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估算在英国整个初级保健中实施先发制人药物遗传学检测的潜在影响。

Estimating the potential impact of implementing pre-emptive pharmacogenetic testing in primary care across the UK.

机构信息

School of Pharmacy, University of East Anglia, Norwich, UK.

Boots UK, Thane Road, Nottingham, UK.

出版信息

Br J Clin Pharmacol. 2021 Jul;87(7):2907-2925. doi: 10.1111/bcp.14704. Epub 2021 Jan 19.

Abstract

AIMS

Pharmacogenetics (PGx) in the UK is currently implemented in secondary care for a small group of high-risk medicines. However, most prescribing takes place in primary care, with a large group of medicines influenced by commonly occurring genetic variations. The goal of this study is to quantitatively estimate the volumes of medicines impacted by implementation of a population-level, pre-emptive pharmacogenetic screening programme for nine genes related to medicines frequently dispensed in primary care in 2019.

METHODS

A large community pharmacy database was analysed to estimate the national incidence of first prescriptions for 56 PGx drugs used in the UK for the period 1 January-31 December 2019. These estimated prescription volumes were combined with phenotype frequency data to estimate the occurrence of actionable drug-gene interactions (DGI) in daily practice in community pharmacies.

RESULTS

In between 19.1 and 21.1% (n = 5 233 353-5 780 595) of all new prescriptions for 56 drugs (n = 27 411 288 new prescriptions/year), an actionable drug-gene interaction (DGI) was present according to the guidelines of the Dutch Pharmacogenetics Working Group and/or the Clinical Pharmacogenetics Implementation Consortium. In these cases, the DGI would result in either increased monitoring, guarding against a maximum ceiling dose or an optional or immediate drug/dose change. An immediate dose adjustment or change in drug regimen accounted for 8.6-9.1% (n = 2 354 058-2 500 283) of these prescriptions.

CONCLUSIONS

Actionable drug-gene interactions frequently occur in UK primary care, with a large opportunity to optimise prescribing.

摘要

目的

英国的药物基因组学(PGx)目前在二级护理中针对一小部分高风险药物实施。然而,大多数处方都在初级保健中开具,其中大量药物受到常见遗传变异的影响。本研究的目的是定量估计实施针对经常在初级保健中开处方的九种与药物相关基因的人群水平、先发制人的药物基因组学筛选计划对 2019 年 9 种药物的影响。

方法

分析大型社区药房数据库,以估计英国在 2019 年 1 月 1 日至 12 月 31 日期间用于 56 种 PGx 药物的全国首诊处方量。这些估计的处方量与表型频率数据相结合,以估计在社区药房的日常实践中出现的可操作药物-基因相互作用(DGI)。

结果

在所有 56 种药物(每年 27411288 个新处方)的新处方中(n=5233353-5780595),根据荷兰药物基因组学工作组和/或临床药物基因组学实施联盟的指南,有 19.1%至 21.1%(n=27411288 个新处方/年)存在可操作的药物-基因相互作用(DGI)。在这些情况下,DGI 将导致增加监测,防止最大上限剂量或可选或立即药物/剂量变化。立即调整剂量或改变药物方案占这些处方的 8.6%-9.1%(n=2354058-2500283)。

结论

在英国初级保健中经常出现可操作的药物-基因相互作用,有很大的机会优化处方。

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