Propofol: Difference between revisions

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==Background==
==General==
*Type: [[Sedative agent]]
*Dosage Forms: 10mg/mL
*Common Trade Names: Diprivan


==Adult Dosing==
===Standard Induction Sedation===
*Induction = 0.5-1 mg/kg IV over 10s, followed by 0.5 mg/kg every 2-3 minutes as needed
*Small incremental doses (10-30 mg) can slowly be administered to effect conscious sedation


-an ultrashort-acting sedative alkylphenol derivative that induces deep sedation
===Other===
*Maintenance dose for sedation between 0.1-0.2 mg/kg/min or 25-50 mg IV PRN in healthy patients < 55 years of age
*Antiemetic dosing, 10-20 mg IV or 10 μg/kg/min infusion


-rapid onset (90-100 seconds) and short duration (2-8 minute half-life)
===Adjunctive medications===
*Fentanyl or morphine (propofol does not provide analgesia)
*NS for transient hypotension
*[[Lidocaine]] flush (to reduce injection pain)


===[[ICU Sedation]]===
*5-50 mcg/kg/min IV, increase 5 mcg/kg/min q10min
*Avoid prolonged use, especially of high doses, to avoid propofol infusion syndrome (PRIS)
*[[PRIS]] usually associated with >65 mcg/kg/min for >24hrs, and critically ill patients with increased endogenous glucocorticoids and catecholamines
**[[PRIS]]: [[Heart failure]], [[Rhabdomyolysis]], [[metabolic acidosis]], renal failure
*Propofol drip of these high dosages can be seen in post-intubation [[status epilepticus]] (drip 2-10mg/kg/hr)


==Contraindications==
==Pediatric Dosing==
*Induction (3-16 yo) at 2.5-3.5 mg/kg IV
*[[Procedural sedation]] 1 mg/kg (max 40 mg), then 0.5 mg/kg PRN (max 20 mg)
*Pediatric population especially at risk for [[Propofol infusion syndrome|propofol infusion syndrome (PRIS)]]


==Special Populations==
*[[Drug Ratings in Pregnancy|Pregnancy Rating]]: Drug of choice for induction in pregnancy (only Category B induction agent)
*[[Lactation risk categories|Lactation risk]]:
*Renal Dosing
**Adult
*** No adjustment necessary
**Pediatric
*** No adjustment necessary
*Hepatic Dosing
**Adult
*** No adjustment necessary
**Pediatric
*** No adjustment necessary


-allergy to soy or eggs
==Contraindications==
 
*Allergy to class/drug
-hypotension
*Allergy to soy or eggs
 
*Hypotension
-aortic stenosis
*Aortic stenosis
 
 
Higher-risk of complications:
 
1. Patients >55 years old
 
2. Debilitated patients
 
3. Patients with significant underlying illness (i.e. ASA physical status score III or IV)
 
 
*Optimize volume status before administration
 
 
==Side Effects==
 
 
1. Respiratory depression
 
2. Transient hypotension
 
3. Pain at injection site (inject lidocaine IV first)
 
 
==Dose==
 
 
induction = 1mg/kg IV, followed by 0.5mg/kg every 2-3 minutes as needed
 
Small incremental doses (10-30mg) can slowly be administered to effect
 
 
Adjunctive medications:
 
-fentanyl or morphine (propofol does not provide analgesia)
 
-NS for transient hypotension
 
-Lidocaine flush (to reduce injection pain)
 
 
==Pediatric Population==
 
 
Safe for procedural sedation in pediatric patients.  Same dosing.


===Higher Risk===
*Patients >55 years old
*Debilitated patients
*Patients with significant underlying illness (i.e. ASA physical status score III or IV)
**Optimize volume status before administration
**Largest decrease in systemic BP (vasodilation with only small increase in HR) compared with other induction drugs



==Adverse Reactions==
*Respiratory depression
*Transient hypotension
*Pain at injection site (inject lidocaine 20-40mg IV and fentanyl 50 mcg IV first)
*[[Hypertriglyceridemia]] - check TG levels in ICU setting
*Cardiac arrest (patients with significant cardiac disease receiving propofol for induction at highest risk)
*[[Propofol infusion syndrome]] (PRIS)


