Neuromuscular blocker

Succinylcholine

Also called sux

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

Indications

Dosing

WhereDose
Airway and RSISuccinylcholine: 1–1.5 mg/kg; avoid in hyperkalemia, burns or crush over 24–72 h old, neuromuscular disease, malignant hyperthermia history

On the quick cards

Mechanism of action

Succinylcholine is two acetylcholine molecules joined through their acetyl groups. It binds the acetylcholine sites on the two α1 subunits of the adult muscle nicotinic receptor (α1, α1, β1, δ, ε) and opens its cation channel, so the end plate depolarizes and the fibers fasciculate. Acetylcholinesterase in the cleft does not hydrolyze it, so the end plate stays depolarized, the surrounding voltage-gated sodium channels stay inactivated and no new action potential can start: the muscle goes flaccid (phase I block). Large or repeated doses desensitize the receptors, and the block takes on nondepolarizing features (phase II).

Pharmacology

Pharmacokinetics

OnsetUnder 1 min IV (30–60 s); 2–3 min IM
PeakFull block about 1 min after an IV dose, held for about 2 min
DurationRecovery over the next 4–6 min, so under 10 min in all after an intubating dose
Half-lifeAbout 47 s in plasma (Torda 1997); undetectable 2.5 min after 1–2 mg/kg
DistributionMostly extracellular fluid; permanently charged and poorly lipid soluble, so little crosses the blood-brain barrier or placenta
MetabolismPlasma cholinesterase (butyrylcholinesterase, made in the liver) hydrolyzes most of a dose before it reaches the end plate: first to succinylmonocholine, a negligible blocker, then more slowly to succinic acid and choline
EliminationThe block ends as drug diffuses from the junction back into plasma; about 10% is excreted unchanged in urine
Cholinesterase variantsHomozygous atypical BCHE genes (about 1 in 2,500–5,000 people) prolong paralysis to several hours; heterozygotes only modestly. Dibucaine number 70–90 normal, 30–70 heterozygous, under 30 homozygous
Low enzyme activityPregnancy (about 24% lower), severe liver or kidney disease, cancer, burns, infection, myxedema; organophosphates, echothiophate, some chemotherapy, MAOIs, chronic steroids or oral contraceptives

Chemistry

Adverse effects and cautions

In the one-pagers

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Sources

  1. FDA label: Anectine (2023)
  2. Torda 1997 (half-life)
  3. Martyn 2006 (hyperkalemia)
  4. MedlinePlus Genetics: pseudocholinesterase deficiency (2025)

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