Hjalmarson A, Franzon M, Westin A, Wiklund O
Department of Heart and Lung Disease, University of Göteborg, Sweden.
Arch Intern Med. 1994 Nov 28;154(22):2567-72.
Nicotine replacement therapies have proved to be of value in smoking cessation. However, not all smokers can use the nicotine gum or nicotine patch owing to side effects. In addition, the absorption of nicotine from these formulas is slow compared with smoking. A nicotine nasal spray delivers nicotine more rapidly. The objective of this study was to evaluate the efficacy and safety of the nicotine nasal spray for smoking cessation.
Subjects were recruited through advertisements in newspapers and among patients referred to the smoking cessation clinic at Sahlgren's Hospital, Göteborg, Sweden. Two hundred forty-eight smokers were treated in small groups with eight counseling sessions over 6 weeks. At their first group session, subjects were randomized to a group receiving nicotine spray (n = 125), 0.5 mg of nicotine per single spray, or to a placebo group (n = 123). The procedure was double blind. Success rates were measured up to 12 months. The nonsmoking status was verified by expired carbon monoxide less than 10 ppm.
Significantly more subjects in the nicotine group were continuously abstinent for 12 months than in the placebo group (27% vs 15%; odds ratio, 2.16; 95% confidence interval, 1.15 to 4.12). Ten of the 34 abstinent subjects in the nicotine group used the spray for 1 year. Mild or moderate side effects were rather frequent for both sprays, but they were significantly more for the nicotine spray. Subjects with high scores (> 7) on Fagerström's tolerance questionnaire had a significantly lower success rate with placebo than with the nicotine spray. For subjects with low scores, there was no difference.
Nicotine nasal spray in combination with group treatment is an effective aid to smoking cessation.
尼古丁替代疗法已被证明在戒烟方面具有价值。然而,由于副作用,并非所有吸烟者都能使用尼古丁口香糖或尼古丁贴片。此外,与吸烟相比,这些剂型中尼古丁的吸收较慢。尼古丁鼻喷雾剂能更迅速地递送尼古丁。本研究的目的是评估尼古丁鼻喷雾剂用于戒烟的疗效和安全性。
通过报纸广告以及向瑞典哥德堡萨尔格伦医院戒烟诊所转诊的患者招募受试者。248名吸烟者被分成小组接受治疗,在6周内进行8次咨询。在他们的第一次小组会议上,受试者被随机分为接受尼古丁喷雾剂组(n = 125),每次喷雾含尼古丁0.5毫克,或安慰剂组(n = 123)。该过程为双盲。测量长达12个月的成功率。通过呼出一氧化碳低于10 ppm来验证非吸烟状态。
尼古丁组持续戒烟12个月的受试者明显多于安慰剂组(27%对15%;优势比为2.16;95%置信区间为1.15至4.12)。尼古丁组34名戒烟受试者中有10人使用该喷雾剂达1年。两种喷雾剂的轻度或中度副作用都相当常见,但尼古丁喷雾剂的副作用明显更多。在法格斯特罗姆耐受问卷上得分高(> 7)的受试者,使用安慰剂的成功率明显低于使用尼古丁喷雾剂的成功率。对于得分低的受试者,没有差异。
尼古丁鼻喷雾剂联合小组治疗是戒烟的有效辅助手段。