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Peer-reviewed veterinary case report

Alfaxalone vs diazepam-fentanyl for anesthesia in high-risk dogs

By Psatha, Evdokia et al.·Published in Veterinary anaesthesia and analgesia·2011·Queen Mother Hospital, United Kingdom·View original on PubMed

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Original publication title: Clinical efficacy and cardiorespiratory effects of alfaxalone, or diazepam/fentanyl for induction of anaesthesia in dogs that are a poor anaesthetic risk.

Species:
dog
Breathing & coughDogs

Plain-English summary

Forty dogs with moderate to severe health issues were given either alfaxalone or a combination of fentanyl, diazepam, and propofol to safely induce anesthesia for surgery. Both methods worked well, with no significant differences in blood pressure or recovery quality between the two treatments. The dogs showed good responses to both anesthesia options, and their vital signs remained stable throughout the procedures. Alfaxalone proved to be a safe and effective choice for inducing anesthesia in dogs that are not in perfect health.

People also search for: dog anesthesia options · alfaxalone for sick dogs · anesthesia recovery in dogs

Abstract

OBJECTIVE: To evaluate the clinical efficacy and cardiorespiratory effects of alfaxalone as an anaesthetic induction agent in dogs with moderate to severe systemic disease. STUDY DESIGN: Randomized prospective clinical study. ANIMALS: Forty dogs of physical status ASA III-V referred for various surgical procedures. METHODS: Dogs were pre-medicated with intramuscular methadone (0.2 mg kg(-1) ) and allocated randomly to one of two treatment groups for induction of anaesthesia: alfaxalone (ALF) 1-2 mg kg(-1) administered intravenously (IV) over 60 seconds or fentanyl 5 &#x3bc;g kg(-1) with diazepam 0.2 mg kg(-1) &#xb1; propofol 1-2 mg kg(-1) (FDP) IV to allow endotracheal intubation. Anaesthesia was maintained with isoflurane in oxygen and fentanyl infusion following both treatments. All dogs were mechanically ventilated to maintain normocapnia. Systolic blood pressure (SAP) was measured by Doppler ultrasound before and immediately after anaesthetic induction, but before isoflurane administration. Parameters recorded every 5 minutes throughout subsequent anaesthesia were heart and respiratory rates, end-tidal partial pressure of carbon dioxide and isoflurane, oxygen saturation of haemoglobin and invasive systolic, diastolic and mean arterial blood pressure. Quality of anaesthetic induction and recovery were recorded. Continuous variables were assessed for normality and analyzed with the Mann Whitney U test. Repeated measures were log transformed and analyzed with repeated measures anova (p<0.05). RESULTS: Treatment groups were similar for continuous and categorical data. Anaesthetic induction quality was good following both treatments. Pre-induction and post-induction systolic blood pressure did not differ between treatments and there was no significant change after induction. The parameters measured throughout the subsequent anaesthetic procedures did not differ between treatments. Quality of recovery was very, quite or moderately smooth. CONCLUSIONS AND CLINICAL RELEVANCE: Induction of anaesthesia with alfaxalone resulted in similar cardiorespiratory effects when compared to the fentanyl-diazepam-propofol combination and is a clinically acceptable induction agent in sick dogs.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/21214707/