Teicoplanin Dosing Recommendations
For standard infections, administer teicoplanin with a loading dose of 6 mg/kg every 12 hours for three doses, followed by 6 mg/kg once daily maintenance; for severe infections including endocarditis and septic arthritis, use 12 mg/kg every 12 hours for three doses, followed by 12 mg/kg once daily maintenance. 1, 2
Standard Dosing Algorithm
Loading Dose Phase
- Standard infections: 6 mg/kg IV every 12 hours for 3 doses (total 18 mg/kg over 36 hours) 1, 3
- Severe infections (endocarditis, septic arthritis, complicated bacteremia): 12 mg/kg IV every 12 hours for 3 doses (total 36 mg/kg over 36 hours) 1, 2, 4
- Loading doses remain the same regardless of renal function and are critical to rapidly achieve therapeutic levels 3
Maintenance Dose Phase
For patients with normal renal function (GFR >90 mL/min):
For patients with moderate renal impairment (GFR 50-90 mL/min):
For patients with severe renal impairment (GFR 10-50 mL/min):
For patients with end-stage renal disease (GFR <10 mL/min):
Infection-Specific Dosing
Complicated Skin and Soft Tissue Infections
- 6-12 mg/kg IV every 12 hours for 3 doses, then once daily 1
- Duration: 7-14 days 1
- For Fournier's gangrene specifically: Loading dose 12 mg/kg every 12 hours for 3 doses, then 6 mg/kg every 12 hours as part of combination therapy 5
Bacteremia
- Uncomplicated: 6-12 mg/kg IV every 12 hours for 3 doses, then once daily for 2 weeks 1
- Complicated: 6-12 mg/kg IV every 12 hours for 3-6 doses, then 6-12 mg/kg once daily for 4-6 weeks 1, 2
Endocarditis and Septic Arthritis
- Critical dosing: 12 mg/kg every 12 hours for 3 doses, then 12 mg/kg once daily 1, 2, 4
- Duration: 3-4 weeks for septic arthritis, longer for endocarditis 1
- Target trough concentration ≥20 mg/L 1, 2
Osteomyelitis
Special Populations
Hemodialysis Patients
CAPD Peritonitis
Continuous Renal Replacement Therapy
Pediatric Patients
Therapeutic Drug Monitoring
Routine monitoring is not generally required but is indicated in specific situations: 1, 3
- S. aureus endocarditis or septic arthritis (target trough ≥20 mg/L) 1, 2
- Major burns 1, 3
- Intravenous drug users 1, 3
- Rapidly changing renal function 1, 3
- Immunocompromised patients 3
Target trough concentrations:
Common Pitfalls to Avoid
- Inadequate loading doses: Failure to provide adequate loading doses leads to subtherapeutic levels regardless of renal function 3
- Underdosing severe infections: Using 6 mg/kg instead of 12 mg/kg for endocarditis or septic arthritis results in treatment failure 4, 6
- Incorrect interval adjustment: Not extending dosing intervals appropriately in renal impairment causes drug accumulation 3
- Overlooking monitoring needs: Missing the need for therapeutic drug monitoring in high-risk situations leads to suboptimal outcomes 1, 3
Evidence Quality Considerations
The higher dosing regimen (12 mg/kg) for severe infections is supported by multiple studies showing that standard 400 mg (approximately 6 mg/kg) daily doses frequently result in subtherapeutic levels 7. Research demonstrates that 600 mg daily doses (approximately 12 mg/kg for a 50 kg patient) achieve therapeutic levels in 68% versus 37% with lower doses, without increased toxicity 7. For endocarditis specifically, trough levels over 20 mg/L are needed for cure rates similar to vancomycin 4, 6.