Department of Microbiology, Armed Forces Institute of Pathology / National University of Medical Sciences, Rawalpindi, Pakistan.
J Coll Physicians Surg Pak. 2024 Sep;34(9):1024-1028. doi: 10.29271/jcpsp.2024.09.1024.
To evaluate the diagnostic accuracy of a commercial real-time polymerase chain reaction (PCR) kit targeting 18S rRNA against Giemsa-stained tissue slides in patients clinically suspected of cutaneous leishmaniasis (CL).
Cross-sectional analytical study. Place and Duration of the Study: Department of Microbiology, Armed Forces Institute of Pathology / National University of Medical Sciences, Rawalpindi, Pakistan, from July to December 2022.
Samples of skin tissue in 98 patients suspected of CL were evaluated. These samples were subjected to Giemsa-staining for microscopy and real-time PCR. Sensitivity, specificity, and accuracy of the PCR were calculated keeping Giemsa-stained tissue slide microscopy as gold standard.
Out of the 98 tissue samples, 37 were found positive for leishmaniasis on PCR while 13 were found Leishmania positive on microscopy of Giemsa-stained slides. The sensitivity, specificity, and accuracy of the PCR for the detection of Leishmania species were 100%, 71.8%, and 91.8%, respectively with 100% negative predictive value.
This study demonstrates that the commercial PCR is a reliable diagnostic test for the diagnosis of CL. The ease, rapidity, and reliability of the PCR make it a dependable tool in diagnostic repertoire of CL.
Giemsa stain, Leishmania spp., Polymerase chain reaction, Viasure.
评估针对 18S rRNA 的商业实时聚合酶链反应 (PCR) 试剂盒在临床上疑似皮肤利什曼病 (CL) 的患者中对吉姆萨染色组织切片的诊断准确性。
横断面分析研究。研究地点和时间:巴基斯坦拉瓦尔品第武装部队病理学院/国立医科大学微生物学系,2022 年 7 月至 12 月。
评估了 98 例疑似 CL 的皮肤组织样本。对这些样本进行吉姆萨染色以进行显微镜检查和实时 PCR。以吉姆萨染色组织切片显微镜检查为金标准,计算 PCR 的敏感性、特异性和准确性。
在 98 个组织样本中,37 个样本的 PCR 结果为利什曼病阳性,13 个样本的吉姆萨染色组织切片显微镜检查为利什曼原虫阳性。PCR 检测利什曼物种的敏感性、特异性和准确性分别为 100%、71.8%和 91.8%,阴性预测值为 100%。
本研究表明,商业 PCR 是一种可靠的 CL 诊断测试。PCR 的简便、快速和可靠性使其成为 CL 诊断组合中的可靠工具。
吉姆萨染色、利什曼属、聚合酶链反应、Viasure。