Severcan Ezgi Ulusoy, Demir Esen, Gülen Figen, Bilgin Raziye Burcu Güven, Tanaç Remziye
Division of Pediatric Allergy and Immunology, Department of Pediatrics, Ege University Faculty of Medicine, İzmir, Turkey.
Department of Pediatrics, Ege University Faculty of Medicine, İzmir, Turkey.
Turk Pediatri Ars. 2020 Sep 23;55(3):251-256. doi: 10.14744/TurkPediatriArs.2019.35467. eCollection 2020.
Recurrent wheezing is a common problem in preschool children.It is classified into two groups because there can be many reasons for wheeze: typical and atypical. The aim of this study was to identify the general features of atypical wheezy children.
Three hundred two children who presented to our clinic between 2000 and 2015 for three or more wheezing attacks and were diagnosed as having an underlying disease such as bronchiectasis, foreign body aspiration, recurrent aspiration pneumonia, cystic fibrosis, bronchopulmonary dysplasia, congenital anomalies, and tuberculosis, were included in the study.
In this study, 127 (42.1%) girls and 175 (57.9%) boys were evaluated. The diagnostic distribution of the patients was as follows: bronchopulmonary dysplasia (21.9%), bronchiolitis obliterans (16.6%), bronchiectasis (14.5%), bronchiolitis obliterans + primary immunodeficiency (12.3%), cystic fibrosis (10.3%), bronchiectasis + primary immunodeficiency (7.9%), recurrent aspiration pneumonia (3.6%) and foreign body aspiration (3.3%), and other diseases (9.6%). Mosaic oligemia, bronchiectasis, atelectasis, bronchiolectasis, and small airway disease were the most distinct findings on high-resolution lung tomography. When the patients were evaluated clinically, radiologically, and according to pulmonary functions after an average period of 40 months, it was seen that 9.2% deteriorated, 33.9% regressed, and 56.7% remained stable. Presentation to hospital after the first attack occurred earlier in patients with bronchopulmonary dysplasia, bronchiolitis obliterans and bronchiolitis obliterans + primary immunodeficiency compared with patients with bronchiectasis, bronchiectasis + primary immunodeficiency, and cystic fibrosis. When presentation time and outcomes were evaluated, it was found that 63.4% of patients who presented to hospital early (0-6 months) and 7.5% of patients who presented late (after 5 years) had regression.
Recurrent wheezy children must be promptly evaluated for an underlying disease. Early diagnosis and treatment influence the prognosis.
反复喘息是学龄前儿童的常见问题。由于喘息的原因可能多种多样,故将其分为两组:典型组和非典型组。本研究的目的是确定非典型喘息儿童的一般特征。
选取2000年至2015年间到我院就诊、有三次或更多次喘息发作且被诊断患有诸如支气管扩张、异物吸入、反复吸入性肺炎、囊性纤维化、支气管肺发育不良、先天性畸形和结核病等基础疾病的302名儿童纳入研究。
本研究共评估了127名(42.1%)女孩和175名(57.9%)男孩。患者的诊断分布如下:支气管肺发育不良(21.9%)、闭塞性细支气管炎(16.6%)、支气管扩张(14.5%)、闭塞性细支气管炎+原发性免疫缺陷(12.3%)、囊性纤维化(10.3%)、支气管扩张+原发性免疫缺陷(7.9%)、反复吸入性肺炎(3.6%)和异物吸入(3.3%),以及其他疾病(9.6%)。马赛克样低灌注、支气管扩张、肺不张、细支气管扩张和小气道疾病是高分辨率肺断层扫描中最明显的表现。在平均40个月后对患者进行临床、放射学及肺功能评估时,发现9.2%的患者病情恶化,33.9%的患者病情好转,56.7%的患者病情保持稳定。与支气管扩张、支气管扩张+原发性免疫缺陷和囊性纤维化患者相比,支气管肺发育不良、闭塞性细支气管炎和闭塞性细支气管炎+原发性免疫缺陷患者首次发作后到医院就诊的时间更早。当对就诊时间和预后进行评估时,发现早期(0至6个月)到医院就诊的患者中有63.4%病情好转,晚期(5年后)到医院就诊的患者中有7.5%病情好转。
反复喘息儿童必须及时评估是否存在基础疾病。早期诊断和治疗会影响预后。