Clinical Microbiology and Infectious Diseases, Hospital General Universitario Gregorio Marañón, Madrid, Spain; Instituto de Investigación Sanitaria Hospital Gregorio Marañón, Madrid, Spain; CIBER Enfermedades Respiratorias - CIBERES (CB06/06/0058), Madrid, Spain.
Clinical Microbiology and Infectious Diseases, Hospital General Universitario Gregorio Marañón, Madrid, Spain; Instituto de Investigación Sanitaria Hospital Gregorio Marañón, Madrid, Spain; CIBER Enfermedades Respiratorias - CIBERES (CB06/06/0058), Madrid, Spain; Medicine Department, School of Medicine, Universidad Complutense de Madrid, Madrid, Spain.
Clin Microbiol Infect. 2017 Dec;23(12):1000.e1-1000.e4. doi: 10.1016/j.cmi.2017.05.006. Epub 2017 May 12.
To investigate the performance of the routine serum galactomannan (sGM) assay in the diagnosis of invasive aspergillosis (IA) in high-risk haematology patients receiving prophylaxis with micafungin.
Retrospective study including all haematological patients who received prophylaxis with micafungin during high-risk IA episodes (neutropenic patients after chemotherapy for acute myeloid leukaemia/myelodysplastic syndrome; allogeneic haematopoietic stem-cell transplantation during early neutropenic phase or graft-versus-host disease requiring high prednisone doses) and for whom at least one sGM result was available. Episodes were classified as follows: true-positive (positive GM in the context of IA), false-positive (positive GM result in patients who had no evidence of IA), true-negative (negative GM test results and no IA), or false-negative (negative GM test in the context of IA). Non-evaluable patients were excluded.
Among 146 evaluable episodes, four were true-positive in the context of probable breakthrough IA (incidence of breakthrough IA, 2.7%); 111/146 high-risk episodes (76%) were considered true-negative and 31/146 (21.2%) were considered false-positive. No false-negative episodes were detected. All but one of the false-positive episodes were detected in surveillance GM tests, leading to high-resolution CT scans in eight cases (8/31; 25.8%), all of which were negative. The positive predictive and negative predictive values of sGM for surveillance and diagnostic approaches were 3.2% (1/31) and 100% (110/110) and 75% (3/4) and 100% (1/1), respectively.
Surveillance of asymptomatic patients receiving prophylaxis with micafungin using sGM is unnecessary, because the results are either negative or false-positive. However, sGM remains useful in the diagnosis of breakthrough IA in symptomatic patients during prophylaxis.
探讨常规血清半乳甘露聚糖(sGM)检测在接受米卡芬净预防治疗的高危血液病患者侵袭性曲霉病(IA)诊断中的应用价值。
本回顾性研究纳入了所有接受米卡芬净预防治疗高危 IA 期(化疗后中性粒细胞减少的急性髓系白血病/骨髓增生异常综合征患者;异基因造血干细胞移植期间的早期中性粒细胞减少期或需要高剂量泼尼松的移植物抗宿主病患者)的血液病患者,且至少有一个 sGM 检测结果。将 IA 期分为以下几类:真阳性(IA 背景下 GM 阳性)、假阳性(IA 证据不足的 GM 阳性结果)、真阴性(GM 检测结果阴性且无 IA)和假阴性(IA 背景下 GM 检测结果阴性)。排除无法评估的患者。
在 146 例可评估的 IA 期中,有 4 例为疑似突破性 IA 的真阳性(IA 突破性发生率为 2.7%);146 例高危 IA 期中的 111 例(76%)被认为是真阴性,31 例(21.2%)被认为是假阳性。未发现假阴性病例。除了 1 例以外,所有假阳性病例均在 GM 监测检测中发现,导致 8 例患者(8/31;25.8%)进行高分辨率 CT 扫描,结果均为阴性。sGM 对监测和诊断方法的阳性预测值和阴性预测值分别为 3.2%(1/31)和 100%(110/110)以及 75%(3/4)和 100%(1/1)。
对于接受米卡芬净预防治疗的无症状患者,使用 sGM 进行监测是不必要的,因为检测结果要么为阴性,要么为假阳性。然而,sGM 在预防治疗期间有症状的患者中对突破性 IA 的诊断仍然有用。