Nakamura Tomoaki, Imai Ryosuke, Kitamura Atsushi, So Clara, Ro Shosei, Okafuji Kohei, Tomishima Yutaka, Jinta Torahiko, Nishimura Naoki
Department of Pulmonary Medicine, Thoracic Center, St. Luke's International Hospital, Tokyo, JPN.
Cureus. 2023 May 10;15(5):e38820. doi: 10.7759/cureus.38820. eCollection 2023 May.
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 DNA; antigen testing for and ; and loop-mediated isothermal amplification method for . 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 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.
关于使用下呼吸道标本的FilmArray呼吸病原体检测板2.1(FARP)的效用的报告很少见。本回顾性研究评估了其作为综合传染病检测板的一部分,用于检测免疫抑制患者支气管肺泡灌洗样本中肺炎病毒病因的情况。方法:本研究纳入了2021年4月1日至2022年4月30日期间接受支气管镜检查进行支气管肺泡灌洗或支气管冲洗的免疫功能低下患者。收集的样本被送去进行综合检测,包括FARP检测;巨细胞病毒、水痘-带状疱疹病毒DNA和单纯疱疹病毒的逆转录聚合酶链反应(RT-PCR);DNA的PCR检测;[具体病原体名称1]和[具体病原体名称]的抗原检测;以及[具体病原体名称]的环介导等温扩增法检测。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性阴影,3例(13%)需要插管。免疫抑制的最常见原因是使用抗癌药物(n = 12,52%)和血液系统肿瘤(n = 11,48%)。通过FARP检测,只有2例(9%)患者的严重急性呼吸综合征冠状病毒2和腺病毒呈阳性。4例(17%)患者通过RT-PCR检测巨细胞病毒呈阳性,但细胞学检查未发现包涵体。9例(39%)患者通过PCR检测[具体病原体名称]呈阳性,但细胞学检查仅在1例中证实有该病原体。结论:使用免疫抑制患者肺部病变采集的支气管肺泡灌洗样本进行的综合传染病检测显示,FARP的阳性检测率较低。目前FARP可检测到的病毒可能较少参与免疫功能低下患者诊断的病毒性肺炎。