British Journal of Anaesthesia, Vol 75, Issue 5 610-615, Copyright © 1995 by The Board of Management and Trustees of the British Journal of Anaesthesia
D. W. Blake, A. F. Van Leeuwen, O. U. Petring, J. Ludbrook and S. Ventura
We have studied in eight rabbits the cardiovascular effects of midazolam,
propofol and alfentanil with graded hypoxia. Central blood volume was
reduced progressively by gradual inflation of a thoracic vena cava cuff so
that cardiac index (CI) decreased at a constant rate. Under control
conditions the haemodynamic response was biphasic. During phase I, mean
arterial pressure (MAP) was maintained by a progressive decrease in
systemic vascular conductance (SVCI). When CI had declined to a critical
level, phase II occurred with an abrupt increase in SVCI and decrease in
MAP. Phase I was prolonged by hypoxia, alfentanil and midazolam, but the
effects were not additive. Phase I was shortened by propofol and this
effect increased with hypoxia. The gradient of the SVCI response in phase I
was also reduced by propofol > midazolam, but not by alfentanil. The
occurrence of phase II was less frequent during alfentanil infusion than
midazolam and propofol with all of the inspired gas mixtures. Thus the
opioid was protective against circulatory collapse with hypoxia and
simulated hypovalaemia.
LABORATORY INVESTIGATIONS
Haemodynamic response to simulated haemorrhage in the rabbit: interaction of i.v. anaesthesia and hypoxia
Department of Anaesthesia, Royal Melbourne Hospital and University of Melbourne, Parkville, Victoria, Australia 3050; Department of Surgery, Royal Melbourne Hospital and University of Melbourne, Parkville, Victoria, Australia 3050
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