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indicated for ADHD, narcolepsy, exogenous obesity, and BED
stimulants
stimulants increase ________________ and _________________ avaoilibility
dopamine, norepi
Dopamine and norepinephrine reuptake inhibitor and releaser (DN-RIRe):
_________-containing
•Inhibits presynaptic reuptake
•Allows neurotransmitters to accumulate in the synapse
MPH
Dopamine and norepinephrine reuptake inhibitor and releaser (DN-RIRe):
_________-containing
•Promote release of dopamine and norepinephrine from storage sites in the presynaptic nerve
AMP
With oral administration of stimulants, the time to peak may be delayed ~ ______ hours by a ________ meal
2-3, high fat
MPH: Transdermal absorption increases when patch applied to inflamed or ________ exposed skin
heat
AMP: Mixed salts of amphetamine and lisdexamfetamine should be avoided in __________
ESRD
Duration of action/effect of stimulants is dependent on the _______________ of each formulation (extended-release products contain both ________ beads and ________ beads - overall duration longer than IR med alone)
delivery system, IR, ER
stimulant contraindication
MAOI within 14d
stimulant warnings
CV
stimulant BBW
abuse potential
stimulant warnings:
•Growth ____________ - children not growing or gaining weight should stop treatment, at least temporarily
•May worsen motor and phonic _________, Tourette’s syndrome
•May worsen symptoms of thought disorder and behavioral disturbance in patients with ___________
•May lower the__________threshold
•May lead to emergence or worsening of activation and ___________
suppression, tics, psychosis, seizure, agitation
stimulant warning mitigation strategies:
•Prescribe _________ and include documentation of appropriate use
•Avoid __________ use
•Provide close __________ for ________ and drug ___________
sparingly, prolonged, monitoring, tolerance, dependence
stimulants may counteract the effects of _____________________
antihypertensives
opioid analgesics and other sympathomimetics ________________ concentrations of stimulants
increase
_______________________ can have an additive effect on the increased BP or HR when taken w stimulants
Psychostimulants (e.g., caffeine, modafanil [Provigil])
Antacids, proton pump inhibitors, and H2 blockers can affect ___________ of stimulants
absorption
when is reduced appetite from stimulants the greatest
lunch
management of reduced appetite and weight loss from stimulant
high cal breakfast and dinner, switch med
management of stomachache from stimulant
decrease dose, take on full stomach
management of N/V from stimulant
take w food, switch med
management of insomnia from stimulant
give earlier, reduce dose, change med, add sedative
management of headache from stimulant
decrease dose, take w food, take analgesic, change md
management of irritability or jitteriness from stimulant
decrease dose, change med
Evaluate need for dosage adjustment of stimulants at least once _________ until symptoms have stabilized, then several times per _______
monthly, yr
Stimulant monitoring:
•Appetite, BP, HR, height, and weight - _________ and each follow-up
•__________ symptoms
•__________ suppression
baseline, cardiac, growth
Stimulant _________________:
•May limit growth suppression
•Reassess symptoms and decrease potential longer-term effects
•Hold medication over the weekend
•Discontinue over the summer
drug holidays
stimulant controlled substance class
C-II
Untreated ADHD increases the risk of ___________________ compared with children with treated ADHD
substance misuse
Sx of stimulant withdrawal typically begin around _________hrs after last use and can last _______d
24, 3-5
S/Sx:
•Agitation
•Irritability, anxiety
•Depression, mood changes, suicidal ideation
•Fatigue
•Hypersomnia or insomnia
•Increased appetite
•Muscle aches
•Poor concentration
stimulant withdrawal
___________ stimulants to avoid withdrawal
taper
Stimulant ____________ following chronic therapeutic use may unmask symptoms of the underlying disorder and may require follow-up and ________________ of treatment
withdrawal, reinstitution
Careful supervision is required during withdrawal from stimulant misuse since severe ____________ may occur
depression
Titrate stimulants at ___________ intervals until clinical response is observed
weekly
stimulants are given _________ times daily depending on formulation
1-3
Short acting stimulants take effect on behavior seen within _______ minutes, persist for ______ hr
30-60, 3-5
Mid-day dosing (~ noon) during school typically required
short acting stimulant
Can be used in addition to longer-acting formulations for symptom control early in the morning or to prolong duration and smooth withdrawal in late afternoon
short acting stimulant
_____ short acting stimulant products are usually given at least twice a day, morning and noon
IR
Preferred stimulants for patients weighing < 16 kg because of limited long-acting stimulants that are available in low enough doses
IR short acting
An ______________ dose of stimulants may be prescribed if rebound symptoms occur, but avoid giving the dose too late in the day (i.e., no less than 6 hours before bedtime) to reduce risk of insomnia
afterschool
________________ stimulants:
•Slower onset, longer duration of action
•Good option for patients who are sensitive to stimulant side effects
