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1.
Rev Med Liege ; 77(10): 565-570, 2022 Oct.
Article in French | MEDLINE | ID: mdl-36226392

ABSTRACT

Atrial fibrillation (AF) is the most common heart rhythm disorder, with an increasing prevalence, currently estimated at 3 % of the world population. It has long been well known, as the holiday heart syndrome, that acute alcohol consumption (binge drinking) may trigger an episode of AF, most often benign, during or immediately after consumption. Meta-analyses of observational studies have clearly shown a significant association between a high level of alcohol consumption and the risk of AF. According to the studies included in meta-analyses, the conclusions may differ regarding the association between low and moderate levels of alcohol consumption and the risk of AF. The association probably only exists from a level of consumption of at least one drink per day. Heavy alcohol consumption appears to increase the risk of complications in patients with AF, while light or moderate alcohol consumption does not. The causal nature of the relationship between alcohol consumption and AF cannot currently be confirmed or denied, given the contradictory results of Mendelian randomization studies published to date. However, in patients diagnosed with AF, the recommendation to abstain from alcohol, resulting in a strong reduction in consumption, made it possible to significantly reduce the recurrence of AF episodes.


: La fibrillation auriculaire (FA) est le trouble du rythme cardiaque le plus fréquent, avec une prévalence croissante, actuellement estimée à 3 % de la population mondiale. La consommation aiguë d'alcool («binge drinking¼) est susceptible de déclencher un épisode de FA, le plus souvent bénin, au cours ou au décours immédiat de la consommation. Les méta-analyses d'études observationnelles ont clairement montré une association significative entre un niveau élevé de consommation d'alcool et le risque de FA. Selon les études incluses dans les méta-analyses, les conclusions peuvent différer concernant l'association entre les niveaux faibles et modérés de consommation d'alcool et le risque de FA. L'association n'existe vraisemblablement qu'à partir d'un niveau de consommation d'au moins 1 verre par jour. Une forte consommation d'alcool semble augmenter le risque de complications chez les patients atteints de FA, contrairement à une consommation faible ou modérée. La nature causale de la relation entre la consommation d'alcool et la FA ne peut actuellement être ni confirmée ni infirmée, compte-tenu des résultats contradictoires des études de randomisation mendélienne publiées à ce jour. En revanche, chez des patients diagnostiqués avec une FA, la recommandation de s'abstenir d'alcool, résultant en une forte réduction de la consommation, a permis de réduire significativement les récurrences de FA.


Subject(s)
Atrial Fibrillation , Alcohol Drinking/adverse effects , Alcohol Drinking/epidemiology , Atrial Fibrillation/epidemiology , Atrial Fibrillation/etiology , Ethanol , Humans , Risk Factors
2.
Rev Med Liege ; 76(4): 287-291, 2021 Apr.
Article in French | MEDLINE | ID: mdl-33830694

ABSTRACT

Tobacco is a risk factor for many chronic diseases and is the leading cause of preventable death. In the same way, periodontal diseases are one of the main chronic inflammatory diseases. The significant positive association between smoking and a higher risk of periodontitis is not any more to show and it appears that if smoking would be eliminated in this population, the risk of periodontitis would be reduced by approximately 14 %. Thus, the management of smoking cessation as well as periodontal treatment have become a public health issue. Motivational interviewing is a method of communication to support the change of health behaviour. The periodontist is then in the first position to set up a motivational interview in conjunction with smoking cessation and periodontal therapy. The taking into account of the risk factors among which tobacco is a stake for the restoration and the maintenance of periodontal health. Published evidence suggests that smoking cessation interventions are effective, highlighting the need for behavioural support in periodontal care. Motivational interviewing becomes an important part of both periodontal and smoking treatment.


