Cefalotin

General

  • Type: 1st generation Cephalosporin
  • Dosage Forms: powder for injection
  • Dosage Strengths: 1g, 2g vial
  • Routes of Administration: IV, IM (IM is painful)
  • Common Trade Names: Keflin

Adult Dosing

General

  • Mild-Mod: 500mg-1g IV/IM q4-6h
  • Severe: 1g-2g IV/IM q4h
  • Max: 12g/day (doses up to 2g q4h have been used in life-threatening infections)

Perioperative Prophylaxis

  • 1-2g IV x 1 (administer 30-60 min before skin incision)
  • intraoperative redosing: q2-3h

Respiratory Tract Infection

  • 500mg IM/IV q6h

Skin/Skin Structure Infection

  • 500mg IM/IV q6h

Pediatric Dosing

General

  • 20-40mg/kg/dose IV/IM q6h
  • Max: 12g/day

Neonatal (<28 Days)

  • Postnatal age <7 days: 20 mg/kg IV q12h
  • Postnatal age >7 days (<2000g): 20 mg/kg/dose IV q12h
  • Postnatal age >7 days (>2000g): 20 mg/kg/dose IV q8h

Special Populations

  • Pregnancy: B
  • Lactation: Probability of harm is low (excreted in breast milk)
  • Renal
    • Adult
      • CrCl >50: No adjustment
      • CrCl 25-50: 1g q6h
      • CrCl 10-25: 1g q12h
      • CrCl 2-10: 500mg q12h
      • CrCl <2: 500mg q24h
      • Hemodialysis: Loading dose 1g, then 500mg q24h
      • Peritoneal dialysis: 500mg q12h
    • Pediatric
      • Renal adjustment required; modify interval based on oliguria/anuria.
  • Hepatic
    • No adjustment usually required

Contraindications

  • Allergy to class/drug (Cephalosporins)
  • History of anaphylaxis to Penicillins

Adverse Reactions

Serious

Common

  • Thrombophlebitis (Frequent with IV administration; more common than with Cefazolin)
  • Nausea and Vomiting
  • Diarrhea
  • Rash/Pruritus
  • Pain at injection site (IM)
  • Eosinophilia

Pharmacology

  • Half-life: 0.5 - 1 hour (shorter than Cefazolin)
  • Metabolism: Hepatic (deacetylation) to active metabolite
  • Excretion: Urine
  • Mechanism of Action: Bactericidal; inhibits cell wall mucopeptide synthesis

Antibiotic Sensitivities[1]

Group Organism Sensitivity
Gram Positive Strep. Group A, B, C, G S
Strep. Pneumoniae S
Viridans strep S
Strep. anginosus gp X1
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 X1
N. meningitidis R
Moraxella catarrhalis I
H. influenzae I
E. coli S
Klebsiella sp S
E. coli/Klebsiella ESBL+ R
E coli/Klebsiella KPC+ R
Enterobacter sp, AmpC neg R
Serratia sp R
Salmonella sp X1
Shigella sp X1
Proteus mirabilis S
Proteus vulgaris R
Providencia sp. R
Morganella sp. R
Citrobacter sp. R
Aeromonas sp R
Acinetobacter sp. R
Pseudomonas aeruginosa R
Burkholderia cepacia R
Stenotrophomonas maltophilia R
Yersinia enterocolitica R
Francisella tularensis X1
Brucella sp. X1
Legionella sp. R
Misc Chlamydophila sp X1
Mycoplasm pneumoniae X1
Rickettsia sp X1
Anaerobes Actinomyces X1
Bacteroides fragilis R
Prevotella melaninogenica X1
Clostridium difficile X1
Clostridium (not difficile) X1
Fusobacterium necrophorum X1
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
  • Epocrates
  • Sanford Guide