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热带地区流感 A 和 B 的快速流感诊断检测评估。

Evaluation of rapid influenza diagnostic tests for influenza A and B in the tropics.

机构信息

Department of Medical Microbiology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.

Diagnostic Virology Laboratory, University Malaya Medical Centre, Kuala Lumpur, Malaysia.

出版信息

J Med Virol. 2019 Aug;91(8):1562-1565. doi: 10.1002/jmv.25495. Epub 2019 May 14.

Abstract

Rapid diagnosis of influenza is important for early treatment and institution of control measures. In developing tropical countries such as Malaysia, influenza occurs all year round, but molecular assays and conventional techniques (such as immunofluorescence and culture) for diagnosis are not widely available. Rapid influenza diagnostic tests (RIDTs) may be useful in this setting. A total of 552 fresh respiratory specimens were assessed from patients with respiratory symptoms at a teaching hospital in Kuala Lumpur, Malaysia from November 2017 to March 2018. Two digital immunoassays (DIAs), STANDARD F Influenza A/B Fluorescence Immunoassay (STANDARD F) and Sofia Influenza A + B Fluorescence Immunoassay (Sofia) and one conventional RIDT (immunochromatographic assay), SD Bioline Influenza Ag A/B/A(H1N1) Pandemic rapid test kit (SD Bioline) were evaluated in comparison with a WHO-recommended reverse transcription quantitative PCR (RT-qPCR). Of the 552 samples, influenza A virus was detected in 47 (8.5%) and influenza B virus in 7 (1.3%). The digital immunoassays STANDARD F and Sofia had significantly higher overall sensitivity rates (71.7% and 70.6%, respectively) than the conventional RIDT SD Bioline and immunofluorescence/viral culture (55.8% and 52.8%, respectively). Sensitivity rates were higher for influenza A than influenza B, and specificity rates were uniformly high, ranging from 98% to 100%. Digital readout RIDTs can be used in tropical settings with year-round influenza if PCR is unavailable.

摘要

快速诊断流感对于早期治疗和实施控制措施非常重要。在马来西亚等热带发展中国家,流感全年都有发生,但用于诊断的分子检测和常规技术(如免疫荧光和培养)并不广泛。快速流感诊断检测(RIDT)在这种情况下可能很有用。2017 年 11 月至 2018 年 3 月,从马来西亚吉隆坡一家教学医院有呼吸道症状的患者中评估了 552 份新鲜呼吸道标本。两种数字免疫测定法(DIAs),STANDARD F 流感 A/B 荧光免疫测定法(STANDARD F)和 Sofia 流感 A+B 荧光免疫测定法(Sofia)以及一种常规 RIDT(免疫层析测定法),SD Bioline 流感 Ag A/B/A(H1N1)大流行快速检测试剂盒(SD Bioline)与世界卫生组织推荐的逆转录定量 PCR(RT-qPCR)进行了比较。在 552 个样本中,检测到 47 个(8.5%)流感 A 病毒和 7 个(1.3%)流感 B 病毒。数字免疫测定法 STANDARD F 和 Sofia 的总体敏感性率(分别为 71.7%和 70.6%)明显高于常规 RIDT SD Bioline 和免疫荧光/病毒培养(分别为 55.8%和 52.8%)。流感 A 的敏感性率高于流感 B,特异性率均很高,范围从 98%到 100%。如果无法进行 PCR,数字读取 RIDT 可在全年有流感的热带环境中使用。

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