ADHD Flashcards

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1
Q

What is ADHD?

A
  • manifests in childhood w/ sxs of hyperactivity, impulsivity, and/or inattention
  • sxs affect cognitive, academic, behavioral, emotional and social fxning
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2
Q

Prevalence of ADHD?

A
- in school aged kids: 8-10%
one of the most common disorders of childhood
- male to female ratio:
4:1 for predom. hyperactive
2:1 for predom inattentive
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3
Q

What other psych disorders is ADHD frequently assoc with?

A
  • oppositional defiant disorder
  • conduct disorder
  • depression
  • anxiety disorder
  • learning disabilities
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4
Q

Neuropathogenesis of ADHD?

A
  • fxnl brain imaging reveals decreased activation in areas of basal ganglion and anterior frontal lobe
  • major neurotransmitters involved in ADHD are dopamine and NE
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5
Q

Fxn of dopamine?

A
  • most of dopamine sensitive neurons are located in the frontal lobe
  • dopamine system is assoc with:
    reward, attention, short term memory tasks, planning and motivation
  • dopamine limits and selects sensory information arriving from the thalamus to the forebrain
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6
Q

Fxn of the frontal lobe?

A
  • ability to project future consequences resulting from current actions
  • choice b/t good and bad actions (or better and best)
  • override and suppression of socially unacceptable responses
  • the determination of similarities and differences b/t things or events
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7
Q

How does ADHD affect the fxn of the brain?

A
  • decreased activation in the areas of the basal ganglion and anterior frontal lobe
  • increase in dopamine transporter activity thus clearing dopamine from the synapse too quickly
  • the dopamine imbalance allows an inappropriate increase in NE activity
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8
Q

The mechanism of ADHD tx wtih methylphenidate?

A
  • increases extracellular dopamine in the brain
  • changes the areas of fxn in the frontal lobe
  • in pts w/o ADHD mehylphenidate doesn’t have same effect on frontal lobe fxn
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9
Q

What is the DSM V criteria for ADHD?

A
  • need 6 or more sxs of inattention or hyperactivity/impulsivity, 5 or more for age 17 and older
  • sxs inappropriate for any given age
  • negatively impacts social and academic or occupational activities
  • sxs developed prior to age 12
  • sxs present in 2 or more settings
  • sxs present for at least 6 months
  • sxs are not better explained by other psychiatric disorders
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10
Q

What are the inattentive sxs for ADHD?

A
  • failure to give close attention to detail
  • difficulty sustaining attention in task
  • failure to listen when spoken to directly
  • failure to follow directions
  • difficulty organizing tasks and activities
  • reluctance to engaage in tasks that reqr sustained mental effort
  • loses things necessary for tasks or activities
  • easy distractibility
  • forgetfulness in daily activities
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11
Q

What are the impulsive-hyperactive sxs of ADHD?

A
  • fidgetiness w/ hands and feet or squirms in seat
  • difficulty remaining seated in class
  • excessive running or climbing in inappropriate situations
  • diff. in engaging in quiet activities
  • is often on the go or acts as if driven by a motor
  • often talks excessively
  • excessive talking and blurting out answers b/f questions have been completed
  • difficulty awaiting turns (while waiting in line)
  • interrupting and intruding on others
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12
Q

Medical eval of pt with suspected ADHD?

A
  • parents and teacher need to fill out a form such as the Vanderbilt form
  • refer for vision and hearing tests
  • complete Hx, ROS, and PE to rule out other causes and psychiatric illnesses
  • if hx suggests may consider the following testing:
    blood lead level
    TSH
    sleep study
    neuro consult if concern for seizures or other neuro disorder
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13
Q

dx and tx of ADHD in adults?

A
  • dx should be made by mental health professional
  • sxs often continue into adulthood and can have significant effects on social and occupational fxning
  • same meds used for adults as for kids
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14
Q

What methods of tx are used in ADHD?

A
  • stimulants (ritalin, adderall, and concerta) are the TOC
  • behavioral therapy tx: hasn’t been show to reduce sxs in absence of concurrent stimulant rx (in conjuction with rx - shown to be helpful)
  • other alt. such as cognitive tx, dietary modification, and mutlivitamins haven’t been shown to be effective in controlled studies
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15
Q

What is the criteria for initiation of pharm therapy for ADHD?

A
  • complete dx assessment that confirms ADHD
  • 6 or older
  • parental consent
  • school is cooperative (if dosing during school hours)
  • no previous sensitivity to the chosen med
  • normal HR and BP
  • no hx of seizure disorder (if so refer to neuro to tx ADHD too)
  • doesn’t have tourette syndrome, autism spectrum disorder, or substance abuse among household members
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16
Q

Before starting stimulant therapy what should be done?