Le tabac est un facteur de risque commun à nombreuses maladies chroniques; c'est la première cause de mortalité évitable. Les maladies parodontales sont l'une des principales maladies inflammatoires chroniques. L'association du tabagisme à une augmentation du risque de parodontite est bien démontrée; on estime que si le tabagisme était éliminé dans cette population, le risque de parodontite serait réduit d'environ 14 %. La prise en charge du sevrage tabagique, comme du traitement parodontal, est devenue un enjeu de santé publique. L'entretien motivationnel est une approche psychologique visant à engager les personnes dans le changement de comportement en matière de santé. Le parodontiste a une position idéale pour mettre en place un entretien motivationnel visant conjointement le sevrage tabagique et la thérapeutique parodontale. La prise en compte des facteurs de risque, dont le tabac, est un enjeu pour la restauration et le maintien de la santé parodontale. Les données publiées suggèrent que les interventions pour la cessation du tabagisme sont efficaces, soulignant ainsi la nécessité d'un soutien comportemental dans les soins parodontaux. L'entretien motivationnel devient une part importante du traitement, à la fois parodontal et tabagique.


Subject(s)
Motivational Interviewing , Smoking Cessation , Chronic Disease , Communication , Humans , Smoking
4.
Rev Mal Respir ; 36(7): 752-800, 2019 Sep.
Article in French | MEDLINE | ID: mdl-31285084

ABSTRACT

Although recognized as less dangerous than conventional cigarettes, the toxicity of the electronic cigarette vapor's toxicity remains to be fully assessed. This review explores vapers' exposition to formaldehyde and acrolein. METHOD: Systematic PubMed search for reports regarding formaldehyde or acrolein or their metabolites in electronic cigarette vapor, in vapers, or in ambient air. RESULTS: Fifty-two publications were selected. Found in almost all studies on vaper, formaldehyde is 8 times out of 11 - and acrolein constantly - in lower amounts than those found in conventional cigarettes. Acrolein's metabolite is found in all studies in vapers. The concentrations of formaldehyde and/or acrolein generated during vapor production may be affected by the characteristics of the E-liquid, voltage, vaping topography, and by the flavor additives. CONCLUSION: In the current state of knowledge, we must continue to support and help smokers to quit smoking, and for those who are engaged in a harm reduction approach, to minimize the duration of their electronic cigarette use.


Subject(s)
Acrolein/toxicity , Electronic Nicotine Delivery Systems , Formaldehyde/toxicity , Occupational Exposure , Vaping/adverse effects , Humans , Occupational Exposure/analysis , Occupational Exposure/statistics & numerical data , Smokers/statistics & numerical data , Smoking Cessation/methods , Vaping/epidemiology
5.
Drug Alcohol Depend ; 167: 42-8, 2016 Oct 01.
Article in English | MEDLINE | ID: mdl-27590745

ABSTRACT

INTRODUCTION: The aim of this study was to clarify the impact of binge drinking, its intensity and frequency, and drinker self-concept on health-related quality-of-life (HRQOL) in students. METHODS: This cross-sectional online survey included 16,930 students. We collected sociodemographics, environmental data, and drinking behaviors. We assessed HRQOL using the Alcohol Quality-of-Life scale, which explicitly explores the subjective negative impact on quality of life one attributes to his relationship with alcohol and the degree to which drinking is a part of an individual's self-concept. Data analyses were performed in 2015 and 2016. We described and compared binge drinkers and non-binge drinkers. Using a regression model we identified the independent factors associated with HRQOL. RESULTS: The impact on HRQOL attributed to alcohol was significantly greater among binge drinkers. Factors of impact on HRQOL subjectively attributed to alcohol by students were: AUDIT-C score, interaction between gender and AUDIT-C score, strong individual identity as a drinker, binge-drinking frequency, financial difficulties, being a foreigner, fewer years since diploma, chronic condition, recent use of cannabis, psychostimulant, poppers or gambling. Sleep quality, ability to work, expenditure on alcohol, shame, and health-related concerns were the most strongly impacted quality of life areas. CONCLUSIONS: Binge-drinking frequency should be considered as an important target in prevention programs. In addition, integrating findings on students' subjective perceptions of impairment of HRQOL by alcohol could enable the development of more acceptable and more relevant prevention messages.


