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通过商业乳胶凝集试验快速诊断轮状病毒肠胃炎。

Rapid diagnosis of rotavirus gastroenteritis by a commercial latex agglutination test.

作者信息

Pai C H, Shahrabadi M S, Ince B

出版信息

J Clin Microbiol. 1985 Nov;22(5):846-50. doi: 10.1128/jcm.22.5.846-850.1985.

Abstract

The Rotalex test, a commercial latex agglutination test for rotavirus, was compared with direct electron microscopy (EM) and the Rotazyme test I, a commercial enzyme immunoassay, for detection of rotavirus in stools of children and neonates. For initial stool specimens from 265 children (less than 3 years old) with diarrhea, the Rotalex test had a sensitivity of 81.7% and specificity of 99.5% compared with EM results. Positive and negative predictive values were 98 and 94.9%, respectively. The Rotalex test was slightly more sensitive and specific than the Rotazyme test. When daily stool specimens from patients with rotavirus gastroenteritis were examined, the sensitivity of the Rotalex test varied depending on the time of stool collection relative to the onset of symptoms. Sensitivity was 100 (20/20), 96 (23/24), and 54% (7/13) during 1 to 4, 5 to 7, and 8 to 18 days, respectively, after the onset of symptoms. The sensitivity of the Rotazyme test varied similarly with days from onset. We also examined 214 EM-negative stool specimens from asymptomatic newborns. False positivity by the Rotalex test was only 3.3% (7/214) compared with 4.2% (9/215) for the Rotazyme test. The Rotalex test was as sensitive and specific as EM for detection of rotavirus during the acute stage of illness and much faster and cheaper than EM or the Rotazyme test. The test appears to be suitable for routine use in small hospitals, emergency wards, or even the physician's office for rapid diagnosis of rotavirus gastroenteritis.

摘要

将用于轮状病毒检测的商业乳胶凝集试验——罗塔列克斯试验(Rotalex test),与直接电子显微镜检查(EM)以及商业酶免疫测定法——罗塔酶试验I(Rotazyme test I)进行比较,以检测儿童和新生儿粪便中的轮状病毒。对于265名腹泻儿童(3岁以下)的初始粪便标本,与电子显微镜检查结果相比,罗塔列克斯试验的灵敏度为81.7%,特异性为99.5%。阳性预测值和阴性预测值分别为98%和94.9%。罗塔列克斯试验比罗塔酶试验略敏感且特异。当检查轮状病毒胃肠炎患者的每日粪便标本时,罗塔列克斯试验的灵敏度根据粪便采集时间相对于症状发作的时间而有所不同。症状发作后1至4天、5至7天和8至18天的灵敏度分别为100%(20/20)、96%(23/24)和54%(7/13)。罗塔酶试验的灵敏度也随症状发作天数有类似变化。我们还检查了214份无症状新生儿的电子显微镜检查阴性的粪便标本。罗塔列克斯试验的假阳性率仅为3.3%(7/214),而罗塔酶试验为4.2%(9/215)。在疾病急性期,罗塔列克斯试验在检测轮状病毒方面与电子显微镜检查一样敏感和特异,并且比电子显微镜检查或罗塔酶试验更快、更便宜。该试验似乎适用于小型医院、急诊病房甚至医生办公室的常规使用,用于快速诊断轮状病毒胃肠炎。

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