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Suxamethonium
Brief presentation
1/27/2019 2
Uses
 Wherever rapid and profound
neuromuscular blockade is required Eg.
To facilitate tracheal intubation
 For modification of fits after
electroconvulsive therapy
Chemical
• The dicholine ester of succinic acid{
equivalent to 2 acetylcholine molecules
joined back to back}
• Presentation
As a clear aqueous solution containing
50mg/ml of Suxamethonium chloride
The preparation should be stored at 4 degree
C
1/27/2019 3
Main action & MOA
 Neuromuscular blockade of brief duration
in skeletal muscle
 Suxamethonium causes prolonged
depolarization of skeletal muscle fibers to
a membrane potential above which an
action potential can be triggered
1/27/2019 4
Route of administration and
doses
• The intravenous dose is 0.5- 2.0 mg/kg
• The onset of action occurs with in 30 sec
and duration of action is 3-5 min
• The intramuscular dose is up to 2.5mg/kg
• The drug may also administered
sublingually at a doses of 2mg/kg
1/27/2019 5
Cardiovascular effects
 With repeated doses of sux, bradycardia
and slight increase in MAP may occur
 Premedication with atropine
 Caution using on the patient already taking
B-blockers
1/27/2019 6
Central nervous system effects
• The adm. Of sux may initially cause
fasciculation which are then followed by
phase I depolarizing block
• The characteristics of the block is
A well sustained tetanus during stimulation at
50 -100hz
The absence of post- tetanic fasciculation
A train of four ratio > 0.7 and
Potentiation by anticholinesterases
1/27/2019 7
• With repeated administration or a large
total dose, phase II block may develop
• The characteristics of this block is
A poorly sustained tetanus
A post tetanic fasciculation
A train of four ratio < 0.3
Reversal by anticholinesterases and
Tachyphylaxis
1/27/2019 8
Other effects
• ICP and IOP are both raised following
administration of sux
• The intragastric pressure increases by 7-
12cmH2O, the lower esophageal sphincter
tone simultaneously decreases with the
use of suxamethonium
• Serum potassium concentration is briefly
increased in normal individual by 0.2-
0.4mmol/l
1/27/2019 9
Toxicity & side effects
• Bradycardia & other dysarrythmia
• Hyperkalemia
• Postoperative myalgia – in women middle
age
• Increases IOP,ICP & IGP
• Triggering agent for malignant
hyperthermia
• Sux apnea
• Anaphylactic reaction1/27/2019 10
Metabolism
• The drug is hydrolyzed by plasma
cholinesterase to succinylmonocholine
{which is weakly active} and choline
• The former is further hydrolyzed by
plasma cholinesterase to succinic acid and
choline
• 80% of administered dose is hydrolyzed
before it reaches the NMJ
1/27/2019 11
Special points
• The incidence of muscle pain after
administration of suxamethonium may be
decreased by pre-treatment with
A low dose {0.2mg/kg} dose of sux
A small dose of a non-depolarizing relaxants
Diazepam
Aspirin or
Vitamin C
1/27/2019 12
1/27/2019 13

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Suxamethonium

  • 2. 1/27/2019 2 Uses  Wherever rapid and profound neuromuscular blockade is required Eg. To facilitate tracheal intubation  For modification of fits after electroconvulsive therapy
  • 3. Chemical • The dicholine ester of succinic acid{ equivalent to 2 acetylcholine molecules joined back to back} • Presentation As a clear aqueous solution containing 50mg/ml of Suxamethonium chloride The preparation should be stored at 4 degree C 1/27/2019 3
  • 4. Main action & MOA  Neuromuscular blockade of brief duration in skeletal muscle  Suxamethonium causes prolonged depolarization of skeletal muscle fibers to a membrane potential above which an action potential can be triggered 1/27/2019 4
  • 5. Route of administration and doses • The intravenous dose is 0.5- 2.0 mg/kg • The onset of action occurs with in 30 sec and duration of action is 3-5 min • The intramuscular dose is up to 2.5mg/kg • The drug may also administered sublingually at a doses of 2mg/kg 1/27/2019 5
  • 6. Cardiovascular effects  With repeated doses of sux, bradycardia and slight increase in MAP may occur  Premedication with atropine  Caution using on the patient already taking B-blockers 1/27/2019 6
  • 7. Central nervous system effects • The adm. Of sux may initially cause fasciculation which are then followed by phase I depolarizing block • The characteristics of the block is A well sustained tetanus during stimulation at 50 -100hz The absence of post- tetanic fasciculation A train of four ratio > 0.7 and Potentiation by anticholinesterases 1/27/2019 7
  • 8. • With repeated administration or a large total dose, phase II block may develop • The characteristics of this block is A poorly sustained tetanus A post tetanic fasciculation A train of four ratio < 0.3 Reversal by anticholinesterases and Tachyphylaxis 1/27/2019 8
  • 9. Other effects • ICP and IOP are both raised following administration of sux • The intragastric pressure increases by 7- 12cmH2O, the lower esophageal sphincter tone simultaneously decreases with the use of suxamethonium • Serum potassium concentration is briefly increased in normal individual by 0.2- 0.4mmol/l 1/27/2019 9
  • 10. Toxicity & side effects • Bradycardia & other dysarrythmia • Hyperkalemia • Postoperative myalgia – in women middle age • Increases IOP,ICP & IGP • Triggering agent for malignant hyperthermia • Sux apnea • Anaphylactic reaction1/27/2019 10
  • 11. Metabolism • The drug is hydrolyzed by plasma cholinesterase to succinylmonocholine {which is weakly active} and choline • The former is further hydrolyzed by plasma cholinesterase to succinic acid and choline • 80% of administered dose is hydrolyzed before it reaches the NMJ 1/27/2019 11
  • 12. Special points • The incidence of muscle pain after administration of suxamethonium may be decreased by pre-treatment with A low dose {0.2mg/kg} dose of sux A small dose of a non-depolarizing relaxants Diazepam Aspirin or Vitamin C 1/27/2019 12