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2
A framework to guide the optimal development and use of real-world evidence for drug coverage and formulary decisions.一个指导为药物覆盖范围和处方集决策优化开发和使用真实世界证据的框架。
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3
Real-world evidence for coverage decisions: opportunities and challenges.用于医保覆盖决策的真实世界证据:机遇与挑战
J Comp Eff Res. 2018 Dec;7(12):1133-1143. doi: 10.2217/cer-2018-0066. Epub 2018 Nov 9.
4
Real-World Evidence and Real-World Data for Evaluating Drug Safety and Effectiveness.用于评估药物安全性和有效性的真实世界证据与真实世界数据。
JAMA. 2018 Sep 4;320(9):867-868. doi: 10.1001/jama.2018.10136.
5
Real-World Evidence: Useful in the Real World of US Payer Decision Making? How? When? And What Studies?真实世界证据:在美国医保支付方决策的现实世界中有用吗?如何有用?何时有用?以及哪些研究有用?
Value Health. 2018 Mar;21(3):326-333. doi: 10.1016/j.jval.2017.08.3013. Epub 2017 Oct 18.
6
AMSTAR 2: a critical appraisal tool for systematic reviews that include randomised or non-randomised studies of healthcare interventions, or both.AMSTAR 2:一种用于系统评价的关键评估工具,该系统评价包括医疗保健干预措施的随机或非随机研究,或两者皆有。
BMJ. 2017 Sep 21;358:j4008. doi: 10.1136/bmj.j4008.
7
Good practices for real-world data studies of treatment and/or comparative effectiveness: Recommendations from the joint ISPOR-ISPE Special Task Force on real-world evidence in health care decision making.治疗和/或比较效果的真实世界数据研究的良好实践:ISPOR-ISPE联合特别工作组关于医疗保健决策中真实世界证据的建议。
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8
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J Manag Care Spec Pharm. 2017 Jun;23(6):613-620. doi: 10.18553/jmcp.2017.16368. Epub 2017 Mar 16.
9
Comparative Effectiveness of Rapid-Acting Insulins in Adults with Diabetes.成人糖尿病患者速效胰岛素的疗效比较。
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ROBINS-I: a tool for assessing risk of bias in non-randomised studies of interventions.ROBINS-I:一种评估干预性非随机研究偏倚风险的工具。
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在线工具合成比较有效性研究的真实世界证据,以加强处方决策。

Online tools to synthesize real-world evidence of comparative effectiveness research to enhance formulary decision making.

机构信息

The Comparative Health Outcomes, Policy and Economics (CHOICE) Institute, University of Washington School of Pharmacy, Seattle.

National Pharmaceutical Council, Washington, DC.

出版信息

J Manag Care Spec Pharm. 2021 Jan;27(1):95-104. doi: 10.18553/jmcp.2021.27.1.095.

DOI:10.18553/jmcp.2021.27.1.095
PMID:33377442
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10391288/
Abstract

Results of randomized controlled trials (RCTs) provide valuable comparisons of 2 or more interventions to inform health care decision making; however, many more comparisons are required than available time and resources to conduct them. Moreover, RCTs have limited generalizability. Comparative effectiveness research (CER) using real-world evidence (RWE) can increase generalizability and is important for decision making, but use of nonrandomized designs makes their evaluation challenging. Several tools are available to assist. In this study, we comparatively characterize 5 tools used to evaluate RWE studies in the context of making health care adoption decision making: (1) Good Research for Comparative Effectiveness (GRACE) Checklist, (2) IMI GetReal RWE Navigator (Navigator), (3) Center for Medical Technology Policy (CMTP) RWE Decoder, (4) CER Collaborative tool, and (5) Real World Evidence Assessments and Needs Guidance (REAdi) tool. We describe each and then compare their features along 8 domains: (1) objective/user/context, (2) development/scope, (3) platform/presentation, (4) user design, (5) study-level internal/external validity of evidence, (6) summarizing body of evidence, (7) assisting in decision making, and (8) sharing results/making improvements. Our summary suggests that the GRACE Checklist aids stakeholders in evaluation of the quality and applicability of individual CER studies. Navigator is a collection of educational resources to guide demonstration of effectiveness, a guidance tool to support development of medicines, and a directory of authoritative resources for RWE. The CMTP RWE Decoder aids in the assessment of relevance and rigor of RWE. The CER Collaborative tool aids in the assessment of credibility and relevance. The REAdi tool aids in refinement of the research question, study retrieval, quality assessment, grading the body of evidence, and prompts with questions to facilitate coverage decisions. All tools specify a framework, were designed with stakeholder input, assess internal validity, are available online, and are easy to use. They vary in their complexity and comprehensiveness. The RWE Decoder, CER Collaborative tool, and REAdi tool synthesize evidence and were specifically designed to aid formulary decision making. This study adds clarity on what the tools provide so that the user can determine which best fits a given purpose. This work was supported by the Health Tech Fund, which was provided to the University of Washington School of Pharmacy by its Corporate Advisory Board. This consortium of pharmaceutical and biotech companies supports the research program of the University of Washington School of Pharmacy across the competitive space. The sponsors seeded the idea for the project and contributed to study design and improvement. The authors had full control of all content development, manuscript drafting, and submission for publication. The REAdi tool was developed by the authors. Chen, Bansal, Barthold, Carlson, Veenstra, Basu, Devine, Yun, Ta, and Beal were supported by a training grant from the University of Washington-Allergan Fellowship, unrelated to this work. Basu reports personal fees from Salutis Consulting, unrelated to this work. Graff is an employee of the National Pharmaceutical Council, which was a partner in the development of the CER Collaborative and funding partner for the CMTP RWE Decoder and the GRACE Checklist. A previous version of this work was presented as an invited workshop at AMCP Nexus 2018; October 22-25, 2018; Orlando, FL.

