Principles and Pharmacology Flashcards
what composes the triad of anaesthesia?
- hypnosis
- paralysis
- analgesia
Outline the drugs used in phase 1: Induction
- inhalation: volatile (sevoflurane) or nitrous oxide
- intravenous: propofol +/- opioid
- +/- muscle relaxant
Outline the drugs used in phase 2: Maintenance
- inhalational: volatile (sevoflurane) +/- opioid
- intravenous: propofol +/- opioid = TIVA
- +/- muscle relaxant
how does propofol/sevoflurane work?
Propofol and sevoflurance bind to and activate the GABAa receptor, activating the channel, allowing lots of Cl- ions to enter the cell.
- The influx of Cl- means membrane potential remains below resting potential of-70mV, so cannot get to threshhold of excitation (-55 mV) > therefore stops any forward transmission of neural signals and pathways.
- Pharmacologically induced state of narcosis.
how does fentanyl work?
Opioids inhibit propagation of pain impulse from peripheral tissue up to the brain.
- morphine and fentanyl act on MOP receptor type.
what opioids are commonly used by anaesthetists?
how does rocuronium work?
- muscle relaxant
- act at NMJ
- block acetylcholine receptors on post-synaptic membrane, blocking acetylcholine from binding and stimulating a muscle contraction
what are the types of muscle relaxants used by anaesthetists?
- non-depolarising - competitive antagonists at ACh receptor e.g. rocuronium, atracurium
- depolarising - ACh receptor agonist e.g. suxamethonium
what agents are used to reverse muscle relaxants?
- neostigmine - ACh inhibitor + glycopyrrolate - muscarinic anticholinergic
- suggamadex
what do anaesthetics do to all components of these two equations?
what drugs can help combat this?
decrease
- sympathetic nervouse system agonists, alpha receptors > vasculature and beta receptors > heart.
THE ONE BIG ANAESTHETIC EMERGENCY THAT EVERYONE LEARNS ABOUT BUT NO ONE SEES?
- malignant hyperthermia
- lethal unless given dantrolene
how does local anaesthetic work?
- can be ionised or unionised
- have to be unionised to cross the cell membrane where they bind to a protein, becoming ionised.
- they then block the sodium channel intracellularly, preventing depolarisation.