Cephamycin

General

  • Type: 2nd generation Cephalosporin
  • Dosage Forms: powder for injection
  • Dosage Strengths: 1g, 2g, 10g
  • Routes of Administration: IV, IM
  • Common Trade Names: Mefoxin (Cefoxitin), Cefotan (Cefotetan)

Adult Dosing

General

  • Cefoxitin: 1-2g IM/IV q6-8h
  • Cefotetan: 1-2g IM/IV q12h
  • Max: 12g/day (Cefoxitin); 6g/day (Cefotetan)

Pelvic Inflammatory Disease (PID)

  • Cefoxitin: 2g IV q6h (plus Doxycycline 100mg PO/IV q12h)
  • Cefotetan: 2g IV q12h (plus Doxycycline 100mg PO/IV q12h)

Surgical Prophylaxis (Colorectal/Appendectomy)

  • Cefoxitin: 2g IV x1 (30-60 min before procedure)
  • Cefotetan: 2g IV x1 (30-60 min before procedure)

Gonorrhea Uncomplicated (Alternative)

Pediatric Dosing

General (>3 Months)

  • Cefoxitin:
    • 80-160 mg/kg/day IM/IV divided q4-6h
    • Max 12g/day
  • Cefotetan:
    • 40-60 mg/kg/day IM/IV divided q12h
    • Max 6g/day

Appendicitis (Complicated)

  • Cefoxitin: 160 mg/kg/day IV divided q6h
  • Cefotetan: 40 mg/kg/day IV divided q12h

Special Populations

  • Pregnancy: B
  • Lactation: Safe
  • Renal
    • Adult (Cefoxitin)
      • CrCl 30-50: 1-2g q8-12h
      • CrCl 10-29: 1-2g q12-24h
      • CrCl <10: 0.5-1g q24h
      • Hemodialysis: Loading dose 1-2g x1, maintenance 1-2g post-dialysis
    • Adult (Cefotetan)
      • CrCl 10-30: Give usual dose q24h
      • CrCl <10: Give usual dose q48h
      • Hemodialysis: Give 500mg supplement (or 1/4 dose) post-dialysis
    • Pediatric
      • Adjust frequency based on GFR similar to adult adjustments
  • Hepatic
    • Not defined

Contraindications

  • Allergy to class/drug
  • History of serious hypersensitivity to penicillin

Adverse Reactions

Serious

Common

Pharmacology

  • Half-life: 0.7-1h (Cefoxitin); 3-4.6h (Cefotetan)
  • Metabolism: Not significantly metabolized (Cefoxitin); No metabolism (Cefotetan)
  • Excretion: Urine
  • Mechanism of Action: Bactericidal; inhibits cell wall mucopeptide synthesis.
  • Class Distinction: Possesses 7-alpha-methoxy group which confers high stability against beta-lactamases (especially those produced by Bacteroides fragilis).

Antibiotic Sensitivities[1]

Group Organism Sensitivity
Gram Positive Strep. Group A, B, C, G S
Strep. Pneumoniae S
Viridans strep S
Strep. anginosus gp S
Enterococcus faecalis R
Enterococcus faecium R
MSSA S
MRSA R
CA-MRSA R
Staph. Epidermidis I
C. jeikeium R
L. monocytogenes R
Gram Negatives N. gonorrhoeae S
N. meningitidis S
Moraxella catarrhalis S
H. influenzae S
E. coli S
Klebsiella sp S
E. coli/Klebsiella ESBL+ R
E coli/Klebsiella KPC+ R
Enterobacter sp, AmpC neg I
Enterobacter sp, AmpC pos R
Serratia sp R
Serratia marcescens R
Salmonella sp S
Shigella sp S
Proteus mirabilis S
Proteus vulgaris S
Providencia sp. S
Morganella sp. I
Citrobacter freundii R
Citrobacter diversus S
Citrobacter sp. I
Aeromonas sp I
Acinetobacter sp. R
Pseudomonas aeruginosa R
Burkholderia cepacia R
Stenotrophomonas maltophilia R
Yersinia enterocolitica S
Francisella tularensis X1
Brucella sp. X1
Legionella sp. R
Pasteurella multocida S
Haemophilus ducreyi X1
Vibrio vulnificus X1
Misc Chlamydophila sp X1
Mycoplasm pneumoniae X1
Rickettsia sp X1
Mycobacterium avium R
Anaerobes Actinomyces S
Bacteroides fragilis S
Prevotella melaninogenica S
Clostridium difficile X1
Clostridium (not difficile) S
Fusobacterium necrophorum S
Peptostreptococcus sp. S

Key

  • S susceptible/sensitive (usually)
  • I intermediate (variably susceptible/resistant)
  • R resistant (or not effective clinically)
  • S+ synergistic with cell wall antibiotics
  • U sensitive for UTI only (non systemic infection)
  • X1 no data
  • X2 active in vitro, but not used clinically
  • X3 active in vitro, but not clinically effective for Group A strep pharyngitis or infections due to E. faecalis
  • X4 active in vitro, but not clinically effective for strep pneumonia

See Also

References

  1. Sanford Guide to Antimicrobial Therapy