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Published on: November 9, 2016
Propylene Glycol-Related Delirium After Esmolol Infusion
Berber Kapitein1, Renee C G Biesmans2, Heleen van der Sijs2
1Erasmus MC-Sophia Children's Hospital, Rotterdam, Netherlands b.kapitein@erasmusmc.nl.
Insights
Intravenous esmolol can cause delirium due to toxic levels of propylene glycol, an excipient. Discontinuation of the drug resolved the patient's symptoms, highlighting the importance of physician education on excipient toxicity.
Area of Science:
- Pharmacology
- Toxicology
- Intensive Care Medicine
Background:
- Excipients in intravenous medications can lead to serious adverse events.
- Propylene glycol accumulation from prolonged infusions can cause toxicity.
Purpose of the Study:
- To report a case of delirium in a pediatric patient secondary to propylene glycol toxicity from intravenous esmolol.
- To assess the causal relationship between esmolol excipients and the adverse event.
Main Methods:
- A 15-year-old boy with hypertrophic cardiomyopathy received continuous intravenous esmolol.
- Delirium developed and was assessed for causality using the Naranjo scale.
- Propylene glycol plasma concentration was measured.
Main Results:
- The patient developed delirium unresponsive to standard treatments.
- High plasma concentration of propylene glycol (4 g/L) was detected.
- A probable relationship (Naranjo score 6) was established between propylene glycol infusion and delirium.
- Delirium resolved spontaneously after esmolol discontinuation.
Conclusions:
- This is the first case linking esmolol excipient toxicity to delirium.
- Physician education on excipient toxicity and readily available information are crucial.
Objective:
Excipients used in oral or intravenous preparations may cause serious adverse events.
Case Summary:
We present the case of a 15-year-old boy with hypertrophic cardiomyopathy. In the pediatric intensive care unit, he received high doses of continuous intravenous esmolol (range = 20-400 µg/kg/min) for cardiac rhythm control. After a few days he developed a delirium not responding to high doses of antipsychotics or discontinuation of benzodiazepines. We eventually realized that the IV esmolol formulation contained high doses of propylene glycol and ethanol, which may accumulate after prolonged infusion and cause intoxication. Intoxication with propylene glycolcan cause neuropsychiatric symptoms. The boy's propylene glycol plasma concentration was approximately 4 g/L, whereas clinical symptoms arise at concentrations above 1 to 1.44 g/L. Application of the Naranjo adverse drug reaction probability scale suggested a probable relationship (score 6) between the propylene glycol infusion and the delirium. After discontinuation of esmolol, the delirium disappeared spontaneously.
Discussion:
This is the first case describing excipient toxicity of esmolol, with an objective causality assessment revealing a probable relationship for the adverse event-namely, delirium-and esmolol.
Conclusion:
Although excipient toxicity is a well-known adverse drug reaction, this case stresses the importance for easily available information for and education of physicians.
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