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Factors influencing the diagnostic accuracy of the rapid influenza antigen detection test (RIADT): a cross-sectional study

机译:影响流感快速抗原检测试验(RIADT)诊断准确性的因素:一项横断面研究

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Objective To evaluate the diagnostic accuracy of the rapid influenza antigen detection test (RIADT) and determine which symptoms are relevant to results. Design Single-centre, cross-sectional study. Setting Primary care centre, Tokyo, Japan. Participants 82 consecutive outpatients presenting with upper respiratory symptoms and fever ≥37°C at any time from symptom onset, between December 2010 and April 2011. Main outcome measures Results of history and physical examination including age, sex, temperature, time of test from symptom onset, vaccination record and current symptoms (sore throat, arthralgia and/or myalgia, headache, chills, cough and/or throat phlegm, nasal discharge) were recorded. The RIADT and a fully automated respiratory virus nucleic acid test (Verigene Respiratory Virus Plus; VRV), the latter being the gold standard, were performed. Patients were divided into four groups: false negative (FN), RIADT? and VRV+; true positive (TP), RIADT+ and VRV+; true negative (TN), RIADT? and VRV?; and false positive, RIADT+ and VRV?. Groups were compared regarding age, sex, temperature, time of test from symptom onset, vaccination record and symptoms. Results RIADT sensitivity, specificity, positive predictive value and negative predictive value were 72.9% (95% CI 61.5% to 84.2%), 91.3% (79.7% to 102.8%), 95.6% (89.5% to 101.6%) and 56.8% (40.8% to 72.7%), respectively. Time from symptom onset to test was shorter for the FN group than the TP group (p=0.009). No significant differences were detected for the other factors assessed. Results revealed higher temperatures for FN than TN patients (p=0.043), and more FN than TN patients had chills (p=0.058). Conclusions The RIADT sensitivity was low, due to early administration of the test. In the epidemic season, the RIADT should not be used for suspected influenza until 12?h after symptom onset. A positive RIADT firmly supports the influenza diagnosis; a negative result does not confirm its absence. High fever and chills might indicate influenza, but additional tests are sometimes necessary.
机译:目的评估快速流感抗原检测试验(RIADT)的诊断准确性,并确定哪些症状与结果相关。设计单中心,横断面研究。设置初级保健中心,日本东京。参与者2010年12月至2011年4月之间,在症状出现后任何时间连续出现上呼吸道症状和发烧≥37°C的连续门诊患者82。主要结果指标病史和体格检查的结果,包括年龄,性别,体温,症状检查时间记录发病,疫苗接种记录和当前症状(喉咙痛,关节痛和/或肌痛,头痛,畏寒,咳嗽和/或喉咙痰,鼻涕)。进行了RIADT和全自动呼吸道病毒核酸测试(Verigene Respiratory Virus Plus; VRV),后者是金标准。患者分为四组:假阴性(FN),RIADT?和VRV +;真阳性(TP),RIADT +和VRV +;真阴性(TN),RIADT?和VRV?以及误报,RIADT +和VRV?比较各组的年龄,性别,体温,症状发作的时间,疫苗接种记录和症状。结果RIADT的敏感性,特异性,阳性预测值和阴性预测值分别为72.9%(95%CI 61.5%至84.2%),91.3%(79.7%至102.8%),95.6%(89.5%至101.6%)和56.8%( 40.8%至72.7%)。 FN组从症状发作到测试的时间短于TP组(p = 0.009)。对于其他评估因素,未发现显着差异。结果显示,FN的温度比TN患者更高(p = 0.043),FN的温度比TN患者更容易发冷(p = 0.058)。结论由于该试验的早期给药,RIADT敏感性较低。在流行季节,RIADT除非症状发作后12小时才用于怀疑的流感。 RIADT阳性可坚定支持流感诊断。阴性结果不能确认其不存在。高烧和发冷可能表示流行性感冒,但有时还需要进行其他检查。

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