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Cytisine for smoking cessation: A 40-day treatment with an induction period.
Tinghino, Biagio; Cardellicchio, Salvatore; Corso, Flavia; Cresci, Chiara; Pittelli, Victoria; Principe, Rosastella; Siracu-Sano, Licia; Zelano, Giovanni; Zagà, Vincenzo; Cattaruzza, Maria Sofia.
Afiliação
  • Tinghino B; Territorial Socio-Health District of Vimercate, ASST Brianza, Italy.
  • Cardellicchio S; Careggi University Hospital, Florence, Italy.
  • Corso F; Addictions Department of Verona, Verona, Italy.
  • Cresci C; Careggi University Hospital, Florence, Italy.
  • Pittelli V; Territorial Socio-Health District of Vimercate, ASST Brianza, Italy.
  • Principe R; UPMC Salvator Mundi International Hospital, Rome, Italy.
  • Siracu-Sano L; Humanitas Research Hospital, Rozzano, Milan, Italy.
  • Zelano G; Servizio Dipendenze ASST di Lecco, Lecco, Italy.
  • Zagà V; Bologna Local Health, Bologna, Italy.
  • Cattaruzza MS; Sapienza University of Rome, Rome, Italy.
Article em En | MEDLINE | ID: mdl-38803387
ABSTRACT

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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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article