Analyze Diet

Pharmacokinetics of cefotaxime in neonatal pony foals.

Abstract: Serum concentrations of cefotaxime and desacetylcefotaxime were measured in 1-week-old pony foals after IV administration of a single dose of cefotaxime. The cefotaxime disposition data conformed to a two-compartment model with elimination half-life of 0.60 hour. The combined cefotaxime and desacetylcefotaxime data was best described by a four-compartment model. The apparent half-life describing the disappearance of desacetylcefotaxime was 1.69 hours. Dosage of 40 mg/kg of body weight given IV every 4 to 6 hours for neonatal foals with gram-negative septicemia and every 2 hours for foals with meningitis is recommended for further study.
Publication Date: 1993-04-01 PubMed ID: 8484578
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research article discusses a study performed on the pharmacokinetics or how the body processes cefotaxime, an antibiotic, in neonatal pony foals. The aim was to understand the drug’s disposition in the body to further optimize its dosage for treating neonatal sepsis and meningitis in ponies.

Research Methodology

  • The researchers administered a single intravenous (IV) dose of cefotaxime to 1-week-old pony foals.
  • The serum concentrations of cefotaxime and its metabolite, desacetylcefotaxime, were then monitored and measured.

Drug Disposition Data

  • The data obtained on cefotaxime comportment in the pony’s body was found to conform to a two-compartment model with an elimination half-life of 0.60 hours.
  • Elimination half-life refers to the time it takes for the drug concentration in the body to decrease by half. Therefore, in about 0.6 hours, half the initial dose of cefotaxime administered would be removed from the pony’s body.
  • The combined data on both the original drug, cefotaxime, and its metabolite, desacetylcefotaxime, fit a more complex four-compartment model. This indicates that both substances are distributed throughout the body and undergo several processes before being fully eliminated.

Dosing Recommendations

  • Based on these findings, the researchers recommended a dosage of 40 mg of cefotaxime per kg of body weight. The frequency was suggested to be every 4 to 6 hours for neonatal foals with gram-negative septicemia while it was set to every 2 hours for foals with meningitis.
  • The researchers have made these recommendations based on the aim to maintain an effective drug concentration in the body throughout the treatment duration. However, these suggested dosages require further analysis and study before they can be employed clinically.

Cite This Article

APA
Gardner SY, Sweeney RW, Divers TJ. (1993). Pharmacokinetics of cefotaxime in neonatal pony foals. Am J Vet Res, 54(4), 576-579.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 54
Issue: 4
Pages: 576-579

Researcher Affiliations

Gardner, S Y
  • Department of Clinical Studies, School of Veterinary Medicine, University of Pennsylvania, Kennett Square 19348.
Sweeney, R W
    Divers, T J

      MeSH Terms

      • Animals
      • Animals, Newborn / metabolism
      • Cefotaxime / analogs & derivatives
      • Cefotaxime / blood
      • Cefotaxime / metabolism
      • Cefotaxime / pharmacokinetics
      • Female
      • Horses
      • Male
      • Metabolic Clearance Rate
      • Models, Biological
      • Time Factors

      Citations

      This article has been cited 0 times.