A
  • comprehensive medical eval - no hx of seizure disorder, tourettes, autism spectrum
  • EKG (rule out arrhythmia)
  • document pretx ht, wt, BP, HR
  • document presence of any of the following sxs prior to tx: general appetite, sleep pattern, HAs, and abdominal pain
  • assess for substance use or abuse: need tx b/f starting ADHD meds
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17
Q

What should be included in the pt’s pretx education?

A
  • tell pt that meds are beign prescribed to help with self control and ability to focus
  • benefits and potential risks:
    emphasize uncertainty about causal assoc b/t serious CV risks to include sudden unexpected death and stimulants for kids with cardiac sxs or positive family hx of heart disease
  • other potential risks: anorexia, insomnia, tics, priapism with methylphenidate or atomoxetine
  • the f/u protocol that is expected
    -pt specific tx goals
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18
Q

TOC in ADHD?

A
  • depends on what pt and parents agree on
  • stimulants are first line agent:
    methylphenidate (ritalin)
    dextroamphetamine (adderall)
  • atomoxetine (strattera) is an alt. (non-stimulant) - use if hx of substance abuse in family
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19
Q

What are general considerations that may affect med choice in ADHD?

A
  • daily duration of coverage needed - completion of homework or driving after school?
  • ability of child to swallow pills or capsules
  • time of day when target sxs occur
  • desire to avoid admin at school
  • coexisting tic disorder (avoid stimulants)
  • coexisting emotional or behavioral condition
  • potential adverse effects
  • hx of substance abuse in pt or household member (avoid stimulants)
  • expense (short acting are least expensive)
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20
Q

What are the pros of pharm therapy for ADHD?

A
  • stimulants have long record of safety and efficacy
  • at least 80% of school age kids and adolescents will respond to stimulant med
  • improves:
    core sxs of ADHD
    parent child interactions
    aggressive behavior
    academic productivity and accuracy
    improved self-esteem
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21
Q

What are the cons of pharm therapy for ADHD?

A
  • insufficient data to judge affect on long term academic performance
  • ADHD sxs tend to improve over time regardless of tx modality
  • doesn’t significantly affect:
    learning problems
    reduced social skills
    oppositional behavior
    emotional problems
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22
Q

How do you choose b/t stimulants?

A
  • providers preference and comfort level

- pt and parent preference: after discussion of meds

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23
Q

Tx preschool kids?

A
  • this age group needs referral to behavioral health specialist
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24
Q

What are the drug classes used in tx of ADHD?

A
  1. stimulants (schedule II controlled substance):
    first line therapy
    methylphenidate
    amphetamines: detroamphetamine and detroamphetamine-amphetamine
  2. atomoxetine
  3. alpha-2-adrenergic agonists (refer for these)
  4. Antidepressants: TCAs, bupropion
25
Q

What are the short acting stimulants - methylphenidate?

A

methylphenidate:
ritalin and methylin are short acting formulations
- tablet, chewable tab or liquid
- time to onset of action ranges from 20-60 min
- duration of action: 3-5 hrs
- half life is 2-3 hrs

26
Q

What are the long acting stimulants -methylphenidate?

A

single pulse: metadate ER, methylin ER and ritalin SR
onset of action 20-60 min, duration: 8 hrs

  • sustained release capsules: focalin XR
    (dexmethylphenidate) , metadate CD, ritalin LA:
  • onset of action 20-60 min, duration: 9 hrs except for focalin XR duration is 12 hrs
  • contain a mix of immediate release and enteric coated delayed release beads
  • approximates BID dosing of short acting
  • osmotic release: concerta - immediate release on outside then uses osmotic pump to slowly release med
  • approximates TID dosing of short acting formula, onset of action 20-60 min, duration of action 12 hrs
  • oral suspension: quillivan XR: onset of action: 60 min, duration: 12 hrs
  • transdermal: daytrana - onset of action 60 min, duration 12 hrs, effects last 3 hrs post removal of the patch
27
Q

Short acting stimulants - amphetamines?

A
  • detroamphetamine: dexedrine, dextrostat, procenta (oral) - onset: 20 min, duration 4-6 hrs
  • amphetamine - dextroamphetamine: adderall, Onset: 20 min, duration: 4-6 hrs
28
Q

What are long acting stimulants - amphetamines?

