Add, Headache, Bipolar Flashcards

1
Q

ADHD

Occurs in-
Funct impairment-

A
  • 6-9% of children aged 5-12 yrs (b:g=4-8:1)
  • 60-80%
  • 50%: symp in adulthood (b:g=1:1)
  • only preschool children w moderate to severe dysfunction are considered for drug treatment
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2
Q

Goals of therapy

A
  • improv in core symp
  • reduc in associated symp
  • impr functional outcomes
  • incr ability of child to exert control when desired as opposed to controlling child
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3
Q

Medication can

A
  • imp short term learning
  • prolong attention span
  • imp concent
  • redu impulsiveness, hyperactivity, aggressive
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4
Q

Stimulant medications

A
  • sche II (monthly prescr)
  • dopamine & NE reuptake inhibitor (prolonging dopamine receptor effects)
  • efficacy> 70%
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5
Q

Methylphenidate-MOA

A

Immediate
Intermediate
Long acting

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6
Q

Methylphenidate-application

A

Patch- for 9 h

DexMethylphenidate- focalin (4-5 h)

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7
Q

Methylphenidate-AD

A
  • headache (12-14%)
    -loss of appetite
  • insomina
  • abdominal pain

Emotional lability & dysphoria seen at beginning of therapy
1-4% pts discontinue due to ADRs

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8
Q

Amphetamines

A

Enters CNS, affects mood n alertness
Study aid in 60’s, appetite suppressant

  • dextroamphetamine
  • addrall
  • lisdexamphetamine
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9
Q

dextroamphetamine

A
  • amphetamine
  • short
  • intermediate
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10
Q

Adderall (racemic mis of amphetamine salts)

A

-amphetamine

  • intermediate
  • long acting
  • racemic mix of amphetamine salts
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11
Q

Modafinil

A
  • amphetamine substitute
  • use in narcolepsy

ADs:

  • less mood changes
  • less insomnia
    -less abuse (than amphetamines)
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12
Q

Lisdexamphetamine

A
  • amphetamine
    -long acting
  • prodrug of dextro-amphetamine (activated in GI)
    -1st pass metabolism

enters CNS to affect mood & alertness

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13
Q

Lisdexamphetamine- application

A
  • noninjectable
    -not ADHD diagnostic
  • study aid in 60s
  • appetite suppressant in 70s
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14
Q

Lisdexamphetamine- ADs

A

misuse
abuse
tolerance

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15
Q

TCA

A

Impramine

Desipramine

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16
Q

Imipramine/ Desipramine (TCA)

A

given to pts who cannot tolerate amphetamines

ADHD (low dose); not comorbid depression or anxiety

ADs: develop tolerance w long term use

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17
Q

SSRIs

A

used alone or given in combo with Methylphenidate

ADs: fewer ADs & reduced toxicity (than TCAs)

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18
Q

Stimulant medi for adhd

A
Methylphenidine
Dextroamphetamine
Adderall
Lisdexamphetamine
Modafinil
Imipramine, desipramine
Ssri
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19
Q

Non stimulant medi

A

Atomoxetine

Clonidine

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20
Q

Atomoxetine

A
  • inhibits reuptake of presynaptic NE
    -not effective when combined with amphetamines: delayed therapeutic effect
  • works well for adolescents
  • AD: decreased appetite, N/V, fatigue
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21
Q

Clonidine

A
  • regulates NE release from locus ceruleus
  • reduces symptoms alone or in combo with stimulants
    -reduces symptoms of aggression & insomnia with stimulants
  • most frequently prescribed for ADHD
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22
Q

Guanfacine (intuniv)

A

-alpha 2 ago (for ADHD)
- 6 yrs -adolescents (oral: extended release)
(ADs)
Cardiovascular- bradycardia, hypo, ortho,syncope
CNS- sedation, drowsiness
Dermatological- skin rash w exfoliation (d/c)

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23
Q

ADHD

Charac-
Symp-
Risk for-

A
  • impulsiveness, heightened distractibility & short atten
  • symp: before 7yrs ( >6 mon)
  • at risk for developing new psychiatric disorders
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24
Q

