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Bedside Snapshot
  • Acetylcholinesterase Inhibitor: Increases acetylcholine at nicotinic (neuromuscular junction) and muscarinic (heart, gut, bronchi) receptors
  • Two Main Critical-Care Uses:
    • Reversal of non-depolarizing neuromuscular blockers (NMBs) like rocuronium/vecuronium at end of anesthesia when sugammadex unavailable
    • Treatment of acute colonic pseudo-obstruction (Ogilvie's syndrome) when conservative therapy fails
  • Always Paired with Antimuscarinic: NMB reversal always combined with glycopyrrolate or atropine due to muscarinic effects (bradycardia, secretions, bronchospasm)
  • Dosing: 0.02-0.07 mg/kg IV (max ~5 mg) for NMB reversal; 2 mg IV slow push over 3-5 minutes for Ogilvie's with continuous ECG monitoring and atropine at bedside
  • Critical Safety: For Ogilvie's, must exclude mechanical obstruction/perforation before administration; severe bradycardia and asystole are well-described
Brand & Generic Names
  • Generic Name: Neostigmine methylsulfate
  • Brand Names: Bloxiverz, Prostigmin, generics
Medication Class

Reversible acetylcholinesterase inhibitor; parasympathomimetic

Pharmacology

Mechanism of Action:

  • Reversibly inhibits acetylcholinesterase, the enzyme that hydrolyzes acetylcholine (ACh) in synaptic clefts
  • At neuromuscular junction: Increased ACh competes with non-depolarizing NMBs (rocuronium, vecuronium) for nicotinic receptors, restoring neuromuscular transmission and skeletal muscle strength
  • At muscarinic receptors: In heart, GI tract, and airways, increased ACh causes parasympathetic effects—bradycardia, bronchoconstriction, increased secretions, increased GI motility
  • In acute colonic pseudo-obstruction: Enhancing ACh in enteric nervous system and smooth muscle increases colonic motility and may relieve functional obstruction

Pharmacokinetics (IV):

  • Onset: Clinical effect begins within 5-10 minutes after IV administration for NMB reversal, depending on depth of neuromuscular blockade
  • Peak effect: Approximately 7-10 minutes after dosing
  • Duration: ~45-90 minutes for neuromuscular reversal; GI motility effects may last several hours
  • Distribution: Quaternary ammonium compound, highly polar; does NOT cross blood-brain barrier meaningfully
  • Metabolism/elimination: Partly hepatic; ~50% excreted unchanged in urine; elimination half-life ~50-90 minutes, prolonged in significant renal impairment
Dosing & Administration

Available Forms:

  • Injection: Commonly 1 mg/mL (e.g., 10 mg/10 mL) vials for IV/IM administration
  • Oral tablets: 15 mg tablets for chronic MG therapy (much less commonly used than pyridostigmine)
  • For both NMB reversal and Ogilvie's syndrome, IV route is standard and preferred

Neostigmine Dosing (Adult):

Indication / Scenario Dose Route / Timing Notes
Reversal of non-depolarizing NMB (typical) 0.02-0.07 mg/kg IV over ≥1-2 min Max ~5 mg; dose guided by depth of block and TOF monitoring
Common flat dosing example 2.5-5 mg IV once Often combined with glycopyrrolate (e.g., 0.2 mg per 1 mg neostigmine)
Acute colonic pseudo-obstruction (Ogilvie's) 2 mg IV slow push over 3-5 min Continuous ECG monitoring; atropine ready; may repeat once after several hours if incomplete response
Total maximum dose for Ogilvie's 4 mg IV (e.g., 2 mg × 2 doses) Lack of response → reconsider diagnosis, rule out mechanical obstruction/perforation
Renal impairment Lower end of dosing range IV Prolonged effect possible; adjust cautiously
Timing for NMB reversal Give when TOF ratio ≥0.2-0.3 Too early in deep block → incomplete reversal and more side effects
Antimuscarinic Required: Always combine with glycopyrrolate or atropine for NMB reversal to prevent bradycardia and other muscarinic effects.
Contraindications

Contraindications:

  • Suspected or confirmed mechanical intestinal obstruction or peritonitis (for GI indication)
  • Urinary tract obstruction (risk of worsening urinary retention)
  • Known hypersensitivity to neostigmine or formulation components

Major Precautions:

  • Bradycardia, AV block: Must have atropine or glycopyrrolate available; bradyarrhythmias are major risk with IV dosing
  • Asthma or severe COPD: Risk of bronchospasm and increased bronchial secretions
  • Recent MI, severe CAD, decompensated heart failure: Bradycardia and hypotension can reduce coronary perfusion
  • In Ogilvie's: Must exclude perforation or mechanical obstruction with imaging before giving neostigmine; otherwise may precipitate perforation
Adverse Effects

Common (Cholinergic):

  • Bradycardia, hypotension
  • Increased salivation and bronchial secretions
  • Nausea, vomiting, abdominal cramping, diarrhea
  • Sweating, miosis

Serious:

  • Symptomatic bradycardia, asystole, AV block
  • Bronchospasm and respiratory distress
  • Severe cholinergic crisis with muscle weakness (overdose or in MG patients)
Monitoring

During and After Administration:

  • Continuous ECG and blood pressure monitoring, especially for Ogilvie's dosing
  • For NMB reversal: Train-of-four (TOF) monitoring if available plus clinical assessment (hand grip, head lift, tidal volume, airway protection)
  • Respiratory status: work of breathing, wheezing/bronchospasm, secretions
  • In Ogilvie's: Abdominal distension, tenderness, and bowel function to gauge response and detect early perforation
Indications / Clinical Uses (ED/ICU/Anesthesia Focus)
  • Reversal of residual non-depolarizing neuromuscular blockade: Rocuronium, vecuronium at end of general anesthesia or procedural paralysis
  • Acute colonic pseudo-obstruction (Ogilvie's syndrome): When conservative measures (NPO, NG/rectal decompression, mobilization, electrolyte correction) have failed
  • Myasthenia gravis: Historically and in some regions as adjunct; pyridostigmine preferred for chronic oral therapy
Clinical Pearls
Ceiling Effect: For NMB reversal, neostigmine has a ceiling effect—beyond a certain point, more drug adds muscarinic toxicity without better reversal; ensure adequate spontaneous recovery before dosing.
Ogilvie's Success: Success rates with neostigmine are high when diagnosis is correct and mechanical obstruction excluded; if it fails, consider endoscopic decompression early.
Draw Atropine First: Always draw up atropine before giving neostigmine for Ogilvie's; severe bradycardia and even asystole are well-described.
Sugammadex vs Neostigmine: Sugammadex has replaced neostigmine in many ORs for rocuronium reversal, but neostigmine remains essential where sugammadex is unavailable, restricted, or cost-prohibitive.
References
  • 1. Lexicomp. (2024). Neostigmine: Drug information. Wolters Kluwer.
  • 2. Ponec, R. J., Saunders, M. D., & Kimmey, M. B. (1999). Neostigmine for the treatment of acute colonic pseudo-obstruction. New England Journal of Medicine, 341(3), 137–141.