Datta S, Basu B, Chandra Y, Nagendra A
Consultant (Clinical Microbiology), Sir Ganga Ram Hospital, New Delhi.
Reader,(Dept of Microbiology), AFMC, Pune-40.
Med J Armed Forces India. 2010 Apr;66(2):129-33. doi: 10.1016/S0377-1237(10)80124-8. Epub 2011 Jul 21.
This study attempts to evaluate and compare the efficacy of polymerase chain reaction (PCR) and quantitative buffy coat (QBC) assay with conventional Giemsa stained peripheral blood smear (PBS) examination in the diagnosis of malaria.
The study was conducted on 50 cases of smear positive malaria (group 1), 50 cases of clinically suspected malaria (group 2) and 15 healthy controls. All were subjected to Giemsa stain slide examination both thick and thin smear, QBC assay and PCR. PBS examination by Giemsa stain was taken as gold standard.
In this study the overall sensitivity and positive predictive value (PPV) of QBC assay in group 1 was 100% and that of PCR was 60% and 100% respectively. In group 2 the sensitivity, specificity, PPV and NPV of QBC assay was 100% and that of PCR was 71%, 100%, 100% and 73% respectively as compared to the gold standard. All the 15 healthy controls were negative by all the three assays showing 100% specificity.
QBC assay was an excellent alternative to the conventional method as it is rapid and less time consuming and can directly demonstrate the parasite. Utility of PCR lies in species-specific diagnosis of falciparum malaria especially when there is a high degree of clinical suspicion and the report is negative by the other two methods.
本研究旨在评估和比较聚合酶链反应(PCR)、定量血沉棕黄层(QBC)检测与传统吉姆萨染色外周血涂片(PBS)检查在疟疾诊断中的疗效。
对50例涂片阳性疟疾患者(第1组)、50例临床疑似疟疾患者(第2组)和15名健康对照者进行研究。所有研究对象均接受吉姆萨染色厚、薄涂片镜检、QBC检测和PCR检测。以吉姆萨染色的PBS检查作为金标准。
在本研究中,第1组QBC检测的总体灵敏度和阳性预测值(PPV)分别为100%,PCR的分别为60%和100%。与金标准相比,第2组中QBC检测的灵敏度、特异度、PPV和阴性预测值(NPV)分别为100%,PCR的分别为71%、100%、100%和73%。所有15名健康对照者的三项检测结果均为阴性,特异度为100%。
QBC检测是传统方法的一种优秀替代方法,因为它快速且耗时少,并且可以直接显示疟原虫。PCR的作用在于对恶性疟进行种特异性诊断,特别是在临床高度怀疑而其他两种方法报告为阴性时。