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首页> 外文期刊>JMIR Research Protocols >Multisite Semiautomated Clinical Data Repository for Duplication 15q Syndrome: Study Protocol and Early Uses
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Multisite Semiautomated Clinical Data Repository for Duplication 15q Syndrome: Study Protocol and Early Uses

机译:多站点半自动化重复15q综合征临床数据存储库:研究方案和早期使用

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Background Chromosome 15q11.2-q13.1 duplication syndrome (Dup15q syndrome) is a rare disorder caused by duplications of chromosome 15q11.2-q13.1, resulting in a wide range of developmental disabilities in affected individuals. The Dup15q Alliance is an organization that provides family support and promotes research to improve the quality of life of patients living with Dup15q syndrome. Because of the low prevalence of this condition, the establishment of a single research repository would have been difficult and more time consuming without collaboration across multiple institutions. Objective The goal of this project is to establish a national deidentified database with clinical and survey information on individuals diagnosed with Dup15q syndrome. Methods The development of a multiclinic site repository for clinical and survey data on individuals with Dup15q syndrome was initiated and supported by the Dup15q Alliance. Using collaborative workflows, communication protocols, and stakeholder engagement tools, a comprehensive database of patient-centered information was built. Results We successfully established a self-report populating, centralized repository for Dup15q syndrome research. This repository also resulted in the development of standardized instruments that can be used for other studies relating to developmental disorders. By standardizing the data collection instruments, it allows us integrate our data with other national databases, such as the National Database for Autism Research. A substantial portion of the data collected from the questionnaires was facilitated through direct engagement of participants and their families. This allowed for a more complete set of information to be collected with a minimal turnaround time. Conclusions We developed a repository that can efficiently be mined for shared clinical phenotypes observed at multiple clinic sites and used as a springboard for future clinical and basic research studies.
机译:背景染色体15q11.2-q13.1复制综合征(Dup15q syndrome)是由15q11.2-q13.1染色体重复引起的罕见疾病,在受影响的个体中导致广泛的发育障碍。 Dup15q联盟是一个提供家庭支持并促进研究以改善患有Dup15q综合征的患者的生活质量的组织。由于这种情况的患病率低,如果没有多个机构之间的协作,建立一个单一的研究资料库将是困难且耗时的。目的该项目的目的是建立一个全国性的身份不明数据库,其中包含有关诊断为Dup15q综合征的个体的临床和调查信息。方法Dup15q联盟发起并支持建立一个多诊所站点资料库,用于Dup15q综合征患者的临床和调查数据。使用协作工作流,通信协议和利益相关方参与工具,建立了以患者为中心的全面信息数据库。结果我们成功地建立了一个自报告填充的集中式资料库,用于Dup15q综合征研究。该知识库还促成了标准工具的开发,该标准工具可用于与发育障碍有关的其他研究。通过标准化数据收集工具,它使我们能够将数据与其他国家数据库(例如国家自闭症研究数据库)集成。参与者及其家人的直接参与促进了从问卷中收集的大部分数据。这样可以在最短的周转时间内收集到更完整的信息。结论我们开发了一个可以有效挖掘在多个诊所站点观察到的共享临床表型的存储库,并可以用作将来临床和基础研究的跳板。

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