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Bupropion for smokers hospitalized with acute cardiovascular disease.

Bupropion for smokers hospitalized with acute cardiovascular disease. Research Abstract Details 

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  • Bupropion for smokers hospitalized with acute cardiovascular disease. Abstract Text:

    nancy a rigottiNancy A Rigotti,anne n thorndikeAnne N Thorndike,susan reganSusan Regan,kathleen mckoolKathleen McKool,richard c pasternakRichard C Pasternak,yuchiao changYuchiao Chang,susan swartzSusan Swartz,nancy torres-finnertyNancy Torres-Finnerty,karen m emmonsKaren M Emmons,daniel e singerDaniel E Singer,

    PURPOSE: Smoking cessation after myocardial infarction reduces cardiovascular mortality, but many smokers cannot quit despite state-of-the-art counseling intervention. Bupropion is effective for smoking cessation, but its safety and efficacy in hospitalized smokers with acute cardiovascular disease is unknown. METHODS: A five-hospital randomized double-blind placebo-controlled trial assessed the safety and efficacy of 12 weeks of sustained-release bupropion (300 mg) or placebo in 248 smokers admitted for acute cardiovascular disease, primarily myocardial infarction and unstable angina. All subjects had smoking counseling in the hospital and for 12 weeks after discharge. Cotinine-validated 7-day tobacco abstinence, cardiovascular mortality, and new cardiovascular events were assessed at 3 months (end-of-treatment) and 1 year. RESULTS: Validated tobacco abstinence rates in bupropion and placebo groups were 37.1% vs 26.8% (OR 1.61, 95% CI, 0.94-2.76; P=.08) at 3 months and 25.0% vs 21.3% (OR, 1.23, 95% CI, 0.68-2.23, P=.49) at 1 year. The adjusted odds ratio, after controlling for cigarettes per day, depression symptoms, prior bupropion use, hypertension, and length of stay, was 1.91 (95% CI, 1.06-3.40, P=.03) at 3 months and 1.51 (95% CI, 0.81-2.83) at 1 year. Bupropion and placebo groups did not differ in cardiovascular mortality at 1 year (0% vs 2%), in blood pressure at follow-up, or in cardiovascular events at end-of-treatment (16% vs 14%, incidence rate ratio [IRR]1.22 (95% CI: 0.64-2.33) or 1 year (26% vs 18%, IRR 1.56, 95% CI 0.91-2.69). CONCLUSIONS: Bupropion improved short-term but not long-term smoking cessation rates over intensive counseling and appeared to be safe in hospitalized smokers with acute cardiovascular disease.

    Bupropion for smokers hospitalized with acute cardiovascular disease. Publishing Authors By Initials

    na rigottiNA Rigotti,an thorndikeAN Thorndike,s reganS Regan,k mckoolK McKool,rc pasternakRC Pasternak,y changY Chang,s swartzS Swartz,n torres-finnertyN Torres-Finnerty,km emmonsKM Emmons,de singerDE Singer,

    For similar behavior and behavior mechanisms: behavior: habits: smoking research abstracts see: behavior and behavior mechanisms: behavior: habits: smoking research

    PUBMED ID PMID:

    MEDLINE DATE:

    Bupropion for smokers hospitalized with acute cardiovascular disease. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: The American journal of medicine

    VOLUME: 119

    Page Numbers: 1080-7

    Journal Abbreviation: Am. J. Med.

    ISSN: 1555-7162

    DAY: 3

    MONTH: Dec

    YEAR: 2006

    Bupropion for smokers hospitalized with acute cardiovascular disease. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 267200

    Bupropion for smokers hospitalized with acute cardiovascular disease. Keywords Mesh Terms:

    KEYWORDS: Smoking

    MESH TERMS: drug therapy

    Chemical & Substance for Abstract: Bupropion for smokers hospitalized with acute cardiovascular disease. Information

    Substance Name: Bupropion

    Registry Number: 34841-39-9

    Grant and Affiliation Information for Bupropion for smokers hospitalized with acute cardiovascular disease.

    AFFILIATION: Tobacco Research and Treatment Center, General Medicine Division, and Cardiology Division, Massachusetts General Hospital and Harvard Medical School, Boston, Mass 02114, USA. nrigotti@partners.org

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NHLBI

    GRANT: R01 HL 61779

    ACRONYM: HL

    MEDLINETA: Am J Med

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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