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General Anesthetics & Pre-Anesthetics
 BY
 ASAWE TEJASWINI L
 DEPARTMENT OF PHARMACOLOGY
 ASSIASTANT PROFESSOR
 SIDHHIS INSTITUTE OF PHARMACY
 THANE
General Anesthetics
 an anaesthetic that affects the whole body and
usually causes a loss of consciousness.
 The goal of general anesthesia is to produce
analgesia, unconsciousness and amnesia
 Loss of pain perception, Loss of awareness of one’s
surrounding, Inability to recall what took place
History of Anesthesia
Stages of Anesthesia
 There are 4 stages of Anesthesia
 Stage 1 : The Analgesia :
 The Analgesia stage begins with the inhalation of anesthesia
 Pain is Progressively abolished during this stage
 Patient remains conscious, can hear and see, and feels like a
dream state
 Stage 2 : The Excitement/Stage of Delirium :
 It starts from loss of consciousness to beginning of regular
respiration.
 Excitement is seen and the patient may shout, struggle and
hold breath, jaws are tightly closed.
 Vomiting, may occur.
 Heart rate & BP may rise and pupils dilate due to
sympathetic stimulation
 Stage 3 : Surgical Anesthesia :
 Moving eyeballs this stage ends when eyes becomes fixed
 Loss of corneal and Laryngeal reflexes
 Pupil start dilating and light reflex is lost.
 Stage 4 : Medullary Paralysis:
 This is the stage between respiratory arrest
and death due to circulatory collapse.
 In this stage medullary paralysis
cardiovascular & respiratory centres in
medulla are suppressed by anesthetics.
CLASSIFICATION OF GENERAL ANETHETICS
Classification
 A) Inhalation anesthetic –
 I. Nitrous oxide
 II. Cyclopropane
 Have rapid onset of action and rapid recovery
 III.Ethylene-
 Less toxic than other gas anesthetics
 B) Liquids
 Ether , Halothane , Isoflurane , Desflurane ,
Methoxyflurane .
 B) Intravenous anesthetic –
 a) Inducing agents
 Thiopentone sodium , Methohexitone sodium ,
Propofol
 b)Slowly Acting Drug –
 i)Benzodiazepins – Diazepam , Lorazepam ,
Midazolam
 ii)Dissociative anesthetics –
 Iii)Opoid analgesia
Anesthetic Agents
 The first attempt to use of “Intravenous Anesthesia” (they
quickly achieve high concentrations in the central nervous
system. ) was Discovered by “WREN” in 1656.
 “THIOPENTAL” is a barbiturate
 It is water soluble & alkaline in nature
 Thiopental produce rapid onset of actions and ultrashorts
recovery period
 It produce mild direct cardiac depression resulting into lower
BP.
 It is used for rapid control of convulsion.
Nitrous Oxide
• widely used
• Potent analgesic
• Produce a light anesthesia
• Do not depress the
respiration/vasomotor center
• Used ad adjunct to supplement
other inhalationals
Halothane
•Halothane is flurinated volatile
liquid with sweet odour , non irritant
, non-flammable, stored in amber
colured bottle .
• It is potent anesthetic .
•Non irritant , controls hypotension
•Potent and speedy recovery .
•Special apparatus is required for
administration.
•Reduce cardiac output
Isoflurane
smooth and rapid induction and
recovery
 very little metabolism (0.2%)
 most widely employed
 It producess less myocardial depression.
 Low nausea and vomitting
 It producess uterine muscle relaxation .
 It is expensive
Enflurane
 Enflurane is non- inflammable with mild sweet odour and boils at
57° C.
 Its action is similar to halothane .
 Rapid, smooth induction and maintenance
 2-10% metabolized in liver
 Introduced as replacement for halothane
 Depresses myocardial force of contraction and sensitize heart to
adrenalin
 Metabolism releases fluoride ion causes renal toxicity
Intravenous Induction Agents
 Commonly used IV induction
agents
Propofol
Thiopental sodium
Ketamine
Intravenous Anesthetics
• Intravenous (i.v.) anesthetics are unique drugs that
induce anesthesia rapidly as they quickly achieve
high concentrations in the central nervous system.
• Most exert their actions by potentiating GABAA
receptor
Thiopental sodium
• rapid onset (20 sec)
• short-acting iv anesthetics.
 Effect terminated not by metabolism but by
redistribution
Side effects
 Hypotension
 apnoea
 airway obstruction
Propofol
 Short-acting agent used for the
induction
 maintenance of GA and
sedation
 Onset within one minute of
injection
 It is highly protein bound in vivo and is metabolised
in the liver
Side-effect
 pain on injection
 hypotension
 transient apnoea following induction
Ketamine
 NMDA Receptor Antagonist
 usually stimulate circulatory system
 “METHOHEXITAL” it is similar to thiopentone and
three times more potent
 It has a quicker 5-8 min action.
