Reuse and integration of healthcare information for subjects in a clinical trial for treatment of recurrent respiratory papillomatosis

Proceedings of the 2014 IEEE 15th International Conference on Information Reuse and Integration (IEEE IRI 2014) Pub Date : 2014-08-01 DOI:10.1109/IRI.2014.7051984

Anatoly D. Goldstein

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Abstract

This paper describes healthcare information reuse and integration in the clinical trial of a drug (Avastin) involving 20 research subjects diagnosed with recurrent respiratory papillomatosis (RRP) of the vocal cords and treated at Massachusetts General Hospital (MGH) Voice Center. The client/server application designed and developed by the author assisted in clinical trial data entry, storage in a relational database, retrieval, and reporting. The developed clinical trial software included data auditing to satisfy FDA requirements. Auxiliary import/export jobs were employed, which allowed to reuse standard MGH outpatient and surgical schedules and increased the efficiency of the clinical trial data management by avoiding data entry duplication. This clinical data processing design allowed the author to preserve integrity of the healthcare data used in the clinical trial. The clinical data integration allowed doctors to track the overall dynamics of the treatment process covering pre-trial, in-trial and post-trial examinations of the research subjects.

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在治疗复发性呼吸道乳头状瘤病的临床试验中，医疗保健信息的重用和集成

本文描述了一种药物(阿瓦斯汀)的临床试验中的医疗信息重用和集成，该试验涉及20名在马萨诸塞州总医院(MGH)语音中心治疗的被诊断为声带复发性呼吸道乳头状瘤病(RRP)的研究对象。作者设计和开发的客户端/服务器应用程序协助临床试验数据输入、存储在关系数据库中、检索和报告。开发的临床试验软件包括数据审计，以满足FDA的要求。采用辅助导入/导出工作，允许重复使用MGH标准门诊和手术时间表，并通过避免数据输入重复提高临床试验数据管理的效率。这种临床数据处理设计使作者能够保持临床试验中使用的医疗保健数据的完整性。临床数据整合使医生能够跟踪治疗过程的整体动态，包括试验前、试验中和试验后对研究对象的检查。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Proceedings of the 2014 IEEE 15th International Conference on Information Reuse and Integration (IEEE IRI 2014)

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