Is there a relationship between serum S-100beta protein and neuropsychologic dysfunction after cardiopulmonary bypass?

Over the past decade, the glial protein S-100beta has been used to detect cerebral injury in a number of clinical settings including cardiac surgery. Previous investigations suggest that S-100beta is capable of identifying patients with cerebral dysfunction after cardiopulmonary bypass. Whether dete...

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Veröffentlicht in:The Journal of thoracic and cardiovascular surgery 2000-01, Vol.119 (1), p.132-137
Hauptverfasser: Westaby, S, Saatvedt, K, White, S, Katsumata, T, van Oeveren, W, Bhatnagar, N K, Brown, S, Halligan, P W
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Sprache:eng
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Zusammenfassung:Over the past decade, the glial protein S-100beta has been used to detect cerebral injury in a number of clinical settings including cardiac surgery. Previous investigations suggest that S-100beta is capable of identifying patients with cerebral dysfunction after cardiopulmonary bypass. Whether detection of elevated levels S-100beta reflects long-term cognitive impairment remains to be shown. The present study evaluated whether perioperative release of S-100beta after coronary artery operations with cardiopulmonary bypass could predict early or late neuropsychologic impairment. A total of 100 patients undergoing elective coronary bypass without a previous history of neurologic events were prospectively studied. To exclude noncerebral sources of S-100beta, we did not use cardiotomy suction or retransfusion of shed mediastinal blood. Serial perioperative measurements of S-100beta were performed with the use of a new sensitive immunoluminometric assay up to 8 hours after the operation. Patients underwent cognitive testing on a battery of 11 tests before the operation, before discharge from the hospital, and 3 months later. No significant correlation was found between S-100beta release and neuropsychologic measures either 5 days or 3 months after the operation. Despite using a sensitive immunoluminometric assay of S-100beta, we found no evidence to support the suggestion that early release of S-100beta may reflect long-term neurologic injury capable of producing cognitive impairment.
ISSN:0022-5223