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Anesthesia
262
GENERAL ANESTHESIA
Def.:
CNS depressant, characterized by: loss of consciousness, loss of sensation &
adequate m. relaxation.
Stages of GA.:
1- Stage I : Stage of induction or analgesia
2- Stage II : Stage of excitement or delirium (Dilated reactive pupil)
3- Stage III: Stage of Surgical anesthesia ( Normal pupil)
It is divided into 4 Planes
4- Stage VI: Stage of medullary paralysis (Dilated non-reactive pupil)
Mechanism of action:
Either : - GABA
- NMDA of Glutamate
Classification:
Inhalation I.V.
Gases Volatile liquide 1- Ultra short Barbiturate
2- Non Barbiturate:
Nitrous 1- Halothane - Benzodiazepines
Oxide 2- Enflurane - Propofol
3- Isoflurane - Propanidid
4- Desflurane - Neurolept analgesia
5- Methoxyflurane - Etomidate
6- Trichloro-ethylene - Ketamine
7- Ethylchloride
8- Ether (obsolete)
9- Chloroform (obsolete)
N.B.:
- Most of anesthetics stop respiration before circulation, while chloroform stops
respiration with circulation
- Recovery occurs in reverse order. CO2 & O2 administration can fasten
recovery in inhalation anesthesia
- The onset of action of anesthetic depends on its solubility in blood, thus:
• N2O has low solubility & rapid onset, while
• Methoxyflurane has high solubility & delayed onset.
Anesthesia
263
Inhalation anesthesia
Halothane N2O
Advantages:
1- Non-inflammable & non-explosive
2- Non-irritant
3- Produces broncho-dilatation
4- Produces controlled hypotension
Advantages:
1- Non-inflammable & non-explosive
2- Non-irritant
3- Rapid induction & recovery
4- Good analgesics in labour
5- Safe on :CVS , Resp., Vital organs
Disadvantage:
1- Weak analgesic
2- Weak sk.m. relaxants
3- Uterine relaxant
4- Cardiotoxic:
- Stage 1: Bradycardia
- Stage 2: sensetize the
heart to catecholamine
arrhythmia
- Stage 3: direct depressant
5- Hepatotoxic
6- Malignant hyperthermia
7- Expensive
Disadvantage:
1- Weak anesthetic
2- Weak sk.m. relaxants
3- Produces Diffusion hypoxia: during
recovery it diffuses rapidly O2
conc. In alveoli Hypoxia, so give
O2 during recovery
4- Megaloblastic anemia
5- Teratogenic: to both patient & doctor
N.B.:
- Enflurane : As Halothane but no hepatic toxicity
& less sensitization of heart to catecholamines
- Isoflurane & Desflurane: As Enflurane but:
do not sensitize heart to catecholamines.
- Methoxyflurane: Cardiotoxic & Nephrotoxic
- Balanced anasthesia : N2O + Halothane
Minimal alveolar anesthetic concentration (MAC):
- Definition: It is the minimal alveolar anesthetic concentration at which 50 % of
patients do not respond to a surgical stimulus
- Importance: it is a measure of anesthetic potency, MAC is small for potent
anesthetics, as halothane & large for weak anesthetics as N2O
Anesthesia
264
I.V. Anesthesia
Advantages:
a. Easy
b. Rapid induction & recovery
c. No irritation of respiratory tract
d. No sensitization of heart to catecholamines
e. No post-operative nausea or vomiting
f. No explosive hazards
Disadvantages: Once injected, cannot be withdrawn
1- Ultrashort Barbiturate
Thiopental, Methohexital & Hexobarbital
*Kinetics: - Rapidly absorbed
- Passes BBB & Placental barrier
- Fate: Redistribution & slow metabolism Accumulation
NB.: 1- Methohexital is metabolized faster Rapid onset – rapid recovery – little effect
on Bl.Pr.
2- Thiopental (highly alkaline, as it is prepared in the form of Na solution) should
not mixed with Succinylcholine (acidic ) in the same syringe
*Actions: - CNS: - Sedation – hypnosis – anesthesia
- Potentiate analgesics
- H.R.C - R.C - VMC
- CVS: - Large dose Sudden hypotension due cardiac contractility
- Respiration: - RC - Bronchospasm
- Sk.m. relaxation
*Uses: 1- Induction of G.A 2- Brief G.A 3- Anticonvulsants
*Side effects: 1- Respiratory complication: Apnea – Bronchospasm
2- Hypotension
3- Irritant: Phlebitis – Thrombophlebitis – Pain – Necrosis & slough
4- Contraindicated in Acute intermittent porphyria
---------------------------------------------------------------------------------------------------------------
2- Benzodiazepines
As: Diazepam – Midazolam – Lorazepam -----------see before
--------------------------------------------------------------------------------------------------------------
3- Propofol
Rapid induction & recovery
--------------------------------------------------------------------------------------------------------------
4- Propanidid
- Rapid induction & recovery
- Metabolised by pseudo-cholinestrase its action is intensified by succinylcholine &
Anti-cholinestrase.
