Required Reading-Drugs Flashcards

1
Q

IV induction agents

A

propofol, etomidate, ketamine, thiopental

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2
Q

IV opioids

A

fentanyl, morphine, hydromorphone, remifentanil

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3
Q

General anesthetics will ensure that pt is _____ and ____ throughout the procedure.

A

unconscious; amnesic

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4
Q

____ and ___ nerve blocks deliver drugs to precise locations along neural transmission pathways; ___ drugs are usually used.

A

Neuraxial (spinal/epidural); peripheral; local anesthetic

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5
Q

Benzodiazepines have ___, ___ and ___ effects due to GABA transmission enhancement. Benefit is ______ therapy.

A

sedative; anxiolytic; amnesic; anticonvulsant

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6
Q

Midazolam (Versed)–IV sedative dose ___; effects last 20-30 min due to ______

A

1-2 mg; redistribution

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7
Q

Benzos do NOT provide ___ effects.

A

analgesia

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8
Q

Monitored anesthesia care [MAC]/general anesthesia can be replaced by ____ to provide sedation/amnesia in OR. This is particularly useful in patients with poor _____ status who may not tolerate enough inhaled agents to be unconscious.

A

benzodiazepines; hemodynamic

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9
Q

Tx for oversedation due to benzos; only lasts about ____, which is particularly a problem with long-lasting benzos (re-sedation), like ____.

A

flumazenil (Romazicon); diazepam (t1/2 about 20hrs)

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10
Q

Opioids have ___ and ___ (not reliable) effects; bind receptors in ___ of brain and ___ of SC.

A

sedative; analgesic; periacqueductal gray; substantia gelatinosa

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11
Q

Opioid binding R cause inhibition of _____ and ____ release.

A

ACh; substance P

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12
Q

Analgesia– short-acting opioids, like ____, are used for pain control ____; long-acting opioids used for _____ pain control.

A

fentanyl; intraoperatively; postop (morphine, hydromorphone, meperidine)

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13
Q

Fentanyl– rapid-acting opioid; given during ___ of anesthesia to blunt sympathetic response during ____. Neg effects: can cause ___ in high doses

A

induction; intubation; apparent chest wall rigidity (>1000mcg; may impair adequate ventilation)

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14
Q

Sufentanil– rapid-acting opioid used for ____ and ____

A

induction; maintenance

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15
Q

Alfentanil– ULTRA rapid-acting opioid (5-10 min); about ___ as potent as fentanyl but with ___ onset; used for ___ and ___

A

25%; fast (1-2 min); induction; maintenance

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16
Q

Morphine– long-acting (peak onset 30 min) opioid; ___-soluble and can accumulate in the presence of _____, causing bradycardia and ___ release

A

lipid; renal failure; histamine; [typical dose postop 5-15mg]

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17
Q

Hydromorphone– long-acting (peak 15-30min) opioid; MC used for ___ pain control

A

postop [typical dose 1-2mg]

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18
Q

Meperidine–must be metabolized to normeperidine; has ___ properties (postop use); can accumulate in pts w/ ____ leading to oversedation or ___ and histamine release. Should be avoided in pts on ______.

A

anti-shivering; renal failure; seizures; type A MAOIs [serotonin-like syndrome hyperthermia, seizures, death]

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19
Q

Remifentanil–ULTRA short-acting (t/12 ~___min) b/c broken down by nonspecific ____, so does not ____ in patients with renal/hepatic failure; good for short intraop cases (~2hrs)

A

4; plasma esterases; accumulate

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20
Q

Accumulating opioids (___> alfentanil/sufentanil > ____) the context-sensitive half-time increases w/ long durations of administration

A

fentanyl; remifentanil

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21
Q

Main adverse effect of opioids is respiratory depression due to a decrease in _____ and an increase in the _____.

A

hypoxic drive; apneic threshold [CO2 level above which patients are stimulated to breathe]

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22
Q

To reverse opioids, use ____, which antagonizes ___ receptors.

A

naloxone; mu

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23
Q

Methylnaltrexone, opioid antagonist like naltrexone, can block peripheral receptors located in the ____ without affecting analgesia.

A

GI tract

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24
Q

Because of blunting of endocrine response, opioids can decrease ____ with minimal effects on baseline ___ status. Good for OR pt w/ ____.

A

stress response; CV; hemodynamic instability

25
Q

Any IV med that causes a patient to be unconscious is considered an _____; benzos and opioids are MC used together

A

induction agent

26
Q

Propofol– enhances ____ receptor; IV rapid-onset (t/12 ___ min) and short DOA due to rapid ___ metabolism and excretion by ___.

A

GABA-A; 2-8; hepatic; kidneys [**few pharmacokinetic changes w/ pts w/ liver or renal dz!!]

27
Q

Propofol is ___philic and provides ___ for gen anesthesia. A common SE is __ after an induction dose.

A

lipo; sedation; apnea

28
Q

Propofol is a potent __ and __ depressant and therefore is avoided when pts need to maintain spontaneous ventilation, are hypotensive or unable to sustain ____ stability.

A

CV; respiratory; hemodynamic

29
Q

Favorable SEs of propofol include anti___ and anti___ properties. MC SEs is pain on injection, for which ___ is added.

