Allen Sharon S, Allen Alicia M, Lunos Scott, Tosun Nicole
Department of Family Medicine and Community Health, Medical School, University of Minnesota, Minneapolis, MN;
Department of Family Medicine and Community Health, Medical School, University of Minnesota, Minneapolis, MN.
Nicotine Tob Res. 2016 Nov;18(11):2145-2153. doi: 10.1093/ntr/ntw156. Epub 2016 Aug 18.
Pregnancy is a strong motivator to quit smoking, yet postpartum relapse rates are high. Growing evidence suggests a role of sex hormones in drug abuse behavior and given the precipitous drop in sex hormones at delivery, they may play a role in postpartum relapse. This pilot study evaluates the feasibility and potential role of exogenous progesterone in postpartum smoking relapse.
This 12-week double-blind placebo-controlled randomized pilot trial randomized 46 abstinent postpartum women to active progesterone (PRO; 200mg twice a day) versus placebo (PBO) for 4 weeks. Participants were followed for relapse for 12 weeks. Main study outcomes include abstinence (point prevalence), feasibility (compliance per number of clinic visits attended, pill counts and Electronic Data Capture [EDC] completed) and self-reported acceptability. Safety was also measured by depressive symptom scores, adverse events, and breastfeeding.
Overall retention rate was 87% at week 12. At week 4, abstinence rates were 75% in the PRO group and 68.2% in the PBO group (p = .75). Medication adherence was 68% and clinic visit attendance was 80%, with no differences by randomization. Depressive symptom scores, adverse events, and breastfeeding did not vary by randomization.
Although the study was not powered to evaluate abstinence rates, we did observe a higher prevalence of abstinence at week 4 in the PRO group. Further, exogenous progesterone was well tolerated and did not adversely affect depressive symptoms or breastfeeding. Thus, the results of this pilot study indicate further investigation into progesterone as a postpartum relapse prevention strategy is warranted.
This innovative pilot trial determined the feasibility of delivering exogenous progesterone as a potential prevention of postpartum smoking relapse. We observed high retention and moderate adherence rates, as well as high acceptability among participants. Further, though not statistically significant, more women in the treatment group remained abstinent from smoking during follow-up. This project adds to the growing body of literature on the role of sex hormones in smoking relapse and also provides support for a fully powered clinical trial.
怀孕是促使戒烟的强大动力,但产后复吸率很高。越来越多的证据表明性激素在药物滥用行为中发挥作用,鉴于分娩时性激素急剧下降,它们可能在产后复吸中起作用。这项初步研究评估了外源性孕酮在产后吸烟复吸中的可行性和潜在作用。
这项为期12周的双盲安慰剂对照随机初步试验将46名产后戒烟女性随机分为活性孕酮组(PRO;每日两次,每次200mg)和安慰剂组(PBO),为期4周。对参与者进行12周的复吸随访。主要研究结果包括戒断(点患病率)、可行性(每次就诊的依从性、药丸计数和完成的电子数据采集[EDC])以及自我报告的可接受性。还通过抑郁症状评分、不良事件和母乳喂养来衡量安全性。
第12周时总体保留率为87%。在第4周时,PRO组的戒断率为75%,PBO组为68.2%(p = 0.75)。药物依从性为68%,就诊率为80%,随机分组之间无差异。抑郁症状评分、不良事件和母乳喂养在随机分组之间没有差异。
尽管该研究没有足够的效力来评估戒断率,但我们确实观察到PRO组在第4周时戒断患病率更高。此外,外源性孕酮耐受性良好,不会对抑郁症状或母乳喂养产生不利影响。因此,这项初步研究的结果表明有必要进一步研究孕酮作为产后预防复吸的策略。
这项创新性的初步试验确定了提供外源性孕酮作为预防产后吸烟复吸的潜在方法的可行性。我们观察到高保留率和中等依从率,以及参与者的高接受度。此外,尽管没有统计学意义,但治疗组中更多女性在随访期间仍保持戒烟。该项目增加了关于性激素在吸烟复吸中作用的文献,并为全面的临床试验提供了支持。