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Non-surgical Correction of Congenital Ear Anomalies: A Review of the Literature
Congenital ear anomalies have been known to cause lasting psychosocial consequences for children. Congenital ear anomalies can generally be divided into malformations (chondro-cutaneous defect) and deformations (misshaped pinna). Operative techniques are the standard for correction at a minimal age...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722567/ https://www.ncbi.nlm.nih.gov/pubmed/33299713 http://dx.doi.org/10.1097/GOX.0000000000003250 |
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author | Feijen, Michelle M.W. van Cruchten, Cas Payne, Phileemon E. van der Hulst, Rene R. W. J. |
author_facet | Feijen, Michelle M.W. van Cruchten, Cas Payne, Phileemon E. van der Hulst, Rene R. W. J. |
author_sort | Feijen, Michelle M.W. |
collection | PubMed |
description | Congenital ear anomalies have been known to cause lasting psychosocial consequences for children. Congenital ear anomalies can generally be divided into malformations (chondro-cutaneous defect) and deformations (misshaped pinna). Operative techniques are the standard for correction at a minimal age of 5–7, exposing the children to teasing and heavy complications. Ear molding is a non-operative technique to treat ear anomalies at a younger age. Having been popularized since the 1980s, its use has increased over the past decades. However, uncertainties about its properties remain. Therefore, this review was conducted to look at what is known and what has been newly discovered in the last decade, comparing different treatment methods and materials. A literature search was performed on PubMed, and 16 articles, published in the last decade, were included. It was found that treatment initiated at an early age showed higher satisfactory outcome rates and a shorter duration of treatment. A shorter duration of treatment also led to higher satisfactory rates, which might be attributable to age at initiation, individual moldability, and treatment compliance. Complications were minor in all articles. Recurrence rate was low and mostly concerned prominent ears, which proved to be the most difficult to correct deformity as well. Malformations, however, were even more difficult to treat than deformations. Our analysis shows ear molding to be a successful treatment method for ear anomalies with a preference for early diagnosis and treatment. |
format | Online Article Text |
id | pubmed-7722567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-77225672020-12-08 Non-surgical Correction of Congenital Ear Anomalies: A Review of the Literature Feijen, Michelle M.W. van Cruchten, Cas Payne, Phileemon E. van der Hulst, Rene R. W. J. Plast Reconstr Surg Glob Open Pediatric/Craniofacial Congenital ear anomalies have been known to cause lasting psychosocial consequences for children. Congenital ear anomalies can generally be divided into malformations (chondro-cutaneous defect) and deformations (misshaped pinna). Operative techniques are the standard for correction at a minimal age of 5–7, exposing the children to teasing and heavy complications. Ear molding is a non-operative technique to treat ear anomalies at a younger age. Having been popularized since the 1980s, its use has increased over the past decades. However, uncertainties about its properties remain. Therefore, this review was conducted to look at what is known and what has been newly discovered in the last decade, comparing different treatment methods and materials. A literature search was performed on PubMed, and 16 articles, published in the last decade, were included. It was found that treatment initiated at an early age showed higher satisfactory outcome rates and a shorter duration of treatment. A shorter duration of treatment also led to higher satisfactory rates, which might be attributable to age at initiation, individual moldability, and treatment compliance. Complications were minor in all articles. Recurrence rate was low and mostly concerned prominent ears, which proved to be the most difficult to correct deformity as well. Malformations, however, were even more difficult to treat than deformations. Our analysis shows ear molding to be a successful treatment method for ear anomalies with a preference for early diagnosis and treatment. Lippincott Williams & Wilkins 2020-11-24 /pmc/articles/PMC7722567/ /pubmed/33299713 http://dx.doi.org/10.1097/GOX.0000000000003250 Text en Copyright © 2020 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Pediatric/Craniofacial Feijen, Michelle M.W. van Cruchten, Cas Payne, Phileemon E. van der Hulst, Rene R. W. J. Non-surgical Correction of Congenital Ear Anomalies: A Review of the Literature |
title | Non-surgical Correction of Congenital Ear Anomalies: A Review of the Literature |
title_full | Non-surgical Correction of Congenital Ear Anomalies: A Review of the Literature |
title_fullStr | Non-surgical Correction of Congenital Ear Anomalies: A Review of the Literature |
title_full_unstemmed | Non-surgical Correction of Congenital Ear Anomalies: A Review of the Literature |
title_short | Non-surgical Correction of Congenital Ear Anomalies: A Review of the Literature |
title_sort | non-surgical correction of congenital ear anomalies: a review of the literature |
topic | Pediatric/Craniofacial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722567/ https://www.ncbi.nlm.nih.gov/pubmed/33299713 http://dx.doi.org/10.1097/GOX.0000000000003250 |
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