Parenteral Manual

Edrophonium chloride

Disclaimer: Official controlled document is the CHEO online copy. It is the responsibility of user to ensure that any paper copy version is the same as the online version before use.

Alternate Name(s): 
TENSILON®, ENLON®
Classification: 
Diagnostic agent for myasthenia gravis; parasympathomimetic to reverse curariform drugs
Original Date: 
August 2005
Indications: 
  • Differential diagnosis of myasthenia gravis, evaluation of treatment of myasthenia gravis
  • Curare antagonist for reversal of neuromuscular blockade produced by tubocurarine, curare, gallamine triethiodide, atracurium, vecuronium, pancuronium
  • Treatment of respiratory depression caused by curare overdose
Reconstitution and Stability: 
  • Stable at room temperature
  • Protect from light
  • Available as 10 mg/mL ampoules and multi-dose vials
Compatibility: 

- Solutions Compatible: D5W, 0.9% NaCl, D5NS, ringer's lactate for 4 hours at room temperature

- Additives/Above Cassette Compatible: no information

- Y-site Compatible: KCl (up to 40 mEq/L), heparin

Incompatible: no information

Administration: 

(For approved routes of administration by nursing personnel, refer to Policy for the Administration of Intravenous Medications.)

SC YES, usually IV
IM YES, usually IV
IV Push

YES
Usual dilution: undiluted
Infusion: 1 minute

IV Intermittant Infusion NO
IV Continuous Infusion NO
Dosage: 

(For neonatal dosages, refer to Neonatal IV Drug Manual.)

Infant:        
- Myasthenia gravis diagnosis:

  • 0.5-1 mg IM/SC OR
  • 0.1 mg IV followed by 0.4 mg (if no response): total dose = 0.5 mg

Pediatric:                          
- Myasthenia gravis diagnosis:

  • <34 kg: 2 mg IM/SC  
  • >34 kg: 5 mg IM/SC OR
  • 0.04 mg/kg IV followed by 0.16 mg/kg IV given within 45 seconds, if no response   
  • Maximum: 10 mg total

Adolescent/Adult :            
- Myasthenia gravis diagnosis:

  • 10 mg IM/SC: if no cholinergic reaction occurs, give 2 mg 30 minutes later to rule out false    negative OR
  • Use 10 mg in tuberculin syringe, 2 mg test dose administered over 15-30 seconds leaving needle in situ; If no reaction in 45 seconds, inject remaining 8 mg.  May repeat in 30 minutes

- Curare antagonist:

  • 10 mg IV over 30-45 seconds.  May repeat Q 5-10 minutes
  • Maximum: 40 mg total dose
Potential hazards of parenteral administration: 
  • Thrombophlebitis
  • Bradycardia and cardiac arrhythmias (antidote-atropine sulphate), A-V block
  • Hypotension
  • Bronchospasm, respiratory distress especially in asthmatics
  • Increased salivary, gastrointestinal, lacrimal and bronchial secretions
  • Weakness and fasciculations
  • Seizures, drowsiness, headaches

 

Notes: 
  • May cause cholinergic crisis (IV atropine should be available)
  • Resuscitation equipment should be readily available
  • Not effective in reversing paralysis caused by succinylcholine
  • Caution in patients with asthma or cardiac arrhythmias
  • Supportive ventilation must be readily available in apneic patients
  • Not recommended for maintenance therapy in myasthenia gravis due to short duration of action
  • Contraindicated in intestinal and urinary obstruction of mechanical type
  • Monitor pre- and post-injection strength, heart rate, respiratory rate, blood pressure, changes in fasciculations
  • Dose may need to be reduced in chronic renal failure

 

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