Geller D E, Kaplowitz H, Light M J, Colin A A
Division of Pediatric Pulmonology, The Nemours Children's Clinic, Orlando, FL 32806, USA.
Chest. 1999 Sep;116(3):639-46. doi: 10.1378/chest.116.3.639.
Using the large database from the Epidemiologic Study of Cystic Fibrosis (ESCF), the objectives of this study were to (1) estimate the reported prevalence of allergic bronchopulmonary aspergillosis (ABPA) in patients with cystic fibrosis (CF); (2) compare reported prevalence rates across geographic regions; (3) compare reported prevalence rates between patient subgroups based on demographic and disease characteristics; and (4) describe the ABPA group with regard to their sex, age, and disease severity.
All patients > or = 5 years of age enrolled in ESCF between December 1993 and May 1996 were eligible. Criteria for the diagnosis of ABPA were defined by the ESCF guidelines. Prevalence rates for ABPA were calculated, and potential risk factors for the diagnosis of ABPA were analyzed, including sex, age, pulmonary function, diagnosis of asthma, presence of wheeze, and positive respiratory culture for Pseudomonas.
There were 14,210 eligible patients enrolled in ESCF during this period, and ABPA was diagnosed in 281 patients (2%). Regional prevalence varied from 0.9% in the Southwest to 4.0% in the West. Increased prevalence rates occurred in female patients, the adolescent age group, and subjects with lower lung function, wheeze, asthma, and positive Pseudomonas cultures. Although most ABPA patients had evidence of airway obstruction, 10% had an FEV1 of > 100% of predicted. The rates of wheeze (17%) and asthma (30%) were lower than expected in the ABPA group.
This observational study found a reported prevalence rate of ABPA of 2% of CF patients in a large database. This rate was lower than the 5 to 15% rate reported in smaller studies, suggesting that ABPA is underdiagnosed in the CF population. There was wide regional variation in reported prevalence rates, which is unexplained at this time. The characteristics of the patients with ABPA and the epidemiologic risk factors for diagnosis of ABPA were described. Simplified diagnostic criteria were adapted for ESCF with the intent of increasing awareness of ABPA among the participants in this study.
利用囊性纤维化流行病学研究(ESCF)的大型数据库,本研究的目的是:(1)估计囊性纤维化(CF)患者中报告的变应性支气管肺曲霉病(ABPA)患病率;(2)比较不同地理区域报告的患病率;(3)比较基于人口统计学和疾病特征的患者亚组之间报告的患病率;(4)描述ABPA组患者的性别、年龄和疾病严重程度。
1993年12月至1996年5月期间纳入ESCF的所有年龄≥5岁的患者均符合条件。ABPA的诊断标准由ESCF指南定义。计算ABPA的患病率,并分析ABPA诊断的潜在危险因素,包括性别、年龄、肺功能、哮喘诊断、喘息的存在以及铜绿假单胞菌呼吸道培养阳性。
在此期间,ESCF共纳入14210例符合条件的患者,其中281例(2%)被诊断为ABPA。区域患病率从西南部的0.9%到西部的4.0%不等。女性患者、青少年年龄组以及肺功能较低、有喘息、哮喘和铜绿假单胞菌培养阳性的受试者患病率增加。虽然大多数ABPA患者有气道阻塞证据,但10%的患者FEV1超过预测值的100%。ABPA组中喘息(17%)和哮喘(30%)的发生率低于预期。
这项观察性研究在一个大型数据库中发现,CF患者中报告的ABPA患病率为2%。该患病率低于较小研究中报告的5%至15%的患病率,表明CF人群中ABPA诊断不足。报告的患病率存在广泛的区域差异,目前尚无法解释。描述了ABPA患者的特征以及ABPA诊断的流行病学危险因素。为ESCF采用了简化的诊断标准,旨在提高本研究参与者对ABPA的认识。