Serum S100B Protein Could Help to Detect Cerebral Complications Associated with Extracorporeal Membrane Oxygenation (ECMO)
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  • 作者:Duc Nam Nguyen (1)
    Luc Huyghens (1)
    Francis Wellens (2)
    Johan Schiettecatte (3)
    Johan Smitz (3)
    Jean-Louis Vincent (4)
  • 关键词:ECMO ; S100B protein ; Cerebral complications
  • 刊名:Neurocritical Care
  • 出版年:2014
  • 出版时间:June 2014
  • 年:2014
  • 卷:20
  • 期:3
  • 页码:367-374
  • 全文大小:
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  • 作者单位:Duc Nam Nguyen (1)
    Luc Huyghens (1)
    Francis Wellens (2)
    Johan Schiettecatte (3)
    Johan Smitz (3)
    Jean-Louis Vincent (4)

    1. Department of Critical Care, University Hospital of Brussels, Laarbeeklaan 101, 1090, Brussels, Belgium
    2. Department of Cardiac Surgery, University Hospital of Brussels, Brussels, Belgium
    3. Department of Radioimmunochemistry, University Hospital of Brussels, Brussels, Belgium
    4. Department of Intensive Care, Erasme University Hospital, Brussels, Belgium
  • ISSN:1556-0961
文摘
Background To investigate if serum S100B protein levels could early detect cerebral complications under treatment extracorporeal membrane oxygenation (ECMO). Methods Serum S100B levels were measured over 5?days in 32 patients with cardiogenic and septic shock, including 15 patients who treated by ECMO and 17 who did not. Cerebral complications included hemorrhage, stroke, encephalopathy with myoclonus, and brain death. Delirium was identified by the positive Confusion Assessment Method in the ICU. Results S100B levels were elevated in 24/32 patients (75?%) at ICU admission. Five patients developed cerebral complications (2 hemorrhages with 1 brain death, 1 encephalopathy with myoclonus in the ECMO group and 2 strokes in the non-ECMO group). At day 5, S100B levels were higher in the 5 patients with cerebral complications than in the 27 without cerebral complications, regardless of ECMO (0.426 [0.421, 0.652] vs. 0.102 [0.085, 0.135] μg/L, p?=?0.011). S100B levels were also more elevated in 3 patients with than in 12 without cerebral complications associated with ECMO (0.799 [0.325, 0.965] vs. 0.102 [0.09, 0.607] μg/L, p?=?0.033). S100B levels were not associated with delirium after sedation withdrawal. Conclusions Measurement serum S100B could be useful to detect cerebral complications in deeply sedated patients associated with ECMO but not for monitoring delirium after sedation withdrawal.

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