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   <subfield code="a">10.1007/s12028-012-9810-1</subfield>
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   <subfield code="a">Outcome of Poor-Grade Subarachnoid Hemorrhage as Determined by Biomarkers of Glucose Cerebral Metabolism</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Gleicy Barcelos, Yannick Tholance, Sebastien Grousson, Bernard Renaud, Armand Perret-Liaudet, Frederic Dailler, Luc Zimmer]</subfield>
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   <subfield code="a">Purpose: The aim of this study was to determine if the measurement of blood biomarkers of glucose cerebral metabolism, performed with retrograde jugular catheter, could predict the outcome of poor-grade aneurysmal subarachnoid hemorrhage (aSAH) patients. Methods: This study was conducted in 68 poor-grade aSAH patients. A total of 4,024 blood samples obtained from jugular and radial catheters were analyzed for glucose, lactate, and oxygen content every 8h for 10±0.5days. Metabolic ratio (MR) and lactate-oxygen index (LOI) were obtained by ratios using arterio-jugular differences. Functional outcome was evaluated at 12months with the Glasgow Outcome Scale. Results: Outcome was unfavorable in 40 patients. In this group of patients, the MR was significantly lower (p&lt;0.0001) and the LOI was significantly higher (p=0.0001) than in the group with favorable outcome. The MR cutoff value, below which the patients are likely to have an unfavorable outcome, was determined to be 3.35. More interestingly, the data obtained in this study demonstrated that the patients achieving an unfavorable outcome were distinguished from those with a favorable outcome by having at least three events of MR inferior to 3.35 (sensitivity=90%, specificity=82.1%). Moreover, in patients who developed cerebral vasospasm, we observed a significant decrease in the MR. Conclusion: Our data provide additional support to the view that the MR is a reliable marker for predicting the outcome of poor-grade aSAH patients. Prospective studies are needed to confirm its value in multimodal monitoring.</subfield>
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   <subfield code="a">Springer Science+Business Media New York, 2013</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Cerebral ischemia</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Glucose metabolism</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Hyperglycolysis</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Neurologic outcome</subfield>
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   <subfield code="a">Subarachnoid hemorrhage</subfield>
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   <subfield code="a">Barcelos</subfield>
   <subfield code="D">Gleicy</subfield>
   <subfield code="u">BioRaN Team, Lyon Neuroscience Research Center, CNRS UMR 5292, INSERM U1028, University Lyon 1, Lyon, France</subfield>
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   <subfield code="a">Tholance</subfield>
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   <subfield code="u">Neurochemistry Unit, Department of Biochemistry, Neurological Hospital, Hospices Civils de Lyon, Lyon, France</subfield>
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   <subfield code="a">Grousson</subfield>
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   <subfield code="a">Renaud</subfield>
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   <subfield code="u">Neurochemistry Unit, Department of Biochemistry, Neurological Hospital, Hospices Civils de Lyon, Lyon, France</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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