vecuronium

Brand: Norcuron

ISMP High Alert Prototype: succinylcholine
Drug Class: neuromuscular blocking agent (NMBA)
Drug Family: neuromuscular blocking agent
Subclass: non-depolarizing NMBA (aminosteroid)
Organ Systems: cnsmusculoskeletal

Mechanism of Action

Intermediate-duration non-depolarizing NMBA; competitive nicotinic antagonist at the NMJ. Minimal cardiovascular effects (no histamine release, no ganglionic blockade). Partially reversed by neostigmine and fully reversed by sugammadex.

nicotinic acetylcholine receptor at NMJ (competitive antagonist)

Indications

  • facilitation of endotracheal intubation
  • intraoperative skeletal muscle relaxation
  • facilitation of mechanical ventilation in ICU

Contraindications

  • hypersensitivity to vecuronium

Adverse Effects

Common

  • residual neuromuscular blockade

Serious

  • prolonged paralysis in liver/renal impairment
  • anaphylaxis (rare)

Pharmacokinetics (ADME)

Absorption IV only
Distribution protein binding ~30%; Vd ~0.27 L/kg
Metabolism hepatic; active metabolite 3-desacetylvecuronium (50-70% potency of parent)
Excretion biliary (~40-75%) and renal (25%)
Half-life 65-75 minutes
Onset 2-3 minutes at 0.1 mg/kg
Peak 3-5 minutes
Duration 25-40 minutes at 0.1 mg/kg
Protein Binding 30%
Vd 0.27 L/kg

Drug Interactions

Drug / Agent Mechanism Severity
aminoglycosides potentiate blockade moderate
succinylcholine (priming) prior succinylcholine enhances subsequent vecuronium effect moderate

Nursing Considerations

  1. Prolonged blockade occurs in hepatic impairment due to accumulation of active 3-desacetylvecuronium metabolite; monitor carefully in liver disease.
  2. Vecuronium can be reversed by neostigmine (with anticholinergic) or sugammadex depending on depth of blockade.
  3. Assess TOF before reversal; ensure respiratory muscle function (TOF ratio >0.9) before extubation.
  4. Dilute in compatible IV fluid; stable in NS, D5W, LR for 24 hours.

Clinical Pearls

  • Vecuronium has minimal cardiovascular effects making it preferred in cardiac patients where tachycardia or histamine release are concerns.
  • The 3-desacetylvecuronium active metabolite accumulates in renal and hepatic failure, causing prolonged blockade (ICU myopathy if combined with corticosteroids).

Safety Profile

Pregnancy use-with-caution
Lactation use-with-caution
Renal Adjustment Required
Hepatic Adjustment Required
TDM Not required