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临床试验/NCT03209622
NCT03209622已完成不适用

Nicotine Replacement Therapy After Acute Coronary Syndrome

University of Monastir1 个研究点 分布在 1 个国家目标入组 89 人开始时间: 2015年1月2日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
89
试验地点
1
主要终点
smoking cessation rates with NRT among patients hospitalized for acute coronary syndrome

研究概览

简要总结

A randomized controlled trial was conducted in cardiology department and smoking cessation center of University Hospital of Monastir (Tunisia). All smokers Hospitalized for ACS were included. Participants were randomly assigned to either group "A", initiating Nicotine replacement therapy (NRT) in intra-hospitalization or a control group "B" that received NRT after hospital discharge. The end point assessment was smoking abstinence at 24 weeks following randomization, defined as self-reported abstinence in the past week before the 24 week clinic visit confirmed by a measured exhaled carbon monoxide ≤8 ppm. Data were analyzed by intention to treat.

详细描述

Background: Smoking is the main preventable cause worldwide of morbidity and premature death (1). It is a major and independent risk factor for coronary heart disease (CHD) (2). More than two-thirds of sudden cardiac death resulting from acute thrombus occurs in smokers (3). Compared to non-smokers the odds ratio (OR) for myocardial infarction is about 2.5, and for cardiovascular diseases overall the OR is about 2 (2) (4). Smoking cessation in persons with known CHD reduces the risk of recurrent myocardial infarctions or cardiovascular death by 30 % to 50 % (5,6) during the subsequent 3 to 7 years (7). Nevertheless, although smoking cessation is potentially the most effective CHD prevention strategy (5), quitting smoking is difficult and two-thirds of patients will return to smoking within one year of their acute coronary syndrome (ACS) (8,9). So, being hospitalized for a major cardiac condition, such as ACS can be an opportunity to prompt many individuals to stop smoking. Through using this "teachable moment" immediately after an ACS, it may be possible to increase smoking abstinence in this high-risk population (9). Cessation rates among smokers hospitalized for ACS, range from 31% without intervention to 60% with sustained intervention post hospitalization, at one year follow-up (10). Although Nicotine replacement therapy (NRT), Bupropion, and Varenicline have demonstrated efficacy medical treatment for smoking cessation compared with placebo (9). NRT improved cessation rates as well with an OR of 1.84 (95% CI 1.71 to 1.99) (2) and no adverse events was found (1). However, the smoking cessation remains a secondary concern in cardiology departments and there is no well strategies offered to these smoker patients with established CHD. Furthermore, there were no difference in cessation rates between this population and the general population despite the proved benefit of smoking cessation on clinical outcomes in CHD patients (11). Many studies have examined the benefits of smoking cessation after ACS and the efficacy of smoking cessation pharmacotherapy's in hospitalized patients with ACS but few randomized controlled trials have examined the efficacy time of smoking cessation in hospitalized patients with ACS either during the hospitalization or after hospital discharge. We aimed at comparing, among patients with ACS, the smoking cessation rates with NRT when began in-hospitalization, against that began after hospital discharge.

  1. Design and study population: We have carried out a randomized controlled trial conducted simultaneously in the smoking cessation center and the department of cardiology at the University Hospital of Monastir (Tunisia). This study was performed from January 2015 to Jun 2016 with a mean of 24 weeks of run-up and 24 weeks of follow-up. We have included patients aged more than 18 years, hospitalized with an ACS actively smoking at the time of inclusion, motivated to quit smoking, able to provide informed consent and willing to participate in a clinical study including a follow-up examination every 2 weeks after hospital discharge. Active smoking was defined as smoking one cigarette or more (or water pipe) per day during the month preceding the hospital stay. Non-inclusion criteria were the refusal of assistance of smoking cessation, inability to follow-up clinical visit (professional, regional or physical hindrance), diagnosis of depression or of serious health condition at admission (ventilated patient, cardiogenic shock, etc).

