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Assessment of Clinical Diagnosis, Microscopy, Rapid Diagnostic Tests, and Polymerase Chain Reaction in the Diagnosis of Plasmodium falciparum in Nigeria

机译:尼日利亚疟原虫疟原虫诊断中临床诊断,显微镜,快速诊断试验和聚合酶链反应的评估

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摘要

This study compares the performance of clinical diagnosis and three laboratory diagnostic methods (thick film microscopy (TFM), rapid diagnostic test (RDT), and polymerase chain reaction (PCR)) for the diagnosis of Plasmodium falciparum in Nigeria. Using clinical criteria, 217 children were recruited into the study out of which 106 (48.8%) were positive by TFM, 84 (38.7%) by RDT, and 125 (57.6%) by PCR. Using a composite reference method generated from the three diagnostic methods, 71 (32.7%) patients were found to be truly infected and 90 (41.5%) truly uninfected, while 56 (25.8%) were misidentified as infected or noninfected. When each of the 3 diagnostic methods was compared with the composite reference, PCR had sensitivity of 97.3%, specificity of 62.5%, positive predictive value (PPV) of 56.8%, and negative predictive value (NPV) of 97.8%; microscopy had sensitivity of 77.2%, specificity of 72%, PPV of 66.9%, and NPV of 81.1%, while RDT had sensitivity of 62.3%, specificity of 87.4%, PPV of 67.7%, and NPV of 84.5%. PCR test performed best among the three methods followed by TFM and RDT in that order. The result of this study shows that clinical diagnosis cannot be relied upon for accurate diagnosis of P. falciparum in endemic areas.
机译:该研究比较了临床诊断的性能和三种实验室诊断方法(厚膜显微镜(TFM),快速诊断试验(RDT)和聚合酶链反应(PCR)),用于尼日利亚疟原虫疟原虫诊断。使用临床标准,将217名儿童招募到该研究中,其中通过TFM,84(38.7%)通过RDT和PCR的125(57.6%)阳性的106(48.8%)。使用从三种诊断方法产生的复合参考方法,发现71名(32.7%)患者被发现真正感染,90例(41.5%)真正无感染,而56(25.8%)被误诊为感染或非感染。当将3种诊断方法中的每一个与复合参考进行比较时,PCR的敏感性为97.3%,特异性为62.5%,阳性预测值(PPV)为56.8%,负预测值(NPV)为97.8%;显微镜敏感性为77.2%,特异性为72%,PPV为66.9%,NPV为81.1%,而RDT的敏感性为62.3%,特异性为87.4%,PPV为67.7%,NPV为84.5%。 PCR测试在三种方法中表现最佳,然后按此顺序进行TFM和RDT。本研究的结果表明,不能依赖临床诊断,以便准确诊断流行区域中的杀菌性疟原虫。

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