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• W2033701812 abstract "Critically ill patients are sedated with intravenous agents because the use of inhaled agents is limited by their potential risk of toxicity. Increasing levels of inorganic fluorides after the metabolism of these agents have been considered potentially nephrotoxic. However, hepatic involvement after prolonged administration of sevoflurane has not yet been studied. The present study evaluated the potential renal and hepatic toxicity caused by prolonged administration (72h) of sevoflurane.For this experimental, prospective, randomized, controlled trial, 22 Landrace x Large-White female pigs were randomly assigned to two groups: intravenous propofol (P) or inhaled sevoflurane via the AnaConDa™ device (S, end-tidal 2.5 vol%). The P group remained sedated for 108h with propofol. In the S group, sevoflurane was administered for 72h and then changed to propofol for the remaining 36h in order to observe the kinetics of fluoride after discontinuation of sevoflurane. Serum creatinine was the primary outcome variable, but inorganic fluoride concentrations and other renal, hepatic, and cardiorespiratory variables were also measured.Both groups of animals were comparable at baseline. No differences were found between the two groups for plasma creatinine and urea or creatinine clearance throughout the study. Fluoride levels were significantly higher in the sevoflurane group. No correlation was found between inorganic fluoride and serum creatinine values. No significant differences were observed for hepatic function. Hemodynamic, respiratory, and blood gas variables were comparable between the groups.Long-term sedation with sevoflurane using AnaConDa™ or propofol does not negatively affect renal or hepatic function." @default.
• W2033701812 created "2016-06-24" @default.
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• W2033701812 date "2015-04-01" @default.
• W2033701812 modified "2023-10-16" @default.
• W2033701812 title "Integridad renal y hepática tras la sedación prolongada con sevoflurano administrado a través del dispositivo AnaConDa®: comparación con la sedación intravenosa con propofol en modelo animal" @default.
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• W2033701812 doi "https://doi.org/10.1016/j.redar.2014.05.009" @default.
• W2033701812 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25146774" @default.
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