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Dexmedetomidine infusion overdose during anesthesia: A case report.
Christine Li1, Michael Clifford2
1University of Melbourne, Parkville, Vic, Australia.
Paediatric Anaesthesia
|December 24, 2019
Summary
A high dose of dexmedetomidine (DEX) in an infant caused temporary hypertension, followed by bradycardia and hypotension, requiring medical intervention. The infant experienced no lasting side effects from this anesthetic adjunct.
Area of Science:
- Anesthesiology
- Pediatric Critical Care
- Pharmacology
Background:
- Dexmedetomidine is an alpha-2 adrenergic agonist used for procedural sedation and as an adjunct in general anesthesia.
- Standard dexmedetomidine infusion rates are typically in the micrograms per kilogram per hour (µg kg⁻¹ h⁻¹) range.
- The use of dexmedetomidine in pediatric anesthesia requires careful dose titration due to potential cardiovascular effects.
Observation:
- An intravenous dexmedetomidine infusion of 0.2 µg kg⁻¹ min⁻¹ was administered to a 12-kg infant during general anesthesia.
- A 60-fold increase in the dexmedetomidine infusion rate was observed.
- This dose escalation resulted in a biphasic cardiovascular response.
Findings:
- The initial response to the increased dexmedetomidine infusion rate was hypertension.
- This was followed by significant bradycardia and hypotension, necessitating inotropic support.
- No adverse postoperative or long-term sequelae were identified in the infant.
Implications:
- This case highlights the potential for significant cardiovascular events with supratherapeutic dexmedetomidine dosing in pediatric patients.
- It underscores the importance of precise dose calculation and monitoring during dexmedetomidine administration, especially in infants.
- Understanding the biphasic cardiovascular effects of dexmedetomidine is crucial for managing anesthetic adjuncts in pediatric populations.
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