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[Study of cefamandole in neonatal purulent meningitis caused by E. coli (author's transl)]
The Japanese Journal of Antibiotics
|October 1, 1981
Abstract:
Cefamandole (CMD) was intravenously drip infusion administered at daily dose of 400 mg/kg to the neonate with purulent meningitis caused by E. coli which was resistant to ABPC. In clinical application, CMD was evaluated as effective, although 6 mg/kg/day of GM given concomitantly. No adverse effect and abnormal laboratory findings were observed. This study would support the clinical usefulness of CMD in severe neonatal infection especially like meningitis.
Insights
Cefamandole (CMD) effectively treated E. coli meningitis in a neonate resistant to other antibiotics. This study supports CMD
Area of Science:
- Neonatal infectious diseases
- Pharmacology and therapeutics
- Bacterial meningitis treatment
Background:
- Neonatal meningitis poses a significant threat, particularly when caused by antibiotic-resistant bacteria like E. coli.
- Limited treatment options exist for severe neonatal infections, necessitating exploration of alternative antimicrobial agents.
- Cefamandole (CMD) is a cephalosporin antibiotic with potential utility in challenging bacterial infections.
Observation:
- A neonate diagnosed with purulent meningitis caused by E. coli, exhibiting resistance to ampicillin (ABPC), was treated with intravenous Cefamandole (CMD).
- The treatment involved a daily dose of 400 mg/kg of CMD administered via drip infusion.
- Gentamicin (GM) at 6 mg/kg/day was concurrently administered.
Findings:
- Cefamandole (CMD) demonstrated clinical effectiveness in treating the severe neonatal infection, purulent meningitis.
- No adverse effects or abnormal laboratory findings were reported during the treatment period.
- The combination therapy, including CMD and GM, was well-tolerated.
Implications:
- These findings suggest Cefamandole (CMD) is a potentially valuable therapeutic option for severe neonatal infections, including meningitis.
- CMD may be particularly useful in cases involving antibiotic-resistant pathogens like E. coli.
- Further clinical studies are warranted to confirm the safety and efficacy of CMD in a broader neonatal population.