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Rapid Laboratory Testing: Always a Good Idea?

机译:快速实验室测试:总是一个好主意吗?

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Anyone involved with infectious disease laboratory testing has heard the above refrain from physicians in the emergency room, intensive care unit, or infectious disease service. Assay manufacturers are constantly developing rapid diagnostic tests for a large variety of infectious diseases. However, an assay's speed does not always correlate with an assay's performance. Magauran et al, in this issue of Infectious Diseases in Clinical Practice, report their experience in using rapid assays for detecting influenza and respiratory syncytial virus (RSV) in their hands during a 2-year time frame. Their laboratory, at the Cleveland Clinic Foundation in Cleveland, Ohio, USA, instituted rapid enzyme immunoassay (EIA) testing for influenza and RSV in the fall of 2004. Specimens that tested negative by the rapid EIA procedures were then subjected to standard direct immunofluorescence testing for RSV and viral culture for influenza. The rapid EIA tests failed to detect 83% of direct fluorescent antibody (DFA)-positive RSV specimens and 64% of the culture-positive influenza specimens. By the end of the 2004 to 2005 season, the clinicians had stopped requesting the rapid EIA tests. Overall, the rapid EIA assays had been performed on less than 11% of the specimens submitted for influenza or RSV analysis during the 2004 to 2005 winter season.
机译:涉及传染病实验室测试的任何人都听说过上述急诊室,重症监护病房或传染病服务机构内医生的克制。化验制造商正在不断开发针对多种传染病的快速诊断测试。但是,化验的速度并不总是与化验的性能相关。 Magauran等人在本期《临床实践中的传染病》中报告了他们在2年时间内使用快速测定法检测手中的流感和呼吸道合胞病毒(RSV)的经验。他们的实验室位于美国俄亥俄州克利夫兰的克利夫兰诊所基金会,于2004年秋季对流感和RSV进行了快速酶免疫测定(EIA)测试。然后,对通过快速EIA程序呈阴性的标本进行了标准直接免疫荧光测试用于RSV,病毒培养用于流感。快速EIA测试未能检测到83%的直接荧光抗体(DFA)阳性RSV标本和64%的培养阳性流感标本。到2004年至2005年季节结束时,临床医生已停止要求进行快速EIA测试。总体而言,在2004年至2005年冬季期间,仅对不到11%提交流感或RSV分析的标本进行了快速EIA分析。

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