Mohammed Hussein, Kassa Moges, Kebede Amha, Endeshaw Tekola
Ethiopian Health and Nutrition Research Institute P. O. Box. 1242, Addis Ababa.
Ethiop J Health Sci. 2012 Jul;22(2):93-8.
Malaria is a major cause of morbidity and mortality in Ethiopia. Rapid diagnostic tests such as Paracheck Pf are the major tools for falciparum malaria diagnosis as an alternative to microscopy in peripheral health facilities. The objective of this study was to evaluate the sensitivity and specificity of Paracheck Pf against microscopy for diagnosis of P.falciparum infection and observe the persistence of the antigen for an elongated period.
Cross sectional study was undertaken in Arbaminch Zuria at Shele health center from October 2008 to January 2009. Paracheck-Pf versus microscopy comparison was done in conjunction with an artemisinin-based combination therapy efficacy monitoring for a period of 28 days. Standard microscopic procedures were done by experienced laboratory technicians and paracheck-Pf was performed in accordance with the manufacturer's instruction.
out of 1293 examined blood films, 400(31%) were found to be malaria positive. Considering microscopy as the gold standard, paracheck-pf showed sensitivity of 94.1 %( 95%CI: 89.9-98.3%) and specificity of 80.0% (95%CI: 67.6-92.4%). The positive and negative predictive values were 93.3 %( 95%CI: 88.8-97.8%) and 82.1% (95%CI: 70-94.1%), respectively. Comparing microscopy results 98.7 % (79/80), 60% (48/80), 48.1% (37/77), and 44.6 %( 33/74) were also found to be positive by paracheck-pf at days7, 14, 21, and 28, respectively.
Paracheck Pf® has a comparable diagnostic performance in detecting P. falciparum infections through the persistence of frequent false positivity is a limitation. Thus, this diagnostic test is not appropriate for monitoring of treatment effect.
疟疾是埃塞俄比亚发病和死亡的主要原因。像Paracheck Pf这样的快速诊断测试是外周医疗机构中作为显微镜检查替代方法用于恶性疟原虫疟疾诊断的主要工具。本研究的目的是评估Paracheck Pf相对于显微镜检查诊断恶性疟原虫感染的敏感性和特异性,并观察抗原的长期持续性。
2008年10月至2009年1月在阿巴明奇祖里亚的谢勒健康中心进行了横断面研究。Paracheck-Pf与显微镜检查的比较是结合基于青蒿素的联合疗法疗效监测进行的,为期28天。标准显微镜检查程序由经验丰富的实验室技术人员进行,Paracheck-Pf按照制造商的说明进行操作。
在1293份检查的血片中,400份(31%)被发现疟疾呈阳性。以显微镜检查为金标准,Paracheck-pf的敏感性为94.1%(95%CI:89.9 - 98.3%),特异性为80.0%(95%CI:67.6 - 92.4%)。阳性和阴性预测值分别为93.3%(95%CI:88.8 - 97.8%)和82.1%(95%CI:70 - 94.1%)。比较显微镜检查结果,在第7天、14天、21天和28天,Paracheck-pf也分别有98.7%(79/80)、60%(48/80)、48.1%(37/77)和44.6%(33/74)呈阳性。
Paracheck Pf®在检测恶性疟原虫感染方面具有可比的诊断性能,但频繁出现假阳性的持续性是一个局限性。因此,这种诊断测试不适用于监测治疗效果。