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GENERAL ANAESTHESIA PowerPoint Presentation

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Description : Check out this medical presentation on Neurology, which is titled "GENERAL ANAESTHESIA", to know about ANAESTHESIA, the reversible loss of response to noxious stimuli.

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GENERAL ANAESTHESIA
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ANAESTHESIA – is the reversible loss of response to noxious stimuli. GENERAL ANAESTHESIA – when anaesthesia is associated with loss of conciousness. LOCAL ANAESTHESIA – when conciousness is maintained during anaesthesia.
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BALANCED ANAESTHESIA Unconciousness Analgesia Muscle relaxation Abolition of compensatory reflex response General anesthetics have therapeutic indices of about 2 - 4.
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PREANAESTHETIC MEDICATION It is the use of drugs prior to anesthesia to make it more safe and pleasant. To relieve anxiety – benzodiazepines. To prevent allergic reactions – antihistaminics. To prevent nausea and vomiting – antiemetics. To provide analgesia – opioids. To prevent acidity – proton pump inhibitor To prevent bradycardia and secretion – atropine.
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STAGES OF ANESTHESIA Stage I : Analgesia Stage II : Excitement, combative behavior – dangerous state Stage III : Surgical anesthesia -Plane 1- roving movements of eyeballs -Plane 2- prog. loss of corneal reflex (surgery) -Plane 3- pupils start dilating, muscle relaxation -Plane4- only abdo respi, fully dilated pupils Stage IV : Medullary paralysis – respiratory and vasomotor control ceases.
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MOLECULAR MECHANISM OF THE GA GABA –A : Potentiation by Halothane, Propofol, Etomidate NMDA receptors : inhibited by Ketamine & N2O
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The main target of anaesthetics is the brain
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CLASSIFICATION There are two types of anaesthetics : Inhalational --- for maintenance Intravenous --- for induction and short procedures Inhalation anaesthetics: Advantage of controlling the depth of anesthesia. Metabolism is very minimal. Excreted by exhalation.
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INHALATIONAL ANAESTHETICS Non-halogenated gas Nitrous oxide Halogenated hydrocarbons Halothane Enflurane Isoflurane Desflurane Sevoflurane Methoxyflurane – nephrotoxicity.
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The important characteristics of Inhalational anaesthetics which govern the anaesthesia are Partial pressure of anaesthetic in inspired gas Pulmonary ventilation Alveolar exchange Solubility in the blood (blood : gas partition co-efficient) Solubility in the fat (oil : gas partition co-efficient)
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BLOOD : GAS PARTITION CO-EFFICIENT It is a measure of solubility in the blood. It determines the rate of induction and recovery of Inhalational anesthetics. Lower the blood : gas co-efficient – faster the induction and recovery – Nitrous oxide. Higher the blood : gas co-efficient – slower induction and recovery – Halothane.
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BLOOD GAS PARTITION CO-EFFICIENT
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Agents with low solubility in blood quickly saturate the blood. The additional anesthetic molecules are then readily transferred to the brain.
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OIL: GAS PARTITION CO-EFFICIENT It is a measure of lipid solubility. Lipid solubility - correlates strongly with the potency of the anesthetic. Higher the lipid solubility – potent anesthetic e.g., halothane
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MAC value is a measure of inhalational anesthetic potency. It is defined as the minimum alveolar anesthetic concentration ( % of the inspired air) at which 50% of patients do not respond to a surgical stimulus. MAC values are additive and lower in the presence of opioids. MAC values 1.1 to 1.2 used during surgery.
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OIL GAS PARTITION CO-EFFICIENT Higher the Oil: Gas Partition Co-efficient lower the MAC . E.g., Halothane 1.4 220 0.8
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Second gas effect Nitrous oxide is very insoluble in blood and other tissues. This results in rapid equilibration. The rapid uptake of N2O from alveolar gas serves to concentrate coadministered halogenated anesthetics. This effect (the "second gas effect") speeds induction of anesthesia.
