Bellanger Anne-Pauline, Gbaguidi-Haore Houssein, Tatoyan Natacha, Berceanu Ana, Scherer Emeline, Millon Laurence
Department of Parasitology-Mycology, Besançon University Hospital, Besançon, France.
Chrono-Environnement CNRS 6249 Research Team, Franche-Comté University, Besançon, France.
Folia Microbiol (Praha). 2018 Nov;63(6):757-761. doi: 10.1007/s12223-018-0618-z. Epub 2018 May 30.
Galactomannan antigen (GM) testing has been used for decades to screen immunocompromised patients for invasive aspergillosis (IA). Recent publications suggested that using a higher cut-off value than 0.5 in bronchoalveolar lavage fluid (BALF) could be more discriminant for hematology patients. We retrospectively analyzed the values of GM in BALF over 7 years (from 2010 to 2016). Performance indicators of the GM in BALF, according to three different cut-off values (0.5, 0.8, 1.5), were calculated using Stata 14.1. IA classification for hematology patients was based on European Organization for Research and Treatment of Cancer/Mycoses Study Group (EORTC/MSG) criteria, as defined in 2008. A number of 716 GM were performed on BALF from 2010 to 2016 (597 patients) and 66 were positive (> 0.5). Among these 597 patients, 27 IA were diagnosed, 13 with a positive GM in BALF, 9 with a negative GM in BALF, and 5 unclassified IA (ICU patients). The analysis of performance indicators, based on our local data, did not demonstrate any significant difference using a higher cut-off value of GM in BALF. This result may be explained by the local recruitment of patients and by pre-analytic variations during BALF realization.
半乳甘露聚糖抗原(GM)检测已被用于筛查免疫功能低下患者的侵袭性曲霉病(IA)数十年。最近的出版物表明,对于血液学患者,在支气管肺泡灌洗液(BALF)中使用高于0.5的临界值可能更具鉴别力。我们回顾性分析了7年(2010年至2016年)期间BALF中GM的值。使用Stata 14.1根据三个不同的临界值(0.5、0.8、1.5)计算BALF中GM的性能指标。血液学患者的IA分类基于2008年定义的欧洲癌症研究与治疗组织/真菌病研究组(EORTC/MSG)标准。2010年至2016年期间对597例患者的BALF进行了716次GM检测,其中66次呈阳性(>0.5)。在这597例患者中,诊断出27例IA,其中13例BALF中GM呈阳性,9例BALF中GM呈阴性,5例IA未分类(ICU患者)。基于我们当地数据的性能指标分析表明,在BALF中使用更高的GM临界值没有显示出任何显著差异。这一结果可能是由于当地患者的招募以及BALF采集过程中的分析前变异所致。