FilmArray Respiratory Panel 2.1

  • 文章类型: Case Reports
    人类偏肺病毒(hMPV)是一种呼吸道病原体,可引起免疫功能正常的成年人的下呼吸道感染和肺炎。据报道,由hMPV引起的肺炎更有可能导致支气管壁增厚和毛玻璃混浊(GGO)。一名44岁无明显病史的女性出现发热,咳嗽,和恶心。胸部计算机断层扫描显示右上叶散布的GGO,左侧舌侧和双侧下叶有空气支气管图浸润的阴影。患者入院作进一步评估。怀疑为非典型肺炎,并开始使用雷舒沙星(LSFX)。多重聚合酶链反应(PCR)使用FilmArray呼吸面板2.1在医院第2天检测hMPV。怀疑由hMPV引起的肺炎,并停用LSFX。患者随后表现出自发改善,并在入院后第6天出院。放电后,肺炎继续好转。使用多重PCR早期检测呼吸道病原体可以帮助确定合适的治疗策略。由于hMPV也会引起大叶性肺炎,在大叶性肺炎的鉴别诊断中,应考虑由hMPV引起的肺炎.
    Human metapneumovirus (hMPV) is a respiratory pathogen that can cause lower respiratory tract infections and pneumonia in immunocompetent adults. Pneumonia caused by hMPV is reportedly more likely to cause bronchial wall thickening and ground-glass opacity (GGO). A 44-year-old woman with no significant medical history developed fever, cough, and nausea. Computed tomography of the chest showed scattered GGOs in the right upper lobe and infiltrating shadows with air bronchograms in the left lingual and bilateral lower lobes. The patient was admitted to our hospital for further evaluation. Atypical pneumonia was suspected and lascufloxacin (LSFX) was started. Multiplex polymerase chain reaction (PCR) detected hMPV on hospital day 2 using the FilmArray Respiratory Panel 2.1. Pneumonia due to hMPV was suspected and LSFX was discontinued. The patient subsequently showed spontaneous improvement and was discharged on hospital day 6 after admission. After discharge, pneumonia continued to improve. Early detection of respiratory pathogens using multiplex PCR can help determine the appropriate treatment strategy. As hMPV can also cause lobar pneumonia, we should consider pneumonia due to hMPV in the differential diagnosis of lobar pneumonia.
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  • 文章类型: Journal Article
    介绍很少有关于FilmArray呼吸面板2.1(FARP)使用下呼吸道标本的有用性的报告。这项回顾性研究评估了其使用情况,作为综合传染病小组的一部分,使用免疫抑制患者的支气管肺泡灌洗样本检测肺炎的病毒原因。方法本研究纳入2021年4月1日至2022年4月30日期间接受支气管镜支气管肺泡灌洗或支气管冲洗的免疫受损患者。收集的样本已提交全面测试,包括FARP测试;巨细胞病毒的逆转录聚合酶链反应(RT-PCR),水痘-带状疱疹病毒DNA,和单纯疱疹病毒;焦氏肺孢子虫DNA的PCR;曲霉和新生隐球菌的抗原检测;军团菌的环介导等温扩增方法。结果23例患者中,16例(70%)在计算机断层扫描上显示双侧浸润阴影,3例(13%)插管。免疫抑制的最常见原因是使用抗癌药物(n=12,52%)和血液肿瘤(n=11,48%)。只有两名(9%)患者通过FARP检测出严重急性呼吸综合征冠状病毒2和腺病毒呈阳性。4名患者(17%)通过RT-PCR检测巨细胞病毒阳性,但细胞学上没有发现包涵体。9名(39%)患者通过PCR检测出jirovecii肺孢子虫阳性,但细胞学只证实了一例.结论传染病综合检测,使用从免疫抑制患者的肺部病变收集的支气管肺泡灌洗样本进行,FARP检测呈低阳性。目前通过FARP可检测到的病毒可能较少涉及在免疫受损患者中诊断的病毒性肺炎。
    Introduction Reports are rare on the usefulness of the FilmArray Respiratory Panel 2.1 (FARP) using lower respiratory tract specimens. This retrospective study assessed its use, as part of a comprehensive infectious disease panel, to detect the viral causes of pneumonia using bronchoalveolar lavage samples from immunosuppressed patients. Methods This study included immunocompromised patients who underwent bronchoalveolar lavage or bronchial washing by bronchoscopy between April 1, 2021, and April 30, 2022. The collected samples were submitted for comprehensive testing, including FARP test; reverse transcription polymerase chain reaction (RT-PCR) for cytomegalovirus, varicella-zoster virus DNA, and herpes simplex virus; PCR for Pneumocystis jirovecii DNA; antigen testing for Aspergillus and Cryptococcus neoformans; and loop-mediated