Psychosis Flashcards

1
Q

define psychosis

A

clinical state of mind characterised by loss of contact with reality

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

explain the 2 perceptual disturances that the pt might eperience ?

A

delusion : are fixed unshakeable beliefs
Hallucinations : are perceptions without adequate stimuli e.g. hearing voices or seeing dead people

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

what negative symptoms they might experience ?

A
  • blunting of affect
  • Avolition (lackk of motivation to complete tasks )
  • alogia ( inability to speak because o cognitive impairement ,mental confusion or aphasia)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what to do when pt has delirium with acute confusion and aggression ?

A

delirium is dengerous more than psychosis because with psychosis the LOC is normal but with delirium they can not maintain normal LOC-> this is a medical emergency
- always look for a cause -> DIMTOP (drugs, infection, metabolic, trauma, oxygen, psychological)

-> OTHER SYMPTOMS :Impaired awareness, confusion, disorientation others (restlessness, agitation and hallucinations, ANS symptoms,aggressiveness )

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

explain the pathogenesis of psychosis

A

UNknown
-Dopamine hypothesis of schizophrenia
Excessive dopaminergic activity
- role of dopamine : the dopamine hypothesisi :
-used to explain that the unusual behaviours in psychosis can be largely explained by dopamine function changes in the brain .

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

name the 2 functional psychotic conditions

A

-Schizophrenia
-Bipolar mood disorder

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

what causes pyschotic disorders

A
  1. medical conditions such as epilepsy, Alzheimer’s dementia, HIV, neurosyphilis,urimia(renal failure),encephalytis
  2. drugs :
    - Illicit drugs –cannabis, mandrax, cocaine, amphetamines(over the counter ,all diet tablets contain them ),PCP(Phencyclidine aka angel’s dust),psilocybin (magic mashrooms ),alcohol( delirium tremors (happens 36 hours later ),thymine definciency and can cause hypoglycaemia in people with poor diet )
    -Prescription drugs- steroids, antiparkinsonism drugs, atropine(anticholinergic ),lithium,all the opiods,Ketamine( used in anesthesia ,excelent analgesic,causes dissociation)
  3. others: e.g. postpartum psychosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

mane the 4 major pathways by which dopamine affects the brain and their function

A

1.mesolimbic pathway - resiponsibile for the negatve symptoms in Schiezophramia -> hyperactive in Schiezophrania -> hallucinations and delusion
2. Mesocortical pathway -> responsible for the positive symptoms of schizophrenia ->behaviour ( symptoms such as lack of motivation and social withdrawal )->underactive in Schiezo
3. Nigrostrial->coordination of voluntary movement->blocked by typical antipsychotics ->extra[yramidal symptoms (deficiency of Dopamine in this pathway can lead to dystonia and parkinson’s symptoms while excess causes dyskinetic symptoms .

  1. Tuberoinfindibular- prolactin secretion -> dopamin in this pthway is responsible for inhibition of prolactin secretion from the pituitary gland .
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what are the indications for neuroleptics ?

A

Primary
Schizophrenia
Mania
Organic psychosis

Others
Nausea and vomiting
Intractable hiccups
Tourette’s syndrome
Behaviour disorders
Anaesthesia

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

explain the approach to management of psychosis

A
  1. Depends on : aetiology and onset of the pyschosis
  2. Acute management (agitated or acutely disturbed pt)
    Goals of therapy is to calm pt down and achieve containment.
    Antipsychotic and/or benzodiazepine of your choice
  3. Chronic management :
    Goal of therapy is to prevent relapse of acute psychotic symptoms i.e. delusions, hallucination so as to maintain functionality
    - Antipsychotic drugs
    - Supportive psychotherapy for patient and family
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what is the difference between classic and atypical neuroleptic drugs ?

A

dopamine receptors that they target .
- classical neuroleptics : (they have high affirnity except for chlorpromazine and Thioridazine )
Dopamine 2 receptors antagonists ,they have the tendency to cause extrapyramidal side effects .
-Atypical neuroleptics :
D2 and D3 receptors antagonists
and D2 (bind weakly )AND serotonin receptor antagonist(strongly ).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

List the traditional neuroleptics (classic neuroleptics )

A
  1. Phenothiazines (side chain)
    - Aliphatic e.g. chlorpromazine
    - Piperazine e.g. prochloperazine, fluphenazine
    - Piperidine e.g. thioridazine*(discontinued due to cardiotoxicity), pericyazine.
  2. Butyrophenones
    - Haloperidol, droperidol
  3. Thioxanthenes
    - Flupenthixol, zuclopenthixol
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what is the formulation for typucal neuroleptics ?