Subject(s)
Alcohol Drinking/psychology , Binge Drinking/psychology , Quality of Life , Self Concept , Students/psychology , Adult , Cross-Sectional Studies , Female , Humans , Male
6.
Rev Mal Respir ; 33(10): 892-898, 2016 Dec.
Article in French | MEDLINE | ID: mdl-27242286

ABSTRACT

INTRODUCTION: Long-term nicotine use has been proposed as a risk-reduction strategy in smokers unwilling or unable to quit. However, its safety remains debated. METHODS: Analysis of publications identified in PubMed, Toxibase, Google Scholar and in the Food and Drug Administration, and French National Authority for Health websites. RESULTS: Nicotine seems to be implicated in the genesis of atherosclerosis. It could be a cancer precursor, could be implicated in cancer proliferation and angiogenesis, in apoptosis reduction, and may be genotoxic. New studies are warranted for more complete assessment of the risk-benefit balance. CONCLUSION: It is difficult to affirm the safety of long term nicotine use. The risk-benefit balance should be assessed in terms of a risk-reduction strategy, as in other domains, notably illicit drug use.


Subject(s)
Long Term Adverse Effects , Nicotine/adverse effects , Smoking Cessation/methods , Tobacco Use Disorder/therapy , Cardiovascular Diseases/chemically induced , Cardiovascular Diseases/epidemiology , Humans , Long Term Adverse Effects/epidemiology , Neoplasms/chemically induced , Neoplasms/epidemiology , Nicotine/administration & dosage , Nicotine/metabolism , Nitrosation/drug effects , Risk Assessment , Smoking Cessation/statistics & numerical data , Time Factors
7.
Qual Life Res ; 25(6): 1549-60, 2016 06.
Article in English | MEDLINE | ID: mdl-26589528

ABSTRACT

PURPOSE: The Alcohol Quality of Life Scale (AQoLS) is a new patient-reported outcome 34-item questionnaire measuring health-related quality of life (HRQOL), specific to patients with an alcohol use disorder, developed from the patients' perspective. This is the first report establishing evidence in support of measurement reliability and validity of the AQoLS. METHODS: A total of 285 randomly selected patients receiving interventions for alcohol use disorder in addiction specialised care settings in France were included in the study (response rate 80.1 %). Exploratory factor analysis was conducted to evaluate the hypothesised-during-development-stage dimensional structure of the AQoLS. Internal consistency of the total score and the dimensions subscores were assessed through Cronbach's alpha coefficients. Construct validity was tested through correlations with the Short-Form 36 Health Survey (SF-36) and EuroQol 5 dimensions (EQ-5D). RESULTS: Exploratory analysis indicated seven observed dimensions which differed slightly from the 7 dimensions defined a priori in the framework hypothesised during the scale development: activities, relationships, living conditions, negative emotions, self-esteem, control and sleep. A major common factor allows the summing of the 34 items to obtain a total score. All the 34 items were acceptable. Cronbach's alpha for the AQoLS total score was 0.96 and ranged from 0.8 to 0.9 for the dimensions subscores. Negative correlations between AQoLS and all dimensions of the SF-36, but general health and positive correlations between AQoLS and all items of the EQ-5D were shown. As expected, the correlations were mostly moderate in magnitude, low with scores referring to physical areas and the highest with the SF-36 MSC. CONCLUSION: This study provides evidence of the measure's psychometric properties in terms of construct validity and internal consistency. The "control" and "self-esteem" dimensions are of particular interest as these concepts are not captured in existing HRQOL. Further longitudinal validation of the scale is necessary to assess sensitivity to change.


Subject(s)
Alcohol-Related Disorders/psychology , Patient Reported Outcome Measures , Psychometrics/instrumentation , Quality of Life/psychology , Surveys and Questionnaires , Adult , Female , France , Health Status , Humans , Male , Middle Aged , Reproducibility of Results , Self Concept , Self-Control/psychology , Sleep , Young Adult
8.
Qual Life Res ; 24(6): 1471-81, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25407634

