What is the specific bacterial coverage of cefoxitin?

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Bacterial Coverage of Cefoxitin

Spectrum of Activity

Cefoxitin provides broad-spectrum coverage against gram-positive cocci (excluding enterococci), gram-negative facultative bacteria (excluding Pseudomonas), and critically, anaerobic bacteria including Bacteroides fragilis, making it particularly valuable for polymicrobial infections. 1

Gram-Positive Coverage

  • Staphylococcus aureus (methicillin-susceptible, including penicillinase-producing strains) 1
  • Staphylococcus epidermidis (methicillin-susceptible isolates only) 1
  • Streptococcus pneumoniae 1
  • Streptococcus pyogenes and other streptococci 1
  • Streptococcus agalactiae (Group B Streptococcus) 1
  • Peptococcus niger and Peptostreptococcus species 1

Gram-Negative Coverage

  • Escherichia coli 1
  • Klebsiella species 1
  • Proteus mirabilis 1
  • Proteus vulgaris 1
  • Morganella morganii 1
  • Providencia species (including P. rettgeri) 1
  • Haemophilus influenzae 1
  • Neisseria gonorrhoeae (including penicillinase-producing strains) 1
  • Eikenella corrodens (non-β-lactamase producers) 1

Anaerobic Coverage

Cefoxitin's distinguishing feature is its excellent activity against anaerobes, particularly Bacteroides fragilis, which sets it apart from many other cephalosporins. 2, 1

  • Bacteroides fragilis 1, 3
  • Bacteroides species (including B. distasonis, B. ovatus, B. thetaiotaomicron) 1
  • Clostridium species (including C. perfringens) 1
  • Prevotella bivia 1

Critical Coverage Gaps

Cefoxitin has NO activity against the following clinically important organisms: 1

  • Enterococcus species (including E. faecalis) - this is a critical gap requiring alternative coverage when enterococcal infection is suspected 1
  • Pseudomonas aeruginosa - documented treatment failures have occurred with Pseudomonas infections 4
  • Chlamydia trachomatis - when treating pelvic inflammatory disease, appropriate anti-chlamydial coverage (doxycycline) must be added 2, 1
  • Methicillin-resistant Staphylococcus aureus (MRSA) - only methicillin-susceptible strains are covered 1

Mechanism of Resistance Stability

Cefoxitin demonstrates high stability against beta-lactamase degradation due to its 7-alpha-methoxyl group, allowing it to remain active against many organisms resistant to other cephalosporins. 1, 5, 3

  • Active against penicillinase-producing staphylococci 1
  • Resistant to most beta-lactamases produced by gram-negative and gram-positive bacteria 1, 3
  • Maintains activity against many cephalothin-resistant gram-negative bacteria 3

Clinical Implications

The combination of aerobic and anaerobic coverage makes cefoxitin particularly effective for polymicrobial infections, especially in intra-abdominal and pelvic infections where mixed flora is common. 6, 7

  • In clinical studies of pelvic infections, an average of 2.5 bacteria per patient were isolated, with 37% having mixed aerobic-anaerobic infections 6
  • The drug achieved 92% clinical response rates in mixed aerobic-anaerobic pelvic infections when used as monotherapy 6
  • However, cefoxitin's anaerobic coverage advantage over ceftriaxone has been questioned, as the clinical necessity of Bacteroides fragilis coverage for all pelvic infections remains unproven 2, 7

Common Pitfalls to Avoid

  • Never use cefoxitin alone for suspected enterococcal infections - add ampicillin or vancomycin if enterococci are likely 1
  • Always add doxycycline when treating pelvic inflammatory disease - cefoxitin has no activity against Chlamydia trachomatis 2, 1
  • Do not use for Pseudomonas infections - documented treatment failures with Serratia and Pseudomonas have occurred 4
  • Resistance can develop during therapy - particularly with initially moderately susceptible organisms like Serratia marcescens 4

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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