用于戒烟的 Cytisine:为期 40 天的诱导期治疗。

IF 1.9 Q3 SUBSTANCE ABUSE
Tobacco Prevention & Cessation Pub Date : 2024-05-27 eCollection Date: 2024-01-01 DOI:10.18332/tpc/187556
Biagio Tinghino, Salvatore Cardellicchio, Flavia Corso, Chiara Cresci, Victoria Pittelli, Rosastella Principe, Licia Siracu-Sano, Giovanni Zelano, Vincenzo Zagà, Maria Sofia Cattaruzza
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引用次数: 0

摘要

简介Cytisine 是一种戒烟药物,目前已在全球范围内使用。根据东欧以往的临床经验,文献中的大多数数据都预测其疗程为 25 天。有关剂量的研究很少,只有最近一些研究人员尝试了更长的治疗时间:这项真实世界的回顾性横断面研究分析了从 2015 年到 2021 年在意大利中北部七个戒烟中心连续收集的数据。这项研究旨在评估为期40天的胞二磷胆碱治疗的有效性和耐受性,其中包括一个诱导阶段和一个较慢的减量计划。研究收集了 871 名接受半胱氨酸、伐尼克兰和尼古丁替代疗法(NRT)治疗的患者的数据。样本未经随机分配。所有患者都接受了行为支持(4-6 次治疗,每次持续 20-30 分钟,外加评估治疗):结果:服用胞二辛(543 人,40 天)、伐伦克林(281 人,12 周)和 NRT(47 人,8 周)的亚组在 6 个月时经生化证实的戒烟率分别为 50.5%、55.9% 和 51.0%,胞二辛与伐伦克林之间的差异具有统计学意义(p结论:这项研究提供的初步证据表明,与伐尼克兰相比,40 天疗程的胞二辛似乎效果较差,但效果的大小相当。其效果和耐受性似乎优于其他大多数研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytisine for smoking cessation: A 40-day treatment with an induction period.

Introduction: 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.

Methods: 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.

Results: 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.

Conclusions: 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.

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来源期刊
CiteScore
1.80
自引率
0.00%
发文量
155
审稿时长
4 weeks
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