IC11 Schizophrenia & Psychosis Flashcards

1
Q

What is psychosis?

A

Psychosis is when a person is out of touch with reality

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2
Q

What is schizophrenia?

A

Schizophrenia is when a person experiences psychosis for prolonged periods of time (at least 6 months).

Schizophrenia is a more severe form of psychosis.

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3
Q

What are possible causes of psychosis?

A
  1. Iatrogenic causes - mistake made in treatment
  2. Alcohol & psychoactive substance misuse
  3. Mood disorders - mania, severe depression
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4
Q

What are the 2 main theories that can lead to schizophrenia?

A

It is the dysregulation of:
1. Dopaminergic (DA) functions
2. Serotonergic (5HT) functions

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5
Q

What are common risk factors that increases the chance of a patient developing schizophrenia?

A
  1. Genetics
  2. Neurodevelopmental effects
  3. Personality
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6
Q

What are possible risk factors that can cause a patient to develop schizophrenia?

A
  1. Tumour or injury
  2. Drug / substance-induced psychosis
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7
Q

What are risk factors that prolong schizophrenia in patients?

A
  1. Poor adherence to antipsychotic medication
  2. Lack of support
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8
Q

What are the criteria to diagnose a patient with schizophrenia?

A

A. 2 or more of the following persisting for 1 month:
- delusions
- hallucinations
- disorganized speech
- disorganized appearance OR catatonic behaviour
- negative symptoms

B. Social / occupational dysfunction

C. Continuous signs of disorder for at least 6 months (inclusive of criteria A)

D. Other possible conditions have been excluded

E. Disorder is NOT due to a medical disorder or substance use

F. If there is pervasive developmental disorder - there must be hallucinations or delusions present for at least 1 month

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9
Q

What should we assess for a patient suspected with schizophrenia?

A
  1. History of present illness
  2. Psychiatric hx
  3. Substance Use hx
  4. Medication hx
  5. Family, occupational hx
  6. Any injury or trauma
  7. Assess for suicidal tendencies***
  8. Lab tests
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10
Q

What are the goals of therapy in treating schizophrenia?

A
  1. Minimize threat to self & others
  2. Minimize acute symptoms
  3. Prevent relapse
  4. Promote medication adherence
  5. Optimise dose and manage ADR
  6. Improve QOL & function
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11
Q

What are non-pharmacological management treatments that we can use?

A
  1. Social support & counselling
  2. Individual Cognitive Behavioural Therapy (CBT)
  3. Electroconvulsive therapy (ECT)
  4. Psychosocial rehabilitation program

CBT can be considered if patient is in a listening state.

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12
Q

What is the main class of drug to use for schizophrenia?

A

Anti-psychotics

Antipsychotics help to relieve symptoms of psychosis & prevent relapse.

Long-term treatment is often necessary

Antipsychotics can be used to treat mania.
Antipsychotics can also be used together with Antidepressants for pt w Major Depression.

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13
Q

How can we overcome the poor adherence to anti-psychotic medications?

A
  1. Use IM long-acting injections
  2. Educate pt & family
  3. Have community nurse provide regular home visits & administer the medication.
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14
Q

Recall what are the 4 dopamine pathways:

A
  1. Nigrostriatal pathway
  2. Mesolimbic pathway
  3. Mesocortical pathway
  4. Tuberoinfundibular pathway
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15
Q

What are the functions of the 4 dopamine pathways?

  1. Nigrostriatal pathway
  2. Mesolimbic pathway
  3. Mesocortical pathway
  4. Tuberoinfundibular pathway
A

Nigrostriatal pathway:
- Nigrostriatal pathway controls movement. Blocking the dopamine receptors in the nigrostriatal pathway will lead to extrapyramidal side effects (EPS)*

Mesolimbic pathway::
- Overactivity of dopamine receptors in this region leads to positive symptoms* of schizophrenia. Main MOA of anti-psychotics is to block dopamine receptor in the mesolimbic pathway

Mesocortical pathway:
- Dopamine blockade of the mesocortical pathway will lead to negative symptoms* in schizophrenia.

Tuberoinfundibular pathway:
- Dopamine blockade in this pathway leads to hyperprolactinemia*

Blockade of the nigrostriatal, mesocortical & tuberoinfundibular pathway will lead to ADR.

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16
Q

Based on your knowledge of the 4 pathways, what are the effects of using dopamine antagonist?
(Name both good and bad effects)

A

Good effect:
- Helps to reduce positive symptoms

Bad effects:
- Extrapyramidal side effects
- Hyperprolactinemia

17
Q

Based on research, dopamine antagonists are effective as antipsychotics if they block _____% of dopamine receptors.

(A) 50%
(B) 60%
(C) 70%
(D) 80%

A

Ans: 60%

If inhibition of dopamine receptors exceed 60%, there will be hyperprolactinemia and EPS.

18
Q

Can you list out the guideline to treat and manage schizophrenia?

A

Upon diagnosis of schizophrenia,

      1. Use a single* FGA or SGA (avoid clozapine)

      2. If it doesn't work, use another single* FGA & SGA (avoid clozapine)

      3. If it doesn't work, use clozapine*

      4. If clozapine doesn't work, use combination therapy
                - FGA + FGA
                - FGA + SGA

If any of the treatment is sufficient w tolerable side effects, we can continue using the same treatment without escalating.

