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GENERAL ANAESTHETICS
Presented by:
Akansh Goel
M.Pharm (Pharmacology)
1st semester 1
Contents
 Introduction
 Stages & Phases of anaesthesia
 Classification
 Pharmacokinetics
 Pharmacodynamics
 Techniques of anaesthesia
 Complications & Contraindications
 Drug Interactions
 Pre-anaesthetics
 Bibliography
2
Introduction
 Reversible, Drug-induced loss of sensations and
consciousness to stimuli.
• Depresses the Nervous System
 Anaesthetic state
• Changes in behaviour or perception.
Amnesia , immobility and muscle relaxation , abolition of
somatic and autonomic reflexes, analgesia, hypnosis.
3
General
Anaesthesia
Pain Relief
Muscle
Relaxation
Sleep
Essential Components Of
Anaesthesia
• Hypnosis – Loss of consciousness
• Reversible loss of sensations
• Amnesia – Loss of memory
• Analgesia – Loss of perception of pain
• Immobility – Loss of motor reflexes
• Skeletal muscle relaxation
• Quick acting and rapid eliminated
• No toxic effects – Large margin of safety
4
• Pleasant, non irritating, no after effects, fast
recovery
For Patient
• Provide - Adequate analgesia, Immobility,
muscle relaxation and non inflammable
For Surgeon
• Easy administration, cheap, stable, safe, easy to
store, long shelf-life
For Anaesthetist
Properties of ideal anaesthetics
5
Stages
1.
• Stage of Analgesia
2.
• Stage of Delirium
3.
• Surgical Anaesthesia
4.
• Medullary Paralysis
6
1.
• Induction
2.
• Maintenance
3.
• Recovery
Phases
MaintaineneInduction Recovery
Duration in Hours
Concentration
Inplasma
Inhalation
Or
Infusion
7
Classification
General
Anaesthetics
Inhalational
agents
Volatile
Liquids
Gaseous
Intravenous
agents
Fast Acting drugs
(Inducing agents)
Slower Acting
Drugs
Benzodiazepines Opioids Neuroleptic
agent
8
Volatile Liquids
- Chloroform
- Ether
- Halothane
- Enflurane
- Isoflurane
- Desflurane
- Sevoflurane
- Methoxyflurane
Inducing agents
- Thiopentone
- Methohexitone
- Propofol
- Etomidate
- Ketamine
(Dissociative)
Gases
- Nitrous oxide
- Entonox
- Xenon
Opioids
- Fentanyl
- Remifentail
- Sufentanil
- Alfentanil
Benzodiazepines
- Diazepam
- Lorazepam
- Midazolam
Neuroleptic agent
- Droperidol
Drugs
9
Pharmacokinetics
• Depth of anaesthesia depends on Potency of the agent
(MAC) and Partial Pressure (PP) attained in the brain.
• Induction and recovery depends on rate of change of
PP in brain.
10
Factors affecting PP of
anaesthetics in Brain
1. PP of anaesthetic in the inspired gas
2. Pulmonary ventilation
3. Alveolar exchange
4. Solubility of anaesthetic in blood –
Blood: gas partition coefficient
5. Solubility in tissues
6. Cerebral blood flow
11
Elimination
• Mostly through lungs in unchanged form.
• Channel of absorption channel of elimination.
• Enter and persists in adipose tissue for long periods –
high lipid solubility and low blood flow.
• They are not metabolized except Halothane.
• Second gas effect
• Diffusion hypoxia
12
Properties of Inhaled Anaesthetics
13
Minimal Alveolar Concentration (MAC)
• Smaller the MAC value more potent is the anaesthetic
and vice versa.
Arteriovenous concentration Gradient(ACG)
• Smaller the ACG value faster will be the onset of
action and vice versa.
Blood – Gas partition coefficient
• Smaller the B/G partition coefficient value faster will
be the onset of action and vice versa.
• Rank order of MAC values(%) of different
inhalational anaesthetics –
High
Methoxyflurane (0.16%)
Halothane (0.75%)
Isoflurane (1.2%)
Enflurane (1.7%)
Sevoflurane (1.9%)
Desflurane (6%)
Nitrous oxide (>100%)
Low
14
Potency
Points to Remember..
Blood solubility – Rate of Induction
Lipid solubility – Potency
A/V Gradient – Rate of Induction
Partial Pressure – Potency
B/G partition coefficient – Rate of Induction
15
Pharmacodynamics
No specific receptor has been identified as the locus
of general anesthetic action. They -
• Increases the activity of GABA receptors.
• Increases the activity of the glycine receptors.
• Blocks postsynaptic nicotinic currents.
• Inhibit the activity of Glutamate receptors.
16
Note: The mechanism by which the anesthetics perform
these modulatory roles is not understood.
