Rodríguez-Escudero Idaliz, Cedeño Julio A, Rodríguez-Nazario Ileana, Reynaldo-Fernández Gledys, Rodríguez-Vera Leyanis, Morales Niretzy, Jiménez-Vélez Braulio, Ruaño Gualberto, Duconge Jorge
School of Pharmacy, University of Puerto Rico, Medical Sciences Campus, San Juan, Puerto Rico.
Institute of Pharmacy and Foods, University of Havana, Cuba.
J Am Coll Clin Pharm. 2020 Sep;3(6):1028-1037. doi: 10.1002/jac5.1250. Epub 2020 May 2.
Pharmacists are poised to be the health care professionals best suited to provide medication-related consults and services based on a patient's genetics. Despite its potential benefits, the implementation of pharmacogenetic (PGx) testing into primary clinical settings has been slow among medically underserved populations. To our knowledge, this is the first time that PGx-driven recommendations have been incorporated into a Comprehensive Medication Management (CMM) service in a Hispanic population.
The aim of this study is to evaluate the clinical utility of adding PGx guidance into pharmacist-driven CMM.
This is a pre- and post-interventional design study. Patients were recruited from a psychologist's clinic. A total of 24 patients had a face-to-face interview with a pharmacist to complete a CMM, Personal Medication Record, and Medication-Related Action Plan (MAP) blind to PGx findings. Collected buccal DNA samples were genotyped using drug-metabolizing enzymes and transporters (DMET) Plus Array.
The pharmacist generated new MAPs for each patient based on PGx results. Genetic variants that could potentially affect the safety and effectiveness of at least one drug in the pharmacotherapy were identified in 96% of patients, for whom the pharmacist changed the initial recommendations. Polymorphisms in genes encoding for isoenzymes CYP2D6, CYP2C19, and CYP2C9 were identified in 83%, 52%, and 41% of patients, respectively. Pharmacists performing CMM identified 22 additional medication problems after PGx determinations. Moreover, they agreed with the clinical utility of PGx in the studied sample based on perceived value of adding PGx to traditional CMM and its utility in the decision-making process of pharmacists.
The study confirmed the critical role to be played by pharmacists in facilitating the clinical usage of relevant genetic information to optimize drug therapy decisions as well as their involvement on many levels of these multidisciplinary implementation efforts, including championing and leading PGx-guided CMM services.
药剂师有望成为最适合根据患者基因提供药物相关咨询和服务的医疗保健专业人员。尽管有潜在益处,但在医疗服务不足的人群中,将药物基因组学(PGx)检测应用于初级临床环境的进展一直缓慢。据我们所知,这是首次将PGx驱动的建议纳入西班牙裔人群的综合药物管理(CMM)服务中。
本研究旨在评估在药剂师主导的CMM中添加PGx指导的临床效用。
这是一项干预前后设计研究。患者从一家心理诊所招募。共有24名患者与药剂师进行了面对面访谈,以完成一份CMM、个人用药记录和与药物相关的行动计划(MAP),且对PGx结果不知情。收集的颊部DNA样本使用药物代谢酶和转运体(DMET) Plus Array进行基因分型。
药剂师根据PGx结果为每位患者制定了新的MAP。在96%的患者中发现了可能影响药物治疗中至少一种药物安全性和有效性的基因变异,药剂师据此改变了初始建议。分别在83%、52%和41%的患者中鉴定出编码同工酶CYP2D6、CYP2C19和CYP2C9的基因中的多态性。进行CMM的药剂师在PGx测定后又发现了22个用药问题。此外,基于将PGx添加到传统CMM的感知价值及其在药剂师决策过程中的效用,他们认可PGx在研究样本中的临床效用。
该研究证实了药剂师在促进相关基因信息的临床应用以优化药物治疗决策方面所起的关键作用,以及他们在这些多学科实施工作的多个层面上的参与,包括支持和引领PGx指导的CMM服务。