Department of Medicine, Mahatma Gandhi Institute of Medical Sciences, Sevagram, Maharashtra 442102, India.
Trans R Soc Trop Med Hyg. 2009 Dec;103(12):1237-44. doi: 10.1016/j.trstmh.2009.04.011. Epub 2009 May 27.
Although highly accurate rapid diagnostic tests (RDT) for Plasmodium falciparum [based on identification of histidine-rich protein-2 (PfHRP2)] have been developed, the accuracy of non-falciparum tests is relatively poor. Recently, a Plasmodium vivax-specific RDT [based on identification of species-specific lactate dehydrogenase (PvLDH)] became available, which along with PfHRP2 may improve malaria diagnosis by identifying the species correctly. A cross-sectional hospital-based study was designed to evaluate the diagnostic accuracy of FalciVax, a commercially available PfHRP2- and PvLDH-based RDT (index test), using malaria microscopy as a reference standard. All consecutive inpatients who presented with fever underwent both the index test and the reference standard. The study sample included 657 patients and the overall sensitivity and specificity of the RDT for diagnosis of any malarial species were 92.9% and 98.4%, respectively. The diagnostic accuracy estimates for correct species identification were lower (sensitivity 91.8%, specificity 96.8%). The accuracy of the PvLDH test to detect P. vivax was low (sensitivity 76.6%, specificity 98.1%).
虽然已经开发出了高度准确的恶性疟原虫 [基于检测组氨酸丰富蛋白-2 (PfHRP2)] 快速诊断检测方法(RDT),但非恶性疟原虫检测方法的准确性相对较差。最近,一种基于鉴定种特异性乳酸脱氢酶(PvLDH)的间日疟原虫 RDT [基于鉴定种特异性乳酸脱氢酶(PvLDH)] 已经问世,PfHRP2 和 PvLDH 可能会通过正确识别物种来提高疟疾诊断的准确性。本研究设计了一项基于医院的横断面研究,以评估 FalciVax 的诊断准确性,FalciVax 是一种市售的基于 PfHRP2 和 PvLDH 的 RDT(标准检测方法),并以疟疾显微镜检查作为参考标准。所有因发热而连续入院的患者均同时接受标准检测方法和参考标准检测。研究样本包括 657 名患者,该 RDT 检测所有疟原虫物种的总体敏感性和特异性分别为 92.9%和 98.4%。正确鉴定物种的诊断准确性估计值较低(敏感性 91.8%,特异性 96.8%)。检测间日疟原虫的 PvLDH 检测方法的准确性较低(敏感性 76.6%,特异性 98.1%)。