What is the half-life of Precedex (dexmedetomidine)?

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Half-Life of Dexmedetomidine (Precedex)

Dexmedetomidine (Precedex) has a terminal elimination half-life of approximately 3 hours in adults, with a shorter redistribution half-life of less than 10 minutes. 1, 2

Pharmacokinetic Profile

Dexmedetomidine's pharmacokinetic profile includes:

  • Onset of action: Less than 5 minutes
  • Peak effects: 15 minutes
  • Distribution half-life: 6-8.6 minutes
  • Terminal elimination half-life: 3-3.7 hours
  • Volume of distribution: 132-223 liters
  • Clearance: 39.7-57.0 L/h

1, 2, 3

Factors Affecting Half-Life

Several factors can influence dexmedetomidine's half-life and clearance:

  • Age: Clearance decreases with increasing age, potentially prolonging half-life in elderly patients 4
  • Cardiac output: Decreased cardiac output reduces clearance 4
  • Albumin levels: Low plasma albumin concentration increases volume of distribution, potentially prolonging elimination half-life 4
  • Infusion duration: While pharmacokinetics remain generally linear even with prolonged infusions, context-sensitive half-time may increase with longer infusions 3

Special Populations

Pediatric Patients

  • Infants have faster clearance of dexmedetomidine compared to adults 5
  • This suggests a potentially shorter half-life in the pediatric population

Critical Care Patients

  • Pharmacokinetics in critically ill patients receiving prolonged infusions remain generally consistent with those observed in healthy volunteers
  • Mean residence time averages 3.86 hours in postoperative ICU patients 2
  • The steady-state volume of distribution may be higher in critically ill patients compared to healthy volunteers 2

Clinical Implications

The relatively short half-life of dexmedetomidine has important clinical implications:

  • Rapid recovery from sedation after discontinuation of short-term infusions
  • Minimal respiratory depression compared to other sedatives 1
  • Patients can be aroused to their baseline level of consciousness when stimulated 1
  • Overdose primarily manifests as oversedation rather than significant hemodynamic instability 6
  • The short redistribution half-life (6-8.6 minutes) allows for rapid resolution of oversedation from brief infusions 6

Metabolite Information

Dexmedetomidine is metabolized to H-3, a practically inactive metabolite with:

  • Elimination half-life of approximately 9.1 hours
  • AUC ratio of H-3 to dexmedetomidine of approximately 1.47 (range 0.29-4.4) 3

The relatively short half-life of dexmedetomidine makes it suitable for procedural sedation and short-term ICU sedation, with predictable offset of action when discontinued.

References

Guideline

Sedation Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Dexmedetomidine overdose in the perioperative setting.

The Annals of pharmacotherapy, 2004

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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