module 6 Flashcards

1
Q

prodromal symptoms

A
  • emerging symptoms that come before the first psychotic episode
  • experience changes in cognition and behaviour
  • may last for a few weeks or slowly worsen over several years
  • first stage of schizophrenia and occurs before any noticeable psychotic symptoms appear
  • 75% of people that have been diagnosed with schizophrenia go through this prodromal stage
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2
Q

examples of prodromal symptoms

A
  • non-specific symptoms
  • social isolation
  • anxiety
  • irritability
  • changes to one’s normal routine
  • sleep problems
  • neglecting personal hygiene
  • mild or poorly formed hallucinations
  • lack of motivation
  • difficulty concentrating
  • erratic behaviours
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3
Q

active symptoms

A
  • intense delusions, hallucinations, fully disorganized speech, etc
  • when an individual experiences a psychotic episode
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4
Q

residual symptoms

A
  • symptoms that remain after a full psychotic episode
  • the psychotic episode has ended and individual continue to experience symptoms with impact similar to the prodromal stage
  • no positive symptoms like hallucinations, delusions or disorganized speech
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5
Q

residual symptoms examples

A
  • lack of motivation
  • low energy
  • depressed mood
  • social withdrawal
  • difficulty concentrating
  • reduced or absent facial expression (flat affect)
  • flat or monotone voice
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6
Q

positive symptoms

A
  • hallucinations and delusions are positive symptoms
  • positive symptoms tend to decrease over time, possible due to natural age related decreases in dopamine
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7
Q

hallucinations as positive symptoms

A
  • experience of sensory events without input from external reality
  • auditory: may include voices, sounds or commands
  • visual: shadows or ghost-like images
  • almost 40% of people have experienced a hallucination
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8
Q

delusions as positive symptoms

A
  • incredibly strongly held beliefs that appear irrational to any reasonable person
  • 5 subtypes of delusions
    1. grandeur/grandiose
    2. persecutory
    3. erotomatic
    4. jealous
    5. somatic
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9
Q

grandeur/grandiose delusions

A

having a great talent or insight, or making some discovery

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10
Q

persecutory delusions

A

being cheated, spied upon, poisoned, harassed or obstructed

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11
Q

erotomatic delusions

A

someone else loves you

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12
Q

jealous delusions

A

lover/spouse is unfaithful

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13
Q

somatic delusions

A
  • involving bodily functions/sensations
  • beliefs that something is wrong with them; can also feed into hallucinations
  • capgras syndrome: believing that everyone around you has been replaced by imposters
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14
Q

disorganized symptoms

A
  1. disorganized speech
  2. inappropriate affect
  3. grossly disorganized behaviour
  4. catatonia
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15
Q

disorganized speech as a disorganized symptom

A
  • illogical speech while jumping from topic to topic
  • tangential speech: when individuals go off on tangents and their replies to questions tend to be totally irrelevant
  • loose associations/derailment: having spontaneous speech with an inability to stay on topic but there are minimal, hard to find, logical connections between thoughts
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16
Q

inappropriate affect as a disorganized symptom

A
  • expressing emotions do not match the context
  • e.g. laughing at a funeral
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17
Q

grossly disorganized behaviour as a disorganized symptom

A
  • largely disorganized behaviour
  • childish/silly behaviour
  • unpredictable agitation
  • hoarding and collecting odd items
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18
Q

catatonia as a disorganized symptom

A
  • waxy flexibility: individuals in a catatonic state are almost as if their bodies are made of soft wax that you can bend into positions
  • pacing, stereotyped behaviours
  • echolalia: repeating back or mimicking sounds you hear
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19
Q

negative symptoms

A
  1. avolition/apathy
  2. alogia
  3. anhedonia
  4. affective flattening/flat affect
  5. asociality
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20
Q

avolition/apathy as a negative symptoms

A
  • little interest in daily functions including hygiene
  • inability to initiate or persist in activities
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21
Q

alogia as a negative symptom

A

little use of speech or interest in conversation

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22
Q

anhedonia

A

little interest in pleasurable activities

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23
Q

affective flattening/flat affect

A

lack of emotional expression

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24
Q

asociality as a negative symptom

A

little interest in socializing and poor social skills

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25
Q

criteria A for a psychotic episode and schizophrenia

A
  • criteria A defines active psychosis
  • two or more of the following during a one month period:
    1. delusions
    2. hallucinations
    3. disorganized speech
    4. grossly disorganized or catatonic behaviour
    5. negative symptoms
  • at least one of either delusions, hallucination or disorganized speech must be present
26
Q