Sample size: We hypothesized that nicotine replacement therapy after ACS during hospitalization would improve the rate of smoking cessation rate comparing to that after hospitalization discharge from 32.7% up to 51% . This was considered realistic because of the previous study reported a rate of 51% among smokers who received the NRT in-hospital smoking cessation intervention (12) and 32.7% among patients receiving treatments after hospital discharge (13). The expected sample size of 68 participants would enable us to identify such an increase in the smoking cessation rate with a power of 0.80 and a two-sided p-value of <0.05. The proportion of patients who dropped out or withdrew was expected to be 30%. Hence a sample size of 89 was estimate to be adequate, we have included 99 consecutive patients (14). Computer randomization was performed, after consent was obtained. Blinding was not possible. Participants randomized to arm "A" have received a smoking cessation counseling and a Nicotine Replacement Therapy (NRT) during intra-hospital stay one day after SCA. Those in arm "B" have benefited a smoking cessation counseling during intra-hospital stay, while the NRT was offered on a mean of 14 days after SCA in the first clinical visit after hospital discharge. All patients received a regular follow-up visits in smoking cessation center after hospital discharge every 2 weeks. Of the 99 patients enrolled in the study, 44 (81.4 %) and 30 (66.6 %) patients had respectively completed the follow-up smoking cessation in arm A and arm B. Loss to follow up was equivalent in two arms (p=0.1) (Fig 1).

Ethical considerations: The study was conducted in accordance with good clinical practice and the ethical standards described in the Helsinki Declaration. 2. Study protocol and data collection:

During the hospital-stay: All patients included in the two arms study, received an individual therapeutic education associated to motivational interview. The therapeutic education aimed to explain tobacco addiction, psychological, physical and behavioral tobacco dependence, the efficiency of NRT in the smoking cessation and introduce examples of behavioral strategies that the patient might adopt when leaving the hospital to overcome his nicotine dependence. Data was collected through a self-administered questionnaire. Patients were asked about their socio-demographic status, history of tobacco use, level of nicotine dependence (Fagerstrom test for Nicotine Dependence: FTNDs) (15), psychological state (using Hospital Anxiety and Depression Scale (HADS) (16), co-addiction (alcohol, drugs, cannabis) and the level of motivation to quit smoking (QMAT scale) (17). Participants in "A" arm have start NRT. The first appointment was scheduled at one week from hospital discharge.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • patients aged more than 18 years, hospitalized with an ACS actively smoking at the time of inclusion, motivated to quit smoking, able to provide informed consent and willing to participate in a clinical study including a follow-up examination every 2 weeks after hospital discharge.

排除标准

  • the refusal of assistance of smoking cessation, inability to follow-up clinical visit (professional, regional or physical hindrance), diagnosis of depression or of serious health condition at admission (ventilated patient, cardiogenic shock, etc).

研究组 & 干预措施

A intervention

Experimental

intervention = Nicotine replacement therapy (NRT): initiated in cardiology intensive care unit, Some hours after acute coronary syndrome.

Drug: One or two pachs for each ARM, depending of number of cigarettes consummed every day. The dose is decreased every 4 weeks. The patient leave with an appointment to the external consultation for follow-up.

干预措施: Nicotine replacement therapy delivred in cardiology intensive care unit versus Nicotine replacement therapy delivered after hospital discharge (Procedure)

A intervention

Experimental

intervention = Nicotine replacement therapy (NRT): initiated in cardiology intensive care unit, Some hours after acute coronary syndrome.

Drug: One or two pachs for each ARM, depending of number of cigarettes consummed every day. The dose is decreased every 4 weeks. The patient leave with an appointment to the external consultation for follow-up.

干预措施: Nicotine patch (Drug)

B: control

Active Comparator

Intervention: Nicotine replacement therapy (NRT) initiated after hospital discharge, some days after acute coronary syndrome. The patient leave with an appointment to the external consultation for follow-up without pach of nicotine.One or two pachs for each ARM, depending of number of cigarettes consummed every day. The dose is decreased every 4 weeks.

干预措施: Nicotine replacement therapy delivred in cardiology intensive care unit versus Nicotine replacement therapy delivered after hospital discharge (Procedure)

B: control

Active Comparator

Intervention: Nicotine replacement therapy (NRT) initiated after hospital discharge, some days after acute coronary syndrome. The patient leave with an appointment to the external consultation for follow-up without pach of nicotine.One or two pachs for each ARM, depending of number of cigarettes consummed every day. The dose is decreased every 4 weeks.

干预措施: the external consultation (Other)

结局指标

主要结局

smoking cessation rates with NRT among patients hospitalized for acute coronary syndrome

时间窗: 24 weeks after acute coronary syndrome

smoking cessation rates with NRT when began in-hospitalization, against that began after hospital discharge

次要结局

  • smoking cessation duration with NRT among patients hospitalized for acute coronary syndrome(24 weeks after acute coronary syndrome)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sriha Belguith_asma

Head of epidemiology and preventive medicine, Principal Investigator, Associate Professor

University of Monastir

研究点 (1)

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