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Exploring perceptions, knowledge, and attitudes regarding pharmacogenetic testing in the medically underserved

Introduction: Pharmacogenetic testing may hold promise in addressing health disparities, as medically underserved patients appear to be prescribed medications with pharmacogenetic guidelines at higher rates. While routine clinical implementation of testing in medically underserved populations has no...

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Autores principales: Gawronski, Brian E., Cicali, Emily J., McDonough, Caitrin W., Cottler, Linda B., Duarte, Julio D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9880414/
https://www.ncbi.nlm.nih.gov/pubmed/36712853
http://dx.doi.org/10.3389/fgene.2022.1085994
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author Gawronski, Brian E.
Cicali, Emily J.
McDonough, Caitrin W.
Cottler, Linda B.
Duarte, Julio D.
author_facet Gawronski, Brian E.
Cicali, Emily J.
McDonough, Caitrin W.
Cottler, Linda B.
Duarte, Julio D.
author_sort Gawronski, Brian E.
collection PubMed
description Introduction: Pharmacogenetic testing may hold promise in addressing health disparities, as medically underserved patients appear to be prescribed medications with pharmacogenetic guidelines at higher rates. While routine clinical implementation of testing in medically underserved populations has not yet been achieved, using patient perspectives to inform implementation should increase the likelihood of success. The aim of this study was to assess the perceptions, knowledge, and attitudes regarding pharmacogenetic testing in medically underserved patients. Methods: We developed a survey instrument to assess respondent views on pharmacogenetic testing. The survey instrument was developed through a process of literature review, expert input, iterative pilot testing, and final refinement. The survey instrument was fielded to US adults with an estimated household income of $42,000 per year or less. Results: During the survey instrument development, 59 pilot testers provided 133 comments which lead to 38 revisions to the survey instrument. The nationwide survey resulted in 1,060 respondents, of which half (49.8%) reported having no health insurance or being on Medicaid. Most patients (78.9%) had not previously heard of pharmacogenetic testing. After being provided an explanation of pharmacogenetic testing, 60.5% were very or moderately interested in receiving testing if there were no cost and 75.8% of respondents agreed or strongly agreed that pharmacogenetic testing should be available to help with medication selection regardless of cost. Respondents shared that their greatest concern with pharmacogenetic testing was that the test would cost them money, which was expressed by over half (52.7%). This was followed by concerns that the results could reveal a risk for a disease, could affect health insurance, and would not improve care. Discussion: Our results indicate a strong interest in pharmacogenetic testing and identify key perceptions, attitudes, concerns, and potential barriers that can be addressed as pharmacogenetic testing is clinically implemented in medically underserved patient populations.
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spelling pubmed-98804142023-01-28 Exploring perceptions, knowledge, and attitudes regarding pharmacogenetic testing in the medically underserved Gawronski, Brian E. Cicali, Emily J. McDonough, Caitrin W. Cottler, Linda B. Duarte, Julio D. Front Genet Genetics Introduction: Pharmacogenetic testing may hold promise in addressing health disparities, as medically underserved patients appear to be prescribed medications with pharmacogenetic guidelines at higher rates. While routine clinical implementation of testing in medically underserved populations has not yet been achieved, using patient perspectives to inform implementation should increase the likelihood of success. The aim of this study was to assess the perceptions, knowledge, and attitudes regarding pharmacogenetic testing in medically underserved patients. Methods: We developed a survey instrument to assess respondent views on pharmacogenetic testing. The survey instrument was developed through a process of literature review, expert input, iterative pilot testing, and final refinement. The survey instrument was fielded to US adults with an estimated household income of $42,000 per year or less. Results: During the survey instrument development, 59 pilot testers provided 133 comments which lead to 38 revisions to the survey instrument. The nationwide survey resulted in 1,060 respondents, of which half (49.8%) reported having no health insurance or being on Medicaid. Most patients (78.9%) had not previously heard of pharmacogenetic testing. After being provided an explanation of pharmacogenetic testing, 60.5% were very or moderately interested in receiving testing if there were no cost and 75.8% of respondents agreed or strongly agreed that pharmacogenetic testing should be available to help with medication selection regardless of cost. Respondents shared that their greatest concern with pharmacogenetic testing was that the test would cost them money, which was expressed by over half (52.7%). This was followed by concerns that the results could reveal a risk for a disease, could affect health insurance, and would not improve care. Discussion: Our results indicate a strong interest in pharmacogenetic testing and identify key perceptions, attitudes, concerns, and potential barriers that can be addressed as pharmacogenetic testing is clinically implemented in medically underserved patient populations. Frontiers Media S.A. 2023-01-13 /pmc/articles/PMC9880414/ /pubmed/36712853 http://dx.doi.org/10.3389/fgene.2022.1085994 Text en Copyright © 2023 Gawronski, Cicali, McDonough, Cottler and Duarte. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Gawronski, Brian E.
Cicali, Emily J.
McDonough, Caitrin W.
Cottler, Linda B.
Duarte, Julio D.
Exploring perceptions, knowledge, and attitudes regarding pharmacogenetic testing in the medically underserved
title Exploring perceptions, knowledge, and attitudes regarding pharmacogenetic testing in the medically underserved
title_full Exploring perceptions, knowledge, and attitudes regarding pharmacogenetic testing in the medically underserved
title_fullStr Exploring perceptions, knowledge, and attitudes regarding pharmacogenetic testing in the medically underserved
title_full_unstemmed Exploring perceptions, knowledge, and attitudes regarding pharmacogenetic testing in the medically underserved
title_short Exploring perceptions, knowledge, and attitudes regarding pharmacogenetic testing in the medically underserved
title_sort exploring perceptions, knowledge, and attitudes regarding pharmacogenetic testing in the medically underserved
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9880414/
https://www.ncbi.nlm.nih.gov/pubmed/36712853
http://dx.doi.org/10.3389/fgene.2022.1085994
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