Achieved dose and treatment discontinuation of candesartan in men and women with chronic heart failure: data from CHARM.

Abstract

Angiotensin receptor blockers have been shown to reduce heart failure hospitalization and cardiovascular mortality in men and women with heart failure with reduced ejection fraction (HFrEF). It is unknown whether there are differences between men and women in achieved dose and treatment discontinuation due to adverse events of candesartan. We conducted a post hoc analysis of the Candesartan in Heart failure: Assessment of Reduction in Mortality and morbidity (CHARM) programme. A total of 3172 men and 1106 women with HFrEF [left ventricular ejection fraction (LVEF)≤40%] in New York Heart Association class II-IV were randomized to candesartan or placebo. Every 2weeks, patients were up-titrated from 4 or 8, to16, to 32mg once daily, unless a higher dose was contraindicated or not tolerated. Women were older (66 vs. 64years), had a higher LVEF (29.9% vs. 28.6%), and had more hypertension (54% vs. 47%) than men. The mean achieved dose of candesartan was 21.5±12.6mg in men and 20.7±12.9mg in women (P=0.19). In both the candesartan and placebo groups, cardiovascular death and heart failure hospitalizations were higher in men and women who achieved lower dose levels. Event rates for achieved dose levels of 0, 4 or 8, 16, and 32mg candesartan were 20.8, 17.2, 14.0, and 10.1 per 100 person-years in men, respectively, and 23.6, 13.7, 14.0, and 9.1 per 100 person-years in women, respectively. In each of the achieved dose levels, there was no sex difference in the proportion of patients with an event, neither in the candesartan group nor in the placebo group (P-value for all>0.05). There was no significant interaction between sex and treatment-related discontinuation for hypotension (P=0.520), an increase in creatinine (P=0.102), and hyperkalaemia (P=0.905). In a randomized clinical trial in patients with HFrEF, men and women achieved similar doses of candesartan. Primary event rates and treatment-related discontinuation due to adverse events were also similar between men and women.