Objective-To characterize the hemodynamic effects of medetomidine admi
nistered intravenously at doses ranging from 1 to 20 mu g/kg, and to d
etermine whether these effects are dose dependent. Study Design-Prospe
ctive randomized multidose trial. Animals-Twenty-five clinically norma
l male beagles (5 groups of 5), aged 1 to 4 years and weighing 13.5 +/
- 1.7 kg. Methods-Medetomidine, at a dose of 1, 2, 5, 10, or 20 mu g/k
g, was administered intravenously at time 0. Heart rate, arterial pres
sure, central venous pressure, mean pulmonary arterial pressure, pulmo
nary capillary wedge pressure, body temperature, cardiac output, and p
acked cell volume were measured immediately before and at selected tim
es after medetomidine administration (3, 7, 10, 20, 30, 40, 50, and 60
minutes in all groups, at 90 minutes for the 10 and 20 mu g/kg groups
, and at 120 minutes for the highest dose). Cardiac index, stroke inde
x, rate-pressure product, systemic vascular resistance index, pulmonar
y vascular resistance index, and left and right ventricular stroke wor
k indices were calculated. The degree of sedation was subjectively sco
red by an observer who was blinded to the treatment used. Results-Hear
t rate, rate-pressure product, cardiac index, and left and right ventr
icular stroke work indices decreased below baseline values. Central ve
nous pressure and systemic vascular resistance index increased above b
aseline measurements. Except in the 2 mu g/kg group, after an initial
and short lasting increase, a prolonged decrease in arterial pressure
was observed. Conclusions-Hemodynamic changes were observed with the i
ntravenous (IV) administration of medetomidine, at any dose. However,
the two lowest doses (1 and 2 mu g/kg) produced less cardiovascular de
pression. Clinical Relevance-Medetomidine is an alpha-2 adrenoceptor a
gonist widely used in dogs, producing sedation, analgesia and cardiova
scular depression. When using IV medetomidine, a reduction of the reco
mmended dosage (ie, +/-30 to 40 mu g/kg) by up to 6 times did not sign
ificantly influence the cardiovascular effects. (C) Copyright 1998 by
The American College of Veterinary Surgeons.