Telmisartan | Enalapril | P-value | |
---|---|---|---|
RAASi standardized dose* | 100% [100–100] | 50% [25–100] | < 0.001 |
Achieving ≥ 50% of the target RAASi dose | 93.5% | 68.6% | 0.002 |
Occurrence of DR | 10.6% | 32.7% | 0.008 |
Composite of DR-DC | 31.9% | 55.1% | 0.018 |
Peak serum creatinine | 1.68 ± 0.57 | 1.63 ± 0.50 | 0.61 |
Estimated GFR | 48.89 ± 12.44 | 54.04 ± 17.86 | 0.11 |
Serum potassium | 4.64 ± 0.56 | 4.57 ± 0.71 | 0.72 |
Rate of WRF (1) | 14% | 20.8% | 0.31 |
Rate of WRF (2) | 8.5% | 12.5% | 0.384 |
Rate of WRF (3) | 6.4% | 22.9% | 0.022 |
Maintaining MRA therapy | 89.4% | 87.5% | 0.51 |
Maintaining BB therapy | 87.2% | 93.8% | 0.23 |
BB standardized dose* | 39.4 ± 33.5% | 43.2 ± 32.4% | 0.569 |
Loop diuretic standardized dose† | 109 ± 126 | 125 ± 113 | 0.362 |
Composite of all-cause death and/or HHF | 22.4% | 28% | 0.343 |
All-cause death | 4% | 4% | 0.684 |
HFH | 18.4% | 28% | 0.185 |
NYHA classification at 3-months [n (%)] | |||
I–II | 30 (63.8%) | 33 (68.8%) | 0.785 |
III | 11 (23.4%) | 8 (16.7%) | |
IV | 6 (12.8%) | 7 (14.6%) | |
NYHA class shifts between baseline-to-3-months | 0 [− 1, 0] | 0 [− 1, 0] | 0.616 |