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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...

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Autores principales: Cyrus, Alissa, Street, Natalie, Quary, Sharon, Kable, Julie, Kenneson, Aileen, Fernhoff, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
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.
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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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