Antidote

Lipid emulsion 20% (Intralipid)

Also called Intralipid

Reviewed by Alex G, BSN, RN, CEN, CCRN, CMC, NREMT-P · From the Reference tab of the app

Indications

Mechanism of action

Infused lipid forms an intravascular lipid phase that pulls lipid-soluble drugs such as bupivacaine out of plasma water, lowering free drug at the heart and brain (the sink), then carries it to muscle and liver (the shuttle). It also raises contractility and vascular tone within minutes and activates prosurvival kinases such as Akt, a postconditioning effect. The older metabolic theory, that fatty acids refuel a heart whose mitochondrial fatty-acid uptake bupivacaine blocks, has weaker support (Fettiplace 2018).

Pharmacology

Pharmacokinetics

OnsetMinutes; the bolus may be repeated once or twice (ASRA)
DurationShort, so toxicity can recur: observe 4–6 h after cardiovascular signs, 2 h after CNS-only signs
Half-lifeTriglycerides about 15–40 min after a bolus in healthy adults
DistributionStays in plasma as chylomicron-sized droplets
MetabolismEndothelial lipoprotein lipase splits triglycerides into free fatty acids and glycerol; the liver clears remnants
ClearanceSaturable; triglycerides rise more with lipid disorders, obesity or diabetes (label)
EliminationFatty acids are oxidized to CO₂ and water or stored

Chemistry

Adverse effects and cautions

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Sources

  1. FDA label: Intralipid 20% (2025)
  2. ASRA LAST checklist (2020)
  3. Fettiplace and Weinberg 2018 (mechanisms)
  4. Grunbaum 2016 (lab interference)

For education and exam preparation only. Follow your institution’s protocols. Typical adult values for study. Follow your local protocols and medical direction.