A
  1. Oral
  2. Injectable - usually IM injection.
    - short acting - acute management
    -long acting depot preparations -preferred if compliance a problem.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

explain the mechanism of action for typical antipsychotics

A

Block the D2 and D1 receptors .
This drugs have high affinity (bind strongly on the receptors )
Side effects :
1. D2 receptor antagonism -> affects the nigrostriatal pathway (mostly high affinity drugs than low )-> causes extrapyramidal ( dystonia , akathisia, parkinson sx)
2. Antimuscarinic effects (low>high)->dry mouth , constipation, blurred vision ,urinary retension .
3. Blocks 5-HT2 (5-hydroxytryptamine )receptors ->mood ,digestion ,sexual health ,sleep-wake cycle , Nausea
4. Alpha 1 receptors antagonist (low>high)->orthostatic hypotension
5. Histamine H receptor antagonist (low>high)
-Weight gain and sedation .

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

what is the potency, duration of onset ,half life and doses for Chlorpromazine?

A
  • potency : low ( this is the oldest neuroleptic of low potency )
  • half life : 30 hrs
  • duration of onset : 30-60min after oral ingestion and 15min after injection
    -Doses : initially 25mg tds but maintenance range 75-300mg.
    IM 25-50mg ,can be repeated 3-4 times in 24hrs as necessary
    USE THE LOWEST EFFECTIVE DOSE
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what are the indications and contraindications for Chlorpromazine ?

A

INDICATIONS :
- Schizophrenia
-Mania
-Organic psychosis etc
-Tranquillization in emergency aggressive behavioural disturbanc
(Tranquilization ->calming or sedative effect)
CONTRAINDICATIONS :
- coma
- severe mental depression
- severe liver impairment
- sugnisicant cardiac disorder
- Glaucoma
- Bone marrow depression

17
Q

what are the Adverse effects of Chlorpromazine ?

A

Adverse effects: EPSEs, sedation, postural hypotension, anticholinergic side effects, epileptogenic, photosensitivity ,jaundice, agranulocytosis

18
Q

which drugs dose Chlorpromazine interact with ?

A

Drug interactions with anticholinergics, antiepileptics, antihypertensives, antiparkinsonism drugs, CNS depressants , enzyme inducers

19
Q

what is the potency, duration of onset ,half life and doses for Haloperidol- butyrophenone?

A
  • potency : very potent
  • duration of onset : Onset of action 10min after IM injection, Tmax 4-6 hrs ofter oral ingestion
  • half life : Half life 13-35hrs. Metabolised in liver extensively
  • Doses : Initially 0.5-5.0mg 2-3X daily then reduce to LOWEST EFFECTIVE DOSE. Usual maintenance dose is 2-10mg daily
    -Advantage is that it is also available in IV formulation
20
Q

what are the indications and contraindications for Haloperidol- butyrophenone ?

A

INDICATIONS :
- Schizophrenia
-Mania
-Organic psychosis etc
-Tranquillization in emergency aggressive behavioural disturbanc
(Tranquilization ->calming or sedative effect)
CONTRAINDICATIONS:
Contraindicated in Parkinson’s and pt with history of EPSEs from neuroleptics
Caution in special groups as ↑ risk of side effects

21
Q

what are the Adverse effects of Haloperidol- butyrophenone ?

A

Adverse effects: less anticholinergic, hypotensive, least epileptogenic BUT increased risk of EPSEs

22
Q

which drugs does Haloperidol- butyrophenone interact with ?

A

Drug interaction:
- Lithium –neurotoxicity
- As with other antipsychotic drugs

23
Q

explain the mechanism of action for atypical antipsychotics

A

Antagonise D2 receptor ->weakly
Antagonise 5HT-2A receptor ->strongly

Side effects :
- Neutropenia /Agranulocytosis ( adverse reaction of clozapine)
- Alpha adrenergic receptor ->orthorstatic hypotension
- 5 HT2-> mood ,digestion ,sexual health ,sleep-wake cycle , Nausea
- Metabolic effects ->weight gain ,dyslipidemia,hyperglycemia
- Antimuscarinic effects-> dry mouth , constipation, blurred vision ,urinary retension .
- HISTAMINE H1 receptor antagonism : weight gain ,sedation

24
Q

what makes the atypical neuroleptics ,use ?

A
  • Newer and expensive
  • effects : Less EPSEs (not devoid of EPSEs), prolactin effects, ↑weight gain
  • Clozapine EDL- reserved for treatment resistant psychosis.
    Major s/e agranulocytosis & neutropenia
  • Associated with QT prolongation
25
Q

what type of drug is Clozapine-dibenzodiazepine?

A

D2 and serotonin receptor antagonist

26
Q

what are the indications and contraindications of Clozapine-dibenzodiazepine?

A
  • Indicated for resistant psychosis
  • Contraindicated in history of drug induced agranulocytosis
27
Q

what are the adverse effect of Clozapine-dibenzodiazepine?

