Dexmedetomidine (Precedex) Dosing
For adult ICU sedation, start with a loading dose of 1 μg/kg over 10 minutes in hemodynamically stable patients, followed by a maintenance infusion of 0.2–0.7 μg/kg/hour, titrating up to 1.5 μg/kg/hour as tolerated; omit the loading dose entirely in hemodynamically unstable patients, elderly patients, or those with severe hepatic impairment. 1
Adult ICU Sedation: Standard Protocol
Loading Dose Decision Algorithm
Hemodynamically stable patients:
- Administer 1 μg/kg IV over 10 minutes 1
- Monitor blood pressure and heart rate every 2–3 minutes during bolus 1
- Have atropine immediately available for bradycardia 1
Hemodynamically unstable patients (hypotension, bradycardia, severe cardiac disease):
- Omit loading dose entirely 1, 2
- Start directly with maintenance infusion at 0.2 μg/kg/hour 1
- Never administer loading dose faster than 5 minutes in any circumstance 1
Maintenance Infusion
- Start at 0.2–0.7 μg/kg/hour 1
- Titrate up to maximum 1.5 μg/kg/hour based on Richmond Agitation-Sedation Scale (RASS) target 1
- Target RASS -2 to +1 for light sedation with easy arousability 1
Standard Preparation
- Dilute to 4 μg/mL concentration using 0.9% normal saline 1
- For 100 μg ampoule: add to 25 mL normal saline 1
- For 200 μg ampoule: add to 50 mL normal saline 1
- Example for 70 kg patient: loading dose = 70 μg = 17.5 mL over 10 minutes; maintenance at 0.5 μg/kg/hour = 35 μg/hour = 8.75 mL/hour 1
Special Populations
Elderly Patients
- Omit or extend loading dose to 15–20 minutes if deemed necessary 1
- Start maintenance at lower end of range (0.2 μg/kg/hour) 1
- Context-sensitive half-time becomes prolonged with age, particularly in those with hypoalbuminemia 1, 3
- Dexmedetomidine clearance decreases with increasing age 3
Hepatic Impairment
- Omit or significantly reduce loading dose due to hemodynamic instability risk 1, 4
- Start maintenance at 0.2 μg/kg/hour (lower end of range) 1, 4
- Severe hepatic dysfunction impairs clearance, requiring lower doses and prolonged monitoring 1, 2, 4
- Elimination half-life is prolonged in patients with hypoalbuminemia 3
- Volume of distribution at steady state increases with low albumin, further prolonging effects 3
Cirrhotic Patients (Specific Considerations)
- Dexmedetomidine preferred over benzodiazepines to preserve cognitive function and reduce delirium (54% vs 76.6%, p<0.001) 4
- Reduces need for benzodiazepines in alcohol withdrawal, preventing hepatic encephalopathy 4
- Hypotension occurs in 10–40% of cirrhotic patients, usually resolving without intervention 4
Pediatric Dosing (≥1 Month)
Ages 1 month to <17 years:
- Loading dose: 0.5–1 μg/kg IV over 10 minutes 1, 5
- Maintenance: 0.2–0.7 μg/kg/hour 1, 5
- May titrate up to 2.0 μg/kg/hour for procedural sedation 5
- Use same 4 μg/mL dilution for precise dosing 1
Neonates (≥28 weeks gestational age to <1 month):
Procedural Sedation (Non-ICU)
Awake Intubation or Airway Procedures
- Bolus: 0.5–1 μg/kg over 5 minutes (faster onset acceptable in controlled airway setting) 1
- Maintenance: 0.3–0.6 μg/kg/hour 1
Perioperative/VATS Surgery
- Single bolus: 1 μg/kg IV 20 minutes before end of surgery reduces postoperative pain and opioid requirements 1
- Alternative: loading dose before induction + 0.5 μg/kg/hour infusion until 20 minutes before surgery end 1
- Postoperative low-dose: 0.15 μg/kg/day reduces pain scores 1
Critical Monitoring Requirements
Cardiovascular Monitoring
- Continuous blood pressure and heart rate monitoring mandatory 1, 2, 4
- Hypotension occurs in 10–20% of patients due to central sympatholytic effects 1, 2
- Bradycardia occurs in 10–18% within 5–15 minutes of administration 1
- More serious arrhythmias include first-degree and second-degree AV block, sinus arrest, AV dissociation, and escape rhythms 1
- Loading doses cause biphasic response: transient hypertension followed by hypotension within 5–10 minutes 1
Respiratory Monitoring
- Continuous pulse oximetry mandatory in non-intubated patients 1
- Dexmedetomidine does not significantly affect respiratory drive, unlike benzodiazepines, propofol, and opioids 1
- Critical caveat: Can cause loss of oropharyngeal muscle tone leading to airway obstruction in non-intubated patients 1, 2
- Monitor for both hypoventilation and hypoxemia 1, 2
- Only sedative approved in the United States for non-intubated ICU patients 1
Contraindications and Precautions
Absolute Contraindications
- Sinus node disease 2
- Second- or third-degree AV block 2
- Active hemodynamic instability (unless loading dose omitted) 1
- Primary sedative for alcohol or benzodiazepine withdrawal delirium 1
Relative Contraindications
- Baseline hypotension or severe bradycardia 1
- Compromised cerebrovascular reserve (dexmedetomidine decreases cerebral blood flow by ~33%) 2
Pharmacokinetics
- Terminal elimination half-life: 1.8–3.1 hours (83–159 minutes) in normal hepatic function 1, 3
- Onset of sedation: within 15 minutes 2
- Peak effects: approximately 1 hour after starting IV infusion 2
- Clearance decreases with decreasing cardiac output and increasing age 3
Clinical Advantages
- Reduces delirium compared to benzodiazepines (9% vs 23%, OR 0.35, p<0.0001) 1
- Opioid-sparing effects, significantly reducing narcotic requirements 1, 2, 4
- Preserves sleep architecture, inducing stage N3 non-REM sleep mimicking natural sleep 1
- Patients remain easily arousable and interactive with minimal respiratory depression 1
- Can continue infusions safely after extubation 1, 2
Combination Therapy Considerations
With Antipsychotics
- Obtain baseline QTc before combining with antipsychotics 1
- Avoid combination if QTc prolonged, concurrent QT-prolonging medications, or history of torsades de pointes 1
- Antipsychotics are adjunctive only, not first-line for delirium 1
With Neuromuscular Blockade
- Must combine with GABA agonist (propofol or midazolam) to provide amnesia 1