B. Pypendop et J. Verstegen, Cardiorespiratory effects of a combination of medetomidine, midazolam, andbutorphanol in dogs, AM J VET RE, 60(9), 1999, pp. 1148-1154
Objective-To characterize cardiorespiratory effects for a combination of me
detomidine, butorphanol, and midazolam and to compare magnitude of cardiore
spiratory depression with that induced by a commonly used inhalation anesth
etic regimen (acepromazine-butorphanol-thiopenral-halothane).
Animals-10 clinically normal dogs(2 groups of 5).
Procedure-In treated dogs, medetomidine was administered (time, 0 minutes);
midazolam and butorphanol were administered when effects of medetomidine w
ere maximal (time, 20), and atipamezole was administered subsequently (time
60). In control dogs, drugs were administered after allowing effects of ea
ch agent to be achieved: acepromazine was given at time 0, butorphanol and
thiopental were administered at time 35, and halothane was administered fro
m time 45 until 110. Various cardiorespiratory and hematologic variables we
re measured or calculated.
Results-Respiratory rate, arterial and venous pH, venous oxygen content, ox
ygen consumption, and oxygen delivery decreased significantly below baselin
e values for treated dogs; end-tidal CO2, afterial and venous Pco(2),, and
O-2,extraction increased significantly above; baseline values. Compared wit
h data obtained after anesthesia, arterial HCO3- concentration, venous Po-2
and So(2), cardiac output, oxygen extraction, and oxygen delivery appeared
more modified in treated dogs. Oxygen consumption and physiologic shunt fr
action were less modified in treated dogs than control dogs.
Conclusions and Clinical Relevance-Medetomidine-butorphanol-midazolam combi
nation induced respiratory depression, comparable in magnitude to that indu
ced by a widely used inhalation anesthetic regimen. Respiratory variables r
emained within acceptable limits during anesthesia; however, those associat
ed with cardiovascular function were more severely affected.