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Clinic-Based Infant Screening for Duchenne Muscular Dystrophy: A Feasibility Study
Purpose. The purpose of this study was to assess the desirability of Duchenne muscular dystrophy (DMD) screening, the effectiveness of the consent process, and the feasibility of conducting DMD screening in a pediatric office. Methods. Infant males who attended a 12-month routine well-child visit at...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3392140/ https://www.ncbi.nlm.nih.gov/pubmed/22866242 http://dx.doi.org/10.1371/4f99c5654147a |
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author | Cyrus, Alissa Street, Natalie Quary, Sharon Kable, Julie Kenneson, Aileen Fernhoff, Paul |
author_facet | Cyrus, Alissa Street, Natalie Quary, Sharon Kable, Julie Kenneson, Aileen Fernhoff, Paul |
author_sort | Cyrus, Alissa |
collection | PubMed |
description | Purpose. The purpose of this study was to assess the desirability of Duchenne muscular dystrophy (DMD) screening, the effectiveness of the consent process, and the feasibility of conducting DMD screening in a pediatric office. Methods. Infant males who attended a 12-month routine well-child visit at a participating pediatric clinic were screened for DMD. Parents and providers completed post-screening questionnaires to assess their experiences with and attitudes toward screening. Results. A total of 264 male infants were screened for DMD. Approximately 78% of parents indicated support of voluntary DMD screening and 91% of providers were in favor of screening for DMD. About 75% of parents correctly answered three of five questions testing their knowledge of DMD screening. Conclusion. DMD screening is feasible in a pediatric office when conducted as part of a research study. Infant screening for DMD eventually could be offered in pediatric health care provider offices as an optional public health service outside of newborn screening. |
format | Online Article Text |
id | pubmed-3392140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33921402012-08-03 Clinic-Based Infant Screening for Duchenne Muscular Dystrophy: A Feasibility Study Cyrus, Alissa Street, Natalie Quary, Sharon Kable, Julie Kenneson, Aileen Fernhoff, Paul PLoS Curr Muscular Dystrophy Purpose. The purpose of this study was to assess the desirability of Duchenne muscular dystrophy (DMD) screening, the effectiveness of the consent process, and the feasibility of conducting DMD screening in a pediatric office. Methods. Infant males who attended a 12-month routine well-child visit at a participating pediatric clinic were screened for DMD. Parents and providers completed post-screening questionnaires to assess their experiences with and attitudes toward screening. Results. A total of 264 male infants were screened for DMD. Approximately 78% of parents indicated support of voluntary DMD screening and 91% of providers were in favor of screening for DMD. About 75% of parents correctly answered three of five questions testing their knowledge of DMD screening. Conclusion. DMD screening is feasible in a pediatric office when conducted as part of a research study. Infant screening for DMD eventually could be offered in pediatric health care provider offices as an optional public health service outside of newborn screening. Public Library of Science 2012-05-02 /pmc/articles/PMC3392140/ /pubmed/22866242 http://dx.doi.org/10.1371/4f99c5654147a Text en http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Muscular Dystrophy Cyrus, Alissa Street, Natalie Quary, Sharon Kable, Julie Kenneson, Aileen Fernhoff, Paul Clinic-Based Infant Screening for Duchenne Muscular Dystrophy: A Feasibility Study |
title | Clinic-Based Infant Screening for Duchenne Muscular Dystrophy: A Feasibility Study |
title_full | Clinic-Based Infant Screening for Duchenne Muscular Dystrophy: A Feasibility Study |
title_fullStr | Clinic-Based Infant Screening for Duchenne Muscular Dystrophy: A Feasibility Study |
title_full_unstemmed | Clinic-Based Infant Screening for Duchenne Muscular Dystrophy: A Feasibility Study |
title_short | Clinic-Based Infant Screening for Duchenne Muscular Dystrophy: A Feasibility Study |
title_sort | clinic-based infant screening for duchenne muscular dystrophy: a feasibility study |
topic | Muscular Dystrophy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3392140/ https://www.ncbi.nlm.nih.gov/pubmed/22866242 http://dx.doi.org/10.1371/4f99c5654147a |
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