Propofol: Difference between revisions

No edit summary
 
(28 intermediate revisions by 10 users not shown)
Line 1: Line 1:
==Background==
==General==
*Rapid onset (90-100 seconds) and short duration (2-8 minute)
*Type: [[Sedative agent]]
*Wake up after induction dose usually 8-10 min
*Dosage Forms: 10mg/mL
*Seizure-like activity possible during induction, but safe in seizure disorder (most studies actually support anticonvulsant effect)
*Common Trade Names: Diprivan
*Has significant anti-emetic activity
 
*Drug of choice for induction in pregnancy (only Category B induction agent)
==Adult Dosing==
*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>
===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
**[[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)
 
==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


==Contraindications==
==Contraindications==
*Allergy to class/drug
*Allergy to soy or eggs
*Allergy to soy or eggs
*Hypotension
*Hypotension
Line 13: Line 51:


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


==Side Effects==
==Adverse Reactions==
*Respiratory depression
*Respiratory depression
*Transient hypotension
*Transient hypotension
*Pain at injection site (inject lidocaine 20-40mg IV and fentanyl 50 mcg IV first)
*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)
*Cardiac arrest (patients with significant cardiac disease receiving propofol for induction at highest risk)
*Propofol infusion syndrome (PRIS): See below
*[[Propofol infusion syndrome]] (PRIS)


==Dose==
==Pharmacology==
===Standard Induction Sedation===
*Half-life: 40 minutes (initial); 24-72 hr (after 10-day infusion)
*Induction = 0.5-1mg/kg IV over 10s, followed by 0.5mg/kg every 2-3 minutes as needed
*Metabolism: Hepatic
*Small incremental doses (10-30mg) can slowly be administered to effect
*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


===Other===
==Comments==
*Maintenance dose for sedation between 0.1-0.2/kg/min or 25-50 mg IV prn in healthy pts < 55 yoa
*Seizure-like activity possible during induction, but safe in seizure disorder (most studies actually support anticonvulsant effect)
*Antiemetic dosing, 10-20 mg IV or 10 μg/kg/min infusion
*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>
===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 pts with increased endogenous glucocorticoids and catecholamines
**PRIS: Heart failure, [[Rhabdomyolysis]], metabolic acidosis, renal failure
*Propofol gtt of these high dosages can be seen in post-intubation status epilepticus (gtt 2-10 mg/kg/hr)
 
==Pediatric Population==
*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)


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


==References==
==References==
*Stoelting RK, Miller RD. Basics of Anesthesia. 5th ed. Philadephia, PA: Churchill Livingstone Elsevier; 2007.
*Brophy GM. Guidelines for the Evaluation and Management of Status Epilepticus. J Neurocrit Care. 2012, Apr;17(1):3-23.
<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.