Psychosis Flashcards

1
Q

State the definition of psychosis.

A

Clinical state of mind characterised by loss of contact with reality. Patients might experience perceptual disturbances (e.g. hallucinations, delusions).
Negative symptoms -blunting of affect, avolition, alogia.
Social or occupational dysfunction.
Clear sensorium

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2
Q

What is the difference between hallucinations and delusions?

A

Delusions are fixed unshakeable beliefs.
Hallucinations are perceptions without adequate stimuli.

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3
Q

What are the symptoms of delirium?

A

Medical emergency
Impaired awareness, confusion, disorientation

Others: restlessness, agitation, hallucinations, aggressiveness, ANS symptoms

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4
Q

List the causes of delirium.

A

DIMTOP

Drugs, Infections, Metabolic, Trauma, Oxygen, Psychological

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5
Q

Explain the pathogenesis of psychosis.

A

Dopamine hypothesis of schizophrenia - excessive dopaminergic activity.

Increased dopamine activity at mesolimbic pathway: leads to positive symptoms (hallucinations, delusions, thought disorders)

Nigrostrial pathway: often affect by antipsychotic treatment which can lead to motor side effects (Parkinsonism)

Tuberinfundibular pathway: involved in regulation of prolactin secretion (dopamine blockage can lead to hyperprolactinemia as side effect)

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6
Q

What are the causes of psychosis?

A

Functional psychosis
- schizophrenia
-bipolar mood disorder

Psychotic disorders due to medial conditions
- medical conditions (epilepsy, Alzheimer’s dementia, HIV, neurosyphilis)
- illicit drugs (cannabis, mantras, cocaine, amphetamines)
-prescription (steroids, antiparkinsonism, atropine)

Other
- postpartum psychosis

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7
Q

Outline the approach to management of psychosis.

A

Depends on aetiology and onset of psychosis.

Acute:
- goals of therapy is to clam the patient down and achieve containment
-antipsychotic and/or benzodiazepine

Chronic:
- goals of therapy is to prevent relapse of acute psychotic symptoms
- antipsychotic drugs & supportive psychotherapy for patient and family

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8
Q

Name the two main classes of neuroleptics? And what is there mechanism of action?

A

Classical neuroleptics
- dopamine 2 receptor antagonists
- tendency to cause extra pyramidal side effects

Atypical neuroleptics
- D2 and D3 receptor antagonists
- D2 and serotonin receptor antagonist

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9
Q

What are the indications for neuroleptics?

A

Primary:
- schizophrenia, mania, organic psychosis

Others:
- nausea + vomiting, intractable hiccups, Tourette’s syndrome, behaviour disorders, anaesthesia

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10
Q

Name of the different classes (with examples) of traditional neuroleptics.

A

Phenothiazines
- alipathic (chlorpromazine)
- piperazine (fluphenazine, prochloperazine)
- piperidine (thioridazine)

Butyrophenones
- haloperidol, droperidol

Thioxanthenes
- flupenthixol, zuclopenthixol

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11
Q

In which cases is the short acting vs long acting depot preparations injectable performed?

A

Short acting - acute management

Long acting - preferred if compliance is a problem

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12
Q

List the indications for using chlorpromazine.

A

Schizophrenia
Mania
Organic psychosis
Transquilization in emergency aggressive behavioural disturbances

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13
Q

What are the contraindications of chlorpromazine?

A

In coma, severe mental depression, severe liver impairment, significant cardiac disorders, glaucoma, bone marrow depression

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14
Q

Name the oldest neuroleptic of low potency.

A

Chlorpromazine

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15
Q

What are the adverse effects of chlorpromazine?

A

EPSEs, sedations, postural hypotension, anticholinergic side effects, epileptogenic, photosensitivity, jaundice, agranulocytosis

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16
Q

Which drug classes does chlorpromazine have drug interactions with?