---------------------------------------------------------------------------------------------------------------
5- Etomidate
Rapid onset short duration
Anesthesia
265
6-Neurolept analgesia
Droperidol + Fentanyl = Thalamonal
- It produces analgesia without loss of consciousness
- Useful in obestatric & minor procedure as bronchoscopy as pt. is cooperative
---------------------------------------------------------------------------------------------------------------
7- Ketamine
Actions:
Produces Dissociative anasthesia : [ loss of sensation & motor activity +
Amnesia + Analgesia without loss of consciousness ]
Side effects: Contra-indication:
1- Emergence phenomenon 1- Mental disorders
(Terrifying hallucination
during recovery )
2- ICT 2- ICT
3- Blood pr. 3- Hypertension
4- IOP 4- Glaucoma
Uses: To provide analgesia for minor procedure esp. in children
Pre-anesthetic medication
Benefits:
1- To produce: sedation , amnesia & analgesia
2- To reduce:
a- amount of anesthesia
b- post-anesthetic complications
c- parasympathetic supply to lungs , salivary gland & heart secretions ,
bronchospasm & reflex vagal stimulation
Drugs used include:
1- Narcotic analgesics: Morphine & Meperidine
2- Anxiolytics :as : - Barbiturate - Benzodiazepines
- Chloralhydrate - Paraldehyde
3- Neuroleptics as: Phenothiazine group
4- Parasympatholytics as : Atropine & Hyoscine
5- Adjuvant drugs:
- Neuromuscular blockers
- Controlled hypotension:[ Trimethaphan – Na Nitroprusside ]
- Hypothermic agents : by Lytic cocktail [Clorpromazine – Promethazine
Meperidine ]
N.B.:
1- Hypotensive drugs as Reserpine may lead to severe hypotension
2- MOA inhibitors potentiate the action of Morphine & Meperidine
3- In Thyrotoxic patients: Hyoscine is used instead of atropine & curare instead of
Gallamine
Anesthesia
266
LOCAL ANESTHESIA
Definition:
Local anesthetics are drugs that cause reversible block of nerve conduction producing
transient localized anesthesia without significantly affecting consciousness.
Structure and Chemical aspects:
They are weak bases formed of lipophylic group connected to ionizable hydrophilic
group by an intermediate chain; which may be amide or ester
Classification:
a) According to their chemical structure.
L.A
Amides Esters
- Lidocaine
- Dibucaine Benzoic a. esters PABA esters
- Prilocaine Cocaine - Procaine
- Mepivacaine - Tetracaine
- Bupivacaine - Benzocaine
-------------------------------------------------------------------------------------------------------
b) According to their solubility and therapeutic application into:
L.A
1- Soluble L.A suitable for
injection:
• Lidocaine
• Dibucaine
• Procaine
• Tetracaine
All these can produce
surface anesthesia
EXCEPT Procaine which is
effective ONLY by injection
2- Soluble L.A used only
topically:
• Cocaine
• Phenacaine
• Butacaine
Mainly used to
produce topical
anesthesia of the Eye
3- Insoluble L.A:
• Benzocaine
• Orthoform
Used as surface anaesthetics
in the form of powders and
ointments for wounds.
Kinetics:
1- Pass easily mucous membrane except Procaine
2- Benzocaine & Orthoform are insoluble & are used on skin only
3- Fate: - Esters By plasma psudocholine Estrase enz. (Shorter duration)
- Amides By hepatic microsomal enzymes.
4- Excreted in urine & Acidification of urine its excretion
Anesthesia
267
Methods of administration:
1- Surface anesthesia:
- By direct application for skin & mucous membrane
2- Infiltration anesthesia:
- By S.C injection to reach fine nerve branches and sensory nerve terminals.
3- Nerve block anesthesia:
- By injection close to the appropriate nerve trunks (Brachial plexus) to produce a
loss of sensation peripherally.
4- Sympathetic block:
It is injected around sympathetic ganglion.
5- Para vertebral block:
It is injected around spinal roots as they emerge
from the paraverterbal foramina.
6- Epidural anesthesia:
- The LA is injected in the epidural space;
between the dura & bony spinal canal
containing fat & connective tissue.
