Brief counseling for smoking cessation and alcohol use reduction concomitant with hospital procedures: a randomized clinical trial.

OBJECTIVE: To evaluate the effect of brief counseling on patient readiness for behavioral change and cessation/reduction of tobacco and alcohol use. METHODS: This clinical trial randomized patients in blocks, stratified by risk factor. Adult smokers or at-risk drinkers undergoing surgical or diagnostic procedures were recruited. Outcome assessments and analyses were blinded. Brief counseling was compared with educational materials for the outcomes progress in stage of change and smoking/alcohol cessation/reduction. RESULTS: Overall, 222 participants were randomly assigned to the intervention group and 218 to the control group. Among them, 28 and 18 patients were lost to follow-up, respectively. Progress in change stage was 94.1% at 1 month in both groups (RR = 1.00; 95%CI 0.95-1.05) and 94.8 vs. 90.5% at 3 months (RR = 1.05; 95%CI 0.99-1.11) in the intervention and control groups, respectively. Smoking cessation and alcohol reduction rates at 3 months were 57.2 vs. 41% (RR = 1.40; 95%CI 1.14-1.71) in the intervention and control groups, respectively. Only brief counseling led to significant differences in smoking cessation (51.4 vs. 35.1%; RR = 1.46; 95%CI 1.12-1.92). CONCLUSIONS: Brief counseling and educational materials improved patient motivation for behavioral change, but brief counseling had a greater effect on smoking cessation.

Brief counseling for smoking cessation and alcohol use reduction concomitant with hospital procedures: a randomized clinical trial

Objective: To evaluate the effect of brief counseling on patient readiness for behavioral change and cessation/reduction of tobacco and alcohol use. Methods: This clinical trial randomized patients in blocks, stratified by risk factor. Adult smokers or at-risk drinkers undergoing surgical or diagnostic procedures were recruited. Outcome assessments and analyses were blinded. Brief counseling was compared with educational materials for the outcomes progress in stage of change and smoking/alcohol cessation/reduction. Results: Overall, 222 participants were randomly assigned to the intervention group and 218 to the control group. Among them, 28 and 18 patients were lost to follow-up, respectively. Progress in change stage was 94.1% at 1 month in both groups (RR = 1.00; 95%CI 0.95-1.05) and 94.8 vs. 90.5% at 3 months (RR = 1.05; 95%CI 0.99-1.11) in the intervention and control groups, respectively. Smoking cessation and alcohol reduction rates at 3 months were 57.2 vs. 41% (RR = 1.40; 95%CI 1.14-1.71) in the intervention and control groups, respectively. Only brief counseling led to significant differences in smoking cessation (51.4 vs. 35.1%; RR = 1.46; 95%CI 1.12-1.92). Conclusions: Brief counseling and educational materials improved patient motivation for behavioral change, but brief counseling had a greater effect on smoking cessation. Clinical trial registration: NCT03521622

Sociodemographic, family and clinical characteristics associated with smoking cessation intention among smokers treated in a quaternary care hospital / Características sociodemográficas, familiares y clínicas asociadas con la intención de cesación del tabaquismo en fumadores atendidos en un hospital de cuarto nivel

Abstract Introduction: Smoking cessation interventions are a priority in medical care settings, including hospitals. Objectives: To describe the sociodemographic, family, and clinical characteristics of smokers treated in a quaternary care hospital and to establish the variables associated with smoking cessation intention in order to optimize the management of this risk factor in the hospital setting. Materials and methods. A cross-sectional study was conducted in 321 active smokers treated between April 2018 and November 2019 in Bogotá D.C., Colombia. Smoking prevalence was calculated, and participants' sociodemographic, family, and clinical information was obtained and subsequently analyzed using descriptive statistics. Associations between said variables and cessation intention were established by means of bivariate (chi-squared test) and multivariate analyses (ordinal logistic regression model with the corresponding 95% confidence intervals). Results: Smoking prevalence was 8.89% (95%CI: 7.97-9.82), (N=3609; n=321 active smokers). Most participants were men (66.67%), had a low or middle socioeconomic status (96.89%) and a basic educational level (52.34%), and 42.06% were between 46 and 64 years old. The majority of active smokers had a mild degree of smoking consumption and low level of nicotine dependence (78.82% and 81.62%, respectively). Furthermore, 78.82% reported previous attempts to quit smoking. Nuclear family was the predominant family type (58.57%), and 40.19% of smokers experienced some degree of family dysfunction. Smokers with more perceived benefits derived from smoking cessation and high self-efficacy are more likely to make a smoking cessation attempt (OR=9.44, 95%CI:1.27-85.03 and OR=3.73, 95%CI:1.55-8.78, respectively). Conclusions: The identification and characterization of smokers in the hospital setting provides useful insights to personalize smoking cessation interventions.

