Effects of intramuscular alfaxalone alone or in combination with diazepam in swine
Article first published online: 15 MAR 2013
© 2013 The Authors. Veterinary Anaesthesia and Analgesia © 2013 Association of Veterinary Anaesthetists and the American College of Veterinary Anesthesia and Analgesia
Veterinary Anaesthesia and Analgesia
Volume 40, Issue 4, pages 399–402, July 2013
How to Cite
Santos González, M., Bertrán de Lis, B. T. and Tendillo Cortijo, F. J. (2013), Effects of intramuscular alfaxalone alone or in combination with diazepam in swine. Veterinary Anaesthesia and Analgesia, 40: 399–402. doi: 10.1111/vaa.12033
- Issue published online: 13 JUN 2013
- Article first published online: 15 MAR 2013
- Manuscript Accepted: 20 NOV 2012
- Manuscript Received: 29 AUG 2012
To describe the use of intramuscular (IM) premedication with alfaxalone alone or in combination with diazepam in pigs.
Twelve healthy 2 month-old Landrace x Large White pigs weighing 21.3 ± 2.4 kg.
Animals were distributed randomly into two groups: group A (n = 6) 5 mg kg−1 of IM alfaxalone; and group AD (n = 6) 5 mg kg−1 of IM alfaxalone + 0.5 mg kg−1 of IM diazepam mixed in the same syringe. The total volume of injectate was standardized at 14 mL by dilution in 0.9% sodium chloride. Pain on injection, the degree of sedation and the quality of and time to induction of recumbency were evaluated. Once pigs were recumbent, reflexes were evaluated. Pulse and respiratory rates and arterial oxygen saturation were recorded at 5 and 10 minutes after drug administration. Pigs were then moved to another room for subsequent anaesthesia.
Two animals of group A and one of group AD showed slight pain on drug injection. Time to lateral recumbency (in seconds) was shorter in group AD (mean 203 ± SD 45 range 140–260) than group A (302 ± 75, range 220–420; p < 0.05). In group AD sedation was deeper, and on recumbency there was better muscle relaxation. When moved for anaesthesia, two pigs in Group A showed slight resistance but did not vocalize. There were no differences in physiologic measurements between groups, although in both groups, respiratory rate was significantly lower at ten compared with five minutes post drug injection. There was no apneoa.
Conclusions and clinical relevance
IM administration of alfaxalone combined with diazepam resulted in a rapid onset of recumbency and deep sedation, with minimal side effects. The combination might be useful for premedication, but volume of injectate will limit its use to small pigs.