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   <subfield code="a">10.1007/s12028-013-9867-5</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/s12028-013-9867-5</subfield>
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   <subfield code="a">Serum Neuron-Specific Enolase Levels from the Same Patients Differ Between Laboratories: Assessment of a Prospective Post-cardiac Arrest Cohort</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Michael Mlynash, Marion Buckwalter, Ami Okada, Anna Caulfield, Chitra Venkatasubramanian, Irina Eyngorn, Marcel Verbeek, Christine Wijman]</subfield>
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   <subfield code="a">Background: In comatose post-cardiac arrest patients, a serum neuron-specific enolase (NSE) level of &gt;33μg/L within 72h was identified as a reliable marker for poor outcome in a large Dutch study (PROPAC), and this level was subsequently adopted in an American Academy of Neurology practice parameter. Later studies reported that NSE &gt;33μg/L is not a reliable predictor of poor prognosis. To test whether different clinical laboratories contribute to this variability, we compared NSE levels from the laboratory used in the PROPAC study (DLM-Nijmegen) with those of our hospital's laboratory (ARUP) using paired blood samples. Methods: We prospectively enrolled cardiac arrest patients who remained comatose after resuscitation. During the first 3days, paired blood samples for serum NSE were drawn at a median of 10min apart. After standard preparation for each lab, one sample was sent to ARUP laboratories and the other to DLM-Nijmegen. Results: Fifty-four paired serum samples from 33 patients were included. Although the serum NSE measurements correlated well between laboratories (R=0.91), the results from ARUP were approximately 30% lower than those from DLM-Nijmegen. Therapeutic hypothermia did not affect this relationship. Two patients had favorable outcomes after hypothermia despite NSE levels measured by DLM-Nijmegen as &gt;33μg/L. Conclusions: Absolute serum NSE levels of comatose cardiac arrest patients differ between laboratories. Any specific absolute cut-off levels proposed to prognosticate poor outcome should not be used without detailed data on how neurologic outcomes correspond to a particular laboratory's method, and even then only in conjunction with other prognostic variables.</subfield>
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   <subfield code="a">Springer Science+Business Media New York, 2013</subfield>
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   <subfield code="a">Cardiac arrest</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Coma</subfield>
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   <subfield code="a">Neuron-specific enolase</subfield>
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   <subfield code="a">Prognosis</subfield>
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   <subfield code="a">Agreement between clinical measurements</subfield>
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   <subfield code="u">Stanford Neurocritical Care Program, Stanford Stroke Center, Department of Neurology and Neurological Sciences, Stanford University Medical Center, Stanford, CA, USA</subfield>
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