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Propylene glycol-induced lactic acidosis in a child receiving a pentobarbital continuous infusion
Courtney J Chandler1, Christopher Cunnyngham2, Jamie Miller2,3
1Children's Medical Center, Dallas, TX, USA.
Insights
Pentobarbital, containing propylene glycol, can cause lactic acidosis and hypotension in children. Monitor osmolar gap and lactate levels during continuous infusions to prevent adverse events.
Area of Science:
- Pediatric Critical Care Medicine
- Clinical Pharmacology
- Neurology
Background:
- Pentobarbital (PB) is used for refractory seizures but contains propylene glycol (PG), a potential cause of lactic acidosis (LA).
- Previous reports of PG-induced LA exist, but not specifically in young children receiving PB continuous infusions (CI).
Observation:
- A 3-year-old male with refractory seizures received escalating doses of intravenous PB CI.
- The patient developed hypotension and elevated lactate levels (3.01 and 6.28 mmol/L) on hospital days 15 and 37, respectively.
- These events coincided with receiving PG doses exceeding the WHO recommended threshold.
Findings:
- The patient's clinical presentation and laboratory values, including elevated osmolar gap, strongly suggest PG-induced LA.
- The Naranjo probability scale indicated a high probability of a drug-related adverse event.
Implications:
- Clinicians should be aware of the risk of PG-induced LA and hypotension in pediatric patients on prolonged or high-dose PB CI.
- Routine monitoring of osmolar gap and lactate levels is recommended for early detection of this adverse event.
- This case highlights the importance of considering the PG content in medications when managing critically ill children.
Abstract:
Pentobarbital (PB) contains 40% propylene glycol (PG) and could result in lactic acidosis (LA). Previous reports have indicated PG-induced LA following PB continuous infusion (CI), but there are no reports in young children. A 3-year-old male was admitted for new-onset seizures. After failing conventional therapy, he was initiated on intravenous PB on hospital day (HD) 3. The seizures continued, and he was initiated on a PB CI on HD 5 to achieve burst suppression. His CI was titrated to 10 mg/kg/hr. On HD 15, he developed hypotension with a mean arterial pressure (MAP) in the 40's and venous lactate of 3.01 mmol/L (normal range: 0.4-2.0 mmol/L). He received epinephrine, and his PB was decreased to 8 mg/kg/hr. Over the next few weeks, he continued to have subclinical seizures and PB was increased to 10 mg/kg/hr. On HD 37, he developed hypotension with a lactate of 6.28 and osmolar gap of 20.4 mOsm/kg. He received a fluid bolus, sodium bicarbonate, and his PB was decreased to 5 mg/kg/hr. His PB was tapered off, and the decision was made to treat clinical seizures only. The World Health Organization recommends a maximum of 25 mg/kg of PG. On HD 15 and 37, our patient received more than this threshold, 1398 and 1604 mg/kg, respectively. The Naranjo probability scale supports a high-probable drug-related adverse event. Practitioners should be aware of this potential adverse event with medications containing PG. Routine monitoring of osmolar gap should be performed for patients with prolonged use or higher PB doses.
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