A

Adverse effects:Weight gain, agranuloctosis and neutropenia, sedation, postural hypotension, anticholinergic s/e.LESS EPSEs

NB. WCC monitoring essential:
- Baseline, weekly for 18wks, then fortnightly, for a yr, then monthly
- STOP if WCC below 3000/mm2 or Neutrophil count is less than 1500 /mm2

28
Q

what is the dose forClozapine-dibenzodiazepine?

A

Adult doses 12.5 -25mg dly then increase to therapeutic levels in 2-3 wks

29
Q

what are the differences among antipsychotics ?

A
  1. All effectively bind D2 receptors but have different affinity for other receptors viz
    - Muscarinic receptors-
    anticholinergic-urinary retention, blurred vision, orthostatic hypotension, erectile dysfunction
    - Histamine receptors- sedation, antiemetic
    - Alpha adrenergic receptor- orthostatic hypotension
    - Serotonin receptors- psuedodepression
  2. Difference in lowering seizure threshold
  3. Difference in tendency to cause metabolic and endocrine effects e.g. weight gain and hyperprolactinaemia resp
  4. Difference in tendency to cause cardiac toxicity e.g. ventricular arrhythmia , QT prolongation
30
Q

one of the complication of antipsychotics is EPSEs , list the symptoms ,onset,risk factors ,treatment options .

A

SYMPTOMS :
Acute dystonic reaction- spasm of muscles of tongue, face, neck, and back (torticollis, protrusion of the tongue, facial grimacing, oculogyric crisis, opisthotonus, truncal dystonia and laryngeal spasm) vs seizure
- ONSET : 24-48hrs
- Risk factor- young male
- Rx –biperiden 2mg IM/IV, benzodiazepine if necessary, if c/o pain analgesia
(Stop neuroleptic until symptoms full resolution)

31
Q

one of the complication of antipsychotics is Parkinsonism , list the symptoms ,onset,risk factors ,treatment options .

A

SYMPTOMS :
Parkinsonism –bradykinesia, rigidity, tremor
- ONSET : weeks or months
- Risk factors - Common in older pts
- TREATMENT :
- reduce dose- lowest effective dose
- Prescribe anticholinergic orphenadrine 50-150mg

32
Q

one of the complication of antipsychotics is Akathisia , list the symptoms ,onset,risk factors ,treatment options .

A

SYMPTOMS :
- Akathisia-motor restlessness vs anxiety
ONSET :
- Onset days-weeks
TREATMENT :
- Reduce dose
- Add anticholinergic if necessary

33
Q

one of the complication of antipsychotics is Tardive dyskinesia, list the symptoms ,onset,treatment options .

A

SYMPTOMS :
- Tardive dyskinesia- syndrome of choreoathetoid and or other involuntary movements, usually of face, lips and tongue +/- arms legs and trunk
ONSET :usually >6/12
Treatment :
PREVENTION N.B. lowest effective dose for the shortest time
- Gradually withdraw
- Consider changing to atypical antipsychotics (less tendency for EPSEs)

(MOA-? Excess dopamine)

34
Q

one of the complication of antipsychotics is Neuroleptic malignant syndrome, list the symptoms ,onset,risk factors ,treatment options .

A

SYMPTOMS : Presents with:
-Hyperpyrexia
-Sweating
-Unstable blood pressure
-Changes in LOC (stupor or catatonia like state)
-Muscle rigidity

ONSET : usually weeks but can occur after 1st dose (Lasts 5-7 days, longer if depot prep used)

RISK : Risk- ↑ambient temp, dehydration, intercurrent mildly febrile illness, catatonia

(Neuroleptic malignant syndrome-Rare BUT mortality >10%. Aetiology unknown-?dopamine blockade in hypothalamus)

35
Q

What are the causes of treatment failure ?

A
  1. Low efficacy rate!!!!! 40-60%
  2. Inter and intraindividual variability
  3. Under dosing- lowest EFFECTIVE dose
  4. Malabsorption- change to depot preparation
  5. Drug interactions
  6. Wrong diagnosis- Rx underlying cause e.g. brain tumours
  7. Non-compliance
    - Lack of insight-consider depot preparation vs tablets
    - Adverse effects- consider changing classes
36
Q

What are the special populations for antipsychotics and why ?

A
  1. Pregnancy or lactation
    - beacuse there are no randomised controlled trials done on them
    - All neuroleptics cross the placenta
    - Phenothiazines are excreted in breast milk-behavioural changes in infants
  2. Children -> Use only if necessary as EPSEs can occur after first dose
  3. Elderly -> More susceptible to cardiovascular side effects and anticholinergic side effects
  4. Hepatic diseases -> dose adjustment may be needed