IV Vancomycin Dosing in CAPD Patients
For CAPD patients requiring IV vancomycin, administer a full loading dose of 15-20 mg/kg (or 25-30 mg/kg for serious infections) based on actual body weight, followed by maintenance dosing of 1 gram every 5-7 days, with mandatory trough monitoring before each subsequent dose to target levels of 15-20 mg/L for serious infections. 1
Loading Dose Strategy
- The loading dose is NOT affected by renal function and must be given at full weight-based dosing to rapidly achieve therapeutic concentrations, even in patients with end-stage renal disease on CAPD. 1
- For serious infections (bacteremia, endocarditis, osteomyelitis, meningitis, pneumonia), administer a loading dose of 25-30 mg/kg based on actual body weight. 1
- For less severe infections, a loading dose of 15-20 mg/kg is appropriate. 1
- Infuse the loading dose over 2 hours to minimize the risk of red man syndrome, particularly with doses exceeding 1 gram. 1, 2
Maintenance Dosing in CAPD Patients
- After the loading dose, maintenance dosing should be 1 gram every 5-7 days based on pharmacokinetic studies in end-stage renal failure patients. 3, 4
- Research demonstrates that vancomycin elimination half-life in end-stage renal failure is approximately 121-131 hours, supporting extended dosing intervals. 3, 4
- Studies show that 500 mg every 7 days may be adequate for some patients, but 1 gram every 7 days provides more consistent therapeutic levels. 4
Therapeutic Monitoring Requirements
- Obtain trough levels immediately before each subsequent dose (every 5-7 days) to guide dosing adjustments. 1
- Target trough concentrations of 15-20 mg/L for serious infections such as CAPD-associated peritonitis, bacteremia, or other invasive infections. 1, 2
- For less severe infections, target trough levels of 10-15 mg/L. 1
- Research shows that 16-42% of patients may have subtherapeutic levels with standard dosing, making monitoring essential. 5, 4
Special Considerations for CAPD-Associated Peritonitis
- If treating CAPD-associated peritonitis specifically, intraperitoneal vancomycin administration is preferred over IV dosing, as IV vancomycin does not consistently achieve therapeutic intraperitoneal concentrations. 6
- Studies demonstrate poor correlation (R² = 0.18) between serum and peritoneal dialysate vancomycin concentrations, with 23% of patients having subtherapeutic peritoneal levels despite adequate serum levels. 6
- If IV vancomycin must be used for peritonitis, more frequent dosing may be necessary to maintain therapeutic peritoneal concentrations. 6
Dosing Adjustment Algorithm
- If trough level is <10 mg/L: Shorten the dosing interval to every 5 days or increase the dose. 1
- If trough level is 10-15 mg/L for non-severe infections: Maintain current regimen. 1
- If trough level is 15-20 mg/L for serious infections: Maintain current regimen. 1
- If trough level is >20 mg/L: Hold the next dose and recheck trough; resume at extended interval once level decreases to target range. 7
Critical Pitfalls to Avoid
- 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
- Do not use fixed 1-gram loading doses without weight-based calculation, as this results in subtherapeutic levels in most patients. 1
- Avoid using vancomycin dosing schedules designed for hemodialysis patients, as CAPD provides continuous but minimal drug clearance (vancomycin clearance averages only 0.086 mL/min/kg in dialysis patients). 8
- Do not assume adequate serum levels guarantee therapeutic peritoneal concentrations when treating peritonitis. 6
- Monitor for nephrotoxicity even in anuric patients, as vancomycin can cause additional renal injury that may affect residual renal function. 1
Alternative Considerations
- If vancomycin MIC is ≥2 μg/mL, consider alternative agents such as daptomycin, linezolid, or ceftaroline, as target AUC/MIC ratios may not be achievable. 1
- For CAPD-associated peritonitis, intraperitoneal vancomycin dosing (loading dose of 30 mg/kg in one exchange, followed by 15-25 mg/L in each subsequent exchange) is the preferred route. 6