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更多阻力之路:国家医疗保健安全网络和临床实验室标准协会标准在制定累积抗菌药物敏感性测试报告和机构抗生素图方面的比较。

The Path of More Resistance: a Comparison of National Healthcare Safety Network and Clinical Laboratory Standards Institute Criteria in Developing Cumulative Antimicrobial Susceptibility Test Reports and Institutional Antibiograms.

机构信息

David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.

Department of Pharmacy, Ronald Reagan UCLA Medical Center, Los Angeles, California, USA.

出版信息

J Clin Microbiol. 2022 Feb 16;60(2):e0136621. doi: 10.1128/JCM.01366-21. Epub 2021 Dec 1.

Abstract

In the absence of antimicrobial susceptibility data, the institutional antibiogram is a valuable tool to guide clinicians in the empirical treatment of infections. However, there is a misunderstanding about how best to prepare cumulative antimicrobial susceptibility testing reports (CASTRs) to guide empirical therapy (e.g., routine antibiogram) versus monitoring antimicrobial resistance, with the former following guidance from the Clinical and Laboratory Standards Institute (CLSI) and the latter from the Centers for Disease Control and Prevention's National Healthcare Safety Network (NHSN). These criteria vary markedly in their exclusion or inclusion of isolates cultured repeatedly from the same patient. We compared rates of nonsusceptibility (NS) using annual data from a large teaching health care system subset to isolates eligible by either NHSN criteria or CLSI criteria. For a panel of the three most prevalent Gram-negative pathogens in combination with clinically relevant antimicrobial agents (or priority pathogen-agent combinations [PPACs]), we found that the inclusion of duplicate isolates by NHSN criteria yielded higher NS rates than when CLSI criteria (for which duplicate isolates are not included) were applied. Patients with duplicate isolates may not be representative of antimicrobial resistance within a population. For this reason, users of CASTR data should carefully consider that the criteria used to generate these reports can impact resulting NS rates and, therefore, maintain the distinction between CASTRs created for different purposes.

摘要

在缺乏抗菌药物敏感性数据的情况下,机构抗菌谱是指导临床医生进行感染经验性治疗的有价值的工具。然而,人们对于如何最好地准备累积抗菌药物敏感性测试报告(CASTR)以指导经验性治疗(例如常规抗菌谱)与监测抗菌药物耐药性存在误解,前者遵循临床和实验室标准协会(CLSI)的指南,后者遵循疾病控制和预防中心的国家医疗保健安全网络(NHSN)的指南。这些标准在排除或包括从同一患者重复培养的分离物方面存在显著差异。我们比较了使用来自大型教学医疗保健系统子集的年度数据和符合 NHSN 标准或 CLSI 标准的分离物的非敏感性(NS)率。对于一组三种最常见的革兰氏阴性病原体与临床相关的抗菌药物(或优先病原体-药物组合[PPAC]),我们发现 NHSN 标准纳入重复分离物会导致更高的 NS 率,而 CLSI 标准(不包括重复分离物)则不会。具有重复分离物的患者可能不能代表人群中的抗菌药物耐药性。因此,CASTR 数据的使用者应仔细考虑用于生成这些报告的标准可能会影响最终的 NS 率,因此应保持为不同目的创建 CASTR 的区别。

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