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Pharmacogenomic-Based Decision Support to Predict Adherence to Medications.
Christian, Carlton; Borden, Brittany A; Danahey, Keith; Yeo, Kiang-Teck J; van Wijk, Xander M R; Ratain, Mark J; O'Donnell, Peter H.
Afiliação
  • Christian C; The University of Chicago Pritzker School of Medicine, Chicago, Illinois, USA.
  • Borden BA; The University of Chicago Center for Personalized Therapeutics, Chicago, Illinois, USA.
  • Danahey K; The University of Chicago Center for Personalized Therapeutics, Chicago, Illinois, USA.
  • Yeo KJ; The University of Chicago Center for Research Informatics, Chicago, Illinois, USA.
  • van Wijk XMR; The University of Chicago Center for Personalized Therapeutics, Chicago, Illinois, USA.
  • Ratain MJ; The University of Chicago Department of Pathology, Chicago, Illinois, USA.
  • O'Donnell PH; The University of Chicago Advanced Technology Clinical Laboratory, Chicago, Illinois, USA.
Clin Pharmacol Ther ; 108(2): 368-376, 2020 08.
Article em En | MEDLINE | ID: mdl-32236960
Poor adherence is associated with worse disease outcomes. Pharmacogenomics provides a possible intervention to address adherence. We hypothesized that pharmacogenomic-informed care could increase adherence. Patients in a prospective case-control study underwent preemptive pharmacogenomic genotyping with results available for provider use at the point of care; controls (not genotyped) were treated by the same providers. Over 6,000 e-prescriptions for 39 medications with actionable pharmacogenomic information were analyzed. Composite adherence, measured by modified proportion of days covered (mPDC), was compared between cases/controls and genomically concordant vs. genomically higher-risk medications. Overall, 536 patients were included. No difference in mean mPDC was observed due to availability of pharmacogenomic guidance. However, case patients prescribed high-risk pharmacogenomic medications were more than twice as likely to have low mPDC for these medications compared with genomically concordant prescriptions (odds ratio = 2.4 (1.03-5.74), P < 0.05). This study is the first to show that composite pharmacogenomic information predicts adherence.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Farmacogenética / Técnicas de Apoio para a Decisão / Adesão à Medicação / Medicina de Precisão / Variantes Farmacogenômicos Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Pharmacol Ther Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Farmacogenética / Técnicas de Apoio para a Decisão / Adesão à Medicação / Medicina de Precisão / Variantes Farmacogenômicos Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Pharmacol Ther Ano de publicação: 2020 Tipo de documento: Article