•Unfortunately, are highly variable in efficacy and duration
intermediate acting
____________________ stimulants most contain a combination of IR plus DR/ER components, i.e. 50/50, 20/80, 40/60
•Example: 50/50 = 50% IR beads plus 50% enteric-coated DR beads
long acting
long acting stimulant onset of action is __________min and duration of action is _______hrs
20-60, 8-16
only stimulant taken at BEDTIME:
DR/ER taken at night to provide effect on awakening and slow release throughout the day
Methylphenidate long-acting (Jornay PM)
stimulants in multiple forms including Cap to sprinkle on food, chewable tab, ODT, oral suspension, transdermal patch
long acting
ODT stimulants:
•Place on ________ immediately after removing from blister pack
•Allow to dissolve, then ________
•Do not ______________ tablet
tongue, swallow, chew or crush
stimulant available as a suspension
MPH-OROS (Concerta)
MPH-OROS (Concerta):
•Avoid in patients with ___________________ or narrowing
•Contains _____________ acid (metabolite of benzyl alcohol)
•Associated with ____________ reactions
GI obstructions, benzoic, allergic
Stimulant transdermal patch:
•Apply the patch to a clean, dry area of the ____________ beneath the underwear, avoid the waistline, and rotate sites ________
•Apply the patch _____ hours before the desired effect needed
•Wear the patch for up to 9 hours: on ____ hr, off ____ hr
•Do not exceed 9 hours
•OK to have on for less time – tailor to patient’s needs
•After removal, fold onto itself and dispose into the toilet or a lidded container
•Effects last ____ hours after removed
lateral hip, daily, 2, 9, 15, 3
Transdermal stimulant ADE:
Mild ____________ should resolve in 24-36 hours after patch removed; patient should be instructed to contact provider if persists > ________
erythema, 2d
Transdermal stimulant ADE:
•_____________________ sensitization characterized by intense local reactions that can spread beyond the patch site
•symptoms include edema, vesicles, and papules at the ______________ site
•Manage by removing the patch, monitoring reaction, and seeking medical attention if symptoms do not resolve within ______ hours
allergic contact, application, 24
Transdermal stimulant ADE:
•Permanent loss of skin color at the site of application
•Difficult to predict - can occur 2 months to 4 years after initiating treatment
chemical leukoderma
An afternoon dose of MPH-_____ may be necessary if symptoms occur
IR
once daily dosing of ____________ can eliminate hassle/difficulties of lunchtime dosing at school
Lisdexamfetamine (Vyvanse)
Patient must take _____________ first thing in the morning - if they delay taking until later in the day, the risk of insomnia is greatly increased
Lisdexamfetamine (Vyvanse)
Selective norepinephrine reuptake inhibitor
Atomoxetine (Strattera)
Atomoxetine (Strattera):
•Inhibits _________ reuptake of _________
•Therapeutic effects in ADHD without _________ potential
presynaptic, norepi, misuse
Atomoxetine (Strattera) metabolism via ______________:
-UM: _________________
-PM: _________________
CYP2D6, less effective, toxic
Atomoxetine (Strattera) contraindications
CV, MAOI within 14d
Atomoxetine (Strattera) bbw
SI
Atomoxetine (Strattera) warnings
liver injury, priapism, hostile/aggressive, psychosis/mania
management of GI discomfort from Atomoxetine (Strattera)
take w food
management of headache, drowsiness, and insomnia from Atomoxetine (Strattera)
take in morning
management of dizziness Atomoxetine (Strattera)
take at night, divide dose
Atomoxetine (Strattera) takes effect in __________
2-4wks
Splitting the Atomoxetine (Strattera) dose twice daily may decrease __________
ADEs
Atomoxetine (Strattera) availability
oral
stimulants have a ____________ onset and are more likely to suppress ___________
quicker, suppress
Atomoxetine (Strattera) has a ___________ onset, ______________ risk of dizziness, fatigue, and sedation, and is a good option for pts w ________________ disorders
delayed, higher, substance misuse
Do NOT discontinue ________________________ abruptly due to risk of rebound hypertension
alpha 2 adrenergic agonists
alpha 2 adrenergic agonists ADE
Dizziness, dry mouth, headache, hypotension, bradycardia
CNS depressants and antihypertensives have additive effects when taken with _________________________________
alpha 2 adrenergic agonists
check _______ and ______ at every visit when taking alpha 2 adrenergic agonists
BP, HR
___________ can be used to treat tics
Guanfacine ER (Intuniv)
Stimulants may result in increased risk of _________ birth and _______ birth weight (Newborns may experience _________ effects)
premature, low, withdrawal
____________________ may decrease breast milk production
amphetamines
Infants may experience increased irritability, agitation, and crying
amphetamines
Atomoxetine in pregnancy and breastfeeding
unknown, use caution
If a stimulant is needed in the elderly, consider _______________ or _____________________
modafinil (Provigil), armodafinil (Nuvigil)
______________________________ should be used with caution in the elderly due to decreased hepatic, renal, and cardiac function
Lisdexamfetamine (Vyvanse)
________ and _________ may be decreased in ADHD and may be used as adjunctive therapy in children and adolescents
omega 3, omega 6
May be used as adjunctive ADHD therapy in children and adolescents at risk for low iron concentrations
ferrous sulfate