Effects of Midazolam on Cerebral Hemodynamics and Cerebral Vasomotor Responsiveness to Carbon Dioxide
Author(s) -
Alain Forster,
O Juge,
Denis R. Morel
Publication year - 1983
Publication title -
journal of cerebral blood flow and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.167
H-Index - 193
eISSN - 1559-7016
pISSN - 0271-678X
DOI - 10.1038/jcbfm.1983.33
Subject(s) - cerebral blood flow , midazolam , anesthesia , hypercarbia , medicine , hemodynamics , hypercapnia , placebo , blood pressure , vasomotor , benzodiazepine , inhalation , alternative medicine , receptor , pathology , sedation , acidosis
Although it is known that hypercarbia increases and benzodiazepines decrease cerebral blood flow (CBF), the effects of benzodiazepines on CBF responsiveness to CO 2 are not well documented. The influence on CBF and CBF-C0 2 sensitivity of placebo or midazolam, which is a new water-soluble benzodiazepine, was measured in eight healthy volunteers using the noninvasive 133 Xe inhalation method for CBF determination. Under normocarbia, midazolam decreased CBF from 40.6 ± 3.2 to 27.0 ± 5.0 ml 100 g −1 min −1 (x̄ ± SD). At a later session under hypercarbia, CBF was 58.8 ± 4.4 ml 100 g −1 min −1 after administration of placebo, and 49.1 ± 10.2 ml 100 g −1 min −1 after midazolam. The mean of the slopes correlating P a co 2 and CBF was significantly steeper with midazolam (2.5 ± 1.2 ml 100 g −1 min −1 mm Hg −1 ) than with placebo (1.5 ± 0.4 ml 100 g −1 min −1 mm Hg −1 ). Our results suggest that midazolam may be a safe agent to use in patients with intracranial hypertension, since it decreases CBF and thus cerebral blood volume; however, it should be administered with caution in nonventilated patients with increased intracranial pressure, since its beneficial effects on cerebrovascular tone can be readily counteracted by the increase in arterial CO 2 tension induced by this drug.
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