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识别药物不良事件:基于计算机的监测器的开发以及与病历审查和激发性自愿报告的比较。

Identifying adverse drug events: development of a computer-based monitor and comparison with chart review and stimulated voluntary report.

作者信息

Jha A K, Kuperman G J, Teich J M, Leape L, Shea B, Rittenberg E, Burdick E, Seger D L, Vander Vliet M, Bates D W

机构信息

Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.

出版信息

J Am Med Inform Assoc. 1998 May-Jun;5(3):305-14. doi: 10.1136/jamia.1998.0050305.

Abstract

BACKGROUND

Adverse drug events (ADEs) are both common and costly. Most hospitals identify ADEs using spontaneous reporting, but this approach lacks sensitivity; chart review identifies more events but is expensive. Computer-based approaches to ADE identification appear promising, but they have not been directly compared with chart review and they are not widely used.

OBJECTIVES

To develop a computer-based ADE monitor, and to compare the rate and type of ADEs found with the monitor with those discovered by chart review and by stimulated voluntary report.

DESIGN

Prospective cohort study in one tertiary-care hospital.

PARTICIPANTS

All patients admitted to nine medical and surgical units in a tertiary-care hospital over an eight-month period.

MAIN OUTCOME MEASURE

Adverse drug events identified by the computer-based monitor, by chart review, and by stimulated voluntary report.

METHODS

A computer-based monitoring program identified alerts, which were situations suggesting that an ADE might be present (e.g., an order for an antidote such as naloxone). A trained reviewer then examined patients' hospital records to determine whether an ADE had occurred. The results of the computer-based monitoring strategy were compared with two other ADE detection strategies: intensive chart review and stimulated voluntary report by nurses and pharmacists. The monitor and the chart review strategies were independent, and the reviewers were blinded.

RESULTS

The computer monitoring strategy identified 2,620 alerts, of which 275 were determined to be ADEs. The chart review found 398 ADEs, whereas voluntary report detected 23. Of the 617 ADEs detected by at least one method, 76 ADEs were detected by both computer monitor and chart review. The computer monitor identified 45 percent; chart review, 65 percent; and voluntary report, 4 percent. The ADEs identified by computer monitor were more likely to be classified as "severe" than were those identified by chart review (51 versus 42 percent, p = .04). The positive predictive value of computer-generated alerts was 16 percent during the first eight weeks of the study; rule modifications increased this to 23 percent in the final eight weeks. The computer strategy required 11 person-hours per week to execute, whereas chart review required 55 person-hours per week and voluntary report strategy required 5.

CONCLUSIONS

The computer-based monitor identified fewer ADEs than did chart review but many more ADEs than did stimulated voluntary report. The overlap among the ADEs identified using different methods was small, suggesting that the incidence of ADEs may be higher than previously reported and that different detection methods capture different events. The computer-based monitoring system represents an efficient approach for measuring ADE frequency and gauging the effectiveness of ADE prevention programs.

摘要

背景

药物不良事件(ADEs)既常见又代价高昂。大多数医院通过自发报告来识别药物不良事件,但这种方法缺乏敏感性;病历审查能识别出更多事件,但成本高昂。基于计算机的药物不良事件识别方法似乎很有前景,但尚未与病历审查进行直接比较,也未得到广泛应用。

目的

开发一种基于计算机的药物不良事件监测器,并将该监测器发现的药物不良事件的发生率和类型与病历审查及激发性自愿报告所发现的进行比较。

设计

在一家三级医疗医院进行的前瞻性队列研究。

参与者

在八个月期间入住一家三级医疗医院九个内科和外科病房的所有患者。

主要观察指标

通过基于计算机的监测器、病历审查和激发性自愿报告识别出的药物不良事件。

方法

一个基于计算机的监测程序识别警报,即提示可能存在药物不良事件的情况(例如,开具纳洛酮等解毒剂的医嘱)。然后,一名经过培训的审查人员检查患者的医院记录,以确定是否发生了药物不良事件。将基于计算机的监测策略的结果与另外两种药物不良事件检测策略进行比较:深入病历审查以及护士和药剂师的激发性自愿报告。监测器和病历审查策略相互独立,审查人员对结果不知情。

结果

计算机监测策略识别出2620个警报,其中275个被确定为药物不良事件。病历审查发现了398个药物不良事件,而自愿报告检测到23个。在至少一种方法检测到的617个药物不良事件中,计算机监测器和病历审查都检测到了76个。计算机监测器识别出45%;病历审查识别出65%;自愿报告识别出4%。与病历审查识别出的药物不良事件相比,计算机监测器识别出的药物不良事件更有可能被归类为“严重”(分别为51%和42%,p = 0.04)。在研究的前八周,计算机生成警报的阳性预测值为16%;通过修改规则,在最后八周该值提高到了23%。计算机策略每周执行需要11人时,而病历审查每周需要55人时,自愿报告策略每周需要5人时。

结论

基于计算机的监测器识别出的药物不良事件比病历审查少,但比激发性自愿报告多得多。使用不同方法识别出的药物不良事件之间的重叠很小,这表明药物不良事件的发生率可能高于先前报告的水平,并且不同的检测方法捕获的是不同的事件。基于计算机的监测系统是一种测量药物不良事件频率和评估药物不良事件预防项目有效性的有效方法。

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