TY - JOUR
T1 - Serum S-100 β protein during coronary artery bypass graft surgery with or without cardiopulmonary bypass
AU - Wang, Kuan Jen
AU - Wu, Hsiang Hua
AU - Fang, Shih Yuan
AU - Yang, Yu Ren
AU - Tseng, A. Chia Chih
PY - 2005/10
Y1 - 2005/10
N2 - Background. Brain damage is a serious complication of cardiac anesthesia. The purpose of this study was to detect brain damage at different surgical stages during coronary artery bypass graft with or without cardiopulmonary bypass. Methods. We conducted a prospective, longitudinal study to evaluate serum S-100 β protein, an early marker of brain injury, in patients electively undergoing off-pump (n = 30) or traditional coronary artery bypass graft (n = 60). Blood was sampled immediately before anesthesia, before and after cardiopulmonary bypass, and on the day after surgery. Results. Serum S-100 β protein was lowest immediately before induction of anesthesia and significantly increased before and after cardiopulmonary bypass, then declined by the first postoperative day in both groups. Peak values were highest in the traditional group directly after coronary artery bypass graft. On the day after surgery, S-100 β protein levels were similar between groups, but were higher than baseline within each group. Significant increase in serum S-100 β protein was also observed even before cardiopulmonary bypass in cardiopulmonary bypass patients, or before manipulation of the heart and aorta in off-pump patients. These reflect the possibility that brain damage may occur before major manipulation (cardiopulmonary bypass or manipulating heart and aorta). Moreover, S-100 β levels did not return to normal on the day after the operation. Conclusions. This prospective study has shown that serum S-100 β protein was not only higher than baseline both after cardiopulmonary bypass and on the day after surgery in both groups of patients but it was also significantly increased before cardiopulmonary bypass or manipulation of the heart or aorta. These findings may have implications for anesthesiologic care during the total course of cardiac surgery.
AB - Background. Brain damage is a serious complication of cardiac anesthesia. The purpose of this study was to detect brain damage at different surgical stages during coronary artery bypass graft with or without cardiopulmonary bypass. Methods. We conducted a prospective, longitudinal study to evaluate serum S-100 β protein, an early marker of brain injury, in patients electively undergoing off-pump (n = 30) or traditional coronary artery bypass graft (n = 60). Blood was sampled immediately before anesthesia, before and after cardiopulmonary bypass, and on the day after surgery. Results. Serum S-100 β protein was lowest immediately before induction of anesthesia and significantly increased before and after cardiopulmonary bypass, then declined by the first postoperative day in both groups. Peak values were highest in the traditional group directly after coronary artery bypass graft. On the day after surgery, S-100 β protein levels were similar between groups, but were higher than baseline within each group. Significant increase in serum S-100 β protein was also observed even before cardiopulmonary bypass in cardiopulmonary bypass patients, or before manipulation of the heart and aorta in off-pump patients. These reflect the possibility that brain damage may occur before major manipulation (cardiopulmonary bypass or manipulating heart and aorta). Moreover, S-100 β levels did not return to normal on the day after the operation. Conclusions. This prospective study has shown that serum S-100 β protein was not only higher than baseline both after cardiopulmonary bypass and on the day after surgery in both groups of patients but it was also significantly increased before cardiopulmonary bypass or manipulation of the heart or aorta. These findings may have implications for anesthesiologic care during the total course of cardiac surgery.
UR - http://www.scopus.com/inward/record.url?scp=25144464457&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=25144464457&partnerID=8YFLogxK
U2 - 10.1016/j.athoracsur.2005.04.011
DO - 10.1016/j.athoracsur.2005.04.011
M3 - Article
C2 - 16181873
AN - SCOPUS:25144464457
SN - 0003-4975
VL - 80
SP - 1371
EP - 1374
JO - Annals of Thoracic Surgery
JF - Annals of Thoracic Surgery
IS - 4
ER -