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Published on: July 31, 2016
Pemoline-associated hepatic injury
Insights
Pemoline can cause liver injury, primarily in children and adolescents. The injury is hepatocellular and likely metabolic, not immunologic.
Area of Science:
- Hepatology
- Pharmacology
- Toxicology
Background:
- Pemoline, a stimulant medication, has been associated with adverse hepatic events.
- Understanding the risk factors and characteristics of pemoline-induced liver injury (APELI) is crucial for patient safety.
Observation:
- A review of 100 cases of hepatic injury linked to pemoline identified 43 suitable for analysis.
- The majority of affected patients were pediatric, with 80% under 12 years old and predominantly male.
- Liver injury onset varied widely, from one week to over a year after pemoline initiation.
Findings:
- The hepatic injury was consistently hepatocellular, indicated by elevated aminotransferase levels.
- One patient experienced fatal massive hepatic necrosis, confirming the severity of the injury.
- The mechanism of injury was deemed idiosyncratic, likely stemming from metabolic processes rather than an immunologic response.
Implications:
- This highlights the significant hepatotoxic potential of pemoline, particularly in pediatric populations.
- Clinicians should be aware of the risk of severe, idiosyncratic liver injury when prescribing pemoline.
- Further research into the metabolic pathways underlying pemoline hepatotoxicity may inform safer drug development.
Abstract:
Among 100 cases of hepatic injury attributed to the administration of pemoline, 43 had sufficient accompanying information to permit analysis. All but two patients were less than 20 years old, and 80% were less than 12 years old. Males predominated the study. Injury appeared as early as 1 week or as late as greater than 1 year of taking the drug. The injury was uniformly hepatocellular as judged by the high values for aminotransferases and by death in massive necrosis in one patient. Mechanism was judged to be idiosyncratic, and the idiosyncrasy was probably metabolic rather than immunologic.
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