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A A Case Rep ; 7(11): 243-246, 2016 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-27749294

RESUMEN

This case report describes a 71-year-old woman who experienced unusual delayed emergence from propofol, which lasted for 3 hours and resulted in admission to the intensive care unit. Because genetic variations of propofol-metabolizing enzymes are proposed to be causal factors, we explored genetic polymorphisms of cytochrome P450 2B6 (CYP2B6) and uridine 5'-diphospho-glucuronosyltransferase 1A9 (UGT1A9). Suggested high-risk factors (advanced age, CYP2B6 516 G/T, and UGT1A9 I399 C/C) were observed in this case of delayed propofol metabolism. Therefore, genetic variants involved in propofol metabolism should be considered in unexplained delayed emergence.


Asunto(s)
Anestésicos Intravenosos/farmacocinética , Citocromo P-450 CYP2B6/genética , Retraso en el Despertar Posanestésico/genética , Glucuronosiltransferasa/genética , Polimorfismo de Nucleótido Simple , Propofol/farmacocinética , Anciano , Anestésicos Intravenosos/sangre , ADN/sangre , ADN/genética , Retraso en el Despertar Posanestésico/enzimología , Femenino , Genotipo , Humanos , Propofol/sangre , UDP Glucuronosiltransferasa 1A9
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