schizophrenia criteria

A
  • level of functioning has deteriorated below what was seen before onset
  • continuous sign of the disorder must be present for at least 6 months either in prodromal, active or residual states
  • rates are equal between men and women
  • life prevalence = 0.3%-1%
27
Q

schizoaffective disorder

A
  • experience an active psychosis (criteria a), concurrent with mood episode (mania or major depressive) to receive a diagnosis
  • hallucinations or delusions must have occurred outside of mood episodes as evidence of a mood disorder outside of a psychotic episode
  • mood episode occurs throughout the majority of the active and residual periods
  • similar negative prognosis as schizophrenia
  • rates are higher in women than men because women are more likely to have depression
  • life% = 0.3%
28
Q

schizophreniform disorder

A
  • active psychosis (criteria a) for at least one month but deterioration in functioning lasts less than 6 months
  • less impairment of functioning
  • often serves as a provisional diagnosis while we wait to see if it develop into schizophrenia
  • effects men and women equally
  • occurs much more in developed countries
  • life prevalence: 0.1%-1%
29
Q

brief psychotic disorder

A
  • experience one or more of the following for at least 1 day, but for less than 1 month:
    1. delusions
    2. hallucinations
    3. disorganized speech
  • may also experience catatonia
  • you can only be diagnosed retrospectively; after the symptoms have remitted
  • symptoms present for less than one month
  • twice as common in men
  • life% = 0.1%-0.5%
30
Q

delusional disorder

A
  • must experience one or more delusions for 1 month or longer
  • apart from the impact of the delusions, functioning is not impaired and behaviour is not odd
  • does not meet criteria for schizophrenia, though hallucinations may be present but they must fit within the delusional themes and more not be prominent
  • delusions tend to not be as bizarre as in schizophrenia
    and are of things that can happen in real life such as being followed, poisoned, infected, loved at a distance, being deceived by a spouse or lover
  • function must better than those with schizophrenia or schizoaffective and have less impairment and have no negative symptoms
  • life% = 0.2%
31
Q

psychological models - etiology

A
  • stress
  • families
32
Q

psychological methods - stress etiology

A
  • stress has a bidirectional relationship with psychosis and relapse
  • stressful events can precede relapse
  • can trigger subsequent psychotic episodes
  • symptoms cause people to drop in socioeconomic status
  • social support from non-family can improve outcomes
33
Q

psychological methods - family etiology

A
  • may see symptoms as intentional
  • attitudes towards loved ones with schizophrenia tend to be negative
  • expressed emotion such as criticism, animosity and intrusiveness
  • individuals with families with high expressed emotion can trigger a relapse quicker
  • in latin american families, criticism had no effect on relapse but lack of warmth did
  • in african american families, expressed emotion decreased relapse
  • this could be because expressed emotion was experienced as compassion and more openness by the individual
34
Q

psychological methods and treatments - historical treatments

A
  1. psychoanalytic/psychodynamic
  2. token economy
35
Q

psychoanalytic/psychodynamic as a historical treatment

A
  • have historically been harmful
  • schizophrenogenic mothers: moms who were characterized as cold, rejecting and overprotective caused their kids to have schizophrenia
36
Q

token economy as a historical treatment

A
  • involve rewarding someone for positive behaviour to get them to continue positive behaviour while punishing negative behaviour
  • formerly used in psychiatric hospitals
37
Q

psychological models and treatments - modern treatments

A
  1. community resources
  2. clinicians
  3. first episode clinics
38
Q

community resources as a modern treatment

A

individuals may be connected with life coaches, peer groups, recreational therapists

39
Q

clinicians as a modern treatment

A
  • help clients detect relapse, manage medications, and deal with stress
  • teach to deconstruct complex social skills and model healthy social skills (e.g. how to make a friend, how to give feedback)
  • initial positive results tend to fade when treatment is done
40
Q

first episode clinics as a modern treatment

A
  • the earlier you can intervene in an illness the more likely you are the decrease relapses
  • provide individuals and family with psychoeducation
  • targets those who have experienced their first active phase episode
  • connect with support systems and community resources
  • prescribe correct medications, offer therapy, help with medication compliance
41
Q

psych. models and treatments - behavioural family therapy

A
  • classroom-type psychoeducation for family members to help understand the disorder
  • may include some training in expressed emotion
  • effective in the short-term and helpful while they are in treatment, but tend to decline when family members leave treatment
42
Q

