Variable | Ketorolac ( n  = 54) | Placebo ( n  = 55) | P value |
---|---|---|---|
Safety endpoint (n, %) | |||
 Total positive patients | 3, 5.56% | 9, 16.36% | 0.135 |
 gastrointestinal ulceration | 0 | 0 | - |
 gastrointestinal bleeding | 0 | 0 | - |
 gastrointestinal perforation | 0 | 0 | - |
 postoperative hemorrhage within 24 h > 1L | 2, 3.70% | 5, 9.09% | 0.449 |
 renal failure | 1, 1.85% | 0 | 0.993 |
 liver failure | 0 | 4, 7.27% | 0.131 |
 drug allergies | 0 | 0 | - |
Efficacy endpoint (n, %) | |||
 Total positive patients | 6, 11.11% | 7, 12.73% | 0.795 |
 in-hospital mortality | 3, 5.56% | 6, 10.91% | 0.505 |
 organ malperfusion syndrome | 2, 3.70% | 4, 7.27% | 0.691 |
 permanent dialysis | 0 | 0 | - |
 tracheotomy | 0 | 2, 3.64% | 0.484 |
 neurological impairment | 0 | 2, 3.64% | 0.484 |
 unplanned cardiac reoperation | 1, 1.85% | 0 | 0.993 |
 mechanical circulatory support | 0 | 2, 3.64% | 0.484 |
 ECMO (n, %) | 0 | 2, 3.64% | 0.484 |
 IABP (n, %) | 0 | 0 | - |
Other Endpoints | |||
 Postoperative peek BP > 140 mmHg (n, %) | 13, 24.07% | 11, 20.00% | 0.778 |
 Postoperative cardiac arrest (n, %) | 0 | 0 | - |
 Pneumonia (n, %) | 4, 7.41% | 12, 21.82% | 0.064 |
 Stroke (n, %) | 0 | 0 | - |
 Mechanical ventilation time [hours, M (Q1, Q3)] | 23.50(12.25–59.75) | 28.00(17.50–79.00) | 0.247 |
 Duration of hospitalization [days, M (Q1, Q3)] | 16.50(15.00–19.00) | 17.50(15.75–22.00) | 0.067 |
 Duration of ICU stay [days, M (Q1, Q3)] | 6.50(5.00–8.00) | 8.00(6.00–10.50) | 0.044 |
 Bleeding in surgery [L, M (Q1, Q3)] | 1.80(1.40–2.00) | 2.00(1.50–3.00) | 0.030 |
 Chest drainage within post-24 h [mL, M (Q1, Q3)] | 320.00(230.00–477.50) | 480.00(350.00–620.00) | 0.001 |
 AKI stage II or IIIb (n, %) | 4, 7.41% | 10, 18.18% | 0.163 |
 CRRT (n, %) | 1, 1.85% | 4, 7.27% | 0.371 |
 Total hospital costs [× 103¥, M (Q1, Q3)] | 170.43 (145.97–190.60) | 187.73 (153.75–220.54) | 0.028 |