Clindamycin Dosing for Staphylococcus aureus Infections
For adults with Staphylococcus aureus infections, administer clindamycin 600 mg IV or PO every 8 hours for complicated infections, or 300-450 mg PO every 6-8 hours for uncomplicated skin infections; for children, use 10-13 mg/kg/dose IV every 6-8 hours (maximum 40 mg/kg/day) or 30-40 mg/kg/day PO divided into 3-4 doses. 1
Adult Dosing by Infection Severity
Complicated Infections (Hospitalized Patients)
- Administer 600 mg IV or PO every 8 hours for complicated skin and soft tissue infections, MRSA pneumonia, osteomyelitis, and septic arthritis 2, 1
- For severe or life-threatening infections, escalate to 900 mg IV every 6-8 hours 1
- This higher dosing (600 mg every 8 hours) supersedes FDA labeling and is based on superior clinical outcomes in IDSA guidelines 3, 1
Uncomplicated Outpatient Infections
- Administer 300-450 mg PO every 6-8 hours (three to four times daily) for uncomplicated purulent cellulitis and simple skin infections 2, 3, 1
- This regimen provides adequate coverage when combined with appropriate incision and drainage 2
Pediatric Dosing
Intravenous Administration
- Administer 10-13 mg/kg/dose IV every 6-8 hours, not to exceed 40 mg/kg/day total for complicated skin and soft tissue infections, pneumonia, osteomyelitis, and septic arthritis 2, 3, 1
- This dosing applies to stable children without ongoing bacteremia or endovascular infection 2, 3
Oral Administration
- Administer 30-40 mg/kg/day divided into 3-4 doses for MRSA and methicillin-susceptible S. aureus (MSSA) infections 2, 3, 1
- Transition to oral therapy once clinical improvement is evident and the strain is confirmed susceptible 2
Duration of Therapy
- 5-10 days for uncomplicated skin and soft tissue infections, with 5 days sufficient if rapid improvement occurs 2, 3
- 7-14 days for complicated skin and soft tissue infections, with longer duration reserved for slow clinical response 3, 1
- Minimum 8 weeks for osteomyelitis 3, 1
- 2-6 weeks for bacteremia and endocarditis, depending on source and presence of metastatic foci 3
Critical Resistance Considerations
Only use clindamycin when local MRSA clindamycin resistance rates are <10% 2, 3, 1. This is a crucial threshold because:
- Inducible macrolide-lincosamide-streptogramin B (MLS_B) resistance in erythromycin-resistant MRSA strains can lead to treatment failure 1, 4
- Resistance patterns vary dramatically by region; some areas report constitutive clindamycin resistance rates exceeding 25% 5
- Against S. aureus isolates with inducible resistance, clindamycin fails to prevent regrowth of resistant phenotypes 4
Important Clinical Caveats
When Clindamycin Should NOT Be Used
- Do not use for suspected infective endocarditis or endovascular source of infection due to high relapse rates and resistance development 3, 6
- Avoid in areas with >10% clindamycin resistance rates as this significantly increases treatment failure risk 1
- Not recommended for S. epidermidis infections (especially septicemia and endocarditis) due to high resistance rates 6
Source Control is Mandatory
- Incision and drainage is the cornerstone of abscess treatment and may be sufficient alone for simple abscesses 3
- Antibiotics provide limited benefit without adequate drainage, with 85-90% cure rates achieved with drainage alone 3
- If no clinical improvement occurs within 48-72 hours, consider inadequate drainage or deeper infection requiring imaging 3
Advantages of Clindamycin
- Provides dual coverage against both MRSA and β-hemolytic streptococci, making it ideal as monotherapy when both pathogens are suspected 2, 3
- Excellent penetration and accumulation within leukocytes, potentially valuable for large abscesses 6
- Particularly useful for mixed staphylococcal and anaerobic infections in skin, subcutaneous tissue, diabetic foot, and bone/joint infections 6
Common Pitfalls to Avoid
- Never underdose serious infections by using 300 mg doses for complicated infections; always use 600 mg every 8 hours for MRSA and serious infections 3, 1
- Do not prematurely discontinue treatment; ensure minimum treatment durations are met based on infection type 1
- Monitor for Clostridium difficile diarrhea, especially in ambulatory long-term treatment of diabetic osteitis and chronic osteomyelitis 6
- Be aware that clindamycin had lower recurrence rates (2.0%) compared to trimethoprim-sulfamethoxazole (7.1%) at 6-8 weeks in clinical trials 7