2008
DOI: 10.1016/j.resuscitation.2007.07.002
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Intranasal selective brain cooling in pigs

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Cited by 45 publications
(28 citation statements)
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“…The methods differ in that the net measurement time per temperature point is 5 s for phase-mapping and 41 s for MRSI with high spatial definition. However, both methods were able to follow the dynamics of temperature decrease observed with intranasal cooling [12,14]. The measurement of absolute brain temperature is not possible with these techniques.…”
Section: Magnetic Resonance Measurementmentioning
confidence: 99%
See 1 more Smart Citation
“…The methods differ in that the net measurement time per temperature point is 5 s for phase-mapping and 41 s for MRSI with high spatial definition. However, both methods were able to follow the dynamics of temperature decrease observed with intranasal cooling [12,14]. The measurement of absolute brain temperature is not possible with these techniques.…”
Section: Magnetic Resonance Measurementmentioning
confidence: 99%
“…An intranasal method for initiating brain cooling where cold saline is circulated within intranasal balloons has previously been successfully applied in pigs [12][13][14]. In the present study, the intranasal balloon catheters circulated with saline at 20°C were applied for 60 min in awake, unsedated volunteers.…”
Section: Introductionmentioning
confidence: 97%
“…In rat models, flushing the nasopharnyx with cold saline 21 , or cold water passed through tygon tubing have both been attempted 22 . Others have extended these findings to large animal (pig) models 23 . Covaciu and colleagues anesthetized twelve pigs and performed selective cooling via a specially designed thin walled balloon catheter, placed in the nasopharnyx 24 examine the effect of high flow oxygen though the nasopharnyx on brain temperature for 11 intubated adult rats.…”
Section: Non Invasive Techniques Of Coolingmentioning
confidence: 83%
“…Experimentally there is some proof that a more immediate and more rapid cooling would be more neuroprotective (Noguchi et al, 2011), but clinically this has not been easy to prove. In spite of this nasal cooling, a method implying a considerably more rapid cooling of the brain has been tried (Castren et al, 2010;Covaciu et al, 2008Covaciu et al, , 2009Weis et al, 2009). Also experimentally mild induced hypothermia has been demonstrated to decrease the ischemia-reperfusion injury on many levels, for example, reduction of extracellular levels of excitatory neurotransmitters; avoidance of proliferation, migration, transformation, and activation of astroglial cells; decrease of p53 protein levels and apoptotic cell death; and mitigating proteins Bcl-2 and cytochrome C and block of proteins responsible for mediating the caspase-independent apoptosis (Gonzalez-Ibarra et al, 2011).…”
Section: Introductionmentioning
confidence: 99%