Migraines

Gender
Onset
Pain location
Type of pain
Duration
A
f (3:1)
Onset-Variable
Loca-Unilateral
Type-Pulsating, N,V, photo, phonophobia aura
Dur- 2h, 3 d
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25
Cluster ``` Gender Onset Pain location Type of pain Duration ```
``` Gender- M (10:1) Onset- During sleep Pain location- behind, around eye Type of pain- stabbing, boring, sweating, flushing, nasal congestion Duration- 15-90 m ```
26
Tension ``` Gender Onset Pain location Type of pain Duration ```
``` Gender- f(2:1) Onset- variable Pain location- bilateral in band Type of pain- non-pulsating, mild photo, phono Duration- 30 m, 7d ```
27
MIGRAINE: 2 TYPES
1. ) Common: without aura. Severe unilateral, pulsating. Can be aggravated by physical activity. Accompanied by N and V, photo and phonophobia. Approx 85% of migraine sufferers do not have aura. 2. ) Classic: with aura. The aura can be visual, sensory, may cause speech or motor problems
28
TREATMENT AND PREVENTION OF MIGRAINES
Goals: be realistic Treatment: with oral meds, relief and normal function within 2 hours Prevention: total prevention unrealistic
29
GENERAL PRINCIPLES OF MIGRAINE MANAGEMENT
-Individual management -Treatment choice depends on: Attack frequency and severity Presence and degree of disability Associated symptoms Prior response and patient preferences Coexistent conditions -Establish dosing limits (2 days/week)
30
TREATMENT: ABORTIVE THERAPY (tries to stop headache) -Must begin at onset to get full effect: 50-80% achieve significant relief Simple analgesics:
Acetominophen-Tylenol NSAIDs: PG inhibitors (decrease serotonin release) Ergotamine ‘Triptans: serotonin system Memantine Misc. agents: Midrin, Metoclopramide, Chlorpromazine, Prochiorperazine
31
TREATMENT: PROPHYLACTIC THERAPY (increase time between headaches)
Beta blockers, Clonidine, Antidepressants, Cyproheptadine, Topiramate (anticonvulsant), Calcium channel blockers, Valproate, Anticonvulsants, NSAIDs, Methysergide
32
CLUSTER HEADACHE
Short, severe, episodic, clustering pain over the eyes and the forehead. Clustering is the predominant feature with cluster periods lasting between 2-3 months in most patients. Remission may last from 2 months to 20 years (usually 2 years). Episodes more common in the spring and fall. A family history is not usually present. Usually at night.
33
TREATMENT
1.) Abortive therapy: Ergotamine, Oxygen, Topical anesthetics, Misc agents-Capsaicin, Prednisone, leuprolide 2.) Prophylactic therapy: Lithium, Ergotamine, Methysergide, Misc agents-non Rx analgesics, B-blockers, antidepressants, Cyproheptadine, Calcium channel blockers, anticonvulsants
34
Migraine- cortical spreading depression
- most common cause of migraine- self propagating wave of depolarizing cortical neurons associated w a large efflux of K ions - dilates middle meningeal artery - opens blood brain barrier - cause aura in susceptible pt
35
ERGOT ALKALOIDS/METHYSERGIDE MOA
action at several types of Rs including agonist, and antagonist actions at alpha adrenergic and serotonin Rs and agonist actions at CNS dopamine Rs. (Can make histamine, ACh) (LSD is an Ergot alkaloid)
36
ERGOT ALKALOIDS/METHYSERGIDE Pharmacokinetics
variably absorbed from the GI tract; aided by administration with caffeine (100mg/mg of ergot). The ergot alkaloids are extensively metabolized in the body (caffeine increases absorption) (Inhaler)
37
ERGOT ALKALOIDS/METHYSERGIDE Effects 1.) CNS: hallucinogenic, bromocriptine and pergolide are best at suppressing prolactin secretion
2. ) Vascular Smooth M: drug, species, vessel dependent. Ergotamine constricts human blood vessels; assoc’d w partial alpha agonist effects; prolonged vasospasm possible(also contract uterine smooth m) 3. ) Uterine Smooth M: alpha agonist +serotonin effect+others. Ergovine most selective in this effect (can be used after delivery to decrease blood loss)
38
ERGOT ALKALOIDS/METHYSERGIDE ADs
1.) GI: NVD 2.) Prolonged vasospasm: especially after overdose 3.) Fibroplastic changes 4.) Ergot Poisoning: often from infected grain (claviceps purpurea) dementia
