School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, Dublin, Ireland.
Faculty of Health, Science, Social Care & Education, Kingston University, London, UK.
Br J Clin Pharmacol. 2024 Sep;90(9):2280-2298. doi: 10.1111/bcp.16122. Epub 2024 Jun 12.
Pharmacogenetics (PGx) is increasingly recognized as a strategy for medicines optimisation and prevention of adverse drug reactions. According to guidelines produced by the Clinical Pharmacogenetics Implementation Consortium (CPIC) and the Dutch Pharmacogenetic Working Group (DPWG), most medicines with drug-gene interactions (DGIs) are prescribed in primary care. This study aimed to estimate the prevalence of potential and actionable DGIs involving all medicines dispensed in Irish primary care.
Dispensings of 46 drugs to General Medical Services (GMS) patients in the Health Service Executive Primary Care Reimbursement Service Irish pharmacy claims database from 01 January 2021 to 31 December 2021 were analysed to estimate the national prevalence of total dispensings and incidence of first-time dispensings of drugs with potential DGIs according to the CPIC and/or DPWG guidelines. Phenotype frequency data from the UK Biobank and the CPIC were used to estimate the incidence of actionable DGIs.
One in five dispensings (12 443 637 of 62 754 498, 19.8%) were medicines with potential DGIs, 1 878 255 of these dispensed for the first time. On application of phenotype frequencies and linked guideline based therapeutic recommendations, 2 349 055 potential DGIs (18.9%) required action, such as monitoring and guarding against maximum dose, drug or dose change. One in five (369 700, 19.7%) first-time dispensings required action, with 139 169 (7.4%) requiring a change in prescribing. Antidepressants, weak opioids and statins were most commonly identified as having actionable DGIs.
This study estimated a high prevalence of DGIs in primary care in Ireland, identifying the need and opportunity to optimize drug therapy through PGx testing.
药物遗传学(PGx)越来越被认为是优化药物治疗和预防药物不良反应的策略。根据临床药物遗传学实施联盟(CPIC)和荷兰药物遗传学工作组(DPWG)制定的指南,大多数具有药物-基因相互作用(DGIs)的药物都在初级保健中开具。本研究旨在估计涉及爱尔兰初级保健中所有配药的潜在和可操作的 DGIs 的流行率。
分析了 2021 年 1 月 1 日至 2021 年 12 月 31 日期间,在健康服务行政部门初级保健报销服务爱尔兰药房索赔数据库中,46 种药物对一般医疗服务(GMS)患者的配药情况,以根据 CPIC 和/或 DPWG 指南估计潜在 DGIs 的总配药和首次配药的全国流行率。从英国生物银行和 CPIC 获得表型频率数据,以估计可操作的 DGIs 的发生率。
五分之一的配药(62754498 份中的 12443637 份,19.8%)是具有潜在 DGIs 的药物,其中 1878255 份为首次配药。在应用表型频率和相关的基于指南的治疗建议后,需要采取行动的潜在 DGIs 有 2349055 个(18.9%),例如监测和防止最大剂量、药物或剂量变化。五分之一(369700 份,19.7%)的首次配药需要采取行动,其中 139169 份(7.4%)需要改变处方。抗抑郁药、弱阿片类药物和他汀类药物最常被确定为具有可操作的 DGIs。
本研究估计了爱尔兰初级保健中 DGIs 的高流行率,确定了通过 PGx 测试优化药物治疗的必要性和机会。