Treatment Regimen for Permacath Infection with Vancomycin and Amikacin
For permacath (tunneled dialysis catheter) infections, use vancomycin 20 mg/kg loading dose during the last hour of dialysis, then 500 mg during the last 30 minutes of each subsequent dialysis session, combined with gentamicin (or amikacin) 1 mg/kg (not exceeding 100 mg) after each dialysis session, along with antibiotic lock therapy using vancomycin 2.5-5.0 mg/mL with heparin. 1
Systemic Antibiotic Dosing
Vancomycin Dosing for Hemodialysis Patients
- Loading dose: 20 mg/kg infused during the last hour of the dialysis session 1
- Maintenance: 500 mg during the last 30 minutes of each subsequent dialysis session 1
- Target trough levels: 15-20 mcg/mL for serious infections including catheter-related bloodstream infections 1
- Monitor trough concentrations before the fourth or fifth dose at steady state 1
Amikacin Dosing for Hemodialysis Patients
- Dose: 1 mg/kg after each dialysis session, not to exceed 100 mg 1
- Alternative: Gentamicin or tobramycin at same dosing 1
- Peak target: 25-35 mg/L 2
- Trough target: 4-8 mg/L 2
- Monitor closely for nephrotoxicity and ototoxicity, especially when combined with vancomycin 1
Antibiotic Lock Therapy (Critical Component)
Antibiotic lock therapy should be added to systemic antibiotics for catheter salvage. 1, 3
Lock Solution Preparation
- Vancomycin concentration: 2.5-5.0 mg/mL (5.0 mg/mL is more efficacious for biofilm eradication) 1
- Heparin: 2,500-5,000 IU/mL 1
- Gentamicin alternative: 1.0 mg/mL with 2,500 IU/mL heparin for gram-negative coverage 1
Lock Therapy Administration
- Instill the antibiotic lock solution into both lumens of the catheter in the exact volume of each lumen 3
- Dwell time: 24 hours between dialysis sessions 3
- Replace lock solution daily 3
- Continue for the entire duration of systemic antibiotic therapy 3
Treatment Duration and Monitoring
Duration
- Minimum: 2 weeks for uncomplicated catheter-related bloodstream infection 1
- Typical range: 13-24 days depending on clinical response and follow-up blood cultures 3
- Continue until blood cultures are negative and clinical signs resolve 3
Monitoring Requirements
- Blood cultures: Draw from both the catheter and peripheral vein before starting antibiotics 3
- Vancomycin levels: Trough before 4th-5th dose, target 15-20 mcg/mL 1
- Amikacin levels: Peak and trough monitoring if available, especially with high-dose therapy 1
- Renal function: Monitor creatinine closely; avoid other nephrotoxic agents 1
- Hepatic enzymes: Check for twofold increases (more common with vancomycin-containing regimens) 4
- Ototoxicity screening: Particularly important with aminoglycoside use 1
Empirical Coverage Rationale
This combination provides:
- Gram-positive coverage (including MRSA): Vancomycin 1
- Gram-negative coverage: Amikacin/gentamicin 1
- Biofilm penetration: Antibiotic lock therapy addresses organisms embedded in catheter biofilm 1
Common Pathogens in Permacath Infections
- Staphylococcus species (most common) 3
- Pseudomonas species 3
- Enterobacter species 3
- Streptococcus species 3
Catheter Management
Attempt catheter salvage with combined systemic and lock therapy before removal. 3
Indications for Catheter Removal
- Hemodynamic instability or septic shock 1
- Persistent bacteremia after 72 hours of appropriate therapy 1
- Fungal infection (Candida species) 1
- Tunnel or exit site infection with purulence 1
Success Rates
- Combined systemic antibiotics plus lock therapy: 90% catheter salvage rate 3
- Systemic antibiotics alone: 71% catheter salvage rate with 29% mortality 3
Important Caveats
- Red man syndrome: Can occur with vancomycin infusion; consider prolonging infusion time to 2 hours and premedication with antihistamine 1
- Nephrotoxicity risk: Significantly increased with vancomycin-aminoglycoside combination; avoid additional nephrotoxic agents 1
- Dialysis schedule: Maintain regular dialysis schedule throughout treatment 3
- Adjust for renal function: These recommendations are specific to hemodialysis patients; different dosing applies to patients with residual renal function 5, 6