Introduction to Anaesthetic Drugs - Pharmacology Of Anaesthetic Drugs | Lecture Notes - YNetStudyHub
Pharmacology Of Anaesthetic Drugs

Introduction to Anaesthetic Drugs

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Overview of the different classes of anaesthetic drugs, their mechanism of action, and common uses in clinical practice.

Introduction to Anaesthetic Drugs
Designed as a quick‑reference guide for students and health‑care professionals.


1. What Is an Anaesthetic?

Aspect Definition
Purpose To induce a reversible loss of sensation (pain, temperature, pressure) and, when required, loss of consciousness.
Types of effects • Analgesia – pain relief
• Amnesia – loss of memory of the event
• Muscle relaxation – facilitates surgery
• Unconsciousness – general anaesthesia
Routes of administration Inhalational (gas/vapour), intravenous (IV), intramuscular (IM), oral, topical, epidural/spinal.

2. Classification of Anaesthetic Drugs

Class Main agents Typical clinical use Key pharmacologic features
Inhalational (volatile) agents Sevoflurane, Desflurane, Isoflurane, Halothane (rare) Maintenance of general anaesthesia (GA) Low blood‑gas partition coefficient → rapid induction/recovery; dose‑dependent respiratory depression; minimal metabolism (except halothane).
Intravenous induction agents Propofol, Etomidate, Thiopental, Ketamine Induction of GA; sedation; procedural anaesthesia • Propofol – rapid onset, anti‑emetic, dose‑dependent hypotension.
• Etomidate – hemodynamically stable, adrenal suppression.
• Thiopental – barbiturate, long‑acting.
• Ketamine – dissociative, stimulates sympathetic tone, preserves airway reflexes.
Opioid analgesics Fentanyl, Sufentanil, Remifentanil, Morphine, Hydromorphone Intra‑operative analgesia; postoperative pain control Potent µ‑receptor agonists; respiratory depression; remifentanil unique for rapid metabolism by plasma esterases.
Neuromuscular blocking agents (NMBAs) Depolarizing: Succinylcholine
Non‑depolarizing: Rocuronium, Vecuronium, Atracurium, Cisatracurium
Facilitate tracheal intubation & muscle relaxation Succinylcholine – rapid onset, short duration, contraindicated in hyperkalemia. Non‑depolarizers – longer acting, reversed with anticholinesterases (neostigmine) or sugammadex (rocuronium, vecuronium).
Adjuncts & adjuvants Midazolam, Dexmedetomidine, Lidocaine, Magnesium, Anticholinergics (glycopyrrolate, atropine) Sedation, anxiolysis, blunting of sympathetic response, reduction of anesthetic dose Benzodiazepines → amnesia, anxiolysis; Dexmedetomidine → sedation with minimal respiratory depression; Lidocaine → IV analgesia, reduces cough on emergence.
Local anaesthetics Lidocaine, Bupivacaine, Ropivacaine, Mepivacaine Regional blocks, infiltration, epidural/spinal anaesthesia Block Na⁺ channels → prevent depolarization. Duration & potency depend on lipid solubility and protein binding.

3. Pharmacokinetic Principles Relevant to Anaesthetics

Parameter Description Clinical implication
Onset of action Determined by drug’s lipid solubility, pKa, and route Faster onset → easier airway
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Unit Syllabus 10 Topics
Introduction to Anaesthetic Drugs
Inhalation Anaesthetics
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Intravenous Anaesthetics
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Neuromuscular Blocking Agents
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Local Anaesthetics
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Adjuvant Drugs in Anaesthesia
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Pharmacodynamics of Anaesthetic Drugs
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Special Considerations in Anaesthetic Pharmacology
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Management of Anaesthetic Emergencies
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Future Trends in Anaesthetic Pharmacology
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