ADHD Therapeutics Flashcards

(61 cards)

1
Q

TRUE OR FALSE

it is very common for people with ADHD to have comorbid mental illness

A

true

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2
Q

decreased _____ drives the disease of ADHD

A

decreased dopamine

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3
Q

ADHD is characterized by inattentiveness, with or without….

A

hyperactivity and impulsivity

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4
Q

ADHD = ___ +____

A

inattentive + hyperactive

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5
Q

name some things that can be misdiagnosed as ADHD

A

autism, tourette’s, conduct disorders

depression, bipolar disorder

anxiety disorder

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6
Q

stimulants will make _____ disorders worse

A

anxiety

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7
Q

name some risks of not treating ADHD

A

difficulty socializing, poor work/school performance, unstable relatioships, substance use disorders, accidents

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8
Q

____ can be the sole intervention for mild-moderate ADHD

what about for moderate-severe cases

A

psychotherapy

for moderate-severe ADHD, psychotherapy should be used alongside medications

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9
Q

first line options for treating ADHD

A

stimulants

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10
Q

as far as stimulants for ADHD, _____ may have a higher incidence of adverse events than _____ preparations

A

amphetamines have a higher risk of AE than methylphenidate

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11
Q

which are more affordable - IR or ER stimulant dosage forms

A

IR more affordable

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12
Q

which formulations are more likely to be misused - IR or ER

A

IR more likely to be abused

use ER/XR if this is a concern

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13
Q

true or false

when stimulants are used for ADHD, there will be an IMMEDIATE RESPONSE

A

true

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14
Q

in children, which dosage formulations are preferred

A

ER/XR

more convenient dosing strategies

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15
Q

the 2 stimulant treatment choices are all variations of ___ or ____

A

methylphenidate or amphetamine

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16
Q

which dopamine firing is preferred and why - tonic or pulsatile

A

tonic is preferred

pulsatile release increases the risk of compulsive use and dependence, and also leads to higher dopamine levels which can cause a stress-like state

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17
Q

BBW of stimulants

A

drug misuse and dependence!

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18
Q

5 warnings for stimulants (not the BBW of dependence and misuse)

A

-ocular effects - can increase IOP or worsen glaucoma

-pts with cardiac conditions - can raise HR and BP! (minimal risk in young pts w no cardiac issues)

-can exacerbate tics in tourette’s

-risk of mania/psychosis in bipolar or schizophrenia

-growth suppression in peds bc decreased appetitie

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19
Q

2 stimulant CONTRAINDICATIONS

A

hypersensitivity

when used during or within 14 days of MAO inhibitors

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20
Q

3 “relative” stimulant contraindications that depend on the patient

A

active psychosis ( can worsen)

active substance use disorder

significant anxiety disorder/sensitivity to stimulants

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21
Q

methylphenidate brand and dexmethylphenidate brand

A

methylphenidate - ritalin

dexmethylphenidate - focalin

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22
Q

MOA of ritalin and focalin

A

noncompetitive dopamine and NE reuptake inhibitor (like buproprion)

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23
Q

which is the more potent enantiomer and what is the dose conversion - methylphenidate or dexmethylphenidate

