1. Psychosis Flashcards

1
Q

Describe: Psychosis (4)

A
  • Psychosis is an interruption from reality that may affect thought process, thought content, behaviors, and/or perceptions.
  • It is manifested by delusions, hallucinations, disorganized thoughts and behaviors, or failed reality testing.
  • Delusions are fixed, false beliefs that fall outside of cultural norms.
  • Psychosis is a symptom and not a Dx.
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2
Q

Schizophrenia is characterized by what? (3)

A
  • positive symptoms (delusions, hallucinations)
  • negative symptoms (affective blunting, anhedonia, avolition, alogia)
  • and cognitive impairment (attention, concentration, processing speed, learning, memory, executive function).
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3
Q

The lifetime prevalence of schizophrenia is what? (1)

A

1% .

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4
Q

Age of onset of psychosis in schizophrenia is when?

A

late teens to mid-30s, and is earlier for men.

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5
Q

A prodrome is often noted in adolescence when? (3)

A
  • when nonspecific symptoms such as social withdrawal, irritability, antagonistic thoughts, and functional decline become noticeable by others
  • Attenuated psychotic signs present during this time such as suspiciousness and perceptual distortions are thought to have a high positive predictive value for schizophrenia.
  • This is an area of active clinical interest as it is thought that a long duration of untreated psychosis is related to adverse outcomes.
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6
Q

The genetic risk for schizophrenia is ___% when both parents are affected, and ___% with a monozygotic twin.

A

The genetic risk for schizophrenia is 50% when both parents are affected, and 60% to 84% with a monozygotic twin.

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7
Q

Name psychosis environmental factors (3)

A
  • perinatal events
  • obstetric complications
  • social stressors.
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8
Q
A
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9
Q

What produces positive symptoms? (1)

A

Hyperdopaminergic state in the D2 striatal system

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10
Q

What leads to cognitive deficits? (2)

A
  • hypodopaminergic state in the prefrontal D1 system
  • Glutamate and GABA have also been investigated, and activity at the glutamater- gic and GABA receptors produces some of the behavioral and cognitive symptoms of schizophrenia.
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11
Q

What explains negative symptoms? (1)

A

However, the dopamine theory does not adequately explain negative systems, and it is thought that other monoamine receptors (serotoninergic, histaminergic, muscarinic, a-adrenergic) are contributory.

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12
Q

What explains the high use of tobacco among patients with schizophrenia? (1)

A

the involvement of acetylcholine is thought to explain

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13
Q

Name changes in imageries in psychosis (4)

A
  • The most common anatomical finding is enlargement of the ventricles.
  • PET studies show reduced frontal lobe activation.
  • Functional MRI studies demonstrate functional circuit disruption rather than localized dysfunction.
  • Diffusion tensor imaging looks at the structural integrity of white matter, and decreased coherence has been shown in the prefrontal cortex and in frontotemporal and frontoparietal tracts
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14
Q

Describe HX of psychosis (17)

A
  • Important notes before beginning the interview:
    • The patient who is psychotic will not be reliable and he or she may have no insight. Collateral information gathered from family, caregivers, ambulance, or available police reports is needed to corroborate information.
    • Make sure that you are safe during the interview. Patients with psychosis may act erratically if they are paranoid, attending to internal stimuli (e.g., command hallucinations).
  • Patient identifiers: name, age, occupation
  • Social and contextual information: relationship status, living arrangement, work or source of income, children, caregivers of children besides the patient
  • Who is looking after the patient’s children? Does social work have to be involved?
  • Ask about the DSM-5 criteria for psychotic disorders
  • Recent and current stressors: personal losses that have occurred or anticipated (e.g., death in family, loss of work, property), role transitions, financial difficulties, interpersonal conflict, isolation
  • Social supports available
  • Suicide
  • Screen for symptoms of depression, mania/hypomania, and anxiety
  • Substance use: Comorbid substance use is common.
  • Forensic history
  • Psychiatric history
    • For the multiepisode patient, it is crucial to know what medications have been tried, which ones worked, the side effects that occurred, and what doses have been tried and for how long.
  • Family psychiatric history: Particularly important in patients with first-break psychosis
  • Medical history
  • Medications
  • Allergies
  • Personal history: childhood relationships, performance in school at different stages, highest level of education, occupations held, relationships in adolescence and adulthood, history of abuse at any stage in life
    • Look for signs of attenuated psychosis in the prodromal period in the first break patient
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15
Q

