Rd. Keegan et al., CARDIOVASCULAR EFFECTS OF EPIDURALLY ADMINISTERED MORPHINE AND A XYLAZINE-MORPHINE COMBINATION IN ISOFLURANE-ANESTHETIZED DOGS, American journal of veterinary research, 56(4), 1995, pp. 496-500
Cardiovascular effects of epidurally administered morphine, a morphine
-xylazine combination, and saline solution (control) during isoflurane
-maintained anesthesia were assessed in 6 healthy dogs. Anesthesia was
induced with isoflurane in O-2 and was maintained at 2.0% end-tidal i
soflurane concentration. Ventilation was controlled to maintain PaCO2
at 35 to 45 mm of Hg. The dorsal pedal artery was cannulated for measu
rement of systolic, mean, and diastolic pressures, and for blood sampl
e collection. Arterial blood pH and gas tensions were determined every
30 minutes. Cardiac output was determined by thermodilution. The EGG,
heart rate, body temperature, central venous pressure, mean pulmonary
artery pressure, pulmonary capillary wedge pressure, end-tidal isoflu
rane concentration, and CO2 tension were monitored. Systemic and pulmo
nary vascular resistance, arterial HCO3- concentration, base excess, a
nd cardiac index were calculated. After baseline measurements were tak
en, morphine (0.1 mg/kg of body weight) in 5 mi of isotonic saline sol
ution, morphine and xylazine (0.1 mg of morphine and 0.02 mg of xylazi
ne/kg) in 5 mi of isotonic saline solution, or 5 mi of isotonic saline
solution was injected into the lumbosacral epidural space. Data were
recorded at 5, 15, 30, 45, 60, 75, 90, 105, and 120 minutes after epid
ural injection. Statistical analysis included ANOVA for repeated measu
res. Significance was set at P < 0.05. None of the measured variables
was significantly different among the 3 treatments at any time. Result
s of the study indicated that epidural administration of morphine or m
orphine and xylazine is not associated with significant cardiovascular
side effects during isoflurane-maintained anesthesia in dogs.