Buchanan-Chell M, Taylor G
University of Alberta Hospitals, Edmonton, Canada.
Am J Infect Control. 1992 Dec;20(6):310-4. doi: 10.1016/s0196-6553(05)80235-4.
Generic medical quality improvement concurrent chart review for adverse patient occurrences was introduced into our hospital. To determine whether this program could be used to augment the surveillance activities of the infection control program, an evaluation of this review was carried out and it was compared with existing surveillance methods.
Analysts were provided with Centers for Disease Control definitions of site infections and were trained in identification. During a 6-month period (period 1) infections in this manner documented were reviewed by infection control program to confirm nosocomial infection as a measure of specificity. Data were also compared with infection control surveillance data when the two programs overlapped (nosocomial bloodstream infections and surgical wound infections) as a check on the sensitivity of the data generated in the medical quality improvement process. A second 6-month review of data (period 2), starting 3 months after completion of period 1, was carried out; this review was limited to areas of overlap and designed to determine whether changes in data occurred with experience.
In period 1, 72% (109/152) of infections detected by chart review were confirmed by infection control methods, and 51% (26/51) of infections detected by the infection control program were also detected by chart review. During period 2 the values were 73% (52/71) for confirmed infections and 61% (43/70) for detected infections. There was no statistical difference between periods 1 and 2. In the two periods 25 bacteremic infections went undetected by chart surveyors.
We conclude that this chart surveillance has only moderate sensitivity and specificity compared with our infection control surveillance methods. Improvements were not demonstrated with experience.
我院引入了针对不良患者事件的通用医疗质量改进同步病历审查。为确定该计划是否可用于加强感染控制计划的监测活动,对此次审查进行了评估,并将其与现有的监测方法进行了比较。
向分析人员提供了疾病控制中心关于部位感染的定义,并对其进行识别培训。在为期6个月的时间段(第1阶段)内,感染控制计划对以这种方式记录的感染进行审查,以确认医院感染情况,作为特异性的一种衡量标准。当两个计划重叠时(医院血流感染和手术伤口感染),还将数据与感染控制监测数据进行比较,以检查医疗质量改进过程中产生的数据的敏感性。在第1阶段完成3个月后,开始了为期6个月的数据第二次审查(第2阶段);此次审查仅限于重叠领域,旨在确定数据是否随经验发生变化。
在第1阶段,通过病历审查检测到的感染中有72%(109/152)经感染控制方法确认,通过感染控制计划检测到的感染中有51%(26/51)也通过病历审查检测到。在第2阶段,确认感染的值为73%(52/71),检测到的感染的值为61%(43/70)。第1阶段和第2阶段之间没有统计学差异。在这两个阶段,有25例菌血症感染未被病历审查人员检测到。
我们得出结论,与我们的感染控制监测方法相比,这种病历监测的敏感性和特异性仅为中等。经验并未显示出改进效果。