Javitz Harold S, Swan Gary E, Zbikowski Susan M, Curry Susan J, McAfee Timothy A, Decker Donna L, Patterson Richard, Jack Lisa M
Center for Health Sciences, SRI International, Menlo Park, Calif 94025, USA.
Am J Manag Care. 2004 Mar;10(3):217-26.
To determine the differential cost effectiveness of 2 dosing regimens of bupropion sustained release (SR) in combination with behavioral interventions of minimal intensity (tailored mailings [TM]) or moderate intensity (proactive telephone calls [PTC]) for smoking cessation in an actual practice setting.
Open-label, randomized trial, with 1-year follow-up, conducted in a large health system based in Seattle, Washington.
A total of 1524 adult smokers interested in quitting smoking were randomly assigned to receive 150 mg bupropion SR daily and PTC (n = 382), 150 mg bupropion SR daily and TM (n = 381), 300 mg bupropion SR daily and PTC (n = 383), or 300 mg bupropion SR daily and TM (n = 378). Sufficient medication for 8 weeks of dosing was provided to patients. The primary outcome measure was self-reported point-prevalence 7-day nonsmoking status at 12 months after the target quit date.
Although the 300-mg dose was associated with a higher 12-month nonsmoking rate relative to the 150-mg dose with both PTC and TM, the additional cost resulted in lower cost effectiveness. The PTC behavioral intervention was more expensive than TM, but the additional effectiveness resulted in almost equivalent cost effectiveness at the 150-mg dose. Costs per additional 12-month nonsmoker (above that expected for placebo) for the 150-mg dose groups averaged 950 dollars and per additional lifetime quitter averaged 1508 dollars; for the 300-mg groups these costs were 1342 dollars and 2129 dollars, respectively. Cost per life-year and quality-adjusted life-years (QALYs) saved varied substantially by age and treatment, but were no greater than 1100 dollars for all treatment groups when averaged across the age and sex distribution for the study population.
Although the cost per life-year and QALYs saved were sufficiently low for all doses to rate these smoking cessation interventions as among the most cost effective of life-saving medical treatments, within the regimens tested 150 mg bupropion combined with either PTC or TM was the most cost effective.
在实际临床环境中,确定安非他酮缓释剂(SR)两种给药方案联合最低强度行为干预(定制邮件[TM])或中等强度行为干预(主动电话随访[PTC])用于戒烟的成本效益差异。
开放标签随机试验,随访1年,在华盛顿州西雅图市的一个大型医疗系统中进行。
共1524名有戒烟意愿的成年吸烟者被随机分配,分别接受每日150mg安非他酮SR联合PTC(n = 382)、每日150mg安非他酮SR联合TM(n = 381)、每日300mg安非他酮SR联合PTC(n = 383)或每日300mg安非他酮SR联合TM(n = 378)。为患者提供了足够服用8周的药物。主要结局指标是在目标戒烟日期后12个月自我报告的7天时点患病率非吸烟状态。
尽管与PTC和TM联合使用时,300mg剂量组相对于150mg剂量组的12个月戒烟率更高,但额外的成本导致成本效益降低。PTC行为干预比TM更昂贵,但额外的疗效使得150mg剂量组的成本效益几乎相当。150mg剂量组每增加一名12个月戒烟者(高于安慰剂预期)的平均成本为950美元,每增加一名终身戒烟者的平均成本为1508美元;300mg剂量组的这些成本分别为1342美元和2129美元。每个生命年和质量调整生命年(QALY)的成本因年龄和治疗方式而异,但在研究人群的年龄和性别分布中进行平均后,所有治疗组的成本均不超过1100美元。
尽管所有剂量的每个生命年和QALY成本都足够低,使这些戒烟干预措施被列为最具成本效益的挽救生命医疗治疗方法之一,但在测试的方案中,150mg安非他酮联合PTC或TM是最具成本效益的。