Congenital Heart Defects Clinical Trial
Official title:
Effect of Sevoflurane Anesthesia in Postoperative Troponin I Levels in Children Undergoing Congenital Heart Defects Surgery: a Randomized Controlled Clinical Trial
The main purpose of this study is to compare myocardial injury of patients undergoing
congenital cardiac defects repair surgery (RACHS Risk Score one, two or three) under total
intravenous anesthesia compared to inhalation anesthesia with sevoflurane. The primary aim of
the study is to evaluate the troponin I levels in patients following congenital heart surgery
and elucidate if one of the two anesthetic techniques (TIVA x inhalation anesthesia) is more
effective in reducing troponin I levels in the first 72h after surgery..
Sixty six are planned to be included in the study and the follow-up will take approximately 3
days for the primary outcome.
As a secondary outcome evaluate the BNP, CPK and CKMB postoperative levels in the same period
(72h), also ICU and hospital lengh of stay (LOS), duration of mechanical ventilation,
inotropic/vasoactive drugs use and incidence of renal injury (according to pediatric RIFLE
score).
n/a
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