Vancomycin Dosing in Dialysis Patients
For patients on intermittent hemodialysis, administer a loading dose of 20-25 mg/kg (actual body weight) followed by weight-based maintenance dosing of 500-1000 mg after each dialysis session, with mandatory trough monitoring before each dialysis to maintain target levels of 15-20 mg/L for serious infections. 1, 2
Loading Dose Strategy
- Administer a full loading dose of 20-25 mg/kg based on actual body weight regardless of dialysis status, as the loading dose is not affected by renal function and is essential to rapidly achieve therapeutic concentrations 3, 1, 4
- The loading dose of 20 mg/kg rapidly and reliably establishes therapeutic pre-dialysis serum levels (10-25 μg/mL) in hemodialysis patients 5
- For seriously ill patients with suspected MRSA infection, consider the higher end of the loading dose range (25-30 mg/kg) 3, 6
Maintenance Dosing Regimen
Weight-based maintenance dosing after each dialysis session is critical, as fixed-dose regimens fail to reach target levels in the majority of hemodialysis patients 4:
- Patients <70 kg: 500 mg after each dialysis session 2
- Patients 70-100 kg: 750 mg after each dialysis session 2
- Patients >100 kg: 1000 mg after each dialysis session 2
This weight-based protocol achieves maintenance (pre-HD) troughs of 10-20 mg/L in 86% of patients, with 65.5% achieving levels between 10-20 mg/L 2
Timing of Administration
- Administer vancomycin during the last hour of the dialysis session rather than after dialysis, as this approach is safe, efficacious, and improves patient quality of life 7
- If administering during dialysis, increase the dose by approximately 25% to compensate for dialysis-related losses (e.g., 1.4 g for a typical patient) 7
- Traditional post-dialysis administration remains acceptable but is less convenient for patients 5
Critical Monitoring Requirements
- Obtain trough levels immediately before each dialysis session (pre-HD) to guide dosing adjustments 5, 2
- Target trough concentrations of 15-20 mg/L for serious infections (bacteremia, endocarditis, osteomyelitis, meningitis, pneumonia) 8, 3, 6
- For non-severe infections, target trough levels of 10-15 mg/L may be acceptable 3
- Monitor serum creatinine at least twice weekly for nephrotoxicity, defined as ≥2-3 consecutive increases of 0.5 mg/dL or 150% from baseline 6
High-Flux Dialysis Considerations
High-flux hemodialysis membranes significantly remove vancomycin, making traditional once-weekly dosing obsolete 5, 9:
- With high-flux membranes, 77% of vancomycin levels fall below 10 μg/mL by five days after a single dose, and 84% are subtherapeutic at one week 5
- Once-weekly vancomycin dosing should be abandoned in the high-flux setting due to consistently subtherapeutic levels 5
- Polyethersulfone high-flux membranes (PES-AP) result in lower vancomycin concentrations compared to medium-low flux membranes 9
Management of Elevated Trough Levels
- If trough exceeds 20 mg/L, hold the next scheduled dose and recheck the trough before administering subsequent doses 8, 6
- Once trough decreases to 15-20 mg/L, resume vancomycin at a reduced dose 8, 6
- Sustained trough concentrations >20 μg/mL significantly increase the risk of nephrotoxicity 8
Infusion Guidelines
- Administer each dose over at least 60 minutes at a rate no faster than 10 mg/min to minimize infusion-related reactions 1
- Use concentrations no greater than 5 mg/mL (up to 10 mg/mL in fluid-restricted patients) 1
- Consider antihistamine premedication for large loading doses to prevent red man syndrome 3, 1
Common Pitfalls to Avoid
- Never use fixed 1-gram dosing every 5-7 days in hemodialysis patients with high-flux membranes, as this results in subtherapeutic levels in the majority of patients 5, 9
- Do not rely on standard nomograms designed for patients with normal renal function, as these will result in inappropriate dosing 6
- Avoid monitoring peak levels, as trough concentrations are the most accurate method for guiding therapy 8, 6
- Do not assume residual renal function is negligible—consider interdialytic interval and any remaining kidney function when dosing 4
Alternative Therapy Considerations
- If vancomycin MIC is ≥2 μg/mL, switch to alternative agents (daptomycin, linezolid, or ceftaroline), as target AUC/MIC ratios of ≥400 are not achievable with conventional dosing 3, 6
- For MRSA pneumonia, consider linezolid as first-line due to superior lung penetration and documented vancomycin limitations 3