School of Social and Community Medicine, University of Bristol, Bristol BS8 2PS, UK.
BMJ. 2013 Oct 11;347:f5704. doi: 10.1136/bmj.f5704.
To compare the risk of suicide, self harm, and depression in patients prescribed varenicline or bupropion with those prescribed nicotine replacement therapy.
Prospective cohort study within the Clinical Practice Research Datalink.
349 general practices in England.
119,546 men and women aged 18 years and over who used a smoking cessation product between 1 September 2006 and 31 October 2011. There were 81,545 users of nicotine replacement products (68.2% of all users of smoking cessation medicines), 6741 bupropion (5.6%), and 31,260 varenicline (26.2%) users.
Outcomes were treated depression and fatal and non-fatal self harm within three months of the first smoking cessation prescription, determined from linkage with mortality data from the Office for National Statistics (for suicide) and Hospital Episode Statistics data (for hospital admissions relating to non-fatal self harm). Hazard ratios or risk differences were estimated using Cox multivariable regression models, propensity score matching, and instrumental variable analysis using physicians' prescribing preferences as an instrument. Sensitivity analyses were performed for outcomes at six and nine months.
We detected 92 cases of fatal and non-fatal self harm (326.5 events per 100,000 person years) and 1094 primary care records of treated depression (6963.3 per 100,000 person years). Cox regression analyses showed no evidence that patients prescribed varenicline had higher risks of fatal or non-fatal self harm (hazard ratio 0.88, 95% confidence interval 0.52 to 1.49) or treated depression (0.75, 0.65 to 0.87) compared with those prescribed nicotine replacement therapy. There was no evidence that patients prescribed bupropion had a higher risk of fatal or non-fatal self harm (0.83, 0.30 to 2.31) or of treated depression (0.63, 0.46 to 0.87) compared with patients prescribed nicotine replacement therapy. Similar findings were obtained using propensity score methods and instrumental variable analyses.
There is no evidence of an increased risk of suicidal behaviour in patients prescribed varenicline or bupropion compared with those prescribed nicotine replacement therapy. These findings should be reassuring for users and prescribers of smoking cessation medicines.
比较处方用伐伦克林或安非他酮与处方用尼古丁替代疗法的患者自杀、自残和抑郁的风险。
在临床实践研究数据链接内进行的前瞻性队列研究。
英格兰 349 家全科诊所。
119546 名年龄在 18 岁及以上的男性和女性,他们在 2006 年 9 月 1 日至 2011 年 10 月 31 日期间使用了戒烟产品。有 81545 名尼古丁替代产品使用者(所有戒烟药物使用者的 68.2%),6741 名安非他酮使用者(5.6%)和 31260 名伐伦克林使用者(26.2%)。
从与国家统计局的死亡率数据(自杀)和医院入院统计数据(非致命性自残住院)的链接中确定,在首次戒烟处方后三个月内,将治疗后的抑郁和致命及非致命自残作为结局。使用 Cox 多变量回归模型、倾向评分匹配和将医生的处方偏好作为工具的工具变量分析来估计风险比或风险差异。对六个月和九个月的结果进行了敏感性分析。
我们发现了 92 例致命和非致命的自残(每 100000 人年有 326.5 例事件)和 1094 例经治疗的抑郁的初级保健记录(每 100000 人年有 6963.3 例)。Cox 回归分析显示,与处方尼古丁替代疗法的患者相比,服用伐伦克林的患者没有更高的致命或非致命自残(危险比 0.88,95%置信区间 0.52 至 1.49)或治疗后抑郁(0.75,0.65 至 0.87)的风险。与处方尼古丁替代疗法的患者相比,服用安非他酮的患者没有更高的致命或非致命自残(0.83,0.30 至 2.31)或治疗后抑郁(0.63,0.46 至 0.87)的风险。使用倾向评分方法和工具变量分析也得到了类似的发现。
与处方尼古丁替代疗法的患者相比,服用伐伦克林或安非他酮的患者自杀行为的风险没有增加。这些发现应该让戒烟药物的使用者和处方者感到放心。