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尼古丁咀嚼胶的随机对照试验。

Randomised controlled trial of nicotine chewing-gum.

作者信息

Jarvis M J, Raw M, Russell M A, Feyerabend C

出版信息

Br Med J (Clin Res Ed). 1982 Aug 21;285(6341):537-40. doi: 10.1136/bmj.285.6341.537.

Abstract

The effectiveness of 2 mg nicotine chewing-gum as an aid to stopping smoking was compared with a placebo containing 1 mg nicotine, but unbuffered, in a double-blind randomised trial. Of 58 subjects given the active gum, 27 (47%) were not smoking at one-year follow-up compared with 12 (21%) of the 58 subjects treated with placebo (p less than 0.025). By the most stringent criterion of outcome, 18 (31%) subjects in the active treatment group and eight (14%) in the placebo group had not smoked at all from the start of treatment to follow-up at one year (p less than 0.05). Subjects receiving the active gum experienced less severe withdrawal symptoms and rated their gum as more helpful than did the placebo group. Minor side effects were common but only gastric symptoms were more frequent with the active gum. Subjects receiving active gum used it for longer than those receiving placebo but most stopped using it within six months and only four (7%) developed longer-term dependence. The number of gums used daily correlated significantly with pretreatment blood nicotine concentrations in the active treatment group and with pretreatment cigarette consumption in the placebo group. A lower pretreatment blood nicotine value was the best predictor of success at one year (p less than 0.001) but there was no significant relation to cigarette consumption, sex, and social class. The results clearly confirm the usefulness of nicotine chewing-gum as an aid to stopping smoking and imply a definite role for nicotine in cigarette dependence and withdrawal. Successful use of the gum requires careful attention to subjects' expectations and clear instructions on how to use it.

摘要

在一项双盲随机试验中,对2毫克尼古丁咀嚼胶作为戒烟辅助手段的有效性与含1毫克未缓冲尼古丁的安慰剂进行了比较。在接受活性口香糖的58名受试者中,27名(47%)在一年随访时不再吸烟,而接受安慰剂治疗的58名受试者中有12名(21%)不再吸烟(p<0.025)。按照最严格的结局标准,活性治疗组中有18名(31%)受试者,安慰剂组中有8名(14%)受试者从治疗开始到一年随访期间完全没有吸烟(p<0.05)。与安慰剂组相比,接受活性口香糖的受试者戒断症状较轻,且认为口香糖更有帮助。轻微副作用很常见,但只有胃肠道症状在活性口香糖组中更频繁。接受活性口香糖的受试者使用时间比接受安慰剂的受试者长,但大多数在六个月内停止使用,只有4名(7%)产生了长期依赖。活性治疗组中每日使用口香糖的数量与治疗前血液尼古丁浓度显著相关,安慰剂组中与治疗前香烟消耗量显著相关。较低的治疗前血液尼古丁值是一年成功戒烟的最佳预测指标(p<0.001),但与香烟消耗量、性别和社会阶层无显著关系。结果清楚地证实了尼古丁咀嚼胶作为戒烟辅助手段的有效性,并表明尼古丁在香烟依赖和戒断中具有明确作用。成功使用口香糖需要密切关注受试者的期望,并就如何使用提供明确指导。

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