Key result
Baseline statin use in patients with systolic chronic heart failure was associated with a significant survival benefit compared to no statin use (HR 0.60; 95% CI 0.39-0.94; P<0.005).
Why the study?
Does statin therapy improve survival in patients with NYHA classes III-IV systolic chronic heart failure?
Cohort (n=2,647)
Does statin therapy improve survival in patients with NYHA classes III-IV systolic chronic heart failure?
Hazard Ratio: 0.6 (95% CI 0.39–0.94)
p-value: p=< 0.005
In a post-hoc analysis of the CIBIS II trial, baseline statin use was associated with improved survival in patients with systolic heart failure, with a potentially favorable interaction when combined with beta-blocker therapy.
BACKGROUND: HMG-CoA reductase inhibitors (statins) are widely prescribed in patients with established systolic chronic heart failure (CHF). However, there is considerable controversy regarding their benefit in this setting. We therefore conducted a post-hoc analysis of outcomes according to statin use within the Second Cardiac Insufficiency Bisoprolol Study of the beta-blocker, bisoprolol, in NYHA classes III-IV systolic CHF patients (left ventricular ejection fraction <35%), receiving background ACE inhibitor and diuretics. METHODS: Analysis of clinical outcomes was performed according to baseline use of statins and subsequent randomisation to placebo or bisoprolol. Cumulative incidence curves for clinical events were constructed using the Kaplan-Meier method and tested for significance by log-rank statistic. Multivariate analysis was performed using the Cox proportional hazards regression model. RESULTS: Two hundred and twenty-six of 2,647 patients were receiving statins at baseline (8.5%). Patients were well-matched in the 4 study groups at baseline for gender, weight, NYHA class and LVEF, however statin/bisoprolol patients were significantly younger (p < 0.05). Statin use at baseline was associated with a significant survival benefit compared with no statin use (p < 0.005, hazard ratio [HR] = 0.60, 95% confidence interval [CI] = 0.39-0.94). This benefit remained after adjusting for other significant predictors of survival (p < 0.05, HR = 0.60, 95%CI = 0.39-0.94). A significant interaction effect was noted with bisoprolol, survival being greatest in the statin/bisoprolol group (p < 0.001, HR = 0.14, 95% CI = 0.03-0.60). Survival was 98.3% in the statin/bisoprolol group, 82.1% in the statin/placebo group, 87.2% in the no statin/bisoprolol group and 82.8% in the no statin/placebo group. The statin/bisoprolol group was also associated with fewer cardiovascular (p < 0.005) and sudden deaths (p < 0.0005) compared with other groups. CONCLUSIONS: Despite the post-hoc, non-randomised nature of this analysis, these observations suggest that statin use appears to be beneficial in CHF. Furthermore, there appears to be a favourable interaction between statins and beta-blockade within the Second Cardiac Insufficiency Bisoprolol Study cohort. Prospective studies of statins are required to definitively address the role of these agents in established CHF.
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Krum et al. (2006) conducted a cohort in systolic chronic heart failure (n=2,647). Statin therapy vs. No statin therapy was evaluated on survival (HR 0.60, 95% CI 0.39-0.94, p=< 0.005). Baseline statin use in patients with systolic chronic heart failure was associated with a significant survival benefit compared to no statin use (HR 0.60; 95% CI 0.39-0.94; P<0.005).
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