Key result
Hyperoxic reoxygenation on CPB in cyanotic infants linked to ~4-fold higher postoperative S100 levels.
Why the study?
Systemic reoxygenation injury from initiating cardiopulmonary bypass in infants with cyanotic heart disease may cause cerebral dysfunction and injury, which can be quantified by serum protein S100 levels. This study assessed protein S100 in cyanotic patients undergoing cardiopulmonary bypass with normoxic versus hyperoxic paO2, in acyanotic cases, and in controls without cardiopulmonary bypass.
Observational (n=43)
Answers are grounded in this paper and cite their sources.
S100 assessment during CPB in cyanotic infants is hypothesis-generating; larger prospective studies needed before clinical adoption.
BACKGROUND: The systemic reoxygenation injury produced by initiating cardiopulmonary bypass (CPB) in infants with cyanotic heart disease may be associated with cerebral dysfunction and injury. Increased protein S100 (S100) serum levels may indicate cerebral and blood brain barrier damage as well as inflammatory changes, therefore serving to quantify these changes. The present clinical study assessed S100 in cyanotic patients undergoing CPB with normoxic versus hyperoxic paO2 in acyanotic cases and in controls without CPB. METHODS: 43 patients with congenital heart disease aged 5 days to 15 years (mean 4.4 years) were enrolled consecutively and divided in four groups: (1) Cyanotic infants undergoing controlled normoxic reoxygenation on CPB (n = 12), (2) cyanotic infants undergoing uncontrolled hyperoxic reoxygenation on CPB (n = 9), (3) acyanotic infants operated with CPB (n = 16) and (4) patients operated without CPB (n = 6). Blood samples were collected after induction of anesthesia (A), up to 4 hours after surgery (B) and at postoperative day one (C). RESULTS: Preoperative S100 serum levels [microg/l] in all groups were below clinical relevance. S100 increased markedly after surgery in groups 1 and 2. Differences in postoperative S100 levels were significant between groups 1 (0.45 +/- 0.13) and 3 (0.35 +/- 0.09; p = 0.018), between groups 2 (1.41 +/- 0.47) and 3 (p = 0.01), and between groups 2 and 4 (0.29 +/- 0.09; p = 0.045). There were no significant differences in postoperative S100 levels (B) between groups 1 and 2 (p = 0.05), groups 1 and 4 (p = 0.05), or groups 3 and 4 (p = 0.93). CONCLUSION: Uncontrolled hyperoxic reoxygenation on CPB for surgical correction of congenital heart defects is associated with higher S100 levels in cyanotic infants as compared to acyanotic patients undergoing comparable operations.
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Matheis et al. (2000) conducted an observational in Congenital heart disease (n=43). Uncontrolled hyperoxic reoxygenation on cardiopulmonary bypass in cyanotic infants vs. Controlled normoxic reoxygenation on CPB in cyanotic infants, acyanotic infants operated with CPB, and patients operated without CPB was evaluated on Postoperative serum protein S100 levels (microg/l) (p=0.01). Uncontrolled hyperoxic reoxygenation on CPB in cyanotic infants was associated with higher postoperative S100 levels than in acyanotic CPB patients.
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