==Pharmacology==
*Half-life: 40 minutes (initial); 24-72 hr (after 10-day infusion)
*Metabolism: Hepatic
*Excretion: Renal
*Mechanism of Action: GABA agonist
*Rapid onset (90-100 seconds) and short duration (2-8 minute)
*Wake up after induction dose usually 8-10 min


==Comments==
*Seizure-like activity possible during induction, but safe in seizure disorder (most studies actually support anticonvulsant effect)
*Has significant anti-emetic activity
*Associated with static or reduced intracranial pressure in head injured patients requiring [[ICU Sedation]]<ref>McKeage, K. and Perry, C. M. (2003) ‘Propofol’, CNS Drugs, 17(4), pp. 235–272. </ref>


==See Also==
*[[Sedation (Main)]]
*[[Ketofol]]
*[[Propofol infusion syndrome]]


[[Category:Drugs]]
==References==
<references/>
[[Category:Pharmacology]]
[[Category:Critical Care]]

Latest revision as of 14:20, 5 December 2023

General

  • Type: Sedative agent
  • Dosage Forms: 10mg/mL
  • Common Trade Names: Diprivan

Adult Dosing

Standard Induction Sedation

  • Induction = 0.5-1 mg/kg IV over 10s, followed by 0.5 mg/kg every 2-3 minutes as needed
  • Small incremental doses (10-30 mg) can slowly be administered to effect conscious sedation

Other

  • Maintenance dose for sedation between 0.1-0.2 mg/kg/min or 25-50 mg IV PRN in healthy patients < 55 years of age
  • Antiemetic dosing, 10-20 mg IV or 10 μg/kg/min infusion

Adjunctive medications

  • Fentanyl or morphine (propofol does not provide analgesia)
  • NS for transient hypotension
  • Lidocaine flush (to reduce injection pain)

ICU Sedation

  • 5-50 mcg/kg/min IV, increase 5 mcg/kg/min q10min
  • Avoid prolonged use, especially of high doses, to avoid propofol infusion syndrome (PRIS)
  • PRIS usually associated with >65 mcg/kg/min for >24hrs, and critically ill patients with increased endogenous glucocorticoids and catecholamines
  • Propofol drip of these high dosages can be seen in post-intubation status epilepticus (drip 2-10mg/kg/hr)

Pediatric Dosing

Special Populations

  • Pregnancy Rating: Drug of choice for induction in pregnancy (only Category B induction agent)
  • Lactation risk:
  • Renal Dosing
    • Adult
      • No adjustment necessary
    • Pediatric
      • No adjustment necessary
  • Hepatic Dosing
    • Adult
      • No adjustment necessary
    • Pediatric
      • No adjustment necessary

Contraindications

  • Allergy to class/drug
  • Allergy to soy or eggs
  • Hypotension
  • Aortic stenosis

Higher Risk

  • Patients >55 years old
  • Debilitated patients
  • Patients with significant underlying illness (i.e. ASA physical status score III or IV)
    • Optimize volume status before administration
    • Largest decrease in systemic BP (vasodilation with only small increase in HR) compared with other induction drugs

Adverse Reactions

  • Respiratory depression
  • Transient hypotension
  • Pain at injection site (inject lidocaine 20-40mg IV and fentanyl 50 mcg IV first)
  • Hypertriglyceridemia - check TG levels in ICU setting
  • Cardiac arrest (patients with significant cardiac disease receiving propofol for induction at highest risk)
  • Propofol infusion syndrome (PRIS)

Pharmacology

  • Half-life: 40 minutes (initial); 24-72 hr (after 10-day infusion)
  • Metabolism: Hepatic
  • Excretion: Renal
  • Mechanism of Action: GABA agonist
  • Rapid onset (90-100 seconds) and short duration (2-8 minute)
  • Wake up after induction dose usually 8-10 min

Comments

  • Seizure-like activity possible during induction, but safe in seizure disorder (most studies actually support anticonvulsant effect)
  • Has significant anti-emetic activity
  • Associated with static or reduced intracranial pressure in head injured patients requiring ICU Sedation[1]

See Also

References

  1. McKeage, K. and Perry, C. M. (2003) ‘Propofol’, CNS Drugs, 17(4), pp. 235–272.