Techniques of
Inhalation GA
Through
Anaesthetic
machines
Open
system
Closed
system
Semiclosed
system
Open drop
method
17
Techniques
Complications
During anaesthesia:
• Respiratory depression
• Cardiac arrhythmias
• Fall in BP & Aspiration
• Laryngospasm and
asphyxia
• Delirium and convulsion
• Fire and explosion
After anaesthesia:
• Nausea and vomiting
• Persisting sedation
• Pneumonia
• Organ damage – liver,
kidney
• Nerve palsies
• Cognitive defects
18
Contraindications
19
M A S
Medical Problems
Like Diabetes, Asthma,
High Blood Pressure
Alcohol
Intake
Smoking
Drug Interactions
1. Patients on antihypertensives given general anaesthetics—
BP may fall markedly.
2. Neuroleptics, opioids, clonidine and monoamine oxidase
inhibitors potentiate anaesthetics.
3. Halothane sensitizes the heart to Adrenaline.
4. Insulin need of a diabetic is increased during GA: switch
over to plain insulin even if the patient is on oral
hypoglycaemics.
20
Pre- anaesthetics
medication
Defination: It is the term applied to the use of drugs
prior to the administration of an anaesthetic agent to
make anaesthesia safer and more agreeable to the
patient.
21
- Analgesia
- Relief of anxiety
- Amnesia for pre and
post operative events
- Decrease secretions
- Antiemetic effects
- Decrease acidity and
volume of gastric juice
Aim
Drugs
 Sedative- antianxiety drugs – Diazepam, Lorazepam
 Opoids – Morphine, Pethidine
 Anticholinergics – Atropine, Hyoscine, Glycopyrrolate
 Neuroleptics – Chlorpromazine, Haloperidol
 H2- blockers / Proton pump inhibitors – Ranitidine,
Famotidine, Omeprazole, Pantoprazole
 Antiemetics – Metoclopramide, Domperidone,
Ondansetron
22
23
Bibliography
• Goodman, L.S., 2011. Goodman and Gilman's the
pharmacological basis of therapeutics (pp. 527-547). New
York: McGraw-Hill.
• Tripathi, K.D., 2018. Essentials of medical pharmacology.
(Pp. 399- 414) Jaypee Brothers Medical Publishers, New
Delhi.
• Garg, G.R. and Gupta, S., 2018. Review of pharmacology. (Pp.
294-300) Jaypee Brothers Medical Publishers (p) Limited.
• Harvey, R.A., Clark, M.A., Finkel, R., Rey, J.A. and Whalen,
K., 2012. Lippincott’s illustrated reviews: Pharmacology
Medicine and Science in Sports and Exercise, 538.
24
Contd..
• https://www.slideshare.net/DeepakKumarGupta2/general-
anaesthesia-52366531 accessed on 14/11/18.
• Katzung, B.G. and Trevor, A.J. eds., 2015. Basic & clinical
pharmacology (pp. 753-756). New York, NY: McGraw-Hill.
• https://www.slideshare.net/mayur238/general-anaesthesia-
46670800 accessed on 17/11/18.
• https://www.slideshare.net/drswarnankparmar/preanaesthetic-
medication-general-anaesthetics accessed on 17/11/18.
25
Thank You
26

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General Anesthetics

  • 1. GENERAL ANAESTHETICS Presented by: Akansh Goel M.Pharm (Pharmacology) 1st semester 1
  • 2. Contents  Introduction  Stages & Phases of anaesthesia  Classification  Pharmacokinetics  Pharmacodynamics  Techniques of anaesthesia  Complications & Contraindications  Drug Interactions  Pre-anaesthetics  Bibliography 2
  • 3. Introduction  Reversible, Drug-induced loss of sensations and consciousness to stimuli. • Depresses the Nervous System  Anaesthetic state • Changes in behaviour or perception. Amnesia , immobility and muscle relaxation , abolition of somatic and autonomic reflexes, analgesia, hypnosis. 3 General Anaesthesia Pain Relief Muscle Relaxation Sleep
  • 4. Essential Components Of Anaesthesia • Hypnosis – Loss of consciousness • Reversible loss of sensations • Amnesia – Loss of memory • Analgesia – Loss of perception of pain • Immobility – Loss of motor reflexes • Skeletal muscle relaxation • Quick acting and rapid eliminated • No toxic effects – Large margin of safety 4
  • 5. • Pleasant, non irritating, no after effects, fast recovery For Patient • Provide - Adequate analgesia, Immobility, muscle relaxation and non inflammable For Surgeon • Easy administration, cheap, stable, safe, easy to store, long shelf-life For Anaesthetist Properties of ideal anaesthetics 5
  • 6. Stages 1. • Stage of Analgesia 2. • Stage of Delirium 3. • Surgical Anaesthesia 4. • Medullary Paralysis 6
  • 7. 1. • Induction 2. • Maintenance 3. • Recovery Phases MaintaineneInduction Recovery Duration in Hours Concentration Inplasma Inhalation Or Infusion 7
  • 9. Volatile Liquids - Chloroform - Ether - Halothane - Enflurane - Isoflurane - Desflurane - Sevoflurane - Methoxyflurane Inducing agents - Thiopentone - Methohexitone - Propofol - Etomidate - Ketamine (Dissociative) Gases - Nitrous oxide - Entonox - Xenon Opioids - Fentanyl - Remifentail - Sufentanil - Alfentanil Benzodiazepines - Diazepam - Lorazepam - Midazolam Neuroleptic agent - Droperidol Drugs 9
  • 10. Pharmacokinetics • Depth of anaesthesia depends on Potency of the agent (MAC) and Partial Pressure (PP) attained in the brain. • Induction and recovery depends on rate of change of PP in brain. 10
  • 11. Factors affecting PP of anaesthetics in Brain 1. PP of anaesthetic in the inspired gas 2. Pulmonary ventilation 3. Alveolar exchange 4. Solubility of anaesthetic in blood – Blood: gas partition coefficient 5. Solubility in tissues 6. Cerebral blood flow 11
  • 12. Elimination • Mostly through lungs in unchanged form. • Channel of absorption channel of elimination. • Enter and persists in adipose tissue for long periods – high lipid solubility and low blood flow. • They are not metabolized except Halothane. • Second gas effect • Diffusion hypoxia 12
  • 13. Properties of Inhaled Anaesthetics 13 Minimal Alveolar Concentration (MAC) • Smaller the MAC value more potent is the anaesthetic and vice versa. Arteriovenous concentration Gradient(ACG) • Smaller the ACG value faster will be the onset of action and vice versa. Blood – Gas partition coefficient • Smaller the B/G partition coefficient value faster will be the onset of action and vice versa.