ABSTRACT

PURPOSE: The development of patient-centred approaches and of reduction in consumption strategies in alcohol use disorder requires giving a larger place to qualitative assessments that are closer to patients' concerns and more clinically relevant than drinking outcomes and generic health-related quality of life instrument. Our purpose was to develop from patients input the Alcohol Quality of Life Scale (AQoLS), a disease-specific measure for alcohol use disorder (AUD). METHODS: Concept elicitation focus groups were conducted with AUD patients in the UK and France. Thematic analysis was used to identify key areas of impact of AUD, and draft items were developed to capture these issues. The draft items underwent expert review to ensure clinical and cross-cultural applicability. Two iterative rounds of cognitive debriefing interviews were conducted with AUD patients in both countries, to assess face and content validity. RESULTS: From focus groups conducted with 38 AUD patients, seven areas of impact emerged, forming the basis for the AQoLS: relationships, activities, looking after self, emotional impact, control, living conditions, and sleep. An initial pool of 90 items was reduced to 50 following the review process. In cognitive interviews, the measure took less than 10 min to complete, and patients reported that items were relevant to their experience. Following Round 1 interviews (n = 16), 14 items were removed because patients felt they were unclear or uneasy to respond to, 2 were combined, 7 were revised, and 4 new items were added. The recall period of 2 weeks was changed to 4 weeks, based on patient comments. Following Round 2 interviews (n = 15), 5 items were removed and 3 were modified to produce the 34-item AQoLS. CONCLUSION: As the only de novo measure of health-related quality of life developed specifically for AUD, the AQoLS offers the potential of increased sensitivity to show the effectiveness of therapeutic interventions from the patient's perspective.


Subject(s)
Alcoholism/psychology , Health Status , Patient Outcome Assessment , Quality of Life , Adult , Aged , Female , Focus Groups , France , Humans , Male , Middle Aged , Psychometrics , Self Report , Surveys and Questionnaires , United Kingdom , Young Adult
11.
Rev Med Brux ; 34(3): 132-40, 2013.
Article in French | MEDLINE | ID: mdl-23951853

ABSTRACT

OBJECTIVES: Assess the effectiveness of hospital detoxification of opiate substitution treatment (OST) in patients who failed to withdraw as outpatients. METHODS: Retrospective study, conducted among patients admitted for withdrawal of OST in an addiction unit between 2005 and 2011. Referent physicians were interviewed about outcomes at M2, M3, M6 and M12. RESULTS: 47 patients were hospitalized for OST withdrawal. The opioid abstinence rates at 2, 6 and 12 months were 60, 28 and 21 %. No death occurred within 12 months after withdrawal. The only variables significantly associated with the M3 opioids abstinence were : age at admission and among the patients admitted for buprenorphine withdrawal, a low dose of buprenorphine at admission. CONCLUSION: OST withdrawal in a specialized inpatient unit among patients with failure of outpatient withdrawal appears as an option, with an efficacy at least comparable to other methods of detoxification. It allows a comprehensive care and to prevent the risk of overdose.


Subject(s)
Buprenorphine/adverse effects , Inpatients , Narcotic Antagonists/adverse effects , Opiate Substitution Treatment/adverse effects , Substance Withdrawal Syndrome/rehabilitation , Adolescent , Adult , Buprenorphine/administration & dosage , Female , Follow-Up Studies , Humans , Male , Middle Aged , Narcotic Antagonists/administration & dosage , Opiate Substitution Treatment/methods , Retrospective Studies , Risk Factors , Substance Withdrawal Syndrome/diagnosis , Time Factors , Treatment Outcome
12.
Drug Alcohol Depend ; 125(3): 192-202, 2012 Oct 01.
Article in English | MEDLINE | ID: mdl-22939877

ABSTRACT

AIM: The purpose of this systematic review was to compare quality-of-life instruments used as outcome measures in randomized clinical trials for alcohol-dependence treatment. METHODS: Randomized controlled clinical trials, indexed in the EMBASE, PubMed and PsycINFO databases since 1981, which aimed at improving the quality of life in alcohol-dependent patients and used as instrument to measure the quality of life, as specifically designated by the authors, were included. RESULTS: Of the 331 articles screened, 18 studies were included in the review. Eight different quality-of-life instruments were used as outcome measures. Twenty-seven life domains were explored. Between-scale heterogeneity was high. The scale most frequently used was the medical outcomes study 36-item short-form health survey (SF-36). Only 1 clinical trial demonstrated a significant difference between intervention groups at all endpoints, using the quality of life enjoyment and satisfaction questionnaire (Q-LES-Q). CONCLUSION: Because many different instruments were used, it is difficult to compare quality-of-life improvement between trials. The most frequently used instrument was a generic health status measure that may not be well suited as a quality-of-life measure for subjects with alcohol dependence. The construction and validation of a specific patient-reported outcome based on alcohol-dependent patients' concerns would effectively contribute to the assessment of treatment efficacy.


