基于改进HICPAC指南评估万古霉素使用的临床决策过程模型医院感染控制实务谘询委员会。

C Salemi, L Becker, R Morrissey, J Warmington
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引用次数: 0

摘要

目的:本研究的目的是利用修改后的医院感染控制实践咨询委员会(HICPAC)指南,评估万古霉素使用适宜性的临床决策过程模型。设计:采用回顾性图表回顾法对所有非透析万古霉素使用情况进行回顾。对HICPAC指南进行了修改,以区分记录感染和疑似感染以及万古霉素最初和治疗3天后使用的适宜性。收集万古霉素使用顺序和万古霉素使用天数数据。单位:446张床位的保健机构教学医院。结果:采用修订后的HICPAC指南对1993 - 1995年间758例万古霉素的使用进行了评价。71%的病例初始使用是适当的,26%用于记录感染,74%用于疑似感染。在最初适当使用万古霉素的536个订单中,176个疗程的万古霉素治疗在3天内适当停止。3天后的持续使用评估显示,45%的病例为适当使用,25%的病例为不适当使用,30%的病例为经验性持续使用。在3天后,70%的病例有足够的临床或实验室数据可以停止使用万古霉素,或从疑似感染或记录感染或适应症重新分类。仅在3天后进行万古霉素使用评价,不能发现537个最初的万古霉素不适宜使用日,占总不适宜使用日的44%。结论:根据HICPAC指南对万古霉素使用的综合评估应包括修改,以包括初始和3天的重新评估,因为大多数初始使用是用于疑似感染,而不是记录感染。HICPAC指南没有解决区分疑似感染和记录感染指征或正在进行的经验性使用的问题。临床决策过程模型是用于使用评估的文档和数据收集的框架,并解决HICPAC万古霉素指南未涵盖的问题。该模型可为其他医疗机构评估万古霉素或其他抗生素提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A clinical decision process model for evaluating vancomycin use with modified HICPAC guidelines. Hospital Infection Control Practice Advisory Committee.

Objective: The objective of this study was to evaluate a clinical decision process model for the appropriateness of vancomycin use, using modified Hospital Infection Control Practice Advisory Committee (HICPAC) guidelines.

Design: All nondialysis vancomycin use was reviewed using the retrospective chart review method. The HICPAC guidelines were modified to distinguish between documented and suspected infections and appropriateness of vancomycin use initially and after 3 days of therapy. Data were collected on both vancomycin-use orders and vancomycin-use days.

Setting: 446-bed health maintenance organization teaching hospital.

Results: 758 uses of vancomycin from 1993 through 1995 were evaluated using the modified HICPAC guidelines. Initial use was appropriate in 71% of the cases, with 26% used for documented infections and 74% for suspected infections. Of the 536 orders of initial appropriate use, 176 courses of treatment with vancomycin were discontinued appropriately within 3 days. Ongoing use evaluation after 3 days revealed appropriate use in 45%, inappropriate ongoing use in 25%, and empirical ongoing use in 30% of the cases. There were adequate clinical or laboratory data available in 70% of cases after 3 days to discontinue vancomycin or to reclassify from suspected to documented infections or indications. Vancomycin-use evaluation solely after 3 days would not have disclosed 537 initial inappropriate vancomycin-use days, which were 44% of the total inappropriate use days.

Conclusions: Comprehensive evaluation of vancomycin use with HICPAC guidelines should include a modification to encompass initial and 3-day reevaluation, because most initial use is for suspected, and not documented, infections. HICPAC guidelines do not address the issues of differentiating suspected from documented infection indications or ongoing empirical use. The clinical decision process model is a framework for documentation and data collection for use evaluation and addresses issues not covered in HICPAC vancomycin guidelines. This model could be used by other medical centers for evaluation of vancomycin or other antibiotics.

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