39
DRUG INTERACTIONS
-Propranolol (+ Ergot): vasoconstriction with pain and cyanosis -Macrolides (Erythromycin, Clarithromycin, Azithromycin) may exacerbate ergot toxicity
40
CLINICAL USES OF ERGOT 1.) Migraine
- Ergot decreases inflammation -Most effective when given during prodrome of an attack - May be repeated; no more than 6mg/attack and 10mg/week - Not usually as prophylaxis
41
CLINICAL USES OF ERGOT 2.) Hyperprolactinemia
: usually seen with anterior pituitary tumors and antipsychotics -Bromocriptine is the drug of choice -Suppress lactation also
42
CLINICAL USES OF ERGOT 3.) Postpartum Hemorrhage:
3.) Postpartum Hemorrhage: never give before delivery; increases mortality of mom and baby
43
SEROTONIN AGONISTS (CHECK THESE TO MAKE SURE)
ADR: taste alterations, N, V, chest tightness, nasal discomfort, increased BP Contraindicated in ischemic heart disease, uncontrolled hypertension, coronary heart disease Don’t take with ergot (b/c additive side effects)
44
1.) THE TRIPTANS
Sumatriptan, Zolmitriptan, Rizatriptan, Naratriptan, Eletriptan, Almotriptan, Frovatriptan These agents have been shown to be effective for the treatment of migraine with or without aura, but have not been studied well in the management of other types of headache. (Zolmitriptan has been shown to be a more potent agonist)
45
TRIPTANS Moa
MOA: selective serotonin-like R agonists (5HT-1D subtype) Structurally similar to serotonin Pharmacokinetics: Sumatriptan is rapidly absorbed after oral or subQ injection. Significant 1st pass effect -Available in Nasal spray, injection, tablets
46
TRIPTANS Pharmacodynamics:
Onset of relief 10-90 minutes after subQ administration, 1.5 to 2 hours after oral and nasal administration (don’t need to know these times) Duration of action shorter than migraine: may need several doses before headache is over. Doesn’t decrease length of headache, makes pain go away.
47
TRIPTANS Adverse Effects/Overdose:
tingling, dizziness, muscle weakness, neck pain, 5% ches pain, >10% hot flashes
48
TRIPTANS Drug Interactions
- May exacerbate prolonged vasospasm if used with other anti-migraine drugs (ergot, propranol, etc), or MAOI’s and SSRIs - Inhibitors of CYP450-3A4 may decrease metabolism of many of these agents
49
The ‘Triptans’: Advantages over Ergot
-More selective pharmacology (so more narrow in focus) -Simple and consistent pharmacokinetics (get where they’re going to) -Evidence based prescribing instructions -Well established efficacy and safety -Fewer and less severe ADR
50
2.) MIDRIN
2.) MIDRIN -A combo product for patients who can’t take ergot or don’t respond to it (less effective) MOA: Isometheptane 65mg: vasoconstrictor Dichlorphenazone 100mg: mild sedative Acetaminophen 325mg: pain relief (not enough; most pt’s need 500-600mg)
51
Midrin ADs
Adverse Effects/Overdose: dizziness, insomnia, N,V, transient numbness Less Effective than ergot
52
EXCEDRIN MIGRAINE
Acetominophen, aspirin and caffeine May be as effective as sumtriptan for treatment of acute migraine in some patients Most useful in patients with infrequent, mild to moderate headaches without nausea
53
SEROTONIN AGONISTS
TRIPTANS | Midrin
54
Bipolar Disorder
- This disorder, previously know as manic depressive illness, is a cyclical disorder with recurrent fluctuations in mood, energy and behavior encompassing the extremes of human experiences. - This disorder is genetically based, environmentally influenced, and the clinical presentation differs from individual to individual.
55
Bipolar disorder -Lifetime prevalence rate of a manic episode 1.6% for men, 1.7% for women
- Rare before puberty and after 65, Usual age range of onset 18-44 yrs - Genetics higher genetic risk than do major depressivedisorders. Approximately80 90% of bipolar patients have a relative, parent, sibling, or child with a mood disorder.
56
Bipolar disorder Bipolar is characterized by mood swings (mania and depression) that are outside the range of normal mood changes.
