Exam 3 Flashcards

1
Q

schizophrenia pathophysiology

A

neurotransmitter: multiple (dopamine, serotonin, glutamate, GABA and ACh-both nicotinic and muscarinic abnormalities)
anatomical:
-decreased brain size asymmetry
-increased ventricle size, decreased gray matter
-hippocampal volume, neuronal pruing
-blood flow/glucose metabolism
-not just “dopamine deficit”

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2
Q

schizophrenia diagnostic criteria

A

two (+) of the following, each present for a significant portion of time during a 1-month period:
-delusions
-hallucinations
-disorganized speech
-grossly disorganized or catatonic behavior
-negative symptoms
For a significant portion of the time since the onset of the disturbance, level of functioning in one or more major areas, such as work, interpersonal relations, or self-care, is markedly below the level achieved prior to the onset

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3
Q

schizophreniform disorder

A

shorter duration (1-6 months)
impaired social/occupational function NOT required

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4
Q

schizoaffective disorder

A

-symptoms meeting criteria for mood episode are present for substantial portion of duration of illness
-uninterrupted period of illness either major depressive or manic episode concurrent with symptoms meeting criteria for schizophrenia
-impaired social/occupational function NOT required

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5
Q

brief psychotic disorder or episode

A

duration between one day and one month with eventual return to premorbid condition

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6
Q

delusional disorder

A

hallucinations not prominent
mildly impaired function, behavior not blatantly bizarre
subtypes: grandiose, jealous, persecutory

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7
Q

schizophrenia patient evaluation

A

-complete patient history
-mental status exam : rating scales (Positive & negative syndrome scale), BPRS (brief psychiatric rating scale)
-rule out other conditions
*corticosteriods, stimulants, marijuana, DA-augmenting agents, hallucinigens
*HIV/AIDS, epilepsy, CVA/TBI, infections, huntington’s disease

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8
Q

positive schizophrenia symptoms

A

hallucinations
delusions
thought disorder
hostility
excitability

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9
Q

negative schizophrenia symptoms

A

affective flattening, alogia, anhedonia, amotivation, asociality

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10
Q

Non-pharmacologic treatment of schizophrenia

A

goal: realistic and time course for target symptom response, avoidance of relapse, increasing function and integration back into the community as well as avoidance of side effects
-psychosocial rehabilitation
-psychoeducation
-targeted cognitive therapy
-active community treatment (ACT)
-therapeutic alliance
-comprehensive care in a multidisciplinary environment that offers psychological services in addition to psychotropic medication management

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11
Q

general schizophrenia treatment approach

A

*SE profiles, drug interactions, adherence, family history, and cost drive therapy choice
-based on optimized monotherapy, combinations only for most treatment resistant
-favor SGA as first line over FGA
-clozapine for treatment resistance or earlier for patients who are suicidal
-long acting injectable antipsychotics for those who prefer them

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12
Q

updates to antipsychotic guidelines

A

-newer agents have not demonstrated increased efficacy over the older traditional agents
-newer agents may have more potential permanent side effects than the older
-though the range of potential risk varies among patients, these all carry the same class warning and potential
-newer agents are more expensive
-polypharmacy of any combination of agent has not demonstrated improved outcomes or efficacy
-no APS is approved for sleep in non-psychiatric conditions

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13
Q

Patho of dopamine

A

nigrostriatal- movement disorders
mesolimbic- relief of psychosis
mesocortical- akathisia, relief of psychosis
tuberoinfundibular- increased prolactin

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14
Q

D2 antagonism

A

positive symptoms efficacy, EPS, endocrine effects High 5HT2A/D2 affinity ration antipsychotic side effects reduced EPS (vs pure D2 antagonism)

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15
Q

D2 partial agonism

A

reduced positive symptoms, lowers risk of EPS

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16
Q

D3 antagonism

A

reduced positive and negative symptoms; + procognitive, antidepressant

17
Q

5-HT1A antagonism

A

reduced EPS and endocrine effects; + antidepressant & anxiolytic effects

18
Q

5-HT2A antagonism

A

reduced EPS and endocrine effects; - cardiometabolic effects

19
Q

5-HT2C antagonism

A

antidepressant effects; - cardiometabolic effects

20
Q

5-HT7 antagonism

A

reduced circadian rhythm dysfunction reduced negative symptoms; + procognitive

21
Q

a1 antagonism

A

reduced nightmares; postural hypotension, dizziness & sedation

22
Q

H1 antagonism

A

hypnotic effects (sedation); -cardimetaboic (weight gain)

