Pharm- general anesthetics Flashcards

1
Q

anesthetic potency is due to

A

lipid solubility

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2
Q

anesthesia potency expressed as ?

A

minimal alveolar concentration or MAC

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3
Q

MAC required to abolish the response to surgical incision in

A

50% of subjects

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4
Q

concentration in the tissues after equilibration (fast in well perfused organs such as brain and heart)

A

inhaled concentration (MAC)

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5
Q

ligand gated RECEPTOR Cl- channels made of two alpha, two beta, and one gamma subunit

A

GABA A

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6
Q

GABA- alpha subunit mutation inhibits_____

A

volatile but not intravenous anesthetics

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7
Q

GABA- beta subunit mutation inhibits_____

A

inhibits both (volatile and intravenous anesthetics)

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8
Q

volatile binds to _____ intravenous binds to ___ subunits

A

volatile- alpha and beta

intravenous just beta

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9
Q

TREK, TASK, or TRESK subunits

A

two pore domain K+ channels

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10
Q

low concentrations of volatile and gaseous anesthetics reducing membrane excitability

A

two pore domain K+ channels

not affected by intravenous

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11
Q

glutamate (major excitatory neurotransmitter)

Important side of action for nitrous oxide, xenon and ketamine

A

NDMA receptors

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12
Q

inhibit sympathetic –> decreased arterial and venous tone = decreased arterial and venous pressure

A

isoflurane and other halogenated

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13
Q

increase sympathetic and plasma noradrenaline –> increase HR and maintain BP

A

nitrous oxide and ketamine

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14
Q

ventricular extra systoles –> increase sensitization to adrenaline

no harm except if catecholamine secretion is excessive increased risk of VF

A

halothane (and others)

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15
Q

fast, unconscousness in 20 s as soon as drug reaches brain

A

intravenous anesthetic agents

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16
Q

Best intravenous anesthetic drug/ fast recovery so it can be used as a continuous infusion (rapidly metabolized)
causes pain at injection site

A

propofol

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17
Q

Drug in which time is sufficient so it can be administered as a single bolus for short operations

A

ketamine

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18
Q

most used intravenous anesthetics act within 20-30 seconds

A

propofol, thiopental, and etomidate

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19
Q

Propofol - IV
Speed of induction and recovery?
Main unwanted effects?

A

fast onset, very fast recovery

cardiovascular and respiratory depression

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20
Q

thiopental - IV
Speed of induction and recovery?
Main unwanted effects?

A

fast (accumulation occurs, giving slow recovery) HANGOVER lasts 5-10 minutes on single dose

cardiovascular end resp. depression

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21
Q

(IV) largely replaced by propofol causes pain at injection site
risk of precipitating porphyria in susceptible patients

A

thiopental

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22
Q

Etomidate- IV
Speed of induction and recovery?
Main unwanted effects?

A

fast onset, fairly fast recovery

excitatory effects during induction and recovery adrenocortical suppression

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23
Q

(IV) less cardiovascular and respiratory depression than with thiopental/ pain at injection site

24
Q

Ketamine- IV
Speed of induction and recovery?
Main unwanted effects?

A

slow onset, after effects common during recovery

psychomimetic effects following recovery postoperative nausea, vomiting and salivation

raised intracranial pressure

25
(IV) produces good analgesia and amnesia with little respiratory depression
ketamine
26
(IV) slower than other agents /little respiratory or cardiovascular depression
midazolam
27
less painful on injection and rapidly converted by alkaline phosphates to propofol in the body
fospropofol
28
prolonged use of drug + critical care patients = severe acidosis, skeletal muscle necrosis, hyperkalemia, renal failure cardiovascular collapse, hepatomegaly
propofol infusion syndrome (1 in 300 patients)
29
only remaining barbiturate
thiopental
30
crosses BBB without delay, blood concentration declines rapidly 80% within 1-2 min
thiopental
31
used to terminate epilepsy and lower intracranial pressure
thiopental
32
if accidentally injected around rather than in vein; pain local tissue necrosis, ulceration or sever arterial spasms and gangrene
thiopental
33
Less hangover than thiopental , less hypotension, suppress production of adrenal steroids: increase in mortality in severely ill patients
etomidate
34
avoid in patients with adrenal insufficiency (sepsis)
etomidate
35
good option in patients with risk of circulatory failure
etomidate
36
has recreational use
ketamine
37
blocks NDMA receptor, low doses treat depression,
ketamine
38
dissociative anesthesia - sensory loss, analgesia and amnesia, without complete loss of cons.
ketamine
39
Increased BP and HR no effect on respiration/ increase intracranial pressure
ketamine
40
important use in pediatrics
ketamine
41
sometimes hallucinations, delirium and irrational behavior during recovery
ketamine
42
small, lipid soluble molecules that cross alveolar membranes
inhalation anesthetics
43
main factor of inhalation anesthetics that determines the rate of induction and recovery
Blood: gas partition coefficient | solubility in blood
44
Low blood: gas partition coefficient means
fast induction and recovery
45
main factor of inhalation anesthetics that determines the potency of the drug
oil: gas partition coefficient High lipid solubility delays recovery influences distribution in body
46
(INHALATION) fast induction recovery, few adverse effects, risk of anemia, accumulation in gas cavities
Nitrous oxide
47
(INHALATION) good analgesic effect, low potency, usually combined with other inhalation agent
nitrous oxide
48
(INHALATION) medium induction and recovery few adverse effects, possible risk of coronary ischemia in susceptible patients
isoflurane
49
widely used replaced halothane
isoflurane
50
(INHALATION) fast induction recovery,respiratory tract irritation, cough, bronchospasm
desflurane
51
(INHALATION) fast induction recovery, few reported adverse effects, theoretical risk of renal toxicity owing to fluoride
sevoflurane
52
(INHALATION) used for day- case surgery because of fast onset and recovery (comparable to NO)
Desflurane | Sevoflurane
53
Fat patients
low bloodflow and high capacity to take up anesthetics, increased fat soluble anesthetic means delayed recovery prolonged hangover
54
increased heat production in skeletal muscle, excessive release of CA 2+ from sarcoplasmic reticulum, muscle contracture, acidosis, increased metabolism and dramatic rise in body temp
malignant hyperthermia
55
halogenated and depolarizing neuromuscular blocking drugs are triggers for
malignant hyperthermia