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Emerging point of care tests for influenza: innovation or status quo

机译:流感的新兴护理点测试:创新还是现状

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摘要

Please cite this paper as: Tayo A et al. (2012) Emerging point of care tests for influenza: innovation or status quo. Influenza and Other Respiratory Viruses 6(4), 291–298. >Background  Point of care tests (POCTs) for influenza potentially offer earlier diagnosis, enabling specific treatment, infection control measures and greater patient convenience and satisfaction. Current POCTs have limited sensitivity, some cannot distinguish influenza types, none differentiate subtypes and are relatively expensive. >Aims  To identify and characterise influenza POCTs expected to be available for clinical use in the UK by mid‐2013, highlighting those with potential benefits over existing tests. >Methods  Potential developers of influenza POCTs were identified through known manufacturers’ websites, Medical Technology trade associations, the EuroScan International Network, an expert advisory group and by searching relevant online sources. Identified companies were asked to provide standard information on relevant technologies. >Results  Fifty‐six companies were identified, and 29 (52%) responded, identifying 57 potentially relevant technologies. Of these, 40 (70%) were already available or had undetermined status and 5 (9%) were excluded as time to results took over 60 minutes. Of the remaining 12 emerging POCTs, 10 (83%) reportedly enabled differentiation of influenza types and eight differentiation of A subtypes. Nasopharyngeal swabs were the most commonly acceptable sample type; the sample volume ranging from 80 μl to 1·4 ml. >Discussion  Most identified emerging influenza POCTs offered differentiation of influenza type and subtype. Tests claiming this capability include several incorporating reverse transcription polymerase chain reaction assays; though, these also had the longest time to result. However, whilst some identified POCTs exhibit high sensitivity and specificity, most lack published clinical data for assessment, and the overall costs of these technologies remains largely unknown.
机译:请将此论文引用为:Tayo A等。 (2012)流感护理新兴点:创新或现状。流感和其他呼吸道病毒6(4),291–298。 >背景流感的即时检验(POCT)可能提供更早的诊断,从而可以进行特定治疗,采取感染控制措施并为患者带来更大的便利和满意度。当前的POCTs的敏感性有限,有些不能区分流感类型,不能区分亚型,而且价格相对昂贵。 >目标:确定并表征预计到2013年中旬可在英国投入临床使用的流感POCT,重点介绍与现有测试相比具有潜在优势的POCT。 >方法通过已知的制造商网站,医疗技术行业协会,EuroScan国际网络,专家咨询小组以及通过搜索相关的在线资源,确定了潜在的流感POCT开发者。要求已识别的公司提供有关技术的标准信息。 >结果已确定了56家公司,有29家(52%)答复了,确定了57种潜在相关技术。其中,有40个(70%)的状态可用或状态未定,而5个(9%)被排除在外,因为结果花费了60分钟以上。在其余的12种新兴POCT中,据报道有10种(占83%)能够区分流感类型和8种区分A亚型。鼻咽拭子是最普遍接受的样品类型。样品体积从80μl到1·4μml不等。 >讨论:大多数已鉴定的新兴流感POCT提供了流感类型和亚型的区分。声称具有这种能力的测试包括几种整合了逆转录聚合酶链反应的检测方法;但是,这些结果也有最长的时间。但是,尽管某些已鉴定的POCT具有很高的敏感性和特异性,但大多数缺乏公开的临床数据进行评估,而这些技术的总成本仍然未知。

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