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Right arrow Neuroanesthesia and Intensive Care
Canadian Journal of Anesthesia 47:125-130 (2000)
© Canadian Anesthesiologists' Society, 2000

Reports of Investigation

Rate of change of cerebral blood flow velocity with hyperventilation during anesthesia in humans

Kwan Y. Chong, MB BS*, Rosemary A. Craen, MB BS*, John M. Murkin, MD*, Donald Lee, MD{dagger}, Michael Eliasziw, PhD{ddagger} and Adrian. W. Gelb, MB CHB*

* From the Departments of Anaesthesia and
{dagger} Diagnostic Radiology, London Health Sciences Centre, University Campus and
{ddagger} Department of Epidemiology and Biostatistics, The University of Western Ontario, London, Ontario, Canada.

Dr. A.W. Gelb, Department of Anaesthesia, London Health Sciences Centre, University Campus, 339 Windermere Rd, London, Ontario, N6A 5A5 Canada. Phone: 519-663-3828; Fax: 519-663-3161; E-mail: agelb{at}julian.uwo.ca

Purpose: Although it has been suggested that the rate at which the cerebral circulation responds to changes in PaCO2 is different with differing anesthetics, there have been no attempts to measure this. Transcranial Doppler allows the continuous measurement of cerebral blood flow velocity (CBFV) and any changes over time. Our aim was to compare the rate of change of CBFV when end-tidal CO2 (PETCO2) was rapidly altered during halothane or isoflurane anesthesia.

Methods: Twenty-eight unpremedicated healthy patients were randomly assigned to receive air/O2 and either 1 - 1.5 MAC halothane or isoflurane as the primary anesthetic. After 15 min of steady state, PETCO2 was rapidly reduced from 45 mmHg to 30 mmHg. CBFV and PETCO2 were recorded every 30 sec for the next 10 min.

Results: The rate of change of normalized CBFV ({Delta} CBFV vs {Delta} time) was more rapid in the isoflurane group (P < 0.0001) especially in the initial few minutes. In all patients anesthetized with isoflurane, and in all but two patients anesthetized with halothane, the reduction in PETCO2 produced a corresponding decrease in CBFV. However, there were no differences in the magnitude of cerebrovascular CO2 reactivity ({Delta} CBFV vs {Delta} PETCO2) between the two groups.

Conclusions: The rate of change of CBFV was faster in the isoflurane than in the halothane group especially in the initial few minutes. Indeed, for two patients in the halothane group Vmca did not change despite a change in PETCO2. This may be of clinical importance when cerebrovascular tone needs to be changed rapidly.




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