Propofol: Difference between revisions
No edit summary |
|||
| (47 intermediate revisions by 12 users not shown) | |||
| Line 1: | Line 1: | ||
== | ==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 | |||
**[[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 | |||
*Hypotension | |||
*Aortic stenosis | |||
===Higher Risk=== | ===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== | ==See Also== | ||
*[[Sedation (Main)]] | *[[Sedation (Main)]] | ||
*[[Ketofol]] | |||
[[ | *[[Propofol infusion syndrome]] | ||
==References== | ==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
- 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 (PRIS)
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
- Adult
- Hepatic Dosing
- Adult
- No adjustment necessary
- Pediatric
- No adjustment necessary
- Adult
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
- ↑ McKeage, K. and Perry, C. M. (2003) ‘Propofol’, CNS Drugs, 17(4), pp. 235–272.
