Evaluation of the BioFire® FilmArray® Pneumonia plus Panel for Detecting Bacterial Etiological Agents of Lower Respiratory Tract Infections in an Oncologic Hospital. Comparison with Conventional Culture Method.

Polish journal of microbiology Pub Date : 2023-12-16 eCollection Date: 2023-12-01 DOI:10.33073/pjm-2023-035
Maria Teresa Szymankiewicz, Anna Szczepanska, Elzbieta Stefaniuk
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Abstract

Conventional methods used to determine pneumonia pathogens are characterized by low sensitivity and long turnaround times. Introducing new tests with better parameters in patients at higher risk of infections is highly anticipated. The results of the conventional quantitative culture method (CM) in determining the bacterial etiology of pneumonia were compared with the results of the Pneumonia plus Panel test (PNP; BioFire® Diagnostics, USA) in 79 samples of bronchoalveolar lavage (BAL). Materials were collected from 79 patients with suspected pneumonia treated in an oncologic hospital due to solid tumors. Only 16/79 BAL samples (20.3%) were true positive (TP) for bacterial etiology in CM vs. 27/79 samples (34.2%) true positive in the PNP test. The total agreement between methods of interpreting the result (positive or negative) was 84.8%. The most prevalent pathogens in both methods were Staphylococcus aureus, followed by Escherichia coli, Pseudomonas aeruginosa, and Haemophilus influenzae. The PNP test identified several respiratory pathogens that were not grown in culture. The semiquantitative value reported by the PNP test was higher than that reported by culture. The PNP test vs. combined test (PNP test and CM methods) demonstrated positive predictive value (PPV) and negative predictive value (NPV) values of 100.0% and 98.1%, and the sensitivity and specificity were 96.4% and 100.0%. The PNP test is a good tool for determining the etiology of bacterial pneumonia and may support the care of an oncologic patient. However, further large-sample studies are needed to research in strictly defined groups of oncologic patients.

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肿瘤医院检测下呼吸道感染细菌病原体的BioFire®FilmArray®肺炎加小组的评估。与传统培养方法的比较。
用于确定肺炎病原体的常规方法具有灵敏度低和周转时间长的特点。在感染风险较高的患者中引入具有更好参数的新检测备受期待。在79份支气管肺泡灌洗(BAL)样本中,将常规定量培养法(CM)确定肺炎细菌病因的结果与肺炎加小组试验(PNP;BioFire®Diagnostics,USA)的结果进行比较。材料收集自79名在肿瘤医院接受治疗的疑似肺炎实体瘤患者。在CM中,只有16/79个BAL样本(20.3%)的细菌病原学真阳性(TP),而在PNP测试中,27/79个样本(34.2%)的真阳性。解释结果的方法(阳性或阴性)之间的总一致性为84.8%。两种方法中最常见的病原体是金黄色葡萄球菌,其次是大肠杆菌、铜绿假单胞菌和流感嗜血杆菌。PNP测试确定了几种未在培养基中生长的呼吸道病原体。PNP试验所报告的半定量值高于培养所报告的值。PNP试验与联合试验(PNP试验和CM方法)的阳性预测值(PPV)和阴性预测值(NPV)分别为100.0%和98.1%,敏感性和特异性分别为96.4%和100.0%。PNP试验是确定细菌性肺炎病因的良好工具,可支持肿瘤学患者的护理。然而,还需要进一步的大样本研究来研究严格定义的肿瘤患者群体。
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