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

Citation
A. Raabe et al., Jugular venous and arterial concentrations of serum S-100B protein in patients with severe head injury: a pilot study, J NE NE PSY, 65(6), 1998, pp. 930-932
Citations number
14
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
ISSN journal
00223050 → ACNP
Volume
65
Issue
6
Year of publication
1998
Pages
930 - 932
Database
ISI
SICI code
0022-3050(199812)65:6<930:JVAACO>2.0.ZU;2-F
Abstract
The objective of this study was to analyse the temporal course of the jugul ar 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 treat ed according to a standard therapy protocol targeted to maintain cerebral p erfusion pressure. The serum concentration of S-100 protein was measured da ily for five consecutive days after injury by a monoclonal two site immunol uminometric assay. Nine patients showed favourable and six unfavourable out come 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). Patie nts showing an unfavourable outcome had significantly higher jugular venous or arterial S-100 values compared with those with a favourable outcome (ju gular venous S-100B 2.78 mu g/l v 1.22 mu g/l, p<0.05; arterial S-100B 2.48 mu g/l v 1.19 mu g/l, p<0.05). All patients with an initial or secondary i ncrease in S-100B value of >2 mu g/l were found to have an unfavourable out come. S-100B was found to be an independent predictor of outcome after seve re head injury. The persisting increase of S-100B for three to five days ev en in patients with favourable outcome and no signs of secondary insults mi ght reflect continuing damage to the blood-brain barrier or ongoing glial c ell death.