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评估Pastorex脑膜炎试剂盒在尼日利亚快速鉴定脑膜炎奈瑟菌C群的性能。

Evaluation of Pastorex meningitis kit performance for the rapid identification of Neisseria meningitidis serogroup C in Nigeria.

作者信息

Uadiale Kennedy, Bestman Agatha, Kamau Charity, Caugant Dominique A, Greig Jane

机构信息

Médecins sans Frontières, Sokoto, Nigeria.

Médecins sans Frontières, Amsterdam, Netherlands.

出版信息

Trans R Soc Trop Med Hyg. 2016 Jul;110(7):381-5. doi: 10.1093/trstmh/trw046.

Abstract

BACKGROUND

Neisseria meningitidis serogroup C (NmC) has caused outbreaks in Nigeria of increasing size in three consecutive years since 2013. Rapid diagnostic tests (RDTs) for meningitis can facilitate quick identification of the causative pathogen; Pastorex can detect N. meningitidis serogroups A, C (NmC), Y/W135, N. meningitidis serogroup B/Escherichia coli K1, Haemophilus influenzae type b (Hib), Streptococcus pneumoniae, and group B Streptococcus. There is no published field evaluation of Pastorex in the identification of NmC. We report our experience with Pastorex in detecting NmC in field conditions.

METHODS

During sequential outbreaks of NmC in Nigeria in 2013, 2014 and 2015, cerebrospinal fluid (CSF) was collected from suspected cases of meningitis that met the case definition. Pastorex latex agglutination rapid test was done in the field and trans-isolate media were inoculated with CSF for culture and/or PCR, which was used as the reference standard for 63 paired samples.

RESULTS

The sensitivity of Pastorex for NmC was 80.0% (95% CI 65.4-90.4%) and the specificity was 94.4% (95% CI 72.7-99.9%). The positive likelihood ratio (LR) was 14.4 (95% CI 2.1-97.3) and negative LR was 0.2 (95% CI 0.1-0.4). The positive and negative predictive values (PPV and NPV) were 97.3% (95% CI 85.8-99.9) and 65.4% (95% CI 44.3-82.8), respectively, with a prevalence estimate of 71.4% (95% CI 58.6-82.1).

CONCLUSION

Pastorex showed good performance in detecting NmC under field conditions. Prepositioning Pastorex at peripheral health facilities during non-epidemic periods is constrained by a short shelf-life of 1 month after the kit is opened. There is need for development of RDTs that are cheaper and with less challenging requirements for storage and usage.

摘要

背景

自2013年以来,C群脑膜炎奈瑟菌(NmC)在尼日利亚已连续三年引发规模不断扩大的疫情。脑膜炎快速诊断检测(RDT)有助于快速鉴定致病病原体;Pastorex检测试剂盒可检测A、C群脑膜炎奈瑟菌(NmC)、Y/W135群脑膜炎奈瑟菌、B/E群大肠杆菌K1、b型流感嗜血杆菌(Hib)、肺炎链球菌及B族链球菌。目前尚无关于Pastorex检测NmC的现场评估报告。我们报告了在现场条件下使用Pastorex检测NmC的经验。

方法

在2013年、2014年和2015年尼日利亚相继发生的NmC疫情期间,从符合病例定义的疑似脑膜炎病例中采集脑脊液(CSF)。在现场进行Pastorex乳胶凝集快速检测,并将CSF接种于转运培养基中进行培养和/或PCR检测,后者作为63对样本的参考标准。

结果

Pastorex检测NmC的灵敏度为80.0%(95%可信区间65.4 - 90.4%),特异性为94.4%(95%可信区间72.7 - 99.9%)。阳性似然比(LR)为14.4(95%可信区间2.1 - 97.3),阴性似然比为0.2(95%可信区间0.1 - 0.4)。阳性和阴性预测值(PPV和NPV)分别为97.3%(95%可信区间85.8 - 99.9)和65.4%(95%可信区间44.3 - 82.8),患病率估计为71.4%(95%可信区间58.6 - 82.1)。

结论

Pastorex在现场条件下检测NmC表现良好。在非流行期间将Pastorex预先放置在外围卫生设施存在限制,因为试剂盒开封后的保质期仅为1个月。需要开发更便宜且对储存和使用要求较低的RDT。

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