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Intravenous
General
Anesthetics
KKK
Overview
• A General Anaesthetic is a drug that produces a
reversible state of unconscious with absence of
pain sensation over the entire body; such agents
have been described as drugs that remove the
most precious human attributes ---- Conscious.
• For a drug to be useful as a general anaesthetic, its
actions must be of rapid onset.
Intravenous Anaesthetics
• Used for induction or maintenance of general
anaesthesia, sedation and to induce amnesia.
Major
Groups
Barbiturates Thiopental
Non-
Barbiturates
KETAMINE
Propofol
Ketamine
• Brand name: KETALAR
• Phencyclidine derivative
• Shorting acting
• Mainly used in children and
elderly adults for short
procedures such as burns
dressing.
• ABUSIVE DRUG
Drug of Abuse!!!!!
• Is a dissociative anaesthetic as it produces a
cataleptic state in which the patient appears to be
awake but is detached from the environment and
is unresponsive to pain.
• Ketamine is frequently described as a "unique
drug" because it has hypnotic, analgesic and
amnesic effects - no other drug used in clinical
practice combines these three important features.
Pharmacokinetics
Given IV or IM therefore:
• Rapid onset of action: 30 to 60 sec.
Distribution
Initially is distributed to highly perfused tissues
such as brain.
Extreme lipid solubility ensures its rapid transfer
across the BBB.
• Volume of distribution: 2.5-3.5 lit/kg
Metabolism
Hepatic microsomal enzymes cytochrome P450
by N-demethylation to form nor ketamine
which is hydroxylated and conjugated to water
soluble glucuronide derivatives and excreted
in urine.
Elimination
• Elimination half
time: 2-3 hours
• High hepatic
clearance rate: 1
L/min
Mode of Action (PD)
• Antagonises N-methyl-
D- aspartate (NMDA)
receptors; also interacts
with muscarinic
receptor, descending
monoaminergic pain
pathways, voltage-
sensitive calcium
channels and opioid
receptors in brain and
spinal cord.
Clinical Uses
• Sedation
• Amnesia
• Immobility
• Analgesic
• Loss of consciousness
• Pain relief in post
operative care (instead
of morphine)
Effect on Body System
Cardiovascular
• Stimulates sympathetic flow, causing
stimulation of heart with increased BP and CO.
• The heart rate is increased by about 20% - the
overall effect is therefore to increase the
workload of the heart.
(Contraindicated in hypertensive or stroke
patient)
Respiratory
• Causes Bronchodilation
(Potent Bronchodilator)
(Beneficial in patients with
hypovolemic or cardiogenic shock
and in asthmatics)
CNS
Lipophilic drug therefore
enters CNS quickly.
This causes hallucinations,
sedations.
Good analgesic effect.
• Potent cerebral
vasodilator & capable of
increasing cerebral blood
flow by 60% in normal
individual
Dosage
• Same doses are used for adults and children.
Induction
IV, 1-4.5mg/kg
IM, 6.5- 12mg/kg
Drug Interaction
Atracurium + Ketamine (will reduce dose of
atracurium)
used for skeletal muscle
relaxation in anaesthesia and intensive care.
Adverse Effects
• BP & Pulse rate
• muscle tone (sometimes
tonic-clonic & resembling
seizures)
• Lacrimation
• Salivation
• Intracranial pressure & IOP
• Nausea & Vomiting 
Reference
• Australian medicines handbook 2016 (2016) 2016th edn.
Australia: Australian Medicines Handbook Pty.
• Knights, K. and Miners, J.O. (2015) Pharmacology for health
professionals Workbook. 4th edn. Australia: Harcourt
Publishers Group (Australia) Pty.
• Whalen, K. and Pharmacology (2014) Lippincott illustrated
reviews: Pharmacology. Edited by Richard A. Harvery. 6th
edn. United States: Lippincott Williams and Wilkins.
• EPSVideoOnline (2014) Club drugs: Ketamine. Available at:
https://www.youtube.com/watch?v=z92LTc1ZX40
(Accessed: 5 May 2016).
