection. RESULTS: Both groups included 44 patients. Except for age at palatoplasty, there were no statistically significant demographic differences between the two groups; however, the rates of fistula formation in the study and control group were 2.3% and 13.6%, respectively. There were no infections among the patients. CONCLUSIONS: The grafting of bFGF-CGS in primary palatoplasty was safe and probably effective in reducing post-operative oronasal fistula formation. |
format | Online Article Text |
id | pubmed-10406600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Japanese Society for Regenerative Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-104066002023-08-09 Interposition grafting of collagen-gelatin sponge impregnated with basic fibroblast growth factor in primary palatoplasty Katsube, Motoki Utsunomiya, Natsuko Katayama, Yasuhiro Yamanaka, Hiroki Tsuge, Itaru Sowa, Yoshihiro Sakamoto, Michiharu Morimoto, Naoki Regen Ther Original Article INTRODUCTION: An oronasal fistula is a challenging post-operative complication of palatoplasty due to impaired velopharyngeal function or its high recurrence rate. Muscle repositioning, a key procedure in palatoplasty, causes dead space at the junction between the hard and soft palates. Consequently, thin oral and nasal mucosae are prone to break down and form fistulas. In this study, we used basic fibroblast growth factor-impregnated collagen gelatin sponge (bFGF-CGS) in primary palatoplasty to reduce fistula formation. METHODS: This retrospective study assessed the complications and efficacy of bFGF-CGS to reduce fistula formation. Patients who underwent primary palatoplasty with bFGF-CGS were included. The same number of patients who underwent primary palatoplasty without bFGF-CGS was included as a control group. The outcomes included post-operative oronasal fistula formation, delayed healing, bleeding, and infection. RESULTS: Both groups included 44 patients. Except for age at palatoplasty, there were no statistically significant demographic differences between the two groups; however, the rates of fistula formation in the study and control group were 2.3% and 13.6%, respectively. There were no infections among the patients. CONCLUSIONS: The grafting of bFGF-CGS in primary palatoplasty was safe and probably effective in reducing post-operative oronasal fistula formation. Japanese Society for Regenerative Medicine 2023-08-04 /pmc/articles/PMC10406600/ /pubmed/37559871 http://dx.doi.org/10.1016/j.reth.2023.07.010 Text en © 2023 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Original Article Katsube, Motoki Utsunomiya, Natsuko Katayama, Yasuhiro Yamanaka, Hiroki Tsuge, Itaru Sowa, Yoshihiro Sakamoto, Michiharu Morimoto, Naoki Interposition grafting of collagen-gelatin sponge impregnated with basic fibroblast growth factor in primary palatoplasty |
title | Interposition grafting of collagen-gelatin sponge impregnated with basic fibroblast growth factor in primary palatoplasty |
title_full | Interposition grafting of collagen-gelatin sponge impregnated with basic fibroblast growth factor in primary palatoplasty |
title_fullStr | Interposition grafting of collagen-gelatin sponge impregnated with basic fibroblast growth factor in primary palatoplasty |
title_full_unstemmed | Interposition grafting of collagen-gelatin sponge impregnated with basic fibroblast growth factor in primary palatoplasty |
title_short | Interposition grafting of collagen-gelatin sponge impregnated with basic fibroblast growth factor in primary palatoplasty |
title_sort | interposition grafting of collagen-gelatin sponge impregnated with basic fibroblast growth factor in primary palatoplasty |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406600/ https://www.ncbi.nlm.nih.gov/pubmed/37559871 http://dx.doi.org/10.1016/j.reth.2023.07.010 |
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