Amanda Ernst Wood, Deepika Agrawal, Alison P Deem, Terri L Dupper Knoper, Rosa F Merino, Hylton E Molzof, Laurie E Maus, Floreen Kim, Zohra Lodin, Sonia Lim
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Psychiatric medication providers were given access to the PGx assay results, including notification of drug-drug-gene interactions computed from an algorithm decision tool, to assist with medication management decisions. Veteran outpatients (N = 53) prescribed polypharmacy (mean = 13.15 medications) were enrolled into the study. In 92.4% of cases, providers changed medications at baseline, with 83% of providers indicating that they changed their original medication plan based on the PGx results. Clinical improvement over the 12-week treatment phase was seen in depression (F(1.63, 45) = 5.45, P = .01, η<sup>2</sup> = .11) and mental health quality of life (F(2.00, 45) = 4.16, P < .05, η<sup>2</sup> = .16). Adverse drug effects were unchanged or improved over time. Rates of polypharmacy remained unchanged. 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引用次数: 1
摘要
在过去的二十年中,多种药物的使用变得越来越普遍,增加了药物相互作用和药物不良反应的风险。药物基因组学(PGx)分析据称能够根据遗传标记预测个体对特定药物的反应,这可能有助于为服用多种药物的患者制定优化的药物方案。这项为期12周的试点研究检查了PGx结果对退伍军人临床管理的影响,这些退伍军人开了精神科综合药物。精神科药物提供者获得了PGx检测结果,包括通过算法决策工具计算的药物-药物-基因相互作用通知,以协助药物管理决策。临床经验丰富的门诊患者53例(平均13.15种药物)被纳入研究。在92.4%的病例中,提供者在基线时改变了药物治疗,83%的提供者表示他们根据PGx结果改变了原来的药物治疗计划。在12周的治疗期内,患者在抑郁(F(1.63, 45) = 5.45, P = 0.01, η2 = 0.11)和心理健康生活质量(F(2.00, 45) = 4.16, P 2 = 0.16)方面均有临床改善。随着时间的推移,药物不良反应没有变化或有所改善。服用多种药物的比率保持不变。结果表明,基于PGx测定的药物变化可能对复杂的患者群体有益。
Medication Optimization Using Pharmacogenomic Testing in a Complex Mental Health Population Prescribed Psychiatric Polypharmacy.
The use of polypharmacy has become significantly more common over the past two decades, increasing the risk of drug-drug interactions and adverse drug reactions. Pharmacogenomic (PGx) assays have the purported benefit of being able to predict an individual's response to a specific medication based on genetic markers, which may facilitate the development of optimized medication regimens for patients prescribed polypharmacy. This 12-week pilot study examined the impact of the PGx results on the clinical management of Veterans who were prescribed psychiatric polypharmacy. Psychiatric medication providers were given access to the PGx assay results, including notification of drug-drug-gene interactions computed from an algorithm decision tool, to assist with medication management decisions. Veteran outpatients (N = 53) prescribed polypharmacy (mean = 13.15 medications) were enrolled into the study. In 92.4% of cases, providers changed medications at baseline, with 83% of providers indicating that they changed their original medication plan based on the PGx results. Clinical improvement over the 12-week treatment phase was seen in depression (F(1.63, 45) = 5.45, P = .01, η2 = .11) and mental health quality of life (F(2.00, 45) = 4.16, P < .05, η2 = .16). Adverse drug effects were unchanged or improved over time. Rates of polypharmacy remained unchanged. The results suggest that medication changes based on the PGx assay may be beneficial in a complex patient population prescribed polypharmacy.
期刊介绍:
The Journal of Clinical Pharmacology (JCP) is a Human Pharmacology journal designed to provide physicians, pharmacists, research scientists, regulatory scientists, drug developers and academic colleagues a forum to present research in all aspects of Clinical Pharmacology. This includes original research in pharmacokinetics, pharmacogenetics/pharmacogenomics, pharmacometrics, physiologic based pharmacokinetic modeling, drug interactions, therapeutic drug monitoring, regulatory sciences (including unique methods of data analysis), special population studies, drug development, pharmacovigilance, womens’ health, pediatric pharmacology, and pharmacodynamics. Additionally, JCP publishes review articles, commentaries and educational manuscripts. The Journal also serves as an instrument to disseminate Public Policy statements from the American College of Clinical Pharmacology.