Aim. To extend the safe period of aortic crossclamping in the porcine model
by intrathecally dilating the spinal arteries, with cooling of the spinal
cord, or using selfotel
Methods. Experimental design and setting: prospective domestic laboratory p
ig study. Interventions: fifteen animals were assigned to a control group (
C, N=5), intrathecal papaverine plus spinal cord cooling group (IP+C, N=5),
or selfotel group (S, N=5). In the IP+C group, a lumbar laminectomy was pe
rformed and an intrathecal catheter placed for intrathecal injection of pap
averine and perfusion with cold Ringer's solution (4 degrees C) prior to ao
rtic crossclamping. In the selfotel group, 20 mg/kg of selfotel was adminis
tered 30 minutes before aortic crossclamping. In all 15 animals, the aorta
was cross-clamped for 60 minutes at normothermia. Measures: immediately aft
er the operation and 24 hours later, lower limb function was evaluated.
Results. All five control animals were paralyzed; all 5 IP+C animals could
stand or walk (p=0.004 versus control); and in the selfotel group, one had
paraparesis, three had paraplegia and one died before evaluation (p=n.s.)
Conclusions. The combination of intrathecal papaverine to dilate spinal art
eries and prevent spasm from the cold solution plus intrathecally cooling t
he spinal cord appears to extend the period of safe aortic cross-clamping.
Selfotel, in this model of extended, severe, spinal cord ischemia, was inef
fective.