首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Utility of Galactomannan Enzyme Immunoassay and (13) β-d-Glucan in Diagnosis of Invasive Fungal Infections: Low Sensitivity for Aspergillus fumigatus Infection in Hematologic Malignancy Patients
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Utility of Galactomannan Enzyme Immunoassay and (13) β-d-Glucan in Diagnosis of Invasive Fungal Infections: Low Sensitivity for Aspergillus fumigatus Infection in Hematologic Malignancy Patients

机译:半乳甘露聚糖酶免疫测定和(13)β-d-葡聚糖在侵袭性真菌感染诊断中的应用:血液恶性肿瘤患者烟曲霉感染的敏感性低

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摘要

Previous studies have reported that galactomannan (GM) enzyme immunoassay and 1,3 beta-glucan (BG) assay may be useful diagnostic tools, but their sensitivities are variable. We compared the performances of both tests. Between October 2002 and May 2005, 82 patients were prospectively monitored for 12 weeks. A total of 414 samples were tested by GM assay and 409 samples were tested by BG assay for the following four groups of patients: those with invasive aspergillosis (IA), those with other mold infections (Fusarium, scedosporium, zygomycosis, etc.), those with candidemia, and control patients. Blood samples were obtained twice on week 1 and once every other week for a total of 12 weeks. Patients in the invasive fungal infection groups had comparable risk factors. The sensitivity of the GM test was significantly higher for patients with IA due to non-fumigatus Aspergillus species than for patients with IA due to Aspergillus fumigatus (49% versus 13%; P < 0.0001) or with other mold infections (49% versus 6%; P < 0.0001). However, the sensitivity range (47% to 64%) and specificity (88%) of the BG assay were comparable among all patients tested, regardless of the infecting pathogen. The performance of GM-based diagnosis appears to be better for detecting non-fumigatus Aspergillus species. The diagnostic marker BG was shown to have a higher sensitivity than that of GM in detecting IA and other mold infections in hematologic malignancy patients.
机译:先前的研究报告称,半乳甘露聚糖(GM)酶免疫测定和1,3β-葡聚糖(BG)测定可能是有用的诊断工具,但它们的敏感性是可变的。我们比较了两个测试的性能。在2002年10月至2005年5月之间,对82例患者进行了为期12周的前瞻性监测。 GM检验共414份样品,BG检验共409份样品,用于以下四类患者:侵袭性曲霉病(IA),其他霉菌感染的患者(镰刀菌,硬皮孢子菌,合子菌等),那些有念珠菌血症的人,并控制病人。在第1周两次采集血样,每隔一周采集一次血样,共12周。侵袭性真菌感染组的患者具有可比的危险因素。非烟曲霉种类导致的IA患者的GM测试的敏感性显着高于烟曲霉种类导致的IA患者的49%对比13%(P <0.0001)或其他霉菌感染的IA患者(49%比6) %; P <0.0001)。但是,无论感染病原体如何,BG测定的灵敏度范围(47%至64%)和特异性(88%)在所有测试患者中均具有可比性。基于GM的诊断性能似乎更好地检测了非烟曲霉菌种。在血液系统恶性肿瘤患者中,诊断标记物BG在检测IA和其他霉菌感染方面比GM具有更高的敏感性。

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