Brainscape's Knowledge GenomeTM

Browse over 1 million classes created by top students, professors, publishers, and experts.


See full index

PBL SEM 3 > 8 - clinical management of schizophrenia > Flashcards

8 - clinical management of schizophrenia Flashcards

1
Q

link between Sz and substance misuse

A

substance misusers (except tobacco):

  • have a greater chance of persistent low grade psychotic symptoms
  • have a greater chance of later Sz
  • earlier start and heavier use increases risk more
  • become ill 2-5 years younger
  • then have worse outcomes in every respect
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what early signs are seen in young people in development who go on to develop Sz later in life?

A
  • walk, talk, potty train later
  • less attentive in school
  • less likely to have a friend
  • develop non-specific symptoms such as anxiety, depression, poor sleep, general disorganisation (start of an at risk mental state ARMS)

> have a gradual decrease in global function compared to peers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

males vs females Sz <40yo

> 40yo?

A

males outnumber females 2:1 under 40

over 40 — very similar

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what’s the most common age of Sz presentation?

A

20

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

there is a 2nd peak in common Sz presentation — when is it and who is it more common in?

A
  • mid 40s-50s
  • particularly women
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

is there a pattern in presentation of psychosis severity by age and sex?

A

no particular pattern

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

is there a pattern for negative symptom severity at presentation in terms of age and sex?

A

-ve symptoms worse the younger you are and if you’re male

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

is there a pattern for disorganisation severity at presentation in terms of age and sex?

A

disorganised thinking and odd behaviour less severe in older patients

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

is there a pattern for excitement symptom severity at presentation in terms of age and sex?

A

older = more hostile and agitated (younger more severe excitement)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

the longer time ill without treatment……

A

the lower the response to initial treatment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

suicide in Sz?

A
  • almost 1% per year initially, eventually 4-6% but this is probably an underestimate (more around 8% in some studies)
  • maybe half serious DSH occurs before 1st treatment
  • more likely if substance misuse, recent suicidal ideation, feel hopeless, trapped and alienated, stop meds
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

40% of people who commit homocide do so when?

A

before 1st treatment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what is the mainstay of treatment?

A

antipsychotic drugs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

how do all antipsychotic drugs work?

A

reversible D2 receptor antagonists

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

dose of antipsychotic drugs is predicted by what?

A

affinity for receptor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

> _______% occupancy of D2 in ______ has an antipsychotic effect

A

> 60%

associative striatum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

> _______% occupancy of other D2 causes what? where are these other D2 receptors?

A
  • > 75%
  • causes motor side effects and hyperprolactinaemia
  • in motor striatum, hypothalamus, pituitary
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

what medication can be taken for agitation?

A

benzodiazepines (sedative, enhance GABA, reduce anxiety)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

how can motor side effects of antipsychotic drugs be treated?

A

reduce dose or anticholinergics, propranolol (beta blocker and 5-HT1a partial agonist)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

how is depression between Sz episodes treated?

A

antidepressants

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

there is less response to antipsychotic drugs for what type of symptoms?

A

-ve symptoms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

clozapine showed a substantial symptom reduction in 30-50% of what type of Sz?

A

treatment resistant schizophrenia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

what else does clozapine reduce and enable people to do?

A
  • reduce impulsivity ; violence, self harm, drug use
  • enables people to engage in rehab activity, improves QoL

however clozapine has lots of side effects

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

what fraction of people relapse after taking antipsychotics? how does this change if long-acting injectable medications are used?

A
  • 1/4
  • 1/6 with long-acting injectable meds
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

CBT for psychosis is not as good as antipsychotic for what?

A

preventing relapse

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

what form of therapy is good for relapse prevention?

A

family intervention

27
Q

social support in Sz

A
  • supported accommodation
  • families
  • groups — meaningful activity, support
  • vocational interventions, employment
  • education and training
28
Q

what kind of symptoms are extremely disruptive and harder to treat?

A

-ve symptoms

29
Q

who is most likely to relapse?

A

people who have less insight and are more severely ill

30
Q

what is a bad predictor for adherance?

A

poor insight

31
Q

insight and adherance

A
  • 40% non-adherent with APS at any given time
  • roughly 60% miss 1 week at some point
  • increases relapse odds x5
  • predicted by:

> don’t see a medication benefit
dont think will relapse
dont like medication and internal LoC (locus of control)
poor insight, poor relationship with prescribe

32
Q

how is life expectancy altered in Sz and why?

A
  • reduced by 15-25 years
  • many have unhealthy lifestyles — drug misuse, inactive, weight gain, smoking (2/3 patients with Sz smoke)
  • also suicide
33
Q

up to ____% respond to treatment initially and ___% remit

about ___% relapse, most develop persistent symptoms

after 15-20 years ____% improve again

A

95% respond 60% remit

80% relapse

15-20% improve again

34
Q

who is most likely to have negative side effects and a bad outcome?

A

male, young, poor premorbid function

35
Q

antipsychotics are best combined with what?

