Chronic Disease Discussion Questions Related

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Dexmedetomidine:

  • A. Is recognized as an α₁ receptor agonist.
  • B. Increases the minimum alveolar concentration of volatile agents.
  • C. Causes bradycardia.
  • D. Has a loading dose of 0.5-1.0 μg kg⁻¹.
Correct Answer: C

Rationale: Dexmedetomidine is a highly selective α₂-adrenergic receptor agonist, not α₁, used for sedation with minimal respiratory depression. It reduces the minimum alveolar concentration of volatile anesthetics by enhancing sedation and analgesia, not increasing it. Bradycardia is a well-known side effect due to its sympatholytic action, decreasing heart rate via vagal stimulation and reduced catecholamine release. The standard loading dose is indeed 0.5-1.0 μg kg⁻¹ over 10 minutes, followed by infusion, aligning with clinical protocols. At high infusion rates, respiratory depression is unlikely, distinguishing it from opioids. Bradycardia's prominence as a side effect stems from its mechanism activation of α₂ receptors in the brainstem and periphery inhibits sympathetic outflow, making it a critical consideration in perioperative management, especially in patients with cardiovascular comorbidities.