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Developing a pediatric pain data repository

机译:开发儿科疼痛数据库

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摘要

The management of pediatric pain typically consists of individualized treatment plans and interventions that have not been systematically evaluated. There is an emerging need to create systems that can support the translation of clinical discoveries, facilitate the assessment of current interventions, and improve the collection of patient-centered data beyond routine clinical information. We present the development of the pediatric pain data repository, a custom-built system developed at Boston Children’s Hospital by a multidisciplinary pain treatment service. The Repository employs a web platform to collect standardized patient-reported outcomes and integrates this with electronic medical record data. To date, we have collected information on 2577 patients and anticipate adding approximately 500 new patients per year. Major strengths of the Repository include collection of extensive longitudinal patient-reported outcomes, automated clinical data abstraction, and integration of the system into clinical workflows to support medical decision making.
机译:小儿疼痛的治疗通常包括尚未得到系统评估的个性化治疗计划和干预措施。迫切需要创建一种系统,以支持临床发现的翻译,促进对当前干预措施的评估并改善常规临床信息以外的以患者为中心的数据收集。我们介绍了小儿疼痛数据存储库的开发,该数据库是由波士顿儿童医院通过多学科疼痛治疗服务开发的定制系统。知识库使用网络平台来收集患者报告的标准化结果,并将其与电子病历数据集成。迄今为止,我们已经收集了2577名患者的信息,并预计每年增加约500名新患者。存储库的主要优势包括收集广泛的纵向患者报告结果,自动临床数据抽象以及将系统集成到临床工作流程中以支持医疗决策。

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