Antibiotics with Good Bone Penetration for Treating Bone Infections
Fluoroquinolones, rifampin, clindamycin, linezolid, fusidic acid, and trimethoprim-sulfamethoxazole have the best bone penetration and should be preferred for treating bone infections when the causative organism is susceptible to these agents. 1, 2
Bone Penetration of Different Antibiotic Classes
Excellent Bone Penetration
- Fluoroquinolones: Bone-to-serum concentration ratios between 0.3-1.2 3
- Macrolides: Bone-to-serum concentration ratios between 0.3-1.2 (higher for azithromycin) 3
- Linezolid: Bone-to-serum concentration ratios between 0.3-1.2 3
- Rifampin: Excellent bone penetration, always recommended to be combined with another agent 1
- Clindamycin: Good bioavailability and bone penetration 1, 2
- Trimethoprim-sulfamethoxazole: Good bioavailability for oral therapy 1, 2
- Fusidic acid: Good bioavailability for oral therapy 1
Moderate Bone Penetration
- Glycopeptides (Vancomycin): Bone-to-serum concentration ratios between 0.15-0.3 3
- Cephalosporins: Bone-to-serum concentration ratios between 0.15-0.3 3
- Daptomycin: Adequate bone penetration 4
Lower Bone Penetration
- Penicillins: Bone-to-serum concentration ratios between 0.1-0.3 3
- Metronidazole: Poor penetration into bone tissue 4
Antibiotic Selection Based on Common Pathogens
For MRSA Osteomyelitis
- Vancomycin IV is recommended as first-line therapy 1, 2
- Consider adding rifampin (600 mg daily or 300-450 mg twice daily) for improved bone penetration and biofilm activity 1, 2
- Alternatives include:
For MSSA and Other Susceptible Organisms
Oral options with good bioavailability:
- Fluoroquinolones (e.g., ciprofloxacin)
- Clindamycin
- Linezolid
- Fusidic acid
- Trimethoprim-sulfamethoxazole 1
For Gram-negative infections:
Treatment Duration and Administration
Initial parenteral therapy for approximately 1 week, then transition to oral antibiotics with good bioavailability if the organism is susceptible 1, 2
Treatment duration:
Important Clinical Considerations
Bone biopsy for culture is essential before starting antibiotics when possible to guide targeted therapy 2
Surgical debridement is a critical component of treatment for most bone infections 1, 2
Combination therapy with rifampin has shown improved outcomes in staphylococcal osteomyelitis, particularly with implant-related infections 1, 5
Cancellous bone typically shows higher antibiotic concentrations than cortical bone for most antibiotics 3
Local antibiotic delivery (e.g., antibiotic-impregnated beads, sponges, or cement) can achieve very high local concentrations and may be considered as an adjunct to systemic therapy 1
Pitfalls and Caveats
Measuring bone levels of antibiotics has limitations, and the correlation between high bone levels and improved outcomes has not been definitively established 1
Biofilm formation significantly impacts treatment success; antibiotics with anti-biofilm activity (like rifampin) should be considered for implant-related infections 1
Penicillins and cephalosporins have significantly lower bone penetration compared to linezolid, fluoroquinolones, and macrolides 3
Antibiotic resistance patterns must be considered when selecting therapy, particularly for empiric treatment 2
Switching to oral therapy should only be done with antibiotics that have good bioavailability 1, 2
By selecting antibiotics with good bone penetration and appropriate activity against the causative pathogen, combined with appropriate surgical intervention when indicated, successful treatment of bone infections can be achieved.