• Title of article

    Time course of cranial ultrasound abnormalities after arterial switch operation in neonates

  • Author/Authors

    Matthias Sigler، نويسنده , , Jaime F. Vazquez-Jimenez، نويسنده , , Ralph G. Grabitz، نويسنده , , Hedwig H. H?vels-Gürich، نويسنده , , Bruno J. Messmer، نويسنده , , G?tz von Bernuth، نويسنده , , Marie-Christine Seghaye، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2001
  • Pages
    4
  • From page
    877
  • To page
    880
  • Abstract
    Background. The object of this study was to investigate the time course and fate of abnormal findings in cranial ultrasound after performing an arterial switch operation in neonates with transposition of the great arteries, and to analyze the relationship to cerebral cell damage. Methods. Cranial ultrasound was performed prospectively in 35 neonates with transposition of the great arteries before the operation as well as 4 hours, 1, 2, and 3 days, and 1 and 2 weeks postoperatively. Blood levels of neuron-specific enolase, a marker of cerebral cell damage, were determined before, during, and 4 and 24 hours postoperatively. Results. In 17 of 35 neonates (49%), early postoperative cranial ultrasound revealed abnormalities indistinguishable from intraventricular hemorrhage. In 11 neonates findings were transient and were normalized 2 weeks postoperatively, whereas in the remaining 6 neonates there was evidence of resolving hemorrhage. In all neonates there was a rise in neuron-specific enolase blood concentrations during and 4 hours after extracorporal circulation without correlation to sonographic findings. Conclusions. Enhanced echogenicity of the choroid plexus or dilatation of the cerebral ventricular system is a frequent early postoperative finding that may be caused by transient plexus edema rather than intraventricular hemorrhage and is not related to cerebral cell damage.
  • Journal title
    The Annals of Thoracic Surgery
  • Serial Year
    2001
  • Journal title
    The Annals of Thoracic Surgery
  • Record number

    604305