Tinghino Biagio, Cardellicchio Salvatore, Corso Flavia, Cresci Chiara, Pittelli Victoria, Principe Rosastella, Siracu-Sano Licia, Zelano Giovanni, Zagà Vincenzo, Cattaruzza Maria Sofia
Territorial Socio-Health District of Vimercate, ASST Brianza, Italy.
Careggi University Hospital, Florence, Italy.
Tob Prev Cessat. 2024 May 27;10. doi: 10.18332/tpc/187556. eCollection 2024.
Cytisine is a smoking cessation drug now used worldwide. Most of the data available in the literature predict a 25-day treatment, accepted on the basis of previous clinical experience in Eastern Europe. There are few studies on dosing, and only recently some researchers have tried a longer treatment period.
This real-world retrospective cross-sectional study analyzed data collected consecutively from 2015 to 2021, in seven smoking cessation centers in north-central Italy. The aim of this study is to evaluate the effectiveness and tolerability of a 40-day cytisine treatment with an induction phase and a slower reduction schedule. Data were collected from a group of 871 patients treated with cysteine, varenicline, and nicotine replacement therapy (NRT). The sample was not randomized. Behavioral support (4-6 sessions, each lasting 20-30 min, plus the evaluation session) was delivered to all patients.
Subgroups taking cytisine (n=543 for 40 days), varenicline (n=281 for 12 weeks), and NRT (n=47 for eight weeks) showed biochemically confirmed smoking abstinence at 6 months of 50.5%, 55.9%, and 51.0%, respectively, with a statistically significant difference between cytisine versus varenicline (p<0.01) but not between cytisine versus NRT (p=0.5597). Adverse events were 4.4% with cytisine and 33.3% with varenicline. Behavioral support was an important factor in effectiveness.
This study produced preliminary evidence that the 40-day regimen of cytisine, appears to have less effectiveness in comparison to varenicline but the magnitude of the effect is comparable. The results and tolerability seem to be better than in most other studies.
金雀花碱是一种目前在全球范围内使用的戒烟药物。文献中现有的大多数数据预测治疗期为25天,这是基于东欧以前的临床经验而被接受的。关于给药剂量的研究很少,直到最近才有一些研究人员尝试了更长的治疗期。
这项真实世界的回顾性横断面研究分析了2015年至2021年期间在意大利中北部七个戒烟中心连续收集的数据。本研究的目的是评估采用诱导期和较慢减量方案的40代金雀花碱治疗的有效性和耐受性。数据收集自一组接受金雀花碱、伐尼克兰和尼古丁替代疗法(NRT)治疗的871名患者。样本未随机分组。为所有患者提供行为支持(4 - 6次,每次持续20 - 30分钟,外加评估环节)。
服用金雀花碱(40天,n = 543)、伐尼克兰(12周,n = 281)和NRT(8周,n = 47)的亚组在6个月时经生化确认的戒烟率分别为50.5%、55.9%和51.0%,金雀花碱与伐尼克兰之间存在统计学显著差异(p < 0.01),但金雀花碱与NRT之间无差异(p = 0.5597)。金雀花碱的不良事件发生率为4.4%,伐尼克兰为33.3%。行为支持是有效性的一个重要因素。
本研究产生了初步证据,表明40天的金雀花碱治疗方案与伐尼克兰相比有效性似乎较低,但效果程度相当。结果和耐受性似乎比大多数其他研究更好。