Impact of Updating Pharmacogenetic Results: Lessons Learned from the PREDICT Program

Pharmacogenomic (PGx) evidence for selective serotonin reuptake inhibitors (SSRIs) continues to evolve. For sites offering testing, maintaining up-to-date interpretations and implementing new clinical decision support (CDS) driven by existing results creates practical and technical challenges. Vande...

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Autores principales: Michelle Liu, Sara L. Van Driest, Cindy L. Vnencak-Jones, Leigh Ann G. Saucier, Bartholomew P. Roland, Cheryl L. Gatto, Shari L. Just, Asli O. Weitkamp, Josh F. Peterson
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/59b4c678d0c74fe7be7ea8ccb90969b1
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spelling oai:doaj.org-article:59b4c678d0c74fe7be7ea8ccb90969b12021-11-25T18:06:44ZImpact of Updating Pharmacogenetic Results: Lessons Learned from the PREDICT Program10.3390/jpm111110512075-4426https://doaj.org/article/59b4c678d0c74fe7be7ea8ccb90969b12021-10-01T00:00:00Zhttps://www.mdpi.com/2075-4426/11/11/1051https://doaj.org/toc/2075-4426Pharmacogenomic (PGx) evidence for selective serotonin reuptake inhibitors (SSRIs) continues to evolve. For sites offering testing, maintaining up-to-date interpretations and implementing new clinical decision support (CDS) driven by existing results creates practical and technical challenges. Vanderbilt University Medical Center initiated panel testing in 2010, added <i>CYP2D6</i> testing in 2017, and released CDS for SSRIs in 2020. We systematically reinterpreted historic <i>CYP2C19</i> and <i>CYP2D6</i> genotypes to update phenotypes to current nomenclature and to launch provider CDS and patient-oriented content for SSRIs. Chart review was conducted to identify and recontact providers caring for patients with current SSRI therapy and new actionable recommendations. A total of 15,619 patients’ PGx results were reprocessed. Of the non-deceased patients reprocessed, 21% (<i>n</i> = 3278) resulted in <i>CYP2C19</i><i>*1/*17</i> reinterpretations. Among 289 patients with an actionable recommendation and SSRI medication prescription, 31.8% (<i>n</i> = 92) did not necessitate contact of a clinician, while 43.2% (<i>n</i> = 125) resulted in clinician contacted, and for 25% (<i>n</i> = 72) no appropriate clinician was able to be identified. Maintenance of up-to-date interpretations and recommendations for PGx results over the lifetime of a patient requires continuous effort. Reprocessing is a key strategy for maintenance and expansion of PGx content to be periodically considered and implemented.Michelle LiuSara L. Van DriestCindy L. Vnencak-JonesLeigh Ann G. SaucierBartholomew P. RolandCheryl L. GattoShari L. JustAsli O. WeitkampJosh F. PetersonMDPI AGarticlepharmacogenomicspharmacogeneticspersonalized medicineprecision medicineSSRIsreprocessingMedicineRENJournal of Personalized Medicine, Vol 11, Iss 1051, p 1051 (2021)
institution DOAJ
collection DOAJ
language EN
topic pharmacogenomics
pharmacogenetics
personalized medicine
precision medicine
SSRIs
reprocessing
Medicine
R
spellingShingle pharmacogenomics
pharmacogenetics
personalized medicine
precision medicine
SSRIs
reprocessing
Medicine
R
Michelle Liu
Sara L. Van Driest
Cindy L. Vnencak-Jones
Leigh Ann G. Saucier
Bartholomew P. Roland
Cheryl L. Gatto
Shari L. Just
Asli O. Weitkamp
Josh F. Peterson
Impact of Updating Pharmacogenetic Results: Lessons Learned from the PREDICT Program
description Pharmacogenomic (PGx) evidence for selective serotonin reuptake inhibitors (SSRIs) continues to evolve. For sites offering testing, maintaining up-to-date interpretations and implementing new clinical decision support (CDS) driven by existing results creates practical and technical challenges. Vanderbilt University Medical Center initiated panel testing in 2010, added <i>CYP2D6</i> testing in 2017, and released CDS for SSRIs in 2020. We systematically reinterpreted historic <i>CYP2C19</i> and <i>CYP2D6</i> genotypes to update phenotypes to current nomenclature and to launch provider CDS and patient-oriented content for SSRIs. Chart review was conducted to identify and recontact providers caring for patients with current SSRI therapy and new actionable recommendations. A total of 15,619 patients’ PGx results were reprocessed. Of the non-deceased patients reprocessed, 21% (<i>n</i> = 3278) resulted in <i>CYP2C19</i><i>*1/*17</i> reinterpretations. Among 289 patients with an actionable recommendation and SSRI medication prescription, 31.8% (<i>n</i> = 92) did not necessitate contact of a clinician, while 43.2% (<i>n</i> = 125) resulted in clinician contacted, and for 25% (<i>n</i> = 72) no appropriate clinician was able to be identified. Maintenance of up-to-date interpretations and recommendations for PGx results over the lifetime of a patient requires continuous effort. Reprocessing is a key strategy for maintenance and expansion of PGx content to be periodically considered and implemented.
format article
author Michelle Liu
Sara L. Van Driest
Cindy L. Vnencak-Jones
Leigh Ann G. Saucier
Bartholomew P. Roland
Cheryl L. Gatto
Shari L. Just
Asli O. Weitkamp
Josh F. Peterson
author_facet Michelle Liu
Sara L. Van Driest
Cindy L. Vnencak-Jones
Leigh Ann G. Saucier
Bartholomew P. Roland
Cheryl L. Gatto
Shari L. Just
Asli O. Weitkamp
Josh F. Peterson
author_sort Michelle Liu
title Impact of Updating Pharmacogenetic Results: Lessons Learned from the PREDICT Program
title_short Impact of Updating Pharmacogenetic Results: Lessons Learned from the PREDICT Program
title_full Impact of Updating Pharmacogenetic Results: Lessons Learned from the PREDICT Program
title_fullStr Impact of Updating Pharmacogenetic Results: Lessons Learned from the PREDICT Program
title_full_unstemmed Impact of Updating Pharmacogenetic Results: Lessons Learned from the PREDICT Program
title_sort impact of updating pharmacogenetic results: lessons learned from the predict program
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/59b4c678d0c74fe7be7ea8ccb90969b1
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