Ketamine

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Ketamine

  • 2. Overview • A General Anaesthetic is a drug that produces a reversible state of unconscious with absence of pain sensation over the entire body; such agents have been described as drugs that remove the most precious human attributes ---- Conscious. • For a drug to be useful as a general anaesthetic, its actions must be of rapid onset.
  • 3. Intravenous Anaesthetics • Used for induction or maintenance of general anaesthesia, sedation and to induce amnesia. Major Groups Barbiturates Thiopental Non- Barbiturates KETAMINE Propofol
  • 4. Ketamine • Brand name: KETALAR • Phencyclidine derivative • Shorting acting • Mainly used in children and elderly adults for short procedures such as burns dressing. • ABUSIVE DRUG
  • 6. • Is a dissociative anaesthetic as it produces a cataleptic state in which the patient appears to be awake but is detached from the environment and is unresponsive to pain. • Ketamine is frequently described as a "unique drug" because it has hypnotic, analgesic and amnesic effects - no other drug used in clinical practice combines these three important features.
  • 7. Pharmacokinetics Given IV or IM therefore: • Rapid onset of action: 30 to 60 sec. Distribution Initially is distributed to highly perfused tissues such as brain. Extreme lipid solubility ensures its rapid transfer across the BBB. • Volume of distribution: 2.5-3.5 lit/kg
  • 8. Metabolism Hepatic microsomal enzymes cytochrome P450 by N-demethylation to form nor ketamine which is hydroxylated and conjugated to water soluble glucuronide derivatives and excreted in urine.
  • 9. Elimination • Elimination half time: 2-3 hours • High hepatic clearance rate: 1 L/min
  • 10. Mode of Action (PD) • Antagonises N-methyl- D- aspartate (NMDA) receptors; also interacts with muscarinic receptor, descending monoaminergic pain pathways, voltage- sensitive calcium channels and opioid receptors in brain and spinal cord.
  • 11. Clinical Uses • Sedation • Amnesia • Immobility • Analgesic • Loss of consciousness • Pain relief in post operative care (instead of morphine)
  • 12. Effect on Body System Cardiovascular • Stimulates sympathetic flow, causing stimulation of heart with increased BP and CO. • The heart rate is increased by about 20% - the overall effect is therefore to increase the workload of the heart. (Contraindicated in hypertensive or stroke patient)
  • 13. Respiratory • Causes Bronchodilation (Potent Bronchodilator) (Beneficial in patients with hypovolemic or cardiogenic shock and in asthmatics)
  • 14. CNS Lipophilic drug therefore enters CNS quickly. This causes hallucinations, sedations. Good analgesic effect. • Potent cerebral vasodilator & capable of increasing cerebral blood flow by 60% in normal individual
  • 15. Dosage • Same doses are used for adults and children. Induction IV, 1-4.5mg/kg IM, 6.5- 12mg/kg Drug Interaction Atracurium + Ketamine (will reduce dose of atracurium) used for skeletal muscle relaxation in anaesthesia and intensive care.
  • 16. Adverse Effects • BP & Pulse rate • muscle tone (sometimes tonic-clonic & resembling seizures) • Lacrimation • Salivation • Intracranial pressure & IOP • Nausea & Vomiting 
  • 17.
  • 18. Reference • Australian medicines handbook 2016 (2016) 2016th edn. Australia: Australian Medicines Handbook Pty. • Knights, K. and Miners, J.O. (2015) Pharmacology for health professionals Workbook. 4th edn. Australia: Harcourt Publishers Group (Australia) Pty. • Whalen, K. and Pharmacology (2014) Lippincott illustrated reviews: Pharmacology. Edited by Richard A. Harvery. 6th edn. United States: Lippincott Williams and Wilkins. • EPSVideoOnline (2014) Club drugs: Ketamine. Available at: https://www.youtube.com/watch?v=z92LTc1ZX40 (Accessed: 5 May 2016).