Primary psychotic disorders
Overview of psychosis
Psychosis makes it difficult for people to differentiate between what is real and what is not. Psychotic disorders include but are not limited to: schizophrenia, schizoaffective disorder, delusional disorder and drug-induced psychosis.
Schizophrenia
Epidemiology of schizophrenia
Genetic and environmental factors both play a role in whether someone develops schizophrenia. Possible environmental factors include but are not limited to: complicated pregnancy and birth, early social services contact, neurodevelopmental difficulties, and cannabis use, especially in adolescence.
Schizophrenia is more common among males. Age of onset varies between genders, with more men experiencing the onset of symptoms in their early-to-mid twenties, and more women experiencing onset of symptoms in their late twenties. Early onset schizophrenia is typically associated with a poorer prognosis (as are presentations with mainly negative symptoms).
Clinical features of schizophrenia
Onset of schizophrenia may be acute or insidious. A prodromal phase often precedes the onset of psychotic symptoms, which may include negative symptoms, social withdrawal, self-neglect, inversion of sleep cycles, anxiety or depression.
As per the ICD-11, for a diagnosis of schizophrenia, symptoms must be present for at least one month. At least two symptoms are needed for diagnosis. At least one of the two symptoms must come from the following list:
- Persistent delusions
- Persistent hallucinations
- Formal thought disorder (e.g. tangentiality, ‘knight’s move thinking’, ‘word salad’)
- Experiences of influence, passivity, or control (e.g. thought withdrawal/broadcasting)
The second of the two symptoms can come from either the above list or from the following symptoms:
- Negative symptoms (e.g. flat affect, poverty or paucity of speech, lack of motivation, social withdrawal and anhedonia)
- Grossly disorganised behaviour that impedes goal-oriented activity
- Psychomotor disturbances (e.g. catatonic restlessness or agitation, posturing, waxy flexibility, negativism, mutism or stupor)
Management of schizophrenia
There is no first-line antipsychotic drug suitable for all patients, and drug choice is shaped by individual circumstances and choices, as well as minimisation of side effects.
There are two main classes of antipsychotic medication:
- First-generation (typical) antipsychotics:
- D2 antagonists (+ other receptors)
- E.g. haloperidol, chlorpromazine, fluphenazine
- Extrapyramidal side effects (EPSEs) are more common
- Second-generation (atypical) antipsychotics
- 5HT2A/D2 antagonists (+ other receptors)
- E.g. aripiprazole, olanzapine, quetiapine, paliperidone, risperidone, lurasidone and clozapine
- Metabolic side effects more common
Key considerations for maintenance therapy include:
- Establishing the minimal effective dose in order to reduce side effects
- Depots (e.g. paliperidone, olanzapine, zuclopenthixol) may help ensure compliance
- Encourage psychotherapy, e.g. CBT, family therapy and psychoeducation
Side effects of antipsychotics
Common side effects of antipsychotics include:
Extrapyramidal symptoms:
- Includes parkinsonian symptoms (bradykinesia and tremor), akathisia (restlessness) and tardive dyskinesia (abnormal involuntary movements of the lips, tongue, face and jaw that can continue after drug discontinuation).
- Also includes dystonia (uncontrolled muscle spasms). This can be very acute in onset. Presentations include but are not limited to: oculogyric crisis (prolonged ‘rolling upwards’ of the eyes), torticollis (neck twisting causing the head to tilt), buccolingual crisis (protruding or pulling sensation of tongue), opisthotonic crisis (whole body spasm causing an arched back, flexed arms and extended lower limbs), scoliosis or lordosis, blepharospasm (eyelid spasm preventing eye opening) and torticopelvic crisis (abdominal pain or rigidity). Laryngeal dystonia causes throat pain, shortness of breath and difficulty talking and is rare but potentially life-threatening.
Consider procyclidine to reduce medication side effects and for acute dystonic reactions.
Metabolic symptoms:
- Weight gain, hypercholesterolemia and diabetes.
Cardiovascular:
- QTc-interval prolongation, postural hypotension.
Neuroleptic malignant syndrome:
- Rare but potentially fatal side effects.
- Presents with hyperthermia, sweating, muscle rigidity (‘lead-pipe rigidity’), hyporeflexia, tachycardia, labile blood pressure and fluctuating consciousness.
- Management includes stopping the antipsychotic, giving IV fluids, cooling, and considering bromocriptine and dantrolene.
Hyperprolactinaemia:
- May cause loss of libido, sexual dysfunction, galactorrhoea and infertility in both sexes. In men may cause oligospermia, reduced ejaculation volume and gynaecomastia. In women may cause oligomenorrhea or amenorrhea, reduced vaginal lubrication, dyspareunia, acne and hirsutism.
