Table 3.
Outcomes of major randomized, placebo-controlled trials in patients with heart failure and reduced ejection fraction
Trial | β-Blocker | N | Mean duration | EF | Primary endpoints | Main outcomes |
---|---|---|---|---|---|---|
CIBIS-II [15] | Bisoprolol | 2647 | 1.3 years | ≤35% | All-cause mortality | 11.8 vs. 17.3% (HR 0.66; p < 0.0001) |
Sudden death | 3.6 vs. 6.3% (HR 0.56; p = 0.0011) | |||||
COPERNICUS [16] | Carvedilol | 2289 | 10.4 months | <25% | Combined risk of death or hospitalization for CV reasons | Cumulative risk 41.6 vs. 30.2% (p = 0.00002) |
Combined risk of death or hospitalization for HF | Cumulative risk 37.9 vs. 25.5% (p = 0.000004) | |||||
MERIT-HF [17] | Metoprolol | 3991 | 1 year | ≤40% | Combined total mortality or all-cause hospitalization | Risk reduction 19% (p < 0.001) |
SENIORS [18] | Nebivolol | 2128 | 21 months | ≤35% in 65% of pts; >35% in 35% of pts | Death or hospitalization for CV reasons | 31.1 vs. 35.3% (HR 0.86; p = 0.039) |
All-cause mortality | 15.8 vs. 18.1% (HR 0.88; p = 0.21) |
CV cardiovascular, EF ejection fraction, HF heart failure, HR hazard ratio, pts patients