Recommended Antibiotic for Burn Infections
For burn wound infections, antibiotic selection should be culture-guided when possible, targeting the polymicrobial flora that typically includes both Gram-positive and Gram-negative organisms, with broad-spectrum beta-lactams like cefepime or piperacillin-tazobactam administered at high doses via continuous infusion being the preferred empiric systemic therapy when infection is documented. 1
Key Principle: Prophylaxis vs. Treatment
Universal antibiotic prophylaxis is NOT recommended for burn wounds. 1 The evidence shows:
- Systemic antibiotic prophylaxis administered in the first 4-14 days significantly reduced mortality by nearly half, but limited perioperative prophylaxis reduced wound infections without affecting mortality 1
- Topical antibiotic prophylaxis (including silver sulfadiazine) applied to burn wounds had no beneficial effects and was associated with increased burn wound infections and longer hospital stays 1
- The Surviving Sepsis Campaign explicitly recommends against sustained systemic antimicrobial prophylaxis in patients with burn injury in the absence of infection 1
When to Initiate Antibiotics
Antibiotics should be reserved for patients with:
- Documented burn wound infection (not just colonization) 1
- Systemic signs of infection (fever, hemodynamic instability, sepsis) 1
- Spreading cellulitis beyond the burn wound 1
- Severe comorbidities or compromised immune status 1
Microbiology of Burn Wound Infections
Burn wound infections are typically polymicrobial: 1
- Early colonization (immediate): Gram-positive bacteria from endogenous skin flora (S. aureus, including MRSA)
- Later colonization (within 1 week): Gram-negative bacteria predominate (Pseudomonas aeruginosa, E. coli, Klebsiella, Enterobacter)
- Anaerobes may also be present in deeper infections
Recommended Antibiotic Regimens
For Documented Burn Wound Infections:
Empiric broad-spectrum coverage targeting both Gram-positive and Gram-negative organisms is required: 1
First-line options:
- Cefepime 2g every 8-12 hours (or higher doses with continuous infusion) 2, 3, 4, 5, 6
- Piperacillin-tazobactam (high doses with continuous infusion preferred) 5
- Meropenem or imipenem-cilastatin (for severe infections or resistant organisms) 5
Critical Dosing Considerations in Burn Patients:
Burn patients have altered pharmacokinetics requiring dose adjustments: 1, 4, 5
- Increased clearance of antibiotics due to hyperdynamic circulation 4
- Increased volume of distribution correlating with percent third-degree burn 4
- High doses and continuous infusion are needed to achieve adequate PK/PD targets 5
- Therapeutic drug monitoring should guide dosing when available 1, 5
For cefepime specifically in burn patients:
- Standard dosing of 1g q8h, 2g q8h, or 2g q12h may be adequate for organisms with lower MICs 4
- However, continuous infusion at higher doses is increasingly recommended to maintain serum concentrations above MIC for >60-70% of the dosing interval 2, 5
MRSA Coverage:
Add MRSA-directed therapy based on: 1
- Local epidemiology (>20% MRSA prevalence) 1
- Previous MRSA colonization or infection
- Failure to respond to initial therapy
MRSA treatment options:
Topical Therapy:
Silver sulfadiazine cream 1% is FDA-approved as an adjunct for prevention and treatment of wound sepsis in second and third-degree burns 7:
- Apply once to twice daily to thickness of 1/16 inch 7
- However, recent evidence shows it may increase infection rates and hospital stay compared to modern dressings 1
- Continue until satisfactory healing or burn site ready for grafting 7
Essential Non-Antibiotic Management
Surgical source control is paramount and more important than antibiotics: 1
- Early excision of eschar substantially decreases invasive burn wound infection 1
- Debridement of necrotic tissue is necessary to remove pathogens 1
- Mechanical reduction of pathogen burden through wound care 1
Culture-Guided Therapy
Bacterial cultures should guide antibiotic selection: 1
- Obtain cultures before initiating antibiotics when possible
- Adjust therapy based on susceptibility results
- This is especially important given increasing bacterial drug resistance 1
Common Pitfalls to Avoid
- Do not use prolonged prophylactic antibiotics without documented infection 1
- Do not rely solely on topical silver sulfadiazine given evidence of harm 1
- Do not use standard dosing regimens without considering altered pharmacokinetics in burn patients 1, 4, 5
- Do not neglect surgical debridement in favor of antibiotics alone 1