Key result
Intra-aortic propofol injection during aortic cross-clamping resulted in higher Tarlov scores at 24 hours compared to saline or intravenous propofol (3.5 vs 0.5 and 1.3; p<0.001).
Why the study?
Does intra-aortic propofol injection prevent spinal cord injury during aortic cross-clamping in a canine model?
Does intra-aortic propofol injection prevent spinal cord injury during aortic cross-clamping in a canine model?
Intra-aortic injection of propofol provides superior protection against spinal cord ischemia during aortic cross-clamping compared to intravenous propofol in a canine model.
Answers are grounded in this paper and cite their sources.
Does not support clinical use; leaves open translation of canine spinal protection to human aortic procedures.
OBJECTIVE: We investigated whether propofol, a widely used anesthetic, injected into clamped aortic segments quickly attenuated transcranial spinal motor-evoked potential (MEP) amplitudes and protected against spinal cord injury during thoracoabdominal aortic surgery. METHODS: Eighteen beagle dogs were divided into three groups (n=6, each group): group 1 (20 ml of saline, intra-aortic injection), group 2 (1.5 mg/kg of propofol, intravenous injection), and group 3 (1.5 mg/kg of propofol, intra-aortic injection). Aortic cross-clamping was performed for 30 min. In each group, MEP amplitudes were recorded before, during, and after aortic cross-clamping. Tarlov score and histopathological examination were used to evaluate the protective effects of intra-aortic propofol injections. RESULTS: MEP amplitudes in group 3 attenuated to a value that was 60% of the control in just a minute after aortic cross-clamping, but maintained 40% of the control value during aortic cross-clamping. However, MEP amplitudes in groups 1 and 2 gradually attenuated and almost disappeared. Groups 1 and 2 amplitudes were lower than those in group 3, 30 min after aortic cross-clamping (p<0.001). Twenty-four hours after ischemia, the Tarlov score in group 3 was 3.5+/-0.5 and was higher than scores from groups 1 and 2, which were 0.5+/-0.5 and 1.3+/-1.2 (mean+/-SD, p<0.001, and p<0.001), respectively. Histopathologically, normal spinal cord motor neurons in group 3 were preserved to a significantly greater extent than in groups 1 and 2 (p=0.0031, and p=0.0282, respectively). There was a strong correlation between Tarlov scores at 24h and the number of normal motor neurons in the anterior horns of spinal cords (r=0.897; p<0.001). CONCLUSIONS: Intra-aortic propofol injections produce the quick suppression of MEP amplitudes and protect spinal cords from ischemia during aortic cross-clamping.
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Kumagai et al. (2006) studied spinal cord injury during thoracoabdominal aortic surgery (n=18). Intra-aortic propofol vs. Intravenous propofol (1.5 mg/kg) or intra-aortic saline (20 ml) was evaluated on Tarlov score at 24 hours (p=<0.001). Intra-aortic propofol injection during aortic cross-clamping resulted in higher Tarlov scores at 24 hours compared to saline or intravenous propofol (3.5 vs 0.5 and 1.3; p<0.001).
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