英国医院的抗菌药物管理标记和医源性肺炎阈值标准:MicroGuideTm 应用程序分析。

IF 3.7 Q2 INFECTIOUS DISEASES JAC-Antimicrobial Resistance Pub Date : 2024-04-16 eCollection Date: 2024-04-01 DOI:10.1093/jacamr/dlae058
Luke S P Moore, Ioannis Baltas, James Amos, Mineli Cooray, Stephen Hughes, Rachel Freeman, Tom Ashfield
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引用次数: 0

摘要

背景:为解决抗菌药耐药性问题,必须实施并遵守抗菌药物管理 (AMS) 原则。临床决策辅助工具(如 MicroGuideTM 应用程序)是这些工作的重要组成部分。我们试图评估 MicroGuide 应用程序中 AMS 核心信息的一致性以及医源性肺炎 (HAP) 分类阈值的多样性:提取并分析了微指南应用程序中与急性髓系白血病和 HAP 相关的指南内容。根据 HAP 命名分类对指南进行特征描述;分析社区获得性肺炎 (CAP) 分类,作为参照组:共有 115 个托管机构(119 家医院)被纳入其中。几乎所有医院都制定了关于急性呼吸系统综合症(n = 112/119,94%)和败血症管理(n = 117/119,98%)的微指南。其他 AMS 部分包括门诊肠外抗菌疗法(47%)、抗真菌管理(70%)、重症监护(23%)和静脉注射到口服的转换疗法(83%)。只有 9% 的医院包含了所确定的 AMS 最多六个关键部分的指南。各医院对 HAP 的定义差异很大,有些医院按发病时间分类,有些医院按严重性或复杂性分类。根据严重性/复杂性进行分类的 HAP 指南所占比例最大(n = 69/119,58%)。相比之下,CAP指南中的定义是统一的:结论:所发现的 HAP 分类的高度异质性表明,英国在确定 HAP 临界值方面的做法并不一致。这使得 HAP 管理和 AMS 实践变得复杂。为了按照急性呼吸系统综合征的原则处理 HAP,应制定一项综合战略,优先考虑统一的临床定义和阈值。
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Antimicrobial stewardship markers and healthcare-associated pneumonia threshold criteria in UK hospitals: analysis of the MicroGuideTm application.

Background: To address antimicrobial resistance, antimicrobial stewardship (AMS) principles must be implemented and adhered to. Clinical decision aids such as the MicroGuideTM app are an important part of these efforts. We sought to evaluate the consistency of core AMS information and the diversity of classification thresholds for healthcare-associated pneumonia (HAP) in the MicroGuide app.

Methods: Guidelines in the MicroGuide app were extracted and analysed for content related to AMS and HAP. Guidelines were characterized according to HAP naming classification; community-acquired pneumonia (CAP) classifications were analysed to serve as a comparator group.

Results: In total, 115 trusts (119 hospitals) were included. Nearly all hospitals had developed MicroGuide sections on AMS (n = 112/119, 94%) and sepsis management (n = 117/119, 98%). Other AMS sections were outpatient parenteral antimicrobial therapy (47%), antifungal stewardship (70%), critical care (23%) and IV to oral switch therapy (83%). Only 9% of hospitals included guidance on the maximum six key AMS sections identified. HAP definitions varied widely across hospitals with some classifying by time to onset and some classifying by severity or complexity. The largest proportion of HAP guidelines based classification on severity/complexity (n = 69/119, 58%). By contrast, definitions in CAP guidelines were uniform.

Conclusions: The high heterogeneity in HAP classification identified suggests inconsistency of practice in identifying thresholds for HAP in the UK. This complicates HAP management and AMS practices. To address HAP in alignment with AMS principles, a comprehensive strategy that prioritizes uniform clinical definitions and thresholds should be developed.

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