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评价在暴发情况下用于艰难梭菌诊断的快速环介导等温扩增检测试剂盒 Illumigene。

Evaluation of the rapid loop-mediated isothermal amplification assay Illumigene for diagnosis of Clostridium difficile in an outbreak situation.

机构信息

Department of Laboratory Medicine, Microbiology, Örebro University Hospital, Örebro, Sweden.

出版信息

APMIS. 2014 Feb;122(2):155-60. doi: 10.1111/apm.12121. Epub 2013 Jun 12.

DOI:10.1111/apm.12121
PMID:23758095
Abstract

An outbreak of Clostridium difficile infection (CDI) at Höglandet Hospital Eksjö in southern Sweden in 2011 was mainly due to a multidrug-resistant PCR ribotype 046 (30% of all samples). Diagnostics used routinely was the Vidas CDAB assay, but to control the outbreak the rapid loop-mediated isothermal amplification (LAMP) assay Illumigene was introduced and both techniques were compared to Toxigenic culture (TC) prospectively. The LAMP assay had a superior sensitivity, that is, 98% compared to 79% for the Vidas CDAB assay. Most importantly, the mean turn-around-time from collecting sample to result was reduced from 59 h to 2 h enabling early isolation of patients and effective hygiene precautions. This may potentially decrease the morbidity and nosocomial transmissions of C. difficile.

摘要

2011 年,瑞典南部埃克斯约的 Höglandet 医院爆发艰难梭菌感染(CDI),主要是由于一种多药耐药的 PCR 核糖体 046 型(占所有样本的 30%)。常规使用的诊断方法是 Vidas CDAB 检测,但为了控制疫情,引入了快速环介导等温扩增(LAMP)检测 Illumigene,并前瞻性地将这两种技术与产毒培养(TC)进行了比较。LAMP 检测的灵敏度更高,为 98%,而 Vidas CDAB 检测的灵敏度为 79%。最重要的是,从采集样本到得出结果的平均周转时间从 59 小时缩短到 2 小时,从而能够更早地隔离患者并采取有效的卫生预防措施。这可能会降低艰难梭菌的发病率和医院内传播。

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