What is the recommended starting dose for a propofol (propofol) drip?

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Propofol Infusion Starting Dose

For ICU sedation in mechanically ventilated adults, initiate propofol at 5 mcg/kg/min (0.3 mg/kg/h) as a continuous infusion, then increase by increments of 5-10 mcg/kg/min every 5 minutes until desired sedation is achieved. 1

ICU Sedation Protocol

Initial Dosing Strategy

  • Start at 5 mcg/kg/min (0.3 mg/kg/h) for intubated, mechanically ventilated adults to minimize hypotension 1
  • Allow a minimum of 5 minutes between dose adjustments for peak drug effect 1
  • Increase by increments of 5-10 mcg/kg/min (0.3-0.6 mg/kg/h) until target sedation level is reached 1

Maintenance Dosing

  • Most adult ICU patients require 5-50 mcg/kg/min (0.3-3 mg/kg/h) for maintenance 1
  • Medical ICU patients or those recovered from general anesthesia may require ≥50 mcg/kg/min for adequate sedation 1
  • Never exceed 4 mg/kg/h (approximately 67 mcg/kg/min) unless benefits clearly outweigh risks 1

Critical Safety Considerations

Propofol Infusion Syndrome (PRIS)

  • Doses >70 mcg/kg/min (4.2 mg/kg/h) for >48 hours dramatically increase PRIS risk, which carries up to 33% mortality 2
  • PRIS presents with metabolic acidosis, rhabdomyolysis, cardiac arrhythmias, myocardial failure, renal failure, and hepatomegaly 3
  • Recent case reports document PRIS at rates as low as 1.9-2.6 mg/kg/h, indicating the safe dosage threshold may need re-evaluation 3

Hemodynamic Monitoring Requirements

  • Propofol causes dose-dependent decreases in cardiac output, systemic vascular resistance, and arterial pressure 2
  • Continuous monitoring of heart rate, blood pressure, and oxygen saturation is mandatory 2
  • Hypotension occurs in 5-7% of patients and is more likely at higher infusion rates 2

High-Risk Populations Requiring Dose Reduction

  • Reduce initial dose by 20-80% in elderly, debilitated, or ASA-PS III-IV patients who demonstrate exaggerated hemodynamic responses 1
  • Patients with compromised myocardial function, intravascular volume depletion, or abnormal vascular tone (e.g., sepsis) are more susceptible to hypotension 1
  • Patients receiving large doses of narcotics require reduced propofol dosing 1

Alternative Dosing for Specific Contexts

Procedural Sedation (Non-ICU)

  • For endoscopic procedures using nurse-administered propofol sedation (NAPS), initial bolus doses range from 10-60 mg, with additional 10-20 mg boluses every 20-30 seconds as needed 4
  • Mean total doses for colonoscopy range from 144-287 mg depending on target sedation depth 4, 2

Palliative Sedation

  • For refractory symptoms at end of life, use a loading dose of 20 mg followed by maintenance infusion of 50-70 mg/h 2, 5

Key Clinical Pitfalls

Analgesic Requirements

  • Propofol has zero analgesic properties and must be combined with opioids or other analgesics for painful procedures 2
  • Adequate pain management with analgesics may reduce propofol requirements 1

Pharmacogenomic Considerations

  • For CYP2B6 poor metabolizers, reduce maintenance infusion to 25 mcg/kg/min (approximately 50% reduction from standard range) 2

Daily Assessment Protocol

  • Evaluate sedation level and CNS function daily to determine minimum effective dose 1
  • Avoid abrupt discontinuation; taper gradually to prevent rapid awakening with anxiety, agitation, and ventilator resistance 1
  • Recovery from sedation is typically rapid, averaging 15.5 minutes after stopping infusion 6

References

Guideline

Propofol Sedation Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Medications Used for Medical Aid in Dying

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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