From: Myocardial protection with phosphocreatine in high-risk cardiac surgery patients: a randomized trial
Placebo (n = 63) | Phosphocreatine (n = 57) | p-value | |
---|---|---|---|
Number of patients requiring vasopressor/inotropic drugs, n (%) | 57 (91%) | 49 (88%) | 0.60 |
LVEF on POD 1, %—median (IQR) | 56 (50–62) | 55 (52–59) | 0.89 |
Inotropic score on POD 1—median (IQR) | 4 (0–10) | 4 (0–7) | 0.47 |
SOFA score on POD 1 – mean ± SD | 5.45 ± 2.65 | 5.25 ± 2.33 | 0.83 |
Mechanical ventilation, hours | 6 (4–10) | 6 (4–11) | 0.70 |
New onset atrial fibrillation, n (%) | 5/43 (12%) | 8/30 (27%) | 0.13 |
Duration of ICU stay, hours—median (IQR) | 17 (16–20) | 18 (16–20) | 0.58 |
Length of hospitalization, days—median (IQR) | 14 (11–16) | 13 (11–15) | 0.64 |
Myocardial infarction, n (%) | 2 (3.2%) | 2 (3.5%) | 0.92 |
Acute kidney injury, n (%) | 6 (9.5%) | 9 (16%) | 0.43 |
Neurological damage type I, n (%) | 0 (0%) | 1 (1.7%) | 0.29 |
Neurological damage type II, n (%) | 4 (6.3%) | 5 (8.8%) | 0.61 |
Mediastinitis, n (%) | 3 (4.8%) | 1 (1.7%) | 0.36 |
Wound infection, n (%) | 2 (3.2%) | 2 (3.5%) | 0.92 |
Pneumonia, n (%) | 2 (3.2%) | 2 (3.5%) | 0.92 |
30-day mortality, n (%) | 1 (4.3%) | 0 (0%) | 0.40 |