Department of Preventive Medicine and Public Health, University of Kansas Medical Center, Kansas City, Missouri.
Department of Biostatistics, University of Kansas Medical Center, Kansas City, Missouri.
JAMA Netw Open. 2018 Sep 7;1(5):e181843. doi: 10.1001/jamanetworkopen.2018.1843.
Smokers with chronic obstructive pulmonary disease (COPD) have particular difficulty quitting. Long-term nicotine replacement therapy (LT-NRT) might offer a strategy for reducing harm from cigarettes and provide a pathway for later cessation.
To compare the effect of LT-NRT vs standard smoking cessation (SSC) on exposure to cigarette smoke, harm related to smoking, and cessation among smokers with COPD.
DESIGN, SETTING, AND PARTICIPANTS: This unblinded, randomized clinical trial recruited smokers who self-reported a diagnosis of COPD at any level of readiness to quit from May 23, 2014, through November 30, 2015. The 12-month follow-up was completed December 6, 2016. Patients were recruited at a clinical research unit of an academic medical center. Analysis was based on intention to treat and performed from March 8 through November 30, 2017.
Standard smoking cessation treatment included 10 weeks of NRT and 4 follow-up counseling sessions for those willing to make a quit attempt. Long-term NRT included 12 months of NRT and 6 follow-up counseling sessions regardless of initial willingness to quit. Overall, 198 patients were randomized to SSC, and 197 were included in the primary analysis; 200 patients were randomized to LT-NRT, and 197 were included in the primary analysis.
The primary outcome was 7-day abstinence verified by carbon monoxide (CO) levels at 12 months. Secondary outcomes included cigarettes smoked per day (CPD), exposure to CO, urinary excretion of 4-methylnitrosamino-1-3-pyridyl-1-butanol (NNAL) (a smoking-related carcinogen), and adverse events.
Among 398 patients who were randomized (59.8% female; mean [SD] age, 56.0 [9.3] years), the mean (SD) CPD was 23.1 (12.3). Twelve-month follow-up was completed by 373 participants (93.7%), and 394 (99.0%) were included in the primary analysis. At 12 months, CO-verified abstinence occurred in 23 of 197 participants (11.7%) in the SSC arm and 24 of 197 (12.2%) in the LT-NRT arm (risk difference, 0.5%; 95% CI, -5.9% to 6.9%). Continuing smokers in the SSC and LT-NRT arms had similar, significantly reduced harms caused by smoking, including cigarette consumption by 12.4 and 14.5 CPD, respectively, exhaled CO level by 5.5 and 7.8 ppm, respectively, and mean urinary NNAL excretion by 21.7% and 23.0%, respectively. In multivariate analyses, continuing smokers with greater adherence to NRT experienced less reduction in NNAL exposure. The frequency of major adverse cardiac events was similar in both groups.
Similar rates of cessation and similar reductions in exposure to tobacco smoke resulted with LT-NRT and SSC. Among continuing smokers, ongoing use of NRT was not associated with reductions in smoke exposure.
ClinicalTrials.gov Identifier: NCT02148445.
患有慢性阻塞性肺疾病(COPD)的吸烟者戒烟特别困难。长期尼古丁替代疗法(LT-NRT)可能提供减少香烟危害的策略,并为以后的戒烟提供途径。
比较 LT-NRT 与标准戒烟(SSC)对 COPD 吸烟者吸烟暴露、与吸烟相关的危害和戒烟的影响。
设计、设置和参与者:这项非盲、随机临床试验招募了自报任何戒烟准备水平的 COPD 患者,招募时间为 2014 年 5 月 23 日至 2015 年 11 月 30 日。12 个月的随访于 2016 年 12 月 6 日完成。患者在学术医疗中心的临床研究单位招募。分析基于意向治疗,并于 2017 年 3 月 8 日至 11 月 30 日进行。
标准戒烟治疗包括 10 周的 NRT 和 4 次随访咨询,适用于愿意尝试戒烟的患者。长期 NRT 包括 12 个月的 NRT 和 6 次随访咨询,无论最初是否愿意戒烟。共有 198 名患者被随机分配至 SSC 组,197 名患者纳入主要分析;200 名患者被随机分配至 LT-NRT 组,197 名患者纳入主要分析。
主要结果是通过 12 个月时的一氧化碳(CO)水平验证的 7 天戒烟。次要结果包括每日吸烟量(CPD)、CO 暴露、尿液中 4-甲基亚硝胺-1-(3-吡啶基)-1-丁醇(NNAL)(一种与吸烟有关的致癌物质)排泄量以及不良事件。
在 398 名随机分组的患者(59.8%为女性;平均[SD]年龄为 56.0[9.3]岁)中,平均(SD)CPD 为 23.1(12.3)。373 名参与者(93.7%)完成了 12 个月的随访,394 名参与者(99.0%)纳入了主要分析。在 12 个月时,SSC 组 197 名参与者中有 23 名(11.7%)、LT-NRT 组 197 名参与者中有 24 名(12.2%)通过 CO 验证实现了戒烟(风险差异,0.5%;95%CI,-5.9%至 6.9%)。继续吸烟的患者在 SSC 和 LT-NRT 组的吸烟危害都显著降低,分别减少了 12.4 和 14.5 CPD 的吸烟量,呼气 CO 水平分别降低了 5.5 和 7.8 ppm,平均尿液 NNAL 排泄量分别降低了 21.7%和 23.0%。在多变量分析中,坚持使用 NRT 的患者 NNAL 暴露量减少幅度更大。两组的主要不良心脏事件发生率相似。
LT-NRT 和 SSC 的戒烟率和吸烟暴露减少程度相似。在继续吸烟的患者中,持续使用 NRT 与减少吸烟暴露无关。
ClinicalTrials.gov 标识符:NCT02148445。