Vancomycin Dosage Recommendations
Standard Dosing for Adults with Normal Renal Function
For adult patients with normal renal function, vancomycin should be dosed at 15-20 mg/kg (actual body weight) every 8-12 hours, not to exceed 2 g per dose, with target trough concentrations of 15-20 μg/mL for serious infections such as bacteremia, endocarditis, osteomyelitis, meningitis, and hospital-acquired pneumonia. 1, 2, 3
Dosing Algorithm by Infection Severity
For serious/severe infections:
- Loading dose: 25-30 mg/kg (actual body weight) for critically ill patients with suspected MRSA to rapidly achieve therapeutic concentrations 2, 3
- Maintenance dose: 15-20 mg/kg every 8-12 hours 1, 2, 4
- Target trough: 15-20 μg/mL 1, 2, 3
- Infusion time: Extend to 1.5-2 hours when individual doses exceed 1 g to minimize red man syndrome 1, 2, 4
For non-severe infections (e.g., uncomplicated cellulitis):
- Standard dose: 1 g IV every 12 hours in non-obese patients with normal renal function 2, 5
- Target trough: 10-15 μg/mL 2, 3
- Monitoring: Trough monitoring not routinely required for uncomplicated skin infections in patients with normal renal function who are not obese 2, 5
Critical Dosing Considerations
Weight-based dosing is mandatory in obese patients because conventional fixed dosing of 1 g every 12 hours results in subtherapeutic levels and treatment failure 2, 3, 5. The traditional 1 g every 12 hours regimen is inadequate for most adults, particularly those weighing >70 kg 2.
Loading doses are not affected by renal function and should be administered based on actual body weight even in patients with renal impairment 2. Only maintenance doses require adjustment for kidney dysfunction 2.
Dosing for Patients with Impaired Renal Function
Dosage adjustment is mandatory in patients with impaired renal function, with dosing intervals extended based on creatinine clearance while maintaining an initial dose of at least 15 mg/kg. 4
Renal Dosing Algorithm
Initial dose: Give at least 15 mg/kg even in patients with mild to moderate renal insufficiency to achieve prompt therapeutic concentrations 4
Maintenance dosing by creatinine clearance (CrCl):
- CrCl 100 mL/min: 1,545 mg/24h 4
- CrCl 70 mL/min: 1,080 mg/24h 4
- CrCl 50 mL/min: 770 mg/24h 4
- CrCl 30 mL/min: 465 mg/24h 4
- CrCl 10 mL/min: 155 mg/24h 4
For functionally anephric patients: After the initial 15 mg/kg dose, the maintenance dose required to maintain stable concentrations is 1.9 mg/kg/24h 4. In anuria, 1,000 mg every 7-10 days has been recommended 4.
For marked renal impairment: It may be more convenient to give maintenance doses of 250-1,000 mg once every several days rather than daily administration 4.
Monitoring in Renal Impairment
Measurement of vancomycin serum concentrations is essential in patients with changing renal function to optimize therapy 4. Trough concentrations should be obtained at steady state, before the fourth or fifth dose 2, 3.
Therapeutic Monitoring Strategy
Trough vancomycin concentrations are the most accurate and practical method to guide dosing and should be obtained at steady state conditions, prior to the fourth or fifth dose 1, 2, 3.
When to Monitor
Mandatory monitoring:
- Serious infections requiring trough levels of 15-20 μg/mL 1, 2, 3
- Morbidly obese patients 2, 3
- Renal dysfunction or fluctuating renal function 2, 3, 4
- Prolonged courses of therapy 1
Monitoring not required:
- Uncomplicated skin and soft tissue infections in non-obese patients with normal renal function 2, 5
- Short-course therapy (≤5 days) targeting trough <15 mg/L 1
Target AUC/MIC Ratio
The AUC/MIC ratio >400 is the pharmacodynamic parameter that best predicts vancomycin efficacy 1, 2, 3, 6. Trough concentrations of 15-20 mg/L should achieve an AUC/MIC of ≥400 for most patients if the MIC is ≤1 mg/L 1.
Critical Pitfalls and Caveats
If the vancomycin MIC is ≥2 μg/mL, alternative therapies must be considered because target AUC/MIC ratios are not achievable with conventional dosing in patients with normal renal function 1, 2, 3.
Trough concentrations >20 μg/mL significantly increase nephrotoxicity risk, especially when combined with other nephrotoxic agents 2. Vancomycin-induced nephrotoxicity should be suspected if multiple (at least 2-3 consecutive) high serum creatinine concentrations (increase of 0.5 mg/dL or 50% increase from baseline) are documented after several days of therapy 1.
Underdosing vancomycin leads to treatment failure and promotes resistance development, particularly when trough concentrations are <10 μg/mL 2, 3. Conversely, unnecessarily targeting high trough levels (15-20 μg/mL) for non-severe infections increases nephrotoxicity risk without clinical benefit 2, 3.
Peak concentration monitoring is not recommended to decrease the frequency of nephrotoxicity 1.