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Cisatracurium
The Near Ideal NMB
Dr. Shaikh Noorulhaque
Secondary DNB Resident in Anaesthesiology
Breach Candy Hospital, Mumbai
PG Guide: Dr. Shilpa Bhojraj
HOD: Dr. Alka Halbe
Introduction
What are Neuromuscular Blocking (NMB) drugs ?
• These are agents that act peripherally at neuromuscular
junction/muscle fibre itself to block neuromuscular transmission.
Why do we need them ?
• In order to facilitate muscle relaxation for Intubation, Surgery & for
Mechanical Ventilation during Surgery or in ICU
The Ideal NMB
• An ideal neuromuscular blocking agent needs to take the shortest time in endotracheal intubation
• The best intubating condition and have the shortest duration of muscle paralysis
• Non-depolarizing mechanism of action
• Rapid onset enabling quick intubation
• Rapid, complete and predictable recovery
• Short elimination half life
• No cumulative effect
• No histamine release
• High potency
• Should have pharmacologically inactive metabolites
• Reversible by cholinesterase inhibitors
• Elimination pathways less dependent on organ function
• Lack clinically important Cardiovascular side effects
Vecuronium
• Aminosteriod
• Onset of action-3-5min/Duration-20-35min
• Dosage:
• Intubation-0.08-0.12mg/kg
• Maintenance-0.04mg/kg
• Infusion-1-2μg/kg/min
• Depends primarily on biliary excretion and secondarily on renal
excretion (no dose reduction required)
• Intermediate acting
• Active metabolites- 3 cis vecuronium responsible for prolonged effect
• Prolonged effect in Old Age, Obesity, Renal Failure, AIDS, Obesity…
Atracurium
• Benzoisoquinoline derivative
• Non-organ dependent elimination
• Non specific estererase:- 60% of elimination
• Hofmann elimination:- spontaneous nonenzymatic chemical breakdown
occurs at physiologic pH and Temperature
• Histamine release at higher clinical dose in 30% of patients (Hypotension,
tachycardia, Bronchospasm)
• Laudanosine toxicity:-
• Breakdown product from Hofmann elimination, assoc. with central nervous
system excitation resulting in elevation of MAC and precipitation of
seizures.
• Temperature and pH sensitivity:- action markedly prolonged in hypothermic or
acidotic patients
Cisatracurium
• It is a stereoisomer of atracurium.
• Four times more potent than atracurium.
• It undergoes Hoffmann elimination like atracurium but ester hydrolysis dose
not occur.
• It dose not produce the histamine and Laudanosine production is 5 times
lesser than atracurium.
• Metabolism and elimination are independent of hepatic and renal failure.
• Does not alter heart rate or blood pressure, nor does it produce autonomic
effects.
• Cisatracurium shares with atracurium the…
– production of Laudanosine,
– pH and temperature sensitivity & chemical incompatibility.
Cisatracurium has
Stable hemodynamics
Cisatracurium has no important hemodynamic side effects
No dose-related effects on Mean Arterial Blood Pressure or Heart Rate
in
• Patients without cardiovascular disease.
• Patients with serious cardiovascular disease
• Children
• NMB of choice for medium-to-long term surgeries on
hemodynamically unstable patients
Cisatracurium has an
Organ independent Hofmann elimination
• Responsible for 77% of the overall elimination of Cisatracurium.
• Minimally dependent on liver and kidneys
• Dependent on pH and Temperature
• Occurs in plasma and tissue
Cisatracurium results in
Uniform Recovery
• Shows spontaneous recovery rates of neuromuscular function
• Number or size of doses minimally affect rate of recovery of neuromuscular
function
• Recovery is predictable irrespective of the age of the patient
• Recovery is independent of renal and hepatic insufficiency
With Cisatracurium there is
Lack of Histamine Release and Laudanosine toxicity
• Cisatracurium does not promote
histamine release even at 8 times the
ED95
• Has no dose-related effects on blood
pressure or heart rate 8
• Laudanosine concentrations are lower
following administration of Cisatracurium
besilate than after administration of
atracurium besilate
Dosage & Storage
• Intubating Dose:- 0.15 - 0.2 mg/Kg
• Onset of Action:- 3-4 minutes
• Results in blockades of intermediate duration i.e., 50 – 60 minutes
• Maintenance Infusion Dose:- 1 -2 mcg/Kg/min
• Storage: Refrigeration (2-8 C)
• Used within 21 days after removal from Refrigeration and exposure to room
temperature
Cisatracurium compare with Vecuronium
Cisatracurium compare with Atracurium
Cisatracurium – Summarizing the benefits in
the OT
• Stable hemodynamics
• Organ independent Hoffman elimination
• Uniform recovery
• Lack of clinically relevant histamine release
• Better hemodynamic stability compared to atracurium and
vecuronium
Cisatracurium
S.O.U.L of the Operation Theatre.
