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非白人人群中戒烟药物疗法的疗效综述。

A review of the efficacy of smoking-cessation pharmacotherapies in nonwhite populations.

作者信息

Robles Gisela I, Singh-Franco Devada, Ghin Hoytin Lee

机构信息

Department of Pharmacy Practice, College of Pharmacy, Nova Southeastern University, Ft. Lauderdale, Florida 33328, USA.

出版信息

Clin Ther. 2008 May;30(5):800-12. doi: 10.1016/j.clinthera.2008.05.010.

Abstract

BACKGROUND

Cigarette smoking continues to be the leading cause of preventable morbidity and mortality in the United States. Research suggests that behavioral support strategies and pharmacotherapy can improve abstinence rates. However, both approaches, especially pharmacotherapy, have been understudied in nonwhite US populations.

OBJECTIVE

The aim of this review was to evaluate the efficacy of smoking-cessation pharmacotherapy in nonwhite US populations.

METHODS

Using search terms smoking cessation, nicotine replacement therapy, bupropion SR, varenicline, minority, ethnicity, African American, black, Hispanic, American Indian, and Alaska Native, a literature search was conducted to identify English-language studies that evaluated the use of smoking-cessation pharmacotherapies in nonwhite patients in MEDLINE (1966\2-December 2007), International Pharmaceutical Abstracts (1980\2-January 2008), Database of Abstracts of Reviews of Effectiveness (1990\2-December 2007), and EMBASE Drugs & Pharmacology (1991\2-third quarter 2007).

RESULTS

Nine studies were identified and assessed. Six studies looked at smoking-cessation pharmacotherapy in black smokers, 1 in Hispanic smokers, 1 in Native American smokers, and 1 in white and nonwhite smokers. In black smokers (N = 410; mean cigarettes per day [cpd], 20.4) who received the nicotine patch versus placebo, the 30-day self-reported abstinence rates were 21.5% versus 13.7% (P = 0.03) at 10 weeks and 17.1% versus 11.7% (P = NS) at 6 months. In black smokers (N = 600; mean [SD] cpd, 16.1 [7.5]) who received sustained-release (SR) bupropion 150 mg BID versus placebo for 7 weeks, the 7-day biochemically verified abstinence rates at weeks 6 and 26 were 36.0% versus 19.0% (Delta, 17%; 95% CI, 9.7\2-24.4; P < 0.001) and 21.0% versus 13.7% (Delta, 7.3%; 95% CI, 1.0\2-13.7; P = 0.02). Predictors of smoking cessation included use of bupropion SR (abstinence rate, 41.5% vs 21.1%; P<0.001); smoking nonmentholated cigarettes (abstinence rate, 28.3% in mentholated smokers [n = 417] vs 41.5% in nonmentholated smokers [n = 118]; P = 0.006); not smoking within 30 minutes of awakening (abstinence rate, 26.4% [n = 420] in those who did vs 48.7% [n = 115] in those who did not; P < 0.001); and lower baseline salivary cotinine levels (256.8 [137.0] ng/mL in those who became abstinent vs 305.6 [143.4] ng/mL in those who remained smokers; P < 0.001). In black light (<or=10 cpd) smokers (N = 753) who received nicotine gum 2 mg, the biochemically verified 7-day abstinence rates at weeks 8 and 26 in mentholated versus nonmentholated smokers were 22.6% versus 26.8% (P = NS) and 11.2% versus 18.8% (P = 0.015), respectively; at week 26, the abstinence rates in those who received gum + mentholated cigarettes (n = 309) versus gum + nonmentholated cigarettes (n = 67) were 14% versus 24% (P = 0.031). In Hispanic smokers (N = 108; mean [SD] cpd, 18.8 [10.2]) who received nicotine patch versus placebo for 10 weeks, 46% versus 26% (chi(2) = 4.01; P = 0.05) were abstinent from weeks 2 to 10 (completed all doses of patch); patients who were more acculturated and received active treatment had a higher abstinence rate than less acculturated patients (63% vs 47%; P value not provided). In Native American smokers (N = 252; cpd not provided) who received nicotine patch + counseling and were followed up at 3, 6, 9, and 12 months, selfreported abstinence rates were 31% (49/156), 30% (21/71), 24% (13/55), and 21% (4/19), respectively (P values not provided). In a 6-month study in white (n = 191) and nonwhite (n = 108) smokers (mean [SD] cpd, 21 [11]) randomized to receive a nicotine patch (n = 144) versus nasal spray (n = 155) for 8 weeks, the carbon monoxide\2-verified 7-day abstinence rates were 34.7% versus 29.0%; at 6 months, these rates were 18.1% versus 15.5% (P = NS). In nonwhite patients, logistic regression analysis at 6 months found that a higher proportion of patients randomized to receive nasal spray did not smoke for >or=7 consecutive days (odds ratio, 0.20; 95% CI, 0.05-0.77; P = 0.02).

CONCLUSIONS

Data from the studies in this review support the use of smoking-cessation pharmacotherapy (nicotine patch and bupropion SR) in nonwhite patients. Black patients, who smoked within 30 minutes of awakening, smoked mentholated cigarettes, and had high salivary cotinine levels may have difficulty quitting regardless of the number of cigarettes smoked per day; therefore, determining the type of cigarettes smoked (mentholated vs nonmentholated) and salivary cotinine levels may be helpful in assessing the severity of smoking addiction and guide pharmacotherapy (eg, starting at higher doses of nicotine-replacement therapy in a light smoker). Other than smoking-cessation behavioral studies, there is a lack of congruent smoking-cessation pharmacotherapy studies in American Indian/Alaska Native, Hispanic, and other ethnic populations.

