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Published on: December 6, 2016
Propofol infusion syndrome in a super morbidly obese patient (BMI = 75)
Ramesh Ramaiah1, Loreto Lollo, Douglas Brannan
1Department of Anesthesiology and Pain Medicine, Harborview Medical Center, University of Washington School of Medicine, Seattle, WA, USA.
Insights
Propofol infusion syndrome (PRIS) is a rare, fatal complication of prolonged, high-dose propofol. A supermorbidly obese patient developed PRIS when propofol was dosed by total body weight, highlighting a critical dosing error.
Area of Science:
- Anesthesiology
- Intensive Care Medicine
- Clinical Pharmacology
Background:
- Propofol infusion syndrome (PRIS) is a rare but serious complication associated with prolonged, high-dose propofol administration.
- Risk factors include young age, critical illness, and certain metabolic conditions.
- PRIS presents with metabolic acidosis, rhabdomyolysis, renal and myocardial failure, and bradycardia.
Observation:
- PRIS is typically seen with doses of 4-5 mg/kg/hr for over 48 hours.
- Pathophysiology involves direct mitochondrial respiratory chain inhibition or impaired fatty acid metabolism.
- A supermorbidly obese patient developed PRIS.
Findings:
- The patient received propofol based on total body weight, not ideal or actual body weight.
- This dosing error likely contributed to the excessive propofol exposure leading to PRIS.
- This case underscores the importance of accurate weight-based dosing in obese patients.
Implications:
- Accurate weight-based dosing of propofol is crucial, especially in supermorbidly obese patients.
- Clinicians should be vigilant for PRIS in high-risk patients and with potential dosing errors.
- This case highlights the need for revised dosing protocols for propofol in extreme obesity.
Abstract:
Propofol infusion syndrome (PRIS) is a rare but often fatal complication as a result of large doses of propofol infusion (4-5 mg/kg/hr) for a prolonged period (>48 h). It has been reported in both children and adults. Besides large doses of propofol infusion, the risk factors include young age, acute neurological injury, low carbohydrate and high fat intake, exogenous administration of corticosteroid and catecholamine, critical illness, and inborn errors of mitochondrial fatty acid oxidation. PRIS manifestation include presence of metabolic acidosis with a base deficit of more than 10 mmol/l at least on one occasion, rhabdomyolysis or myoglobinuria, acute renal failure, sudden onset of bradycardia resistant to treatment, myocardial failure, and lipemic plasma. The pathophysiology of PRIS may be either direct mitochondrial respiratory chain inhibition or impaired mitochondrial fatty acid metabolism mediated by propofol. We report a case of supermorbidly obese patient who received propofol infusion by total body weight instead of actual body weight and developed PRIS.
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