A
  • lisdexamfetamine (vyvanase): prodrug of dextroamphetamine, pharm. activated after oral ingestion, designed to discourage drug misuse, onset: 1 hr, duration: 10-12 hrs
  • dextroamphetamine SR (dexedrine spansule): combo of immediate and continuous release meds, onset: 20 minutes, duration: 6-8 hrs
  • amphetamine-dextroamphetamine (adderall XR): combo of immediate and continuous release meds, onset: 20 min, duration: 8-10 hrs
    this is most commonly rx, well tolerated
29
Q

What is first line therapy in ADHD tx?

A
  • methylphenidate, dexmethylphenidate, and amphetamines are equally effective
  • have similar side effect profiles
  • short acting agents: initial rx in kids younger than 6, or can be used to determine optimal dosing b/f switching to longer acting agent
  • longer acting prep: may be used initially in ages over 6, starting at lowest dose and titrating up
30
Q

Nonstimulant meds used fo ADHD tx?

A
  • second line: atomoxetine (strattera)
  • third line:
    alpha-2-adrenergic agonists - clonidine (catapres), guanfacine (tenex)
  • antidepressants: imipramine (tofranil), desipramine (norpramin)
  • bupropion (wellbutrin)
31
Q

How long may it take b/f effects of strattera are noted?

A
  • 1-2 wks
  • pop. in younger kids since it is a non-stimulant
  • dosing by wt (older than 6)
32
Q

How do you monitor the response to therapy and assess for SEs?

A
  • assess weekly during titration stage (can last 1-3 months)
  • monitored behavior through parent and teacher feedback
  • after titration stage pts seen monthly to monitor wt, HR, BP until stable dose w/o new SEs
  • optimal dose is where there are favorable outcomes with minimal side effects
  • ?s to ask: when does side effect occur in relation to admin? Is effect related to coexisting disorder or enviro stressor?
  • mild adverse effects may resolve w/ time or adjusting any of the following:
    dose
    time of administration
    formulation of med
33
Q

What side effects should you eval for at every visit?

A
  • decreased appetite
  • poor growth
  • dizziness
  • insomnia/nightmares
  • mood lability
  • rebound
  • tics
  • psychosis
  • diversion and misuse
34
Q

How do you manage a pt with the side effect of decreased appetite?

A
  • give med at or after meal
  • encourage child to eat nutrient dense foods (no empty calories)
  • offer food that child likes for noon meal
35
Q

How do you manage SE: poor growth?

A
  • drug holidays may be beneficial
36
Q

How do you manage SE: dizziness?

A
  • monitor BP and pulse (make sure you took a good hx - any arrhythmias?)
  • ensure adequate fluid intake
  • if assoc with peak effect, try longer acting prep
37
Q

How do you manage insomnia or nightmares as SE of meds?

A
  • establish a bedtime routine
  • good sleep hygiene habits
  • omit or reduce the last dose of the day
  • if using long acting preparation consider short acting
38
Q

How do you manage mood lability as SE of meds?

A
  • sxs that may occur as med wears off can be averted by using longer acting formulation or increasing from BID to TID if short acting:
    sadness
    irritability
    increased activity
  • sometimes mood changes can occur at peak concentration - try reducing dose or switching to longer acting
39
Q

How do you manage rebound sxs from meds?

A
  • this may improve by stepping dose down at end of the day
40
Q

How do you manage tics as SE of meds?

A
  • conduct a drug trial at different doses included no med to be sure that they are related to meds
41
Q

How do you manage psychosis as SE of meds?

A
  • Psychosis: suicidality, hallucinations, increased aggression
  • verify dose is approp and med is admin as prescribed: if so d/c stimulant (can be done abruptly)
  • refer to mental health specialist
42
Q

Diversion and misuse of stimulants - educating pts?

A
  • have to monitor sxs and prescribe refills - to look for evidence of misuse or diversion
  • long acting stimulants have less potential for abuse
  • keep track of rx dates
  • open discussion with pt
43
Q

What are reasons for tx failure?

A
  • lack of adherence to med regimen
  • possibility of med diversion
  • are tx goals and expectations realistic?
  • is there a comorbid psych dx?
  • can try another stimulant med
  • if fail mult stimulants or intolerable side effects then trial atomoxetine or an alpha-2 adrenergic
44
Q

What are drug holidays?

A
  • d/c of stimulant med on weekends or during summer
  • decide on a case by case basis
  • not an option for atomoxetine or alpha-2-adrenergic agonists becuase of extended half life
45
Q

Maintenance of drug therapy?

A
  • once on a stable dose:
    follow up in office should be 3-6 months
  • continue to monitor ht, wt, BP, and HR
46
Q

How should you terminate ADHD meds?

