Abstract

In de voorliggende studie werd de kwaliteit van de inductie en de recovery vergeleken bij 146 paarden na totale intraveneuze anesthesie met guaifenesine, ketamine en detomidine, ten behoeve van computertomografie (CT). Ze werden willekeurig ingedeeld, waarbij de ene groep romifidine (n=110) en de andere groep detomidine (n=36) als premedicatie kreeg. De anesthesie werd geïnduceerd met een combinatie van ketamine/midazolam. De gemiddelde anesthesieduur van de CT was kort (gemiddeld +/- SD: 23,5 +/- 8,8 minuten). Er bleek geen significant verschil te zijn voor de inductiescore. Wel bleken paarden gepremediceerd met romifidine een significant betere recoveryscore te hebben.

Highlights

  • Alpha-2 agonists are synthetic drugs that cause sedation, analgesia and myorelaxation due to their interaction with alpha-2 adrenoreceptors that are widely distributed throughout the body

  • Analgesia is thought to be the result of actions on the supraspinal and spinal sites in the central nervous system, while sedation is the effect of supraspinal stimulation of alpha-2 receptors in the locus coeruleus (Williams et al, 1985)

  • A study by Luna et al (1996) is consistent with that of Taylor and Watkins (1992), both demonstrating that a combination of guaifenesin, ketamine and detomidine is a reliable alternative to halothane anesthesia

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Summary

Introduction

Alpha-2 agonists are synthetic drugs that cause sedation, analgesia and myorelaxation due to their interaction with alpha-2 adrenoreceptors that are widely distributed throughout the body. Alpha-2 agonists are generally used in veterinary practice to tranquilize animals (i.e. pharmacologic restraint). This facilitates diagnostic examinations of minimally invasive and minor surgical procedures, and limits stress experienced by the patient (Nannarone et al, 2007). A study by Luna et al (1996) is consistent with that of Taylor and Watkins (1992), both demonstrating that a combination of guaifenesin, ketamine and detomidine is a reliable alternative to halothane anesthesia. Pharmacokinetic studies performed during TIVA using the original infusion rates described by Greene et al (1986), indicated that guaifenesin concentrations increased, reaching dangerously high values after two hours of anesthesia (Taylor et al, 1995). A lower infusion rate of guaifenesin is more likely to facilitate a better recovery (Luna et al, 1996)

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