摘要

随机对照试验(RCT)的结果提供了 2 种或多种干预措施的有价值比较,以告知医疗保健决策;然而,需要进行的比较比进行这些比较的时间和资源多得多。此外,RCT 的普遍性有限。使用真实世界证据(RWE)的临床疗效比较研究(CER)可以提高普遍性,对决策很重要,但使用非随机设计会使其评估具有挑战性。有几种工具可用于协助评估。在这项研究中,我们比较了 5 种用于评估在制定医疗保健采用决策时使用真实世界证据研究的工具:(1)GRACE 清单,(2)IMI GetReal RWE 导航器(导航器),(3)医疗技术政策中心(CMTP)RWE 解码器,(4)CER 协作工具,以及(5)真实世界证据评估和需求指南(REAdi)工具。我们描述了每一个工具,然后比较了它们在 8 个方面的特点:(1)目标/用户/上下文,(2)开发/范围,(3)平台/演示,(4)用户设计,(5)证据的研究水平内部/外部有效性,(6)总结证据体,(7)协助决策,(8)结果共享/改进。我们的总结表明,GRACE 清单有助于利益相关者评估单个 CER 研究的质量和适用性。导航器是一系列教育资源,用于指导有效性的证明,是支持药物开发的指导工具,也是 RWE 的权威资源目录。CMTP RWE 解码器有助于评估 RWE 的相关性和严谨性。CER 协作工具有助于评估可信度和相关性。REAdi 工具有助于完善研究问题、检索研究、评估质量、对证据体进行分级,并通过提问提示来促进覆盖决策。所有工具都指定了一个框架,是在利益相关者的投入下设计的,评估内部有效性,可在线使用,并且易于使用。它们在复杂性和全面性方面有所不同。RWE 解码器、CER 协作工具和 REAdi 工具综合证据,专门用于帮助制定处方决策。这项研究更清楚地说明了这些工具提供了什么,以便用户可以确定哪个工具最适合给定的目的。这项工作得到了健康技术基金的支持,该基金由其企业顾问委员会提供给华盛顿大学药学院。该制药和生物技术公司联盟支持华盛顿大学药学院在竞争领域的整个研究计划。赞助商提出了这个项目的想法,并为研究设计和改进做出了贡献。作者对所有内容的开发、手稿的起草和提交发表拥有完全的控制权。REAdi 工具由作者开发。Chen、Bansal、Barthold、Carlson、Veenstra、Basu、Devine、Yun、Ta 和 Beal 得到了华盛顿大学-艾尔建奖学金的培训资助,与这项工作无关。Basu 报告了来自 Salutis Consulting 的个人酬金,与这项工作无关。Graff 是国家药品理事会的员工,该理事会是 CER 协作工具和资助伙伴的开发合作伙伴,也是 CMTP RWE 解码器和 GRACE 清单的资助伙伴。这项工作的一个早期版本作为一个特邀研讨会在 AMCP Nexus 2018 上展示;2018 年 10 月 22 日至 25 日;佛罗里达州奥兰多。