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Prevention of atrial fibrillation in patients with symptomatic chronic heart failure by candesartan in the Candesartan in Heart failure: Assessment of Reduction in Mortality and morbidity (CHARM) program

Ducharme, A. (author)
Swedberg, Karl, 1944 (author)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för akut och kardiovaskulär medicin,Institute of Medicine, Department of Emergeny and Cardiovascular Medicine
Pfeffer, M. A. (author)
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Cohen-Solal, A. (author)
Granger, C. B. (author)
Maggioni, A. P. (author)
Michelson, E. L. (author)
McMurray, J. J. (author)
Olsson, L. (author)
Rouleau, J. L. (author)
Young, J. B. (author)
Olofsson, B. (author)
Puu, M. (author)
Yusuf, S. (author)
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 (creator_code:org_t)
2006
2006
English.
In: American heart journal. - 1097-6744. ; 152:1, s. 86-92
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND: Atrial fibrillation (AF) is frequent in patients with chronic heart failure (CHF). Experimental and small patient studies have demonstrated that blocking the renin-angiotensin-aldosterone system may prevent AF. In the CHARM program, the effects of the angiotensin receptor blocker candesartan on cardiovascular mortality and morbidity were evaluated in a broad spectrum of patients with symptomatic CHF. CHARM provided the opportunity to prospectively determine the effect of candesartan on the incidence of new AF in this CHF population. METHODS: 7601 patients with symptomatic CHF and reduced or preserved left ventricular systolic function were randomized to candesartan (target dose 32 mg once daily, mean dose 24 mg) or placebo in the 3 component trials of CHARM. The major outcomes were cardiovascular death or CHF hospitalization and all-cause mortality. The incidence of new AF was a prespecified secondary outcome. Median follow-up was 37.7 months. A conditional logistic regression model for stratified data was used. RESULTS: 6379 patients (83.9%) did not have AF on their baseline electrocardiogram. Of these, 392 (6.15%) developed AF during follow-up, 177 (5.55%) in the candesartan group and 215 (6.74%) in the placebo group (odds ratio 0.812, 95% CI 0.662-0.998, P = .048). After adjustment for baseline covariates, the odds ratio was 0.802 (95% CI 0.650-0.990, P = .039). There was no heterogeneity of the effects of candesartan in preventing AF between the 3 component trials (P = .57). CONCLUSIONS: Treatment with the angiotensin receptor blocker candesartan reduced the incidence of AF in a large, broadly-based, population of patients with symptomatic CHF.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Keyword

Aged
Angiotensin II Type 1 Receptor Blockers/pharmacology/*therapeutic use
Atrial Fibrillation/epidemiology/physiopathology/*prevention & control
Benzimidazoles/pharmacology/*therapeutic use
Comorbidity
Female
Heart Failure
Congestive/*drug therapy/epidemiology
Humans
Logistic Models
Male
Middle Aged
Prospective Studies
Randomized Controlled Trials
Renin-Angiotensin System/drug effects/physiology
Tetrazoles/pharmacology/*therapeutic use

Publication and Content Type

ref (subject category)
art (subject category)

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