Sutherland G, Stapleton J A, Russell M A, Jarvis M J, Hajek P, Belcher M, Feyerabend C
Health Behaviour Unit, National Addiction Centre, London.
Lancet. 1992 Aug 8;340(8815):324-9. doi: 10.1016/0140-6736(92)91403-u.
Studies with nicotine chewing gum and nicotine skin patches indicate that nicotine replacement can help people to give up smoking. The rapidity with which nicotine is absorbed when given as a nasal spray suggests that it might be effective for those for whom the other means of replacement are too slow. The efficacy and safety of a nasal nicotine spray as an adjunct to group treatment for stopping smoking were assessed in a randomised, double-blind, placebo-controlled trial in which 227 cigarette smokers attending the Maudsley Hospital Smokers Clinic received 4 weeks of supportive group treatment plus active nicotine (0.5 mg per shot) or placebo nasal spray. The main end-point was biochemically validated complete abstinence from smoking from the third week of group treatment until the 12-month follow-up. Side-effects were assessed by self-reports and, where necessary, by physical examination. Of subjects assigned to active treatment 26% (n = 30) were validated abstinent throughout the year, compared with 10% (n = 11) of those assigned to placebo (relative abstinence rate 2.6, 95% CI 1.5-4.5, p less than 0.001). The advantage of the active spray was greatest in the heaviest smokers. Plasma nicotine concentrations from the spray were typically between one-half and three-quarters of baseline smoking levels. Tobacco-withdrawal symptoms, craving for cigarettes, and weight gain in abstinent subjects were reduced by the active spray. Minor irritant side-effects were frequent in both active and placebo sprays, but only 2 subjects had the spray discontinued as a result. No serious adverse effects were encountered. Nasal nicotine spray combined with supportive group treatment is an effective aid to smoking cessation.
对尼古丁口香糖和尼古丁透皮贴剂的研究表明,尼古丁替代疗法有助于人们戒烟。以鼻喷雾剂形式给药时,尼古丁的吸收速度很快,这表明它可能对其他替代方法效果过慢的人群有效。在一项随机、双盲、安慰剂对照试验中,评估了鼻用尼古丁喷雾剂作为戒烟群体治疗辅助手段的疗效和安全性。在该试验中,227名前往莫兹利医院吸烟者诊所就诊的吸烟者接受了为期4周的支持性群体治疗,并同时使用活性尼古丁(每次注射0.5毫克)或安慰剂鼻喷雾剂。主要终点是经生化验证,从群体治疗第三周直至为期12个月的随访期间完全戒烟。通过自我报告评估副作用,必要时进行体格检查。在接受活性治疗的受试者中,26%(n = 30)在全年经证实成功戒烟,而接受安慰剂治疗的受试者中这一比例为10%(n = 11)(相对戒烟率2.6,95%可信区间1.5 - 4.5,p < 0.001)。活性喷雾剂的优势在吸烟量最大的人群中最为明显。喷雾剂产生的血浆尼古丁浓度通常在基线吸烟水平的二分之一至四分之三之间。活性喷雾剂减轻了戒烟者的烟草戒断症状、对香烟的渴望和体重增加。活性喷雾剂和安慰剂喷雾剂都经常出现轻微刺激性副作用,但只有2名受试者因此停止使用喷雾剂。未出现严重不良反应。鼻用尼古丁喷雾剂联合支持性群体治疗是戒烟的有效辅助手段。