First-episode psychosis
Psychosis recognition and early intervention: the AU general practice approach
Psychosis — hallucinations, delusions, and negative symptoms — peaks in onset between ages 15 and 25. Medical, substance-induced, and mood-related causes must be excluded before attributing symptoms to a primary psychotic disorder.
Duration of untreated psychosis (DUP) is the strongest predictor of long-term outcome. The GP's role is rapid recognition, urgent referral to an early intervention service (Orygen, headspace Early Psychosis), and workup to exclude organic causes.
Second-generation antipsychotics are first-line. Psychosocial interventions and cardiometabolic monitoring are integral; schizophrenia carries a 15–20 year premature mortality burden.
Psychosis in the GP setting
For most people, the first contact when psychotic symptoms develop is a general practitioner — not a psychiatrist, and not an emergency department. The consultation might be framed by the patient as “I haven’t been sleeping well” or “things just feel strange,” or it might be a parent who has noticed their teenager withdrawing from friends and failing school. Recognising the possibility of an emerging psychotic illness early — before the full episode becomes entrenched — is one of the highest-impact things a GP can do in mental health care.
The evidence from Orygen’s EPPIC research program and the international OPUS and RAISE trials is consistent: duration of untreated psychosis (DUP) is the single strongest modifiable predictor of long-term outcome. Shorter DUP is associated with better symptomatic recovery, faster remission, improved vocational functioning, and lower hospitalisation rates. Every week a young person spends in an untreated psychotic state carries measurable cost to their recovery trajectory. GPs who recognise early and refer promptly are intervening at the point where intervention makes the most difference.
This article covers the recognition of psychosis and its prodrome, the initial workup, the early intervention model in Australia, treatment principles, and the GP’s ongoing role in physical health monitoring.
A. Core clinical — the AU general-practice framework
What psychosis is and what it is not
Psychosis refers to a syndrome of impaired reality testing characterised by one or more of:
- Delusions — fixed false beliefs held with conviction despite contrary evidence; persecutory, referential, grandiose, somatic, or relating to thought interference or control
- Hallucinations — perceptions without stimulus; auditory hallucinations (voices) are most characteristic of schizophrenia; visual, tactile, and olfactory hallucinations more commonly suggest organic or substance-related causes
- Disorganised thinking — loose associations, tangentiality, derailment, or in severe cases, word salad
- Grossly disorganised or catatonic behaviour
- Negative symptoms — avolition, anhedonia, alogia, affective flattening, social withdrawal
Psychosis is a syndrome, not a diagnosis. The underlying diagnosis — schizophrenia, schizoaffective disorder, substance-induced psychosis, psychosis due to a general medical condition, brief psychotic disorder — is established after careful workup.
The prodromal phase
Months to years before threshold psychotic symptoms, most people experience an at-risk mental state (ARMS) or clinical high-risk (CHR-P) phase. Features are non-specific but clinically recognisable:
- Unexplained significant decline in academic or work performance
- New or intensifying social withdrawal without obvious cause
- Unusual perceptual experiences (“things feel dreamlike,” “voices seem muffled or strange”)
- Sub-threshold suspicious or odd beliefs the person can still partially test
- Persistent anxiety, depression, or irritability refractory to standard treatment
- Sleep disturbance
- Deteriorating self-care
The CAARMS (Comprehensive Assessment of At-Risk Mental States) criteria operationalise this; Orygen and headspace Early Psychosis services can apply these formally. As a GP, the appropriate action when you notice these features in a young person is to refer to the early intervention service rather than waiting to confirm a diagnosis.
Initial assessment priorities
When a person presents with possible first-episode psychosis, structure the initial assessment around:
- Risk — suicidality (5–10% lifetime completed suicide in schizophrenia, highest in early years), risk to others, self-neglect, vulnerability to exploitation
- Capacity — ability to consent and to engage with care
- Organic exclusion — medical and substance causes must be ruled out before attributing symptoms to a primary psychotic disorder
- Functional impact — how severely is daily life affected?
