lecture 66 Flashcards

Ott - pharmacotherapy of ADHD

1
Q

how does the etiology of ADHD mainfest?

A

multifactorial so environmental, genetics, and physiological all come into play
higher rate of diagnosis if a first-degree relative also has ADHD

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2
Q

what co-morbid conditions are associated with ADHD?

A

increased risk of SUD and antisocial personality disorder if ADHD is left untreated

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3
Q

when is it most likely that a person with ADHD will be diagnosed?

A

usually in childhood
but 1/3 of children will be diagnosed in adulthood

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4
Q

what is the diagnostic criteria for ADHD?

A
  1. for each symptom domain, must have at least 6 symptoms present and present in 2 or more settings
  2. for older adolescents and adults (17+), at least 5 symptoms are required for either of the two specifiers
  3. severeal inattentive or hyperactive symptoms must be present prior to age 12 years and present in 2 or more settings
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5
Q

how is inattention and hyperactivity/impuslivity defined in ADHD?

A

six or more of the following symptoms for at least 6 months inconsistent with developmental level and negatively impacting daily functioning

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6
Q

how are stimulants dosed in pediatric patients?

A

calculating based on mg/kg not found to be helpful as variations in dosing not found to be due to height or weight

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7
Q

for pts weighing under 16kg, what should the stimulants be dosed?

A

IR preferred due to limited low-dose availability of long-acting stimulants

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8
Q

when should stimulants be given?

A

avoid giving dose too late in the day (Due to insomnia)
may give an afterschool dose

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9
Q

what stimulant dosage form should be given for late afternoon symptoms?

A

longer-acting formulations

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10
Q

should two different stimulants be utilized?

A

no
can use two different dosage form of the same stimulant

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11
Q

when should 12.6 of Mydayis (mixed amphetamine salts) be used?

A

if pt age 13-17 with a CrCl between 15-30 mL/min

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12
Q

what is the formulation of daytrana (methylphenidate)?

A

patch

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13
Q

what is unique about vyvanse (lisdexfetamine)?

A

prodrug that is converted to dextroampetamine via first pass metabolism

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14
Q

what is unique about jornay (methylphenidate HCL)?

A

take dose in the evening between 6:30pm and 9:30pm

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15
Q

what are the AE of stimulants?

A

appetite loss
sleep disturbances
decreased growth
increase BP/HR

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16
Q

how would reduced appetite/weight loss be managed?

A

high-calorie meal when stimulant effects are low (breakfast, dinner)

17
Q

how would insomnia be managed?

A

dose earlier in the day
lower last dose of day or give earlier
consider sedating med at bedtime

18
Q

how should rebound symptoms be managed?

A

longer-acting stimulant trial
atomoxetine
antidepressants

19
Q

how should increased BP/HR be managed?

A

reduce dose
change stimulant

20
Q

how should hallucinations be managed?

A

d/c stimulant
reassess diagnosis

21
Q

how should risk for sudden cardiac death be managed?

A

risk no greater in clinical trials than general population
ass risk of cardiac structural abnormality and family hx
if concern, cardiac echo

22
Q

what should be monitored in stimulants?

A

appetite
behavior
BP
growth rate (height/weight)
HR
sleep ECG may be considered based on cardiac risk

23
Q

what drugs are alpha 2 agonists?

A

guanfacine ER
clonidine ER

24
Q

what is important to note about alpha 2 agonists?

A

must be tapered if d/c to avoid rebound HTN
guanfacine ER is a 3A4 substrate

25
what drugs are NE reuptake inhibitors?
atomoxetine viloxazine
26
what is important to note about atomoxetine?
2D6 substrate has weight based dosing for over an dunder 70 kg
27
what is important to note about viloxazine?
capsules that need to be swallowed whole or put in applesauce 2D6/UGT substrate and strong 1A2 inhibitor
28
what are the AE of NE reuptake inhibitors?
increase HR/BP increase in suicidal thinking (BW)
29
what are the SE of alpha 2 agonists?
decrease HR/BP, orthostasis somnolence dizziness rebound HTN if abrupt D/c
30
what drug classes make up non-stimulants?
alpha 2 agonists NE reuptake inhibitors
31
what are monitoring parameters for non-stimulants?
appetite BP HR LFTs (atomoxetine only)
32
what are important CP of bupropion?
not FDA-approved for ADHD 2D6 inhibitor CI in seizure disorders and eating disorders
33
what are important CP of TCAs?
less effective than methylphenidate cardiac concerns - sudden cardiac death in children, lethal in overdose
34
what is important to note about using mood stabilizer/atypical antipsychotics in ADHD therapy?
may be useful if there is comorbid BPD, conduct disorder, or intermittent explosive disorder should not use as monotherapy to treat ADHD
35
what is the first line treatment according to the AAP for preschool age children?
methylphenidate
36
what is the treatment guidelines according to the AAP for elementary/middle school/adolescent?
first line -- stimulants second-line -- atomoxetine, guanfacine ER, clonidine ER
37
what is the AAP recommendation for adjunctive treatment?
only guanfacine ER and clonidine ER have evidence as adjunct to stimulants
38
what is the NICE:ADHD guidelines 2018 for adults?
use Methylphenidate OR lidexamfetamine then trial dextroamphetamine then atomoxetine if no response