2003
DOI: 10.1016/s0140-6736(03)14284-5
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Effects of candesartan in patients with chronic heart failure and reduced left-ventricular systolic function intolerant to angiotensin-converting-enzyme inhibitors: the CHARM-Alternative trial

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Cited by 1,557 publications
(637 citation statements)
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“…Even in clinical trials, this is problematic; e.g. in the CHARM‐Alternative study, 59% of the candesartan group reached target dose 4. In the PARADIGM‐HF trial, 12% of the patients withdrew during the run‐in phase owing to adverse events of enalapril or sacubitril–valsartan 10.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Even in clinical trials, this is problematic; e.g. in the CHARM‐Alternative study, 59% of the candesartan group reached target dose 4. In the PARADIGM‐HF trial, 12% of the patients withdrew during the run‐in phase owing to adverse events of enalapril or sacubitril–valsartan 10.…”
Section: Discussionmentioning
confidence: 99%
“…Standard heart failure therapy is effective and refers to an angiotensin‐converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB), a beta‐blocker, and a mineralocorticoid antagonist 2. Even though standard treatment reduces risk of death and heart failure hospitalization by up to 10–37%,3, 4, 5, 6, 7, 8, 9 mortality is high, and many patients suffer from severe symptoms on a daily basis. New and more effective heart failure treatments are needed.…”
Section: Introductionmentioning
confidence: 99%
“…There is good evidence from CHARM-Alternative [13] in patients with CHF and VALIANT [14] in patients after acute myocardial infarction to show that ARBs are a good alternative in patients who cannot tolerate an ACE inhibitor. Furthermore, CHARM-Added [15] showed that ARBs in addition to ACE inhibitors reduce cardiovascular mortality in patients with CHF and Val-HeFT [16] and VALIANT [14] showed that the combination reduced hospital admissions for worsening heart failure in patients with CHF and after acute myocardial infarction, respectively.…”
Section: Discussionmentioning
confidence: 99%
“…81 The candesartan-based regimen resulted in a lower primary end point of total mortality, as well as any secondary end points other than the placebo-based regimen (P ¼ 0.01). In a substudy, 2025 patients intolerant to ACEIs were randomized to either candesartan 32 mg/day (n ¼ 1013) or placebo (n ¼ 1015) and followed for 33.7 months; 82 candesartan reduced the composite end point of cardiovascular death or hospital admissions for CHF by 30% compared to placebo (Po0.0001). The results of the recently published VALIANT study 83 were somewhat different from the Val-HeFT and CHARM studies.…”
Section: Heart Failurementioning
confidence: 99%