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Longitudinal follow-up of muscle echotexture in infants with congenital muscular torticollis
Unilateral fibrous contracture of the sternocleidomastoid (SCM) muscle is the major pathophysiology in infants with congenital muscular torticollis (CMT). Physical examination is not always sufficient to detect minimal muscle fibrosis in involved SCM muscles. A prospective study for SCM muscle fibro...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5313018/ https://www.ncbi.nlm.nih.gov/pubmed/28178161 http://dx.doi.org/10.1097/MD.0000000000006068 |
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author | Hu, Ching-Fang Fu, Tieh-Cheng Chen, Chung-Yao Chen, Carl Pai-Chu Lin, Yu-Ju Hsu, Chih-Chin |
author_facet | Hu, Ching-Fang Fu, Tieh-Cheng Chen, Chung-Yao Chen, Carl Pai-Chu Lin, Yu-Ju Hsu, Chih-Chin |
author_sort | Hu, Ching-Fang |
collection | PubMed |
description | Unilateral fibrous contracture of the sternocleidomastoid (SCM) muscle is the major pathophysiology in infants with congenital muscular torticollis (CMT). Physical examination is not always sufficient to detect minimal muscle fibrosis in involved SCM muscles. A prospective study for SCM muscle fibrosis in CMT infants by quantifying echotexture and muscle thickness during the course of treatment is highlighted in the study. Convenience samples of 21 female and 29 male infants with CMT, who were 1 to 12 months old, underwent physiotherapy for at least 3 months and were followed for 4.7 ± 0.4 months. All infants had at least 2 clinical assessments and ultrasonographic examinations for bilateral SCM muscles during follow-up. The K value, derived from the difference in echo intensities between the involved and uninvolved SCM muscles on longitudinal sonograms, was used to represent the severity of muscle fibrosis. Bilateral SCM muscle thickness and ratio of involved to uninvolved muscle thickness (Ratio I/U) were obtained simultaneously. Clinical outcome was also recorded. No subjects underwent surgical intervention during follow-up. The K value decreased from 6.85 ± 0.58 to 1.30 ± 0.36 at the end of follow-up (P < 0.001), which reflected the decrease of muscle fibrosis. The Ratio I/U decreased from 1.11 ± 0.04 to 0.97 ± 0.02 during treatment, which was possibly related to the increased uninvolved SCM muscle thickness. In conclusion, echotexture is an efficient indicator for reflecting a wide degree of muscle fibrosis in infants with CMT and is informative during the treatment course. |
format | Online Article Text |
id | pubmed-5313018 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-53130182017-02-21 Longitudinal follow-up of muscle echotexture in infants with congenital muscular torticollis Hu, Ching-Fang Fu, Tieh-Cheng Chen, Chung-Yao Chen, Carl Pai-Chu Lin, Yu-Ju Hsu, Chih-Chin Medicine (Baltimore) 6200 Unilateral fibrous contracture of the sternocleidomastoid (SCM) muscle is the major pathophysiology in infants with congenital muscular torticollis (CMT). Physical examination is not always sufficient to detect minimal muscle fibrosis in involved SCM muscles. A prospective study for SCM muscle fibrosis in CMT infants by quantifying echotexture and muscle thickness during the course of treatment is highlighted in the study. Convenience samples of 21 female and 29 male infants with CMT, who were 1 to 12 months old, underwent physiotherapy for at least 3 months and were followed for 4.7 ± 0.4 months. All infants had at least 2 clinical assessments and ultrasonographic examinations for bilateral SCM muscles during follow-up. The K value, derived from the difference in echo intensities between the involved and uninvolved SCM muscles on longitudinal sonograms, was used to represent the severity of muscle fibrosis. Bilateral SCM muscle thickness and ratio of involved to uninvolved muscle thickness (Ratio I/U) were obtained simultaneously. Clinical outcome was also recorded. No subjects underwent surgical intervention during follow-up. The K value decreased from 6.85 ± 0.58 to 1.30 ± 0.36 at the end of follow-up (P < 0.001), which reflected the decrease of muscle fibrosis. The Ratio I/U decreased from 1.11 ± 0.04 to 0.97 ± 0.02 during treatment, which was possibly related to the increased uninvolved SCM muscle thickness. In conclusion, echotexture is an efficient indicator for reflecting a wide degree of muscle fibrosis in infants with CMT and is informative during the treatment course. Wolters Kluwer Health 2017-02-10 /pmc/articles/PMC5313018/ /pubmed/28178161 http://dx.doi.org/10.1097/MD.0000000000006068 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 6200 Hu, Ching-Fang Fu, Tieh-Cheng Chen, Chung-Yao Chen, Carl Pai-Chu Lin, Yu-Ju Hsu, Chih-Chin Longitudinal follow-up of muscle echotexture in infants with congenital muscular torticollis |
title | Longitudinal follow-up of muscle echotexture in infants with congenital muscular torticollis |
title_full | Longitudinal follow-up of muscle echotexture in infants with congenital muscular torticollis |
title_fullStr | Longitudinal follow-up of muscle echotexture in infants with congenital muscular torticollis |
title_full_unstemmed | Longitudinal follow-up of muscle echotexture in infants with congenital muscular torticollis |
title_short | Longitudinal follow-up of muscle echotexture in infants with congenital muscular torticollis |
title_sort | longitudinal follow-up of muscle echotexture in infants with congenital muscular torticollis |
topic | 6200 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5313018/ https://www.ncbi.nlm.nih.gov/pubmed/28178161 http://dx.doi.org/10.1097/MD.0000000000006068 |
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