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Rapid detection of respiratory organisms with FilmArray respiratory panel and its impact on clinical decisions in Shanghai, China, 2016-2018.
Qian, Yiyi; Ai, Jingwen; Wu, Jing; Yu, Shenglei; Cui, Peng; Gao, Yan; Jin, Jialin; Weng, Xinhua; Zhang, Wenhong.
  • Qian Y; Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.
  • Ai J; Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.
  • Wu J; Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.
  • Yu S; Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.
  • Cui P; Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.
  • Gao Y; Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.
  • Jin J; Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.
  • Weng X; Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.
  • Zhang W; Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.
Influenza Other Respir Viruses ; 14(2): 142-149, 2020 03.
Article in English | MEDLINE | ID: covidwho-830213
ABSTRACT

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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia / Respiratory Tract Infections / Multiplex Polymerase Chain Reaction Type of study: Diagnostic study / Experimental Studies / Prognostic study / Randomized controlled trials Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Asia Language: English Journal: Influenza Other Respir Viruses Journal subject: Virology Year: 2020 Document Type: Article Affiliation country: Irv.12701

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia / Respiratory Tract Infections / Multiplex Polymerase Chain Reaction Type of study: Diagnostic study / Experimental Studies / Prognostic study / Randomized controlled trials Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Asia Language: English Journal: Influenza Other Respir Viruses Journal subject: Virology Year: 2020 Document Type: Article Affiliation country: Irv.12701