TY - JOUR
T1 - Dexamethasone reduces postoperative troponin levels in children undergoing cardiopulmonary bypass
AU - Checchia, Paul A.
AU - Backer, Carl L.
AU - Bronicki, Ronald A.
AU - Baden, Harris P.
AU - Crawford, Susan E.
AU - Green, Thomas P.
AU - Mavroudis, Constantine
PY - 2003/6/1
Y1 - 2003/6/1
N2 - Objective: We previously demonstrated that dexamethasone treatment before cardiopulmonary bypass in children reduces the postoperative systemic inflammatory response. The purpose of this study was to test the hypothesis that dexamethasone administration before cardiopulmonary bypass in children correlates with a lesser degree of myocardial injury as measured by a decrease in cardiac troponin I release. Design: A prospective, randomized, double-blind study. Setting: The cardiac surgery operating room and intensive care unit of a pediatric referral hospital. Subjects: Twenty-eight patients who underwent open-heart surgery for congenital heart defects. Interventions: Patients received either placebo (group I, n = 13) or dexamethasone, 1 mg/kg iv (group II, n = 15), 1 hr before initiation of cardiopulmonary bypass. Plasma cardiac troponin I samples were obtained at three time points: immediately before study agent (sample 1), 10 mins after protamine sulfate administration after cardiopulmonary bypass (sample 2), and 24 hrs postoperatively (sample 3). Measurements and Main Results: Mean cardiac troponin I levels (±SD) were significantly lower at sample time 3 in group II (dexamethasone; 33.4 ± 20.0 ng/mL) vs. group I (control; 86.9 ± 81.1) (p = .04). Conclusion: Dexamethasone administration before cardiopulmonary bypass in children resulted in a significant decrease in cardiac troponin I levels at 24 hrs postoperatively. We postulate that this may represent a decrease in myocardial injury, and, thus, a possible cardioprotective effect produced by dexamethasone.
AB - Objective: We previously demonstrated that dexamethasone treatment before cardiopulmonary bypass in children reduces the postoperative systemic inflammatory response. The purpose of this study was to test the hypothesis that dexamethasone administration before cardiopulmonary bypass in children correlates with a lesser degree of myocardial injury as measured by a decrease in cardiac troponin I release. Design: A prospective, randomized, double-blind study. Setting: The cardiac surgery operating room and intensive care unit of a pediatric referral hospital. Subjects: Twenty-eight patients who underwent open-heart surgery for congenital heart defects. Interventions: Patients received either placebo (group I, n = 13) or dexamethasone, 1 mg/kg iv (group II, n = 15), 1 hr before initiation of cardiopulmonary bypass. Plasma cardiac troponin I samples were obtained at three time points: immediately before study agent (sample 1), 10 mins after protamine sulfate administration after cardiopulmonary bypass (sample 2), and 24 hrs postoperatively (sample 3). Measurements and Main Results: Mean cardiac troponin I levels (±SD) were significantly lower at sample time 3 in group II (dexamethasone; 33.4 ± 20.0 ng/mL) vs. group I (control; 86.9 ± 81.1) (p = .04). Conclusion: Dexamethasone administration before cardiopulmonary bypass in children resulted in a significant decrease in cardiac troponin I levels at 24 hrs postoperatively. We postulate that this may represent a decrease in myocardial injury, and, thus, a possible cardioprotective effect produced by dexamethasone.
KW - Cardiopulmonary bypass
KW - Dexamethasone
KW - Postcardiopulmonary bypass inflammatory response
KW - Troponin
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U2 - 10.1097/01.CCM.0000063443.32874.60
DO - 10.1097/01.CCM.0000063443.32874.60
M3 - Article
C2 - 12794414
AN - SCOPUS:0038724162
SN - 0090-3493
VL - 31
SP - 1742
EP - 1745
JO - Critical care medicine
JF - Critical care medicine
IS - 6
ER -