Lorazepam Dosing for ICU Sedation
For ICU sedation, lorazepam should be administered at an initial IV loading dose of 0.02-0.04 mg/kg (maximum 2 mg), followed by maintenance dosing of 0.01-0.1 mg/kg/hr continuous infusion (maximum 10 mg/hr) or 0.02-0.06 mg/kg every 2-6 hours as needed. 1
Pharmacology and Administration
Lorazepam is a benzodiazepine with the following characteristics:
- Onset of action: 15-20 minutes after IV administration
- Elimination half-life: 8-15 hours
- No active metabolites (unlike midazolam and diazepam)
- Loading dose: 0.02-0.04 mg/kg (≤ 2 mg)
- Maintenance dosing options:
- Continuous infusion: 0.01-0.1 mg/kg/hr (not exceeding 10 mg/hr)
- Intermittent dosing: 0.02-0.06 mg/kg every 2-6 hours as needed
Efficacy and Clinical Considerations
While lorazepam has traditionally been used for ICU sedation, current evidence suggests that non-benzodiazepine sedatives may offer advantages:
- Propofol vs. lorazepam: Fewer ventilator days (5.8 vs. 8.4 days) 1
- Dexmedetomidine vs. lorazepam: More days alive without delirium or coma (7.0 vs. 3.0 days) 1
Important Adverse Effects
- Respiratory depression and hypotension, particularly when combined with opioids 1
- Propylene glycol-related acidosis and nephrotoxicity with continuous infusion 1
- Can occur with total daily IV doses as low as 1 mg/kg
- Monitor osmol gap (>10-12 mOsm/L suggests significant propylene glycol accumulation)
- Delayed emergence from sedation due to:
- Prolonged administration (tissue saturation)
- Advanced age
- Hepatic dysfunction
- Renal insufficiency 1
Current Recommendations
The 2013 Society of Critical Care Medicine guidelines suggest that non-benzodiazepine sedatives (propofol or dexmedetomidine) may be preferred over benzodiazepines (midazolam or lorazepam) to improve clinical outcomes in mechanically ventilated ICU patients 1. This recommendation is based on evidence showing:
- Shorter ICU length of stay (by approximately 0.5 days)
- Reduced duration of mechanical ventilation
- Lower incidence of delirium
Practical Dosing Algorithm
Initial sedation:
- Loading dose: 0.02-0.04 mg/kg IV (not exceeding 2 mg)
- Assess response after 15-20 minutes (onset time)
Maintenance options:
- Continuous infusion: Start at 0.01-0.02 mg/kg/hr and titrate to desired effect
- Intermittent dosing: 0.02-0.06 mg/kg every 2-6 hours as needed
Titration:
- Target light sedation (patient arousable and able to follow simple commands)
- Use validated sedation scales (e.g., RASS, SAS) to guide dosing
- Adjust dose every 8 hours if sedation is adequate, or every 2 hours if inadequate 2
Maximum dose:
- Do not exceed 10 mg/hr for continuous infusion 1
- Consider alternative agents if adequate sedation not achieved at maximum dose
Monitoring
- Assess sedation level using validated scales
- Monitor for respiratory depression and hypotension
- Check for signs of propylene glycol toxicity:
- Metabolic acidosis
- Acute kidney injury
- Elevated osmol gap (>10-12 mOsm/L)
- Evaluate for delayed emergence, particularly with prolonged use
Caution
While lorazepam dosing information is provided as requested, current evidence suggests that non-benzodiazepine sedatives like propofol and dexmedetomidine may be preferred first-line agents for ICU sedation due to improved clinical outcomes including reduced delirium, shorter ventilator days, and potentially decreased mortality 1.