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首页> 外文期刊>Mycoses: Diagnosis, therapy and prophylaxis of fungal diseases >Direct comparison of galactomannan performance in concurrent serum and bronchoalveolar lavage samples in immunocompromised patients at risk for invasive pulmonary aspergillosis
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Direct comparison of galactomannan performance in concurrent serum and bronchoalveolar lavage samples in immunocompromised patients at risk for invasive pulmonary aspergillosis

机译:直接比较存在侵袭性肺曲霉病风险的免疫功能低下患者血清和支气管肺泡灌洗液中半乳甘露聚糖的性能

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摘要

Invasive pulmonary aspergillosis (IPA) is a life-threatening infection mainly affecting immunocompromised patients. Early diagnosis is critical, but the diagnostic gold standard (histopathology and culture) is time consuming and cannot offer early confirmation of IPA. Fungal biomarkers like galactomannan (GM) are a promising extension to the diagnostic repertoire. However, it still remains under discussion if biomarker analysis from the site of the infection is superior to testing blood samples. We retrospectively evaluated the diagnostic performance of concurrent serum GM and bronchoalveolar lavage (BAL) GM (obtained within 24 h) of immunocompromised patients at high risk of IPA. Twenty-six proven/probable patients and eight patients with no IPA according to the EORTC/MSG 2008 criteria were included in this study. Sensitivity, specificity, positive predictive value, negative predictive value and diagnostic odds ratio were for BAL GM: 85%, 88%, 96%, 64% and 38.5, and for serum GM: 23%, 88%, 88%, 26% and 2.1 respectively. BAL GM proved to be significantly more sensitive for the detection of IPA compared to same-day serum GM in patients at high risk of IPA (P < 0.0001). Our data show that BAL GM testing is significantly superior to serum GM implying that diagnostic efforts should focus on specimens from the site of infection.
机译:侵袭性肺曲霉病(IPA)是威胁生命的感染,主要影响免疫功能低下的患者。早期诊断至关重要,但是诊断金标准(组织病理学和培养)非常耗时,无法早期确认IPA。像半乳甘露聚糖(GM)这样的真菌生物标记物是诊断库中有希望的扩展。但是,从感染部位进行的生物标志物分析是否优于检测血样,仍处于讨论中。我们回顾性评估了高危人群IPA并发血清GM和支气管肺泡灌洗(BAL)GM(24小时内获得)的诊断性能。根据EORTC / MSG 2008标准,本研究包括26例确诊/可能的患者和8例没有IPA的患者。 BAL GM的敏感性,特异性,阳性预测值,阴性预测值和诊断比值比分别为85%,88%,96%,64%和38.5,血清GM为23%,88%,88%,26%和2.1。与IPA高风险患者的当天血清GM相比,BAL GM被证明对IPA的检测更为敏感(P <0.0001)。我们的数据表明,BAL GM测试显着优于血清GM,这意味着诊断工作应集中在感染部位的标本上。

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