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Development, analysis, refinement, and utility of an interdisciplinary amyotrophic lateral sclerosis database

机译:跨学科的肌萎缩性侧索硬化数据库的开发,分析,完善和实用性

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摘要

The current status of evaluation and management provided by individual health-care professionals (HCP) at amyotrophic lateral sclerosis (ALS) centers and clinics needs to be analyzed. This paper describes one ALS center's experiences with the development, analysis, refinement, and utility of an interdisciplinary, HCP-driven ALS database. The purpose and conceptual framework of the database, the general data that needed to be collected, and the types of reports that needed to be generated were determined, and, in collaboration with a computer programmer, data entry and database management systems were developed. Data were collected on 234 patients between September 1996 and August 1998, and were analyzed by a biostatistician. Based on review of the biostatistician's report and discussion of problems encountered with the systems the database was then refined. Benefits of the database system included: systematization of data collection and reporting reduction of redundant data collection by individuals, decreased variability of evaluation methods and management decisions from patient to patient, and increased availability of a variety of uniform patient information to assist team members in making care decisions. Ongoing refinement will ensure that this HCP-driven ALS database continues to be informative, practical and effective for decision-making and enhancing delivery of care.
机译:需要分析由肌萎缩性侧索硬化症(ALS)中心和诊所的个人医疗保健专业人员(HCP)提供的评估和管理的现状。本文介绍了一个ALS中心在跨学科,由HCP驱动的ALS数据库的开发,分析,改进和实用性方面的经验。确定了数据库的目的和概念框架,需要收集的常规数据以及需要生成的报告的类型,并与计算机程序员合作开发了数据输入和数据库管理系统。在1996年9月至1998年8月之间收集了234例患者的数据,并由生物统计学家进行了分析。基于对生物统计学家报告的审阅以及对系统遇到的问题的讨论,然后对数据库进行了完善。数据库系统的好处包括:数据收集的系统化和报告的减少,减少了个人的冗余数据收集;减少了评估方法和管理决定因患者而异的可变性;以及增加了各种统一的患者信息以帮助团队成员进行决策护理决定。不断完善将确保这个由HCP驱动的ALS数据库继续为决策和增强护理提供信息,实用和有效。

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