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Diffusional hypoxia On discontinuation of N2O administration, nitrous oxide gas can diffuse from blood to the alveoli, diluting O2 in the lung. This can produce an effect called diffusional hypoxia. To avoid hypoxia, 100% O2 should be administered when N2O is discontinued.
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INHALATIONAL ANESTHETICS Nitrous oxide: Safest inhalational anaesthetic. Noninflammable, nonirritating Low potency anaesthetic, poor muscle relaxant but a good analgesic. No toxic effect on the heart, liver and kidney. A/E- diffusional hypoxia, megaloblastic anemia.
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INHALATIONAL ANESTHETICS Ether Potent anaesthetic, good analgesic, good muscle relaxants. Irritant, inflammable, explosive Induction is very slow and unpleasant (highly soluble in blood) Recovery is slow
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INHALATIONAL ANESTHETICS Halothane: It is a potent anesthetic. Poor analgesic, poor muscle relaxant. Induction is pleasant. It sensitizes the heart to catecholamines. It dilates bronchus – preferred in asthmatics. It inhibits uterine contractions. Halothane hepatitis and malignant hyperthermia can occur.
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INHALATIONAL ANESTHETICS Enflurane: Sweet and ethereal odor. Generally do not sensitizes the heart to catecholamines. Seizures occurs at deeper levels –contraindicated in epileptics. Caution in renal failure due to fluoride.
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INHALATIONAL ANESTHETICS Isoflurane: It is commonly used with oxygen or nitrous oxide. It do not sensitize the heart to catecholamines. Its pungency can irritate the respiratory system.
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INHALATIONAL ANESTHETICS Desflurane: It is delivered through special vaporizer. It is a popular anesthetic for day care surgery. Induction and recovery is fast, cognitive and motor impairment are short lived It irritates the air passages producing cough and laryngospasm.
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INHALATIONAL ANESTHETICS Sevoflurane: Induction and recovery is fast. It is pleasant and acceptable due to lack of pungency. It does not cause air way irritancy. Concerns about nephrotoxicity.
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PARENTERAL ANAESTHETICS (IV) These are used for induction of anesthesia. Rapid onset of action. Recovery is mainly by redistribution. Also reduce the amount of inhalation anesthetic for maintenance. E.g., thiopental, midazolam propofol, etomidate, ketamine.
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PARENTERAL ANAESTHETICS Thiopental (Pentothal): It is an ultra short acting barbiturates. Consciousness regained within 10-20 mins by redistribution to skeletal muscle. It do not increase ICT. It is eliminated slowly from the body by metabolism and produce hang over. It can be used for rapid control of seizures. A/E – Laryngospasm, acute intermittent porphyria -- pain, necrosis, gangrene on extravasation & inadvertant arterial injection
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PARENTERAL ANAESTHETICS Propofol : Most commonly used IV anesthetic. Unconsciousness in ~ 45 seconds and lasts ~15 minutes. Anti-emetic in action. Non-irritant to airways. Suited for day care surgery - residual impairment is less marked. A/E- pain during injection, fall in BP
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PARENTERAL ANAESTHETICS Ketamine : Dissociative anesthesia Produce - profound analgesia, immobility, amnesia with light sleep. Acts by blocking NMDA receptors Heart rate and BP are elevated due to sympathetic stimulation. Respiration is not depressed and reflexes are not abolished.
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PARENTERAL ANAESTHETICS Ketamine Emergence delirium, hallucinations and involuntary movements occurs during recovery (can be minimized by diazepam or midazolam). It is useful for burn dressing and trauma surgery. Dangerous for hypertensive and IHD.