Resumen Introducción. Las intervenciones dirigidas a la cesación del tabaquismo son una prioridad en los escenarios de atención médica, incluido el hospitalario. Objetivos. Describir las características sociodemográficas, familiares y clínicas de fumadores atendidos en un hospital de cuarto nivel y establecer las variables asociadas con la intención de cesación del tabaquismo con el fin de optimizar el manejo de este factor de riesgo en el entorno hospitalario. Materiales y métodos. Estudio transversal realizado en 321 fumadores activos atendidos entre abril de 2018 y noviembre de 2019 en Bogotá D.C., Colombia. Se calculó la prevalencia de tabaquismo y se obtuvo información sociodemográfica, familiar y clínica, la cual fue analizada mediante estadística descriptiva. Se establecieron asociaciones entre dichas variables y la intención de cesación mediante un análisis bivariado (prueba X2) y uno multivariado (modelo de regresión logística ordinal con sus correspondientes intervalos de confianza al 95%). Resultados. La prevalencia de tabaquismo activo fue de 8.89% (IC95%: 7.97-9.82), (N=3 609; n=321 fumadores activos). La mayoría fueron hombres (66.67%), de estrato socioeconómico bajo o medio (96.89%), con nivel educativo básico (52.34%) y el 42.06% estaban entre los 46 y 64 años. La mayoría de los fumadores activos tenían un grado leve de tabaquismo y un bajo nivel de dependencia a la nicotina (78.82% y 81.62%, respectivamente); además, el 78.82% reportó intentos previos de cesación. El tipo de familia predominante fue la nuclear (58.57%) y 40.19% de los fumadores experimentaban algún grado de disfuncionalidad familiar. Los fumadores con mayor percepción de beneficios derivados de dejar de fumar y con alta autoeficacia tienen una mayor probabilidad de realizar un intento de cesación de tabaquismo (OR=9.44; IC95%: 1.27-85.03 and OR=3.73; 95%CI: 1.55-8.78, respectivamente). Conclusiones. La identificación y caracterización de fumadores en el entorno hospitalario brinda claves para personalizar las intervenciones de cesación del tabaquismo.

Efectividad de la consejería breve en el ámbito hospitalario para la cesación del tabaquismo y la disminución del consumo riesgoso de alcohol: Protocolo de un experimento clínico aleatorizado / Effectiveness of Brief Counseling in a Hospital Setting for Smoking Cessation and Risky Alcohol Drinking Reduction: Randomized Clinical Trial Protocol

Resumen Introducción: Las enfermedades crónicas son un problema de salud pública; el 80% de ellas se relacionan con factores de riesgo modificables, como una dieta poco saludable, la inactividad física, el tabaquismo y el consumo riesgoso de alcohol. La intervención en el tabaquismo y el consumo riesgoso de alcohol se ha demostrado efectiva en el cuidado primario, pero se desconoce si funciona de la misma manera en el contexto hospitalario. Objetivo: Evaluar la efectividad de la consejería breve para modificar el estadio de cambio en pacientes fumadores y bebedores en riesgo atendidos en un hospital de alta complejidad. Métodos: Experimento clínico aleatorizado, que evalúa la efectividad de 4 modalidades de consejería breve para la cesación de tabaquismo y el consumo riesgoso de alcohol en comparación con el cuidado habitual, seleccionadas según el estadio de cambio del sujeto. El resultado primario es la proporción de pacientes en cada uno de los grupos (intervención y control) en los cuales se identifica el avance en el estadio de cambio; además se analizará la reducción de consumos. Protocolo registrado en ClinicalTrials.gov (NCT03521622). Resultados: Los resultados se publicarán en revistas de literatura científica y su aplicación pretende generar protocolos de intervenciones conductuales en factores de riesgo modificables en hospitales de alta complejidad. El experimento fue presentado y aprobado por el Comité de Ética e Investigación de la Pontificia Universidad Javeriana y el Hospital Universitario de San Ignacio (aprobación 01/2018).

Abstrac Introduction: Chronic diseases are a public health problem, and 80% of them are related to modifiable risk factors such as unhealthy diet, physical inactivity, smoking, and risky alcohol consumption. Although the intervention in smoking and hazardous alcohol drinking has proven to be effective in Primary Care, it is unknown whether it works in the same way in the hospital setting. Objective: To evaluate the effectiveness of brief counselling in order to modify the stage of change in smokers and at-risk drinkers treated in a high complexity hospital. Methods: A Randomized controlled trial to be conducted, in which an evaluation is made of four brief counselling strategies for smoking cessation and risky alcohol consumption compared to usual care, selected according to the patient's stage of change. The primary result will be the proportion of patients in each of the groups (intervention and control) with identified progress in the stage of change. The reduction of consumption will be also be analyzed. Protocol registered at ClinicalTrials.gov (NCT03521622). Results: The results will be published in scientific journals, and its application aims to generate behavioral intervention protocols for modifiable risk factors in high complexity hospitals. The trial was presented and approved by the Ethics and Research Committee of the Pontificia Universidad Javeriana and Hospital Universitario de San Ignacio, Bogota, Colombia (Approval 01/2018).

Effectiveness of Brief Counseling in a Hospital Setting for Smoking Cessation and Risky Alcohol Drinking Reduction: Randomized Clinical Trial Protocol. / Efectividad de la consejería breve en el ámbito hospitalario para la cesación del tabaquismo y la disminución del consumo riesgoso de alcohol: Protocolo de un experimento clínico aleatorizado.

INTRODUCTION: Chronic diseases are a public health problem, and 80% of them are related to modifiable risk factors such as unhealthy diet, physical inactivity, smoking, and risky alcohol consumption. Although the intervention in smoking and hazardous alcohol drinking has proven to be effective in Primary Care, it is unknown whether it works in the same way in the hospital setting. OBJECTIVE: To evaluate the effectiveness of brief counselling in order to modify the stage of change in smokers and at-risk drinkers treated in a high complexity hospital. METHODS: A Randomised controlled trial to be conducted, in which an evaluation is made of four brief counselling strategies for smoking cessation and risky alcohol consumption compared to usual care, selected according to the patient's stage of change. The primary result will be the proportion of patients in each of the groups (intervention and control) with identified progress in the stage of change. The reduction of consumption will be also be analysed. Protocol registered at ClinicalTrials.gov (NCT03521622). RESULTS: The results will be published in scientific journals, and its application aims to generate behavioural intervention protocols for modifiable risk factors in high complexity hospitals. The trial was presented and approved by the Ethics and Research Committee of the Pontificia Universidad Javeriana and Hospital Universitario de San Ignacio, Bogota, Colombia (Approval 01/2018).