FINAL: Exam 1 Flashcards

(47 cards)

1
Q

A protein or other substance that binds to an endogenous chemical or a drug is a ____________

A

receptor

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2
Q

Which drugs experience high levels of first pass metabolism?

Stoelting (3)

Nagelhout (12)

A

Propranolol
Lidocaine
Nitroglycerin (po)

Aspirin
Lidocaine
Morphine
Midazolam

Hydralazine
Metoprolol
Verapamil

Glyceryl trinitrate
Levodopa
Cimetidine
Felodipine
Neostigmine

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3
Q

Alignment of a drug with its receptor is aided by various bonding forces, which bonding forces play a prominent role in this alignment? (there are 5, which 2 most prominent?)

A

Van der Waals ()
Hydrophobic
Hydrogen
Ionic (
)
Covalent

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4
Q

The dosage range of a drug that provides safe effective therapy with minimal adverse effects is?

A

Therapeutic window

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5
Q

Volume of distribution of a mathematical calculation which equals _____/ ______

A

Dose of drug/Plasma concentration of drug

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6
Q

______ ________ are similar in molecular structure to their corresponding agonist drugs; they have receptor affinity, but lack intrinsic activity or efficacy

A

Pure antagonists

(Sits on receptor site but nothing happens)

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7
Q

_______ _________ occurs when a drug’s action is blocked and no receptor activity is involved

A

Chemical antagonism

(ex: protamine, sugammadex)

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8
Q

Drug is regarded as fully eliminated when approximately ___% has been eliminated

Usually occurs in ___ -___ half-lives

A

95

4-5

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9
Q

1:10,000 epinephrine = ____ mcg?

A

100 mcg

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10
Q

Opioids work as agonists on opioid receptors at pre and post synaptic sites in the central nervous system:
_________
_________

A

Brain stem
Spinal cord

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11
Q

Mu receptors principally responsible for:
________ analgesia
________ analgesia

A

supraspinal
spinal

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12
Q

Respiratory depression characteristic of ____ receptor activation

and ____ and ____

A

mu

mu2, delta

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13
Q

Respiratory depression less prominent with ____ receptor activation

A

kappa

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14
Q

Opioid receptors normally activated by endogenous peptide opioid receptor ligands (3)

A

Enkephalins (Delta)
Endorphins (Mu)
Dynorphins (Kappa)

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15
Q

Most common side effects of opioid allergy (3)

A

Localized histamine release
Orthostatic hypotension
Nausea and vomiting

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16
Q

________ is not an indication of pain control

A

Sedation

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17
Q

Morphine produces a histamine release from tissue mast cells, which can cause _______ _____, ________, and _______

A

decreased SVR
hypotension
tachycardia

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18
Q

Morphine Epidural dosing
Bolus: __ - __ mg q__-___h
Infusion: ___-___ mg/h

A

2-6 mg q8-24h
0.2-1mg/h

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19
Q

Dose of meperidine for adult postoperative shivering

A

12.5-25 mg IV

20
Q

Fentanyl intrathecal dose

21
Q

Bolusing remifentanil can cause: (3)

A

Bradycardia/hypotension
Ventilatory depression
Muscle rigidity

22
Q

Methadone is a ________ opioid

23
Q

Oxycodone is ______ as potent as oral morphine

24
Q

Codeine has good ________ activity

2 drugs that suppress cough:

A

antitussive

codeine, heroin (?), dextromethorphan (?)

25
Buprenorphine Epidural dose: ____ Buprenorphine Intrathecal dose: ____
0.3 mg 0.15 mg
26
_______ _____-_______ ______ (______) are among the most commonly prescribed drugs in the world
Nonsteroidal anti-inflammatory drugs (NSAIDs)
27
NSAIDs inhibit the biosynthesis of __________ by preventing the substrate _________ _____ from binding _________ (_____) enzyme active site
prostaglandins arachidonic acid cyclooxygenase (COX)
28
The COX enzyme exists as: (2)
COX-1 isoenzyme COX-2 isoenzyme
29
COX-1 isoenzyme functions: -Maintenance of normal ______ function in the _______ -________ protection in the _______ tract -Production of proaggregatory ________ ___ in the __________
renal, kidneys Mucosal, gastrointestinal thromboxane A2, platelets
30
Hypersensitivity reactions to NSAIDs _____ occur, and they are more common in individuals with _________ or __________
rarely nasal polyps asthma
31
_________ is the leading cause of acute liver failure in the United States, and nearly half of _________ - associated cases are due to ________ overdose
Acetaminophen Acetaminophen unintentional
32
There is evidence supporting the use of _________ in the multimodal analgesia protocols to contribute to postoperative recovery of patients by minimizing opioid doses and, therefore, side effects
corticosteroids
33
Lidocaine produces analgesia by suppressing the activity of ______ channels in neurons that respond to noxious stimuli, thereby preventing _______ conduction and ______ transmission
sodium nerve pain
34
__________ acts as a selective partial alpha2-receptor agonist
Clonidine (Ex: neuraxially) (Precedex also selective alpha2-receptor agonist = more selective than clonidine)
35
In patients taking NSAIDs, GI perforation exists in what % of people?
1%-2%
36
__________ does not increase catecholamines (opioid)
Morphine
37
Opioid induced bradycardia/hypotension occurs through stimulation of :
vagal stimulation
38
__________ is the acute tolerance; rapid appearance of a progressive decrease in response to a given dose of a drug after continuous or repetitive administration
Tachyphylaxis
39
Drugs that cause least amount of biliary pressure increase
Meperidine Naloxone (reverses pressure)
40
Which opioid receptors are responsible for urinary retention?
Mu1 Delta
41
NSAIDs decrease clearance of _______, leading to toxicity
lithium
42
What irreversibly inactivates COX1, leading to prolonged inhibition of platelet aggregation?
Acetylsalicylic acid (Aspirin)
43
This drug has been shown to be beneficial in neurologic pain
Methadone (d/t NMDA receptor antagonism) or Ketamine (NMDA antagonist) or Magnesium (NMDA antagonist)
44
Two drugs that undergo extensive first-pass metabolism
Lidocaine Morphine
45
Things to consider when prescribing a drug (4)
Age Gender Weight Ethnicity
46
*1+1 = 3: _______* 1+ 0 = 3: _______ 1+1 = 0: ________ 1+1 = 2: ________
*Synergism* Potentiation Antagonism Addition
47
___-_______ is the process by which a cell increases the number of receptors to a given drug __- _______ is the process by which a cell decreases the number of receptors for a given drug in response to chronic stimulation
Up-regulation (beta-adrenergic receptors up-regulate in presence of antagonists) Down-regulation (beta-adrenergic receptors down-regulate in presence of agonists)