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用于临床样本中登革热早期检测的商用登革热诊断测试的性能评估

Performance Evaluation of Commercial Dengue Diagnostic Tests for Early Detection of Dengue in Clinical Samples.

作者信息

Mat Jusoh Tuan Nur Akmalina, Shueb Rafidah Hanim

机构信息

Department of Microbiology and Department of Medical Microbiology and Parasitology, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, Kubang Kerian, Malaysia.

出版信息

J Trop Med. 2017;2017:4687182. doi: 10.1155/2017/4687182. Epub 2017 Dec 12.

Abstract

The shattering rise in dengue virus infections globally has created a need for an accurate and validated rapid diagnostic test for this virus. Rapid diagnostic test (RDT) and reverse transcription-polymerase chain reaction (RT-PCR) diagnostic detection are useful tools for diagnosis of early dengue infection. We prospectively evaluated the diagnostic performance of nonstructural 1 (NS1) RDT and real-time RT-PCR diagnostic kits in 86 patient serum samples. Thirty-six samples were positive for dengue NS1 antigen while the remaining 50 were negative when tested with enzyme-linked immunosorbent assay (ELISA). Commercially available RDTs for NS1 detection, RTK ProDetect™, and SD Bioline showed high sensitivity of 94% and 89%, respectively, compared with ELISA. GenoAmp® Trioplex Real-Time RT-PCR and RealStar® Dengue RT-PCR tests presented a comparable kappa agreement with 0.722. The result obtained from GenoAmp® Real-Time RT-PCR Dengue test showed that 14 samples harbored dengue virus type 1 (DENV-1), 8 samples harbored DENV-2, 2 samples harbored DENV-3, and 1 sample harbored DENV-4. 1 sample had a double infection with DENV-1 and DENV-2. The NS1 RDTs and real-time RT-PCR tests were found to be a useful diagnostic for early and rapid diagnosis of acute dengue and an excellent surveillance tool in our battle against dengue.

摘要

全球登革热病毒感染率急剧上升,因此需要一种针对该病毒的准确且经过验证的快速诊断测试。快速诊断测试(RDT)和逆转录聚合酶链反应(RT-PCR)诊断检测是诊断早期登革热感染的有用工具。我们前瞻性地评估了非结构蛋白1(NS1)RDT和实时RT-PCR诊断试剂盒在86份患者血清样本中的诊断性能。36份样本登革热NS1抗原呈阳性,其余50份样本用酶联免疫吸附测定(ELISA)检测时呈阴性。用于NS1检测的市售RDT,RTK ProDetect™和SD Bioline与ELISA相比,分别显示出94%和89%的高灵敏度。GenoAmp®三重实时RT-PCR和RealStar®登革热RT-PCR测试的kappa一致性相当,为0.722。GenoAmp®实时RT-PCR登革热测试结果显示,14份样本携带1型登革热病毒(DENV-1),8份样本携带DENV-2,2份样本携带DENV-3,1份样本携带DENV-4。1份样本同时感染了DENV-1和DENV-2。NS1 RDT和实时RT-PCR测试被发现是急性登革热早期快速诊断的有用诊断方法,也是我们抗击登革热斗争中的出色监测工具。

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