ADHD Meds Flashcards

1
Q

Symptoms of ADHD by Category
- inattention
- hyperactivity

A

pts. can be primarily hyperactive, inattentive or both
Inattention
- cannot focus on details; careless mistakes
- cannot finish tasks which require attention
- difficuty oragnizing tasks and to dos
- cannot listen when spoken too
- easily distracted
- forgetful in daily activities

Hyperactvity
- figet/squiring
- leaves seat when not supposed to
- talks excessively
- trouble waiting their turn, inturrupts others
- runs, climbs when no appropriate/restless

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2
Q

Diagnosis of ADHD
- for those 4-16
- those 17+

A

Diagnosis : Age 4-16
- 6 or MORE symptoms of inattention/hyperactivity/impuslivity for at least 6months inappropriate for developmental level

Diagnosis: Age 17+
- 5 or MORE symptoms of inattention/hyperactivity/impulsivity

___________________________________
with the following criteria also being met
- occuring in 2+ settings like at school/work and at home
- not another disorder
- clear evidence that these sx. interfer with social, school or work
- the symptoms of inattentive/hyperactive were present before the age of 12 for those diagnosed after 12

rating scales such as the ADHD scale, Connors & Vandervbilt Scale are used to help dx. ADHD

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3
Q

Treatment Approach to ADHD

A

Rule out other conditions
- behavior/mood d/o
- autism
- learning disabilities

discuss treatment v no treatment

Goals of Treatment
- to reduce symtpoms: remain seated in class, finish HW etc.

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4
Q

Treatment by Age for ADHD
4-6 y/o
6-12
12-18

A

most stimulant medicationsa re approved for ages 6+

For those age 4-6
- initiate nonpharm first: with evidence based parent-training in behavior management (PTBM) + classroom modification
- methlypehnidate (stimulant) can be used if behavior intervention does not provide significnat improvement

For those age 6-12
- behavioral modification + FDA_approved meds

For those 12-18
- behavioral modification/interventions + FDA-approved meds

all ages: stimulant medications preferred over non-stimulant meds first line
need to be titrated to acheive max benefit with tolerate side effects

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5
Q

Non-Pharmacologic Interventions for ADHA management

A

Combined behavioral thearpy + stimualnt therapy has best improvements & combo with therapy decreases the dose needed of the medication to use

Preschool & School age
- PTBM
- classroom management instructions from teacher

Adolsecent
- breaking up homewokr assignments & using structured organizer/scheduler

Adults and Adolecents
- ADHA specific CBT and metacognitive therapy

not a LO

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6
Q

ADHA Medications: two classes
- what meds in each class

A

ADHA Meds

Stimulants (first line, preferred)
- methylphenidate
- amphetamines
- come short and long acting formulations: Class II substances
- long acting formualtions: containt a mix of IR and ER

Non-Stimulants
- SNRIs (atomoxetine/viloxazine)
- Alpha-2-agonists (clonidine/guanfacine)

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7
Q

ADHD Medications: Stimulants
Initiating Stimulants
considerations for : Dose, Duration and Formulation

A

Initiating Stimulants

Dose: low doses initally, titrating up to the effective doses to best dose with minimal side effects

Duration: deside how long you need the medication to work
- once daily med long-acting vs multiple short acting
- this duration can influence adverse effects

Formulation
- tablets, capsules, liquids, patches
- medication adhearance (are they taking long-acting s. short)
- generic vs. brand

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8
Q

ADHD Meds: Stimulants
- discuss pt. response to stimulants, generics, formulations and tolerance

A

Stimulant Med
- methylpendiate v amphetamines

Pt. Reponse
- can vary between the methylpenidate and the ampetamines
- can vary based on genertic and name brand

Benefits
- typically seen within 1-3 weeks of initiation while adjusting dose

Tolerance
- can occur over time, and may need adjustments of dosing
- some side effects can become more tolerable and diaappear with continued use
- in general: ADHD symptoms tend to decrease with age & lead to less of a need for medication

not a LO

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9
Q

Stimulant ADHD meds: MOA

A

Methlyphenidate MOA
- Blocks the reuptake of NE (norepi) and DA (dopamine) into the presynaptic neuron
- this seems to increase time in cleft, and stimulat the cortex and subcortical structures similar to how the amphetamines do

Amphetamines: MOA
- promote RELEASE of catecholamines (NE and DA) from the storage site in teh presynaptic neuron into the cleft

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10
Q

Stimulant ADHD Medications
BBW

A

BBW: CNS stimulants have a high abuse potential and dependence
- specifcally amphatamines: misue can lead to sudden death/cardiovascual effects

Take Caution in…
- those with hx. of drug dependence or alcoholism
- longer acting formulations are preferred in this pop.

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11
Q

Contraindications of Methylpenidate & Amphetamines

A

Methylphenidate
- cannot be used with 14 days of MAOI or during treatment with MAOI
- cannot be used in those with marked anxiety, tension, agitation
- Cannot be used in those with glaucoma
- tourretes hx. or family hx. of tourettes/tics

Amphetamines
- cannot be used within 14 days of or during MAOI theray
- cannot be used in those with marked anxiet, tension or agitation
- cannot be used in those with glaccoma
- not for those with advnaced atherosclerosis, symptomatic CVD, mod/severe HTn
- not for those withhyperthyroid
- those with hx. of drug abuse

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12
Q

Stimulant Abuse Potentiatl & Symptoms of Abuse

A

Stimulat Abuse
- CNS stimulants have high abuse potential, and potential addiciotn

Symptoms of amphetamine abuse
- increased HR, RR, BP or sweating
- hyperactivity, restlessless, tremor or insomnia
- dilated pupils
- decreased appetite
- flushing, abd pain or vomiting
- anxiety, psychosis, aggression, sucidial or homicidal ideation

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13
Q

Names
methylpenidate
amphetamines
not a lecture ob.

