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EFFECT OF NITROUS OXIDE ON CEREBRAL BLOOD FLOW IN NORMAL HUMANS
We have studied the effect of nitrous oxide on cerebral haemodynamics in 24 healthy male volunteers. Hemispherical cerebral blood flow (CBF) was measured using the xenon-133 inhalation technique, blood flow velocities in the right middle cerebral artery were calculated using transcranial Doppler ult...
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Published in: | British journal of anaesthesia : BJA 1993-02, Vol.70 (2), p.154-159 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | We have studied the effect of nitrous oxide on cerebral haemodynamics in 24 healthy male volunteers. Hemispherical cerebral blood flow (CBF) was measured using the xenon-133 inhalation technique, blood flow velocities in the right middle cerebral artery were calculated using transcranial Doppler ultrasound and the pulsatility index (PI) the inverse of which is theoretically proportional to flow in the vessel under investigation–was derived from analysis of the spectrally analysed velocity pulse wave form obtained from the middle cerebral artery. Each variable was measured with the subject inhaling 100% oxygen (1st baseline), 30% nitrous oxide in oxygen, 100% oxygen (2nd baseline) and 60% nitrous oxide in oxygen. CBF was significantly greater with 30% (0.01 ≥ P ≥ 0.001) and 60% nitrous oxide (P ≤ 0.001) compared with baseline, athough the difference between 30% and 60% nitrous oxide was not significant. Changes in 1/PI correlated closely with those in hemispherical CBF. Blood flow velocities increased significantly with 30% (P > 0.001) and 60% nitrous oxide (0.005 > P % 0.001), the difference between 30% and 60% nitrous oxide also being significant (0.005 > P > 0.001). We observed a plateau in the change in CBF caused by nitrous oxide and suggest that this may be explained by activation of intact auto-regulative mechanisms in healthy human brain. (Br. J. Anaesth. 1993; 70: 154–159) |
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ISSN: | 0007-0912 1471-6771 |
DOI: | 10.1093/bja/70.2.154 |