疑似疟疾患者的快速诊断测试灵敏度调查

Gülnaz Çulha, Yusuf Önlen, Mehmet Çabalak, Tuğba Kaya, Burcu Küçükeser
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引用次数: 0

摘要

目标:截至 2010 年,土耳其已根除疟疾,但仍有输入性病例。本研究旨在比较 SD Bioline Malaria Ag Pf/Pan (SD-Pf/Pan) 和 SD Bioline Malaria Ag Pf/Pv (SD-Pf/Pv) 两种快速检测方法与显微镜检查和实时聚合酶链反应 (RT-PCR) 的诊断价值:方法:采集所有参与者的血液样本。制备厚滴涂片。在光学显微镜下检查厚滴涂片,以区分疟疾阳性/阴性。然后进行两种快速诊断测试(SD-Pf/Pan 和 SD-Pf/Pv)。从血液样本中提取 DNA 后,进行 RT-PCR 分型。数据使用 SPSS 21 统计程序进行评估:在 66 例疑似疟疾病例中,共有 30 例经显微镜和 RT-PCR 检测呈阳性。27 名患者的 SD-Pf/Pan 和 SD-Pf/Pv 检测结果均为阳性。以显微镜检测结果作为参考方法,SD-Pf/Pan 和 SD-Pf/Pv 快速诊断检测的灵敏度为 90%,特异性为 100%,阳性预测值为 100%,阴性预测值为 92.86%。在检测恶性疟原虫方面,以 RT-PCR 结果为参考方法,两种检测方法的灵敏度均为 95.65%,特异性均为 100%,PPV 均为 100%,NPV 均为 88.89%。此外,SD-Pf/Pv 检测间日疟原虫的灵敏度、特异性、PPV 和 NPV 均为 100%;SD-Pf/Pan 检测 PAN 的灵敏度为 77.78%,特异性为 61.90%,PPV 为 46.67%,NPV 为 86.67%:因此,这两种试剂盒在诊断由恶性疟原虫和间日疟原虫引起的疟疾感染时都具有较高的灵敏度和特异性。快速诊断试剂盒可安全地用于诊断,但诊断时应辅以显微镜检查和 RT-PCR 方法。
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Investigation of Sensitivity of Rapid Diagnosis Tests in Patients with Suspected Malaria

Objective: Malaria has been eradicated in Türkiye as of 2010, but there are imported cases. In this study, we aimed to compare the diagnostic value of two rapid tests; SD Bioline Malaria Ag Pf/Pan (SD-Pf/Pan) and SD Bioline Malaria Ag Pf/Pv (SD-Pf/Pv) with microscopy and real time-polymerase chain reaction (RT-PCR).

Methods: Blood samples were taken from all participants. Thick drop smears were prepared. Thick drop smears were examined for malaria positive/negative distinction under the light microscopy. Then, two rapid diagnostic tests (SD-Pf/Pan and SD-Pf/Pv) were performed. After DNA extraction from blood samples, RT-PCR was typed. The data were evaluated with SPSS 21 program of statistics.

Results: A total of 30 cases out of 66 suspected malaria cases were detected as positive with microscopy and RT-PCR. Twenty-seven patients were found positive with both SD-Pf/Pan and SD-Pf/Pv tests. Based on the microscopic results as a reference method, SD-Pf/Pan and SD-Pf/Pv rapid diagnostic tests had a 90% sensitivity, 100% specificity, 100% positive predictive value (PPV), and 92.86% negative predictive value (NPV). Based on the RT-PCR results as a reference method, for detection of P. falciparum, both tests had a 95.65% sensitivity, 100% specificity, 100% PPV, and 88.89% NPV. Moreover, while SD-Pf/Pv had a sensitivity, specificity, PPV, and NPV of 100% in detection of P. vivax; SD-Pf/Pan has a 77.78% sensitivity of, 61.90% specificity of, 46.67% PPV, and 86.67% NPV SD-Pf/Pan for detection of PAN.

Conclusion: As a result, high sensitivity and specificity were detected in both kits in the diagnosis of malaria infections caused by P. falciparum and P. vivax. Rapid diagnostic tests can be used safely in diagnosis however the diagnosis should be supported by microscopy and RT-PCR methods when they are applicable.

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来源期刊
Turkiye parazitolojii dergisi
Turkiye parazitolojii dergisi Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
48
审稿时长
15 weeks
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