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How is genetic testing evaluated? A systematic review of the literature

Given the rapid development of genetic tests, an assessment of their benefits, risks, and limitations is crucial for public health practice. We performed a systematic review aimed at identifying and comparing the existing evaluation frameworks for genetic tests. We searched PUBMED, SCOPUS, ISI Web o...

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Autores principales: Pitini, Erica, De Vito, Corrado, Marzuillo, Carolina, D’Andrea, Elvira, Rosso, Annalisa, Federici, Antonio, Di Maria, Emilio, Villari, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945588/
https://www.ncbi.nlm.nih.gov/pubmed/29422659
http://dx.doi.org/10.1038/s41431-018-0095-5
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author Pitini, Erica
De Vito, Corrado
Marzuillo, Carolina
D’Andrea, Elvira
Rosso, Annalisa
Federici, Antonio
Di Maria, Emilio
Villari, Paolo
author_facet Pitini, Erica
De Vito, Corrado
Marzuillo, Carolina
D’Andrea, Elvira
Rosso, Annalisa
Federici, Antonio
Di Maria, Emilio
Villari, Paolo
author_sort Pitini, Erica
collection PubMed
description Given the rapid development of genetic tests, an assessment of their benefits, risks, and limitations is crucial for public health practice. We performed a systematic review aimed at identifying and comparing the existing evaluation frameworks for genetic tests. We searched PUBMED, SCOPUS, ISI Web of Knowledge, Google Scholar, Google, and gray literature sources for any documents describing such frameworks. We identified 29 evaluation frameworks published between 2000 and 2017, mostly based on the ACCE Framework (n = 13 models), or on the HTA process (n = 6), or both (n = 2). Others refer to the Wilson and Jungner screening criteria (n = 3) or to a mixture of different criteria (n = 5). Due to the widespread use of the ACCE Framework, the most frequently used evaluation criteria are analytic and clinical validity, clinical utility and ethical, legal and social implications. Less attention is given to the context of implementation. An economic dimension is always considered, but not in great detail. Consideration of delivery models, organizational aspects, and consumer viewpoint is often lacking. A deeper analysis of such context-related evaluation dimensions may strengthen a comprehensive evaluation of genetic tests and support the decision-making process.
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spelling pubmed-59455882018-06-20 How is genetic testing evaluated? A systematic review of the literature Pitini, Erica De Vito, Corrado Marzuillo, Carolina D’Andrea, Elvira Rosso, Annalisa Federici, Antonio Di Maria, Emilio Villari, Paolo Eur J Hum Genet Review Article Given the rapid development of genetic tests, an assessment of their benefits, risks, and limitations is crucial for public health practice. We performed a systematic review aimed at identifying and comparing the existing evaluation frameworks for genetic tests. We searched PUBMED, SCOPUS, ISI Web of Knowledge, Google Scholar, Google, and gray literature sources for any documents describing such frameworks. We identified 29 evaluation frameworks published between 2000 and 2017, mostly based on the ACCE Framework (n = 13 models), or on the HTA process (n = 6), or both (n = 2). Others refer to the Wilson and Jungner screening criteria (n = 3) or to a mixture of different criteria (n = 5). Due to the widespread use of the ACCE Framework, the most frequently used evaluation criteria are analytic and clinical validity, clinical utility and ethical, legal and social implications. Less attention is given to the context of implementation. An economic dimension is always considered, but not in great detail. Consideration of delivery models, organizational aspects, and consumer viewpoint is often lacking. A deeper analysis of such context-related evaluation dimensions may strengthen a comprehensive evaluation of genetic tests and support the decision-making process. Springer International Publishing 2018-02-08 2018-05 /pmc/articles/PMC5945588/ /pubmed/29422659 http://dx.doi.org/10.1038/s41431-018-0095-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, and provide a link to the Creative Commons license. You do not have permission under this license to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Review Article
Pitini, Erica
De Vito, Corrado
Marzuillo, Carolina
D’Andrea, Elvira
Rosso, Annalisa
Federici, Antonio
Di Maria, Emilio
Villari, Paolo
How is genetic testing evaluated? A systematic review of the literature
title How is genetic testing evaluated? A systematic review of the literature
title_full How is genetic testing evaluated? A systematic review of the literature
title_fullStr How is genetic testing evaluated? A systematic review of the literature
title_full_unstemmed How is genetic testing evaluated? A systematic review of the literature
title_short How is genetic testing evaluated? A systematic review of the literature
title_sort how is genetic testing evaluated? a systematic review of the literature
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945588/
https://www.ncbi.nlm.nih.gov/pubmed/29422659
http://dx.doi.org/10.1038/s41431-018-0095-5
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