- Social context — family support, accommodation, employment, trauma history
Differential diagnosis — do not miss organic causes
The eTG psychotropic chapter and NICE CG178 both emphasise that organic causes of psychosis must be actively excluded. Key differentials:
- Substance-induced — methamphetamine, cannabis (especially high-potency), synthetic cannabinoids, LSD, MDMA, cocaine, alcohol withdrawal; also corticosteroids, dopaminergic agents used in Parkinson’s disease, anticholinergics, levetiracetam
- Autoimmune encephalitis — anti-NMDA receptor encephalitis is critically important to recognise; classically in young women, may have teratoma, presents with movement disorder, autonomic instability, and seizures alongside psychiatric features; check anti-NMDA receptor antibodies when atypical features are present
- Delirium — fluctuating level of consciousness, inattention, visual hallucinations more common than auditory; medical illness usually identifiable
- Mood disorder with psychotic features — major depression or mania with mood-congruent psychosis
- Temporal lobe epilepsy — ictal and postictal psychosis; focal neurological symptoms; history of seizures
- CNS infection — HIV, neurosyphilis, viral encephalitis
- Endocrine disorders — hyperthyroidism, Cushing’s syndrome, Addison’s crisis, hypoglycaemia
- Metabolic — hyponatraemia, hypercalcaemia, uraemia, hepatic encephalopathy
- Brain tumour, stroke, traumatic brain injury
B. Early intervention — what the evidence shows
The early intervention model
Australia has world-leading early psychosis infrastructure. Orygen in Melbourne pioneered the EPPIC (Early Psychosis Prevention and Intervention Centre) model, which demonstrated through rigorous research that specialised, intensive, early-phase treatment produces substantially better outcomes than standard care. The model comprises:
- Assertive case management by a consistent clinical team
- Low-dose second-generation antipsychotic therapy
- CBT for psychosis (CBTp)
- Family psychoeducation and family work
- Supported education and employment (Individual Placement and Support model)
- Peer support workers
- Harm-reduction approach to substance use
- Proactive physical health monitoring
headspace Early Psychosis (hEP) extends this model to approximately 14 metropolitan centres across Australia, primarily for young people aged 12–25. State-funded EPPIC equivalents operate in various forms in most states.
Antipsychotic medication — principles
Second-generation antipsychotics are first-line for first-episode psychosis. Key principles from RANZCP guidelines:
- Start low, go slow — people with first-episode psychosis are more sensitive to antipsychotics and typically respond at lower doses than people with established schizophrenia
- Allow adequate trial time — 4–6 weeks at a therapeutic dose before declaring treatment failure; some response may be gradual
- Choose based on side-effect profile and patient preference — aripiprazole and ziprasidone have lower metabolic burden; olanzapine is highly effective but causes more weight gain and metabolic dysregulation
- Long-acting injectable (LAI) antipsychotics — aripiprazole monthly (Abilify Maintena), paliperidone palmitate monthly or three-monthly (Invega Sustenna, Trinza), risperidone fortnightly — should be considered early for adherence, not only after demonstrated non-adherence
Psychosocial treatments
CBT for psychosis (CBTp) is a standard component of care — it reduces symptom distress and improves coping, though it is an adjunct to medication rather than a replacement. Family intervention (psychoeducation, communication training, expressed-emotion reduction) reduces relapse and hospitalisation. Supported employment using the Individual Placement and Support (IPS) model improves real-world employment outcomes significantly.
C. Cardiometabolic health — the mortality gap
The 15–20 year premature mortality in schizophrenia is predominantly from preventable cardiovascular disease — not from suicide, as is often assumed. NPS MedicineWise and RANZCP both emphasise that cardiometabolic care is part of psychosis management, not separate from it.
Mandatory monitoring
Per eTG, at baseline and every 3–6 months on antipsychotics:
- Weight and BMI
- Waist circumference
- Blood pressure
- Fasting lipids
- Fasting glucose and HbA1c
- ECG if QT-prolonging agent used
- Prolactin (with risperidone, paliperidone, or first-generation antipsychotics)
Specific clozapine monitoring: full blood count weekly for 18 weeks, then monthly for life — managed through the Australian Clozapine Patient Monitoring System. Troponin and ECG at 4 weeks (myocarditis surveillance). Constipation surveillance — clozapine-induced bowel obstruction has caused deaths and is often under-recognised.
Smoking cessation
Approximately 50% of people with schizophrenia smoke — roughly double the general population rate. Smoking is the largest single contributor to the cardiovascular mortality gap. Varenicline is the most effective pharmacotherapy and is well-tolerated in schizophrenia despite historical concerns about neuropsychiatric effects — the FDA resolved those concerns after the large EAGLES trial. Nicotine replacement therapy and behavioural support are also appropriate and should be offered proactively at every contact.