Name DDx of psychosis (Figure)

A
  • Psychiatric
    • Psychotic disorders
      • Schizophrenia
      • Schizophreniform
      • Brief psychotic disorder
      • Delusional disorder
      • Schizoaffective disorder
    • Bipolar I disorder with psychotic features
    • Major depression with psychotic features
    • OCD
    • Mental retardation
    • Autism spectrum disorder
    • Personality disorders
      • Schizotypal, Schizoid, Borderline, Paranoid
    • Malingering, factitious
  • Substance/Medications
    • Substance of abuse
      • Alcohol, sedative withdrawal
      • Cannabis
      • Stimulants, hallucinogens, ketamine
      • Anxiolytics
    • Prescription medications
      • Anesthetics, analgesics, anticonvulsants
      • Anticholinergics
      • Antihistamines
      • CV medications
      • Steroids
      • Dopamine agonists, MAOIs
      • Digitalis toxicity
    • Toxins
      • Organophosphates
      • CO, CO2
      • Volatiles, fumes, paint
  • General medical conditions
    • CNS
      • Lesions
      • Infections: HIV, Neurosyphilis
      • Seizures*
      • Strokes
    • Systemic illness
      • Autoimmune diseases
      • Metabolic abnormalities*
      • Endocrine abnormalities*
      • Vitamin deficiencies
      • Sepsis
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16
Q

Describe: General observation and physical exam of psychosis (4)

A
  • Mental status exam
  • Vital signs, pupils, neurologic exam, signs of self-harm behavior, stigmata of drug or alcohol use, signs of hyperthyroidism, or other metabolic abnormalities
  • The Canadian Journal of Psychiatry Clinical Practice Guidelines also recommends the following physical exams or assessments at baseline: neuropsychological test- ing, ocular exam, exam for Parkinsonism and extrapyramidal symptoms, BMI, and waist circumference measurement.
  • A functional inquiry into endocrine and sexual functions is also recommended at baseline and monthly for 3 mo when starting a new antipsychotic.
17
Q

Describe: Mental status exam of psychosis (14)

A
  • dishevelled
  • unkempt
  • attending to internal stimuli
  • poor hygiene
  • nicotine stains on fingers
  • speech is slow, decreased spontaneity, increased latency in response
  • affect may be restricted or blunted
  • may appear perplexed
  • hallucinations in any sensory modality but particularly auditory
  • misperceptions of environmental stimulus
  • thought form may show derailment from linear thinking and incoherence
  • various pathologies such as echolalia, neologisms, word salad, or there may be thought blocking
  • there may be delusionary content or a lack of spontaneous thought
  • often there is no insight and judgment may be impaired by attending to command hallucinations or internal stimulus
18
Q

Describe investigation of psychosis (13)

A
  • The Canadian Journal of Psychiatry Clinical Practice Guidelines for schizophre nia recommends the following investigations at baseline:
    • CBC
    • electrolytes
    • renal function tests
    • toxicology screen
    • liver function tests
    • thyroid function tests
    • fasting plasma glucose
    • lipid panel
    • testing for syphilis and HIV.
    • These may be repeated as indicated clinically.
  • Other investigations recommended at baseline may include a
    • head CT or MRI for structural brain abnormalities,
    • ECG
    • clinical screening for chromosome 22q11 (with testing if indicated clinically).
19
Q

Describe A simplified Dx tree of psychotic psychiatric disorders. (Figure)

A
20
Q

Describe: Management of psychotic patient/thought disorders (7)

