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Genetic Counselors’ Experience with and Opinions on the Management of Newborn Screening Incidental Carrier Findings

Newborn screening (NBS) is a public health program whose aim is to identify infants who will be clinically affected with a serious metabolic, genetic, or endocrine disorder; however, the technology utilized by many NBS programs also detects infants who are heterozygous carriers for autosomal recessi...

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Autores principales: Leppert, Kristen, Bisordi, Katharine, Nieto, Jessica, Maloney, Kristin, Guan, Yue, Dixon, Shannan, Egense, Alena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209045/
https://www.ncbi.nlm.nih.gov/pubmed/29687313
http://dx.doi.org/10.1007/s10897-018-0258-0
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author Leppert, Kristen
Bisordi, Katharine
Nieto, Jessica
Maloney, Kristin
Guan, Yue
Dixon, Shannan
Egense, Alena
author_facet Leppert, Kristen
Bisordi, Katharine
Nieto, Jessica
Maloney, Kristin
Guan, Yue
Dixon, Shannan
Egense, Alena
author_sort Leppert, Kristen
collection PubMed
description Newborn screening (NBS) is a public health program whose aim is to identify infants who will be clinically affected with a serious metabolic, genetic, or endocrine disorder; however, the technology utilized by many NBS programs also detects infants who are heterozygous carriers for autosomal recessive conditions. Discussion surrounding disclosure of these incidental carrier findings remains controversial. The purpose of this study was to assess genetic counselors’ attitudes about disclosure of carrier status results generated by NBS and to gather data on their experiences with incidental carrier findings. An electronic survey was distributed to genetic counselors of all specialties via the NSGC listserv, and a total of 235 survey responses were analyzed. Quantitative data were analyzed using IBM SPSS v24, and qualitative data were manually analyzed for thematic analysis. Results show that the counselor participants were overall in favor of routine disclosure. Those with experience in NBS were much more likely to strongly agree with one or more reasons for disclosure (p < 0.001), whereas those with five or fewer years of experience were more likely to strongly agree with one or more reasons for non-disclosure (p = 0.031). Qualitative analysis identified key motivating factors for disclosure, including helping parents to understand a positive screen, parents may otherwise be unaware of reproductive risk and they may not otherwise have access to this information, and, while genetic testing is inherently a complex and ambiguous process, this does not justify non-disclosure. The main motivating factor for non-disclosure was the need for better counseling and informed consent. The data suggest that implementation of an “opt-in/out” policy for parents to decide whether or not to receive incidental findings would be beneficial. The results of this study support the continued disclosure of incidental carrier findings; however, additional research is necessary to further determine and implement the most effective disclosure practices.
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spelling pubmed-62090452018-11-13 Genetic Counselors’ Experience with and Opinions on the Management of Newborn Screening Incidental Carrier Findings Leppert, Kristen Bisordi, Katharine Nieto, Jessica Maloney, Kristin Guan, Yue Dixon, Shannan Egense, Alena J Genet Couns Original Research Newborn screening (NBS) is a public health program whose aim is to identify infants who will be clinically affected with a serious metabolic, genetic, or endocrine disorder; however, the technology utilized by many NBS programs also detects infants who are heterozygous carriers for autosomal recessive conditions. Discussion surrounding disclosure of these incidental carrier findings remains controversial. The purpose of this study was to assess genetic counselors’ attitudes about disclosure of carrier status results generated by NBS and to gather data on their experiences with incidental carrier findings. An electronic survey was distributed to genetic counselors of all specialties via the NSGC listserv, and a total of 235 survey responses were analyzed. Quantitative data were analyzed using IBM SPSS v24, and qualitative data were manually analyzed for thematic analysis. Results show that the counselor participants were overall in favor of routine disclosure. Those with experience in NBS were much more likely to strongly agree with one or more reasons for disclosure (p < 0.001), whereas those with five or fewer years of experience were more likely to strongly agree with one or more reasons for non-disclosure (p = 0.031). Qualitative analysis identified key motivating factors for disclosure, including helping parents to understand a positive screen, parents may otherwise be unaware of reproductive risk and they may not otherwise have access to this information, and, while genetic testing is inherently a complex and ambiguous process, this does not justify non-disclosure. The main motivating factor for non-disclosure was the need for better counseling and informed consent. The data suggest that implementation of an “opt-in/out” policy for parents to decide whether or not to receive incidental findings would be beneficial. The results of this study support the continued disclosure of incidental carrier findings; however, additional research is necessary to further determine and implement the most effective disclosure practices. Springer US 2018-04-23 2018 /pmc/articles/PMC6209045/ /pubmed/29687313 http://dx.doi.org/10.1007/s10897-018-0258-0 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research
Leppert, Kristen
Bisordi, Katharine
Nieto, Jessica
Maloney, Kristin
Guan, Yue
Dixon, Shannan
Egense, Alena
Genetic Counselors’ Experience with and Opinions on the Management of Newborn Screening Incidental Carrier Findings
title Genetic Counselors’ Experience with and Opinions on the Management of Newborn Screening Incidental Carrier Findings
title_full Genetic Counselors’ Experience with and Opinions on the Management of Newborn Screening Incidental Carrier Findings
title_fullStr Genetic Counselors’ Experience with and Opinions on the Management of Newborn Screening Incidental Carrier Findings
title_full_unstemmed Genetic Counselors’ Experience with and Opinions on the Management of Newborn Screening Incidental Carrier Findings
title_short Genetic Counselors’ Experience with and Opinions on the Management of Newborn Screening Incidental Carrier Findings
title_sort genetic counselors’ experience with and opinions on the management of newborn screening incidental carrier findings
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209045/
https://www.ncbi.nlm.nih.gov/pubmed/29687313
http://dx.doi.org/10.1007/s10897-018-0258-0
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