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肺部健康研究中的肺量计检查:II. 个体内短期变异性的决定因素

Spirometry in the Lung Health Study: II. Determinants of short-term intraindividual variability.

作者信息

Enright P L, Connett J E, Kanner R E, Johnson L R, Lee W W

机构信息

Respiratory Sciences Center, University of Arizona, Tucson.

出版信息

Am J Respir Crit Care Med. 1995 Feb;151(2 Pt 1):406-11. doi: 10.1164/ajrccm.151.2.7842199.

DOI:10.1164/ajrccm.151.2.7842199
PMID:7842199
Abstract

The Lung Health Study (LHS) is a randomized clinical trial designed to determine whether a smoking intervention program and use of an inhaled bronchodilator (BD) can reduce the rate of decline of FEV1 in cigarette smokers with airflow limitation. During recruitment, spirometry was performed at second and third screening visits, a mean of 21 d apart. A total of 5,887 smokers, 35 to 60 yr of age and of whom 63% were men, met the study eligibility requirements. Smokers taking physician-prescribed BDs or with an FEV1 < 50% or > 90% predicted were excluded, as were those whose FEV1/FVC ratio was greater than 70%. Two inhalations of isoproterenol were given to determine BD response during the second visit. A serial dilution methacholine challenge test was done during the third visit to determine nonspecific airway reactivity. Ninety-five percent of the differences between FEV1 measured at the two visits were within 240 ml for women and within 320 ml for men (coefficients of repeatability). The best independent predictors of the mean short-term (between visit) intraindividual FEV1 variability were factors indicating intrinsic airway reactivity of the participants: bronchodilator response, methacholine reactivity, and the presence of wheezing; as well as factors influenced by the quality of spirometry testing: the difference between the highest and second highest FEV1s and peak flows during baseline spirometry, and the time to reach peak flow (PEFT).

摘要

肺部健康研究(LHS)是一项随机临床试验,旨在确定吸烟干预计划和使用吸入性支气管扩张剂(BD)是否可以降低气流受限的吸烟者中第一秒用力呼气容积(FEV1)的下降速率。在招募期间,在第二次和第三次筛查访视时进行肺功能测定,两次访视平均间隔21天。共有5887名年龄在35至60岁之间的吸烟者符合研究入选要求,其中63%为男性。正在服用医生开具的BD的吸烟者或FEV1低于预计值的50%或高于预计值的90%的吸烟者被排除,FEV1/用力肺活量(FVC)比值大于70%的吸烟者也被排除。在第二次访视期间给予两次异丙肾上腺素吸入以确定BD反应。在第三次访视期间进行系列稀释乙酰甲胆碱激发试验以确定非特异性气道反应性。两次访视时测量的FEV1差异的95%在女性中为240 ml以内,在男性中为320 ml以内(重复性系数)。个体内FEV1短期(访视间)变异性的最佳独立预测因素是表明参与者固有气道反应性的因素:支气管扩张剂反应、乙酰甲胆碱反应性和喘息的存在;以及受肺功能测定测试质量影响的因素:基线肺功能测定期间最高和第二高的FEV1与峰值流速之间的差异,以及达到峰值流速的时间(PEFT)。

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