Effects of candesartan on mortality and morbidity in patients with chronic heart failure: the CHARM-Overall programme
- PMID: 13678868
- DOI: 10.1016/s0140-6736(03)14282-1
Effects of candesartan on mortality and morbidity in patients with chronic heart failure: the CHARM-Overall programme
Erratum in
- Lancet. 2009 Nov 21-2009 Nov 27;(9703):1744
Abstract
Background: Patients with chronic heart failure (CHF) are at high risk of cardiovascular death and recurrent hospital admissions. We aimed to find out whether the use of an angiotensin-receptor blocker could reduce mortality and morbidity.
Methods: In parallel, randomised, double-blind, controlled, clinical trials we compared candesartan with placebo in three distinct populations. We studied patients with left-ventricular ejection fraction (LVEF) 40% or less who were not receiving angiotensin-converting-enzyme inhibitors because of previous intolerance or who were currently receiving angiotensin-converting-enzyme inhibitors, and patients with LVEF higher than 40%. Overall, 7601 patients (7599 with data) were randomly assigned candesartan (n=3803, titrated to 32 mg once daily) or matching placebo (n=3796), and followed up for at least 2 years. The primary outcome of the overall programme was all-cause mortality, and for all the component trials was cardiovascular death or hospital admission for CHF. Analysis was by intention to treat.
Findings: Median follow-up was 37.7 months. 886 (23%) patients in the candesartan and 945 (25%) in the placebo group died (unadjusted hazard ratio 0.91 [95% CI 0.83-1.00], p=0.055; covariate adjusted 0.90 [0.82-0.99], p=0.032), with fewer cardiovascular deaths (691 [18%] vs 769 [20%], unadjusted 0.88 [0.79-0.97], p=0.012; covariate adjusted 0.87 [0.78-0.96], p=0.006) and hospital admissions for CHF (757 [20%] vs 918 [24%], p<0.0001) in the candesartan group. There was no significant heterogeneity for candesartan results across the component trials. More patients discontinued candesartan than placebo because of concerns about renal function, hypotension, and hyperkalaemia.
Interpretation: Candesartan was generally well tolerated and significantly reduced cardiovascular deaths and hospital admissions for heart failure. Ejection fraction or treatment at baseline did not alter these effects.
Comment in
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Candesartan and heart failure: the allure of CHARM.Lancet. 2003 Sep 6;362(9386):754-5. doi: 10.1016/S0140-6736(03)14294-8. Lancet. 2003. PMID: 13678864 No abstract available.
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The CHARM programme.Lancet. 2003 Nov 15;362(9396):1675-6; author reply 1678-9. doi: 10.1016/S0140-6736(03)14808-8. Lancet. 2003. PMID: 14630453 No abstract available.
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The CHARM programme.Lancet. 2003 Nov 15;362(9396):1676; author reply 1678-9. doi: 10.1016/s0140-6736(03)14809-x. Lancet. 2003. PMID: 14630454 No abstract available.
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The CHARM programme.Lancet. 2003 Nov 15;362(9396):1676-7; author reply 1678-9. doi: 10.1016/S0140-6736(03)14810-6. Lancet. 2003. PMID: 14630455 No abstract available.
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The CHARM programme.Lancet. 2003 Nov 15;362(9396):1677-8; author reply 1678-9. doi: 10.1016/S0140-6736(03)14812-X. Lancet. 2003. PMID: 14630457 No abstract available.
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The CHARM programme.Lancet. 2003 Nov 15;362(9396):1678; author reply 1678-9. doi: 10.1016/S0140-6736(03)14813-1. Lancet. 2003. PMID: 14630459 No abstract available.
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The CHARM programme.Lancet. 2003 Nov 15;362(9396):1679. doi: 10.1016/S0140-6736(03)14815-5. Lancet. 2003. PMID: 14630460 No abstract available.
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Clinical trials report. CHARM-Overall Programme.Curr Hypertens Rep. 2004 Feb;6(1):46. Curr Hypertens Rep. 2004. PMID: 14972090 No abstract available.
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Clinical trials report. CHARM-Alternative Trial.Curr Hypertens Rep. 2004 Feb;6(1):47. Curr Hypertens Rep. 2004. PMID: 14972091 No abstract available.
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Candesartan reduced mortality and hospital admissions in chronic heart failure.ACP J Club. 2004 Mar-Apr;140(2):32-3. ACP J Club. 2004. PMID: 15122853 No abstract available.
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