Andrea McCracken, Julien Heidt, Elizabeth Eldridge, Charlie Hurmiz, Nicole Duran, Adam Reich, Efe Eworuke
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While robust feasibility is required to justify the relevance of a data source for a specific research question, the reliability of the data, including the chain of custody and data journey prior to reaching the end user, is of equal importance for drawing valid, meaningful conclusions.</p><p><strong>Aims: </strong>Recently, Castellanos et al. constructed a definition of RWD quality by synthesizing definitions across published guidelines to characterize quality attributes of Flatiron Health RWD. In this paper, the transparent reporting of how data quality attributes (as defined by Castellanos et al.) are met in a single RWD source is replicated for the Guardian Research Network (GRN), a database of aggregated electronic health records (EHRs) collected from a geographically representative consortium of regional community health systems with experienced cancer research programs.</p><p><strong>Materials & methods: </strong>We first describe GRN, including the data elements collected, timeliness of data availability, representativeness, and data access considerations. 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Structured, transparent reporting can support more informed feasibility assessments and facilitate regulator confidence in RWE generation.</p><p><strong>Conclusion: </strong>Continued development of structured approaches to identifying data fit for regulatory use underscores the need for comprehensive information about putative data sources during feasibility to inform decision making, study design, and elicit transparent conversations with regulators.</p>","PeriodicalId":19782,"journal":{"name":"Pharmacoepidemiology and Drug Safety","volume":"34 9","pages":"e70202"},"PeriodicalIF":2.4000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12417101/pdf/","citationCount":"0","resultStr":"{\"title\":\"The Guardian Research Network: A Real-World Data Source for Pharmacoepidemiologic Research and Regulatory Applications.\",\"authors\":\"Andrea McCracken, Julien Heidt, Elizabeth Eldridge, Charlie Hurmiz, Nicole Duran, Adam Reich, Efe Eworuke\",\"doi\":\"10.1002/pds.70202\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>The quality of real-world data (RWD) directly impacts the value of real-world evidence (RWE) generated for regulatory decision-making. 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引用次数: 0
摘要
背景:真实世界数据(RWD)的质量直接影响为监管决策生成的真实世界证据(RWE)的价值。数据所有者和调查人员在为监管目的提交辅助数据时,必须准备好向监管机构提供数据质量评估文件。虽然需要强有力的可行性来证明数据源与特定研究问题的相关性,但数据的可靠性,包括到达最终用户之前的监管链和数据旅程,对于得出有效、有意义的结论同样重要。目的:最近,Castellanos等人通过综合已发表指南中的定义,构建了RWD质量的定义,以表征Flatiron Health RWD的质量属性。在本文中,关于数据质量属性(由Castellanos等人定义)如何在单一RWD来源中得到满足的透明报告被卫报研究网络(GRN)复制,该网络是一个汇总电子健康记录(EHRs)的数据库,从具有经验丰富的癌症研究项目的区域社区卫生系统的地理代表性联盟中收集。材料与方法:我们首先描述GRN,包括收集的数据元素、数据可用性的及时性、代表性和数据访问考虑因素。然后,我们描述了如何在GRN中确保和评估数据可靠性(准确性、可追溯性、及时性、完整性)和相关性(可用性、充分性、代表性),包括相关数据质量检查的说明性示例。结果:GRN数据质量过程的描述展示了确保可靠性和相关性的结构化方法,与已发布的指南保持一致。说明性示例强调了特定质量检查的应用及其对GRN数据的结果。讨论:这些发现说明了记录和交流用于监管用途的RWD来源的数据质量属性的重要性。结构化、透明的报告可以支持更明智的可行性评估,并促进监管机构对RWE发电的信心。结论:识别适合监管使用的数据的结构化方法的持续发展强调了在可行性过程中需要关于假定数据源的全面信息,以便为决策、研究设计提供信息,并引发与监管机构的透明对话。
The Guardian Research Network: A Real-World Data Source for Pharmacoepidemiologic Research and Regulatory Applications.
Background: The quality of real-world data (RWD) directly impacts the value of real-world evidence (RWE) generated for regulatory decision-making. Data owners and investigators must be prepared to provide documentation on data quality assessments to regulators when submitting secondary data for regulatory purposes. While robust feasibility is required to justify the relevance of a data source for a specific research question, the reliability of the data, including the chain of custody and data journey prior to reaching the end user, is of equal importance for drawing valid, meaningful conclusions.
Aims: Recently, Castellanos et al. constructed a definition of RWD quality by synthesizing definitions across published guidelines to characterize quality attributes of Flatiron Health RWD. In this paper, the transparent reporting of how data quality attributes (as defined by Castellanos et al.) are met in a single RWD source is replicated for the Guardian Research Network (GRN), a database of aggregated electronic health records (EHRs) collected from a geographically representative consortium of regional community health systems with experienced cancer research programs.
Materials & methods: We first describe GRN, including the data elements collected, timeliness of data availability, representativeness, and data access considerations. We then provide descriptions of how data reliability (accuracy, traceability, timeliness, completeness) and relevance (availability, sufficiency, representativeness) are ensured and assessed in GRN, including illustrative examples of relevant data quality checks.
Results: Descriptions of GRN's data quality processes demonstrate structured approaches to ensuring both reliability and relevance, aligned with published guidelines. Illustrative examples highlight the application of specific quality checks and their outcomes for GRN data.
Discussion: These findings illustrate the importance of documenting and communicating data quality attributes for RWD sources intended for regulatory use. Structured, transparent reporting can support more informed feasibility assessments and facilitate regulator confidence in RWE generation.
Conclusion: Continued development of structured approaches to identifying data fit for regulatory use underscores the need for comprehensive information about putative data sources during feasibility to inform decision making, study design, and elicit transparent conversations with regulators.
期刊介绍:
The aim of Pharmacoepidemiology and Drug Safety is to provide an international forum for the communication and evaluation of data, methods and opinion in the discipline of pharmacoepidemiology. The Journal publishes peer-reviewed reports of original research, invited reviews and a variety of guest editorials and commentaries embracing scientific, medical, statistical, legal and economic aspects of pharmacoepidemiology and post-marketing surveillance of drug safety. Appropriate material in these categories may also be considered for publication as a Brief Report.
Particular areas of interest include:
design, analysis, results, and interpretation of studies looking at the benefit or safety of specific pharmaceuticals, biologics, or medical devices, including studies in pharmacovigilance, postmarketing surveillance, pharmacoeconomics, patient safety, molecular pharmacoepidemiology, or any other study within the broad field of pharmacoepidemiology;
comparative effectiveness research relating to pharmaceuticals, biologics, and medical devices. Comparative effectiveness research is the generation and synthesis of evidence that compares the benefits and harms of alternative methods to prevent, diagnose, treat, and monitor a clinical condition, as these methods are truly used in the real world;
methodologic contributions of relevance to pharmacoepidemiology, whether original contributions, reviews of existing methods, or tutorials for how to apply the methods of pharmacoepidemiology;
assessments of harm versus benefit in drug therapy;
patterns of drug utilization;
relationships between pharmacoepidemiology and the formulation and interpretation of regulatory guidelines;
evaluations of risk management plans and programmes relating to pharmaceuticals, biologics and medical devices.