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The Journal of Thoracic and Cardiovascular Surgery, Vol 89, 228-234, Copyright © 1985 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
EA Grossi, KH Krieger, JN Cunningham Jr, AT Culliford, IM Nathan and FC Spencer
In the present study, we examined the effects of various levels of oxygen
tension on spinal cord blood flow while using somatosensory evoked
potentials to monitor spinal cord sensory function during hypoxia. In this
experiment, six adult, mongrel dogs were heparinized and placed on right
atrial-femoral artery bypass with an oxygenator in the bypass circuit. The
aorta was cross-clamped proximal to the left subclavian artery, and bypass
flow and fluid balance were adjusted so as to maintain a distal aortic
perfusion pressure of greater than 80 mm Hg. Oxygen flow to the oxygenator
was lowered by graded decrements to provide decreasing levels of oxygen
tension, which ultimately approached pure venoarterial bypass. Each
successive oxygen level was maintained for 30 minutes. Spinal cord blood
flow was measured with radioactive microspheres, and latency and amplitude
of somatosomatic evolved potentials were continuously monitored. The
somatosensory evolved potential signal was invariably present as long as
the distal aortic pressure was greater than 80 mm Hg; there were several
transient hypotensive episodes (less than 5 minutes), which were
accompanied by reversible loss of somatosensory evolved potentials. The
spinal cord blood flow increased from 13.6 to 119.7 ml/100 gm/min as the
distal oxygen tension fell to a mean value of 30 mm Hg, while latency of
somatosensory evolved potentials increased 19.3% and amplitude decreased
43.3%. These results suggest the following conclusions: (1) In response to
hypoxia, spinal cord blood flow dramatically increases and somatosensory
evolved potentials deteriorate (increase in latency and decrease in
amplitude). (2) However, during prolonged hypoxia, spinal cord sensory
function can be maintained by sufficiently high flow rates and perfusion
pressures. (3) Somatosensory evolved potentials can be used to monitor
continuously spinal cord sensory function under these conditions.
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