psych. models and treatments - becks CBT

A
  • targets negative symptoms along with the same lines as CBT for depression since symptoms are similar (i.e. automatic thoughts)
  • targets positive symptoms with very gentle questioning of beliefs with evidence
  • provides a sense of self-control
  • can lead to significant improvements that appear to last although many tend to require more significant interventions due to the nature of the disorder
43
Q

age of onset for psychotic disorders

A
  • late teens to late twenties
  • men = early twenties
  • women = late twenties
44
Q

psychotic disorders as neurodegenerative disorders

A
  • not supported by research
  • most have moderate to severe levels of impairment and levels of functioning that stay stable through life after the first episode is experienced
  • positive symptoms may sometimes decrease in severity with age
  • men tend to have the worst outcomes prognosis wise
45
Q

differences in prevalence of psychotic disorders cross-culturally

A

usually members of minority or marginalized groups are more likely to be forced into hospitalization and given injections as well as receive the worst treatment

46
Q

bio models and treatment etiology

A
  • genetic contribution
  • dopamine
  • glutamate
  • brain structure
  • viral infection
47
Q

bio models etiology - family studies as a genetic contribution

A

parents who have more severe forms of schizophrenia predisposes their children broadly to psychotic disorders

48
Q

bio models etiology - twin studies as a genetic contribution

A

identical twins are more at risk of having schizophrenia, followed by fraternal twins who are slightly more at risk then siblings due to shared in utero environment and upbringing

49
Q

bio models etiology - adoption studies as a genetic contribution

A

individuals can still be at risk of developing schizophrenia/psychotic disorder if their bio parents had schizophrenia but being adopted into healthy environments can delay the onset and decrease severity of the disorder

50
Q

bio models etiology - genes and cannabis as a genetic contribution

A
  • 10% of the population is a carrier for some genes
  • most people who smoke cannabis don’t become psychotic, however use during sensitive periods (i.e. teen years) can increase chances of onset within a specific group with specific genetic profiles
51
Q

bio models etiology - dopamine as a genetic contribution

A
  • individuals with schizophrenia have excessive stimulation of D2 receptor sites and under stimulation of D1 receptor sites
  • d2 sites are located in the basal ganglia and tend to be associated with positive or disorganized symptoms
  • d1 sites are located in the prefrontal cortex in our limbic system and tend to be associated with negative symptoms
52
Q

bio models etiology - glutamate as a genetic contribution

A
  • under stimulation of NMDA receptor sites
  • PCP and ketamine are NMDA antagonists and block glutamate
  • related to positive and negative symptoms
53
Q

bio models etiology - brain structure as a genetic contribution

A
  • proposed 3 points of brain structure as causes of schizophrenia:
    1. enlarged ventricles
    2. decreased frontal lobe activity
    3. 22q deletion syndrome
54
Q

brain structure as a cause of schizophrenia - enlarged ventricles

A
  • enlarged ventricles cause schizophrenia because researchers have found through brain dissection that a lot of people with schizo. have them
  • however this could be due to atrophied brain areas, brain areas that never fully developed or prenatal influenza
55
Q

brain structure as a cause of schizophrenia - decreased frontal lobe activity

A
  • linked to negative symptoms
  • could be the result of viral infections
56
Q

brain structure as a cause of schizophrenia - 22q deletion syndrome

A
  • rare genetic disorder where children are born with 1 copy of chromosome 22 that is missing a segment that includes anywhere between 30-40 genes
  • have a 25-33% chance of developing schizophrenia making it the most common genetic risk factor for the development of schizophrenia
  • also often born with heart defects, increased chance of learning and cognitive disabilities
57
Q

bio models etiology - viral infection as a genetic contribution

A

2nd trimester prenatal influenza has been linked to schizophrenia

58
Q

bio models & treatments - conventional antipsychotics

A
  • work for about 60-70% of clients with the intention to prevent relapse as much as possible while mitigating symptoms
  • can cause severe side effects that make medication compliance difficult
  • can cause extrapyramidal symptoms & tardive dyskinesia, grogginess, difficulty thinking, weight gain, sexual issues & blurred vision
59
Q

extrapyramidal symptoms

A

e.g. parkinsons, expressionless face, slow movements, monotone speech and spasms

60
Q

tardive dyskinesia

A
  • results in excessive eye blinking, protrusions of the tongue, puffing of cheeks, or chewing movements
  • 3-5% will develop these symptoms within 5 years and they may be irreversible
  • longer someone is on the meds the higher likelihood they will develop it
61
Q

bio models & treatments - newer antipsychotics

A
  • fewer side effects, work as well if not better
  • though they can technically cause similar side effects it is less common
  • may work on both positive and negative symptoms