J. Levanen et al., DEXMEDETOMIDINE PREMEDICATION ATTENUATES KETAMINE-INDUCED CARDIOSTIMULATORY EFFECTS AND POSTANESTHETIC DELIRIUM, Anesthesiology, 82(5), 1995, pp. 1117-1125
Background: Dexmedetomidine is a new potent and highly selective alpha
(2)-adrenoceptor agonist with sedative-hypnotic and anesthetic sparing
properties. Because of its sympathoinhibitory activity, it may prove
useful in balancing the cardiostimulatory effects and attenuating the
adverse central nervous system effects of ketamine. Methods: A double-
blind, randomized and comparative parallel-group study design was empl
oyed in 40 volunteers with ASA physical status 1 who were scheduled fo
r elective superficial surgery under ketamine anesthesia. Dexmedetomid
ine (2.5 mu g/kg, n = 20) or midazolam (0.07 mg/kg, n = 20) was admini
stered intramuscularly 45 min before induction of anesthesia. Anesthes
ia was induced with 2 mg/kg ketamine intravenously, and muscle relaxat
ion was achieved with vecuronium. After tracheal intubation, anesthesi
a was maintained with nitrous oxide/oxygen (2:1) and additional 1 mg/k
g intravenous ketamine boluses according to clinical and cardiovascula
r criteria. Hypotension and bradycardia were treated by increasing the
intravenous infusion rate of crystalloids and intravenous atropine, r
espectively. Sedative and anxiolytic properties, intra- and postoperat
ive drug requirements, psychomotor and cognitive impairments, and card
iovascular effects were compared between the two groups. Results: Dexm
edetomidine and midazolam proved to have equal sedative and anxiolytic
effects after intramuscular administration, but dexmedetomidine induc
ed significantly less preoperative psychomotor impairment and less ant
erograde amnesia than did midazolam. Compared to midazolam, dexmedetom
idine decreased the need for intraoperative ketamine and was more effe
ctive in reducing ketamine-induced adverse central nervous system effe
cts. Dexmedetomidine also was superior to midazolam in attenuating the
hemodynamic responses to intubation and the cardiostimulatory effects
of ketamine in general, but it increased the incidence of intra- and
postoperative bradycardia. Conclusions: These results suggest that pre
medication with 2.5 mu g/kg dexmedetomidine is effective in attenuatin
g the cardiostimulatory and postanesthetic delirium effects of ketamin
e. However, because of its propensity to cause bradycardia, routine us
e of an anticholinergic drug should be considered.