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本文引用的文献

1
A multiplex polymerase chain reaction assay for antibiotic stewardship in suspected pneumonia.一种用于疑似肺炎抗生素管理的多重聚合酶链反应检测方法。
Diagn Microbiol Infect Dis. 2020 Dec;98(4):115179. doi: 10.1016/j.diagmicrobio.2020.115179. Epub 2020 Aug 16.
2
Performance and impact of a multiplex PCR in ICU patients with ventilator-associated pneumonia or ventilated hospital-acquired pneumonia.在 ICU 中,多重 PCR 对呼吸机相关性肺炎或医院获得性肺炎患者的表现和影响。
Crit Care. 2020 Jun 19;24(1):366. doi: 10.1186/s13054-020-03067-2.
3
Randomized Trial Evaluating Clinical Impact of RAPid IDentification and Susceptibility Testing for Gram-negative Bacteremia: RAPIDS-GN.随机试验评估革兰氏阴性菌血培养快速鉴定和药敏检测的临床影响:RAPIDS-GN。
Clin Infect Dis. 2021 Jul 1;73(1):e39-e46. doi: 10.1093/cid/ciaa528.
4
Practical Comparison of the BioFire FilmArray Pneumonia Panel to Routine Diagnostic Methods and Potential Impact on Antimicrobial Stewardship in Adult Hospitalized Patients with Lower Respiratory Tract Infections.BioFire FilmArray肺炎检测板与常规诊断方法的实际比较及其对成年住院下呼吸道感染患者抗菌药物管理的潜在影响
J Clin Microbiol. 2020 Jun 24;58(7). doi: 10.1128/JCM.00135-20.
5
Multicenter Evaluation of the BioFire FilmArray Pneumonia/Pneumonia Plus Panel for Detection and Quantification of Agents of Lower Respiratory Tract Infection.BioFire FilmArray肺炎/肺炎加检测板用于下呼吸道感染病原体检测和定量的多中心评估
J Clin Microbiol. 2020 Jun 24;58(7). doi: 10.1128/JCM.00128-20.
6
Evaluation of the BioFire FilmArray Pneumonia Panel for Detection of Viral and Bacterial Pathogens in Lower Respiratory Tract Specimens in the Setting of a Tertiary Care Academic Medical Center.在三级医疗学术医学中心环境下,评估BioFire FilmArray肺炎检测板对下呼吸道标本中病毒和细菌病原体的检测能力。
J Clin Microbiol. 2020 Jun 24;58(7). doi: 10.1128/JCM.00343-20.
7
Evaluation of the Biofire Filmarray Pneumonia panel plus for lower respiratory tract infections.评价生物梅里埃 Filmarray 肺炎检测 panel 试剂盒(plus)在下呼吸道感染中的应用。
Infect Dis (Lond). 2020 Jul;52(7):479-488. doi: 10.1080/23744235.2020.1755053. Epub 2020 Apr 22.
8
Diagnosis of ventilator-associated pneumonia in critically ill adult patients-a systematic review and meta-analysis.诊断重症成年患者呼吸机相关性肺炎:系统评价和荟萃分析。
Intensive Care Med. 2020 Jun;46(6):1170-1179. doi: 10.1007/s00134-020-06036-z. Epub 2020 Apr 18.
9
Species Identification and Antibiotic Resistance Prediction by Analysis of Whole-Genome Sequence Data by Use of ARESdb: an Analysis of Isolates from the Unyvero Lower Respiratory Tract Infection Trial.利用 ARESdb 通过全基因组序列数据分析进行物种鉴定和抗生素耐药性预测:来自 Unyvero 下呼吸道感染试验的分离株分析。
J Clin Microbiol. 2020 Jun 24;58(7). doi: 10.1128/JCM.00273-20.
10
Evaluation of the BioFire FilmArray Pneumonia Panel for rapid detection of respiratory bacterial pathogens and antibiotic resistance genes in sputum and endotracheal aspirate specimens.评价生物梅里埃 FilmArray 肺炎Panel 快速检测痰和气管抽吸物标本中呼吸道细菌病原体和抗生素耐药基因。
Int J Infect Dis. 2020 Jun;95:326-331. doi: 10.1016/j.ijid.2020.03.024. Epub 2020 Mar 14.

多中心评估 Unyvero 平台在支气管肺泡灌洗液检测中的应用。

Multicenter Evaluation of the Unyvero Platform for Testing Bronchoalveolar Lavage Fluid.

机构信息

Curetis GmbH, Holzgerlingen, Germany.

OpGen, Inc., Gaithersburg, Maryland, USA.

出版信息

J Clin Microbiol. 2021 Feb 18;59(3). doi: 10.1128/JCM.02497-20.

DOI:10.1128/JCM.02497-20
PMID:33328178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8106704/
Abstract

Bronchoalveolar lavage (BAL) culture is a standard, though time-consuming, approach for identifying microorganisms in patients with severe lower respiratory tract (LRT) infections. The sensitivity of BAL culture is relatively low, and prior antimicrobial therapy decreases the sensitivity further, leading to overuse of empirical antibiotics. The Unyvero LRT BAL Application (Curetis GmbH, Germany) is a multiplex molecular panel that detects 19 bacteria, 10 antibiotic resistance markers, and a fungus, , in BAL fluid in ∼4.5 h. Its performance was evaluated using 1,016 prospectively collected and 392 archived specimens from 11 clinical trial sites in the United States. Overall positive and negative percent agreements with culture results for identification of bacteria that grow in routine cultures were 93.4% and 98.3%, respectively, with additional potential pathogens identified by Unyvero in 21.7% of prospectively collected specimens. For detection of , the positive percent agreement with standard testing was 87.5%. Antibiotic resistance marker results were compared to standard antibiotic susceptibility test results to determine positive predictive values (PPVs). PPVs ranged from 80 to 100%, based on the microorganism and specific resistance marker(s). The Unyvero LRT BAL Application provides accurate detection of common agents of bacterial pneumonia and of The sensitivity and rapidity of this panel suggest significant clinical value for choosing appropriate antibiotics and for antibiotic stewardship.

摘要

支气管肺泡灌洗(BAL)培养是一种标准的方法,尽管耗时,但可用于鉴定严重下呼吸道(LRT)感染患者的微生物。BAL 培养的敏感性相对较低,并且先前的抗菌治疗进一步降低了敏感性,导致经验性抗生素的过度使用。Unyvero LRT BAL 应用程序(Curetis GmbH,德国)是一种多重分子面板,可在大约 4.5 小时内检测 BAL 液中的 19 种细菌、10 种抗生素耐药标志物和一种真菌。它的性能在美国 11 个临床试验地点的 1016 份前瞻性收集和 392 份存档标本中进行了评估。对于在常规培养中生长的细菌的鉴定,与培养结果的总体阳性和阴性百分比一致性分别为 93.4%和 98.3%,Unyvero 还在 21.7%的前瞻性采集标本中鉴定了其他潜在病原体。对于检测,与标准检测的阳性百分比一致性为 87.5%。抗生素耐药标志物的结果与标准抗生素药敏试验结果进行比较,以确定阳性预测值(PPV)。根据微生物和特定耐药标志物,PPV 范围从 80%到 100%。Unyvero LRT BAL 应用程序提供了对细菌性肺炎常见病原体和的准确检测。该面板的敏感性和快速性表明,在选择合适的抗生素和抗生素管理方面具有重要的临床价值。