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尼古丁吸入器与安非他酮用于戒烟及预防复吸的随机对照研究

Randomized comparison of a nicotine inhaler and bupropion for smoking cessation and relapse prevention.

作者信息

Croghan Ivana T, Hurt Richard D, Dakhil Shaker R, Croghan Gary A, Sloan Jeff A, Novotny Paul J, Rowland Kendrith M, Bernath Albert, Loots Mary L, Le-Lindqwister Nguyet A, Tschetter Loren K, Garneau Stewart C, Flynn Kathleen A, Ebbert Larry P, Wender Donald B, Loprinzi Charles L

机构信息

Nicotine Research Center, Mayo Clinic College of Medicine, 200 First St SW, Rochester, MN 55905, USA.

出版信息

Mayo Clin Proc. 2007 Feb;82(2):186-95. doi: 10.4065/82.2.186.

Abstract

OBJECTIVE

To compare the combination of a nicotine inhaler and bupropion to either treatment alone for initiating smoking abstinence and relapse prevention.

METHODS

Smokers were randomized to receive a nicotine inhaler, bupropion, or both for 3 months. At 3 months, smoking-abstinent study participants were randomized to their initial medications or placebo. Participants who were smoking at 3 months were randomized to an alternative treatment regimen or placebo. This study was conducted from July 2001 to January 2003.

RESULTS

A total of 1700 smokers were randomized to treatment (phase 1) for 3 months. Among the 941 study participants eligible for randomization to the phase 2 trial, 837 continued in the study. For the phase 2 trial, 405 smoking-abstinent participants were randomized to relapse prevention for 9 additional months, and 432 smokers were randomized to re-treatment for an additional 3 months. At the end of the initial 3 months of treatment (phase 1), 82 (14%) of 566, 145 (26%) of 567, and 194 (34%) of 567 study participants receiving a nicotine inhaler, bupropion, or both, respectively, were abstinent from smoking. Of the 405 smoking-abstinent participants at the end of 3 months, the bupropion group had more smokers than the placebo group (mean No. of smokers, 1.5 vs 1.1; P < .001), and the nicotine inhaler group had higher smoking abstinence rates at 12 months than the placebo group. Those receiving combination therapy had reduced rates of relapse to smoking for the first 3 months of relapse prevention, but this difference disappeared after the initial 3 months. Of the 432 study participants who were smoking at the end of 3 months and who received an alternative treatment regimen, the 223 smokers initially assigned to a nicotine inhaler were more likely to stop smoking at 6 months if they were re-treated with bupropion instead of placebo (8 [7%] of 111 vs 0 [0%] of 112; P = .003), and the 209 smokers initially treated with bupropion and re-treated with a nicotine inhaler did not have significantly higher smoking abstinence rates (6 [6%] of 104 vs 3 [3%] of 105; P = -.50).

CONCLUSION

Combined therapy with a nicotine inhaler and bupropion increased smoking abstinence rates. Continuation of the initial combination therapy does not appear to prevent relapse to smoking. Timing of re-treatment and alternative approaches to relapse prevention should be further examined.

摘要

目的

比较尼古丁吸入器与安非他酮联合使用与单独使用其中任何一种治疗方法在启动戒烟及预防复吸方面的效果。

方法

吸烟者被随机分为三组,分别接受尼古丁吸入器、安非他酮或两者联合治疗,为期3个月。3个月时,已戒烟的研究参与者被随机分配继续使用初始药物或使用安慰剂。3个月时仍在吸烟的参与者被随机分配接受替代治疗方案或安慰剂。本研究于2001年7月至2003年1月进行。

结果

共有1700名吸烟者被随机分配接受为期3个月的治疗(第一阶段)。在941名符合第二阶段试验随机分组条件的研究参与者中,837人继续参与研究。在第二阶段试验中,405名已戒烟的参与者被随机分配接受为期9个月的预防复吸治疗,432名吸烟者被随机分配接受为期3个月的再次治疗。在初始治疗的3个月结束时(第一阶段),接受尼古丁吸入器、安非他酮或两者联合治疗的566名、567名和567名研究参与者中,分别有82人(14%)、145人(26%)和194人(34%)成功戒烟。在3个月结束时的405名已戒烟参与者中,安非他酮组吸烟的人数比安慰剂组多(吸烟者平均人数分别为1.5人和1.1人;P <.001),尼古丁吸入器组在12个月时的戒烟率高于安慰剂组。接受联合治疗的参与者在预防复吸的前3个月吸烟复吸率较低,但在最初3个月后这种差异消失。在3个月结束时仍在吸烟且接受替代治疗方案的432名研究参与者中,最初被分配使用尼古丁吸入器的223名吸烟者,如果接受安非他酮再次治疗而非安慰剂,在6个月时更有可能戒烟(111人中8人[7%] vs 112人中0人[0%];P =.003),而最初接受安非他酮治疗并接受尼古丁吸入器再次治疗的209名吸烟者的戒烟率没有显著提高(104人中6人[6%] vs 105人中3人[3%];P = 0.50)。

结论

尼古丁吸入器与安非他酮联合治疗可提高戒烟率。继续使用初始联合治疗似乎无法预防吸烟复吸。应进一步研究再次治疗的时机及预防复吸的替代方法。

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