A

pruritic; emetic; lidocaine

30
Q

Thiopental– __ drug class; rapid onset; CV and respiratory depression; most use for effect of prolonged _____

A

barbiturate; cognitive disarray

31
Q

Thiopental is used in ____ sx cases because it is cerebro-protective

A

brain

32
Q

Main problem with thiopental is that because it is ____, it can precipitate and occlude catheters if mixed with _____.

A

alkaline; paralytic agents (acidic)

33
Q

Thiopental induces the enzyme _____ and therefore is contraindicated in pt w/ inducible porphyrias

A

ALAS [RLS in prophyrin synthesis]

34
Q

Thiopental may result in delayed effects due to high ____ and low _____

A

protein binding; hepatic excretion ratio

35
Q

Etomidate– ___ drug class [inc GABA transmission]; unlike propofol/thiopental, has MINIMAL ___ and ____.

A

imidazole; CV depression; respiratory depression [Therefore it is safer in hemodynamically unstable pts]

36
Q

Etomidate is used in these three patient populations:

A

(1) elderly (2) trauma patients (3) severely volume depleted/on vasopressors

37
Q

After a single bolus, the clinical effect of etomidate is terminated by ____ and rapid _____.

A

redistribution; hepatic metabolism

38
Q

A SE of transient _____ after etomidate is due to enzyme inhibition; therefore try not to use with ___ drugs or those with ______. MC SE is myoclonus and postop ___ and ___.

A

adrenal suppression; steroid; adrenal insufficiency; nausea; vomiting

39
Q

Ketamine– acts as antagonist at ____ R; SEs are ____, like those due to PCP [related], ___ and increase in ICP

A

NMDA; hallucinatory; salivation

40
Q

Ketamine is the ONLY ___ stimulant because it inhibits NE reuptake and has minimal effect on respiratory drive; also a potent ___ and ____

A

CV; analgesic; bronchodilator

41
Q

Ketamine is used in these two patient populations

A

(1) trauma [sedation, analgesia, amnesia, CV support] (2) pediatrics [hallucinations not as scary]

42
Q

Ketamine is AVOIDED in these two pt populations

A

(1) cardiac issues [arrhythmias, HTN] (2) where pt is going to emerge from anesthesia soon after admin [short cases]

43
Q

NMBs are used to facilitate ____. Adequacy of relaxation can be determined by use of a _____.

A

intubation; nerve stimulator

44
Q

Succinylcholine– depolarizing NMBs; prevents junctional ____ b/c drug isn’t hydrolyzed by true AChE; used almost exclusively for ______

A

repolarization; intubation

45
Q

Succinylcholine has quick onset ___ seconds and duration ___ min; if repeated doses are administered, ___ blockade may occur leading to a slow recovery

A

30-45; five; phase II [prolonged end-plate depol leads to conformational changes w/in AChR]

46
Q

___ is the enzyme that breaks down succinylcholine; some pple have a partial/total deficiency and thus can experience prolonged paralysis: ___ min for hetero and ___ hrs for homozygotes

A

Pseudocholinesterase; 20-30; 6-8

47
Q

SE of succinylcholine is elevation in ____ after admin. Must be used in caution with ___ patients or those with ___ or ___ injury.

A

potassium; burn; denervation; muscle

48
Q

SEs of note are succinylcholine are bradycardia and ______

A

malignant hyperthermia

49
Q

Nondepolarizing NMBs are AChR antagonists that inhibit junctional _____; they are divided into benzylisoquinoliniums (______) and steroidals (______, _____ and ______)

A

depolarization; cisatracurium; rocuronium, vecuronium, pancuronium

50
Q

Onset time and duration of action of nondepol NMBs are: ____ > _____ > _____ > _____

A

pancuronium; cisatracurium; vecuronium; rocuronium

51
Q

___ is simultaneously administered with neostigmine to prevent muscarinic overactivity [bradycardia, asytole, bronchospasm] when reversing NMB agents.

A

Glycopyrrolate [also atropine]

52
Q

____ is a NMB is that is degraded in the plasma and is used when there is severe renal/hepatic dysfunction.

A

Cisatracurium

53
Q

Cholinergic crisis post-tx neostigmine consists of these symptoms:

A

bradycardia, bronchospasm, emesis, miosis, muscle weakness

54
Q

Neostigmine and glycopyrrolate [paired] have a ___ onset and ___ duration compared to edrophonium and atropine [paired]

A

slower; longer

55
Q

Central anticholinergic syndrome is due to atropine [unlike ___] overdose because it crosses the _____. Symptoms include ____. Treat with physostigmine.

A

glycopyrrolate; BBB; delirium, excitation, fever, flushing, tachycardia

56
Q

Complete anesthesia includes ___, ____ and ____.

A

hypnosis [sedative], analgesia [opioids], muscle relaxation

57
Q

Which opioids would be best to use for 1.5hr case? Postop?

A

sufentanil, alfentanil, remifentanil (need relatively flat context-sensitive half time curves); fentanyl, morphine, hydromorphone

58
Q

You conduct emergence from anesthesia via ____, ____ and possibly ____ if needed

A

reverse NMB; discontinue opioid infusion; small dose longer-acting analgesia [esp if using remifentanil]