classification of general anaesthetics and pharmacokinetics

24
CLASSIFICATION OF CLASSIFICATION OF GENERAL ANAESTHETICS GENERAL ANAESTHETICS

Upload: bhavyalatha

Post on 27-May-2015

18.242 views

Category:

Education


2 download

TRANSCRIPT

Page 1: Classification of general anaesthetics and pharmacokinetics

CLASSIFICATION OF CLASSIFICATION OF GENERAL ANAESTHETICSGENERAL ANAESTHETICS

Page 2: Classification of general anaesthetics and pharmacokinetics

1.INHALATIONAL

Gases: N2O,Cyclopropane,Xenon

Liquids: Ether, Halothane,

Enflurane, Desflurane,

Isoflurane, Sevoflurane,

Methoxyflurane

Page 3: Classification of general anaesthetics and pharmacokinetics

2.INTRAVENOUS

Inducing Agents: Thiopentone sodium,

Methohexitone sodium,

Propofol, Etomidate

Dissociative Anaesthesia:Ketamine

Neuroleptanalgesia: Fentanyl+Droperidol

(Analgesic)(Neuroleptic)

BZDs: Diazepam,Lorazepam,Midazolam

Page 4: Classification of general anaesthetics and pharmacokinetics

Pharmacokinetics• Rapidly diffuse across the alveoli

• Alveoli blood brain

• Depth of anaesthesia-potency & pp

• Induction & Recovery-rate of change of pp

Page 5: Classification of general anaesthetics and pharmacokinetics

Minimum Alveolar Concentration

• Conc of the inhalational GA that renders 50% of the subjects immobile when exposed to a strong noxious stimulus Halothane 0.75%

Ether 1.9%

Enflurane 1.68%

Isoflurane 1.2%

Desflurane 6%

Sevoflurane 2%

Nitrous oxide 105%

Page 6: Classification of general anaesthetics and pharmacokinetics

• 0.3 MAC→mild analgesia

• 0.5 MAC→amnesia

• 1.0 MAC→50% patients immobile even after stimulation

• 1.3 MAC→sympathetically mediated response blunted

• 2.0 MAC→potentially lethal

• MAC α 1/Potency

Page 7: Classification of general anaesthetics and pharmacokinetics

Minimum Alveolar Concentration

limitations1. Leaves 50% subjects

2. At 1.3MAC awareness & recall may still exist

3. Large no. of patients receive muscle relaxants

4. Other indicators of awareness-highly suggestive when present but not definitive when absent

5. A patient who moves with incision is not necessarily awake &one who does not move is not necessarily unconscious

Page 8: Classification of general anaesthetics and pharmacokinetics

Factors affecting pp of anaesthetic in brain

• PP of anaesthetic in inspired air• Pulmonary ventilation rate• Alveolar exchange• Solubility of anaesthetic in blood• Solubility of anaesthetic in tissues• Cerebral blood flow

Page 9: Classification of general anaesthetics and pharmacokinetics

1.PP of the anaesthetic in 1.PP of the anaesthetic in inspired airinspired air

Page 10: Classification of general anaesthetics and pharmacokinetics

PP of the anaesthetic in inspired air

• Increase in inspired anaesthetic conc increases the rate of induction of anaesthesia by increasing the rate of transfer into blood according to Fick’s Law

• Used for mod soluble-halothane- 3-4% →1-2%

Page 11: Classification of general anaesthetics and pharmacokinetics

Fick’s Law of Diffusion

Flux=diff in conc x A x Permeability

• Thickness of the path

Page 12: Classification of general anaesthetics and pharmacokinetics

2.PULMONARY VENTILATION

lung animation.gif

Page 13: Classification of general anaesthetics and pharmacokinetics

2.Pulmonary Ventilation Rate

• The rate of rise of anaesthetic gas conc in the arterial blood is directly dependent on both rate & depth of ventilation

• Effects- solubility

• 4x ↑ In VR 2x T of halothane bt only 15% ↑ in T of nitrous oxide

Page 14: Classification of general anaesthetics and pharmacokinetics

3.ALVEOLAR EXCHANGE

Page 15: Classification of general anaesthetics and pharmacokinetics

ALVEOLAR EXCHANGE

• GAs diffuse freely across alveoli

• Ventilation Perfusion mismatch delays the attainment of equilibrium between blood and alveoli

Page 16: Classification of general anaesthetics and pharmacokinetics

4.SOLUBILITY IN BLOOD

Page 17: Classification of general anaesthetics and pharmacokinetics

SOLUBILITY IN BLOOD

• One of the most important factor

• Blood:Gas Partition co efficient –index of solubility

• When an anaesthetic with low solubility diffuses from alveoli into arterial blood, relatively few molecules are required to raise its partial pressure and therefore its arterial tension rises rapidly

Page 18: Classification of general anaesthetics and pharmacokinetics

5.SOLUBILITY IN TISSUES5.SOLUBILITY IN TISSUES

Page 19: Classification of general anaesthetics and pharmacokinetics

SOLUBILITY IN TISSUES

• Relative solubility of the anaesthetic in blood and tissue determines its conc in the tissue at equilibrium

• expressed as tissue : blood pc

• =ly soluble in lean tissue & blood. More soluble in fat

• Conc ↑ in white than in grey matter

Page 20: Classification of general anaesthetics and pharmacokinetics

6.CEREBRAL BLOOD FLOW6.CEREBRAL BLOOD FLOW

Page 21: Classification of general anaesthetics and pharmacokinetics

CEREBRAL BLOOD FLOW

• Brain is highly perfused

• GAs are quickly delivered

• CO2 inhalation

Page 22: Classification of general anaesthetics and pharmacokinetics

Second gas effect

• When certain gases like nitrous oxide are administered in high conc, the other anaesthetic gases are also pulled in and their alveolar tension rises more rapidly

• Eg: halothane when given with N2O, delivered at same rate

Page 23: Classification of general anaesthetics and pharmacokinetics

Concentration effect

• When an anaesthetic is administered in high conc, its alveolar tension rises more rapidly than when the same gas is inhaled in lower conc.

Page 24: Classification of general anaesthetics and pharmacokinetics

eElimination• gradients reversed

• Through lungs- unchanged,

• Metabolism-halothane>20% in liver

• Lipid soluble anaesthetic-delayed recovery