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The Veterinary clinics of North America. Equine practice1994; 10(1); 87-107; doi: 10.1016/s0749-0739(17)30370-x

Drug therapy in the neonatal foal.

Abstract: The neonatal period in foals refers to the first 7 days of postnatal life. The effects of drugs (pharmacologic agents) may be different in neonatal foals, particularly during the first 3 days of postnatal life, from those in older foals and adult horses. The changed drug effects decrease as the physiologic processes that affect absorption, distribution, and elimination (metabolism and excretion) of drugs mature. Dosage regimens should take into account the altered pharmacokinetic profiles of drugs, and because of wide individual variation, the response to therapy should be closely monitored for signs of toxicity. In conjunction with the prudent use of drugs, good nursing care and the provision of supportive therapy are critical in the management of neonatal foal diseases. Over-crowding imposes stress upon young foals and predisposes them to an increased incidence of bacterial and parasitic infections. The collection of specimens for precise microbiologic diagnosis and correction of deficits in serum immunoglobulins should precede antimicrobial therapy. Although E. coli is by far the most common cause of bacterial infections in neonatal foals, other bacterial pathogens of unpredictable susceptibility often cause infection. The selection of an antimicrobial drug for specific therapy should be based on both the microbiologic (quantitative susceptibility) and pharmacologic (pharmacokinetic) properties of the drug. The use of an antimicrobial drug or combination of drugs that will produce a bactericidal effect is highly desirable. Whenever possible, a parenteral preparation that can be administered intravenously should be chosen. The bioavailability and selectivity of action of pharmacologic agents are influenced by the dosage form and route of administration. Diazepam is the sedative drug of choice for neonatal foals. Cimetidine, an H2-receptor antagonist, may be indicated in foals diagnosed to have gastric ulcers; hepatic microsomal oxidative metabolism of drugs administered concurrently with cimetidine is decreased. Nonsteroidal anti-inflammatory drugs (flunixin, phenylbutazone) have a higher incidence of toxicity in foals and, when indicated, should be used at lower dosage than in adult horses. Even though it is highly important to maintain hydration status and electrolyte balance, intravenous infusion should always be performed slowly. Immature renal function decreases the ability of the neonatal animal to excrete excess fluid. The use of drugs in neonatal foals requires greater precision in dosage, more attention to the route and rate of administration, and close monitoring of pharmacologic effects.
Publication Date: 1994-04-01 PubMed ID: 8039037DOI: 10.1016/s0749-0739(17)30370-xGoogle Scholar: Lookup
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Summary

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The research article studies the unique effects of drug treatments in neonatal foals, especially in their first week of life, and recommends appropriate dosages, careful administration, and close monitoring due to these foals’ physiological sensitivity and differences from older horses.

Understanding Neonatal Foal Pharmacokinetics

  • The research primarily targets the study of pharmacokinetics—at how prepubescent animals absorb, distribute, and eliminate drugs—in neonatal foals (horse offspring within 7 days of being born).
  • The study acknowledges that drug effects vary between neonatal foals and older horses, especially during the foals’ first three days of life. These differences are attributed to the maturational changes happening within the young horses, whose physiological processes adapt over time.
  • The researchers insist on a unique dosage regimen for neonates that takes into account their distinct pharmacokinetic profile of drugs, further highlighting the need for constant monitoring of their response to treatments for early spotting of signs of toxicity.

Managing Neonatal Foal Diseases

  • In managing neonatal foal diseases, the study stresses the significance of maintaining good nursing practices and providing supportive therapies.
  • Specific environmental factors, such as overcrowding, could cause stress among foals, making them susceptible to bacterial and parasitic infections. Hence, it is essential to control these external factors.
  • The study emphasizes the importance of microbiological diagnosis prior to the administration of antimicrobial therapy. The most common bacterial infection in neonatal foals is caused by E.coli, but other bacterial pathogens may also cause unpredictable infections. Thus, a thorough diagnosis is required.
  • The selection of antimicrobial drugs should be based on both microbiological (quantitative susceptibility) and pharmacological (pharmacokinetic) properties of the drug, aiming for a bactericidal effect.

Choice of Drugs and Route of Administration

  • The study identifies diazepam as the preferred sedative for neonatal foals. For gastric ulcers, cimetidine, an H2-receptor antagonist, may be used, though it reduces the metabolic breakdown of other concurrently administered drugs.
  • Nonsteroidal anti-inflammatory drugs, such as flunixin and phenylbutazone, have a higher incidence of toxicity in neonatal foals, so their administration should be at lower dosages than for adult horses.
  • The research also focuses on the importance of slow intravenous infusions to maintain hydration and electrolyte balance, asserting that neonatal foals have reduced renal functions, limiting their ability to excrete excessive fluids.
  • Given these details, the researchers stress the need for precision in drug dosages, mindful administration routes and rates, and careful monitoring of pharmacologic effects when treating neonatal foals.

Cite This Article

APA
Baggot JD. (1994). Drug therapy in the neonatal foal. Vet Clin North Am Equine Pract, 10(1), 87-107. https://doi.org/10.1016/s0749-0739(17)30370-x

Publication

ISSN: 0749-0739
NlmUniqueID: 8511904
Country: United States
Language: English
Volume: 10
Issue: 1
Pages: 87-107

Researcher Affiliations

Baggot, J D
  • Irish Equine Centre, Johnstown, County Kildare.

MeSH Terms

  • Animals
  • Animals, Newborn / physiology
  • Anti-Infective Agents / pharmacology
  • Anti-Infective Agents / therapeutic use
  • Horse Diseases / drug therapy
  • Horses / physiology
  • Pharmacokinetics

References

This article includes 56 references

Citations

This article has been cited 4 times.
  1. Gold JR, Grubb T, Court MH, Villarino NF. Pharmacokinetics of acetaminophen after a single Oral administration of 20 or 40 mg/kg to 7-9 Day-old foals. Front Vet Sci 2023;10:1198940.
    doi: 10.3389/fvets.2023.1198940pubmed: 37483288google scholar: lookup
  2. Song Y, Day CM, Afinjuomo F, Tan JE, Page SW, Garg S. Advanced Strategies of Drug Delivery via Oral, Topical, and Parenteral Administration Routes: Where Do Equine Medications Stand?. Pharmaceutics 2023 Jan 4;15(1).
    doi: 10.3390/pharmaceutics15010186pubmed: 36678815google scholar: lookup
  3. Ekstrand C, Nostell K, Gehring R, Bondesson U, Bröjer J. The disposition of trimethoprim and sulfadiazine in neonatal foals after intravenous administration. Vet Med Sci 2022 May;8(3):1065-1071.
    doi: 10.1002/vms3.763pubmed: 35152563google scholar: lookup
  4. Igarza L, Soraci A, Auza N, Zeballos H. Pharmacokinetic parameters of (R)-(-) and (S)-(+)-flurbiprofen in dairy bovines. Vet Res Commun 2006 Jul;30(5):513-22.
    doi: 10.1007/s11259-006-3241-4pubmed: 16755363google scholar: lookup