Low Trough (N = 48) | High Trough (N = 55) | Odds Ratio | 95% Confidence Interval | p-value | |
---|---|---|---|---|---|
Clinical Outcomes | |||||
• Clinical Cure (Primary Outcome) | 42 (88%) | 48 (87%) | 1.02 | 0.32–3.28 | > 0.99 |
• Survival | 48 (100%) | 54 (98%) | 2.67 | 0.11–67.13 | > 0.99 |
• Readmission within 30 days for same indication as original course of vancomycin | 0 (0%) | 2 (4%) | 0.22 | 0.01–4.71 | 0.50 |
Microbiological Outcome | |||||
• Patients With Positive Non-Screening Cultures for Resistant Gram positive Isolatesa identified up to 2 weeks after discontinuation of vancomycin | 0 | 0 | – | – | – |
Vancomycin Use and Dosing | |||||
• Final Total Daily Dose, medianb (mg) (Range) | 2000 (500–3000) | 2000 (666–4500) | 0.46 | ||
• Number of Patients With Daily Dose ≥3 g/dayc | 4 (8%) | 14 (25%) | 0.27 | 0.08–0.88 | 0.04 |
• Initial Steady State Trough (mg/L)d | 7.13 ± 2.24 | 12.20 ± 5.30 | <0.0001e | ||
• Final Steady State Trough (mg/L)d | 7.38 ± 1.95 | 16.56 ± 6.56f | < 0.0001f | ||
• Duration of Vancomycin Therapy (days)g | 7 ± 3 | 7 ± 3 | 0.73 | ||
• # Patients Requiring Dose Adjustment | 7 (15%) | 22 (40%) | 0.26 | 0.10–0.67 | 0.005 |
• # of Dose Adjustments Per Patientb | 0.17 ± 0.43 | 0.55 ± 0.79 | 0.02f | ||
• Time Estimate for Dose Adjustments Per Patient (minutes)b | 9 ± 23 | 29 ± 42 | 0.02f | ||
Renal Function Outcomes | |||||
• Final Serum Creatinine (mmol/L) | 71 ± 28 | 83 ± 46 | 0.11e | ||
• % Change in Serum Creatinine | −5 ± 18 | 3 ± 30 | 0.13e | ||
• At Risk for Kidney Injuryh | 0 (0%) | 4 (7%) | 0.12 | 0.01–2.25 | 0.12 |