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The REporting of Studies Conducted Using Observational Routinely-Collected Health Data (RECORD) Statement: Methods for Arriving at Consensus and Developing Reporting Guidelines.

机译:使用常规收集的观察性健康数据(RECORD)声明进行的研究报告:达成共识和制定报告指南的方法。

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摘要

OBJECTIVE: Routinely collected health data, collected for administrative and clinical purposes, without specific a priori research questions, are increasingly used for observational, comparative effectiveness, health services research, and clinical trials. The rapid evolution and availability of routinely collected data for research has brought to light specific issues not addressed by existing reporting guidelines. The aim of the present project was to determine the priorities of stakeholders in order to guide the development of the REporting of studies Conducted using Observational Routinely-collected health Data (RECORD) statement.METHODS: Two modified electronic Delphi surveys were sent to stakeholders. The first determined themes deemed important to include in the RECORD statement, and was analyzed using qualitative methods. The second determined quantitative prioritization of the themes based on categorization of manuscript headings. The surveys were followed by a meeting of RECORD working committee, and re-engagement with stakeholders via an online commentary period.RESULTS: The qualitative survey (76 responses of 123 surveys sent) generated 10 overarching themes and 13 themes derived from existing STROBE categories. Highest-rated overall items for inclusion were: Disease/exposure identification algorithms; Characteristics of the population included in databases; and Characteristics of the data. In the quantitative survey (71 responses of 135 sent), the importance assigned to each of the compiled themes varied depending on the manuscript section to which they were assigned. Following the working committee meeting, online ranking by stakeholders provided feedback and resulted in revision of the final checklist.CONCLUSIONS: The RECORD statement incorporated the suggestions provided by a large, diverse group of stakeholders to create a reporting checklist specific to observational research using routinely collected health data. Our findings point to unique aspects of studies conducted with routinely collected health data and the perceived need for better reporting of methodological issues.
机译:目的:出于行政和临床目的而定期收集的健康数据,没有先验研究的特定问题,越来越多地用于观察,比较有效性,健康服务研究和临床试验。日常收集的研究数据的迅速发展和可用性已经发现了现有报告指南未解决的特定问题。本项目的目的是确定利益相关者的优先顺序,以指导使用常规收集的观察性健康数据(RECORD)陈述进行的研究报告的开发。方法:向利益相关者发送了两次修改的电子德尔菲调查。首先确定的重要主题被认为包含在RECORD语句中,并使用定性方法进行了分析。第二个基于手稿标题的分类确定主题的定量优先级。调查之后,召开了RECORD工作委员会会议,并通过在线评论期与利益相关方重新接触。结果:定性调查(发送了123个调查中的76个答复)产生了10个总体主题,而13个主题来自现有的STROBE类别。收录率最高的总体项目包括:疾病/暴露识别算法;数据库中包括的人口特征;和数据特征。在定量调查中(发送了135个答复,共71个),分配给每个已编译主题的重要性根据分配主题的稿件部分而有所不同。在工作委员会会议之后,利益相关者的在线排名提供了反馈,并导致了最终清单的修订。结论:RECORD声明结合了一大批不同利益相关者提供的建议,以使用常规收集的观察研究创建报告清单。健康数据。我们的发现指出了使用常规收集的健康数据进行的研究的独特方面,以及人们认为需要更好地报告方法学问题。

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