- It can be performed in sacral hiatus (Caudal anesthesia)
7- Spinal:
- The LA is injected in the subarachnoid space
in the lumbar region
- The level of spinal anesthesia depends upon:
i. Posture of the patient.
ii. Specific gravity of the injected solution.
Mechanism of action:
- They act from inside the nerve
& inhibit Na influx
membrane stabilization
- Fibers are affected in this sequence
(Sensory, cold, touch, pressure & lastly motor) & unmyelinated before myelinated.
- Recovery occurs in the reverse direction
Factors modifying action:
1- Extracellular pH: increased pH (alkaline medium) the action due to non-
ionised forms their absorption to act from inside & vice versa
**(Acidosis as in inflammation the action)
2- Extracellular ions: - Ca antagonize the action
- K enhance the action
3- Intracellular pH: tissue level of CO2 intracellular acidosis
accumulation of ionized form the action
4- Hyaluronidase enz. Onset, spread & depth of action
5- V.C. as Adrenaline prolongation of action
Na+
LA
-
Anesthesia
268
Actions
1- Local anesthetic action
2- C.N.S.: stimulation (tremors , convulsions) followed by depression
3- C.V.S.: - Heart Quinidine like except Cocaine
- Bl.V. VD except Cocaine which produce VC
4- Smooth muscle: spasmolytic
Toxicity of L.A.:
A- Systemic:
1- Allergy: esp. with ester type
2- Methaemoglobinemia with Prilocaine
3- C.V.S.: - Shock
- Vasovagal syncope [ Bradycardia – Hypotension – fainting]
4- C.N.S.: stimulation then depression
NB.: PABA esters as procaine are hydrolysed into PABA, so antagonize the
effect of sulphonamiides
B- Local:
1- Pain at site of injection
2- Persistent paraesthesia or anesthetic effect.
3- Haematoma.
4- Oedema.
C- Toxicity of spinal anesthesia:
a- Early:
- Hypotension: due to arterio-dilatation & veino-dilatation
ttt by [ elevate legs – I.V. fluids –sympathomimetics]
- Respiratory paralysis
b- Late:
- Septic meningitis
- Headache in 10% of patients
Contraindications:
1- Advanced liver disease (no enzyme to metabolize it).
2- In hypertensive patients give L.A. alone without adrenaline or
noradrenaline
3- Thyrotoxicosis and heart disease give L.A. with noradrenaline but NOT
adrenaline

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خلاصه انستیزی عمومیComplete review of General Anesthesia.pdf

  • 1. Anesthesia 262 GENERAL ANESTHESIA Def.: CNS depressant, characterized by: loss of consciousness, loss of sensation & adequate m. relaxation. Stages of GA.: 1- Stage I : Stage of induction or analgesia 2- Stage II : Stage of excitement or delirium (Dilated reactive pupil) 3- Stage III: Stage of Surgical anesthesia ( Normal pupil) It is divided into 4 Planes 4- Stage VI: Stage of medullary paralysis (Dilated non-reactive pupil) Mechanism of action: Either : - GABA - NMDA of Glutamate Classification: Inhalation I.V. Gases Volatile liquide 1- Ultra short Barbiturate 2- Non Barbiturate: Nitrous 1- Halothane - Benzodiazepines Oxide 2- Enflurane - Propofol 3- Isoflurane - Propanidid 4- Desflurane - Neurolept analgesia 5- Methoxyflurane - Etomidate 6- Trichloro-ethylene - Ketamine 7- Ethylchloride 8- Ether (obsolete) 9- Chloroform (obsolete) N.B.: - Most of anesthetics stop respiration before circulation, while chloroform stops respiration with circulation - Recovery occurs in reverse order. CO2 & O2 administration can fasten recovery in inhalation anesthesia - The onset of action of anesthetic depends on its solubility in blood, thus: • N2O has low solubility & rapid onset, while • Methoxyflurane has high solubility & delayed onset.
