British Journal of Anaesthesia, Vol 82, Issue 4 542-545, Copyright © 1999 by The Board of Management and Trustees of the British Journal of Anaesthesia
H. J. Skinner, K. J. Girling, A. Whitehurst and M. H. Nathanson
Mivacurium is metabolized by plasma cholinesterase (PCHE). Metoclopramide
inhibits PCHE in vitro and in vivo. We have assessed the effect of
metoclopramide on duration of action of mivacurium and measured PCHE at
baseline and at the time of maximal block. In a randomized, double-blind
study, 30 patients received metoclopramide 0.15 mg kg-1 i.v. or saline,
followed by propofol anaesthesia and mivacurium 0.15 mg kg-1. Using a
TOF-Guard accelerometer, times to recovery of TI to 25%, 75% and 90% were
13.4, 19.3 and 21.9 min in the saline group and 17.8, 25.3 and 28.8 min in
the metoclopramide group (P < 0.01, P < 0.05, P < 0.05,
respectively). There were no differences in onset time or recovery index
between the groups. PCHE activity at the time of maximum block decreased
within each group (P < 0.01) but there was no difference between groups.
In a second biochemical study of eight patients, a small decrease in PCHE
activity was detected after metoclopramide 0.15 mg kg-1, but before
administration of mivacurium (P < 0.025). We conclude that
metoclopramide prolongs the duration of action of mivacurium.
CLINICAL INVESTIGATIONS
Influence of metoclopramide on plasma cholinesterase and duration of action of mivacurium
University Department of Anaesthesia, Queen's Medical Centre and Nottingham City Hospital, Nottingham NG7 2UH, UK; Department of Clinical Chemistry, Nottingham City Hospital, Nottingham NG5 1PB, UK; Department of Anaesthesia, Queen's Medical Centre, Nottingham NG7 2UH, UK
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