Victorian Infectious Diseases Reference Laboratory, Parkville, Vic, Australia; Department of Infectious Diseases, Perth Children's Hospital, Nedlands, WA, Australia.
Department of Infectious Diseases, Perth Children's Hospital, Nedlands, WA, Australia.
Pathology. 2020 Apr;52(3):370-372. doi: 10.1016/j.pathol.2020.01.438. Epub 2020 Feb 24.
Investigating fever in the returned traveller can be difficult and costly. Dengue is one of the most frequently reported aetiologies. NS1 is a non-structural dengue virus protein detectable during acute infection. The aim of this report is to describe the utility of the Platelia Dengue NS1 antigen enzyme immunoassay (EIA) for detection of dengue in a non-endemic region compared to a composite gold standard of contemporaneous molecular testing and seroconversion. We performed a retrospective analysis of all dengue serology tests from 6 February 2012 to 5 December 2018. Dengue serology and in-house flavivirus molecular results were identified using the laboratory information management system. Dengue serology was performed using the Bio-Rad Platelia Dengue NS1 antigen EIA, and Abbott Panbio Dengue IgG and IgM EIA. True positive NS1 result was defined as positive molecular test within one week of the positive NS1 result or seroconversion within 120 days. NS1 negative samples that remained negative to all dengue markers on repeat more than 10 and up to 120 days after were labelled as true negatives. More than 75% of cases had a serology pattern consistent with primary dengue. Sensitivity and specificity of NS1 Ag EIA was 96.4% (95% CI 92.3-98.7%) and 98.4% (95% CI 94.5-99.8%), respectively. Performance was poorer in serotype 4 infections (sensitivity 50%). Platelia Dengue NS1 antigen EIA test performance in the returned traveller cohort fulfils the remit as a single diagnostic test for acute dengue infection.
对旅行者归来后的发热进行调查可能较为困难且代价高昂。登革热是最常报告的病因之一。NS1 是非结构的登革热病毒蛋白,可在急性感染期间检测到。本报告的目的是描述在非流行地区,与同时进行的分子检测和血清转换的综合金标准相比,Platelia Dengue NS1 抗原酶免疫分析(EIA)检测登革热的效用。我们对 2012 年 2 月 6 日至 2018 年 12 月 5 日所有登革热血清学检测进行了回顾性分析。使用实验室信息管理系统确定登革热血清学和内部黄病毒分子检测结果。登革热血清学采用伯乐 Platelia Dengue NS1 抗原 EIA 法和雅培 Panbio Dengue IgG 和 IgM EIA 法进行检测。真正的 NS1 阳性结果定义为在 NS1 阳性结果的一周内分子检测阳性或在 120 天内血清转换。NS1 阴性样本在重复检测中仍为所有登革热标志物阴性,且在 10 天至 120 天后为阴性,则标记为真正阴性。超过 75%的病例具有与原发性登革热一致的血清学模式。NS1 Ag EIA 的敏感性和特异性分别为 96.4%(95%CI 92.3-98.7%)和 98.4%(95%CI 94.5-99.8%)。4 型血清型感染的性能较差(敏感性 50%)。Platelia Dengue NS1 抗原 EIA 试验在旅行者归来者队列中的性能符合急性登革热感染的单一诊断试验要求。