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Rapid detection of respiratory organisms with FilmArray respiratory panel and its impact on clinical decisions in Shanghai, China, 2016‐2018

机译:电影阵列呼吸道呼吸生物的快速检测及其对上海,中国上海临床决策的影响,2016 - 2018年

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Background In this study, we evaluated the diagnostic potential and clinical impact of an automated multiplex PCR platform (the FilmArray Respiratory Panel; FA‐RP), specially designed for pathogen detection in respiratory tract infections in adults with unexplained pneumonia (UP). Methods A total of 112 UP patients in Shanghai, China, were enrolled prospectively and assessed using the FA‐RP from October 2016 to March 2018. We examined the test results and their influence on clinical decisions. Furthermore, as a control group, we retrospectively obtained the clinical data of 70 UP patients between October 2014 and March 2016 (before the FA‐RP was available). The two patient groups were compared with respect to factors, including general antimicrobial use and defined daily dose (DDD) numbers. Results Between October 2016 and March 2018, the positive rate obtained using FA‐RP for UP was 76.8%. The primary pathogens in adults with UP were Influenza A/B (47.3%, 53/112). Compared with the patients before FA‐RP was available, patients who underwent FA‐RP testing had higher rates of antiviral drug use and antibiotic de‐escalation during clinical treatment. FA‐RP significantly decreased the total DDDs of antibiotic or antifungal drugs DDDs by 7?days after admission (10.6?±?2.5 vs 14.1?±?8.8, P ?.01). Conclusions The FA‐RP is a rapid and sensitive nucleic acid amplification test method for UP diagnosis in adults. The application of FA‐RP may lead to a more accurately targeted antimicrobial treatment and reduced use of antibiotic/antifungal drugs.
机译:背景技术在本研究中,我们评估了自动多重PCR平台(Fimbarray呼吸面板; FA-RP)的诊断潜力和临床影响,专门为成人呼吸道感染的病原体检测,具有未解释的肺炎(UP)。方法对中国上海的112例患者共征收,并从2016年10月至2018年3月使用FA-RP进行评估。我们研究了测试结果及其对临床决策的影响。此外,作为对照组,我们回顾性地获得了2014年10月至2016年10月至2016年3月期间70名患者的临床资料(在FA-RP可用之前)。将两种患者组相当于因素进行比较,包括一般抗微生物使用和定义的每日剂量(DDD)数。结果2016年10月至2018年3月,使用FA-RP获得的阳性率为76.8%。含有Up的成人的主要病原体是流感A / B(47.3%,53/112)。与FA-RP之前的患者相比,接受FA-RP测试的患者在临床治疗期间具有更高的抗病毒药物使用和抗生素脱升率。在入院后7-8天(10.6?±2.5​​,14.1?±8.8,P <α.01),将抗生素或抗真菌药物DDDs的总DDDs DDDS DDDS的总DDDs DDDs DDDs的总DDDs降低结论FA-RP是一种快速敏感的核酸扩增试验方法,用于成人诊断。 FA-RP的应用可能导致更准确的靶向抗微生物治疗和减少使用抗生素/抗真菌药物。

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