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The Journal of Thoracic and Cardiovascular Surgery, Vol 103, 1143-1146, Copyright © 1992 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
CK Mezrow, M Mazzoni, D Wolfe, HH Shiang, RS Litwak and RB Griepp
Poloxamer 188, an amphipathic copolymer with cytoprotective properties, was
investigated as a means of improving neurologic outcome after a prolonged
period (150 minutes) of deep hypothermic circulatory arrest. Dogs were
perfusion cooled and surface cooled to 10 degrees C, the heart was arrested
for 150 minutes, and then the dogs were rewarmed and weaned from bypass.
Seven dogs were treated with poloxamer 188 before and after deep
hypothermic circulatory arrest. Six control dogs were treated with saline.
Surviving dogs were evaluated for 1 week after deep hypothermic circulatory
arrest for neurologic deficits or behavioral changes. Neurologic outcome
was graded by the following system: grade 1, death within the observation
period; grade 2, comatose; grade 3, holds head up; grade 4, sits up; grade
5, stands; grade 6, normal in both behavior and gait. There were no deaths
in the seven poloxamer 188-treated animals versus three deaths in the six
control dogs. Poloxamer 188-treated dogs also manifested significantly less
neurologic dysfunction after deep hypothermic circulatory arrest than did
the control group (p less than 0.003). This study shows that poloxamer 188
has a significant impact in improving neurologic outcome after
exceptionally long periods of deep hypothermic circulatory arrest.
ARTICLES
Poloxamer 188 improves neurologic outcome after hypothermic circulatory arrest
Department of Cardiothoracic Surgery, Mount Sinai Medical Center, New York, NY 10029.
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