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疟疾诊断:尼日利亚恶性疟患者中Parasight-F检测的假阴性结果

Malaria diagnosis: false negative parasight-F tests in falciparum malaria patients in Nigeria.

作者信息

Happi C T, Gbotosho G O, Sowunmi A, Falade C O, Akinboye D O, Oladepo O, Oduola A M J

机构信息

Malaria Research Laboratories, Postgraduate Institute for Medical Research and Training, College of Medicine, University of Ibadan, Nigeria.

出版信息

Afr J Med Med Sci. 2004 Mar;33(1):15-8.

Abstract

This study was designed to assess the relative reliability of microscopy, the dipstick technique based on the detection of Plasmodium falciparum-specific histidine rich protein II (HRPII) (Parasight-F) and PCR assays in diagnosing falciparum malaria infections in Nigerian children. The prevalence of P. falciparum infections in enrolled patients was 100% by microscopy. Parasite density ranged from 329 to 81,194 parasites/microL of blood, with a geometric mean parasite density of 5168 parasites/microL of blood. The sensitivity of the HRPII based dipstick, PCR and microscopy were 80%, 92% and 100% respectively. A false negative rate of 20% was observed with Parasight-F as compared with microscopy. The parasitemia in patients with false negative Parasight-F tests ranged from 319 to 54,680 parasites/microL of blood. Detailed PCR analysis of Isolates obtained from five out of the eight patients who exhibited a negative Parasight-F test, showed that the average numbers of P. falciparum clones in these five isolates were: 1.7 +/- 1.02 with MSPI, 3.2 +/- 1.3 with MSP2 and 1.4 +/- 1.72 with GLURP. Comparison of microscopy and HRPII results showed a significant (p=0.009) difference as opposed to microscopy and PCR (p=0.239). This study showed that caution should be exercised when excluding P. falciparum infections on the basis of HRPII based dipstick results alone. Microscopy or PCR diagnosis where possible, should be carried out in order to confirm negative P. falciparum HRPII-based dipstick tests.

摘要

本研究旨在评估显微镜检查、基于检测恶性疟原虫特异性富含组氨酸蛋白II(HRPII)的试纸条技术(Parasight - F)和聚合酶链反应(PCR)检测法在诊断尼日利亚儿童恶性疟原虫感染中的相对可靠性。通过显微镜检查,入选患者中恶性疟原虫感染的患病率为100%。寄生虫密度范围为每微升血液329至81,194个寄生虫,几何平均寄生虫密度为每微升血液5168个寄生虫。基于HRPII的试纸条、PCR和显微镜检查的敏感性分别为80%、92%和100%。与显微镜检查相比,Parasight - F的假阴性率为20%。Parasight - F检测结果为假阴性的患者的寄生虫血症范围为每微升血液319至54,680个寄生虫。对8例Parasight - F检测结果为阴性的患者中的5例所分离出的样本进行详细的PCR分析,结果显示这5个分离株中恶性疟原虫克隆的平均数量分别为:MSPI为1.7±1.02,MSP2为3.2±1.3,GLURP为1.4±1.72。显微镜检查和HRPII结果的比较显示存在显著差异(p = 0.009),而显微镜检查和PCR结果的比较则无显著差异(p = 0.239)。本研究表明,仅根据基于HRPII的试纸条结果排除恶性疟原虫感染时应谨慎。如有可能,应进行显微镜检查或PCR诊断以确认基于HRPII的恶性疟原虫试纸条检测结果为阴性的情况。

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