Mohindra Ritin, Capoor Malini R, Puri Shikha, Raheja Hitesh, Gupta Dinesh K, Gupta B, Chowdhury Ranadip
Department of Hematology, VMMC and Safdarjung Hospital, New Delhi, India.
Department of Microbiology, VMMC and Safdarjung Hospital, New Delhi, India.
Indian J Med Microbiol. 2017 Apr-Jun;35(2):237-242. doi: 10.4103/ijmm.IJMM_17_47.
Invasive aspergillosis (IA) is an increasingly common and fatal opportunistic fungal infection in patients with haematological diseases. Early diagnosis is difficult as mycological culture techniques have low sensitivity and the radiological tools have low specificity. Galactomannan enzyme immunoassay (GEI) detects galactomannan in the human serum with a reported sensitivity and specificity between 30% and 100%.
The aim of this study was to analyse the role of GEI in diagnosis of IA in patients with febrile neutropenia and to evaluate the role of GEI in the diagnosis of IA as per the revised (2008) European Organization for Research and Treatment of Cancer-Mycoses Study Group (EORTC-MSG) criteria at two different optical density (OD) cut-offs of 0.5 and 1.0.
This prospective study was conducted in Safdarjung Hospital, New Delhi, India.
GEI testing was performed in adult patients of febrile neutropenia with evidence of IA. Results at two different OD indices (ODIs) of 0.5 and 1.0 were analysed. The evaluation of the diagnostic parameter, that is, GEI was measured in terms of sensitivity, specificity and positive and negative predictive value and was validated with the revised (2008) EORTC-MSG diagnostic criteria of IA.
One hundred and eleven patients had evidence of IA, of which 79 patients were GEI positive when cut-off ODI was 0.5, whereas with cut-off ODI 1.0, 55 patients were GEI positive.
ODI of 1.0 should be considered as positive while in patients with OD between 0.5 and 1.0, repeat sampling from the patient is recommended.
侵袭性曲霉病(IA)在血液系统疾病患者中是一种日益常见且致命的机会性真菌感染。由于真菌培养技术敏感性低且放射学检查特异性低,早期诊断困难。半乳甘露聚糖酶免疫测定(GEI)可检测人血清中的半乳甘露聚糖,其报道的敏感性和特异性在30%至100%之间。
本研究旨在分析GEI在发热性中性粒细胞减少症患者IA诊断中的作用,并根据修订的(2008年)欧洲癌症研究与治疗组织-真菌病研究组(EORTC-MSG)标准,在0.5和1.0两个不同光密度(OD)临界值下评估GEI在IA诊断中的作用。
本前瞻性研究在印度新德里的萨夫达容医院进行。
对有IA证据的发热性中性粒细胞减少症成年患者进行GEI检测。分析了0.5和1.0两个不同OD指数(ODI)时的结果。根据敏感性、特异性、阳性和阴性预测值对诊断参数即GEI进行评估,并根据修订的(2008年)EORTC-MSG的IA诊断标准进行验证。
111例患者有IA证据,当ODI临界值为0.5时,79例患者GEI阳性;而当ODI临界值为1.0时,55例患者GEI阳性。
ODI为1.0时应视为阳性,而对于OD在0.5至1.0之间的患者,建议对患者重复采样。