首页> 外文期刊>The Korean Journal of Parasitology >Comparative Assessment of Diagnostic Performances of Two Commercial Rapid Diagnostic Test Kits for Detection of Plasmodium spp. in Ugandan Patients with Malaria
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Comparative Assessment of Diagnostic Performances of Two Commercial Rapid Diagnostic Test Kits for Detection of Plasmodium spp. in Ugandan Patients with Malaria

机译:两种商用快速诊断检测试剂盒检测疟原虫的诊断性能的比较评估。在乌干达疟疾患者中

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Prompt diagnosis of malaria cases with rapid diagnostic tests (RDTs) has been widely adopted as an effective malaria diagnostic tool in many malaria endemic countries, primarily due to their easy operation, fast result output, and straightforward interpretation. However, there has been controversy about the diagnostic accuracy of RDTs. This study was conducted to evaluate the diagnostic performances of the 2 commercially available malaria RDT kits, RapiGEN Malaria Ag Pf / Pv ( p LDH/ p LDH) and Asan EasyTestsupTM/sup Malaria Ag Pf / Pv (HRP-2/ p LDH) for their abilities to detect Plasmodium species in blood samples collected from Ugandan patients with malaria. To evaluate the diagnostic performances of these 2 RDT kits, 229 blood samples were tested for malaria infection by microscopic examination and a species-specific nested polymerase chain reaction. The detection sensitivities for P. falciparum of Malaria Ag Pf / Pv ( p LDH/ p LDH) and Asan EasyTestsupTM/sup Malaria Ag Pf / Pv (HRP-2/ p LDH) were 87.83% and 89.57%, respectively. The specificities of the 2 RDTs were 100% for P. falciparum and mixed P. falciparum / P. vivax infections. These results suggest that the 2 RDT kits showed reasonable levels of diagnostic performances for detection of the malaria parasites from Ugandan patients. However, neither kit could effectively detect P. falciparum infections with low parasitaemia (500 parasites/μl).
机译:通过快速诊断测试(RDT)迅速诊断疟疾病例已被许多疟疾流行国家广泛用作有效的疟疾诊断工具,这主要是由于它们易于操作,快速输出结果和易于理解。但是,关于RDT的诊断准确性一直存在争议。本研究旨在评估2种市售疟疾RDT试剂盒RapiGEN Malaria Ag Pf / Pv(p LDH / p LDH)和Asan EasyTest TM Malaria Ag Pf / Pv(HRP-)的诊断性能。 2 / p LDH)具有检测从乌干达疟疾患者那里采集的血液样本中疟原虫种类的能力。为了评估这两种RDT试剂盒的诊断性能,通过显微镜检查和特定物种的巢式聚合酶链反应对229个血液样本进行了疟疾感染测试。疟疾Ag Pf / Pv(p LDH / p LDH)和Asan EasyTest TM 疟疾Ag Pf / Pv(HRP-2 / p LDH)对恶性疟原虫的检出灵敏度分别为87.83%和89.57% , 分别。对于恶性疟原虫和混合性恶性疟原虫/间日疟原虫感染,两种RDT的特异性为100%。这些结果表明,两种RDT试剂盒在检测乌干达患者的疟原虫方面显示出合理水平的诊断性能。但是,这两种试剂盒都不能有效地检测出低寄生虫血症(<500寄生虫/μl)的恶性疟原虫感染。

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