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The Annals of Thoracic Surgery, Vol 58, 116-120, Copyright © 1994 by The Society of Thoracic Surgeons
T Ueno, K Furukawa, Y Katayama, H Suda and T Itoh
We present a clinically available method to protect the spinal cord against
ischemic or reperfusion injury and to prevent paraplegia after
cross-clamping of the aorta. We separated 35 rabbits into five equal groups
and clamped each animal's abdominal aorta distal to the left renal artery.
We also occluded the aortas 2 cm above the iliac bifurcation for 45 minutes
with inflated 5F balloon catheters. Through the catheter port distal to
each balloon one of four different solutions was infused at 3 degrees C for
3 minutes at a rate of 5 mL/min (group I, uninfused control; group II,
lactated Ringer's solution; group III, lactated Ringer's solution + 30
mg/kg of methylprednisolone; group IV, lactated Ringer's
solution+methylprednisolone + 3 mL of 20% mannitol; group V, lactated
Ringer's solution+methylprednisolone+mannitol + 10 mg/kg of vitamins E and
C). We assessed the neurologic status of the hind limbs on the second
postoperative day using Tarlov's criteria. The neurologic status in groups
III, IV, and V was significantly superior to that of group I (p < 0.05,
groups III versus I; p < 0.01, groups IV and V versus I). Spastic
paraplegia occurred in 71% of group I, in 43% of group II, in 29% of group
III, in 14% of group IV, and not at all in group V. The infusion of our
specially blended solution with several spinal cord neuroprotective
properties (hypothermia, methylprednisolone, mannitol, and vitamins E and
C) achieved the best spinal cord protection against ischemic or reperfusion
injury and prevented postoperative paraplegia.
ARTICLES
Spinal cord protection: development of a paraplegia-preventive solution
Department of Surgery, Saga Medical School, Japan.
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