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Autologous Platelet-Poor Plasma Gel for Injection Laryngoplasty
PURPOSE: To overcome the potential disadvantages of the use of foreign materials and autologous fat or collagen, we introduce here an autologous plasma gel for injection laryngoplasty. The purpose of this study was to present a new injection material, a plasma gel, and to discuss its clinical effect...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Yonsei University College of Medicine
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3809861/ https://www.ncbi.nlm.nih.gov/pubmed/24142660 http://dx.doi.org/10.3349/ymj.2013.54.6.1516 |
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author | Woo, Seung Hoon Kim, Jin Pyeong Park, Jung Je Chung, Phil-Sang Lee, Sang-Hyuk Jeong, Han-Sin |
author_facet | Woo, Seung Hoon Kim, Jin Pyeong Park, Jung Je Chung, Phil-Sang Lee, Sang-Hyuk Jeong, Han-Sin |
author_sort | Woo, Seung Hoon |
collection | PubMed |
description | PURPOSE: To overcome the potential disadvantages of the use of foreign materials and autologous fat or collagen, we introduce here an autologous plasma gel for injection laryngoplasty. The purpose of this study was to present a new injection material, a plasma gel, and to discuss its clinical effectiveness. MATERIALS AND METHODS: From 2 mL of blood, the platelet poor serum layer was collected and heated at 100℃ for 12 min to form a plasma gel. The plasma gel was then injected into a targeted site; the safety and efficacy thereof were evaluated in 30 rats. We also conducted a phase I/II clinical study of plasma gel injection laryngoplasty in 11 unilateral vocal fold paralysis patients. RESULTS: The plasma gel was semi-solid and an easily injectable material. Of note, plasma gel maintains the same consistency for up to 1 year in a sealed bottle. However, exposure to room air causes the plasma gel to disappear within 1 month. In our animal study, the autologous plasma gel remained in situ for 6 months in animals with minimal inflammation. Clinical study showed that vocal cord palsy was well compensated for with the plasma gel in all patients at two months after injection with no significant complications. Jitter, shimmer, maximum, maximum phonation time (MPT) and mean voice handicap index (VHI) also improved significantly after plasma gel injection. However, because the injected plasma gel was gradually absorbed, 6 patients needed another injection, while the gel remained in place in 2 patients. CONCLUSION: Injection laryngoplasty with autologous plasma gel may be a useful and safe treatment option for temporary vocal cord palsy. |
format | Online Article Text |
id | pubmed-3809861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Yonsei University College of Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-38098612013-11-01 Autologous Platelet-Poor Plasma Gel for Injection Laryngoplasty Woo, Seung Hoon Kim, Jin Pyeong Park, Jung Je Chung, Phil-Sang Lee, Sang-Hyuk Jeong, Han-Sin Yonsei Med J Original Article PURPOSE: To overcome the potential disadvantages of the use of foreign materials and autologous fat or collagen, we introduce here an autologous plasma gel for injection laryngoplasty. The purpose of this study was to present a new injection material, a plasma gel, and to discuss its clinical effectiveness. MATERIALS AND METHODS: From 2 mL of blood, the platelet poor serum layer was collected and heated at 100℃ for 12 min to form a plasma gel. The plasma gel was then injected into a targeted site; the safety and efficacy thereof were evaluated in 30 rats. We also conducted a phase I/II clinical study of plasma gel injection laryngoplasty in 11 unilateral vocal fold paralysis patients. RESULTS: The plasma gel was semi-solid and an easily injectable material. Of note, plasma gel maintains the same consistency for up to 1 year in a sealed bottle. However, exposure to room air causes the plasma gel to disappear within 1 month. In our animal study, the autologous plasma gel remained in situ for 6 months in animals with minimal inflammation. Clinical study showed that vocal cord palsy was well compensated for with the plasma gel in all patients at two months after injection with no significant complications. Jitter, shimmer, maximum, maximum phonation time (MPT) and mean voice handicap index (VHI) also improved significantly after plasma gel injection. However, because the injected plasma gel was gradually absorbed, 6 patients needed another injection, while the gel remained in place in 2 patients. CONCLUSION: Injection laryngoplasty with autologous plasma gel may be a useful and safe treatment option for temporary vocal cord palsy. Yonsei University College of Medicine 2013-11-01 2013-10-01 /pmc/articles/PMC3809861/ /pubmed/24142660 http://dx.doi.org/10.3349/ymj.2013.54.6.1516 Text en © Copyright: Yonsei University College of Medicine 2013 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Woo, Seung Hoon Kim, Jin Pyeong Park, Jung Je Chung, Phil-Sang Lee, Sang-Hyuk Jeong, Han-Sin Autologous Platelet-Poor Plasma Gel for Injection Laryngoplasty |
title | Autologous Platelet-Poor Plasma Gel for Injection Laryngoplasty |
title_full | Autologous Platelet-Poor Plasma Gel for Injection Laryngoplasty |
title_fullStr | Autologous Platelet-Poor Plasma Gel for Injection Laryngoplasty |
title_full_unstemmed | Autologous Platelet-Poor Plasma Gel for Injection Laryngoplasty |
title_short | Autologous Platelet-Poor Plasma Gel for Injection Laryngoplasty |
title_sort | autologous platelet-poor plasma gel for injection laryngoplasty |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3809861/ https://www.ncbi.nlm.nih.gov/pubmed/24142660 http://dx.doi.org/10.3349/ymj.2013.54.6.1516 |
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