OBJECTIVE: The main objective of this study was to evaluate the effect of switching from parenteral to enteral feeding on liver blood flow and propofol steady-state blood concentrations in patients in the intensive care unit (ICU). DESIGN AND PATIENTS: Steady-state blood concentrations of propofol were measured in eight ICU patients before (on days D -3, D -2, and D -1) and after (on days D + 1, D + 2, and D + 3) switching from parenteral to enteral feeding (on day DO). All patients received a continuous intravenous infusion of propofol (4.5 mg x kg(-1) x h(-1)) from several days before the start of the study, continuing throughout the experimental period. Hepatic blood flow was estimated by measuring steady-state D-sorbitol hepatic clearan...
Background. About 98 % of plasma propofol is bound to albumin. We investigated if severe hypoalbumin...
ABSTRACT: Propofol is a lipid-based sedative that pro-vides 1.1 kcal/mL. Because propofol has rapid ...
Background: Conventional compartmental pharmacokinetic models wrongly assume instantaneous drug mixi...
Objective To investigate the effect of cardiac output and liver blood flow on propofol concentration...
We have compared the pharmacokinetics of propofol as an infusion in 10 control and 10 patients with ...
Propofol is a rapidly acting general anesthetic which is widely used as an intravenous agent for bot...
The disposition of the intravenous anesthetic propofol was studied when administered as a constant r...
We have investigated extrahepatic metabolism of propofol in 10 patients undergoing orthotopic liver ...
The amount of lipid delivered to patients varies considerably depending on the non-nutritional intak...
OBJECTIVE: Results from clinical pharmacokinetic studies of propofol indicate that this i.v. anaesth...
As oversedation is still common and significant variability between and within critically ill patien...
Background Maintaining adequate perioperative hepatic blood flow (HBF) supply is essential for pres...
Propofol, a commonly used sedative in the intensive care unit, is formulated in a 10% lipid emulsion...
Background: The aim of this study was to prospectively evaluate and report the experience of the use...
Objective: To investigate the concentrations of triglyceride, cholesterol, and high-density lipoprot...
Background. About 98 % of plasma propofol is bound to albumin. We investigated if severe hypoalbumin...
ABSTRACT: Propofol is a lipid-based sedative that pro-vides 1.1 kcal/mL. Because propofol has rapid ...
Background: Conventional compartmental pharmacokinetic models wrongly assume instantaneous drug mixi...
Objective To investigate the effect of cardiac output and liver blood flow on propofol concentration...
We have compared the pharmacokinetics of propofol as an infusion in 10 control and 10 patients with ...
Propofol is a rapidly acting general anesthetic which is widely used as an intravenous agent for bot...
The disposition of the intravenous anesthetic propofol was studied when administered as a constant r...
We have investigated extrahepatic metabolism of propofol in 10 patients undergoing orthotopic liver ...
The amount of lipid delivered to patients varies considerably depending on the non-nutritional intak...
OBJECTIVE: Results from clinical pharmacokinetic studies of propofol indicate that this i.v. anaesth...
As oversedation is still common and significant variability between and within critically ill patien...
Background Maintaining adequate perioperative hepatic blood flow (HBF) supply is essential for pres...
Propofol, a commonly used sedative in the intensive care unit, is formulated in a 10% lipid emulsion...
Background: The aim of this study was to prospectively evaluate and report the experience of the use...
Objective: To investigate the concentrations of triglyceride, cholesterol, and high-density lipoprot...
Background. About 98 % of plasma propofol is bound to albumin. We investigated if severe hypoalbumin...
ABSTRACT: Propofol is a lipid-based sedative that pro-vides 1.1 kcal/mL. Because propofol has rapid ...
Background: Conventional compartmental pharmacokinetic models wrongly assume instantaneous drug mixi...