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尼古丁鼻喷雾剂戒烟疗效:一项安慰剂对照双盲试验

Efficacy of a nicotine nasal spray in smoking cessation: a placebo-controlled, double-blind trial.

作者信息

Schneider N G, Olmstead R, Mody F V, Doan K, Franzon M, Jarvik M E, Steinberg C

机构信息

West LA VA Medical Center, Los Angeles, California 90073, USA.

出版信息

Addiction. 1995 Dec;90(12):1671-82. doi: 10.1046/j.1360-0443.1995.901216719.x.

Abstract

Laboratory trials have demonstrated the efficacy of nicotine replacement in smoking cessation but absolute success rates are low. For many, nicotine gum is hard to use and transdermal nicotine is slow-acting and passive. A new, faster-acting nicotine nasal spray (NNS) can provide easily self-administered relief from cigarette withdrawal. The NNS was tested for safety and efficacy in smoking cessation. Two hundred and fifty-five smokers were randomized to NNS or a piperine placebo. Drug use was limited to 8-32 doses/day for 6 months. Subjects were tested while smoking and at post-cessation daily (week 1) with follow-up at weeks 2, 3, 6 and at 3 months, 6 months and 1 year. Continuous abstinence analyses (CO < or = 8 ppm; no slips) showed that NNS significantly enhanced success rates over placebo overall (p < 0.001) and at all test intervals. Differences at key intervals between active and placebo were: 63% vs. 40% (day 5), 51% vs. 30% (week 3), 43% vs. 20% (6 weeks), 34% vs. 13% (3 months), 25% vs. 10% (6 months) and 18% vs. 8% (1 year). Side effects were common but tolerable. Cotinine measures showed that replacement of nicotine approximated 30% of smoking levels. Hazard functions revealed relapse risks peaked at day 1, day 5 and 3 weeks for strict abstinence. It is concluded NNS is safe, efficacious and a viable alternative treatment for smoking cessation.

摘要

实验室试验已证明尼古丁替代疗法在戒烟方面的有效性,但绝对成功率较低。对许多人来说,尼古丁口香糖使用起来很困难,而经皮尼古丁起效缓慢且作用被动。一种新型、起效更快的尼古丁鼻喷雾剂(NNS)可以为戒烟者提供易于自我给药的缓解。对NNS进行了戒烟安全性和有效性测试。255名吸烟者被随机分为NNS组或胡椒碱安慰剂组。药物使用限制为每天8 - 32剂,持续6个月。在吸烟时以及戒烟后每天(第1周)对受试者进行测试,并在第2、3、6周以及3个月、6个月和1年进行随访。持续戒烟分析(一氧化碳含量≤8 ppm;无复吸)表明,总体而言,NNS比安慰剂显著提高了成功率(p < 0.001),并且在所有测试间隔均如此。活性药物组与安慰剂组在关键间隔的差异为:第5天,63%对40%;第3周,51%对30%;第6周,43%对20%;3个月,34%对13%;6个月,25%对10%;1年,18%对8%。副作用常见但可耐受。可替宁测量结果显示,尼古丁替代量约为吸烟量的30%。风险函数显示,严格戒烟的复发风险在第1天、第5天和第3周达到峰值。结论是,NNS安全、有效,是一种可行的戒烟替代治疗方法。

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