Subject(s)
Alcoholism/psychology , Neuropsychological Tests/standards , Quality of Life/psychology , Clinical Trials as Topic , Health Status , Humans , Personal Satisfaction , Randomized Controlled Trials as Topic , Reproducibility of Results , Surveys and Questionnaires
13.
Rev Med Brux ; 33(2): 87-96, 2012.
Article in French | MEDLINE | ID: mdl-22812054

ABSTRACT

Religion's impact on mental health has been largely studied, but results are often difficult to interpret due to methodological concerns: definition of religion and of spirituality ; measuring issues ; identification of specific components such as social dimension, cognitive schemas influencing world perception and meditating behaviors such as prayers. Furthermore, correlations between religious dimensions and mental health variables are too often considered as evidence of causality. Despite all those methodological problems, it appears that religiosity, defined as a global concept encompassing all aspects of religious life, might be a protective factor against several mental health problems, namely substance abuse, depression, suicide and anxiety disorders. This protective property isn't likely due to religions per se, but to associated components: risky behaviors' prevention due to shared moral standards, social support, sense of meaning, purposefulness and control, and meditation habits, exercising an inhibiting influence on chronic stress.


Subject(s)
Mental Health , Religion and Psychology , Humans , Morals , Social Support
14.
Rev Med Liege ; 67(4): 195-201, 2012 Apr.
Article in French | MEDLINE | ID: mdl-22670447

ABSTRACT

Fear of not controlling stress is the most frequently reported obstacle to smoking cessation. We report a retrospective study involving 70 smokers whose files were randomly selected from a smoking cessation clinic's recruitment. Stress management as a motive to smoke (SMMS) was systematically explored at the first visit, before quit date. SMMS mean score was 7.36 (+/- 2.4) on a 10 point scale. The score was higher in females than in males (p = 0,048). A multivariate logistic regression showed that SMMS was explained by two variables: physical dependence as measured with the FTND score (OR = 1.7, 95% CI = 1.18-2.46), and anxiety as measured with the HAD scale (OR = 1.27, 95% CI = 1.03-1.56). In conclusion, the high frequency and impact of perceived stress on smoking behavior call for a systematic clinical evaluation of perceived stress when engaging a treatment for smoking dependence. Our work has confirmed the importance for the smokers of perceived stress on their smoking behavior, particularly in females. Perceived stress showed a strong relationship with nicotine dependence and anxiety. Further investigation is warranted for a better understanding of the relationship between perceived stress and anxiety in smokers.


Subject(s)
Smoking Cessation/psychology , Smoking/psychology , Stress, Psychological/complications , Adult , Anxiety/psychology , Female , Humans , Male , Middle Aged , Retrospective Studies
15.
Encephale ; 37(5): 379-87, 2011 Oct.
Article in French | MEDLINE | ID: mdl-22032281

ABSTRACT

INTRODUCTION: In substance use disorders, the lack of empirically supported treatments and the minimal utilization of available programs indicate that innovative approaches are needed. Mindfulness based therapies have been used in addictive disorders for the last 10years. Mindfulness can be defined as the ability to focus open, non-judgmental attention to the full experience of internal and external phenomena, moment by moment. Several therapies based on mindfulness have been developed. The aim of this study is to review the existing data on the use of these programs in addictive disorders. METHODS: We have reviewed the literature published from January 1980 to January 2009, using the following keywords: mindfulness, mindfulness based stress reduction program, dialectical behavior therapy, acceptance and commitment therapy, mindfulness based cognitive therapy, addiction, substance use, alcohol and smoking. RESULTS: Results of six clinical trials evaluating four different programs were found. Five studies were controlled and four were randomized. Drop-out rates were relatively high (from 28 to 55%). In five cases out of six, the program significantly reduced substance use. In four comparative trials out of five, interventions based on mindfulness proved more effective than control conditions. The effectiveness of interventions based on mindfulness and the differential improvement across conditions became greater and was maintained during follow-up when it was long enough. Participants in mindfulness programs were less likely to endorse the importance of reducing emotions associated with smoking and reported significant decreases in avoidance of thoughts which partially mediated alcohol use reduction. Psychiatric symptoms and the level of perceived stress were also significantly reduced. DISCUSSION: Mindfulness may help substance abusers to accept unusual physical sensations that might be confused with withdrawal symptoms, decentre from a strong urge and not act impulsively. It may reduce an individual's susceptibility to act in response to a drug cue. Practice of mindfulness may develop the ability to maintain perspective in response to strong emotional states and mood fluctuations and increase the saliency of natural reinforcers. Mindfulness based programs require an intensive participation, and should therefore be proposed to highly motivated patients. In smoking cessation, they should be used in patients who were unable to quit with less intensive interventions. Some programs are specifically designed for patients with co-occurring psychiatric disorders. CONCLUSION: The first clinical studies testing mindfulness based interventions in substance use disorders have shown promising results. They must be confirmed by larger controlled randomized clinical trials. By developing a better acceptance of unusual physical sensations, thoughts about drugs and distressing emotions, mindfulness may help in reducing the risk of relapse.