  • 14. • Rank order of MAC values(%) of different inhalational anaesthetics – High Methoxyflurane (0.16%) Halothane (0.75%) Isoflurane (1.2%) Enflurane (1.7%) Sevoflurane (1.9%) Desflurane (6%) Nitrous oxide (>100%) Low 14 Potency
  • 15. Points to Remember.. Blood solubility – Rate of Induction Lipid solubility – Potency A/V Gradient – Rate of Induction Partial Pressure – Potency B/G partition coefficient – Rate of Induction 15
  • 16. Pharmacodynamics No specific receptor has been identified as the locus of general anesthetic action. They - • Increases the activity of GABA receptors. • Increases the activity of the glycine receptors. • Blocks postsynaptic nicotinic currents. • Inhibit the activity of Glutamate receptors. 16 Note: The mechanism by which the anesthetics perform these modulatory roles is not understood.
  • 18. Complications During anaesthesia: • Respiratory depression • Cardiac arrhythmias • Fall in BP & Aspiration • Laryngospasm and asphyxia • Delirium and convulsion • Fire and explosion After anaesthesia: • Nausea and vomiting • Persisting sedation • Pneumonia • Organ damage – liver, kidney • Nerve palsies • Cognitive defects 18
  • 19. Contraindications 19 M A S Medical Problems Like Diabetes, Asthma, High Blood Pressure Alcohol Intake Smoking
  • 20. Drug Interactions 1. Patients on antihypertensives given general anaesthetics— BP may fall markedly. 2. Neuroleptics, opioids, clonidine and monoamine oxidase inhibitors potentiate anaesthetics. 3. Halothane sensitizes the heart to Adrenaline. 4. Insulin need of a diabetic is increased during GA: switch over to plain insulin even if the patient is on oral hypoglycaemics. 20
  • 21. Pre- anaesthetics medication Defination: It is the term applied to the use of drugs prior to the administration of an anaesthetic agent to make anaesthesia safer and more agreeable to the patient. 21 - Analgesia - Relief of anxiety - Amnesia for pre and post operative events - Decrease secretions - Antiemetic effects - Decrease acidity and volume of gastric juice Aim
  • 22. Drugs  Sedative- antianxiety drugs – Diazepam, Lorazepam  Opoids – Morphine, Pethidine  Anticholinergics – Atropine, Hyoscine, Glycopyrrolate  Neuroleptics – Chlorpromazine, Haloperidol  H2- blockers / Proton pump inhibitors – Ranitidine, Famotidine, Omeprazole, Pantoprazole  Antiemetics – Metoclopramide, Domperidone, Ondansetron 22
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  • 24. Bibliography • Goodman, L.S., 2011. Goodman and Gilman's the pharmacological basis of therapeutics (pp. 527-547). New York: McGraw-Hill. • Tripathi, K.D., 2018. Essentials of medical pharmacology. (Pp. 399- 414) Jaypee Brothers Medical Publishers, New Delhi. • Garg, G.R. and Gupta, S., 2018. Review of pharmacology. (Pp. 294-300) Jaypee Brothers Medical Publishers (p) Limited. • Harvey, R.A., Clark, M.A., Finkel, R., Rey, J.A. and Whalen, K., 2012. Lippincott’s illustrated reviews: Pharmacology Medicine and Science in Sports and Exercise, 538. 24
  • 25. Contd.. • https://www.slideshare.net/DeepakKumarGupta2/general- anaesthesia-52366531 accessed on 14/11/18. • Katzung, B.G. and Trevor, A.J. eds., 2015. Basic & clinical pharmacology (pp. 753-756). New York, NY: McGraw-Hill. • https://www.slideshare.net/mayur238/general-anaesthesia- 46670800 accessed on 17/11/18. • https://www.slideshare.net/drswarnankparmar/preanaesthetic- medication-general-anaesthetics accessed on 17/11/18. 25