Vancomycin Renal Dosing
For patients with impaired renal function, administer a full loading dose of 25-30 mg/kg (actual body weight) regardless of renal dysfunction, then extend the maintenance dosing interval based on creatinine clearance while maintaining the weight-based dose of 15-20 mg/kg. 1
Loading Dose Strategy in Renal Impairment
- The loading dose is NOT affected by renal function and must be given at full weight-based dosing (25-30 mg/kg actual body weight) even in severe renal dysfunction, including patients with creatinine clearance <30 mL/min. 1, 2
- This loading dose is designed to fill the volume of distribution, which remains unchanged regardless of kidney function. 1
- Never reduce or omit the loading dose based on renal function—this is the most common error and leads to delayed achievement of therapeutic levels. 1
- Research demonstrates that loading doses >20 mg/kg in patients with severe renal impairment (CrCl <30 mL/min) actually reduce nephrotoxicity risk compared to lower doses (7.2% vs 13.8%, p<0.01). 2
Maintenance Dosing Adjustments
Dosing Interval Extension Based on Creatinine Clearance
The FDA-approved dosing table provides specific guidance: 3
- CrCl 100 mL/min: 1,545 mg/24h (standard 15-20 mg/kg every 8-12h)
- CrCl 90 mL/min: 1,390 mg/24h
- CrCl 80 mL/min: 1,235 mg/24h
- CrCl 70 mL/min: 1,080 mg/24h
- CrCl 60 mL/min: 925 mg/24h
- CrCl 50 mL/min: 770 mg/24h
- CrCl 40 mL/min: 620 mg/24h
- CrCl 30 mL/min: 465 mg/24h
- CrCl 20 mL/min: 310 mg/24h
- CrCl 10 mL/min: 155 mg/24h
Practical Dosing Approach
- The vancomycin dose per day in mg is approximately 15 times the glomerular filtration rate in mL/min. 3, 4
- After the loading dose, extend the dosing interval to 24-48 hours or longer based on creatinine clearance, rather than reducing individual doses. 1
- In marked renal impairment, it may be more convenient to give maintenance doses of 250-1,000 mg once every several days rather than daily. 3
- In anuria, a dose of 1,000 mg every 7-10 days has been recommended. 3
Therapeutic Monitoring Requirements
- Mandatory trough monitoring before the fourth dose is essential in all patients with renal impairment. 1
- Target trough concentrations of 15-20 mg/L for serious infections (bacteremia, endocarditis, osteomyelitis, meningitis, pneumonia). 1, 5
- Monitor serum creatinine at least twice weekly throughout therapy. 5
- Recheck trough with each dose adjustment. 5
Creatinine Clearance Estimation
When only serum creatinine is available, use the Cockcroft-Gault formula: 3
- Men: [Weight (kg) × (140 – age in years)] / [72 × serum creatinine (mg/dL)]
- Women: 0.85 × above value
Important caveat: This calculated clearance overestimates actual clearance in patients with shock, severe heart failure, oliguria, obesity, liver disease, edema, ascites, debilitation, malnutrition, or inactivity. 3
Nephrotoxicity Prevention
- Sustained trough concentrations >20 μg/mL significantly increase nephrotoxicity risk. 6, 7
- If trough exceeds 20 mg/L, immediately hold the next dose and recheck trough before administering subsequent doses. 6, 5
- Concomitant nephrotoxic medications (aminoglycosides, piperacillin-tazobactam, CT contrast, amphotericin B, NSAIDs) substantially increase nephrotoxicity risk. 1
- Monitor for nephrotoxicity defined as increases in serum creatinine of ≥0.5 mg/dL or 150% increase from baseline. 6
Special Populations
Dialysis Patients
- For functionally anephric patients, give an initial dose of 15 mg/kg to achieve prompt therapeutic concentrations. 3
- The dose required to maintain stable concentrations is 1.9 mg/kg/24h. 3
- In patients on CRRT, monitor trough levels at least twice weekly. 5
- Vancomycin clearance in dialysis patients averages 0.086 mL/min/kg. 4
Elderly Patients
- Greater dosage reductions than expected may be necessary because of decreased renal function. 3
- Measurement of vancomycin serum concentrations is particularly helpful in optimizing therapy in elderly patients with changing renal function. 3
Critical Pitfalls to Avoid
- Never use fixed 1-gram doses in renal impairment—this results in either subtherapeutic or toxic levels. 1
- Do not reduce the loading dose based on renal dysfunction. 1, 2
- Avoid targeting trough levels >20 mg/L, as this dramatically increases nephrotoxicity risk without improving efficacy. 6, 7
- Never rely on peak level monitoring—it provides no clinical value. 5
- If vancomycin MIC ≥2 μg/mL, switch to alternative agents (daptomycin, linezolid, ceftaroline) as target AUC/MIC ratios are not achievable. 1, 5