ISOFLURANE VERSUS SODIUM-NITROPRUSSIDE FOR THE CONTROL OF PROXIMAL HYPERTENSION DURING THORACIC AORTIC CROSS-CLAMPING - EFFECTS ON SPINAL-CORD ISCHEMIA
Ji. Simpson et al., ISOFLURANE VERSUS SODIUM-NITROPRUSSIDE FOR THE CONTROL OF PROXIMAL HYPERTENSION DURING THORACIC AORTIC CROSS-CLAMPING - EFFECTS ON SPINAL-CORD ISCHEMIA, Journal of cardiothoracic and vascular anesthesia, 9(5), 1995, pp. 491-496
Citations number
26
Categorie Soggetti
Anesthesiology,"Peripheal Vascular Diseas","Cardiac & Cardiovascular System
Objective: This study was designed to compare the effects of isofluran
e and nitroprusside on spinal cord ischemia when they are used to cont
rol proximal hypertension during thoracic aortic cross-cramping (TACC)
. Design: Prospective, randomized, blinded experimental study. Setting
: Laboratory and animal research facility. Participants: Adult mongrel
dogs. Interventions: Two groups of eight dogs had TACC for 45 minutes
. Proximal aortic, distal aortic, and cerebrospinal fluid (CSF) pressu
res were monitored. Spinal cord perfusion pressure was calculated as t
he distal mean pressure minus the CSF pressure. Group 1 received nitro
prusside and group 2 received isoflurane to control proximal hypertens
ion during cross-clamping. The dogs were neurologically evaluated 24 a
nd 48 hours later by an observer blinded as to the study group. Spinal
cord segments were obtained for histopathologic examination. Measurem
ents and Main Results: Distal perfusion pressure and spinal cord perfu
sion pressure were significantly higher in the isoflurane group (p <.0
05). At 24 hours, seven of eight dogs in group 1 had severe neurologic
injury tie, paraplegia), with the eighth having mild neurologic injur
y. This is in contrast to group 2, where 6 of 8 dogs had either minima
l or no injury, one had mild injury, and one had severe injury. Simila
r results were observed at 48 hours (p <.005). Conclusions: Isoflurane
, when used to control proximal hypertension during TACC, produces a h
igher spinal cord perfusion pressure and is associated with a lower in
cidence of neurologic injury than nitroprusside in this canine model.
(C) 1995 by WB. Saunders Company