A

Methylpenidate
- ritalin, IR or ER
- concerta (ER)
- short acting: give 30 mins before meals
- long acting: give in the AM with food

ampehtamines
- adderall (IR)
- mixed amephtamines adderall ER
- vyvanse (prodrug: less abuse potentil)
- short acting: with or without food
- long acting: am with food

efficacy of long acting 1 daily or short acitn BID is viratully the same

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14
Q

Side Effects of Stimulants
3 most common seen
others

A

Side Effects of Stimulant Meds

Psychatric
- mood disturbances (aggitation/irriable - depression)
- anxiety or panic attacks
- psychosis

Cardiovascualr
- increased HR and BP

Growth Suppression
- due to decreased appetite, decreased high/weight

____________________________________________

GI-related
- dry mouth
- decreasd appetite
- nausea

CNS
- insomina
- sombie-like
- tics/abnormal movements

peripheral vasculpathy: decrease peripheral flow

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15
Q

Managing the Side Effects of the Stimulant Medications

reduced appetite/WL

insomina/agitation

rebound sx./wearing off

A

Managing Side Effects

Reduced Appetite
- give high cal. meal at low-times (breakfast/bed)
- scheudle snacks

Insomina/Jittery
- decrease the dose
- give it earlier in the day
- avoid other stimulants (coffee)
- change fro IR to ER
- assedd for comorbid conditions: bipolar

Rebound/effects wearing off
- consider long-acting
- add a dose of short-acting in the PM

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16
Q

Medication Holiday from Stimulants and Discontinuing therapy

A

Stimulant
- can be held during times: summer vacation for example
- potential decrease in the growth stunting effect if this is done

How to Taper: Stimulants
- tapers them down to decreased teh side effects and withdraw feelings: fatigue

How to Taper: Alpha-2 agonists
- Must be tapered when discontinuing therapy due to significant side effect of rebound hypertension

NONSTIMULANT meds shoud not be put on a medication holiday: they need to be taken continuously for clincial effect

17
Q

Monitoring Stimulant Thearpy
efficacy
safety
growth

A

Efficacy
- patient/parent and teacher reports
- improveed behavior/attention
- duration of medication effect? too long, too short

Safety
- adverse effects
- growth (Height/weight) and changes in appetite
- EKG in those who develop CV symptoms

assess these things monthly and when initiation a dose or tapering

18
Q

Non-Stimulant ADHD Medications
SNRIs
Alpha-2-Agonists

A

Non-Stimulants
- 2nd line after stimulant medications

When can they be used
- in combo with stimulants
- in those who cannot tolerate stimulats or have sub-optimal response
- when stimlants are contraindicated: high risk of misuse or CV issues

SNRIs
- Atomoxetine (Strattera)
- Viloxazine

Alpha 2 Agonists
- clonidine
- guanfacine

19
Q

Non-Stimulant Medications: MOA
& dosage/when to take

A

SNRIs (atomoxetine, viloxzine) MOA

Atomoxetine
- selective inhibition of the NE reuptake
- dosage: kids take less; can tae 2nd dose in the late afternoon/early evening

Viloxazine
- selective inhibition of the NE and serotoin reuptake

20
Q

Atomoxetine (Strattera)
BBW
Contraindcations

A

BBW
- increased risk of suicidal indeation in children/adolescents

Contraindications
- use with MAOI in 14 days
- narrow angel glaucoma
- phenchromocytoma
- conditions of CV that may deteriorate if increased BP or HR occurs

take 2-4 weeks to work, full effect in 6-12 weeks

21
Q

Atmoxetine: Side Effects

A

Side Effects

GI-Related
- N/V/C/D
- decreased appetite & WL

CNS
- insomnia
- drowsy/fatigue
- HA
- irritability
- emontional lability

CV
- increased BP and HR

Others
- sweating, dry mouth, sexual dysnfcion, rarely liver injury

22
Q

Viloxazine
BBW
Contraindications
Side Effects

A

BBW
- increased risk fo suicidal ideation in kids

Contraindications
- use with MAOI in 14 days or in combo

Side Effects
- drowsy/somnolence
- decreased appetite
- N/V
- insomnia
- irrability
- increased HR and BP

potentailly quicker onset of action
more action on serotoni than NE

23
Q

Monitoring Parameters for Individuals on Atomoxetine or Violxazine

A

Monitoring: baseline
- EKG: in those with history or suggestive cardiac disease
- BP and HR
- weight and height
- asses fam & personal hx. of comorbid psych.

Monitoring: during
- new onset/change in chest pain/cardiac sx.
- suicidal behaior, thoughts, agitation
- BP and HR
- changes in weight/appetite
- adverse reactions and response

24
Q

Non-stimulant Medications: Alpha 2 agonists MOA
clonodine
guanfacine

A

MOA: Clonadine
- postsynaptic alpha-2 agonist stimulation
- regulated subcortical activity in the cortex

MOA: Guanfacine
- stimulates postsynaptic alpha2a receptors in teh cortex: improves delay-related firing in the neurons

25
Q

Alpha 2 Agonists
formuation and alterations

A

only the XR formulation of ADHD
- cannot abruptly disconitnue the med: reboudn HTN a possibility: need to taper down

only avalibe: for those 6-17 y/o as adjust or monothearp for adhd

26
Q

Alpha 2 Agonists

Adverse Effects & Monitoring

A

Adverse Effects
- sedation and hypotension : dose-dependent
- sedation: can go away after a few weeks
- GI: N/C/abd. pain
- BP & HR: can decrease
- changes in behavior: aggression/irritable

Monitor
BP and HR with these