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Varenicline for Smoking Cessation in Hospitalized Patients With Acute Coronary Syndrome.
Eisenberg, Mark J; Windle, Sarah B; Roy, Nathalie; Old, Wayne; Grondin, François R; Bata, Iqbal; Iskander, Ayman; Lauzon, Claude; Srivastava, Nalin; Clarke, Adam; Cassavar, Daniel; Dion, Danielle; Haught, Herbert; Mehta, Shamir R; Baril, Jean-François; Lambert, Charles; Madan, Mina; Abramson, Beth L; Dehghani, Payam.
Afiliação
  • Eisenberg MJ; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Windle SB; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Roy N; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Old W; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Grondin FR; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Bata I; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Iskander A; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Lauzon C; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Srivastava N; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Clarke A; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Cassavar D; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Dion D; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Haught H; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Mehta SR; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Baril JF; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Lambert C; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Madan M; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Abramson BL; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
  • Dehghani P; From Jewish General Hospital/McGill University, Montréal, QC, Canada (M.J.E., S.B.W.); Centre de santé et de services sociaux de Chicoutimi, Chicoutimi, QC, Canada (N.R.); Sentara Cardiovascular Research Institute, Norfolk, VA (W.O.); CISSS Chaudière-Appalaches, Hôtel-Dieu de Lévis site, QC, Canada
Circulation ; 133(1): 21-30, 2016 Jan 05.
Article em En | MEDLINE | ID: mdl-26553744
ABSTRACT

BACKGROUND:

Less than one-third of smokers hospitalized with an acute coronary syndrome (ACS) remain abstinent following discharge. We assessed whether varenicline, begun in-hospital, is efficacious for smoking cessation following ACS. METHODS AND

RESULTS:

We conducted a multi-center, double-blind, randomized, placebo-controlled trial in which smokers hospitalized with an ACS were randomized to varenicline or placebo for 12 weeks. All patients received low-intensity counseling. The primary end point was point-prevalence smoking abstinence assessed at 24 weeks by 7-day recall and biochemical validation using expired carbon monoxide. A total of 302 patients were randomized (mean age 55±9 years; 75% male; 56% ST-segment elevation myocardial infarction; 38% non-ST-segment elevation myocardial infarction; 6% unstable angina). Patients smoked a mean of 21±11 cigarettes/d at the time of hospitalization and had been smoking for a mean of 36±12 years. At 24 weeks, patients randomized to varenicline had significantly higher rates of smoking abstinence and reduction than patients randomized to placebo. Point-prevalence abstinence rates were 47.3% in the varenicline group and 32.5% in the placebo group (P=0.012; number needed to treat=6.8). Continuous abstinence rates were 35.8% and 25.8%, respectively (P=0.081; number needed to treat=10.0), and rates of reduction ≥50% in daily cigarette consumption were 67.4% and 55.6%, respectively (P=0.05; number needed to treat=8.5). Adverse event rates within 30 days of study drug discontinuation were similar between groups (serious adverse events varenicline 11.9%, placebo 11.3%; major adverse cardiovascular events varenicline 4.0%, placebo 4.6%).

CONCLUSIONS:

Varenicline, initiated in-hospital following ACS, is efficacious for smoking cessation. Future studies are needed to establish safety in these patients. CLINICAL TRIAL REGISTRATION URL http//www.clinicaltrials.gov. Unique identifier NCT00794573.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Abandono do Hábito de Fumar / Agonistas Nicotínicos / Síndrome Coronariana Aguda / Dispositivos para o Abandono do Uso de Tabaco / Vareniclina / Hospitalização Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Abandono do Hábito de Fumar / Agonistas Nicotínicos / Síndrome Coronariana Aguda / Dispositivos para o Abandono do Uso de Tabaco / Vareniclina / Hospitalização Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article