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诺如病毒爆发诊断中的概率

Probabilities in norovirus outbreak diagnosis.

作者信息

Duizer Erwin, Pielaat Annemarie, Vennema Harry, Kroneman Annelies, Koopmans Marion

机构信息

Center for Infectious Diseases Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands.

出版信息

J Clin Virol. 2007 Sep;40(1):38-42. doi: 10.1016/j.jcv.2007.05.015. Epub 2007 Jul 12.

Abstract

BACKGROUND

Noroviruses are recognized as the most common cause of outbreaks of acute gastroenteritis. Yet, diagnostic testing for norovirus is based mostly on RNA detection by RT-PCR, which is not widely available. While antigen detection tests (ELISAs) are easier to perform, they are in general less sensitive.

OBJECTIVES

Our aim was to provide a scientific basis for declaring norovirus as the causative agent of an outbreak of acute gastroenteritis.

STUDY DESIGN

Statistical analysis used binomial distribution to determine the minimal number of positive samples, and the probability of detecting the required number of positive samples, for different tests, required to assign norovirus as the causative agent of an outbreak of acute gastroenteritis.

RESULTS

For either a standard RT-PCR or a commercially available ELISA, finding only 1 sample positive out of 2, 3 or 4 samples is sufficient to assign norovirus as the causative agent of an outbreak of acute gastroenteritis. However, when ELISA is used, the probability of detecting this required minimum number of positive samples is low when small numbers of samples are tested (57% when 2 samples are tested; 72% when 3 samples are tested). In order to reach a 90% probability of detecting a norovirus outbreak (false negativity at outbreak level <10%), at least 3 samples should be tested using RT-PCR, and 6 samples when using an ELISA.

CONCLUSIONS

The sensitivity for NoV outbreak diagnosis will increase from 57% to 92%, or from 84% to 96%, for ELISA or RT-PCR respectively, when sample size increases from 2 to 6. Thus, using ELISA instead of RT-PCR for the detection of norovirus in stool samples will result in considerable numbers of false negative outbreaks unless a minimum of 6 samples are tested per outbreak.

摘要

背景

诺如病毒被认为是急性胃肠炎暴发的最常见病因。然而,诺如病毒的诊断检测主要基于逆转录聚合酶链反应(RT-PCR)进行RNA检测,而这种检测方法并未广泛普及。虽然抗原检测试验(酶联免疫吸附测定,ELISA)操作更简便,但总体而言敏感性较低。

目的

我们的目的是为将诺如病毒宣布为急性胃肠炎暴发的病原体提供科学依据。

研究设计

统计分析采用二项分布来确定将诺如病毒认定为急性胃肠炎暴发病原体时,不同检测方法所需的阳性样本最小数量以及检测到所需数量阳性样本的概率。

结果

对于标准RT-PCR或市售ELISA,在2份、3份或4份样本中仅发现1份样本呈阳性就足以将诺如病毒认定为急性胃肠炎暴发的病原体。然而,使用ELISA时,检测少量样本(检测2份样本时为57%;检测3份样本时为72%)时检测到所需最小数量阳性样本的概率较低。为了达到90%的概率检测到诺如病毒暴发(暴发水平的假阴性率< 10%),使用RT-PCR时至少应检测3份样本,使用ELISA时则应检测6份样本。

结论

当样本量从2份增加到6份时,ELISA或RT-PCR检测诺如病毒暴发的敏感性将分别从57%提高到92%,或从84%提高到96%。因此,在粪便样本中使用ELISA而非RT-PCR检测诺如病毒会导致大量假阴性暴发,除非每次暴发至少检测6份样本。

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