A

psychosocial interventions

36
Q

DSM 5 vs ICD 11 classification of schizophrenia

A

DSM 5 = american classification. 2 of:
- delusions, hallucinations, disorganised speech, disorganised or catatonic behaviour, negative symptoms
—> must include 1 of the first 3 most of the time for at least 1 month with an episode of illness lasting at least 6 months (under 6 months - schizophreniform disorder)

ICD 11 = based on “core symptoms” of:
- persistent delusions, persistent hallucinations, thought disorder, and experiences of influence, passivity or control
—> at least one symptom must have persisted for a month or more to make the diagnosis, without being caused by something else

37
Q

what do passivity/influence experiences include?

A

impulses, sensations, intentions, emotions or thoughts influenced directly by some kind of external agent

38
Q

____ in every 100,000 adults come to services with new Sz each year

A

10-20/100,000

39
Q

what % of adults in the Uk habe Sz at any one point?

A

0.4%

40
Q

the proportion of Sz is higher in who?

A

2nd generation ethnic minorities

41
Q

what is the lifetime risk of Sz for the general population?

A

1%

42
Q

male:female Sz overall?

A

1.4 : 1

(but females outnumber males over 40)

43
Q

genes associated with an increased risk of Sz fall into what 3 categories?

A
  1. connected to Glu, DA or GABA neurotransmitter function
  2. to neurone structure (often at synapses), plasticity or general synaptic function (eg. some calcium channels)
  3. to inflammatory/immune response
44
Q

what environmental events increase the risk of Sz?

A
  • child sexual abuse, being taken into care
  • cannabis or other substance misuse
  • being 2nd generation of UK ethnic minority
  • migration
  • peri-natal O2 deprivation (ie. birth asphyxia), maternal starvation while in utero
  • urban living, overcrowding, parental separation, general deprivation as a child
45
Q

list the main Sz symptoms

A
  • psychotic — delusions, hallucinations
  • disorganised — incoherent speech, bizarre, unpredictable behaviour
  • negative — apathetic, unsociable, enjoying little, speaking little, not looking after oneself but not depressed
  • excitement and agitation
  • depression sometimes
46
Q

during psychosis too much _____ is made and released in a certain brain area called the _____

A
  • dopamine
  • dorsal striatum
47
Q

adverse effects of antipsychotics due to effects on the DA system — CHAPART

A

C - constipation

H - hyperprolactinaemia (at high doses causes sexual side effects and affects periods in women)

A - anti-nausea effect

P - parkinsonism (when doses are too high)

A - akathisia

R - rarely, Neuroleptic Malignant Syndrome (NMS) (rapid onset of coma, high temp, rigidity and potentially death. often follows initiation or rapid increase in dose of potent antipsychotic like risperidone, haloperidol)

T - tardive dyskinesia

48
Q

akathisia vs tardive dyskinesia

A

akathisia — inner restlessness and constant movement, usually involving the legs. know they’re moving

tardive dyskinesia — gradual development of abnormal movements, often chewing, tongue or arm/leg movements often months, years or decades after onset dont realise they’re moving

49
Q

what are the cholinergic SE?

A
  • urinary retention
  • dry mouth
  • blurred vision
  • constipation
  • tachycardia
50
Q

when is clozapine used?

A

licensed for Treatment Resistant Schizophrenia (TRS) — if 2 antipsychotics fail or cant be tolerated at full dose

51
Q

what are some of the many side effects of clozapine?

A
  • sedation
  • hunger
  • hypersalivation
  • diabetes
52
Q

what is a rare SE of clozapine?

A

agranulocytosis — hence rigorous blood monitoring regime

53
Q

clozapine cant be dispensed without what?

A

a clear FBC

54
Q

what does clozapine bind best to? what is the clinical importance of this?

A
  • binds best to D4
  • therefore if respond poorly to CLZ, add a second APS, a clean D2/D3 antagonist like sulpiride/amisulpride to “fill in” the gap
55
Q

men and the young are more likely to oresent with what symptoms?

A

negative and disorganisation

56
Q

life expectancy in SZ?

A

around 60

57
Q

section 5(2) vs section 5(4) of the Mental Health Act?

A
  • section 5(2) — allows a consulatant or their “nominated deputy” to detain an inpatient for 72hrs until further assessed
  • section 5(4) — allows a nurse to do this
58
Q

section 2 of the MHA

A

allows 2 doctors (either, both specially trained in the MHA and mental health, or one psychiatrist and the patient’s GP) and an “approved Mental Health Professional” (usually social worker) to detain someone in hospital for 28 days for assessment (inc assessing response to a treatment) if they believe they might have a mental illness or “sufficient nature and degree” and are at risk of harming themselves or others

59
Q

section 3 of MHA

A

allows same professionals as in section 2 to detain someone in hospital for 6 months for treatment if they definitely have a specific mental illness that causes a risk to others pr their own “health or safety” and there is appropriate treatment available

60
Q

what is a Community Treatment Order?

A

allows someone discharged from section 3 to be readmitted if they don’t obey specific conditions (usually adherence to medication)

61
Q

deterioration in working memory SE?

A

antagonism of DA receptors in the mesocortical pathway

62
Q

sedation SE?

A

antagonism of H1 and alpha-adrenergic receptors

63
Q

weight gain SE?

A

antagonism of histamine H1 and serotonin 5-HT2c receptors plus effects on leptin

PBL SEM 3 (49 decks)

Brainscape helps you reach your goals faster, through stronger study habits.
© 2024 Bold Learning Solutions. Terms and Conditions