Research PaperCardiopulmonary effects of dexmedetomidine and ketamine infusions with either propofol infusion or isoflurane for anesthesia in horses
Introduction
Infusions of sedative, analgesic and anesthetic drugs can provide a stable plane of anesthesia or analgesia depending on the drugs used. Infusions can be used to provide total intravenous anesthesia (TIVA) without the need for administration of volatile anesthetic agents or used as part of an inhalation anesthetic technique. Using an inhalation agent with partial intravenous anesthesia (PIVA) can reduce some adverse effects produced by volatile drugs resulting in reduced response to noxious stimuli and hemodynamic stability in horses, especially with infusions of analgesic drugs. Both the TIVA and PIVA techniques have been comprehensively reviewed in previous articles (Bettschart-Wolfensberger & Larenza 2007; Lerche 2013; Valverde 2013).
Alpha2-adrenergic agonist drugs are particularly useful for PIVA techniques in horses. A medetomidine infusion enabled reduced concentrations of volatile anesthetic agent to be used and produced superior skeletal muscle relaxation while maintaining hemodynamic stability and body temperature (Creighton et al. 2012). Dexmedetomidine also provided good quality of PIVA with stable hemodynamic variables and smooth recovery from anesthesia (Marcilla et al. 2010, 2012; Gozalo-Marcilla et al. 2013). Alpha2-adrenergic agonist drugs have also been used in combination with infusions of other injectable drugs to provide good quality anesthetic conditions for surgery (Valverde et al. 2010; Benmansour & Duke-Novakovski 2013).
Propofol is a suitable drug for PIVA and TIVA techniques because of its ideal pharmacokinetic profile (Oku et al. 2005, 2006; de Vries et al. 2013). Its use in larger animals as the sole anesthetic agent is limited by the low concentration of the available commercial formulation to deliver an appropriate infusion rate and by its lack of analgesic properties, resulting in unacceptable induction and anesthetic qualities (Mama et al. 1995, 1996). Techniques have been developed to reduce the amount of propofol required, prevent physiological responses to surgery and yet still make use of the anesthetic and rapid recovery properties of propofol (Bettschart-Wolfensberger et al. 2003, 2005a; Oku et al. 2011). Ketamine is an effective anesthetic and analgesic agent in horses, but also requires to be given with other drugs such as alpha2-adrenergic agonists to reduce any adverse effects such as muscle rigidity and excitement (Mama et al. 2005). Ketamine has been co-administered with propofol to provide a suitable quality of induction for endotracheal intubation (Wagner et al. 2002; Posner et al. 2013). Furthermore, ketamine infusions have been used as part of PIVA and TIVA techniques alongside propofol (Nolan et al. 1996; Flaherty et al. 1997; Ohta et al. 2004; Umar et al. 2006, 2007; de Vries et al. 2013).
This crossover study was designed to compare the use of propofol, ketamine and dexmedetomidine infusions for anesthesia (TIVA) with a PIVA technique by replacing the propofol infusion with isoflurane in horses undergoing two arthroscopy procedures several weeks apart.
Section snippets
Material and methods
Six mixed breed horses (three mares and three geldings) aged 7 ± 4.2 years (mean ± SD; range 3–14 years), and weighing 488.3 ± 29.1 kg (mean ± SD, range 460–535 kg) were used for this study. The horses were deemed healthy according to physical and hematological examinations, kept outdoors in paddocks and brought indoors for the study (altitude 482 m above sea level). Horses were fed hay with free access to water and were fasted for 12 hours prior to induction of anesthesia, but not denied
Results
Data are presented as mean ± SD in Tables Table 1, Table 2, Table 3, Table 4. No differences existed between groups for volume of fluid administered, and times to extubation, sternal recumbency and standing. Mean Fe’Iso was approximately 1% (range, 0.5–1.3%) throughout the 60 minute study period. The FIO2 rapidly increased over time (Table 4).
Arterial pH was significantly lower at 30 and 60 minutes after induction in group PROKD compared to group ISOKD (p=0.0099), and PaO2 was significantly
Discussion
Both anesthetic protocols provided suitable conditions for arthroscopy. A shared pre-induction baseline was limited to HR, CT, t, pulmonary arterial and mean RA pressures. The remaining data was compared to the first reading available (10 minutes post-induction) although horses were receiving different treatments at this point. The accuracy of using the right ventricle for sampling mixed venous blood had been previously confirmed (unpublished observations) and avoided accidental
Acknowledgements
The authors would like to acknowledge the support of the WCVM Equine Health Research Fund, the animal care and anesthesia technical staff and Dr. J Bracamonte for their assistance.
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