- First-line treatment is stopping or reducing the antipsychotic and changing to another medication. If this is not feasible, low-dose aripiprazole can also be used as an add-on medication to treat symptomatic hyperprolactinaemia.
Sexual dysfunction.
| Clozapine is a second-generation antipsychotic. It can be very effective, but needs careful titration and monitoring due to side effects. It is trialled when two different antipsychotics have failed.
Common side effects include:
Rare but potentially life-threatening side effects include:
Interactions include:
Clozapine is contraindicated with previous blood dyscrasias, severe cardiac disease (including a history of myocarditis, pericarditis or cardiomyopathy), severe renal disease, or severe/progressive liver disease. People taking clozapine are managed in secondary care. Frequent monitoring of FBC for neutropenia or agranulocytosis is required, especially during titration. |
Box 1 Key facts about clozapine
Monitoring of antipsychotics
There are specific guidelines on monitoring for different antipsychotics, but NICE recommends the following as a guide, in addition to baseline measurements:
| Criteria | Initiation | 3 months | 6 months | Annually | Additional info |
|---|---|---|---|---|---|
| Prolactin | Yes | Yes | Not needed for aripiprazole, clozapine, quetiapine & <20 mg OD olanzapine | ||
| U&Es, FBC, LFTs | Yes | FBC is frequently monitored for patients on clozapine, especially during titration | |||
| Lipids, glucose, HbA1c | Yes | Yes | Needed at one month for clozapine & olanzapine | ||
| BMI | Weekly for the first 6 weeks | Yes | Yes | ||
| HR & BP | After dose changes | Not needed for amisulpride, aripiprazole, trifluoperazone & sulpride | |||
| ECG | After dose changes | Yes |
Table 3 NICE guidelines for monitoring with antipsychotics.
Schizoaffective disorder
As per the ICD-11, schizoaffective disorder is ‘an episodic disorder in which the diagnostic requirements of schizophrenia and a manic, mixed, or moderate or severe depressive episode are met within the same episode of illness, either simultaneously or within a few days of one another.’ Psychomotor disturbances, including catatonia, may be present. Symptoms must have been present for at least one month.
General management is the same as for schizophrenia. However, manic or depressive episodes are managed as in bipolar disorder. The condition tends to have a non-deteriorating course, with prognosis being better than for schizophrenia, although generally worse than for primary mood disorders.
Delusional disorder
Delusional disorder is defined by the ICD-11 as the ‘presence of a delusion or set of related delusions, typically persisting for at least 3 months or often much longer, in the absence of a depressive, manic or mixed episode.’ Delusions are ‘variable in content across individuals, while showing remarkable stability within individuals, although they may evolve over time.’
Characteristic symptoms of schizophrenia (e.g. persistent hallucinations, formal thought disorder, negative symptoms, and experiences of influence, passivity or control) will be absent. However, specific hallucinations typically related to the delusion may be present. Affect, speech and behaviour are typically unaffected, apart from when directly related to the delusions.
Eponymous and miscellaneous delusional conditions
| Syndrome | Description |
|---|---|
| Othello | Delusions of infidelity and paranoid jealousy |
| Cotard’s | Delusions that the person is dead, does not exist, is decaying, or that body parts are missing |
| Capgras | Delusions that someone close to them has been replaced by an identical imposter |
| de Clerambault | Delusions that somebody, especially of higher social status, desires or loves them |
| Folie à deux | Delusions (and sometimes hallucinations) are transmitted from one person to another |
Table 4 Eponymous and miscellaneous delusional conditions (Sims’ Symptoms in the Mind)
References
- British National Formulary. Psychoses and related disorders. Online [cited 16 January 2022]. Available from: https://bnf.nice.org.uk/treatment-summary/psychoses-and-related-disorders.html
- ICD-11. Schizophrenia. Online [cited 17 December 2023]. Available at: https://icd.who.int/browse11/l-m/en#/http%3a%2f%2fid.who.int%2ficd%2fentity%2f1683919430
- ICD-11. Schizoaffective Disorder. Online [cited 17 December 2023]. Available at: https://icd.who.int/browse11/l-m/en#/http://id.who.int/icd/entity/106339515
- National Institute for Health and Care Excellence. Psychosis and schizophrenia: what monitoring is required? [Internet]. NICE. September 2021 [cited 17 December 2023]. Available from: https://cks.nice.org.uk/topics/psychosis-schizophrenia/prescribing-information/monitoring/
- Oyebode F. Delusions and Other Erroneous Ideas. In: Sims’ Symptoms in the Mind. Edinburgh: Elsevier; 2018. Pp. 105-128
- Schizophrenia and Related Psychoses. In: Oxford Handbook of Psychiatry. 4th ed. Ed. Semple D and Smyth R. Oxford: Oxford University Press; 2019. Pp 179-241
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