Aguiar Simone Santana, Damaceno Neiva, Forte Wilma Carvalho Neves
Setor de Pneumologia do Departamento de Pediatria e Puericultura da Irmandade da Santa Casa de Misericórdia de São Paulo, SP, Brasil.
Equipe Multidisciplinar do Serviço de Referência de Tratamento de Fibrose Cística do Setor de Pneumologia do Departamento de Pediatria e Puericultura da Irmandade da Santa Casa de Misericórdia de São Paulo, SP, Brasil.
Rev Paul Pediatr. 2017 Jul-Sep;35(3):252-257. doi: 10.1590/1984-0462/;2017;35;3;00003. Epub 2017 Jul 13.
To evaluate the results of the tests used to identify the IgE mediated sensitization to Aspergillus fumigatus in patients with cystic fibrosis.
This is a cross-sectional descriptive study with a convenience sample of 86 patients diagnosed with cystic fibrosis in the Reference Service in Cystic Fibrosis at a tertiary teaching hospital. The following tests were performed to assess the sensitization to A. fumigatus in patients with cystic fibrosis: Total serum IgE, eosinophil count, fungus detection through oropharyngeal swab or sputum culture, serum-specific IgE, and immediate-type hypersensitivity (IgE) skin tests. We compared the results of the different tests performed.
In 33 (38.4%) patients with cystic fibrosis, with ages ranging from 1 to 33 years (median of 8 years), the IgE-mediated A. fumigatus sensitization test results were: in 16 patients, there was an increase in serum-specific IgE (>0.35 kU/L); in 23, skin tests were positive; and six had sensitization in both tests. We observed two patients with eosinophilia (>1,000 eosinophils/mm3) and seven with increasing total serum IgE (>1,000 IU/mL), all of whom obtained negative results in skin tests and had no IgE increase specific to A. fumigatus. A. fumigatus was not detected in oropharyngeal swabs and/or sputum culture of any patients.
We conclude that, among the tests used to assess sensitization to A. fumigatus in cystic fibrosis patients, both serum-specific IgE and immediate-type hypersensitivity (IgE) skin tests are required. Serum eosinophilia and respiratory secretion culture were not essential in this study.
评估用于识别囊性纤维化患者中烟曲霉IgE介导致敏作用的检测结果。
这是一项横断面描述性研究,便利样本来自一家三级教学医院囊性纤维化参考服务中心确诊的86例囊性纤维化患者。进行了以下检测以评估囊性纤维化患者对烟曲霉的致敏作用:血清总IgE、嗜酸性粒细胞计数、通过口咽拭子或痰培养检测真菌、血清特异性IgE以及速发型超敏反应(IgE)皮肤试验。我们比较了所进行的不同检测的结果。
在33例(38.4%)年龄从1岁至33岁(中位数为8岁)的囊性纤维化患者中,烟曲霉IgE介导致敏试验结果如下:16例患者血清特异性IgE升高(>0.35 kU/L);23例皮肤试验呈阳性;6例在两项检测中均呈致敏状态。我们观察到2例嗜酸性粒细胞增多(>1000个嗜酸性粒细胞/mm³)以及7例血清总IgE升高(>1000 IU/mL)的患者,他们在皮肤试验中均获得阴性结果且烟曲霉特异性IgE未升高。在任何患者的口咽拭子和/或痰培养中均未检测到烟曲霉。
我们得出结论,在用于评估囊性纤维化患者对烟曲霉致敏作用的检测中,血清特异性IgE和速发型超敏反应(IgE)皮肤试验均为必需。在本研究中,血清嗜酸性粒细胞增多和呼吸道分泌物培养并非必要。