  • 2. Anesthesia 263 Inhalation anesthesia Halothane N2O Advantages: 1- Non-inflammable & non-explosive 2- Non-irritant 3- Produces broncho-dilatation 4- Produces controlled hypotension Advantages: 1- Non-inflammable & non-explosive 2- Non-irritant 3- Rapid induction & recovery 4- Good analgesics in labour 5- Safe on :CVS , Resp., Vital organs Disadvantage: 1- Weak analgesic 2- Weak sk.m. relaxants 3- Uterine relaxant 4- Cardiotoxic: - Stage 1: Bradycardia - Stage 2: sensetize the heart to catecholamine arrhythmia - Stage 3: direct depressant 5- Hepatotoxic 6- Malignant hyperthermia 7- Expensive Disadvantage: 1- Weak anesthetic 2- Weak sk.m. relaxants 3- Produces Diffusion hypoxia: during recovery it diffuses rapidly O2 conc. In alveoli Hypoxia, so give O2 during recovery 4- Megaloblastic anemia 5- Teratogenic: to both patient & doctor N.B.: - Enflurane : As Halothane but no hepatic toxicity & less sensitization of heart to catecholamines - Isoflurane & Desflurane: As Enflurane but: do not sensitize heart to catecholamines. - Methoxyflurane: Cardiotoxic & Nephrotoxic - Balanced anasthesia : N2O + Halothane Minimal alveolar anesthetic concentration (MAC): - Definition: It is the minimal alveolar anesthetic concentration at which 50 % of patients do not respond to a surgical stimulus - Importance: it is a measure of anesthetic potency, MAC is small for potent anesthetics, as halothane & large for weak anesthetics as N2O
  • 3. Anesthesia 264 I.V. Anesthesia Advantages: a. Easy b. Rapid induction & recovery c. No irritation of respiratory tract d. No sensitization of heart to catecholamines e. No post-operative nausea or vomiting f. No explosive hazards Disadvantages: Once injected, cannot be withdrawn 1- Ultrashort Barbiturate Thiopental, Methohexital & Hexobarbital *Kinetics: - Rapidly absorbed - Passes BBB & Placental barrier - Fate: Redistribution & slow metabolism Accumulation NB.: 1- Methohexital is metabolized faster Rapid onset – rapid recovery – little effect on Bl.Pr. 2- Thiopental (highly alkaline, as it is prepared in the form of Na solution) should not mixed with Succinylcholine (acidic ) in the same syringe *Actions: - CNS: - Sedation – hypnosis – anesthesia - Potentiate analgesics - H.R.C - R.C - VMC - CVS: - Large dose Sudden hypotension due cardiac contractility - Respiration: - RC - Bronchospasm - Sk.m. relaxation *Uses: 1- Induction of G.A 2- Brief G.A 3- Anticonvulsants *Side effects: 1- Respiratory complication: Apnea – Bronchospasm 2- Hypotension 3- Irritant: Phlebitis – Thrombophlebitis – Pain – Necrosis & slough 4- Contraindicated in Acute intermittent porphyria --------------------------------------------------------------------------------------------------------------- 2- Benzodiazepines As: Diazepam – Midazolam – Lorazepam -----------see before -------------------------------------------------------------------------------------------------------------- 3- Propofol Rapid induction & recovery -------------------------------------------------------------------------------------------------------------- 4- Propanidid - Rapid induction & recovery - Metabolised by pseudo-cholinestrase its action is intensified by succinylcholine & Anti-cholinestrase. --------------------------------------------------------------------------------------------------------------- 5- Etomidate Rapid onset short duration
  • 4. Anesthesia 265 6-Neurolept analgesia Droperidol + Fentanyl = Thalamonal - It produces analgesia without loss of consciousness - Useful in obestatric & minor procedure as bronchoscopy as pt. is cooperative --------------------------------------------------------------------------------------------------------------- 7- Ketamine Actions: Produces Dissociative anasthesia : [ loss of sensation & motor activity + Amnesia + Analgesia without loss of consciousness ] Side effects: Contra-indication: 1- Emergence phenomenon 1- Mental disorders (Terrifying hallucination during recovery ) 2- ICT 2- ICT 3- Blood pr. 3- Hypertension 4- IOP 4- Glaucoma Uses: To provide analgesia for minor procedure esp. in children Pre-anesthetic medication Benefits: 1- To produce: sedation , amnesia & analgesia 2- To reduce: a- amount of anesthesia b- post-anesthetic complications c- parasympathetic supply to lungs , salivary gland & heart secretions , bronchospasm & reflex vagal stimulation Drugs used include: 1- Narcotic analgesics: Morphine & Meperidine 2- Anxiolytics :as : - Barbiturate - Benzodiazepines - Chloralhydrate - Paraldehyde 3- Neuroleptics as: Phenothiazine group 4- Parasympatholytics as : Atropine & Hyoscine 5- Adjuvant drugs: - Neuromuscular blockers - Controlled hypotension:[ Trimethaphan – Na Nitroprusside ] - Hypothermic agents : by Lytic cocktail [Clorpromazine – Promethazine Meperidine ] N.B.: 1- Hypotensive drugs as Reserpine may lead to severe hypotension 2- MOA inhibitors potentiate the action of Morphine & Meperidine 3- In Thyrotoxic patients: Hyoscine is used instead of atropine & curare instead of Gallamine
