Hurt R D, Dale L C, Croghan G A, Croghan I T, Gomez-Dahl L C, Offord K P
Nicotine Dependence Center and Division of Community Internal Medicine, Mayo Clinic Rochester, Minnesota 55905, USA.
Mayo Clin Proc. 1998 Feb;73(2):118-25. doi: 10.1016/S0025-6196(11)63642-2.
To determine the extent of side effects during the initial use of nicotine nasal spray for smoking cessation.
We performed a one-sample, noncomparative, open-label evaluation of the pattern of use, side effects, relief of withdrawal symptoms, and cotinine levels with nicotine nasal spray.
Adult smokers were recruited to use the nicotine nasal spray for smoking cessation at a dosage of 1 to 2 mg/h. Subjects completed daily diaries, which included an assessment of nicotine withdrawal symptoms, previously reported irritant effects of the nicotine nasal spray, and symptoms of nicotine toxicity. A plasma cotinine level was measured at baseline and at day 7 for calculation of percentage replacement.
The mean age of the 50 study subjects was 43.7 years, 46% were women, and the mean baseline smoking rate was 28.5 cigarettes per day. We found an increase in five symptoms (runny nose, nasal irritation, throat irritation, watering eyes, and sneezing) that had been essentially absent before initiation of use of the nicotine nasal spray. All but throat irritation decreased significantly during days 0 through 7 of the study. The mean daily frequency of nicotine nasal spray use for the first week was 15.0 doses. Use of the nasal spray decreased significantly (P<0.001) during the initial 8 weeks of treatment. The mean percentage cotinine replacement for those subjects who were abstinent at day 7 was 38.6%.
Although nicotine nasal spray causes substantial irritant side effects during the first few days of use, these adverse effects decrease significantly within the first week. Despite these side effects, subjects continued to use the nicotine nasal spray and experienced a high rate of initial abstinence from smoking.
确定初次使用尼古丁鼻喷雾剂戒烟期间的副作用程度。
我们对尼古丁鼻喷雾剂的使用模式、副作用、戒断症状缓解情况及可替宁水平进行了单样本、非对照、开放标签评估。
招募成年吸烟者使用尼古丁鼻喷雾剂戒烟,剂量为1至2毫克/小时。受试者完成每日日志,内容包括对尼古丁戒断症状、先前报道的尼古丁鼻喷雾剂刺激作用以及尼古丁中毒症状的评估。在基线和第7天测量血浆可替宁水平,以计算替代百分比。
50名研究对象的平均年龄为43.7岁,46%为女性,平均基线吸烟率为每天28.5支香烟。我们发现有五种症状(流鼻涕、鼻刺激、咽喉刺激、流泪和打喷嚏)在开始使用尼古丁鼻喷雾剂前基本不存在,而使用后有所增加。在研究的第0至7天,除咽喉刺激外,其他症状均显著减轻。第一周尼古丁鼻喷雾剂的平均每日使用频率为15.0剂。在治疗的最初8周内,鼻喷雾剂的使用量显著减少(P<0.001)。在第7天戒烟的受试者,其可替宁替代的平均百分比为38.6%。
尽管尼古丁鼻喷雾剂在使用的最初几天会引起严重的刺激副作用,但这些不良反应在第一周内会显著减轻。尽管有这些副作用,受试者仍继续使用尼古丁鼻喷雾剂,且初期戒烟率较高。