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评估聚合酶链反应检测直肠拭子中产碳青霉烯酶肠杆菌科的直接筛选:诊断荟萃分析。

Evaluation of polymerase chain reaction assays for direct screening of carbapenemase-producing Enterobacteriaceae from rectal swabs: a diagnostic meta-analysis.

机构信息

IAME, UMR 1137, Université Paris 13, Sorbonne Paris Cité, France; Service de Microbiologie Clinique et Unité de Contrôle et de Prévention du risque Infectieux, Groupe Hospitalier Paris Seine Saint-Denis, AP-HP, Bobigny, France; Laboratoire des agents pathogènes, Faculty of Pharmacy, Saint-Joseph University, Beirut, Lebanon.

Service d'épidémiologie et d'hygiène hospitalière, CHU hôpital d'enfants, Dijon, France.

出版信息

J Hosp Infect. 2020 Mar;104(3):381-389. doi: 10.1016/j.jhin.2019.11.017. Epub 2019 Nov 29.

Abstract

Recently, molecular assays have been demonstrated to be reliable for rapid detection of carbapenemase-producing Enterobacteriaceae (CPE) directly from positive blood cultures, reducing significantly the time for identification. Few studies have tested their performance on rectal swabs and no comprehensive conclusions have been reached regarding their utility for infection control management. Our aim was to review and assess the overall diagnostic test accuracy of polymerase chain reaction for the detection of CPE in rectal swabs. The electronic database PubMed was searched, up to October 1, 2019, without language restriction or publication date restrictions. First, the concepts of the research questions were defined: 'carbapenemase-producing Enterobacteriaceae', 'molecular testing', 'test detection', and 'rectal screening'. Two reviewers independently screened studies, extracted data, and assessed quality using the QUADAS-2 instrument. Statistical analyses were carried out in Stata software using the bivariate model. In all, 143 articles were screened and 16 studies were included. Five (31%) of the studies were conducted in the context of a CPE outbreak; one study (6%) included patients pre-identified with CPE in clinical samples (blood or tracheal secretions), whereas the rest (63%) collected rectal swabs from patients considered at high risk of colonization. The molecular assays evaluated had a relatively good sensitivity of 0.95 (95% confidence interval (CI): 0.902-0.989), and an excellent specificity of 0.994 (95% CI: 0.965-1). Molecular techniques seem to be a useful, accurate diagnostic tool in screening for carriage of CPE in contact patients around a fortuitous discovery of a non-isolated hospitalized carrier patient.

摘要

最近,分子检测法已被证明可直接从阳性血培养物中快速检测产碳青霉烯酶肠杆菌科(CPE),大大缩短了鉴定时间。少数研究已经在直肠拭子上测试了它们的性能,但对于它们在感染控制管理中的应用还没有得出全面的结论。我们的目的是回顾和评估聚合酶链反应检测直肠拭子中产碳青霉烯酶肠杆菌科的总体诊断测试准确性。电子数据库 PubMed 被搜索,截至 2019 年 10 月 1 日,无语言限制或出版日期限制。首先,定义了研究问题的概念:“产碳青霉烯酶肠杆菌科”、“分子检测”、“检测测试”和“直肠筛查”。两名审查员独立筛选研究,使用 QUADAS-2 仪器提取数据并评估质量。使用 Stata 软件中的双变量模型进行统计分析。总共筛选了 143 篇文章,纳入了 16 项研究。其中 5 项(31%)研究是在 CPE 爆发的情况下进行的;一项研究(6%)包括在临床样本(血液或气管分泌物)中预先确定的 CPE 患者,而其余研究(63%)从被认为有定植高风险的患者中收集直肠拭子。评估的分子检测具有相对较高的敏感性 0.95(95%置信区间(CI):0.902-0.989)和极好的特异性 0.994(95%CI:0.965-1)。分子技术似乎是一种有用的、准确的诊断工具,可用于筛选偶然发现的非隔离住院携带者周围接触患者的 CPE 定植情况。

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