A case of propofol toxicity: further evidence for a causal mechanism
Davinia E Withington1, Mary K Decell, Tareq Al Ayed
1Department of Anaesthesia, Montreal Children's Hospital, Montreal, Quebec, Canada. davinia.withington@mcgill.ca
Insights
A 5-month-old boy experienced severe organ failure after propofol sedation for cleft lip repair. Early diagnosis of acylcarnitine metabolism abnormality and charcoal hemoperfusion improved his condition.
Area of Science:
- Pediatric Anesthesiology
- Metabolic Disorders
- Critical Care Medicine
Background:
- Propofol is a common anesthetic agent used in pediatric procedures.
- Cleft lip repair is a routine surgical intervention in infants.
- Metabolic disorders can present with severe complications during anesthesia.
Observation:
- A 5-month-old boy developed metabolic acidosis, cardiac dysrhythmias, and hepatic/renal failure post-propofol sedation.
- Escalating doses of propofol and fentanyl were required during the 48-hour post-operative period.
- Symptoms gradually resolved after propofol discontinuation and charcoal hemoperfusion.
Findings:
- The infant's condition improved significantly with charcoal hemoperfusion.
- Investigations revealed an underlying acylcarnitine metabolism abnormality.
- This metabolic abnormality is similar to a previously reported case.
Implications:
- This case highlights the potential risk of propofol in infants with undiagnosed metabolic disorders.
- Acylcarnitine metabolism abnormalities may predispose infants to propofol-induced toxicity.
- Early recognition and intervention, including charcoal hemoperfusion, can be life-saving.
Abstract:
A 5-month-old boy required sedation after a cleft lip repair. He was sedated with propofol and intermittent fentanyl, requiring escalating doses over the subsequent 48 h. On the second post-operative day he developed a metabolic acidosis followed by multiple cardiac dysrhythmias, hepatic and renal failure. Propofol was stopped. His multisystem organ failure gradually resolved after initiation of charcoal haemoperfusion. Further investigation demonstrated an abnormality in acylcarnitine metabolism, similar to that found in one previous case report.
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