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Prevalence and types of inconsistencies in clinical pharmacogenetic recommendations among major U.S. sources
Clinical implementation of pharmacogenomics (PGx) is slow. Previous studies have identified some inconsistencies among clinical PGx recommendations, but the prevalence and types of inconsistencies have not been comprehensively analyzed among major PGx guidance sources in the U.S. PGx recommendations...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603298/ https://www.ncbi.nlm.nih.gov/pubmed/33145028 http://dx.doi.org/10.1038/s41525-020-00156-7 |
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author | Shugg, Tyler Pasternak, Amy L. London, Bianca Luzum, Jasmine A. |
author_facet | Shugg, Tyler Pasternak, Amy L. London, Bianca Luzum, Jasmine A. |
author_sort | Shugg, Tyler |
collection | PubMed |
description | Clinical implementation of pharmacogenomics (PGx) is slow. Previous studies have identified some inconsistencies among clinical PGx recommendations, but the prevalence and types of inconsistencies have not been comprehensively analyzed among major PGx guidance sources in the U.S. PGx recommendations from the Clinical Pharmacogenetics Implementation Consortium, U.S. Food and Drug Administration drug labels, and major U.S. professional medical organizations were analyzed through May 24, 2019. Inconsistencies were analyzed within the following elements: recommendation category; whether routine screening was recommended; and the specific biomarkers, variants, and patient groups involved. We identified 606 total clinical PGx recommendations, which contained 267 unique drugs. Composite inconsistencies occurred in 48.1% of clinical PGx recommendations overall, and in 93.3% of recommendations from three sources. Inconsistencies occurred in the recommendation category (29.8%), the patient group (35.4%), and routine screening (15.2%). In conclusion, almost one-half of clinical PGx recommendations from prominent U.S. guidance sources contain inconsistencies, which can potentially slow clinical implementation. |
format | Online Article Text |
id | pubmed-7603298 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76032982020-11-02 Prevalence and types of inconsistencies in clinical pharmacogenetic recommendations among major U.S. sources Shugg, Tyler Pasternak, Amy L. London, Bianca Luzum, Jasmine A. NPJ Genom Med Article Clinical implementation of pharmacogenomics (PGx) is slow. Previous studies have identified some inconsistencies among clinical PGx recommendations, but the prevalence and types of inconsistencies have not been comprehensively analyzed among major PGx guidance sources in the U.S. PGx recommendations from the Clinical Pharmacogenetics Implementation Consortium, U.S. Food and Drug Administration drug labels, and major U.S. professional medical organizations were analyzed through May 24, 2019. Inconsistencies were analyzed within the following elements: recommendation category; whether routine screening was recommended; and the specific biomarkers, variants, and patient groups involved. We identified 606 total clinical PGx recommendations, which contained 267 unique drugs. Composite inconsistencies occurred in 48.1% of clinical PGx recommendations overall, and in 93.3% of recommendations from three sources. Inconsistencies occurred in the recommendation category (29.8%), the patient group (35.4%), and routine screening (15.2%). In conclusion, almost one-half of clinical PGx recommendations from prominent U.S. guidance sources contain inconsistencies, which can potentially slow clinical implementation. Nature Publishing Group UK 2020-10-30 /pmc/articles/PMC7603298/ /pubmed/33145028 http://dx.doi.org/10.1038/s41525-020-00156-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. 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/4.0/. |
spellingShingle | Article Shugg, Tyler Pasternak, Amy L. London, Bianca Luzum, Jasmine A. Prevalence and types of inconsistencies in clinical pharmacogenetic recommendations among major U.S. sources |
title | Prevalence and types of inconsistencies in clinical pharmacogenetic recommendations among major U.S. sources |
title_full | Prevalence and types of inconsistencies in clinical pharmacogenetic recommendations among major U.S. sources |
title_fullStr | Prevalence and types of inconsistencies in clinical pharmacogenetic recommendations among major U.S. sources |
title_full_unstemmed | Prevalence and types of inconsistencies in clinical pharmacogenetic recommendations among major U.S. sources |
title_short | Prevalence and types of inconsistencies in clinical pharmacogenetic recommendations among major U.S. sources |
title_sort | prevalence and types of inconsistencies in clinical pharmacogenetic recommendations among major u.s. sources |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603298/ https://www.ncbi.nlm.nih.gov/pubmed/33145028 http://dx.doi.org/10.1038/s41525-020-00156-7 |
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