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Propofol-induced hyperamylasaemia in a general intensive care unit
S Nanas1, E Angelopoulos, S Tsikriki
1First Critical Care Department, Medical School, National and Kapodistrian University, Evangelismos Hospital, Athens, Greece. snanas@cc.uoa.gr
Anaesthesia and Intensive Care
|December 19, 2007
Summary
Propofol sedation in intensive care unit (ICU) patients is linked to a higher incidence of hyperamylasemia, a marker of pancreatic injury. Monitoring amylase levels in these patients is recommended.
Area of Science:
- Critical Care Medicine
- Pharmacology
- Biochemistry
Background:
- Hyperamylasemia, elevated serum amylase levels, can indicate pancreatic dysfunction.
- Propofol is a commonly used sedative in intensive care units (ICUs).
- The relationship between propofol administration and hyperamylasemia requires further investigation.
Purpose of the Study:
- To investigate the incidence of hyperamylasemia in intensive care unit patients receiving propofol.
- To determine if propofol infusion is associated with biochemical evidence of pancreatic injury.
- To assess the need for amylase level monitoring in propofol-sedated patients.
Main Methods:
- A study was conducted on 172 consecutive general ICU patients staying over 24 hours.
- Patients with pre-existing conditions causing elevated amylase or on medications affecting amylase levels were excluded.
- Thirty eligible patients received continuous propofol infusion for sedation; 14 served as a control group.
Main Results:
- Of 30 patients receiving propofol, 16 (53%) developed hyperamylasemia (125-466 IU/l) after 2-9 days.
- The incidence of hyperamylasemia in the propofol group was significantly higher than in the 14 control patients (14%, P = 0.021).
- Liver and kidney function remained normal in all observed patients.
Conclusions:
- Continuous propofol infusion in ICU patients is associated with biochemical evidence of pancreatic injury.
- Hyperamylasemia in propofol-treated patients appears to be a direct effect of the sedative.
- Monitoring of serum amylase levels is warranted in intensive care unit patients sedated with propofol.
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