Hays J T, Croghan I T, Schroeder D R, Offord K P, Hurt R D, Wolter T D, Nides M A, Davidson M
Mayo Clinic, Rochester, MN 55905, USA.
Am J Public Health. 1999 Nov;89(11):1701-7. doi: 10.2105/ajph.89.11.1701.
The purpose of this study was to determine the efficacy and safety of the nicotine patch for smoking cessation in an over-the-counter environment. The years of study were 1994 to 1995.
Parallel 6-week trials were conducted: a placebo-controlled trial of no-cost 22-mg, 24-hour nicotine patch therapy and an open label trial of the same therapy with patches purchased by subjects. Participants (n = 958) were 18 years or older, had smoked at least 15 cigarettes daily for at least 6 months, and were enrolled at 3 study sites. The main outcome measure was self-reported smoking abstinence confirmed by expired carbon monoxide measurements.
Smoking cessation rates in the placebo-controlled trial were 16.8% and 9.6% at week 6 and 8.7% and 4.3% at week 24 for the active patch and placebo groups, respectively. Smoking cessation rates in the open label-pay trial were 19.0% and 10.8% at weeks 6 and 24, respectively. A slight increase in adverse cardiovascular events was noted only in the open label-pay group in comparison with the placebo group.
In an over-the-counter environment, the 22-mg, 24-hour nicotine patch is effective and safe for smoking cessation treatment.
本研究旨在确定在非处方环境下尼古丁贴片戒烟的有效性和安全性。研究时间为1994年至1995年。
进行了为期6周的平行试验:一项免费的22毫克、24小时尼古丁贴片疗法的安慰剂对照试验,以及一项受试者购买贴片进行相同疗法的开放标签试验。参与者(n = 958)年龄在18岁及以上,每天至少吸15支烟至少6个月,并在3个研究地点登记。主要结局指标是通过呼出一氧化碳测量确认的自我报告戒烟情况。
在安慰剂对照试验中,活性贴片组和安慰剂组在第6周时的戒烟率分别为16.8%和9.6%,在第24周时分别为8.7%和4.3%。在开放标签付费试验中,第6周和第24周的戒烟率分别为19.0%和10.8%。与安慰剂组相比,仅在开放标签付费组中发现不良心血管事件略有增加。
在非处方环境下,22毫克、24小时尼古丁贴片用于戒烟治疗是有效且安全的。