A

dexmethylphenidate (focalin) is more potent

1mg focalin = 2mg ritalin

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24
Q

which has a LONGER half life - amphetamines or focalin/ritalin

A

amphetamine has longer

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25
true or false ritalin and focalin have MINIMAL CYP drug interactions
true
26
is buproprion used in ADHD
can be used off label for MILD ADHD not really effective in severe
27
true or false methylphenidate can cause weight gain
FALSE - weight loss bc it decreases appetite
28
what are the only 3 trade names of dexmethylphenidate
azstarys focalin focalin XR
29
true or false jornay and quillivant are brand for methylphenidate
true
30
true or false concerta is brand for dexmethylphenidate
FALSE - methylphenidate
31
what is unique about jornay
the drug doesn't actually start working until around 10 hours after taken. taken at night and then starts to take effect in the morning hours - and lasts until evening
32
which has higher potential for abuse - ritalin/focalin or amphetamine
amphetamine
33
MOA amphetamines
COMPETITIVE dopamine and NE reuptake inhibitor. amphetamine can actually get in the synaptic terminal and at high doses it can displace dopamine from the vesicles causing MORE dopamine release so higher potential for abuse and misuse!
34
which amphetamine is the most psychoactive enantiomer
dextroamphetamine so mixed salts are used
35
amphetamine is more prone to DDI than ritalin/focalin which enzyme
CYP2D6
36
what decreases the absorption of amephetamine? does this apply to lisdexamfetamine?
acidic food and drinks (bc basic structure) DOES NOT apply to lisdexamfetamine
37
what INCREASES the absorption of amphetamines
antacids
38
both methyl/dexmethylphenidate and amphetamines have similar adverse effects. however.....
amphetamine AE's happen more often
39
what's the only stimulant indicated for moderate/severe binge-eating disorder
lisdexamfetamine
40
structurally, what is lesdexamfetamine
a prodrug of dextroamphetamine. has a lysine attached therefore, can't be injected! must be ingested. less abuse potential
41
is methamphetamine indicated for ADHD
yes - actually is but not really used in practice bc of misuse
42
most often, what formulations of amphetamine are used
mixed amphetamine salts
43
long active mixed amphetamine salts capsule
mydayis
44
true or false adderall is mixed amphetamine salts
true
45
can ER mixed-amphetamine capsules be opened
yes - but do not crush or chew
46
what are considered 2nd line for ADHD
"NRIs" --- selective norepinephrine reuptake inhibitors (note - NOT SNRI's!!!) can be used as monotherapy OR as an adjunct to stimulants
47
explain when NRIs would be used as an adjunct to stimulants when would they be considered FIRST LINE as monotherapy?
adjunct -- if the pt had some response from a stimulant but can't tolerate a higher dose NRI's are first line monotherapy for patients with substance use disorders or have a CI to a stimulant (or just prefer a non-stimulant)
48
true or false NRIs are stimulants
FALSE - they are not
49
name the 2 NRI's
atomoxetine viloxazine
50
are NRI's effective at treating depression
no
51
can strattera capsules be opened what about viloxazine
NO - must be swallowed whole viloxazine can be opened
52
name 2 alpha 2 agonists that can potentially be used for ADHD
guanfacine and clonidine
53
which alpha 2 agonist is generally preferred over the other and why
guanfacine preferred over clonidine bc less AE
54
for ADHD, alpha 2 agonists tend to improve _____ symptoms more than ______ symptoms
improve behavioral, impulse symptoms more than the inattentive
55
true or false alpha 2 agonists are considered 2nd line for ADHD
true
56
alpha 2 agonists are approved in kids how young
6 years and older
57
AE of clonidine
orthostasis, hypotension, headache, dizziness, dry mouth, sedation, nightmares rebound hypertension if not tapered properly! guanfacine has these side effects too, but they are less severe bc more selective for a2a receptors in the prefrontal cortex and not the rest of the body
58
a pediatric patient was given methylphenidate oral solution 5mg twice daily. in the afternoons, his symptoms have still not improved what to do
increase the frequency to 5mg TID
59
pediatric patient got methylphenidate 5mg TID after 5mg BID was not working in the afternoons at school now, they come back to the clinic and the afternoon symptoms STILL haven't improved and now he is having trouble sleeping at night also, the child refuses to get pulled from class to take the med bc he's embarrassed what should we do
switch to methylphenidate ER tablets (concerta) 18mg QD (dont increase the dose of the solution! will just increase AE)
60
patient was prescribed methylphenidate QD he's been throwing it up an hour after taking. what should we do
if he's throwing up that soon after taking - he's barely getting any drug. it's not working switch to methylphenidate ER suspension 20mg ONCE A DAY when he can actually take the med - it seems to work. stick on methylphenidate. he was previously on a liquid and not throwing up
61