Department of Psychiatry, Yale School of Medicine,40 Temple Street, Suite 6B, New Haven, CT, 06510, United States.
Department of Psychiatry, Yale School of Medicine,40 Temple Street, Suite 6B, New Haven, CT, 06510, United States.
Psychoneuroendocrinology. 2017 Dec;86:96-103. doi: 10.1016/j.psyneuen.2017.09.012. Epub 2017 Sep 14.
Close to half of women who were smokers prior to conception quit smoking in pregnancy, when endogenous progesterone levels are high. However, at least half resume pre-pregnancy smoking levels within weeks after delivery and when progesterone levels drop. The current pilot study tested the feasibility and preliminary efficacy of postpartum progesterone replacement in preventing relapse to smoking in postpartum women with a history of pre-pregnancy smoking.
This was an 8-week, double-blind, parallel, randomized, placebo-controlled pilot trial of 41 women with a history of pre-pregnancy smoking who achieved abstinence by 32 weeks of gestation. Immediately following delivery women were randomized to oral micronized progesterone (200mg twice daily) or placebo via computerized urn randomization program. The main outcome measures were descriptions of study feasibility: recruitment and retention. Secondary outcomes were 7-day point prevalence of abstinence at week 8, time to relapse and smoking cravings.
The trial was feasible with adequate randomization, 64% (41/64) of eligible women, and trial retention, 78% (32/41) completed the trial. Women taking progesterone were 1.8 times more likely to be abstinent during week 8 and took longer to relapse (10 vs. 4 weeks) compared to the placebo group, although these differences did not reach statistical significance. After adjusting for age and pre-quit smoking level, the number needed to treat was 7. There was a 10% greater decline per week in craving ratings in the progesterone group compared to placebo (β=-0.10, 95% CI: -0.15, -0.04, p<0.01). No serious adverse events occurred during the trial.
These preliminary findings support the promise of progesterone treatment in postpartum smokers and could constitute a therapeutic breakthrough.If these preliminary findings can be evaluated and replicated in a larger study with sufficient power, this may constitute an acceptable and safe smoking relapse prevention strategy for use during lactation.
近半数在受孕前吸烟的女性会在怀孕期间戒烟,此时内源性孕酮水平较高。然而,至少有一半的女性会在产后数周内,当孕酮水平下降时,恢复到孕前的吸烟水平。本项先导性研究旨在测试产后孕激素替代治疗在预防有孕前吸烟史的产后妇女复吸方面的可行性和初步疗效。
这是一项为期 8 周、双盲、平行、随机、安慰剂对照的先导性试验,纳入了 41 名在妊娠 32 周时达到戒烟的有孕前吸烟史的女性。分娩后,女性立即通过计算机化 urn 随机分组程序接受口服微粒化孕酮(200mg,每日两次)或安慰剂治疗。主要结局是描述研究的可行性:招募和保留情况。次要结局是第 8 周时 7 天点的戒烟率、复发时间和吸烟渴求程度。
该试验具有足够的可行性,完成了充分的随机分组(64%,41/64)和试验保留(78%,32/41)。与安慰剂组相比,服用孕激素的女性在第 8 周时更有可能保持不吸烟状态,且复发时间更长(10 周 vs. 4 周),尽管这些差异没有达到统计学意义。调整年龄和戒烟前的吸烟水平后,治疗所需人数为 7 人。与安慰剂组相比,孕激素组的渴求评分每周下降 10%(β=-0.10,95%CI:-0.15,-0.04,p<0.01)。试验期间未发生严重不良事件。
这些初步发现支持孕激素治疗在产后吸烟者中的应用前景,并可能构成治疗上的突破。如果这些初步发现能够在一项具有足够效能的更大研究中得到评估和复制,这可能构成一种在哺乳期使用的可接受且安全的预防复吸策略。