Sharew Bekele, Legesse Mengistu, Animut Abebe, Jima Daddi, Medhin Girmay, Erko Berhanu
Aklilu Lemma Institute of Pathobiology, Addis Ababa University, P.O. Box 1176, Addis Ababa, Ethiopia.
Acta Trop. 2009 Sep;111(3):321-4. doi: 10.1016/j.actatropica.2009.05.014. Epub 2009 May 29.
To evaluate the diagnostic performance of CareStart Malaria Pf/Pv Combo test relative to microscopy for the diagnosis of falciparum and vivax malaria in Ethiopia.
668 febrile patients visiting two health centers in Wondo Genet, southern Ethiopia, involved in this study in 2008. Giemsa-stained thin and thick blood smears were prepared and microscopically examined under a 100x oil immersion microscope objective for Plasmodium species identification and determination of parasitaemia, respectively. CareStart Malaria Pf/Pv Combo test and Paracheck Pf test were performed as per the manufacturers' instruction.
The diagnostic validity of CareStart Malaria Pf/Pv Combo test for the diagnosis of Plasmodium falciparum were very good with sensitivity of 99.4%, specificity of 98%, positive predictive value of 94.4% and negative predictive value of 99.8%. Sensitivity, specificity, positive predictive value and negative predictive value of the test for the diagnosis of P. vivax were 99.4%, 98.2%, 94.5% and 99.8%, respectively. The diagnostic performance of CareStart Malaria Pf/Pv Combo test is comparable to that of Paracheck Pf test for the diagnosis of P. falciparum (sensitivity 99.4%, specificity 98.2%).
Although CareStart Malaria Pf/Pv Combo test and Paracheck Pf test have comparable diagnostic performance for the diagnosis of P. falciparum, CareStart Malaria Pf/Pv Combo test has the added advantage of diagnosing P. vivax. Hence, it is preferable to use CareStart Malaria Pf/Pv Combo test for the diagnosis of malaria in areas where microscopy is not accessible and where malaria due to P. falciparum and P. vivax are co-endemic as in Ethiopia.
评估CareStart疟原虫Pf/Pv组合检测相对于显微镜检查在埃塞俄比亚诊断恶性疟和间日疟的诊断性能。
2008年,668名到埃塞俄比亚南部翁多杰内特的两个健康中心就诊的发热患者参与了本研究。制备吉姆萨染色的薄血膜和厚血膜,并分别在100倍油镜下进行显微镜检查,以鉴定疟原虫种类并确定疟原虫血症。按照制造商的说明进行CareStart疟原虫Pf/Pv组合检测和Paracheck Pf检测。
CareStart疟原虫Pf/Pv组合检测诊断恶性疟的诊断有效性非常好,敏感性为99.4%,特异性为98%,阳性预测值为94.4%,阴性预测值为99.8%。该检测诊断间日疟的敏感性、特异性、阳性预测值和阴性预测值分别为99.4%、98.2%、94.5%和99.8%。CareStart疟原虫Pf/Pv组合检测在诊断恶性疟方面的诊断性能与Paracheck Pf检测相当(敏感性99.4%,特异性98.2%)。
尽管CareStart疟原虫Pf/Pv组合检测和Paracheck Pf检测在诊断恶性疟方面具有相当的诊断性能,但CareStart疟原虫Pf/Pv组合检测具有诊断间日疟的额外优势。因此,在像埃塞俄比亚这样无法进行显微镜检查且恶性疟和间日疟共同流行的地区,使用CareStart疟原虫Pf/Pv组合检测来诊断疟疾更可取。