Multiplex lateral flow test sensitivity and specificity in detecting influenza A, B and SARS-CoV-2 in adult patients in a UK emergency department.

IF 2.7 3区 医学 Q1 EMERGENCY MEDICINE Emergency Medicine Journal Pub Date : 2025-01-21 DOI:10.1136/emermed-2024-214177
Rahul Batra, Edward Blandford, Raghavendran Kulasegaran-Shylini, Matthias E Futschik, Abbie Bown, Matthew Catton, Hermione Conti-Frith, Alexandra Alexandridou, Rebecca Gill, Clara Milroy, Sean Harper, Holly Gettings, Maryann Noronha, Hooi-Ling Harrison, Sam Douthwaite, Gaia Nebbia, Paul E Klapper, Sarah Tunkel, Richard Vipond, Susan Hopkins, Tom Fowler
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Abstract

Background: Rapid identification of individuals with acute respiratory infections is crucial for preventing nosocomial infections. For rapid diagnosis, especially in EDs, lateral flow devices (LFDs) are a convenient, inexpensive option with a rapid turnaround. Several 'multiplex' LFDs (M-LFDs) now exist, testing for multiple pathogens from a single swab sample. We evaluated the real-world performance of M-LFD versus PCR testing in detecting influenza A, B and SARS-CoV-2) in the ED setting.

Methods: After preliminary evaluation of an M-LFD (SureScreen) with laboratory-grown virus and PCR-negative clinical samples, it was evaluated in a real-world setting at the ED of St Thomas' Hospital (London, UK) from 1 December 2022 to 21 April 2023. Eligible participants were ≥18 years of age, admitted with respiratory symptoms and received concurrent M-LFD and PCR tests. Main endpoints were sensitivity to detect influenza A/B (primary) and SARS-CoV-2 (secondary) versus PCR. The probability of a true positive in relation to viral concentration (expressed as PCR cycle threshold (Ct)) was analysed using logistic regression.

Results: In total, 808 symptomatic participants were included (49.8% female; mean age 46.9 years). Test sensitivity (95% CI) was 67.0% (56.9% to 76.1%) for influenza A (n=100), 94.1% (71.3% to 99.9%) for influenza B (n=17) and 48.2% (39.7% to 56.8%) for SARS-CoV-2 (n=141). Sensitivity for SARS-CoV-2 was significantly lower than that for influenza A and B (p=0.0057 and p=0.00088, respectively). The probability of a true positive was 98% for Ct<25 for influenza A and SARS-CoV-2 (influenza B non-evaluable). No co-infections were identified by PCR or M-LFD.

Conclusion: The real-world performance of SureScreen M-LFD was consistent with laboratory evaluation and achieved a high sensitivity for individuals with high viral concentration, most likely to be infectious. Given the representative UK population sample, results could be generalised for use in other settings.

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多重侧流试验检测英国急诊科成年患者甲型流感、乙型流感和SARS-CoV-2的敏感性和特异性
背景:快速识别急性呼吸道感染个体对于预防医院感染至关重要。为了快速诊断,特别是在急诊科,侧流装置(lfd)是一种方便、廉价、快速周转的选择。目前存在几种“多重”lfd (m - lfd),从单个拭子样本检测多种病原体。我们评估了M-LFD与PCR检测在急诊科环境中检测甲型流感、乙型流感和SARS-CoV-2的实际性能。方法:在对实验室培养的病毒和pcr阴性临床样本对M-LFD (SureScreen)进行初步评估后,于2022年12月1日至2023年4月21日在英国伦敦圣托马斯医院(St Thomas’Hospital, London, UK)的急诊室进行了实际环境评估。符合条件的参与者年龄≥18岁,有呼吸道症状,同时接受M-LFD和PCR检测。主要终点是检测流感A/B(原发性)和SARS-CoV-2(继发性)与PCR的敏感性。使用逻辑回归分析与病毒浓度相关的真阳性概率(以PCR周期阈值(Ct)表示)。结果:共纳入808名有症状的受试者(女性49.8%;平均年龄46.9岁)。A型流感(n=100)的检测灵敏度(95% CI)为67.0% (56.9% ~ 76.1%),B型流感(n=17)为94.1% (71.3% ~ 99.9%),SARS-CoV-2 (n=141)为48.2%(39.7% ~ 56.8%)。SARS-CoV-2的敏感性显著低于甲型流感和乙型流感(p=0.0057和p=0.00088)。结论:SureScreen M-LFD的实际表现与实验室评估一致,对病毒浓度高、最有可能具有传染性的个体具有很高的敏感性。鉴于具有代表性的英国人口样本,结果可以推广到其他情况下使用。
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来源期刊
Emergency Medicine Journal
Emergency Medicine Journal 医学-急救医学
CiteScore
4.40
自引率
6.50%
发文量
262
审稿时长
3-8 weeks
期刊介绍: The Emergency Medicine Journal is a leading international journal reporting developments and advances in emergency medicine and acute care. It has relevance to all specialties involved in the management of emergencies in the hospital and prehospital environment. Each issue contains editorials, reviews, original research, evidence based reviews, letters and more.
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