Antibiotic Treatment for Septic Bursitis
For septic bursitis, empiric therapy should begin with an antistaphylococcal penicillin (such as cloxacillin or nafcillin) administered intravenously at a dose of 2g every 4-6 hours until clinical improvement, followed by oral therapy to complete a 7-10 day course. 1
Pathogen Considerations
- Staphylococcus aureus is the most common causative organism in septic bursitis, accounting for approximately 80-90% of cases 1, 2
- Beta-hemolytic Streptococcus and Staphylococcus epidermidis are less common pathogens 3
- Cultures should be obtained prior to initiating antibiotics if this can be done without delaying treatment beyond one hour 4
Initial Antibiotic Selection
For non-severe cases:
For severe cases with extensive cellulitis or systemic symptoms:
Administration and Dosing
- Administer the first dose of antibiotics as soon as possible after diagnosis, ideally within one hour 4
- Use appropriate loading doses in critically ill patients 4
- For intravenous cloxacillin: 2g every 4-6 hours until clinical improvement 1
- For oral step-down therapy: 1g every 6 hours until resolution 1
Duration of Therapy
- Total duration of 7-10 days is typically adequate 4, 1
- Longer courses (14-21 days) may be necessary for:
- Patients with slow clinical response
- Immunocompromised hosts
- Cases with extensive surrounding cellulitis 4
Adjunctive Measures
Treatment Monitoring and De-escalation
- Reassess antibiotic therapy daily based on clinical response and culture results 4
- De-escalate to targeted therapy once culture and sensitivity results are available 4
- Consider transition from IV to oral therapy when:
- Patient shows clinical improvement
- Fever has resolved
- Inflammatory markers are decreasing 4
Common Pitfalls
- Misdiagnosis as non-septic bursitis despite characteristic bursal fluid leukocytosis (>1000 cells/mm³) 2
- Inadequate drainage leading to treatment failure 3, 6
- Premature switch to oral antibiotics in severe cases 1, 6
- Failure to obtain cultures before starting antibiotics 4
- Inadequate empiric coverage for potential MRSA in high-prevalence areas 5