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ATRACURIUM
DR.FARWA SHABBIR
HOUSE OFFICER ANAESTHESIOLOGY
ROAD MAP
? INTRODUCTION
? STRUCTURE
? MODE OF ACTION
? PHARMACOKINETICS
? METABOLISM AND EXCRETION
? DOSAGE
? INDICATIONS
? SIDE EFFECTS
INTRODUCTION
non-depolarizing
Neuro-muscular blocking agent
Metabolism Rapid
Onset Moderately Rapid
Duration Moderately Rapid
Histamine release slow
Vagal Blockade None
STRUCTURE
? Quaternary Ammonium
compound
? benzylisoquinoline structure
PHARMACOKINETICS
? Bioavailability: poorly absorbed from the GI
tract
? Half-life: approximately 20 minutes
? Distribution: into extracellular fluid, minimally
crosses the placenta
? Elimination Route: excreted principally in
urine and also in feces via biliary elimination
MODE OF ACTION
Atracurium
MODE OF REVERSAL
METABOLISM AND EXCRETION
Ester Hydrolysis
This action is catalyzed by nonspecific esterases
Hofmann Elimination
A spontaneous non-enzymatic chemical breakdown
occurs at physiological pH and temperature.
DOSAGE AND ADMINISTRATION
? A dose of 0.5 mg/kg is administered
intravenously for intubation
? incremental doses of 0.1 mg/kg every 10C20
min after administration of succinylcholine
? An infusion of 5C10 mcg/kg/min can
effectively replace intermittent boluses
INDICATIONS
Endotracheal Intubation
Mechanical Ventilation
Skeletal muscle relaxation during surgery
CONTRAINDICATIONS
No documented contraindications except in such
conditions;
?Allergy
?Myasthenia Gravis
?Asthma
CLINICAL SIDE EFFECTS
Hypotension and Tachycardia
Bronchospasm
Laudanosine Toxicity
Temperature and pH Sensitivity
Chemical Incompatibility
Allergic Reactions
Atracurium

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