D. Australian operations
MBS items for psychosis management
MBS Online items relevant to psychosis care in general practice:
- Items 23/36/44 — standard consultation levels B, C, D
- Items 2715/2717 — Mental Health Treatment Plan (preparation and review)
- Items 80000–80020 — Better Access psychology (10 sessions per year)
- Item 81335 — telehealth psychology
- Items 132/133 — consultant physician (psychiatry) initial and subsequent
- Items 291/293 — psychiatrist consultation
- Items 965/967 — GPCCMP (Chronic Condition Management Plan) for cardiometabolic care in established illness
- Item 715 — ATSI Health Assessment (includes mental health screening)
PBS prescribing authority
Most antipsychotics require Authority (Streamlined or telephone) for PBS subsidy with a schizophrenia or psychosis indication. Relevant PBS items:
- Oral olanzapine, risperidone, paliperidone — Authority Required (Streamlined)
- Aripiprazole, quetiapine — Authority Required (Streamlined or telephone)
- Paliperidone palmitate LAI (Invega Sustenna, Trinza) — Authority Required for schizophrenia
- Aripiprazole LAI (Abilify Maintena) — Authority Required
- Clozapine — Authority Required, specialist initiation, mandatory monitoring system
Crisis pathways
Each state and territory has a 24-hour mental health crisis line — Vic 1300 369 012, NSW 1800 011 511, Qld 1300 642 255, SA 13 14 65, WA 1800 676 822. For acute psychosis with risk, the emergency department under the relevant Mental Health Act is the appropriate pathway.
Community supports
SANE Australia provides peer support, education, and resources. Mental Illness Fellowship of Australia (MIFA) supports families and carers. NDIS eligibility applies for persistent psychosocial disability impairing daily function in those under 65.
E. Special populations
Adolescents — onset in adolescence often disrupts education and social development at critical periods. NICE CG155 provides guidance on psychosis in children and young people; dose considerations, safeguarding, and family involvement are particularly important. headspace and Orygen both serve adolescents.
Women of reproductive age — antipsychotics vary in teratogenic risk; clozapine and olanzapine have more data than newer agents. Prolactin elevation from some antipsychotics can suppress ovulation; women may assume they cannot become pregnant. Contraceptive counselling and preconception planning are part of holistic care.
Substance use — methamphetamine and cannabis are the most commonly encountered complicating substances in Australian practice. Substance-induced psychosis can be clinically indistinguishable from primary psychosis in the acute phase. A harm-reduction approach to substance use is standard; abstinence from cannabis is advice supported by evidence given its strong dose-response relationship with psychosis risk and course.
Cultural and linguistic diversity — psychosis presentations and explanatory models vary across cultural backgrounds. Interpreter services and culturally safe assessment are important, particularly in the refugee and migrant populations who are disproportionately represented in first-episode services.
When to escalate
Refer or escalate urgently when:
- Suicidal ideation with plan or intent, or command hallucinations directing self-harm
- Active homicidal ideation
- Severe agitation or aggression risking safety
- Suspected catatonia — benzodiazepine challenge (lorazepam IM) is first-line; ECT for refractory catatonia
- Suspected neuroleptic malignant syndrome — fever, rigidity, autonomic instability, raised CK; medical emergency
- Suspected autoimmune encephalitis — urgent neurology or immunology workup
- Any acute delirium or organic cause suspected — acute medical workup
- First-episode psychosis in a young person — refer to headspace Early Psychosis or equivalent for specialist assessment
What this article is and is not
This is general health information drawn from Australian and international clinical guidelines — RANZCP, Orygen Early Psychosis Clinical Guidelines, NICE CG178/CG155, eTG Psychotropic, and headspace program literature. It is not personal medical advice and does not create a doctor–patient relationship. Treatment decisions for people with psychotic illness require specialist mental health input; GPs play a vital role in recognition, physical health, and coordination but should work alongside psychiatry and early intervention services rather than managing psychotic illness independently.
If you or someone you know needs support: Lifeline 13 11 14 (available 24 hours), Beyond Blue 1300 22 4636, or 13YARN 13 92 76 (First Nations peoples, 24 hours). For a mental health emergency: call 000 or go to the nearest emergency department.
For consumer support: SANE Australia, HealthDirect — Psychosis, or state mental health crisis lines.
Sources cited
- RANZCP — Clinical Practice Guidelines for Schizophrenia and Related Disorders
- Orygen — Early Psychosis Clinical Guidelines
- headspace — Early Psychosis programs
- Therapeutic Guidelines (eTG) — Psychotropic: schizophrenia and psychosis
- Australian Medicines Handbook
- NICE CG178 — Psychosis and schizophrenia in adults
- NICE CG155 — Psychosis and schizophrenia in children and young people
- NPS MedicineWise — Antipsychotic medications
- RACGP — Mental health resources
- HealthDirect — Psychosis
- SANE Australia
- MBS Online
Frequently asked questions
-
What are the early warning signs of psychosis that a GP should recognise?