Subject(s)
Alcoholism/rehabilitation , Attention , Awareness , Cognitive Behavioral Therapy/methods , Meditation , Smoking Cessation/psychology , Substance-Related Disorders/rehabilitation , Adaptation, Psychological , Alcoholism/psychology , Controlled Clinical Trials as Topic , Emotions , Humans , Internal-External Control , Motivation , Randomized Controlled Trials as Topic , Substance-Related Disorders/psychology
16.
Alcohol Alcohol ; 46(5): 586-91, 2011.
Article in English | MEDLINE | ID: mdl-21771742

ABSTRACT

AIM: Assessing acceptance of controlled drinking (CD) among French alcohol specialists. METHODS: On-line survey of 547 French alcohol specialists. We searched factors associated with acceptance of CD, and factors that affected the specialists' selection of treatment goal. Criteria for success used by specialists in clinical practice were compared with criteria expected to be used in clinical trials. RESULTS: CD was accepted as a treatment goal by 48.6% of alcohol specialists (n = 105, n = 216), and 61.9% practiced CD for their own patients (n = 130, n = 210). Factors in selecting outcome goals were: patient's choice, perceived self-efficacy, relapse history and severity of dependence. Age, profession and basis of specialists' opinion on CD were associated with acceptance of CD. CONCLUSION: Half of French alcohol specialists accept CD as a goal. Acceptance was associated with specialists' personal and professional characteristics. The criteria for success specialists use in their clinical practice differ from those they expect to be used in clinical trials.


Subject(s)
Alcohol Drinking/therapy , Alcoholism/therapy , Goals , Temperance/psychology , Adult , Alcohol Drinking/metabolism , Alcohol Drinking/psychology , Alcoholism/metabolism , Alcoholism/psychology , Attitude of Health Personnel , Clinical Trials as Topic , Data Collection , Electronic Mail , France , Humans , Internet , Middle Aged , Software , Specialization
17.
Thorax ; 63(8): 717-24, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18263663

ABSTRACT

BACKGROUND: Varenicline, a new treatment for smoking cessation, has demonstrated significantly greater efficacy over placebo and sustained release bupropion (bupropion SR). A study was undertaken to compare a 12-week standard regimen of varenicline with a 10-week standard regimen of transdermal nicotine replacement therapy (NRT) for smoking cessation. METHODS: In this 52-week, open-label, randomised, multicentre, phase 3 trial conducted in Belgium, France, The Netherlands, UK and USA, participants were randomly assigned (1:1) to receive varenicline uptitrated to 1 mg twice daily for 12 weeks or transdermal NRT (21 mg/day reducing to 7 mg/day) for 10 weeks. Non-treatment follow-up continued to week 52. The primary outcome was the biochemically confirmed (exhaled carbon monoxide < or = 10 ppm) self-reported continuous abstinence rate (CAR) for the last 4 weeks of the treatment period in participants who had taken at least one dose of treatment. Secondary outcomes included CAR from the last 4 weeks of treatment through weeks 24 and 52, and measures of craving, withdrawal and smoking satisfaction. RESULTS: A total of 376 and 370 participants assigned to varenicline and NRT, respectively, were eligible for analysis. The CAR for the last 4 weeks of treatment was significantly greater for varenicline (55.9%) than NRT (43.2%; OR 1.70, 95% CI 1.26 to 2.28, p<0.001). The week 52 CAR (NRT, weeks 8-52; varenicline, weeks 9-52) was 26.1% for varenicline and 20.3% for NRT (OR 1.40, 95% CI 0.99 to 1.99, p = 0.056). Varenicline significantly reduced craving (p<0.001), withdrawal symptoms (p<0.001) and smoking satisfaction (p<0.001) compared with NRT. The most frequent adverse event was nausea (varenicline, 37.2%; NRT, 9.7%). CONCLUSIONS: The outcomes of this trial established that abstinence from smoking was greater and craving, withdrawal symptoms and smoking satisfaction were less at the end of treatment with varenicline than with transdermal NRT. TRIAL REGISTRATION NUMBER: NCT00143325.


