Characteristic | |
Initial dose (daily), n (%) | |
  1000–2000 mg | 4 (5.1) |
  2001–3000 mg | 50 (64.1) |
   > 3000 mg | 24 (30.8) |
Average daily dosage (mg/kg, q12h) | 15.18 ± 3.29 |
 | 15.38 [14.29–19.27] |
Average trough concentration (mg/L) | 8.26 ± 5.01 |
 | 6.90 [5.28–11.20] |
Ctrough, n (%) | |
   < 10 mg/L | 54 (69.2) |
  10–15 mg/L | 15 (19.2) |
  15–20 mg/L | 8 (10.3) |
   > 20 mg/L | 1 (1.3) |
 AUC, n (%) | |
   < 400 | 52 (66.7) |
  400–600 | 24 (30.7) |
   > 600 | 2 (2.6) |
Clinical Outcomes | |
 Primary endpoints | |
  Clinical success rate, n (%) | 58 (74.4) |
  28-day all-cause mortality, n (%) | 4 (5.1) |
  Composite outcome of new-onset AKI or RRT, n (%) | 7 (9.0) |
 Secondary endpoints | |
  Duration of vasoactive agent (day) | 4 [2-5] |
  Duration of ventilation (day) | 4 [3-5] |
  Duration of antibiotics (day) | 5 [5-7] |