首页> 美国卫生研究院文献>Indian Journal of Hematology Blood Transfusion >Performance of Galactomannan Antigen Beta-d-Glucan and Aspergillus-Lateral-Flow Device for the Diagnosis of Invasive Aspergillosis
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Performance of Galactomannan Antigen Beta-d-Glucan and Aspergillus-Lateral-Flow Device for the Diagnosis of Invasive Aspergillosis

机译:半乳甘露聚糖抗原β-d-葡聚糖和曲霉侧流装置在侵袭性曲霉病诊断中的性能

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摘要

Aspergillus lateral-flow device (LFD) was recently introduced as a practical tool for the diagnosis of invasive aspergillosis (IA). We investigated the performance of Aspergillus-LFD as a point-of-care test for the diagnosis of IA. Serum samples were collected twice weekly from patients who received intensive chemotherapy for acute leukemia, or recepients of allogeneic stem cell transplantation. Aspergillus galactomannan (GM) antigen, 1,3-beta-d-glucan and Aspergillus-LFD tests were carried out according to manufacturers’ recommendations. GM testing was repeated with a modified procedure which was proven to increase the sensitivity. Aspergillus-LFD was performed without applying any pretreatment procedure to allow the kit to fit as a point-of-care test. Fungal infections were categorized according to European Organization for Research and Treatment of Cancer/Invasive Fungal Infections Cooperative Group and the National Institute of Allergy and Infectious Diseases Mycoses Study Group (EORTC/MSG) criteria. A total of 75 neutropenia episodes in 64 patients were prospectively followed between February 2012 and January 2013. Probable IA was diagnosed in 11 patients, probable pulmonary fungal disease was diagnosed in one patient, and rhinocerebral aspergillosis was diagnosed in one patient. Fungemia was detected in two patients. Aspergillus-LFD was positive in serum of a patient with probable IA and in the bronchoalveolar lavage fluid of an other patient with probable IA. Aspergillus-LFD was false positive in serum of two patients. Although there was no radiological finding of IA or documented fungemia, fever resolved after empirical caspofungin therapy in one of these patients. The sensitivity of Aspergillus-LFD as a point-of-care test without any pretreatment of serum sample is low.Electronic supplementary materialThe online version of this article (doi:10.1007/s12288-016-0653-3) contains supplementary material, which is available to authorized users.
机译:最近引入曲霉侧流装置(LFD)作为诊断侵袭性曲霉病(IA)的实用工具。我们调查了曲霉LFD作为IA诊断的即时检验的性能。每周两次从接受了急性白血病强化化疗或同种异体干细胞移植受体的患者中收集血清样品。根据制造商的建议进行了半乳曲霉半乳甘露聚糖(GM)抗原,1,3-β-d-葡聚糖和Aspergillus-LFD测试。使用改进的程序重复进行GM测试,事实证明该方法可以提高灵敏度。在不应用任何预处理程序的情况下进行了曲霉-LFD试验,以使该试剂盒适合作为即时检验。真菌感染的分类根据欧洲癌症/侵袭性真菌感染研究与治疗组织和国家过敏与传染病研究所真菌病研究组(EORTC / MSG)的标准进行。在2012年2月至2013年1月之间共追踪了64例患者的75例中性粒细胞减少症发作。11例患者诊断为IA,1例诊断为肺真菌病,1例诊断为鼻脑曲霉病。在两名患者中检测到真菌病。曲霉毒素-LFD在可能患有IA的患者血清中和在另一位可能患有IA的患者的支气管肺泡灌洗液中呈阳性。两名患者的血清曲霉LFD呈假阳性。尽管没有放射学检查发现IA或有真菌感染,但其中一名患者的经验性卡泊芬净治疗后发烧消失。未对血清样品进行任何预处理的曲霉菌LFD作为即时检验的敏感性较低电子补充材料本文的在线版本(doi:10.1007 / s12288-016-0653-3)包含补充材料可供授权用户使用。

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