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儿童早期哮喘预防研究:儿童哮喘研究与教育网络的设计、基本原理及方法

The Prevention of Early Asthma in Kids study: design, rationale and methods for the Childhood Asthma Research and Education network.

作者信息

Guilbert Theresa W, Morgan Wayne J, Krawiec Marzena, Lemanske Robert F, Sorkness Chris, Szefler Stanley J, Larsen Gary, Spahn Joseph D, Zeiger Robert S, Heldt Gregory, Strunk Robert C, Bacharier Leonard B, Bloomberg Gordon R, Chinchilli Vernon M, Boehmer Susan J, Mauger Elizabeth A, Mauger David T, Taussig Lynn M, Martinez Fernando D

机构信息

Division of Pediatric Pulmonary Medicine, Arizona Respiratory Center, University of Arizona, 1501 N Campbell Avenue, PO Box 245073, Tucson, AZ 85724, USA.

出版信息

Control Clin Trials. 2004 Jun;25(3):286-310. doi: 10.1016/j.cct.2004.03.002.

Abstract

Pediatric asthma remains an important public health concern as its prevalence and cost to the health care system is rising. In order to promote innovative research in asthma therapies, the National Heart, Lung and Blood Institute created the Childhood Asthma Research and Education Network in 1999. As its first study, the steering committee of the Childhood Asthma Research and Education Network designed a randomized clinical trial to determine if persistent asthma could be prevented in children at a high risk to develop the disease. This communication presents the design of its first clinical trial, the Prevention of Asthma in Kids (PEAK) trial and the organization of the Childhood Asthma Research and Education Network that developed and implemented this trial. Studies of the natural history of asthma have shown that, in persistent asthma, the initial asthma-like symptoms and loss of lung function occur predominately during the first years of life. Therefore, in the Prevention of Asthma in Kids study, children 2 and 3 years old with a positive asthma predictive index were randomized to twice daily treatment with fluticasone 88 microg or placebo via metered-dose inhaler and Aerochamber for 2 years. The double blind treatment period was followed by a 1-year observational period. Lung function was measured by spirometry and oscillometry technique at 4-month intervals throughout the study. Bronchodilator reversibility and exhaled nitric oxide (ENO) studies were performed at the end of the treatment and observation periods. The primary outcome measure was the number of asthma-free days. Other secondary outcomes included number of exacerbations, use of asthma medications and lung function. These measures were chosen to reflect the progression of the disease from intermittent wheezing to persistent asthma and measurement of the extent of airflow limitation and airway reactivity.

摘要

小儿哮喘仍然是一个重要的公共卫生问题,因为其患病率和对医疗保健系统造成的成本正在上升。为了促进哮喘治疗方面的创新性研究,美国国立心肺血液研究所于1999年创建了儿童哮喘研究与教育网络。作为其第一项研究,儿童哮喘研究与教育网络的指导委员会设计了一项随机临床试验,以确定是否可以预防有高发病风险的儿童患持续性哮喘。本通讯介绍了其第一项临床试验——儿童哮喘预防(PEAK)试验的设计,以及开展和实施该试验的儿童哮喘研究与教育网络的组织情况。哮喘自然史研究表明,在持续性哮喘中,最初的哮喘样症状和肺功能丧失主要发生在生命的最初几年。因此,在儿童哮喘预防研究中,哮喘预测指数呈阳性的2至3岁儿童被随机分为两组,通过定量吸入器和储物罐,每天两次接受88微克氟替卡松或安慰剂治疗,为期2年。双盲治疗期之后是1年的观察期。在整个研究过程中,每隔4个月通过肺活量测定法和振荡法测量肺功能。在治疗期和观察期结束时进行支气管扩张剂可逆性和呼出一氧化氮(ENO)研究。主要结局指标是无哮喘天数。其他次要结局包括发作次数、哮喘药物使用情况和肺功能。选择这些指标是为了反映疾病从间歇性喘息发展为持续性哮喘的进程,以及测量气流受限和气道反应性的程度。

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