摘要

背景

在美国,吸烟仍是可预防的发病和死亡的主要原因。研究表明,行为支持策略和药物治疗可提高戒烟率。然而,这两种方法,尤其是药物治疗,在美国非白人人群中的研究较少。

目的

本综述的目的是评估美国非白人人群中戒烟药物治疗的疗效。

方法

使用搜索词“戒烟”、“尼古丁替代疗法”、“安非他酮缓释片”、“伐尼克兰”、“少数群体”、“种族”、“非裔美国人”、“黑人”、“西班牙裔”、“美国印第安人”和“阿拉斯加原住民”,在MEDLINE(1966年2月至2007年12月)、《国际药学文摘》(1980年1月至2008年1月)、《循证医学数据库》(1990年2月至2007年12月)和EMBASE药物与药理学数据库(1991年2月至2007年第三季度)中进行文献检索,以确定评估非白人患者使用戒烟药物治疗的英文研究。

结果

共确定并评估了9项研究。6项研究观察了黑人吸烟者的戒烟药物治疗,1项观察了西班牙裔吸烟者,1项观察了美国原住民吸烟者以及1项观察了白人和非白人吸烟者。在接受尼古丁贴片与安慰剂治疗的黑人吸烟者(N = 410;平均每日吸烟量[cpd],20.4)中,10周时30天自我报告的戒烟率分别为21.5%和13.7%(P = 0.03),6个月时分别为17.1%和11.7%(P =无统计学意义)。在接受150 mg缓释(SR)安非他酮每日两次与安慰剂治疗7周的黑人吸烟者(N = 600;平均[标准差]cpd,16.1 [7.5])中,第6周和第26周经生化验证的7天戒烟率分别为36.0%和19.0%(差值,17%;95%置信区间,9.7 - 24.4;P < 0.001)以及21.0%和13.7%(差值,7.3%;95%置信区间,1.0 - 13.7;P = 0.02)。戒烟的预测因素包括使用安非他酮缓释片(戒烟率,41.5%对21.1%;P<0.001);吸非薄荷醇香烟(薄荷醇吸烟者[n = 417]的戒烟率为28.3%,非薄荷醇吸烟者[n = 118]的戒烟率为41.5%;P = 0.006);醒来后30分钟内不吸烟(吸烟者中,吸烟者[n = 420]的戒烟率为26.4%,不吸烟者[n = 115]的戒烟率为48.7%;P < 0.001);以及较低的基线唾液可替宁水平(戒烟者为256.8 [137.0] ng/mL,仍吸烟者为305.6 [143.4] ng/mL;P < 0.001)。在接受2 mg尼古丁口香糖的黑人轻度(≤10 cpd)吸烟者(N = 753)中,薄荷醇吸烟者与非薄荷醇吸烟者在第8周和第26周经生化验证的7天戒烟率分别为22.6%和26.8%(P =无统计学意义)以及11.2%和18.8%(P = 0.015);在第26周,接受口香糖 + 薄荷醇香烟(n = 309)与口香糖 + 非薄荷醇香烟(n = 67)的吸烟者的戒烟率分别为14%和24%(P = 0.031)。在接受尼古丁贴片与安慰剂治疗10周的西班牙裔吸烟者(N = 108;平均[标准差]cpd,18.8 [10.2])中,第2至10周(完成所有贴片剂量)的戒烟率分别为46%和26%(χ² = 4.01;P = 0.05);文化适应程度较高且接受积极治疗的患者的戒烟率高于文化适应程度较低的患者(63%对47%;未提供P值)。在接受尼古丁贴片 + 咨询并在3、6、9和12个月进行随访的美国原住民吸烟者(N = 252;未提供cpd)中,自我报告的戒烟率分别为31%(49/156)、30%(21/71)、24%(13/55)和21%(4/19)(未提供P值)。在一项针对白人(n = 191)和非白人(n = 108)吸烟者(平均[标准差]cpd,21 [11])的6个月研究中,随机接受尼古丁贴片(n = 144)与鼻喷雾剂(n = 155)治疗8周,经一氧化碳验证的7天戒烟率分别为34.7%和29.0%;在6个月时,这些比率分别为18.1%和15.5%(P =无统计学意义)。在非白人患者中,6个月时的逻辑回归分析发现,随机接受鼻喷雾剂的患者中,连续≥7天不吸烟的比例较高(比值比,0.20;95%置信区间,0.05 - 0.77;P = 0.02)。

结论

本综述中的研究数据支持在非白人患者中使用戒烟药物治疗(尼古丁贴片和安非他酮缓释片)。无论每日吸烟量如何,醒来后30分钟内吸烟、吸薄荷醇香烟且唾液可替宁水平较高的黑人患者可能难以戒烟;因此,确定所吸香烟的类型(薄荷醇与非薄荷醇)和唾液可替宁水平可能有助于评估吸烟成瘾的严重程度并指导药物治疗(例如,轻度吸烟者从较高剂量的尼古丁替代疗法开始)。除了戒烟行为研究外,在美国印第安人/阿拉斯加原住民、西班牙裔和其他种族人群中,缺乏一致的戒烟药物治疗研究。

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