医院环境中药物基因检测的实施与评估策略:范围审查。

IF 2.8 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Therapeutic Drug Monitoring Pub Date : 2024-09-11 DOI:10.1097/FTD.0000000000001243
Angela Wu, Edward J Raack, Colin J D Ross, Bruce C Carleton
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引用次数: 0

摘要

背景:临床环境中的药物基因检测提高了药物治疗的安全性和有效性。越来越多的研究对药物基因学的实施进行了评估,并找出了障碍和促进因素。然而,还没有一篇综述着重于弥补在确定检测的障碍和促进因素与采取的临床应对策略之间的差距。本综述旨在了解药物基因检测项目的实施和评估策略:方法:进行了符合 PRISMA 标准的范围界定综述。纳入的研究讨论了在医院环境中实施的药物基因检测项目。研究方法包括定量、定性和混合设计方法:在 7043 篇描述临床药物基因项目的文章中,共有 232 篇被纳入。介绍药物遗传学实施情况最常见的专科是精神病学(26%)和肿瘤学(16%),尽管许多研究介绍了在多个专科实施的机构项目(19%)。不同的专科报告了不同的临床结果,但所有专科都报告了类似的项目绩效指标,如测试吸收率和遵循测试建议的次数。通过研究人员、药剂师和电子警报提供检测结果有利有弊,但要将药物基因学结果纳入临床决策,医生的积极参与是必要的:结论:需要对药物基因检测计划的维护和可持续性开展进一步研究。这些研究结果概述了不同专科的实施和评估策略,可用于改善药物基因检测。
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Implementation and Evaluation Strategies for Pharmacogenetic Testing in Hospital Settings: A Scoping Review.

Background: Pharmacogenetic testing in clinical settings has improved the safety and efficacy of drug treatment. There is a growing number of studies evaluating pharmacogenetic implementation and identifying barriers and facilitators. However, no review has focused on bridging the gap between identifying barriers and facilitators of testing and the clinical strategies adopted in response. This review was conducted to understand the implementation and evaluation strategies of pharmacogenetic testing programs.

Methods: A PRISMA-compliant scoping review was conducted. The included studies discussed pharmacogenetic testing programs implemented in a hospital setting. Quantitative, qualitative, and mixed design methods were included.

Results: A total of 232 of the 7043 articles that described clinical pharmacogenetic programs were included. The most common specialties that described pharmacogenetic implementation were psychiatry (26%) and oncology (16%), although many studies described institutional programs implemented across multiple specialties (19%). Different specialties reported different clinical outcomes, but all reported similar program performance indicators, such as test uptake and the number of times the test recommendations were followed. There were benefits and drawbacks to delivering test results through research personnel, pharmacists, and electronic alerts, but active engagement of physicians was necessary for the incorporation of pharmacogenetic results into clinical decision making.

Conclusions: Further research is required on the maintenance and sustainability of pharmacogenetic testing initiatives. These findings provide an overview of the implementation and evaluation strategies of different specialties that can be used to improve pharmacogenetic testing.

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来源期刊
Therapeutic Drug Monitoring
Therapeutic Drug Monitoring 医学-毒理学
CiteScore
5.00
自引率
8.00%
发文量
213
审稿时长
4-8 weeks
期刊介绍: Therapeutic Drug Monitoring is a peer-reviewed, multidisciplinary journal directed to an audience of pharmacologists, clinical chemists, laboratorians, pharmacists, drug researchers and toxicologists. It fosters the exchange of knowledge among the various disciplines–clinical pharmacology, pathology, toxicology, analytical chemistry–that share a common interest in Therapeutic Drug Monitoring. The journal presents studies detailing the various factors that affect the rate and extent drugs are absorbed, metabolized, and excreted. Regular features include review articles on specific classes of drugs, original articles, case reports, technical notes, and continuing education articles.
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