23
Q

M1 antagonism

A

anticholinergic side effects (cognitive impairment)

24
Q

M3 antagonism

A

reduced EPS; - cardiometabolic, constipation, sedation, dry mouth blurred vision (anticholinergic effects)

25
Q

M4 agonism

A

clozapine only, increased hypersalivation

26
Q

D1 receptor

A

dependent modulator of glutamate, other

27
Q

sigma-1 antagonism/ inverse agonism

A

opposite effect of an agonist and are called inverse agonists
a drug can be simultaneously an agonist, an antagonist, and an inverse agonist acting at the same receptor. this means that drugs have an additional level of selectivity (signaling selectivity or “functional selectivity”)

28
Q

stabilization and maintenance of schizophrenia

A

6-12 weeks or longer; chronically ill patients may take 3-6 months
Partial responders should be evaluated for medication adherence and other confounding conditions
Relapse rate (18-32% after 12 months)
Tx for 1st episode: 12 months after remission (some support 5 years if robust response to RX), chronic lifelong therapy in most patients with severe illness
Treatment resistance generally considered lack of improvement with at least 2 APS from different classes at optimal dose for >/= 8 weeks
Rating scales to track progress (BPRS, PANSS, CGI)
Discontinuation should be gradual if possible
No “optimal” recommendations to switch agents, but gradual taper off while other agent is slowly titrated p is one option

29
Q

first generation antipsychotics

A

chlorpromazine (thorazine)
fluphenazine (prolixin)
haloperidol (haldol)
perphenazine (trilafon)
thioridazine (mellaril)
thiothixene (navane)

30
Q

FGA class related side effects

A

EPS
QTc prolongation
prolactin elevation
dermatologic
photosensitivity
blue-gray skin
orthostatic hypotension
altered thermoregulation
*Black Box: dementia related psychosis (elderly patients with dementia receiving these drugs for behavioral problems, not primary SMI)

31
Q

second generation antipsychotics

A

aripiprazole (abilify)
asenapine (saphris)
brexiparozole (rexulti)
cariprazine (vraylar)
clozapine (clozaril, fazaclo)
iloperidone (fanapt)
lumateperone (caplyta)
lurasidone (latuda)
olanzapine (zyprexa)
paliperidone (invega)
quetipine (seroquel)
risperidone (risperdal)
ziprasidone (geodon)

32
Q

SGA class related side effects

A

metabolic syndrome: hypertriglyceridemia, hyperglycemia, weight gain (waist circumference)
QTc prolongation
blood dyscrasia/ neutropenias
seizure threshold
anticholinergic effects
sedation
prolactin elevation
ophthalmic effects
*black box: dementia related psychosis

33
Q

aripiprazole (abilify)

A

activating; less sedating. may cause insomnia, akathisia & restlessness. Associated with impulsivity
Oral tablet, solution, Mycite, Initio injection and LAI

34
Q

asenapine (saphris)

A

less weight gain, less anticholinergic & sedation. Do not drink/ eat after SL dos (10mins) CI in severe hepatic disease, high risk QTc, monitor for anaphylaxis after 1st dose. Skin site reactions also seen; do not apply heat to patch area
SL tab, topical patch

35
Q

brexiprazole (rexulti)

A

long half life, akathisia (dose related), less metabolic side effects. Associated with impulsivity
Oral tablet

36
Q

cariprazine (vraylar)

A

long half life and metabolites also attributed to the late occuring adverse effects when these accumulate, akathisia (dose related), less metabolic side effects
Oral capsule

37
Q

clozapine (clozaril, fazaclo)

A

gold standard for refractory illness or sooner if suicidal risk. metabolic risks (greatest), FDA boxed warnings for blood dyscrasias (REMS program includes specific schedule based on frequency of monitoring), QTc prolongation, bradycardia, myocarditis. seizure risk with higher serum concentrations (greater than 600mg daily dose), constipation, GI hypomotility with severe complications (impaction) hypersalivation. hepatotoxicity, fever, PE, anticholinergic toxicity. Dose interruption greater than 48 hours requires re-titration from starting dose, regardless of reason for gap
Tablet, ODT, oral suspension

38
Q

iloperidone (fanapt)

A

orthostatic hypotension, priapism, no prolactin elevation reported, QTc warning, less sedation, 50% dose reduction with conflicting CYP inhibitors avoid in hepatic impairment. slow titration required
Oral tablet

39
Q
A