Fredrickson P A, Hurt R D, Lee G M, Wingender L, Croghan I T, Lauger G, Gomez-Dahl L, Offord K P
Nicotine Dependence Center, Mayo Clinic Jacksonville, Florida 32224, USA.
Psychopharmacology (Berl). 1995 Dec;122(3):215-22. doi: 10.1007/BF02246542.
Transdermal nicotine has been shown to relieve nicotine withdrawal and to double smoking cessation rates compared to placebo in clinical trials. A 21 or 22 mg/day dose provides a steady state serum nicotine that is less than obtained from smoking. Limited information is available about higher nicotine patch doses. To define better the optimal dosing of nicotine patch therapy, we undertook an open-label study to determine the safety and tolerability of 44 mg/day dose for smoking cessation in subjects smoking > or = 20 cigarettes per day. Forty smokers received 44 mg/day of transdermal nicotine for 4 weeks followed by 4 weeks of 22 mg/day. Of the 40 subjects enrolled, 38 (95%) completed the 4 weeks of 44 mg patch therapy and 36 (90%) completed the entire 8 weeks of patch therapy. Non-smokers at week 4 had a mean serum nicotine level of 23.4 +/- 11.7 ng/ml and cotinine of 152.2 +/- 87.3 ng/ml. Percent replacement was calculated by dividing the steady state level at week 4 by the baseline level while the subjects were smoking their usual number of cigarettes. Percent nicotine replacement for non-smokers at week 4 (while on 44 mg nicotine patch) averaged 158% +/- 108.4, and for cotinine was 112.0 +/- 73.8. For nicotine, 33% of non-smokers at week 4 had < or = 100% nicotine replacement and for cotinine 63% < or = 100% replacement. Biochemically confirmed point prevalence smoking cessation rates were 65% and 55% at weeks 4 and 8 of patch therapy, respectively, and self-reported smoking cessation at 3 months was 50%. The most common effect was skin irritation at the patch site. A single subject was admitted for myocardial infarction following step-down from 44 to 22 mg of replacement nicotine. The subject was not smoking and the adverse event was deemed to be not related to the patch therapy. Sleep complaints were reported in 33% of subjects during the 44 mg phase. Other complaints were infrequent. We conclude that 44 mg per 24-h nicotine patch therapy in heavy smokers is safe, tolerable, and without significant adverse events.
在临床试验中,经皮尼古丁已被证明可缓解尼古丁戒断症状,且与安慰剂相比,戒烟成功率可提高一倍。21或22毫克/天的剂量可使血清尼古丁达到稳态水平,且低于吸烟所获得的水平。关于更高剂量尼古丁贴片的信息有限。为了更好地确定尼古丁贴片疗法的最佳剂量,我们进行了一项开放标签研究,以确定每天44毫克剂量用于每天吸烟≥20支的受试者戒烟的安全性和耐受性。40名吸烟者接受了4周每天44毫克的经皮尼古丁治疗,随后是4周每天22毫克的治疗。在入组的40名受试者中,38名(95%)完成了4周的44毫克贴片治疗,36名(90%)完成了整个8周的贴片治疗。第4周时非吸烟者的平均血清尼古丁水平为23.4±11.7纳克/毫升,可替宁水平为152.2±87.3纳克/毫升。替代百分比通过将第4周的稳态水平除以受试者按其通常吸烟量吸烟时的基线水平来计算。第4周(使用44毫克尼古丁贴片时)非吸烟者的尼古丁替代百分比平均为158%±108.4,可替宁为112.0±73.8。对于尼古丁,第4周时33%的非吸烟者尼古丁替代率≤100%,对于可替宁,63%≤100%。经生化确认的时点患病率戒烟率在贴片治疗的第4周和第8周分别为65%和55%,3个月时自我报告的戒烟率为50%。最常见的效应是贴片部位的皮肤刺激。一名受试者在从44毫克降至22毫克替代尼古丁后因心肌梗死入院。该受试者当时不吸烟,且不良事件被认为与贴片治疗无关。在44毫克阶段,33%的受试者报告有睡眠问题。其他问题较少见。我们得出结论,重度吸烟者每天24小时使用44毫克尼古丁贴片疗法是安全、可耐受的,且无明显不良事件。