调整商业上可用的软件程序以改进ADR报告。

Formulary Pub Date : 1995-11-01
A J Ries, M A Kraynak
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引用次数: 0

摘要

为了便于长期存储、检索和分析药物不良反应(ADR)数据,位于圣安东尼奥的德克萨斯大学健康科学中心的药物信息服务部门选择了一种能够编译关系数据库集的计算机软件程序。我们创建了五个子集来形成ADR数据库——患者人口统计、药物、美国医院处方服务分类、不良反应和病例报告。这个计算机化的系统允许快速的信息检索以及每月ADR报告的生成。有了这些信息,就可以确定adr的趋势,并有针对性地开展干预计划,以改善患者护理,并遵守JCAHO的要求。
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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Adapting a commercially available software program to improve ADR reporting.

To facilitate the long-term storage, retrieval, and analysis of adverse drug reaction (ADR) data, the drug information service at the University of Texas Health Science Center at San Antonio selected a computer software program with the capability to compile sets of relational databases. Five subsets were created to form the ADR database--patient demographics, medications, American Hospital Formulary Service classifications, adverse reactions, and case reports. This computerized system allows for quick information retrieval as well as the generation of monthly ADR reports. With such information, trends in ADRs can be identified and targeted for intervention programs to improve patient care and to comply with JCAHO requirements.

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来源期刊
Formulary
Formulary 医学-药学
自引率
0.00%
发文量
14
审稿时长
>12 weeks
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