general anaesthetics Flashcards

1
Q

what does inhalant GA produce towards painful stimuli?

A

unconsciousness and analgesia (inability to feel pain)

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2
Q

what is needed for inhalant GA to produce therapeutic effects?

A

inhalant GA must reach CNS concentration sufficient enough to suppress neuronal excitability

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3
Q

which has higher potency – inhalant GA with higher or lower minimum alveolar concentration (MAC)?

A

lower MAC

recall that MAC is minimum concentration of drug in alveolar air that will produce immobility in 50% of patients exposed to a painful stimulus

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4
Q

GA mechanism of action

A
  1. enhance neurotransmission at inhibitory synpases by allosterically increasing GABA receptor sensitivity to GABA action. binding of GABA neurotransmitter causes greater entry of Cl- which hyperpolarises cell, making it more difficult to depolarise –> reduces neuronal excitability
  2. depressing neurotransmission at excitatory synpases via blocking the NMDA receptor hence preventing glutamate neurotransmitter from acting on and activating NMDA receptor

ref to point 1 (since GABA neurotransmission is inhibitory, this will reduce overall synaptic activity of the brain)

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5
Q

list types of inhalant GA

A

halothane, enflurane, desflurane, isoflurane, sevoflurane, nitrous oxide

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6
Q

adverse effects of halothane?

A
  1. respiratory depression at high doses
  2. hepatotoxicity
  3. relaxation of skeletal muscles
  4. depression of cardiac output decreasing blood pressure
  5. bradycardia, arrhythmias leading to hypotension and dysrhythmias
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7
Q

adverse effects of sevoflurane?

A

nephrotoxicity

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7
Q

halothane has _____ analgesia until patient becomes unconsciousness

A

little to no analgesia

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8
Q

differentiating feature of NO gas

A

not potent but has high analgesic potency

due to very high MAC, NO alone gives analgesia (and amnesia) but not complete unconsciousness or surgical anaesthesia

hence patients undergoing GA get NO to SUPPLEMENT analgesic effects of primary anaesthetic

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9
Q

5 factors affecting inhalant GA action

A
  1. solubility
  2. concentration in inspired air
  3. rate and depth of pulmonary ventilation
  4. pulmonary blood flow
  5. arteriovenous concentration gradient in tissue (for uptake)
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10
Q

absorption pathway of inhalant GA

A

first goes to lungs, then to blood, then to brain and other tissues.

the higher the drug’s solubility in blood, the slower the onset because drug will take longer to get to the brain

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11
Q

what does intravenous GA produce towards painful stimuli?

A

unconsciousness ONLY

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12
Q

list types of IV GAs

A

thiopentone (sodium thiopental)
propofol
ketamine

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13
Q

specific MOA of each IV GA?

A

thiopentone + propofol = GABA MOA
ketamine = NMDA MOA

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14
Q

2 advantages of IV GAs

A
  1. allows for dose reduction of inhalant GAs
  2. can produce effects that cannot be achieved with inhalation alone
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15
Q

thiopentone and propofol have __ onset of action and __ duration of action

A

rapid; very short/short (for propofol)

note that due to the very short/short duration of action, it has to be taken in multiple doses

16
Q

adverse effect of propofol?

A

hypotension

17
Q

in what type of patients do we use propofol with caution?

A
  1. elderly
  2. patients with compromised cardiac function
18
Q

what extra effect does propofol have other than its effect as an anaesthetic

A

antiemetic (prevents vomiting)

19
Q

difference between ketamine and other IV GAs

A
  1. produces altered consciousness instead of unconsciousness –> patient feels disassociated from environment
  2. has analgesic property
20
Q

adverse effects of ketamine

A

psychologic reactions including hallucination, disturbing dreams, delirium

can be reduced through prescribing diazepam or midazolam

21
Q

anaesthetic adjuncts include…

A

benzodiazepines (midazolam), alpha-2 adrenergic agonists, analgesics, neuromuscular blocking agents