Propofol = 2,6- diisopropyl phenol
1% / 2% emulsion in a lipid vehicle containing soybean oil, egg lecithin, and glycerol.
therefore - bacterial growth (thus discard after 6hrs)
Only IV use.
Pain on injection which can be decreased by :
Only IV use.
Pain on injection which can be decreased by :
- injecting in larger vein.
- Mixing with lignocaine
- by cooling propofol
Other points:
- Recovery is rapid and clear (Therefore DOC for Day Care Surgery)
- Hepatic and Extrahepatic (Lungs) clearance.
- Decrease BP and Decrease Heart rate ( propofol blunts carotid body receptor response & hence no compensatory increase in heart rate)
- Causes maximum depression of upper airway reflexes (therefore DOC - for LMA insertion)
- Antiemitic & Antipruritic
- No anticonvulsant.
- Decrease IOP.(intraoccular pressure)
- AntiOxidant
- DOC in hepatic disease/Liver transplant (because it can be metabolized extrahepatic too.)
- Potentiates NMDR and fentanyl.
- DOC in Acute intermittent porphyria (here Thiopentone is Contraindicated)
Propofol Infusion syndrome :
Triad of
- Metabolic Acidosis
- Skeletal Myopathy
- Acute Cardiomyopathy
On prolonged infusion (>48hrs) of high dose in child.
Occurs due to failure of metabolism of free fatty acids.
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