LA, GA Flashcards

1
Q

When pt is having inhaled GA, develops hypertention, tachycardia, hyperthermia, severe muscle rigidity and acidosis. What happen to pt? How to manage?

A
  1. Malignant hyperthermia
  2. Treat with dantrolene (to reduce release of Calcium) + supportive measurement
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2
Q

IV GA is used for:

A
  1. Induction (faster onset of action)

Most IV GA lacks of analgesic properties , can be combined with inhaled or local anesthetics for short procedures

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3
Q

Pt with intracranial bleeding, need for RSI, what induction agent to use?

A
  1. Barbiturate
    Or
  2. Propofol
    Or
  3. Etomidate

Not to use ketamine

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4
Q

What is the MOA of thiopental (e.g. of barbiturate)?

A
  1. Binds to GABAa receptors and facilitates actions of GABA by increasing the duration of GABA gated chloride channel opening
  2. Also works on AMPA receptor to depress glutamate mediated excitation
  3. Non synaptic membrane effects
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5
Q

Benzodiazepine is used for

A
  1. Pre anaesthetic medication and adjuvants during procedure under LA , due to their effects on sedation, anxiolytic and amnestic properties
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6
Q

How to accerate the recovery from large dose of benzodiazepam be given to elderly esp?

A
  1. Benzodiazepine antagonist ( flumazenil) can be given
  2. Need to closely monitor and multiple dosing as flumazenil has short duration of action (<90min)
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7
Q

Ketamine, MOA

A

NMDA Receptor antagonist producing disassociative anesthesia

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8
Q

Effects of ketamine

A
  1. Catatonia
  2. Amnesia
  3. Analgesia

No Loss of consciousness

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9
Q

Ketamine can be used for elderly pt or those with cardiogenic or septic shock due to:

A

Ketamine stimulate cardiovascular system through the cental sympathetic nervous system, and inhibiting reuptake of NorA ( does not reduce BP)

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10
Q

Disavdvantage of ketamine:

A
  1. Increase cerebral blood flow, o2 consumption and ICP
  2. Decrease RR
  3. A/W post OP disorientation, illusion and dream
  4. Higher risk for drug abuse ( chemically r/t phencyclidine (PCP)
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11
Q

Instead of GA, the alternative anaesthesia mothods:

A
  1. Balanced anesthsia (IV induction, inhaled, LA , muscle relaxants and cardiovascular drugs)
  2. Monitored anesthesia care: ( midazolam, propofol infusion for mod to deep sedation , opioid or ketamine)
  3. Conscious sedation: smaller doses of sedatives with mild altered LOC. ( midazolam, propofol, and opioid analgesics)
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12
Q

LA effects:

A
  1. Analgesics and paralysis can be achieved using specific pathways
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13
Q

ADE of LA

A
  1. Localized prolonged anesthesia or parasthesia due to infection via injection site, excessive fluid pressure in confined cavity, and severing of nerves and support tissues during injection
  2. Systemic reaction: depressed CNS effect, allergic reaction, vasovagal episode and cyanosis due to LA toxicity
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14
Q

LA is usually injected around nerves, what is derermined by Asborption and distribution?

A
  1. Off set of action and systemic toxicity

(Not onset of action)

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15
Q

MOA of LA:

A
  1. Binds to receptors near the intracellular end of Na channels
  2. Voltage and time dependent blockage (effect is more marked in rapidly firing fibers)
  3. Reduce depolarization
  4. Prolonged repolarization
  5. Anti inflammatory effects
  6. Effects on other channels [leads to ADE)
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16
Q

Factors determine the choice of LA

A
  1. Duration of effect required (procaine
17
Q

Lidocaine

A
  1. Amide type LA
  2. DOA: 30 TO 60MIN (medium action)
  3. Toxicity: light headedness, seizure, tongue numbness, hypotension, arrhythmia,