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2
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Malariaworld J. 2018 Mar 1;9:1. eCollection 2018.
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本文引用的文献

1
Routine parallel diagnosis of malaria using microscopy and the malaria rapid diagnostic test SD 05FK60: the experience of Médecins Sans Frontières in Myanmar.使用显微镜和疟疾快速诊断测试SD 05FK60对疟疾进行常规平行诊断:无国界医生组织在缅甸的经验。
Malar J. 2013 May 21;12:167. doi: 10.1186/1475-2875-12-167.
2
Over-diagnosis of malaria by microscopy in the Kilombero Valley, Southern Tanzania: an evaluation of the utility and cost-effectiveness of rapid diagnostic tests.坦桑尼亚南部基隆贝罗谷地区显微镜法过度诊断疟疾:快速诊断检测的实用性和成本效益评估。
Malar J. 2013 May 10;12:159. doi: 10.1186/1475-2875-12-159.
3
Low quality of routine microscopy for malaria at different levels of the health system in Dar es Salaam.不同卫生系统层级常规显微镜检用于疟疾的低质量。
Malar J. 2011 Nov 2;10:332. doi: 10.1186/1475-2875-10-332.
4
Laboratory demonstration of a prozone-like effect in HRP2-detecting malaria rapid diagnostic tests: implications for clinical management.实验室证明 HRP2 检测疟疾快速诊断检测中存在类前带效应:对临床管理的影响。
Malar J. 2011 Sep 29;10:286. doi: 10.1186/1475-2875-10-286.
5
Prozone in malaria rapid diagnostics tests: how many cases are missed?疟疾快速诊断检测中的前带现象:漏检了多少病例?
Malar J. 2011 Jun 15;10:166. doi: 10.1186/1475-2875-10-166.
6
A research agenda for malaria eradication: diagnoses and diagnostics.消除疟疾研究议程:诊断与诊断方法。
PLoS Med. 2011 Jan 25;8(1):e1000396. doi: 10.1371/journal.pmed.1000396.
7
Assessment of the prozone effect in malaria rapid diagnostic tests.疟疾快速诊断检测中前带效应的评估。
Malar J. 2009 Nov 30;8:271. doi: 10.1186/1475-2875-8-271.
8
Rapid Diagnosis of Malaria.疟疾的快速诊断
Interdiscip Perspect Infect Dis. 2009;2009:415953. doi: 10.1155/2009/415953. Epub 2009 Jun 11.
9
Quantitative detection of Plasmodium falciparum DNA in saliva, blood, and urine.唾液、血液和尿液中恶性疟原虫DNA的定量检测。
J Infect Dis. 2009 Jun 1;199(11):1567-74. doi: 10.1086/598856.
10
PCR detection of Plasmodium falciparum in human urine and saliva samples.人尿液和唾液样本中恶性疟原虫的聚合酶链反应检测
Malar J. 2006 Nov 8;5:103. doi: 10.1186/1475-2875-5-103.

尼日利亚东南部用于诊断发热个体疟疾的尿液疟疾检测(UMT)试剂盒性能评估:横断面分析研究。

The performance evaluation of a urine malaria test (UMT) kit for the diagnosis of malaria in individuals with fever in south-east Nigeria: cross-sectional analytical study.

作者信息

Oguonu Tagbo, Shu Elvis, Ezeonwu Bertilla U, Lige Bao, Derrick Anne, Umeh Rich E, Agbo Eddy

机构信息

Department of Pediatrics, University of Nigeria Teaching Hospital, Enugu, Nigeria.

出版信息

Malar J. 2014 Oct 15;13:403. doi: 10.1186/1475-2875-13-403.

DOI:10.1186/1475-2875-13-403
PMID:25316216
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4203939/
Abstract

BACKGROUND

Accurate rapid diagnosis is one of the important steps in the effort to reduce morbidity and mortality of malaria. Blood-specific malaria rapid diagnostic tests (RDTs) are currently in use but other body fluid specific diagnostic test kits are being developed. The aim of the present study was to evaluate the performance characteristics of a one-step Urine Malaria Test™ (UMT) dipstick in detecting Plasmodium falciparum HRP2, a poly-histidine antigen in urine of febrile patients for malaria diagnosis.

METHODS

This was an observational study in which a urine-based malaria test kit was used in malaria diagnosis in a normal field setting. Two hundred and three individuals who presented with fever (≥37.5°C) at seven outpatient clinics in Enugu State during periods of high and low transmission seasons in Southeastern Nigeria were enrolled. Matched samples of urine and blood of consecutively enrolled subjects were tested with UMT and blood smear microscopy.

RESULTS

With the blood smear microscopy as standard, the disease prevalence was 41.2% and sensitivity for the UMT was 83.75% (CI: 73.81 to 91.95%, Kappa 0.665, p =0.001). The UMT had an LLD of 120 parasites/μl but the sensitivity at parasite density less than ≤200 parasites/μl was 50% and 89.71% at density ≥201 parasites/μl with specificity of 83.48%. The positive and negative predictive values were 77.91% and 88.07%, respectively.

CONCLUSION

The UMT showed moderate level of sensitivity compared with blood smear microscopy. The test kit requires further improvement on its sensitivity in order to be deployable for field use in malaria endemic regions.

摘要

背景

准确快速诊断是降低疟疾发病率和死亡率的重要步骤之一。目前正在使用血液特异性疟疾快速诊断检测(RDT),但其他体液特异性诊断试剂盒也在研发中。本研究的目的是评估一步式尿液疟疾检测(UMT)试纸条在检测恶性疟原虫组氨酸丰富蛋白2(HRP2)方面的性能特征,HRP2是一种多组氨酸抗原,存在于发热患者尿液中,用于疟疾诊断。

方法

这是一项观察性研究,在正常现场环境中使用基于尿液的疟疾检测试剂盒进行疟疾诊断。在尼日利亚东南部传播季节高低不同时期,对埃努古州七家门诊诊所中出现发热(≥37.5°C)的203名个体进行了登记。对连续登记受试者的尿液和血液匹配样本进行UMT检测和血涂片显微镜检查。

结果

以血涂片显微镜检查为标准,疾病患病率为41.2%,UMT的敏感性为83.75%(CI:73.81至91.95%,Kappa 0.665,p = 0.001)。UMT的最低检测限为120个寄生虫/微升,但在寄生虫密度小于或等于200个寄生虫/微升时敏感性为50%,在密度≥201个寄生虫/微升时敏感性为89.71%,特异性为83.48%。阳性和阴性预测值分别为77.91%和88.07%。

结论

与血涂片显微镜检查相比,UMT显示出中等水平的敏感性。该检测试剂盒需要进一步提高其敏感性,以便能够在疟疾流行地区用于现场检测。