[Abstinence rates with varenicline compared to bupropion and nicotine replacement therapy for quitting smoking in primary care]
- PMID: 21382649
- PMCID: PMC7024938
- DOI: 10.1016/j.aprim.2010.09.010
[Abstinence rates with varenicline compared to bupropion and nicotine replacement therapy for quitting smoking in primary care]
Abstract
Objective: The objective of this study was to estimate the continuous abstinence rates of varenicline, bupropion and nicotine replacement therapy (NRT) in smoking cessation in 2 Primary Care (PC) External Support Units.
Design: Observational, multicentre, longitudinal study using a retrospective review of medical records.
Setting: Six Primary Care Centres.
Participants: Patients > 18 years, who began smoking cessation treatment between 1/01/2006 and 1/12/2008 with varenicline, bupropion or NRT were included in the analysis. CONTINUATION: Patient follow-up was conducted from time-baseline (day 1) and assessed at 6 and 12 months.
Main variables: comorbidities, effectiveness (continuous abstinence) and pharmacological tolerability.
Statistical analysis: logistic regression models and Kaplan-Maier survival curves; P<.05.
Results: A total of 957 smokers treated with NRT (53.0%), bupropion (25.1%) and varenicline (21.9%) were included in the analysis. Mean age: 47.6 (11.3) years; 58.6% men. 32.0% of smokers attended due to physical dependence. Average duration of smoking: 19.5 (6.7) years. At 6 months, 61.2% (95% CI: 54.6-67.8%) of participants in the varenicline group continuously abstained from smoking compared with 56.9% (95% CI: 50.6-63.2%) in the bupropion group, and 52.3% (95% CI: 48.0-56.6%) in the NRT group; P=.003. At 12 months, the rate of continuous abstinence was 57.4% (95% CI: 50.7-64.1%) in the varenicline group compared with 52.9% (95% CI: 46.6-59.2%) in the bupropion group and 47.1% (95% CI: 42.8-51.4%) in the NRT group; P=.002.
Conclusion: One year-follow up results suggest that varenicline is an appropriate alternative compared with bupropion and NRT on smoking cessation in the PC setting.
Objetivo: Determinar las tasas de abstinencia continua conseguidas con vareniclina, bupropión y terapia de sustitución nicotínica (TSN) en la cesación del consumo de tabaco en 2 unidades externas de apoyo a atención primaria (AP).
Diseño: Estudio observacional, multicéntrico, longitudinal, a partir de la revisión retrospectiva de registros médicos.
Emplazamiento: Seis centros de AP.
Participantes: Se incluyeron pacientes > 18 años que iniciaron tratamiento de cesación del hábito tabáquico entre 1/01/2006 y 31/12/2008 con vareniclina, bupropión o TSN.
Mediciones principales: Principales medidas: sociodemográficas, comorbilidad, efectividad (abstinencia continua) y tolerabilidad farmacológica. Se evaluó la abstinencia a los 6 y 12 meses de seguimiento. Análisis estadístico: modelos de regresión logística y curva de supervivencia de Kaplan-Meier.
Resultados: Se incluyeron 957 pacientes fumadores, tratados con TSN (53,0%), bupropión (25,1%) y vareniclina (21,9%). Su media de edad era 47,6 (DE: 11,3) años, y el 58,6% eran hombres. Un 32,0% acudieron por dependencia física y el tiempo medio de fumadores fue de 19,5 (DE: 6,7) años. A los 6 meses, la abstinencia continua con vareniclina fue del 61,2% (IC: 54,6-67,8%), con bupropión del 56,9% (IC: 50,6-63,2%) y con TSN del 52,3% (IC: 48,0-56,6%); p = 0,003. A los 12 meses, fue del 57,4% (IC: 50,7-64,1%), 52,9% (IC: 46,6-59,2%) y 47,1% (IC: 42,8-51,4%), respectivamente, p = 0,002.
Conclusiones: Los resultados tras un año de seguimiento sugieren que vareniclina es una alternativa adecuada frente al bupropión y la TSN en la cesación del tabaco en el ámbito de la AP.
Copyright © 2010 Elsevier España, S.L. All rights reserved.
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