Moolchan Eric T, Robinson Miqun L, Ernst Monique, Cadet Jean Lud, Pickworth Wallace B, Heishman Stephen J, Schroeder Jennifer R
Teen Tobacco Addiction Research Clinic, Clinical Pharmacology and Therapeutics Research Branch, National Institute on Drug Abuse, Intramural Research Program, 5500 Nathan Shock Dr, Baltimore, Maryland 21224, USA.
Pediatrics. 2005 Apr;115(4):e407-14. doi: 10.1542/peds.2004-1894.
To determine the safety and efficacy of the nicotine patch and gum for adolescents who want to quit smoking.
Double-blind, double-dummy, randomized, 3-arm trial with a nicotine patch (21 mg), nicotine gum (2 and 4 mg), or a placebo patch and gum; all participants received cognitive-behavioral group therapy.
Inner-city, outpatient clinic on the East Coast. Subjects. Thirteen- to 17-year-old adolescents who smoked > or =10 cigarettes per day (CPD), scored > or =5 on the Fagerstrom Test of Nicotine Dependence, and were motivated to quit smoking. Intervention. Twelve weeks of nicotine patch or gum therapy with cognitive-behavioral therapy, with a follow-up visit at 6 months (3 months after the end of treatment).
Safety assessed on the basis of adverse event reports for all 3 groups, prolonged abstinence, assessed through self-report and verified with exhaled carbon monoxide (CO) levels of < or =6 ppm, in intent-to-treat analyses, and smoking reduction (CPD and thiocyanate concentrations) among trial completers.
A total of 120 participants were randomized (72% white, 70% female; age: 15.2 +/- 1.33 years; smoking: 18.8 +/- 8.56 CPD; Fagerstrom Test of Nicotine Dependence score: 7.04 +/- 1.29) from 1999 to 2003. Participants started smoking at 11.2 +/- 1.98 years of age and had been smoking daily for 2.66 +/- 1.56 years; 75% had at least 1 current psychiatric diagnosis. Mean compliance across groups was higher for the patch (mean: 78.4-82.8%) than for the gum (mean: 38.5-50.7%). Both the patch and gum were well tolerated, and adverse events were similar to those reported in adult trials. Changes in mean saliva cotinine concentrations throughout treatment were not statistically significant. Intent-to-treat analyses of all randomized participants showed CO-confirmed prolonged abstinence rates of 18% for the active-patch group, 6.5% for the active-gum group, and 2.5% for the placebo group; the difference between the active-patch and placebo arms was statistically significant. There was no significant effect of patch versus gum or gum versus placebo on cessation outcomes. Abstinence rates at the 3-month follow-up assessment were sustained but were not significantly associated with treatment group. Mean smoking rates, but not CO or thiocyanate concentrations, decreased significantly in all 3 arms but not as a function of treatment group.
Nicotine patch therapy combined with cognitive-behavioral intervention was effective, compared with placebo, for treatment of tobacco dependence among adolescent smokers. Decreases in the numbers of cigarettes smoked appeared to be offset by compensatory smoking. Additional study of nicotine gum, with enhanced instructional support, is needed to assess its efficacy among adolescent smokers.
确定尼古丁贴片和口香糖对想要戒烟的青少年的安全性和有效性。
双盲、双模拟、随机、三臂试验,使用尼古丁贴片(21毫克)、尼古丁口香糖(2毫克和4毫克)或安慰剂贴片和口香糖;所有参与者均接受认知行为团体治疗。
东海岸市中心的门诊诊所。受试者:每天吸烟≥10支、在尼古丁依赖的Fagerstrom测试中得分≥5且有戒烟意愿的13至17岁青少年。干预措施:进行为期12周的尼古丁贴片或口香糖治疗并结合认知行为疗法,在6个月时(治疗结束后3个月)进行随访。
根据所有三组的不良事件报告评估安全性;在意向性分析中,通过自我报告评估并经呼出一氧化碳(CO)水平≤6 ppm验证的长期戒烟情况;以及试验完成者中的吸烟减少情况(每日吸烟支数和硫氰酸盐浓度)。
1999年至2003年,共有120名参与者被随机分组(72%为白人,70%为女性;年龄:15.2±1.33岁;吸烟量:18.8±8.56支/日;尼古丁依赖的Fagerstrom测试得分:7.04±1.29)。参与者开始吸烟的年龄为11.2±1.98岁,每日吸烟已达2.66±1.56年;75%目前至少有一种精神疾病诊断。各组的平均依从性方面,贴片组(平均:78.4 - 82.8%)高于口香糖组(平均:38.5 - 50.7%)。贴片和口香糖耐受性均良好,并与成人试验中报告的不良事件相似。整个治疗过程中平均唾液可替宁浓度的变化无统计学意义。对所有随机分组参与者的意向性分析显示,活性贴片组经CO确认的长期戒烟率为18%,活性口香糖组为6.5%,安慰剂组为2.5%;活性贴片组与安慰剂组之间的差异具有统计学意义。贴片与口香糖或口香糖与安慰剂在戒烟结果上无显著影响。3个月随访评估时的戒烟率得以维持,但与治疗组无显著关联。所有三组的平均吸烟率均显著下降,但CO或硫氰酸盐浓度未下降,且与治疗组无关。
与安慰剂相比,尼古丁贴片疗法联合认知行为干预对青少年吸烟者的烟草依赖治疗有效。吸烟支数的减少似乎被代偿性吸烟所抵消。需要对尼古丁口香糖进行更多研究,并加强指导支持,以评估其在青少年吸烟者中的疗效。