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Cardiopulmonary and gastrointestinal motility effects of xylazine/ketamine-induced anesthesia in horses previously treated with glycopyrrolate.

Abstract: To assess the usefulness of glycopyrrolate (GLY) in preventing the decrease in cardiac index (CI) usually caused by xylazine (XYL)/ketamine (KET)-induced anesthesia in horses. Methods: 6 healthy horses. Methods: Horses were treated with saline solution or 2.5 micrograms of GLY/kg of body weight, administered i.v. 15 minutes later, XYL (1 mg/kg) was administered i.v., followed 5 minutes later by KET (2 mg/kg) administration. The horses were positioned in left lateral recumbency, insufflated with 15 L of oxygen/min, and maintained for 30 minutes on the infusion of 0.05 mg of XYL and 0.1 mg of KET/kg/min. Mean, systolic, and diastolic arterial blood pressures, mean pulmonary arterial and central venous pressures, heart rate, CI, and arterial and mixed venous blood gas tensions were recorded up to 40 minutes after anesthesia induction. Intestinal motility was assessed by auscultation of 4 abdominal quadrants for 24 hours after induction. Data were analyzed by Wilcoxon's rank-sum test for nonparametric observations, and by ANOVA for repeated measures and Scheffé's test for continuous parametric variables. Results: Horses given GLY had significantly higher heart rate; mean, systolic, and diastolic arterial blood pressures; CI; oxygen delivery; and mixed venous oxygen tensions, with significantly less tissue oxygen extraction, compared with saline-treated horses. Both groups had complete loss of intestinal motility associated with general anesthesia. Conclusions: GLY significantly reduced the cardiovascular dysfunction attributable to general anesthesia with XYL and KET. The return of intestinal motility was delayed by 3 to 6 hours without causing any serious side effects.
Publication Date: 1996-12-01 PubMed ID: 8950432
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research explores the influence of the drug glycopyrrolate on maintaining heart function in horses undergoing anesthesia with xylazine and ketamine. The study found that the use of glycopyrrolate before administering anesthesia resulted in improved heart function and higher oxygen levels in the horses, even though intestinal movement was still inhibited during the anesthesia period.

Methodology

Six healthy horses were used in the study. The horses were first given either a saline solution or a dosage of glycopyrrolate, based on their body weight. Fifteen minutes later, they were administered the anesthetic mix of xylazine and ketamine. After anesthetization, the horses were given oxygen and maintained by an infusion of both xylazine and ketamine.

  • Various health indicators such as mean arterial pressures, central venous pressures, heart rate, cardiac index, and arterial and mixed venous blood gas tensions were monitored for up to 40 minutes after inducing anesthesia.
  • Intestinal motility was also observed by auscultating four abdomen quadrants for 24 hours post-anesthesia induction.

The collected data were then analyzed using multiple statistical methods suitable for analyzing continuous and non-parametric variables.

Results

The observations showed:

  • Horses given glycopyrrolate demonstrated significantly improved health parameters such as heart rate, mean arterial blood pressures, cardiac index, oxygen delivery and mixed venous oxygen tensions.
  • Horses also showed less tissue oxygen extraction in comparison to those treated with a saline solution.
  • Despite the improvements, it was observed that both groups of horses (those given glycopyrrolate and those given only saline) still exhibited a complete loss of intestinal motility, a common side effect of general anesthesia.

Conclusions

The research concluded that the use of glycopyrrolate significantly reduced cardiovascular dysfunction caused by general anesthesia using xylazine and ketamine in horses. Despite this positive effect however, the return of intestinal motility was delayed by 3 to 6 hours in both groups, indicating that glycopyrrolate treatment had no noticeable effects on improving this common side effect. Overall, the use of glycopyrrolate prior to anesthesia administration didn’t cause any severe side effects and can potentially improve the cardiovascular stability of horses during anesthesia.

Cite This Article

APA
Singh S, McDonell WN, Young SS, Dyson DH. (1996). Cardiopulmonary and gastrointestinal motility effects of xylazine/ketamine-induced anesthesia in horses previously treated with glycopyrrolate. Am J Vet Res, 57(12), 1762-1770.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 57
Issue: 12
Pages: 1762-1770

Researcher Affiliations

Singh, S
  • Department of Clinical Studies, Ontario Veterinary College, University of Guelph, Ontario, Canada.
McDonell, W N
    Young, S S
      Dyson, D H

        MeSH Terms

        • Acid-Base Equilibrium / drug effects
        • Adjuvants, Anesthesia / pharmacology
        • Analysis of Variance
        • Anesthesia, General / veterinary
        • Anesthetics / pharmacology
        • Animals
        • Blood Pressure / drug effects
        • Carbon Dioxide / blood
        • Cross-Over Studies
        • Female
        • Gastrointestinal Motility / drug effects
        • Glycopyrrolate / pharmacology
        • Heart Rate / drug effects
        • Hemodynamics / drug effects
        • Hemoglobins / metabolism
        • Horses
        • Ketamine / pharmacology
        • Oxygen / blood
        • Oxygen Consumption / drug effects
        • Partial Pressure
        • Premedication / veterinary
        • Pulmonary Artery / drug effects
        • Pulmonary Artery / physiology
        • Random Allocation
        • Respiration / drug effects
        • Single-Blind Method
        • Statistics, Nonparametric
        • Time Factors
        • Xylazine / pharmacology

        Citations

        This article has been cited 1 times.
        1. Dyson DH, Pascoe PJ, McDonell WN. Effects of intravenously administered glycopyrrolate in anesthetized horses. Can Vet J 1999 Jan;40(1):29-32.
          pubmed: 9919364