Cisatracurium - The Near Ideal NMB

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Cisatracurium - The Near Ideal NMB

  • 1. Cisatracurium The Near Ideal NMB Dr. Shaikh Noorulhaque Secondary DNB Resident in Anaesthesiology Breach Candy Hospital, Mumbai PG Guide: Dr. Shilpa Bhojraj HOD: Dr. Alka Halbe
  • 2. Introduction What are Neuromuscular Blocking (NMB) drugs ? • These are agents that act peripherally at neuromuscular junction/muscle fibre itself to block neuromuscular transmission. Why do we need them ? • In order to facilitate muscle relaxation for Intubation, Surgery & for Mechanical Ventilation during Surgery or in ICU
  • 3. The Ideal NMB • An ideal neuromuscular blocking agent needs to take the shortest time in endotracheal intubation • The best intubating condition and have the shortest duration of muscle paralysis • Non-depolarizing mechanism of action • Rapid onset enabling quick intubation • Rapid, complete and predictable recovery • Short elimination half life • No cumulative effect • No histamine release • High potency • Should have pharmacologically inactive metabolites • Reversible by cholinesterase inhibitors • Elimination pathways less dependent on organ function • Lack clinically important Cardiovascular side effects
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  • 7. Vecuronium • Aminosteriod • Onset of action-3-5min/Duration-20-35min • Dosage: • Intubation-0.08-0.12mg/kg • Maintenance-0.04mg/kg • Infusion-1-2μg/kg/min • Depends primarily on biliary excretion and secondarily on renal excretion (no dose reduction required) • Intermediate acting • Active metabolites- 3 cis vecuronium responsible for prolonged effect • Prolonged effect in Old Age, Obesity, Renal Failure, AIDS, Obesity…
  • 8. Atracurium • Benzoisoquinoline derivative • Non-organ dependent elimination • Non specific estererase:- 60% of elimination • Hofmann elimination:- spontaneous nonenzymatic chemical breakdown occurs at physiologic pH and Temperature • Histamine release at higher clinical dose in 30% of patients (Hypotension, tachycardia, Bronchospasm) • Laudanosine toxicity:- • Breakdown product from Hofmann elimination, assoc. with central nervous system excitation resulting in elevation of MAC and precipitation of seizures. • Temperature and pH sensitivity:- action markedly prolonged in hypothermic or acidotic patients
  • 9. Cisatracurium • It is a stereoisomer of atracurium. • Four times more potent than atracurium. • It undergoes Hoffmann elimination like atracurium but ester hydrolysis dose not occur. • It dose not produce the histamine and Laudanosine production is 5 times lesser than atracurium. • Metabolism and elimination are independent of hepatic and renal failure. • Does not alter heart rate or blood pressure, nor does it produce autonomic effects. • Cisatracurium shares with atracurium the… – production of Laudanosine, – pH and temperature sensitivity & chemical incompatibility.
  • 10. Cisatracurium has Stable hemodynamics Cisatracurium has no important hemodynamic side effects
  • 11. No dose-related effects on Mean Arterial Blood Pressure or Heart Rate in • Patients without cardiovascular disease. • Patients with serious cardiovascular disease • Children • NMB of choice for medium-to-long term surgeries on hemodynamically unstable patients
  • 12. Cisatracurium has an Organ independent Hofmann elimination • Responsible for 77% of the overall elimination of Cisatracurium. • Minimally dependent on liver and kidneys • Dependent on pH and Temperature • Occurs in plasma and tissue
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  • 14. Cisatracurium results in Uniform Recovery • Shows spontaneous recovery rates of neuromuscular function • Number or size of doses minimally affect rate of recovery of neuromuscular function • Recovery is predictable irrespective of the age of the patient • Recovery is independent of renal and hepatic insufficiency
  • 15. With Cisatracurium there is Lack of Histamine Release and Laudanosine toxicity • Cisatracurium does not promote histamine release even at 8 times the ED95 • Has no dose-related effects on blood pressure or heart rate 8 • Laudanosine concentrations are lower following administration of Cisatracurium besilate than after administration of atracurium besilate
  • 16. Dosage & Storage • Intubating Dose:- 0.15 - 0.2 mg/Kg • Onset of Action:- 3-4 minutes • Results in blockades of intermediate duration i.e., 50 – 60 minutes • Maintenance Infusion Dose:- 1 -2 mcg/Kg/min • Storage: Refrigeration (2-8 C) • Used within 21 days after removal from Refrigeration and exposure to room temperature
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  • 21. Cisatracurium – Summarizing the benefits in the OT • Stable hemodynamics • Organ independent Hoffman elimination • Uniform recovery • Lack of clinically relevant histamine release • Better hemodynamic stability compared to atracurium and vecuronium
  • 22. Cisatracurium S.O.U.L of the Operation Theatre.