支气管肺泡灌洗液中粘菌属 qPCR 在诊断肺粘液瘤病方面的性能。

IF 2.7 3区 医学 Q3 INFECTIOUS DISEASES Medical mycology Pub Date : 2024-01-27 DOI:10.1093/mmy/myae006
Xavier Brousse, Sébastien Imbert, Nahéma Issa, Edouard Forcade, Maxime Faure, Jeremy Chambord, Hanta Ramaroson, Hannah Kaminski, Pierre-Yves Dumas, Elodie Blanchard
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引用次数: 0

摘要

评估支气管肺泡液(BALF)中粘孢子菌 PCR 的常规诊断性能。这是一项单中心回顾性研究,包括2021年1月至2022年5月期间所有年龄大于18岁、在BALF中接受过粘孢子菌PCR检测的连续患者。指标检测是使用 MycoGENIE 曲霉菌属-粘菌属 PCR 进行的前瞻性检测。参照标准是评审委员会对肺粘孢子菌病的诊断。对 938 名患者的 BALF 进行了粘菌 PCR 检测,938 名患者中有 21 名(2.2%)呈阳性。诊断出 11 例肺粘孢子菌病(包括 1 例播散性肺粘孢子菌病)。根据 EORTC/MSGERC 2019 标准,其中 1 例(9.1%)被归类为已证实的粘孢子菌病,3 例(27.3%)被归类为可能的粘孢子菌病,7 例(63.6%)被归类为可能的粘孢子菌病。主要宿主因素是血液恶性肿瘤(11 例中有 10 例,占 90.9%)。8 名患者(72.7%)的血清中粘菌 PCR 呈阳性。三名患者的肺泡液 PCR 呈阳性,但血清 PCR 呈阴性。粘孢子菌病的平均周期阈值明显低于假阳性病例。灵敏度为 72.7%(95% 置信区间 [CI],43.4-90.3%),特异性为 98.6%(95% 置信区间 [CI],97.6-99.2%)。阳性和阴性预测值分别为 38.1%(95% CI,20.8-59.1%)和 99.7%(95% CI,99.1-99.9%)。BALF 中的粘孢子菌 PCR 对粘孢子菌病有良好的诊断效果,尤其是与血清 PCR 结合使用时。鉴于气道中可能存在带菌情况,对阳性结果的解释应谨慎。不过,其较高的阴性预测值和特异性表明,BALF 中的粘孢子菌 PCR 在诊断肺粘孢子菌病方面具有实用价值。
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Performance of Mucorales spp. qPCR in bronchoalveolar lavage fluid for the diagnosis of pulmonary mucormycosis.

To estimate the diagnostic performance of Mucorales polymerase chain reaction (PCR) in Bronchoalveolar lavage fluid (BALF) in routine practice. This was a single-center retrospective study including all consecutive patients >18 years who underwent Mucorales PCR assay in BALF between January 2021 and May 2022. Index testing was prospectively performed using the MycoGENIE Aspergillus spp.-Mucorales spp. PCR. The reference was the diagnosis of pulmonary mucormycosis by the Adjudication Committee. Mucorales PCR in BALF was performed for 938 patients and was positive for 21 of 938 (2.2%). Eleven pulmonary mucormycosis (including one disseminated) were diagnosed. Among them, one (9.1%) was classified as proven mucormycosis, three (27.3%) as probable, and seven (63.6%) as possible according to the EORTC/MSGERC 2019 criteria. The main host factor was hematological malignancy (10 of 11, 90.9%). Mucorales PCR was positive in serum for eight patients (72.7%). Three patients had positive PCR in BALF, but negative in serum. The mean cycle threshold value was significantly lower in mucormycosis than false-positive cases. Sensitivity was 72.7% (95% confidence interval [CI], 43.4-90.3%), and specificity was 98.6% (95% CI, 97.6-99.2%). The positive and negative predictive values were 38.1% (95% CI, 20.8-59.1%) and 99.7% (95% CI, 99.1-99.9%), respectively. Mucorales PCR in BALF showed good diagnostic performance for mucormycosis, particularly in combination with serum PCR. A positive result should be interpreted with caution, given the possibility of carriage in the airway. However, its high negative predictive value and specificity suggest the utility of Mucorales PCR in BALF in the diagnosis of pulmonary mucormycosis.

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来源期刊
Medical mycology
Medical mycology 医学-兽医学
CiteScore
5.70
自引率
3.40%
发文量
632
审稿时长
12 months
期刊介绍: Medical Mycology is a peer-reviewed international journal that focuses on original and innovative basic and applied studies, as well as learned reviews on all aspects of medical, veterinary and environmental mycology as related to disease. The objective is to present the highest quality scientific reports from throughout the world on divergent topics. These topics include the phylogeny of fungal pathogens, epidemiology and public health mycology themes, new approaches in the diagnosis and treatment of mycoses including clinical trials and guidelines, pharmacology and antifungal susceptibilities, changes in taxonomy, description of new or unusual fungi associated with human or animal disease, immunology of fungal infections, vaccinology for prevention of fungal infections, pathogenesis and virulence, and the molecular biology of pathogenic fungi in vitro and in vivo, including genomics, transcriptomics, metabolomics, and proteomics. Case reports are no longer accepted. In addition, studies of natural products showing inhibitory activity against pathogenic fungi are not accepted without chemical characterization and identification of the compounds responsible for the inhibitory activity.
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