The prodromal or 'at-risk mental state' typically precedes a full psychotic episode by months to years. Warning signs include a marked unexplained decline in school or work performance, new social withdrawal in a young person, unusual beliefs or perceptual oddities ('things look or feel strange'), brief odd or suspicious thoughts that the person can still partially dismiss, persistent anxiety or depression that doesn't respond to standard treatment, and deteriorating personal hygiene. When a young person's functioning drops noticeably without a clear trigger, think about the possibility of an emerging psychotic illness and refer to a specialist early intervention service promptly.
-
What should the initial workup for first-episode psychosis include?
The purpose of the initial workup is to exclude organic and medical causes before attributing symptoms to a primary psychotic disorder. Investigations include full blood count, urea and electrolytes, liver function tests, thyroid function tests, fasting glucose, calcium, magnesium, vitamin B12 and folate, vitamin D, ferritin, syphilis serology (RPR/VDRL), HIV serology if risk factors present, urine drug screen (methamphetamine and cannabis are the most commonly encountered in AU practice), and urine beta-hCG in women of reproductive age. Baseline ECG is required before starting antipsychotics. Brain CT or MRI is indicated to exclude structural pathology. If atypical features are present — movement disorder, autonomic instability, or a recent viral prodrome — an autoimmune encephalitis panel should be requested.
-
What are the early intervention services available in Australia?
Australia has a well-developed early psychosis intervention infrastructure. [Orygen](https://www.orygen.org.au) in Melbourne is the national and international centre of excellence, combining clinical services with research and training. The [headspace Early Psychosis (hEP) program](https://headspace.org.au) operates in approximately 14 metro sites across Australia — Sydney, Melbourne, Brisbane, Adelaide, Perth, Hunter Valley, Townsville, and others — primarily serving people aged 12–25. State-funded EPPIC (Early Psychosis Prevention and Intervention Centre) equivalent services exist in some states. These multidisciplinary services provide specialist assessment, low-dose antipsychotic medication, CBT for psychosis, family intervention, supported education and employment, and peer support — typically for a 2–5 year intensive period.
-
Which antipsychotic should be considered first and what monitoring is needed?
Second-generation (atypical) antipsychotics are first-line for first-episode psychosis — olanzapine, risperidone, aripiprazole, paliperidone, and quetiapine are most commonly used. Start at the lowest effective dose and increase slowly; people experiencing their first psychotic episode are often more sensitive to both therapeutic effects and side effects than those with longer illness. Cardiometabolic monitoring is mandatory given significant weight gain, dyslipidaemia, and glucose dysregulation from most antipsychotics: measure weight, waist circumference, blood pressure, fasting lipids, and fasting glucose at baseline and every three to six months. Prolactin monitoring is appropriate with risperidone and paliperidone. ECG monitoring is relevant for agents with QT-prolonging potential.
-
When is clozapine used and what does it require?
Clozapine is reserved for treatment-resistant schizophrenia, defined as inadequate response after two adequate trials of different antipsychotics — each at therapeutic dose for at least six weeks — including at least one second-generation agent. It has the strongest evidence for reducing symptoms, relapse, and suicide risk in refractory illness. However, it requires specialist initiation and mandatory haematological monitoring — full blood count weekly for the first 18 weeks then monthly for life — because of a ~1% risk of agranulocytosis. Myocarditis risk (particularly in the first four weeks), severe constipation, and seizures are additional significant concerns. Clozapine prescribing in Australia is managed through the Australian Clozapine Patient Monitoring System.
-
Why does physical health matter so much in psychosis management?
People with schizophrenia and related psychotic disorders die on average 15–20 years earlier than the general population, predominantly from preventable cardiovascular disease. This mortality gap reflects a combination of antipsychotic-induced metabolic effects, high rates of smoking (~50% in schizophrenia), poor access to preventive health care, and the illness-related reduction in self-care. Smoking cessation — using varenicline, nicotine replacement therapy, and behavioural support — addresses the single largest modifiable mortality cause. Annual cardiovascular risk assessment, blood pressure monitoring, glucose and lipid management, and proactive preventive care are part of every consultation with a person who has a psychotic illness.
Source quality
Sources grouped by evidence tier. AU primary tier first; international where AU is silent or lagging; named-author reconstruction where guidelines have not yet caught up. How tiers work.
-
T1 AU primary 9 sources - RANZCP — Clinical Practice Guidelines for Schizophrenia and Related Disorders
- Orygen — Early Psychosis Clinical Guidelines
- headspace — Early Psychosis programs
- Therapeutic Guidelines (eTG) — Psychotropic: schizophrenia and psychosis
- Australian Medicines Handbook
- RACGP — Mental health resources
- HealthDirect — Psychosis
- SANE Australia
- NPS MedicineWise — Antipsychotic medications
-
T2 International primary 1 source