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J Neurol Neurosurg Psychiatry 1998;65:930-932 doi:10.1136/jnnp.65.6.930
  • Short report

Jugular venous and arterial concentrations of serum S-100B protein in patients with severe head injury: a pilot study

  1. Andreas Raabea,
  2. David K Menonb,
  3. Sanjeeva Guptab,
  4. Marek Czosnykaa,
  5. John D Pickarda
  1. aDepartment of Neurosurgery, bDepartment of Anaesthesia, Addenbrookes Hospital, University of Cambridge, England
  1. Dr Andreas Raabe, Department of Neurosurgery, University of Leipzig, Johannisallee 34, 04103 Leipzig, Germany. Telephone 0049 341 9712000; fax 0049 341 9712009; emailaraa{at}server3.medizin.uni-leipzig.de
  • Received 16 January 1998
  • Revised 22 May 1998
  • Accepted 15 June 1998

Abstract

The objective of this study was to analyse the temporal course of the jugular venous-arterial gradient of S-100B protein after severe head injury and the correlation between the absolute concentrations of serum S-100B protein and outcome, CT findings, and clinical variables.

 Fifteen patients were included in this pilot study. All patients were treated according to a standard therapy protocol targeted to maintain cerebral perfusion pressure. The serum concentration of S-100 protein was measured daily for five consecutive days after injury by a monoclonal two site immunoluminometric assay. Nine patients showed favourable and six unfavourable outcome after 6 months with a mortality rate of 33% (five patients). The mean gradient between jugular venous and arterial blood was 8.2% (p<0.05). Patients showing an unfavourable outcome had significantly higher jugular venous or arterial S-100 values compared with those with a favourable outcome (jugular venous S-100B 2.78 μg/l v 1.22 μg/l, p<0.05; arterial S-100B 2.48 μg/l v 1.19 μg/l, p<0.05). All patients with an initial or secondary increase in S-100B value of >2 μg/l were found to have an unfavourable outcome. S-100B was found to be an independent predictor of outcome after severe head injury. The persisting increase of S-100B for three to five days even in patients with favourable outcome and no signs of secondary insults might reflect continuing damage to the blood-brain barrier or ongoing glial cell death.

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