Patients usually experience periods of mood elevations (called mania or hypomania) that alternate with normal mood states -Individuals can differ in symptoms, course, severity, and response to treatment
57
Bipolar disorder Bipolar I,II,Cyclothymic disorder
Bipolar I-at least one manic episode, major depression is common Bipolar II- major depression along with hypomania Cyclothymic disorder- non major depression and hypomania Bipolar NOS (not otherwise specified) usually milder features
58
BIPOLAR DISORDER Clinical presentation
Clinical presentation- Does not require a history of depression, but mania or hypomania that is not caused by any other medical condition, substance, or mental disorder. Several medications and withdrawal syndromes can mimic manic and hypomanic symptoms.
59
Acute Bipolar Depression Mood stabilizer
Lithium, valproic acid, extended release carbamazepine
60
Acute Bipolar Depression Antipsychotics
Olanzapine, aripiprazole, riseridone, quetiapine
61
Acute Bipolar Depression Antidepressants
Combo mood stabilizer (olanzapine n fluoxetine)
62
Long term treatment
Monotherapy w lithium, valproic acid, lamotrigine, aripiprazole Combinatioon w olanzapine Extended release cabamazepine
63
Treatment Medication/ psychotherapy, thyroid work up needed
Manic episode - 1st episodes: lithium plus benzodiazepines (clonazepam) for sleep - if no response in 2-3 wks add a 2nd agent
64
Treatment | Recurrent or severe episodes - Prophylactic therapy/ or maintenance
Prophylactic therapy/ or maintenance - If 2 major episodes try maintenance therapy - For breakthrough episodes add antipsychotics, benzodiazepines (check for Li induced hypothyroidism)
65
Lithium 1st truly antimanic drug for bipolar depression
Efficacy- 70-80% :prevents and treats both mania and depression Long term- more effective Other uses- schizophrenia, migraine impulse control, steroid induced mania, aggressive disorders
66
Pharmacokinetics
Solutions absorbed better than regular or slow release formulations Not affected by food Renally excreted- not metabolized Renal dysfunction can double T 1/2
67
Pharmacodynamics Onset 5/7 d
Affects synthesis, storage, release, uptake of NE, serotonin, dopamine, ACH, and GABA Competes with Ca, Mg, K, Na in body tissues and binding sites Stabilized post synaptic receptor sensitivity Antimanic effect 10 after 28 days;antidepressant after 21 days;
68
Adverse Effects Lithium | -early
Gi upset, nausea, polydipsia, polyuria, nocturia, dry mouth, fine hand tremor, leukocytosis, m weak, difficulty concentrating, impaired memory
69
Adverse Effects Lithium - long term
Weigt gain, rash, acne, hypothyroidism, psoriasis, alopecia,
70
Lithium Adverse effect Overdose problems
Toxicity- severe drowsiness, coarse hand tremor, m twitching, myoclonus, choreoathetosis, cogwheel rigidity, vomiting, hyperreflexia, nystagmus, seizures, coma Mid toxicity- dec memory n concentration
71
Lithium Adverse effect Overdose problems
>1.5mEq agitation, confusion, headache,nystagmus, tremors | >3 mEq/L tonic/clonic twitching, seizures, irreversible brain damage, respiratory complications, coma death
72
Lithium Adverse effect Overdose problems
Dialysis can help but need to correct fluid and electrolyte abnormalities
73
Monitoring Decrease dose in elderly and those on diuretics, with renal disease, dehydration, or poor cardiac output.
ECG-every 6-12 m ( >50 yrs), cardiac ds | Vital signs, CBC with differential, weight, thyroid functions, renal function and urinalysis
74
SERUM CONCENTRATION MONITORING
-Narrow therapeutic index -Levels every 2-3 days in patients prone to toxicity- range is 0.6-1.2mEq/L 12 hours after the last dose -In acutely manic patients levels should be at least 0.8mEq/L and as high as 1.5mEq/L toxicity
75
Lithium Use Cautions
Acute mania, maintenance | Narrow therapeutic index, thyroid tox
76
Valproate Use Cautions
Acute mania | Liver, pancreas tox, sedation wt gain
77
Lamotrigine Use Cautions
Maintenance | Rash
78
CBZ Use Cautions
Acute mania | Sedation, heme effects