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用于鉴定 COVID-19 重症患者肺炎致病细菌病原体的多重聚合酶链反应(PCR)面板的性能。

Performance of a multiplex polymerase chain reaction panel for identifying bacterial pathogens causing pneumonia in critically ill patients with COVID-19.

机构信息

Department of Microbiology, Saint-Louis-Lariboisière Hospital Group, Assistance Publique-Hôpitaux de Paris, Paris, France; University of Paris, INSERM 1137, IAME, Paris, France.

Department of Anesthesiology and Critical Care and Burn Unit, Saint-Louis-Lariboisière Hospital Group, Assistance Publique-Hôpitaux de Paris, Paris, France.

出版信息

Diagn Microbiol Infect Dis. 2021 Jan;99(1):115183. doi: 10.1016/j.diagmicrobio.2020.115183. Epub 2020 Aug 21.

Abstract

The FilmArray® Pneumonia Plus (FA-PP) panel can provide rapid identifications and semiquantitative results for many pathogens. We performed a prospective single-center study in 43 critically ill patients with coronavirus disease 2019 (COVID-19) in which we performed 96 FA-PP tests and cultures of blind bronchoalveolar lavage (BBAL). FA-PP detected 1 or more pathogens in 32% (31/96 of samples), whereas culture methods detected at least 1 pathogen in 35% (34/96 of samples). The most prevalent bacteria detected were Pseudomonas aeruginosa (n = 14) and Staphylococcus aureus (n = 11) on both FA-PP and culture. The FA-PP results from BBAL in critically ill patients with COVID-19 were consistent with bacterial culture findings for bacteria present in the FA-PP panel, showing sensitivity, specificity, and positive and negative predictive value of 95%, 99%, 82%, and 100%, respectively. Median turnaround time for FA-PP was 5.5 h, which was significantly shorter than for standard culture (26 h) and antimicrobial susceptibility testing results (57 h).

摘要

FilmArray® 肺炎 PLUS (FA-PP) 检测 panel 可快速鉴定和半定量检测多种病原体。我们对 43 例 2019 冠状病毒病 (COVID-19) 危重症患者进行了前瞻性单中心研究,对这些患者进行了 96 次 FA-PP 检测和盲支气管肺泡灌洗 (BBAL) 培养。FA-PP 在 32% (96 个样本中的 31 个) 的样本中检测到 1 种或多种病原体,而培养方法在 35% (96 个样本中的 34 个) 的样本中至少检测到 1 种病原体。在 FA-PP 和培养物上最常见的细菌是铜绿假单胞菌 (n = 14) 和金黄色葡萄球菌 (n = 11)。来自 COVID-19 危重症患者 BBAL 的 FA-PP 结果与 FA-PP 检测 panel 中存在的细菌的细菌培养结果一致,显示出 95%、99%、82%和 100%的敏感性、特异性、阳性预测值和阴性预测值。FA-PP 的中位周转时间为 5.5 小时,明显短于标准培养 (26 小时) 和抗菌药物敏感性试验结果 (57 小时)。

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