A
  • Pharmacologic
    • Antipsychotics: Typical, Atypical
  • Psychosocial
  • Hospitalization
  • Others
    • Psychoeducation for patient, caregiver, and family about nature and natural history of psychosis
    • Rehab and day programs, case management, supportive housing, ACT teams, community support groups for patients and family members, sheltered work programs
    • Emotional support
    • Select patients who need specialized care
21
Q

Describe plasma peak of antipsychotics (2)

A
  • Oral (peak plasma levels after 1–4 h)
  • intramuscular (peak plasma levels after 30 min, with clinical effects starting after 15–30 min).
22
Q

Between atypical and typical antipsychotics, why one is used first? Why? (2)

A
  • An atypical antipsychotic is often used first (less chance in developing extrapyramidal symptoms and tardive dyskinesias that can be debilitating).
  • The trade-off is an increase in metabolic side effects.
23
Q

How long should you use antipsychotics before changing?

A

6–8 wk at an optimized therapeutic dose

24
Q

After two failed trials of different antipsychotics (i.e., 6–8 wk at an optimized therapeutic dose), what can be tried? (3)

A
  • clozapine may be tried.
  • Clozapine is the most efficacious medication for treatment of schizophrenia, but has serious side effects that need regular and consistent monitoring (e.g., agranulocytosis, seizures, myocarditis).
  • Specialist involvement is necessary for clozapine management. Once started, withdrawal is not to be taken lightly as it is a “last-line” medication.
25
Q

Name Typical—high potency antipsychotics (2)

A
  • haloperidol (haldol)
  • fluphenazine (Modecate)
26
Q

Name indications/CI/adverse effects: Typical—high potency antipsychotics (2)

A
  • Indications:
    • Positive symptoms
    • pregnancy (haloperidol)
  • CI: Preexisting movement disorder/TD
  • Adverse effects:
    • Higher risk of EPS/TD
    • hyperprolactinemia
27
Q

Name examples Typical antipsychotic —low potency (2)

A
  • chlorpromazine (Largactil)
  • thioridazine (Mellaril)
28
Q

Name indications/CI/adverse effects: Typical antipsychotic —low potency (2)

A
  • Indications: Positive symptoms
  • CI: Preexisting movement disorder/TD
  • Adverse effects:
    • Lower risk of EPS/TD
    • postural hypotension
    • sedation
    • anticholinergic (blind as a bat, mad as a batter, dry as a bone, red as a beet, hot as a hare)
29
Q

Name examples: Atypical antipsychotics (7)

A
  • olanzapine (Zyprexa)
  • Risperidone (Risperdal)
  • Ziprasidone (Zeldox®)
  • Clozapine (Clozaril®)
  • Quetiapine (Seroquel®, Seroquel XR®)
  • Amisulpride (Solian)
  • aripiprazole (Abilify)
30
Q

Name indications/CI/adverse effects: Atypical antipsychotics

A
  • Indications:
    • Positive or negative or cognitive symptoms
    • preexisting movement disorders sensitivity (quetiapine or clozapine)
    • treatment-refractory (clozapine)
    • suicidality (clozapine)
  • CI: Diabetes (relative not absolute)
  • Adverse effects:
    • Low risk of EPS/TD
    • weight gain/hyperglycemia/hyperlipidemia/diabetes
    • sedation
    • agranulocytosis (clozapine—need weekly CBC for 6 mo then ≥biweekly CBC)
    • prolonged QT interval (especially quetiapine—need ECG monitoring)
31
Q

Describe Psychosocial tx of psychosis (2)

A
  • Supportive psychotherapy—reassure, explain, clarify, guide, and suggest
  • CBT—same as supportive and also to gradually help patient challenge their delusional beliefs by examining evidence for them
32
Q

Who to hospitalize in psychotic patients? (2)

A
  • For suicidal or aggressive patients and patients who cannot care for themselves outside hospital
  • For stabilization of acute episodes