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评估BD Max艰难梭菌检测试剂盒在检测人类粪便标本中产毒艰难梭菌方面的性能。

Evaluation of the BD Max Cdiff assay for the detection of toxigenic Clostridium difficile in human stool specimens.

作者信息

Putsathit Papanin, Morgan Justin, Bradford Damien, Engelhardt Nelly, Riley Thomas V

机构信息

1Microbiology and Immunology, School of Pathology and Laboratory Medicine, The University of Western Australia, Crawley 2Department of Microbiology and Infectious Diseases, PathWest Laboratory Medicine, Royal Perth Hospital, Perth 3Department of Microbiology, PathWest Laboratory Medicine, Queen Elizabeth II Medical Centre, Nedlands 4Department of Microbiology, PathWest Laboratory Medicine, Fremantle Hospital, Fremantle, WA, Australia.

出版信息

Pathology. 2015 Feb;47(2):165-8. doi: 10.1097/PAT.0000000000000214.

Abstract

The Becton Dickinson (BD) PCR-based GeneOhm Cdiff assay has demonstrated a high sensitivity and specificity for detecting Clostridium difficile. Recently, the BD Max platform, using the same principles as BD GeneOhm, has become available in Australia. This study aimed to investigate the sensitivity and specificity of BD Max Cdiff assay for the detection of toxigenic C. difficile in an Australian setting. Between December 2013 and January 2014, 406 stool specimens from 349 patients were analysed with the BD Max Cdiff assay. Direct and enrichment toxigenic culture were performed on bioMérieux ChromID C. difficile agar as a reference method. isolates from specimens with discrepant results were further analysed with an in-house PCR to detect the presence of toxin genes. The overall prevalence of toxigenic C. difficile was 7.2%. Concordance between the BD Max assay and enrichment culture was 98.5%. The sensitivity, specificity, positive predictive value and negative predictive value for the BD Max Cdiff assay were 95.5%, 99.0%, 87.5% and 99.7%, respectively, when compared to direct culture, and 91.7%, 99.0%, 88.0% and 99.4%, respectively, when compared to enrichment culture. The new BD Max Cdiff assay appeared to be an excellent platform for rapid and accurate detection of toxigenic C. difficile.

摘要

基于Becton Dickinson(BD)聚合酶链反应(PCR)的GeneOhm艰难梭菌检测法已显示出在检测艰难梭菌方面具有高灵敏度和特异性。最近,采用与BD GeneOhm相同原理的BD Max平台已在澳大利亚上市。本研究旨在调查BD Max艰难梭菌检测法在澳大利亚环境中检测产毒艰难梭菌的灵敏度和特异性。2013年12月至2014年1月期间,使用BD Max艰难梭菌检测法对349例患者的406份粪便标本进行了分析。以生物梅里埃公司的ChromID艰难梭菌琼脂进行直接和增菌产毒培养作为参考方法。对结果不一致的标本分离株进一步采用内部PCR检测毒素基因的存在情况。产毒艰难梭菌的总体患病率为7.2%。BD Max检测法与增菌培养之间的一致性为98.5%。与直接培养相比,BD Max艰难梭菌检测法的灵敏度、特异性、阳性预测值和阴性预测值分别为95.5%、99.0%、87.5%和99.7%;与增菌培养相比,分别为91.7%、99.0%、88.0%和99.4%。新的BD Max艰难梭菌检测法似乎是快速准确检测产毒艰难梭菌的优秀平台。

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