19
Q

What are the rules to follow in the treatment guideline of schizophrenia?

      1. Use a single* FGA or SGA (avoid clozapine)

      2. If it doesn't work, use another single* FGA & SGA (avoid clozapine)

      3. If it doesn't work, use clozapine*

      4. If clozapine doesn't work, use combination therapy
                - FGA + FGA
                - FGA + SGA

If any of the treatment is sufficient w tolerable side effects, we can continue using the same treatment without escalating.

A

These are the rules to follow when using the treatment guideline:

  1. Medication selection is individualized
  2. Pt to be on a medication for at least 2-6 weeks at therapeutic doses, before we consider it as ineffective***
  3. Help patients to manage side effects. If intolerable, switch to another agent
  4. Consider long acting injectable anti-psychotics to improve compliance
  5. ***Only consider clozapine in treatment resistant pt that have failed ≥2 types of antipsychotics. Monitor pt on clozapine closely and regularly.
20
Q

What is the most significant ADR of clozapine?

A

Agranulocytosis

21
Q

What are adjunctive medications that we can use in:
(1) Cooperative patient
(2) Uncooperative patient

A

(1) Cooperative pt:
- Oral lorazepam
- Oral risperidone

(2) Uncooperative pt:
- IM lorazepam
- IM olanzapine
- IM haloperidol

22
Q

What are the 3 common characteristics of oral antipsychotics?

A
  1. 1-3 hours to reach peak concentration
    - Most oral antipsychotics take 1-3hrs to reach peak concentration
  2. Long half-life
    - Most oral anti-psychotics have long half-life
  3. Drowsiness
    - Most antipsychotics have drowsiness effect. Advice patient to take the medication at night.
23
Q

List out first generation antipsychotics (FGA) and second generation antipsychotics (SGA).

A

FGA:
1. Haloperidol
- Haloperidol often comes as haloperidol decanoate, where the phenol group of the compound is esterified

SGA:
1. Clozapine
2. Quetiapine
3. Risperidone

24
Q

What is the difference in terms of side effects between FGA & SGA?

A

In general, FGA have more SE than SGA.

  1. FGA has more EPS than SGA***.
  2. FGA has more severe hyperprolactinemia SE than SGA
  3. The FGA that we learn in this IC do not cause weight gain, whereas SGA medication - clozapine and olanzapine can lead to severe weight gain

All SE are dose dependent!

25
How to manage these side effects: 1. Dystonia (involuntary muscle contraction) - EPS 2. Pseudo-parkinsonism - EPS 3. Akathisia (inability to remain still) - EPS 4. Tardive dyskinesia (involuntary movements of the tongue, lips, face, trunk, and extremities ) - EPS 5. Hyperprolactinemia 6. Metabolic 7. CNS - neuroleptic malignant syndrome (NMS) - NMS is life-threatening and associated w muscle rigidity, fever, autonomic dysfunction, altered consciousness, ↑CK 8. Haematological - ↓WBC, agranulocytosis, ↓absolute neutrophil count
[Those w * are ones I should prioritise memorising] 1. Dystonia (involuntary muscle contraction) - EPS - *Use IM anticholinergics 2. Pseudo-parkinsonism - EPS - ↓ antipsychotic dose OR switch to SGA - *Use anticholinergics PRN 3. Akathisia (inability to remain still) - EPS - ↓ antipsychotic dose OR switch to SGA - *Clonazepam PRN 4. Tardive dyskinesia (involuntary movements of the tongue, lips, face, trunk, and extremities ) - EPS - *Discontinue any anticholinergics - *Use valbenazine - ↓ antipsychotic dose OR switch to SGA - Clonazepam PRN 5. Hyperprolactinemia - Switch to apriprazole - a SGA 6. Metabolic - *Treat diabetes & hyperlipidemia - *Switch to lower risk agents - Modify lifestyle 7. CNS - neuroleptic malignant syndrome (NMS) - NMS is life-threatening and associated w muscle rigidity, fever, autonomic dysfunction, altered consciousness, ↑CK - Use IV dantrolene - Switch to 2nd SGA 8. Haematological - ↓WBC, agranulocytosis, ↓absolute neutrophil count - Discontinue antipsychotic if severe
26
What can we use to monitor SE of antipsychotics use? (Think of the ADRs and what we can use to monitor them)
1. EPS exam 2. BMI - to measure weight gain 3. Fasting blood sugar - to monitor DM 4. Lipid panel 5. WBC & absolute neutrophil count (ANC)
27
What are drugs that may interact with antipsychotics?
1. Drugs with CNS depressant effects - e.g benzodiazepines, alcohol, opioids 2. Drugs that inhibits M1, H1, a1-adrenoceptors 3. Dopamine augmenting agents - e.g levodopa 4. Anti-hypertensives - can worsen hypotensive effects 5. CYP1A2 inhibitors - fluvoxamine, quinolones, macrolides 6. Carbamazepine - avoid use w clozapine, can worsen agranulocytosis
28
What are the improvements that we can observe in a patient initiated on antipsychotics after: (1) 1 week (2) 2-4 weeks (3) 6-12 weeks
After 1 week of taking anti-psychotics: - ↓ agitation, aggression After 2-4 weeks of taking anti-psychotics: - ↓ paranoia, hallucinations After 6-12 weeks of taking antipsychotics: - ↓ delusions, improvement in -ve symptoms