General and Local Anesthetics Flashcards

1
Q

General Anesthesia

A

reversible response of depression of CNS function resulting in loss of function and perception of external stimuli

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2
Q

Local anesthetics

A

lidocaine, bupivicaine, ropivacaine, cocaine, benzocaine

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3
Q

General anesthetics

A

halothane, enflurane, isoflurane, desflurane, sevoflurane, NO

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4
Q

IV anesthetics

A

barbiturates, etomidate, ketamine, propofol

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5
Q

Several anesthesia considerations

A

Amnesia, immobilty, attenuation of response to noxious stimuli, analgesia, unconsciousness

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6
Q

Local Anest.

A

hydrophilic and lipophilic lipophilicity increases potency and duration of action (amides have two i’s in the name, esters do not)

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7
Q

Local Anest.

A

hydrophilic and lipophilic lipophilicity increases potency and duration of action (amides have two i’s in the name, esters do not)

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8
Q

Local Anesthesia MOA

A

decrease conduction at cell membrane, reduce or prevent Na permeability, leads to loss of sensation in the area supplied by nerve

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9
Q

Local anesthesia MOA cont’d

A

anesthesia molecule gains access when the channel is open, stabilizes the inactive state, more blockage produced in highly stimulated nerves

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10
Q

Routes

A

Surface: Topical, Infiltration: injected under surface, Conduction: deep injection (drug bathes nerve itself), Spinal

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11
Q

Amides

A

biotransformed by liver enzymes, longer acting

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12
Q

Duration of action of Local anest.

A

dependent upon- blood flow, temp. affects blood vessel size, protein binding (the stronger the bond between drug and protein on Na channel the longer the duration

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13
Q

Local anest. and use with vasoconstrictor

A

ie. epinephrine, vasoconstriction, decr. systemic absorption, localized action, incr. duration of action (all local anest. are vasodilators except cocaine)

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14
Q

Buffered lidocaine

A

NaHCO3 decreases pain at injection site, shortens onset, decreased stability, ph to 7.2-7.4

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15
Q

Bupivicaine

A

more potent and longer acting than lidocaine, preferred for longer procedures

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16
Q

ADE

A

dose related toxicity, Excitation- tachycardia/tremors, Depression-circulatory shock, respiratory depression

17
Q

General Anesthesia

A

generalized loss of felling or sensation accompanied by loss of consciousness during which surgery can be performed (no loss of consciousness with local anesthesia)

18
Q

Progression of Anesthesia

A

Induction, Maintenance, Emergence

19
Q

Mechanism of general Anesthesia

A

hyperpolarization of neurons, reduce synaptic transmission (pre-synaptic or post-synaptic)

20
Q

Molecular Targets of General Anest.

A

increase sensitivity of receptor to GABA, Inhibition of glutamate receptors (ketamine/NO)

21
Q

Inhaled Anest.

A

for maintenance of anesthesia, low TI in and out of lungs

22
Q

NO

A

weak anesthetic, gas, increased post-op NV

23
Q

Fluorinated Hydrocarbons

A

use via vaporizer, combined with NO, Very strong, increased stability, decreased toxicity, ADE-respiratory depression and malignant hyperthermia

24
Q

Isoflurane

A

most potent of the volatile anesthetics, high solubility, odorous

25
Q

Desflurane

A

rapid onset, not for induction of anesthesia

26
Q

Sevoflurane

A

for induction and maintenance, rapid onset and recovery

27
Q

IV anesthesia

A

move to lipophilic areas of CNS and spinal cord, termination of anesthesia is due to redistribution NOT metabolism

28
Q

IV anesthesia Properties

A

faster acting than inhalation, for short procedures, preferred for induction

29
Q

Brevital

A

methohexital, Barbiturate, works on GABA

30
Q

Diprivan

A

propofol, GABAa, most common for induction, hypnotic, decr. BP, respirator depression, PRIS

31
Q

Etomidate

A

GABAa, hypnotic, quick on and off, little CV effects, causes acute adrenal suppression

32
Q

Ketalar

A

ketamine, inhibits NMDA, good analgesia, amnesia, may have open eyes, increase BP and HR

33
Q

Local anesthetics

A

work by acting on Na Channels, activity is prolonged with use of vasoconstrictors like Epi

34
Q

General anesthetics

A

can be given via inhalation or IV and work primarily by acting on GABAa or NMDA receptors