isothermal amplification method for Legionella. Results Out of 23 patients, 16 (70%) showed bilateral infiltrative shadows on computed tomography and three (13%) were intubated. The most common causes of immunosuppression were anticancer drug use (n=12, 52%) and hematologic tumors (n=11, 48%). Only two (9%) patients tested positive for severe acute respiratory syndrome coronavirus 2 and adenovirus by FARP. Four patients (17%) tested positive for cytomegalovirus by RT-PCR, but no inclusion bodies were identified cytologically. Nine (39%) patients tested positive for Pneumocystis jirovecii by PCR, but cytology confirmed the organism in only one case. Conclusions Comprehensive infectious disease testing, performed using bronchoalveolar lavage samples collected from lung lesions in immunosuppressed patients, showed low positive detection by FARP. The viruses currently detectable by FARP may be less involved in viral pneumonia diagnosed in immunocompromised patients.
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  • 文章类型: Journal Article
    UNASSIGNED:我们的目的是使用多重PCR检测方法,调查日本一家急性护理医院在COVID-19大流行期间按季节和年龄划分的呼吸道感染流行病学。
    UNASSIGNED:我们使用基于多重PCR的FilmArrayRespiratoryPanel2.1(bioMérieux),在奈良县综合医学中心的有呼吸道症状的门诊患者标本中检测到21种病原体。
    未经批准:在3177个案例中,1215人(38.2%)感染了至少一种致病病毒,检测到1641种病毒。检测到的最常见病毒是人鼻病毒/肠道病毒(n=655)和严重急性呼吸道综合症冠状病毒2(SARS-CoV-2)(n=264)。此外,这些病例中有321例(10.1%)感染了两种或多种重叠病毒。SARS-CoV-2和其他病毒共同感染23例。在2020年12月至2021年3月的冬季,检测到的病毒数量相对较低,其次是人类鼻病毒/肠道病毒的激增,呼吸道合胞病毒(RSV),和副流感3型在2021年春季和夏季。虽然人类鼻病毒/肠病毒的数量在2021年夏季之后仍然相对较高,自2021年9月以来检测到的其他病毒数量较低。2021年12月后,SARS-CoV-2的数量迅速增加。
    UNASSIGNED:持续监测呼吸道感染的流行病学对于了解COVID-19大流行的长期影响很重要。
    UNASSIGNED: We aimed to investigate the epidemiology of respiratory infections by season and age during the COVID-19 pandemic in a Japanese acute care hospital using multiplex PCR testing.
    UNASSIGNED: We detected 21 pathogens in specimens from outpatients with respiratory symptoms at the Nara Prefecture General Medical Center using the multiplex PCR-based FilmArray Respiratory Panel 2.1 (bioMérieux).
    UNASSIGNED: Of the 3177 cases, 1215 (38.2%) were infected with at least one causative virus, and 1641 viruses were detected. The most common viruses detected were human rhinovirus/enterovirus (n = 655) and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (n = 264). Additionally, 321 (10.1%) of these cases were infected with two or more overlapping viruses. There were 23 cases of co-infection with SARS-CoV-2 and other viruses. In the winter months from December 2020 to March 2021, the number of detected viruses was relatively low, followed by the surge of human rhinovirus/enterovirus, respiratory syncytial virus (RSV), and parainfluenza type 3 in the spring and summer of 2021. While the number of human rhinovirus/entero-virus remained relatively high after the 2021 summer, the number of other viruses detected since September 2021 was low. After December 2021, the number of SARS-CoV-2 increased rapidly.
    UNASSIGNED: Continuous monitoring of the epidemiology of respiratory infection is important to understand the prolonged impact of the COVID-19 pandemic.
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