Anthonisen N R, Connett J E, Kiley J P, Altose M D, Bailey W C, Buist A S, Conway W A, Enright P L, Kanner R E, O'Hara P
University of Manitoba, Winnipeg.
JAMA. 1994 Nov 16;272(19):1497-505.
To determine whether a program incorporating smoking intervention and use of an inhaled bronchodilator can slow the rate of decline in forced expiratory volume in 1 second (FEV1) in smokers aged 35 to 60 years who have mild obstructive pulmonary disease.
Randomized clinical trial. Participants randomized with equal probability to one of the following groups: (1) smoking intervention plus bronchodilator, (2) smoking intervention plus placebo, or (3) no intervention.
Ten clinical centers in the United States and Canada.
A total of 5887 male and female smokers, aged 35 to 60 years, with spirometric signs of early chronic obstructive pulmonary disease.
Smoking intervention: intensive 12-session smoking cessation program combining behavior modification and use of nicotine gum, with continuing 5-year maintenance program to minimize relapse. Bronchodilator: ipratropium bromide prescribed three times daily (two puffs per time) from a metered-dose inhaler.
Rate of change and cumulative change in FEV1 over a 5-year period.
Participants in the two smoking intervention groups showed significantly smaller declines in FEV1 than did those in the control group. Most of this difference occurred during the first year following entry into the study and was attributable to smoking cessation, with those who achieved sustained smoking cessation experiencing the largest benefit. The small noncumulative benefit associated with use of the active bronchodilator vanished after the bronchodilator was discontinued at the end of the study.
An aggressive smoking intervention program significantly reduces the age-related decline in FEV1 in middle-aged smokers with mild airways obstruction. Use of an inhaled anticholinergic bronchodilator results in a relatively small improvement in FEV1 that appears to be reversed after the drug is discontinued. Use of the bronchodilator did not influence the long-term decline of FEV1.
确定一项包含吸烟干预和使用吸入性支气管扩张剂的方案能否减缓35至60岁患有轻度阻塞性肺病的吸烟者一秒用力呼气量(FEV1)的下降速率。
随机临床试验。参与者以相等概率随机分为以下几组:(1)吸烟干预加支气管扩张剂组;(2)吸烟干预加安慰剂组;或(3)无干预组。
美国和加拿大的10个临床中心。
共有5887名年龄在35至60岁之间、有早期慢性阻塞性肺病肺量计体征的男性和女性吸烟者。
吸烟干预:强化的12节戒烟课程,结合行为矫正和使用尼古丁口香糖,并持续进行5年的维持计划以尽量减少复发。支气管扩张剂:异丙托溴铵,通过定量吸入器每日给药三次(每次两喷)。
5年期间FEV1的变化率和累积变化。
两个吸烟干预组的参与者FEV1的下降幅度明显小于对照组。这种差异大部分发生在进入研究后的第一年,且归因于戒烟,实现持续戒烟的人受益最大。与使用活性支气管扩张剂相关的微小非累积益处在研究结束停用支气管扩张剂后消失。
积极的吸烟干预方案可显著降低中年轻度气道阻塞吸烟者中与年龄相关的FEV1下降。使用吸入性抗胆碱能支气管扩张剂可使FEV1有相对较小的改善,但在停药后这种改善似乎会逆转。使用支气管扩张剂并未影响FEV1的长期下降。