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商业性细菌和真菌广谱 PCR(Micro-Dx™)检测正常无菌部位培养阴性标本:诊断价值及对抗菌药物治疗的影响。

Commercial bacterial and fungal broad-range PCR (Micro-Dx™) used on culture-negative specimens from normally sterile sites: diagnostic value and implications for antimicrobial treatment.

机构信息

Department of Clinical Microbiology, Slagelse Hospital, Region Zealand, Denmark; Department of Clinical microbiology, Odense University Hospital, Odense, Denmark; Department of Clinical microbiology, Vejle Hospital, Vejle, Denmark.

Department of Clinical Microbiology, Slagelse Hospital, Region Zealand, Denmark; Department of Clinical Microbiology, Herlev and Gentofte Hospital, Herlev, Denmark.

出版信息

Diagn Microbiol Infect Dis. 2020 Jun;97(2):115028. doi: 10.1016/j.diagmicrobio.2020.115028. Epub 2020 Feb 22.

Abstract

The aim of this study was to evaluate the clinical value of partial 16S/18S rRNA gene sequencing with the commercial kit Micro-Dx™ used with the SelectNA™plus instrument on culture-negative samples. A retrospective study of microbiological and clinical data from a 2.5-year period was performed. Assessment of the clinical relevance of the 16S/18S rRNA gene sequencing results was based on evaluation of the results in the clinical context and changes in antimicrobial therapy. Included were 529 samples from 223 patients, representing 251 episodes. In 191 samples (36.1%), bacterial/fungal DNA was detected. Positive results were judged clinically relevant in 79 (31.5%) episodes. Antimicrobial treatment was adjusted according to the 16S/18S rRNA gene sequence analysis result in 42 (16.7%) episodes. The results from 16S/18S rRNA gene sequence analysis were highly clinically relevant. These findings support the use of this analysis in a routine setting.

摘要

本研究旨在评估使用商业试剂盒 Micro-Dx™ 和 SelectNA™plus 仪器对培养阴性样本进行部分 16S/18S rRNA 基因测序的临床价值。对 2.5 年期间的微生物学和临床数据进行了回顾性研究。根据临床背景评估 16S/18S rRNA 基因测序结果的临床相关性,并评估抗菌治疗的变化。共纳入 223 名患者的 529 份样本,代表 251 个感染部位。在 191 份样本(36.1%)中检测到细菌/真菌 DNA。79 个(31.5%)感染部位的阳性结果被判断为具有临床相关性。根据 16S/18S rRNA 基因序列分析结果,42 个(16.7%)感染部位调整了抗菌治疗。16S/18S rRNA 基因序列分析的结果具有高度的临床相关性。这些发现支持在常规环境中使用该分析。

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