管制物质电子处方的采用和增加使用

S. Achar, Nikhil Sinha, W. Norcross
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引用次数: 0

摘要

管制物质的电子处方(EPCS)现在正在美国大多数卫生保健实践和药房实施。本综述旨在详细介绍EPCS采用所需的步骤,并综合最新的关于其采用的好处和挑战的文献。我们对1990年至2020年期间发表的七项研究进行了系统回顾,发现EPCS在减少错误、欺诈、过度处方、成本和效率提高方面的好处。关于挑战的已发表证据有限,例如实施成本和开处方者负担。随着EPCS成为一个全国性的过程,需要进一步的研究,以最大限度地提高EPCS的有效性,并探索额外的好处和挑战。我们使用了“Cochrane干预措施系统评价手册”中强调的系统评价的GRADE(推荐、评估、发展和评价分级)系统的修改版本来评估所评价的主要研究的质量每位作者的任务是确定所审查的每个初步研究的质量,并分配高、中或低质量的质量分数。来自随机对照试验的证据开始时质量高,而来自观察性研究的证据开始时质量低。5个因素可降低质量:偏倚风险、不精确风险、不一致性风险、间接性风险和发表偏倚风险,并可通过大的效应强度和明显的剂量-反应梯度提高质量。我们从原始出版物的文本、表格和图表中提取数据。附录A说明了研究的质量。审查的数据库包括PubMed、b谷歌Scholar、Cochrane和SCOPUS。这项研究始于1990年,当时出现了第一波阿片类药物流行和首次发表的电子处方研究,并一直持续到2020年。关键词“管制药物电子处方”、“管制药物电子处方”、“管制药物欺诈处方”、“EPCS与PDMP”和“药物与管制药物电子处方的相互作用”被用作检索在线学术数据库文章的纳入标准。仅包括用英语撰写的报告、评论和研究的主要和次要数据。疾病控制中心(CDC)、国家药物滥用研究所(NIDA)、缉毒局(DEA)、药物滥用和精神卫生服务管理局(SAMHSA)、美国家庭医学学会(AAFP)和全国代表性的卫生信息网络被用来获取有关EPCS的最新统计数据。
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The Adoption and Increased Use of Electronic Prescribing of Controlled Substances
The electronic prescribing of controlled substances (EPCS) is now becoming implemented in most health care practices and pharmacies in the United States. This review aims to detail the steps needed for EPCS adoption and synthesize the most current literature on the benefits and challenges associated with its adoption. Our systematic review of seven published studies from 1990 to 2020 notes the benefits of EPCS in the reduction of errors, fraud, overprescribing, cost and efficiency improvements. There is limited published evidence of challenges, such as the cost of implementation and prescriber burden. With EPCS becoming a nationwide process, further research needs to be conducted to maximize the effectiveness of EPCS and explore additional benefits and challenges. We used a modified version of the GRADE (Grading of Recommendations, Assessment, Development and Evaluations) system for systematic reviews highlighted in the “Cochrane Handbook for Systematic Reviews of Interventions” to assess the quality of the primary studies reviewed.1 Each author was tasked with determining the quality of each primary study reviewed and assigning a quality score of either high, moderate or low quality. Evidence stemming from randomized controlled trials starts as high quality while evidence from observational studies starts as low quality. Quality can be lowered by five factors: risk of bias, imprecision, inconsistency, indirectness, and publication bias and can be raised by a large magnitude of effect and a clear dose-response gradient. We extracted data from the text, tables and graphs of the original publications. Appendix A illustrates the quality of the studies. Databases reviewed included PubMed, Google Scholar, Cochrane and SCOPUS. The search was started in 1990, with the first wave of the opioid epidemic and the first published studies of e-prescribing, and continued to the year of 2020. The key phrases “electronic prescribing of controlled substances,” “e-prescribing of controlled substances,” “fraudulent prescribing of controlled substances,” “EPCS with PDMP,” and “drug interactions with e-prescribing of controlled drugs” were used as an inclusion criterion to search online scholarly databases for articles. Only primary and secondary data from reports, reviews and research studies written in English were included. The Centers for Disease Control (CDC), National Institute on Drug Abuse (NIDA), Drug Enforcement Administration (DEA), Substance Abuse and Mental Health Services Administration (SAMHSA), American Academy of Family Medicine (AAFP), and nationally represented health information networks were used to obtain updated statistics regarding EPCS.
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