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Transitioning Pharmacogenomics into the Clinical Setting: Training Future Pharmacists

Pharmacogenomics, once hailed as a futuristic approach to pharmacotherapy, has transitioned to clinical implementation. Although logistic and economic limitations to clinical pharmacogenomics are being superseded by external measures such as preemptive genotyping, implementation by clinicians has me...

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Autores principales: Frick, Amber, Benton, Cristina S., Scolaro, Kelly L., McLaughlin, Jacqueline E., Bradley, Courtney L., Suzuki, Oscar T., Wang, Nan, Wiltshire, Tim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976536/
https://www.ncbi.nlm.nih.gov/pubmed/27551265
http://dx.doi.org/10.3389/fphar.2016.00241
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author Frick, Amber
Benton, Cristina S.
Scolaro, Kelly L.
McLaughlin, Jacqueline E.
Bradley, Courtney L.
Suzuki, Oscar T.
Wang, Nan
Wiltshire, Tim
author_facet Frick, Amber
Benton, Cristina S.
Scolaro, Kelly L.
McLaughlin, Jacqueline E.
Bradley, Courtney L.
Suzuki, Oscar T.
Wang, Nan
Wiltshire, Tim
author_sort Frick, Amber
collection PubMed
description Pharmacogenomics, once hailed as a futuristic approach to pharmacotherapy, has transitioned to clinical implementation. Although logistic and economic limitations to clinical pharmacogenomics are being superseded by external measures such as preemptive genotyping, implementation by clinicians has met resistance, partly due to a lack of education. Pharmacists, with extensive training in pharmacology and pharmacotherapy and accessibility to patients, are ideally suited to champion clinical pharmacogenomics. This study aimed to analyze the outcomes of an innovative pharmacogenomic teaching approach. Second-year student pharmacists enrolled in a required, 15-week pharmaceutical care lab course in 2015 completed educational activities including lectures and small group work focusing on practical pharmacogenomics. Reflecting the current landscape of direct-to-consumer (DTC) genomic testing, students were offered 23andMe genotyping. Students completed surveys regarding their attitudes and confidence on pharmacogenomics prior to and following the educational intervention. Paired pre- and post-intervention responses were analyzed with McNemar's test for binary comparisons and the Wilcoxon signed-rank test for Likert items. Responses between genotyped and non-genotyped students were analyzed with Fisher's exact test for binary comparisons and the Mann-Whitney U-test for Likert items. Responses were analyzed for all student pharmacists who voluntarily completed the pre-intervention survey (N = 121, 83% response) and for student pharmacists who completed both pre- and post-intervention surveys (N = 39, 27% response). Of those who completed both pre- and post-intervention surveys, 59% obtained genotyping. Student pharmacists demonstrated a significant increase in their knowledge of pharmacogenomic resources (17.9 vs. 56.4%, p < 0.0001) and confidence in applying pharmacogenomic information to manage patients' drug therapy (28.2 vs. 48.7%, p = 0.01), particularly if the student had received genotyping. Student pharmacists understanding of the risks and benefits of using personal genome testing services significantly increased (55.3 vs. 86.8%, p = 0.001) along with agreement that personal genomics would likely play an important role in their future career (47.4 vs. 76.3%, p = 0.01), particularly among students who participated in genotyping. The educational intervention, including personal genotyping, was feasible, and positively enhanced students' reflections, and attitudes toward pharmacogenomics in a professional pharmacy program.
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spelling pubmed-49765362016-08-22 Transitioning Pharmacogenomics into the Clinical Setting: Training Future Pharmacists Frick, Amber Benton, Cristina S. Scolaro, Kelly L. McLaughlin, Jacqueline E. Bradley, Courtney L. Suzuki, Oscar T. Wang, Nan Wiltshire, Tim Front Pharmacol Pharmacology Pharmacogenomics, once hailed as a futuristic approach to pharmacotherapy, has transitioned to clinical implementation. Although logistic and economic limitations to clinical pharmacogenomics are being superseded by external measures such as preemptive genotyping, implementation by clinicians has met resistance, partly due to a lack of education. Pharmacists, with extensive training in pharmacology and pharmacotherapy and accessibility to patients, are ideally suited to champion clinical pharmacogenomics. This study aimed to analyze the outcomes of an innovative pharmacogenomic teaching approach. Second-year student pharmacists enrolled in a required, 15-week pharmaceutical care lab course in 2015 completed educational activities including lectures and small group work focusing on practical pharmacogenomics. Reflecting the current landscape of direct-to-consumer (DTC) genomic testing, students were offered 23andMe genotyping. Students completed surveys regarding their attitudes and confidence on pharmacogenomics prior to and following the educational intervention. Paired pre- and post-intervention responses were analyzed with McNemar's test for binary comparisons and the Wilcoxon signed-rank test for Likert items. Responses between genotyped and non-genotyped students were analyzed with Fisher's exact test for binary comparisons and the Mann-Whitney U-test for Likert items. Responses were analyzed for all student pharmacists who voluntarily completed the pre-intervention survey (N = 121, 83% response) and for student pharmacists who completed both pre- and post-intervention surveys (N = 39, 27% response). Of those who completed both pre- and post-intervention surveys, 59% obtained genotyping. Student pharmacists demonstrated a significant increase in their knowledge of pharmacogenomic resources (17.9 vs. 56.4%, p < 0.0001) and confidence in applying pharmacogenomic information to manage patients' drug therapy (28.2 vs. 48.7%, p = 0.01), particularly if the student had received genotyping. Student pharmacists understanding of the risks and benefits of using personal genome testing services significantly increased (55.3 vs. 86.8%, p = 0.001) along with agreement that personal genomics would likely play an important role in their future career (47.4 vs. 76.3%, p = 0.01), particularly among students who participated in genotyping. The educational intervention, including personal genotyping, was feasible, and positively enhanced students' reflections, and attitudes toward pharmacogenomics in a professional pharmacy program. Frontiers Media S.A. 2016-08-08 /pmc/articles/PMC4976536/ /pubmed/27551265 http://dx.doi.org/10.3389/fphar.2016.00241 Text en Copyright © 2016 Frick, Benton, Scolaro, McLaughlin, Bradley, Suzuki, Wang and Wiltshire. http://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) or licensor 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 Pharmacology
Frick, Amber
Benton, Cristina S.
Scolaro, Kelly L.
McLaughlin, Jacqueline E.
Bradley, Courtney L.
Suzuki, Oscar T.
Wang, Nan
Wiltshire, Tim
Transitioning Pharmacogenomics into the Clinical Setting: Training Future Pharmacists
title Transitioning Pharmacogenomics into the Clinical Setting: Training Future Pharmacists
title_full Transitioning Pharmacogenomics into the Clinical Setting: Training Future Pharmacists
title_fullStr Transitioning Pharmacogenomics into the Clinical Setting: Training Future Pharmacists
title_full_unstemmed Transitioning Pharmacogenomics into the Clinical Setting: Training Future Pharmacists
title_short Transitioning Pharmacogenomics into the Clinical Setting: Training Future Pharmacists
title_sort transitioning pharmacogenomics into the clinical setting: training future pharmacists
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976536/
https://www.ncbi.nlm.nih.gov/pubmed/27551265
http://dx.doi.org/10.3389/fphar.2016.00241
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