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FebriDx:一种用于鉴别急性呼吸道感染中细菌和病毒病因的快速诊断测试。

FebriDx: A Rapid Diagnostic Test for Differentiating Bacterial and Viral Aetiologies in Acute Respiratory Infections.

机构信息

Springer Nature, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand.

出版信息

Mol Diagn Ther. 2019 Dec;23(6):803-809. doi: 10.1007/s40291-019-00433-x.

Abstract

FebriDx is a rapid, point-of-care diagnostic test that is designed to aid in the differentiation of bacterial and viral acute respiratory infections (ARIs), thus helping to guide decisions regarding the prescription of antibiotics in the outpatient setting. FebriDx carries a CE mark for use in the EU and is also approved in several other countries, including Canada, Saudi Arabia and Singapore. It is indicated for use in patients > 2 years old with symptoms consistent with a community-acquired ARI. The test involves the use of an immunoassay on a fingerstick blood sample to provide simultaneous, qualitative measurement of elevated levels of C-reactive protein (CRP) and myxovirus resistance protein A (MxA). In two prospective, multicentre studies in patients with acute upper respiratory tract infections, FebriDx was shown to be both sensitive and specific in identifying patients with a clinically significant infection and in differentiating between infections of bacterial and viral aetiology. The test is simple, requires no additional equipment and produces actionable results in ~ 10 min. As was demonstrated in a small, retrospective analysis, FebriDx results can help guide (improve) antibiotic prescribing decisions. Reducing the unnecessary or inappropriate prescription of antibiotics for ARIs of probable viral aetiology is important for antibiotic stewardship and can also reduce the unnecessary exposure of patients to the risk of antibiotic-related adverse events. FebriDx thus represents a useful diagnostic tool in the outpatient setting.

摘要

FebriDx 是一种快速的即时诊断检测方法,旨在帮助区分细菌和病毒引起的急性呼吸道感染(ARI),从而有助于指导门诊处方抗生素的决策。FebriDx 获得了欧盟的 CE 标志,也在包括加拿大、沙特阿拉伯和新加坡在内的其他几个国家获得批准。它适用于症状符合社区获得性 ARI 的> 2 岁患者。该检测方法涉及使用手指采血进行免疫测定,以同时定性测量 C 反应蛋白(CRP)和粘病毒抗性蛋白 A(MxA)的升高水平。在两项针对急性上呼吸道感染患者的前瞻性、多中心研究中,FebriDx 被证明在识别具有临床显著感染的患者以及区分细菌和病毒病因感染方面具有敏感性和特异性。该检测方法简单,无需额外设备,大约 10 分钟即可获得可操作的结果。如小型回顾性分析所示,FebriDx 结果可帮助指导(改善)抗生素处方决策。减少对可能为病毒病因的 ARI 的不必要或不适当的抗生素处方对于抗生素管理非常重要,还可以减少患者不必要地接触抗生素相关不良反应的风险。因此,FebriDx 是门诊环境中的一种有用的诊断工具。

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