A

Anticholinergics
Anti-epileptics
Anti hypertensives
Anti Parkinsonism
CNS depressants
Enzyme inducers

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17
Q

What is onset of action in chlorpromazine? Also mention their half life. `

A

Onset 30-60 hours after oral ingestion and 15min after injections

18
Q

At what doses should chlorpromazine be taken?

A

Initially 25mg TDS but maintenance range 75-300mg
IM 25-50mg be respected 3-4 times in 24 hours as necessary

19
Q

Name a very potent antipsychotic drug.

A

Haloperidol

20
Q

In which patients is haloperidol contraindicated?

A

In Parkinson’s and patient with history of EPSEs from neuroleptics

21
Q

What are the adverse effects of haloperidol?

A

Less anticholinergic, hypotensive, least epileptogenic but increased risk of EPSEs

22
Q

Which drug does haloperidol have drug interactions with?

A

Lithium -neurotoxicity

23
Q

What are the adult doses of haloperidol ?

A

Initially 0.5 - 5mg 2-3 times daily then reduce to lowest effective dose. Usual maintenance dose is 2-10mg daily

24
Q

Describe the onset of action of haloperidol . Also mention its half life.

A

Onset of action - 10 minutes after IM injection
Max 4-6 hours after oral ingestion.
Half life 13-35 hours. Metabolised in liver extensively

25
Name an atypical neuroleptic.
Clozapine
26
Indication for clozapine?
Resistant psychosis
27
Contraindication in clozapine?
In history of drug induced agranulocytosis.
28
What are the adverse effects of clozapine?
Weight gain, Agranulocytosis Neutropenia Sedation Postural hypotension Anticholinergic
29
What are the adult doses for clozapine?
12.5 - 25mg daily then increase to therapeutic levels in 2 - 3 weeks.
30
List the complications of EPSEs.
Acute dystopia reaction - spasm of uncles of tongue, face, neck and back Onset 25-48 hours Risk factor (young male)
31
List the complications of Parkinsonism.
Bradykinesia, rigidity, tremor Onset: weeks or moths Common in older patients
32
List the complications of akathisia.
Motor restlessness vs anxiety Onset: days - weeks
33
What is the treatment for the complication of EPSEs?
Biperiden 2mg IM/IV, Benzodiazepine if necessary (f complains of pain (analgesia) Stop neuroleptic until symptoms full resolution
34
What is the treatment for the complication of Parkinsonism?
Reduce dose - lowest effective dose Prescribe anticholinergic orphenadrine 50-150 mg
35
What is the treatment for the complication of akathsia?
Reduce dose, add anticholinergic if necessary
36
What are the risks of neuroleptic malignant syndrome?
Increased ambient temperature Dehydration Intercurrent mildly febrile illness Catatonia
37
How does neuroleptic malignant syndrome present?
hyperpyrexia Sweating Unstable BP Changes in LOC (stupor or catatonia like state) Muscle rigidity
38
How long do the synonyms of NMS last for?
5-7 days, longer if depot prep used
39
How do the atypical neuroleptics compare to the typical?
Newer + expensive Less EPSEs, prolactin effects. Increased weight gain, associated with QT prolongation
40
List the special populations which should be accounted of when prescribing?
Pregnancy or lactation - all neuroleptics cross the placenta - phenothiazoines are excreted in breast milk behavioural changes in infants Children - use only if necessary as EPSEs can occur after 1st dose Elderly - more susceptible to cardiovascular side effects +anticholinergic side effects Hepatic diseases - need dose adjustment
41
List the causes of treatment failure.
Low efficiency rate (40-60%) Inter and intra individual variability Under dosing - lowest effective dose Malabosrptiom Drug interactions ‘wring diagnosis Non compliance
42
List the causes of treatment failure.
Low efficiency rate (40-60%) Inter and intra individual variability Under dosing - lowest effective dose Malabosrptiom Drug interactions ‘wring diagnosis Non compliance