British Journal of Anaesthesia, Vol 77, Issue 5 625-631, Copyright © 1996 by The Board of Management and Trustees of the British Journal of Anaesthesia
L. Arendt-Nielsen, J. Nielsen, S. Petersen-Felix, T. W. Schnider and A. M. Zbinden
We have compared the analgesic efficacy of the racemic mixture and the
stereoisomer (S+) of the NMDA antagonist ketamine. In a double-blind,
three-way crossover, placebo-controlled study, we assessed the following:
pain evoked by small/large area pressure stimuli, pain detection threshold
and pain ratings to small/large area of heat stimuli, pain detection
threshold and pain rating to heat stimuli of brief/long duration, summation
pain threshold and pain ratings to repeated heat/electrical stimuli, side
effects and reaction time. Plasma concentrations of 350 ng ml-1 for
ketamine (racemic) and 180 ng ml-1 for ketamine (S+) were tried. We found
that ketamine (racemic) prolonged the reaction time more than ketamine
(S+). Both drugs affected pain caused by repeated stimuli or stimuli of
long duration equally or more than a single stimulus of short duration.
They also affected pain evoked from large areas equally or more than pain
evoked from small areas. The (S+)-isomer was approximately twice as potent
as the racemic mixture of ketamine in inhibiting central summation.
CLINICAL INVESTIGATIONS
Effect of racemic mixture and the (S+)-isomer of ketamine on temporal and spatial summation of pain
Laboratory for Experimental Pain Research, Aalborg University, Aalborg, Denmark; Department of Anaesthesiology, Inselspital Bern, Switzerland
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