Cl. Tyner et al., MULTICENTER CLINICAL COMPARISON OF SEDATIVE AND ANALGESIC EFFECTS OF MEDETOMIDINE AND XYLAZINE IN DOGS, Journal of the American Veterinary Medical Association, 211(11), 1997, pp. 1413
Objective-To evaluate analgesic and sedative effects of medetomidine h
ydrochloride in dogs and to compare effects with those of xylazine hyd
rochloride. Design-Randomized, controlled trial. Animals-184 dogs that
required sedation or analgesia for completion of minor diagnostic or
therapeutic procedures. Procedure-Dogs were sedated with medetomidine,
IV (750 mu g/m(2) of body surface area) or IM (1,000 mu g/m(2)) or wi
th xylazine, IV (1.1 mg/kg [0.5 mg/lb] of body weight) or IM (2.2 mg/k
g [1 mg/lb]). Sedative effects were measured by scoring posture and re
sponse to noise. Durations of effects were determined by measuring tim
e intervals between drug administration and changes in posture. Analge
sic effects were measured by determining toe-pinch pressure needed to
elicit a withdrawal response. Clinicians rated sedative and analgesic
effects and ease with which diagnostic or therapeutic procedures could
be performed. Results-Posture and response to noise scores were signi
ficantly higher for dogs given medetomidine, IM, than for dogs given x
ylazine, IM, and for dogs given medetomidine, IV, than for dogs given
xylazine, IV. Time to regaining sternal recumbency and time to regaini
ng ability to stand were longest after IM administration of medetomidi
ne. Toe-pinch pressures were not significantly different among groups.
Clinicians rated overall analgesic and sedative effects as excellent
significantly more often after administration of medetomidine than aft
er administration of xylazine, Prevalence of adverse effects did not d
iffer among groups. Clinical Implications-Medetomidine and xylazine, a
t doses tested, were effective and safe, but results of subjective mea
surements indicated that medetomidine provided better sedation and ana
lgesia than did xylazine. Specific alpha(2)-adrenergic antagonists (at
ipamezole, yohimbine) are available for control of adverse cardiovascu
lar effects.