Subject(s)
Benzazepines/administration & dosage , Nicotine/administration & dosage , Nicotinic Agonists/administration & dosage , Quinoxalines/administration & dosage , Smoking Cessation/methods , Smoking Prevention , Administration, Cutaneous , Adolescent , Adult , Aged , Female , Humans , Male , Middle Aged , Patient Compliance , Reinforcement, Psychology , Substance Withdrawal Syndrome/etiology , Treatment Outcome , Varenicline
18.
Gynecol Obstet Fertil ; 34(12): 1126-30, 2006 Dec.
Article in French | MEDLINE | ID: mdl-17113811

ABSTRACT

OBJECTIVE: To investigate the smoking cessation period during pregnancy. PATIENTS AND METHODS: Questionnaire-based, descriptive study of 979 pregnant women in four regions of France. The variables analysed included the characteristics of the mother and neonate at delivery, the smoking habits of the mother before and during pregnancy, the perception of risk linked to smoking, and the reasons for giving up smoking. RESULTS: Eighteen percent of women smoked until delivery. Forty-five percent of women gave up smoking during pregnancy, usually in the first trimester. More precisely, about one woman who smoked out of 50 gives up in order to prepare pregnancy. The proportion of women who stop smoking in each of the three trimesters of pregnancy is 84,1, 8,8 and 7,1% respectively. DISCUSSION AND CONCLUSION: Most women appear to stop smoking before any intervention therapy is possible. The first contact with a midwife or an obstetrician takes place whereas smoking cessation is already successful.


Subject(s)
Mothers/psychology , Motivation , Prenatal Exposure Delayed Effects , Smoking Cessation/statistics & numerical data , Smoking/psychology , Adult , Female , France , Humans , Pregnancy , Pregnancy Trimester, First , Pregnancy Trimester, Second , Pregnancy Trimester, Third , Surveys and Questionnaires , Time Factors
20.
Sleep Med ; 7(2): 147-54, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16458598

ABSTRACT

BACKGROUND AND PURPOSE: Sleep disturbance is a common symptom of tobacco withdrawal and might contribute to early relapse vulnerability in abstinent smokers. This study was designed to compare the effects on sleep of nicotine patches applied either for 24 h (Nicopatch) or 16 h (Nicorette). PATIENTS AND METHODS: During a short smoking cessation period (48 h), this open-label, randomised, two-period crossover study compared the effects on sleep of the two nicotine patches in 20 heavy smokers (9 women, 11 men). During each period, polysomnographic recordings were performed from 12 pm to 7 am for two consecutive nights (baseline and treatment nights). Smoking cessation started from 8 pm the day of the baseline sleep recordings, and treatments were applied around 8 am the following morning. RESULTS: Compared to the 16-h nicotine patch, smokers who received the 24-h nicotine patch experienced significantly less microarousals, a greater proportion of slow wave sleep, a higher REM density and higher rapid eye movement (REM) beta activities. CONCLUSIONS: The results of this study suggest that a 24-h nicotine patch is more efficient than a 16-h nicotine patch to alleviate tobacco withdrawal-induced sleep disturbances.


Subject(s)
Ganglionic Stimulants/pharmacology , Ganglionic Stimulants/therapeutic use , Nicotine/pharmacology , Nicotine/therapeutic use , Polysomnography/methods , Sleep, REM/drug effects , Smoking Cessation/methods , Smoking Prevention , Administration, Cutaneous , Administration, Topical , Adult , Cross-Over Studies , Drug Administration Schedule , Female , Ganglionic Stimulants/administration & dosage , Humans , Male , Nicotine/administration & dosage , Surveys and Questionnaires , Time Factors
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