What is the recommended dose of Keflex (cefalexin) for a patient with a traumatic wound, status post debridement, and normal renal function (creatinine level 0.8), with a wound gap and signs of infection?

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Keflex Dosing for Infected Traumatic Wound Post-Debridement

For an infected traumatic wound status post debridement with normal renal function (creatinine 0.8), administer cephalexin 500 mg orally every 6 hours for 5-7 days. 1

Rationale for Dosing Selection

The FDA-approved dosing for cephalexin in skin and soft tissue infections is 250 mg every 6 hours for mild infections, but 500 mg every 6 hours is appropriate for more severe infections or those caused by less susceptible organisms 1. Your clinical scenario—a traumatic wound with established infection requiring debridement—qualifies as a more severe infection requiring the higher dose.

Treatment Duration

  • For contaminated traumatic wounds with established infection (Class III/IV wounds), antibiotic therapy should continue for 5-7 days 2, 3
  • This differs from prophylaxis in clean wounds, where 2-3 days suffices 3
  • The presence of infection post-debridement indicates therapeutic (not prophylactic) antibiotic use 2

Why This Dose is Appropriate

  • Cephalexin achieves urinary concentrations of 500-1000 mcg/mL following 250-500 mg oral doses, providing tissue levels many times the minimum inhibitory concentration for common wound pathogens 4
  • The drug is completely absorbed from the upper intestine and rapidly distributed to tissues (excluding CSF), making it ideal for soft tissue infections 4
  • For infected wounds requiring debridement, the higher 500 mg dose ensures adequate tissue penetration against Staphylococcus aureus and Streptococcus species 1, 5

Renal Function Consideration

  • With a creatinine of 0.8 mg/dL (normal renal function), no dose adjustment is necessary 4
  • Dose reduction is only required when creatinine clearance falls below 30 mL/min 4

Critical Management Points Beyond Antibiotics

  • Ensure adequate surgical debridement was performed, as antibiotics serve only as adjunct to mechanical removal of contaminated tissue 2
  • The wound should remain open or loosely approximated—primary closure is contraindicated in contaminated/infected traumatic wounds 6, 7
  • Monitor closely for signs of deeper infection including osteomyelitis or septic arthritis, which would require extended therapy (4-6 weeks for osteomyelitis, 3-4 weeks for septic arthritis) 6

Alternative Regimen if Cephalexin Fails

  • If clinical improvement is not seen within 48-72 hours, consider switching to amoxicillin-clavulanate 875/125 mg twice daily for broader anaerobic coverage 2, 6
  • This is particularly important if the wound was contaminated with soil, feces, or involved deeper structures 2

Common Pitfall to Avoid

Do not use the 250 mg every 12 hours dosing regimen listed in the FDA label for "uncomplicated" skin infections 1—your patient has a complicated, infected traumatic wound requiring the more aggressive 500 mg every 6 hours regimen to prevent treatment failure and potential complications like osteomyelitis.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

The pharmacology of cephalexin.

Postgraduate medical journal, 1983

Guideline

Management of Superficial Cat Bites on the Ankle

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Treatment of Facial Laceration from Dog Bite

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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