  • 5. Anesthesia 266 LOCAL ANESTHESIA Definition: Local anesthetics are drugs that cause reversible block of nerve conduction producing transient localized anesthesia without significantly affecting consciousness. Structure and Chemical aspects: They are weak bases formed of lipophylic group connected to ionizable hydrophilic group by an intermediate chain; which may be amide or ester Classification: a) According to their chemical structure. L.A Amides Esters - Lidocaine - Dibucaine Benzoic a. esters PABA esters - Prilocaine Cocaine - Procaine - Mepivacaine - Tetracaine - Bupivacaine - Benzocaine ------------------------------------------------------------------------------------------------------- b) According to their solubility and therapeutic application into: L.A 1- Soluble L.A suitable for injection: • Lidocaine • Dibucaine • Procaine • Tetracaine All these can produce surface anesthesia EXCEPT Procaine which is effective ONLY by injection 2- Soluble L.A used only topically: • Cocaine • Phenacaine • Butacaine Mainly used to produce topical anesthesia of the Eye 3- Insoluble L.A: • Benzocaine • Orthoform Used as surface anaesthetics in the form of powders and ointments for wounds. Kinetics: 1- Pass easily mucous membrane except Procaine 2- Benzocaine & Orthoform are insoluble & are used on skin only 3- Fate: - Esters By plasma psudocholine Estrase enz. (Shorter duration) - Amides By hepatic microsomal enzymes. 4- Excreted in urine & Acidification of urine its excretion
  • 6. Anesthesia 267 Methods of administration: 1- Surface anesthesia: - By direct application for skin & mucous membrane 2- Infiltration anesthesia: - By S.C injection to reach fine nerve branches and sensory nerve terminals. 3- Nerve block anesthesia: - By injection close to the appropriate nerve trunks (Brachial plexus) to produce a loss of sensation peripherally. 4- Sympathetic block: It is injected around sympathetic ganglion. 5- Para vertebral block: It is injected around spinal roots as they emerge from the paraverterbal foramina. 6- Epidural anesthesia: - The LA is injected in the epidural space; between the dura & bony spinal canal containing fat & connective tissue. - It can be performed in sacral hiatus (Caudal anesthesia) 7- Spinal: - The LA is injected in the subarachnoid space in the lumbar region - The level of spinal anesthesia depends upon: i. Posture of the patient. ii. Specific gravity of the injected solution. Mechanism of action: - They act from inside the nerve & inhibit Na influx membrane stabilization - Fibers are affected in this sequence (Sensory, cold, touch, pressure & lastly motor) & unmyelinated before myelinated. - Recovery occurs in the reverse direction Factors modifying action: 1- Extracellular pH: increased pH (alkaline medium) the action due to non- ionised forms their absorption to act from inside & vice versa **(Acidosis as in inflammation the action) 2- Extracellular ions: - Ca antagonize the action - K enhance the action 3- Intracellular pH: tissue level of CO2 intracellular acidosis accumulation of ionized form the action 4- Hyaluronidase enz. Onset, spread & depth of action 5- V.C. as Adrenaline prolongation of action Na+ LA -
  • 7. Anesthesia 268 Actions 1- Local anesthetic action 2- C.N.S.: stimulation (tremors , convulsions) followed by depression 3- C.V.S.: - Heart Quinidine like except Cocaine - Bl.V. VD except Cocaine which produce VC 4- Smooth muscle: spasmolytic Toxicity of L.A.: A- Systemic: 1- Allergy: esp. with ester type 2- Methaemoglobinemia with Prilocaine 3- C.V.S.: - Shock - Vasovagal syncope [ Bradycardia – Hypotension – fainting] 4- C.N.S.: stimulation then depression NB.: PABA esters as procaine are hydrolysed into PABA, so antagonize the effect of sulphonamiides B- Local: 1- Pain at site of injection 2- Persistent paraesthesia or anesthetic effect. 3- Haematoma. 4- Oedema. C- Toxicity of spinal anesthesia: a- Early: - Hypotension: due to arterio-dilatation & veino-dilatation ttt by [ elevate legs – I.V. fluids –sympathomimetics] - Respiratory paralysis b- Late: - Septic meningitis - Headache in 10% of patients Contraindications: 1- Advanced liver disease (no enzyme to metabolize it). 2- In hypertensive patients give L.A. alone without adrenaline or noradrenaline 3- Thyrotoxicosis and heart disease give L.A. with noradrenaline but NOT adrenaline