A
  • may abruptly d/c stimulants or atomoxetine

- alpha-2-adrenergic agonists and TCAs should taper off over several weeks

47
Q

MOA of ritalin (methylphenidate)?

A
  • short and long acting available
  • acts on dopamine and NE to block reuptake
  • 70% of pts experience significant benefit
    (shortest acting: ritalin and methylin
    longest acting: concerta, quillivan XR, daytrana)
48
Q

SEs of ritalin?

A
  • anxiety
  • wt loss
  • psych sxs: psychosis, aggression, hallucinations
  • heart problems in at risk people
  • easy bruising
  • high potentiatl for addiction and abuse - schedule II drug
49
Q

Use of adderral (amphetamine-dextroamphetamine) -Pros? Downside? SEs?

A
  • high potential for abuse (II)
  • may lead to drug dependence
  • extremely popular
  • may be slightly more effective than ritalin
  • SEs:
    anxiety, wt loss, psychosis, hallucinations, aggression
  • ** heart problems in at risk people (sudden death)
50
Q

Use of dexedrine? super dangerous SE?

A
  • previously used for OTC diet pill
  • among most effective tx for ADHD
  • schedule II
  • sudden death in people that have heart problems or cardiac defects
51
Q

What SEs are concerning with dexedrine?

A
  • heart related problems including:
    sudden death in people that have heart problems or defects, sudden death, stroke and heart attack in adults.
    increased BP and HR
  • psych probs: new or worse behavior and thought problems, new or worse behavior
  • kids and teens:
    seeing things or hearing things
    believing things that aren’t true, new manic sxs
52
Q

MOA of Lisdexamphetamine (vyvanase)?

A
  • converted to dextroamphetamine after oral ingestion
  • no generic
  • less addictive but still schedule II
  • amphetmaines cause release of catecholamines (primarily dopamine and NE) from their storage sites in presynaptic nerve terminals
  • a less significant mechanism may include their ability to block the reuptake of catecholamines by competitive inhibition
53
Q

Use of atomoxetine (strattera)? MOA? BBW? Most common SEs?

A
  • initially only approved non stimulant tx until Intuniv
  • works on NE
  • initially tested for depression but didn’t do much
  • BBW: increased risk of suicidal behavior under 25 YOs
  • may not be as effective as stimulant meds
  • expensive
  • most common SEs: dry mouth, insomnia, nausea, decreased appetite, constipation, decreased libido, ED, urinary hesitancy, dizziness, and sweating 1-2 wks to notice effects
  • other SEs: chest pain, SOB, irregular heart beat, unusual thoughts or behavior, aggression, hallucinations, nausea, abdominal pain, loss of appetite, jaundice
54
Q

Why should atomoxetine (strattera) be used with some caution?

A
  • risk of suicidal ideation in kids and adolescents
  • weigh risks vs benefits
  • should be monitored closely for suicidal thinking and behavior
  • families and caregivers should be advised of need for close observation and communication with provider
55
Q

Pros and cons of ADHD tx?

A
  • ritalin: temporary effects - sleep not interrupted, inexpensive, effects and safety have been studied for decades, may cause jitters after snorting
  • adderall XR: most popular study drug, very similar to vyvanse but comparatively more addictive, inexpensive generics available, increases dopamine levels in the brain, can impact sleep patterns
  • vyvanse: expensive, no generics, some insurance plans don’t cover vyvanse. Smoother absorption than adderall and less addictive, can suppress appetite drastically
  • focalin XR: expensive, no generics available. SEs include loss of appetite, jitters and headache
56
Q

What is extended release guanfacine (intuniv)?

A
  • alpha-2-adrenergic agoinst (antiHTN)
  • approved for tx of ADHD
  • SEs:
    fast or slow HR
    pounding heartbeat, chest tightness
    numbness or tingling
    high rate of fainting
    depression
    BP problems (low)
  • caution with kidney or liver disease
57
Q

Use of bupropion (wellbutrin)?

A
  • alt tx for ADHD, other uses - Major depressive disorder cessation
  • MOA: inhibits reuptake of dopamine
  • mildly stimulating so good for pts with fatigue, hypersomnia, or poor concentration
  • no sexual side effects or wt gain
  • SEs: anxiety, insomnia, lowers seizure threshold, avoid in bulemia
58
Q

When should you not use stimulants in ADHD pts?

A
  • hx of substance abuse
  • structural heart defects
  • arryhthmia or increased CV risk profile
59
Q

ADHD screening for parents and teachers?

A

Vanderbilt assessment scales