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PARENTERAL ANAESTHETICS Neuroleptanalgesia It is characterized by calmness, psychic indifference and intense analgesia without total loss of consciousness. Combination of Fentanyl and Droperidol. A/E- chest wall rigidity
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PARENTERAL ANAESTHETICS Neuroleptanalgesia It is associated with decreased motor functions, suppressed autonomic reflexes, cardiovascular stability with mild amnesia. It causes drowsiness but respond to commands. Used for endoscopies, angiography and minor operations.
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STAGES OF ANESTHESIA
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Alcohol
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Effects of alcohol CNS Depressant excitation and euphoria are experienced at lower plasma concentrations promotes GABAA receptor inhibits NMDA receptors Turnover of NA in brain is enhanced.
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CVS Moderate doses -tachycardia -mild rise in BP Large doses -direct myocardial & vasomotor centre depression -fall in BP chronic alcoholism -hypertension -cardiomyopathy -cardiac arrhythmias
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GIT dilute alcohol (10%) -↑gastric secretion Higher concentrations(20%) -↓ gastric secretion - vomiting - gastritis heavy drinking -Acute pancreatitis
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Acute alcoholic toxicity Signs & Symptoms Treatment Hypotension Gastritis respiratory Depression coma and death. Gastric lavage Fluid glucose PPR
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Withdrawl syndrome Anxiety sweating Tremor Confusion Hallucinations delirium tremens convulsions Collapse Treatment benzodiazepines Chordiazepoxide or diazepam
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Disulfiram- Aldehyde dehydrogenase inhibitor Aldehyde syndrome flushing burning sensation headache Perspiration tightness in chest Dizziness vomiting, visual disturbances Mental confusion Collapse
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Methanol poisoning Toxic effects are due to formic acid vomiting, headache, epigastric pain, uneasiness, dyspnoea, bradycardia and hypotension, delirium blindness death due to respiratory failure Treatment Symptomatic Ethanol Haemodialysis Fomepizole (4-methylpyrazole) Folate therapy (Calcium leucovorin)
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MCQs Q1. Preanaesthetic medication is given: to decrease the duration of surgery to make the anaesthetic procedure pleasant and safe to control patients comorbidity to maintain blood pressure Ans. B
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Q2. Which of the following is NOT used as preanaesthetic medication: Glycopyrrolate Pethidine Pantoprazole Adrenaline Ans. D
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Q3. Dissociative anaesthesia' is induced by: Thiopentone Midazolam Ketamine Nitrous oxide Ans. C
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Q4. Malignant hyperthermia may be a complication of use of the following anaesthetic: A. Ether B. Halothane C. Nitrous oxide D. Propofol Ans. B
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Q5. The following general anaesthetic has good analgesic but poor muscle relaxant action: Halothane Nitrous oxide Ether Isoflurane Ans. B
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Q6. 'Second gas effect' is exerted by the following gas when coadministered with halothane: A. Nitrogen B. Nitrous oxide C. Nitric oxide D. CO2 Ans. B
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Q7. Which general anaesthetic selectively inhibits excitatory NMDA receptors: Propofol Halothane Desflurane Ketamine Ans. D
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Q8. Which of the following is NOT a component of anaesthetic state? Amnesia Analgesia Hyperthermia Unconsciousness Ans. C
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Q9. The minimal alveolar concentration of an inhalational anaesthetic is a measure of Therapeutic index Potency Efficacy Diffusibuity Ans. B
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Thank you
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Bibliography Essentials of Medical Pharmacology -7th edition by KD Tripathi Goodman & Gilman's the Pharmacological Basis of Therapeutics 12th edition by Laurence Brunton (Editor) Lippincott's Illustrated Reviews: Pharmacology - 6th edition by Richard A. Harvey Basic and Clinical pharmacology 11th edition by Bertram G Katzung Rang & Dale's Pharmacology -7th edition by Humphrey P. Rang Clinical Pharmacology 11th edition By Bennett and Brown, Churchill Livingstone Principles of Pharmacology 2nd edition by HL Sharma and KK Sharma Review of Pharmacology by Gobind Sparsh