 It more rapidly metabolized than Thiopentone
 “ETOMIDATE” it has direct CNS depressant & GABA
agonist
 “PROPOFOL” produce rapid onset and short duration
action
 It is also produces minimal nausea and vomiting
Slow Action Drugs
 “BENZODIAZEPINE(BZD)”
 produce sedation & amnesia by potentiating GABA receptors
 BDZ are poor analgesic
 BDZ decrease muscle tone by central action
 They do not provoke postoperative nausea or vomiting
 “DIAZEPAM” it is water insoluble produce venous irritation
 It is metabolized by liver and it is not redistributed
 “LORAZEPAM” it is similar to DIAZEPAM it is water insoluble produce
venous irritation
 “MIDAZOLAM” it is more potent than diazepam & lorazepam.
 It has minimal cardiac effects.
Dissociative Anesthesia
 “KETAMINE” pharmacologically katamine is
related to hallucinogen phencyclidine
 Ketamine has been recommended for operation on
the head & neck has bleed , and asthmatic patients
 It is good for repeated use particularly suitable for
burn dressing
 It may be dangerous for hypertensive & ischemic
heart.
Pre-Anesthetics/Pre-operative Medications
 SEDATIVE-HYPNOTIC
 OPIOIDS
 ANTIMETIC
 ANTICHOLINERGICS
 ANTIHISTAMINES
 NUROLEPTICS
This use of medication is IMP due to following
reasons
 For relief of Anxiety
 Decrease the Secretion
 Decrease Acidity & volume of Juice
 “SEDATIVE-ANTIANXIETY DRUGS”:
 They decreases the anxiety , providing amnesia,
 BZDs drug for preanesthetics, anxiolytics, sedation .
 Ex. Lorazepam , midazolam
 “OPIOIDS” :
 Morphine relieve anxiety.
 Reduce the dose of anesthesia
 It produce Pre- & Post-Operative analgesia
 Presurgical pain
 “ANTIMETIC” :
 Antiemetic enhance gastric emptying .
 They are prevent nausea , vomiting in patient
 Metaclopramide is effective in reducing Post-Operative vomiting.
 Ex. metoclopramide 10-20mg
 Domperidone
 “ANTICHOLINERGICS” :
 are drugs that block and inhibit the activity of the
neurotransmitter acetylcholine (ACh) at both central and
peripheral nervous system synapses.
 Atropine or Hyoscine has been used primarily to reduce salivary
& bronchial secretions.
 “ANTIHISTAMINES” : These are H2 blockers
 Ranitidine or Famotidine given in night
 Raising pH of gastric juice
 “NUROLEPTICS” :
Chlorpromazine,Trifluoprazine or Haloperidol's
are frequently use in premedication
 Relieve Anxiety
 Have Antiemetic action i.e. controls nausea and
vomiting
Thank you have nice day

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GA & Pre A.pptx

  • 1. General Anesthetics & Pre-Anesthetics  BY  ASAWE TEJASWINI L  DEPARTMENT OF PHARMACOLOGY  ASSIASTANT PROFESSOR  SIDHHIS INSTITUTE OF PHARMACY  THANE
  • 2. General Anesthetics  an anaesthetic that affects the whole body and usually causes a loss of consciousness.  The goal of general anesthesia is to produce analgesia, unconsciousness and amnesia  Loss of pain perception, Loss of awareness of one’s surrounding, Inability to recall what took place
  • 4.
  • 5. Stages of Anesthesia  There are 4 stages of Anesthesia  Stage 1 : The Analgesia :  The Analgesia stage begins with the inhalation of anesthesia  Pain is Progressively abolished during this stage  Patient remains conscious, can hear and see, and feels like a dream state  Stage 2 : The Excitement/Stage of Delirium :  It starts from loss of consciousness to beginning of regular respiration.  Excitement is seen and the patient may shout, struggle and hold breath, jaws are tightly closed.  Vomiting, may occur.  Heart rate & BP may rise and pupils dilate due to sympathetic stimulation
  • 6.  Stage 3 : Surgical Anesthesia :  Moving eyeballs this stage ends when eyes becomes fixed  Loss of corneal and Laryngeal reflexes  Pupil start dilating and light reflex is lost.  Stage 4 : Medullary Paralysis:  This is the stage between respiratory arrest and death due to circulatory collapse.  In this stage medullary paralysis cardiovascular & respiratory centres in medulla are suppressed by anesthetics.
  • 8. Classification  A) Inhalation anesthetic –  I. Nitrous oxide  II. Cyclopropane  Have rapid onset of action and rapid recovery  III.Ethylene-  Less toxic than other gas anesthetics  B) Liquids  Ether , Halothane , Isoflurane , Desflurane , Methoxyflurane .
  • 9.  B) Intravenous anesthetic –  a) Inducing agents  Thiopentone sodium , Methohexitone sodium , Propofol  b)Slowly Acting Drug –  i)Benzodiazepins – Diazepam , Lorazepam , Midazolam  ii)Dissociative anesthetics –  Iii)Opoid analgesia
  • 10. Anesthetic Agents  The first attempt to use of “Intravenous Anesthesia” (they quickly achieve high concentrations in the central nervous system. ) was Discovered by “WREN” in 1656.  “THIOPENTAL” is a barbiturate  It is water soluble & alkaline in nature  Thiopental produce rapid onset of actions and ultrashorts recovery period  It produce mild direct cardiac depression resulting into lower BP.  It is used for rapid control of convulsion.
