2014
DOI: 10.2174/2210309004666140616232339
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Biomarkers of Organ Injury

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Cited by 5 publications
(7 citation statements)
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“…Deliberate hypothermic cardiac arrest is used for repair of complex cardiovascular conditions, and for cerebral protection the safe use of cardiac arrest for up to 60 min at 8–13 °C 37 39 has been documented. In the present experiment biomarkers of brain injury disclose no pathological changes as GFAP and UCHL1 (Table 3 ), both highly selective for CNS injury 40 , are within normal control levels in pigs 41 .…”
Section: Discussionsupporting
confidence: 49%
“…Deliberate hypothermic cardiac arrest is used for repair of complex cardiovascular conditions, and for cerebral protection the safe use of cardiac arrest for up to 60 min at 8–13 °C 37 39 has been documented. In the present experiment biomarkers of brain injury disclose no pathological changes as GFAP and UCHL1 (Table 3 ), both highly selective for CNS injury 40 , are within normal control levels in pigs 41 .…”
Section: Discussionsupporting
confidence: 49%
“…Deliberate hypothermic cardiac arrest is used for repair of complex cardiovascular conditions, and for cerebral protection the safe use of cardiac arrest for up to 60 min at 8-13 °C [40][41][42] has been documented. In the present experiment biomarkers of brain injury disclose no pathological changes as GFAP and UCHL1 (Table 3), both highly selective for CNS injury [24], are within normal control levels in pigs [43].…”
Section: Restitution Of Organ Blood Ow After Rewarmingsupporting
confidence: 49%
“…The selection of biomarkers to monitor organ function and to detect organ injury were based on a previous report [24]. Alanine aminotransferase (ALAT), aspartate aminotransferase (ASAT), alkaline phosphatase (ALP), amylase, total bilirubin, creatinine, lipase, urea, and γ-glutamyl transferase (γ GT) were analysed by a colorimetric method in plasma samples using a Cobas 8000 analyser (Roche Diagnostics GmbH, Mannheim, Germany).…”
Section: Biochemistrymentioning
confidence: 99%
“…Standard clinical neuroimaging methods such as computed tomography (CT) and conventional MRI are the primary clinical neuroimaging methods for lesion detection after TBI and continue to provide diagnostic and prognostic information, particularly for patients with more severe TBI (Jeter et al, 2013;Mayer et al, 2018). Additionally, advanced MRI techniques such as volumetric MRI analysis, susceptibility-weighted imaging (microhemorrhages), diffusion tensor imaging (DTI) and tractography (white matter injury), functional MRI (network connectivity), and perfusion imaging (blood flow or volume) have produced sets of imaging biomarkers used to predict neurological and/or neuropsychological outcome across all severities of brain injury (Hunter, Wilde, Tong, & Holshouser, 2012;Kou et al, 2010).…”
Section: Mrs As a Biomarker Of Injurymentioning
confidence: 99%