Mivacurium
Mivacron
Benzylisoquinolinium non-depolarizing NMB (short-acting)
Competitive nicotinic antagonist. UNIQUE among non-depolarizers: metabolized by PLASMA CHOLINESTERASE (like succinylcholine) → shortest-acting NDMR.
Indications
- •Short procedures needing brief non-depolarizing relaxation
Dosing
| Context | Adult | Pediatric |
|---|---|---|
| Intubation | 0.15–0.2 mg/kg IV | — |
| Maintenance | Infusion 5–7 mcg/kg/min | — |
Pharmacokinetics
Onset 2–3 min. Duration 15–20 min (shortest NDMR). Plasma-cholinesterase metabolism → PROLONGED in pseudocholinesterase deficiency (like sux).
Hemodynamic effects
Histamine release with rapid/large doses → hypotension, flushing.
Side effects
- !Histamine release (dose/rate-dependent)
- !PROLONGED block in pseudocholinesterase deficiency
- !Prolonged by anticholinesterases (neostigmine paradoxically prolongs it)
Contraindications
- ×Pseudocholinesterase deficiency (relative)
- ×Reactive airway (histamine)
Clinical pearls
- ★Only non-depolarizer metabolized by plasma cholinesterase → shortest-acting, but PROLONGED in atypical/deficient pseudocholinesterase (same populations as succinylcholine).
- ★Neostigmine can PROLONG it (inhibits the plasma cholinesterase that clears it) — reversal is nuanced.
Other drugs in Muscle Relaxants & Reversals
- Succinylcholine
Acetylcholine receptor agonist at the NMJ; sustained depolarization → fasciculations → flaccid paralysis. Hydrolyzed by plasma cholinesterase.
- Rocuronium
Competitive antagonist at the NMJ nicotinic receptor.
- Sugammadex
Encapsulates rocuronium > vecuronium > pancuronium in 1:1 complex. No effect on cisatracurium, atracurium, sux.
- Cisatracurium
Competitive antagonist at the post-synaptic nicotinic ACh receptor at the neuromuscular junction. Single cis-cis isomer of atracurium (4× more potent, lower laudanosine production).
- Vecuronium
Competitive nicotinic ACh-receptor antagonist at the NMJ. Aminosteroid → reversible by sugammadex.
- Atracurium
Competitive nicotinic antagonist. Eliminated by HOFMANN elimination (spontaneous, temp/pH-dependent) + ester hydrolysis → organ-independent clearance.
- Pancuronium
Competitive nicotinic antagonist. Also blocks cardiac muscarinic receptors (vagolytic) → tachycardia.
Browse all classes: /reference/drugs
Suggested reading
- •Stoelting & Hines, Pharmacology & Physiology in Anesthetic Practice, 6e
- •Miller's Anesthesia, 9e
- •FDA package insert



