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National Database for Autism Research (NDAR): Big Data Opportunities for Health Services Research and Health Technology Assessment

机译:国家自闭症研究数据库(NDAR):健康服务研究和健康技术评估的大数据机会

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摘要

The National Database for Autism Research (NDAR) is a US National Institutes of Health (NIH)-funded research data repository created by integrating heterogeneous datasets through data sharing agreements between autism researchers and the NIH. To date, NDAR is considered the largest neuroscience and genomic data repository for autism research. In addition to biomedical data, NDAR contains a large collection of clinical and behavioral assessments and health outcomes from novel interventions. Importantly, NDAR has a global unique patient identifier that can be linked to aggregated individual-level data for hypothesis generation and testing, and for replicating research findings. As such, NDAR promotes collaboration and maximizes public investment in the original data collection. As screening and diagnostic technologies as well as interventions for children with autism are expensive, health services research (HSR) and health technology assessment (HTA) are needed to generate more evidence to facilitate implementation when warranted. This article describes NDAR and explains its value to health services researchers and decision scientists interested in autism and other mental health conditions. We provide a description of the scope and structure of NDAR and illustrate how data are likely to grow over time and become available for HSR and HTA.
机译:国家自闭症研究数据库(NDAR)是美国国立卫生研究院(NIH)资助的研究数据库,通过自闭症研究者与NIH之间的数据共享协议整合异构数据集而创建。迄今为止,NDAR被认为是自闭症研究中最大的神经科学和基因组数据库。除生物医学数据外,NDAR还包含大量临床和行为评估以及新干预措施对健康的影响。重要的是,NDAR具有全局唯一的患者标识符,可以将其链接到汇总的个人级别数据以进行假设生成和检验,以及复制研究结果。因此,NDAR促进了协作并最大程度地增加了原始数据收集的公共投资。由于筛查和诊断技术以及针对自闭症儿童的干预措施的价格昂贵,因此需要健康服务研究(HSR)和健康技术评估(HTA)来产生更多证据,以在有需要时促进实施。本文介绍了NDAR,并说明了其对自闭症和其他精神健康状况感兴趣的卫生服务研究人员和决策科学家的价值。我们提供了NDAR的范围和结构的说明,并说明了数据可能会随着时间增长并变为可用于HSR和HTA。

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