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Clonidine transdermal patch poisoning
1Division of Emergency Medicine, University of Utah School of Medicine, Salt Lake City.
Insights
An infant experienced severe hypotension after exposure to a discarded adult clonidine transdermal patch. Dopamine infusion was necessary to stabilize the infant, highlighting risks associated with transdermal medication disposal.
Area of Science:
- Toxicology
- Pharmacology
- Pediatrics
Background:
- Clonidine is an antihypertensive medication often delivered via transdermal patches.
- Transdermal systems offer continuous drug delivery but pose risks if not properly managed.
- Accidental exposure, particularly in children, can lead to significant toxicity.
Observation:
- A case report details an infant's exposure to a clonidine transdermal patch previously worn by an adult for five days.
- The infant presented with severe hypotension, indicated by a systolic blood pressure of 38 mm Hg.
- Management required a six-hour dopamine infusion to maintain adequate blood pressure.
Findings:
- Infant clonidine poisoning occurred due to contact with a discarded transdermal patch.
- Severe bradycardia and hypotension are key clinical manifestations of clonidine toxicity in infants.
- Transdermal delivery systems can retain significant amounts of active drug even after prolonged use.
Implications:
- This case underscores the critical importance of safe disposal practices for transdermal medications.
- Healthcare providers should counsel patients on the risks of accidental exposure and proper patch disposal.
- Enhanced poison prevention strategies are needed to mitigate risks associated with potent medications in transdermal formulations.
Abstract:
A case of infant clonidine poisoning from a transdermal patch that had been worn for five days by an adult and then discarded is described. The infant became hypotensive with a systolic blood pressure of 38 mm Hg, and a dopamine infusion was required for six hours to maintain adequate blood pressure. The infant was discharged 24 hours after admission. Clonidine toxicity, transdermal delivery system pharmacokinetics, and poison prevention are discussed.
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