  • 11. Nitrous Oxide • widely used • Potent analgesic • Produce a light anesthesia • Do not depress the respiration/vasomotor center • Used ad adjunct to supplement other inhalationals
  • 12. Halothane •Halothane is flurinated volatile liquid with sweet odour , non irritant , non-flammable, stored in amber colured bottle . • It is potent anesthetic . •Non irritant , controls hypotension •Potent and speedy recovery . •Special apparatus is required for administration. •Reduce cardiac output
  • 13. Isoflurane smooth and rapid induction and recovery  very little metabolism (0.2%)  most widely employed  It producess less myocardial depression.  Low nausea and vomitting  It producess uterine muscle relaxation .  It is expensive
  • 14. Enflurane  Enflurane is non- inflammable with mild sweet odour and boils at 57° C.  Its action is similar to halothane .  Rapid, smooth induction and maintenance  2-10% metabolized in liver  Introduced as replacement for halothane  Depresses myocardial force of contraction and sensitize heart to adrenalin  Metabolism releases fluoride ion causes renal toxicity
  • 15. Intravenous Induction Agents  Commonly used IV induction agents Propofol Thiopental sodium Ketamine
  • 16. Intravenous Anesthetics • Intravenous (i.v.) anesthetics are unique drugs that induce anesthesia rapidly as they quickly achieve high concentrations in the central nervous system. • Most exert their actions by potentiating GABAA receptor
  • 17. Thiopental sodium • rapid onset (20 sec) • short-acting iv anesthetics.  Effect terminated not by metabolism but by redistribution
  • 18. Side effects  Hypotension  apnoea  airway obstruction
  • 19. Propofol  Short-acting agent used for the induction  maintenance of GA and sedation  Onset within one minute of injection
  • 20.  It is highly protein bound in vivo and is metabolised in the liver Side-effect  pain on injection  hypotension  transient apnoea following induction
  • 21. Ketamine  NMDA Receptor Antagonist  usually stimulate circulatory system
  • 22.  “METHOHEXITAL” it is similar to thiopentone and three times more potent  It has a quicker 5-8 min action.  It more rapidly metabolized than Thiopentone  “ETOMIDATE” it has direct CNS depressant & GABA agonist  “PROPOFOL” produce rapid onset and short duration action  It is also produces minimal nausea and vomiting
  • 23. Slow Action Drugs  “BENZODIAZEPINE(BZD)”  produce sedation & amnesia by potentiating GABA receptors  BDZ are poor analgesic  BDZ decrease muscle tone by central action  They do not provoke postoperative nausea or vomiting  “DIAZEPAM” it is water insoluble produce venous irritation  It is metabolized by liver and it is not redistributed  “LORAZEPAM” it is similar to DIAZEPAM it is water insoluble produce venous irritation  “MIDAZOLAM” it is more potent than diazepam & lorazepam.  It has minimal cardiac effects.
  • 24. Dissociative Anesthesia  “KETAMINE” pharmacologically katamine is related to hallucinogen phencyclidine  Ketamine has been recommended for operation on the head & neck has bleed , and asthmatic patients  It is good for repeated use particularly suitable for burn dressing  It may be dangerous for hypertensive & ischemic heart.
  • 25. Pre-Anesthetics/Pre-operative Medications  SEDATIVE-HYPNOTIC  OPIOIDS  ANTIMETIC  ANTICHOLINERGICS  ANTIHISTAMINES  NUROLEPTICS
  • 26. This use of medication is IMP due to following reasons  For relief of Anxiety  Decrease the Secretion  Decrease Acidity & volume of Juice
  • 27.  “SEDATIVE-ANTIANXIETY DRUGS”:  They decreases the anxiety , providing amnesia,  BZDs drug for preanesthetics, anxiolytics, sedation .  Ex. Lorazepam , midazolam  “OPIOIDS” :  Morphine relieve anxiety.  Reduce the dose of anesthesia  It produce Pre- & Post-Operative analgesia  Presurgical pain
  • 28.  “ANTIMETIC” :  Antiemetic enhance gastric emptying .  They are prevent nausea , vomiting in patient  Metaclopramide is effective in reducing Post-Operative vomiting.  Ex. metoclopramide 10-20mg  Domperidone  “ANTICHOLINERGICS” :  are drugs that block and inhibit the activity of the neurotransmitter acetylcholine (ACh) at both central and peripheral nervous system synapses.  Atropine or Hyoscine has been used primarily to reduce salivary & bronchial secretions.
  • 29.  “ANTIHISTAMINES” : These are H2 blockers  Ranitidine or Famotidine given in night  Raising pH of gastric juice  “NUROLEPTICS” : Chlorpromazine,Trifluoprazine or Haloperidol's are frequently use in premedication  Relieve Anxiety  Have Antiemetic action i.e. controls nausea and vomiting
  • 30. Thank you have nice day