Home Clinical Examination The Psychiatric History and Mental State Examination

The Psychiatric History and Mental State Examination

πŸ“‹ Key Information Summary

πŸ“‹
  • The psychiatric history is the single most important diagnostic tool in psychiatry β€” more than 80% of diagnoses can be established from a thorough history alone.
  • Always begin with the presenting complaint in the patient's own words, then systematically explore mood, anxiety, psychotic symptoms, substance use, and personal/social history.
  • Assess for risk of harm to self or others at every consultation β€” suicide risk assessment is a mandatory component of every psychiatric evaluation.
  • The Mental State Examination (MSE) is the psychiatric equivalent of the physical examination and must cover appearance, behaviour, speech, mood/affect, thought form and content, perception, cognition, insight, and judgement.
  • Mood disorders (major depressive disorder and bipolar disorder) are the most common psychiatric presentations in Australian primary care, affecting approximately 1 in 7 Australians.
  • Anxiety disorders are the most prevalent class of mental illness in Australia, with lifetime prevalence around 15–20%.
  • Psychotic disorders affect approximately 3% of the Australian population; first-episode psychosis requires urgent specialist referral and early intervention.
  • Substance use disorders frequently co-occur with other psychiatric conditions (dual diagnosis) β€” always screen for comorbid substance misuse.
  • The Mini-Mental State Examination (MMSE) and frontal lobe assessments (e.g., clock drawing, verbal fluency, Luria hand sequences) are essential bedside cognitive screens.
  • Aboriginal and Torres Strait Islander Australians experience psychological distress and suicide at 2–3 times the rate of non-Indigenous Australians; culturally safe assessment is essential.
  • Organic (secondary) causes of psychiatric symptoms β€” delirium, substance intoxication/withdrawal, metabolic and endocrine disorders β€” must always be excluded before attributing symptoms to a primary psychiatric condition.
  • Collateral history from family, carers, or other health professionals is invaluable and should be sought (with appropriate consent) in all psychiatric assessments.
  • Document risk assessment using a structured framework (e.g., the SAD PERSONS scale or the Royal Australian and New Zealand College of Psychiatrists' guidelines) and formulate a clear safety plan.

Introduction & Australian Epidemiology

Psychiatry is unique among medical specialties in that the primary diagnostic instrument is the clinical interview. Unlike cardiology or respiratory medicine, there is no single laboratory test or imaging modality that confirms most psychiatric diagnoses. The systematic collection of a psychiatric history and the performance of a Mental State Examination (MSE) form the bedrock of psychiatric assessment, diagnosis, treatment planning, and risk management.

In Australian general practice and emergency medicine, mental health presentations are among the most common and most time-consuming consultations. General practitioners manage the majority of mental health conditions in Australia, with approximately 12.5% of all GP encounters involving a mental health-related diagnosis.

Australian Epidemiology

According to the Australian Bureau of Statistics (ABS) National Study of Mental Health and Wellbeing (2020–2022):

  • 43% of Australians aged 16–85 years have experienced a mental disorder at some point in their lifetime.
  • 22% of Australians had a 12-month mental disorder, with anxiety disorders (17%) being the most prevalent class, followed by affective disorders (8%) and substance use disorders (3.3%).
  • Suicide was the leading cause of death for Australians aged 15–44 years in 2022, with 3,249 deaths registered β€” a rate of 12.5 per 100,000 population.
  • Aboriginal and Torres Strait Islander Australians die by suicide at approximately twice the rate of non-Indigenous Australians.
  • Mental health conditions cost the Australian economy an estimated 0–220 billion annually (Productivity Commission, 2020).
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Key principle: Always exclude organic (medical) causes of psychiatric symptoms before diagnosing a primary psychiatric disorder. Delirium, medication side effects, thyroid disease, electrolyte disturbances, and substance intoxication/withdrawal can mimic virtually any psychiatric presentation.

Psychiatric History

A thorough psychiatric history follows a systematic structure. The interview should ideally be conducted in a quiet, private environment with adequate time allocated (45–60 minutes for a comprehensive initial assessment). Begin with open-ended questions and progress to more specific enquiries as the clinical picture emerges.

Presenting Complaint

Document the presenting complaint in the patient's own words. Explore the history of presenting complaint using a biopsychosocial framework:

  • Onset: Acute vs. insidious; date of onset; precipitating factors
  • Course: Episodic, continuous, or progressive; any previous episodes
  • Duration: How long have symptoms been present?
  • Severity: Impact on daily functioning, work, relationships, and self-care
  • Treatment to date: Previous and current treatments, response, and adherence

Mood Assessment

Systematically screen for depressive and manic symptoms:

  • Depression screen: Low mood, anhedonia, hopelessness, guilt, worthlessness, suicidal ideation, sleep disturbance (early morning wakening), appetite/weight change, reduced energy, poor concentration, psychomotor retardation or agitation
  • Mania/hypomania screen: Elevated or irritable mood, decreased need for sleep, grandiosity, pressured speech, racing thoughts, increased goal-directed activity, reckless behaviour (spending, sexual disinhibition), flight of ideas
  • Validated tools: Patient Health Questionnaire-9 (PHQ-9), Mood Disorder Questionnaire (MDQ) for bipolar screening

Anxiety Assessment

Screen across the anxiety spectrum:

  • Generalised anxiety: Excessive worry, restlessness, fatigue, muscle tension, irritability, sleep disturbance, difficulty concentrating
  • Panic attacks: Sudden onset of intense fear with palpitations, sweating, trembling, dyspnoea, chest pain, dizziness, derealisation, fear of dying or losing control
  • Specific phobias: Excessive fear of specific objects or situations (heights, needles, flying, animals)
  • Social anxiety: Fear of scrutiny or embarrassment in social situations
  • Agoraphobia: Avoidance of situations where escape might be difficult
  • Validated tools: Generalized Anxiety Disorder 7-item scale (GAD-7), Kessler Psychological Distress Scale (K10)

Psychotic Symptoms

Enquire directly about positive and negative psychotic symptoms:

  • Positive symptoms: Auditory hallucinations (voices), visual hallucinations, paranoid or grandiose delusions, thought insertion, thought broadcasting, thought withdrawal, passivity phenomena
  • Negative symptoms: Alogia, avolition, affective flattening, social withdrawal, anhedonia
  • Disorganisation: Tangential or incoherent speech, bizarre behaviour, disorganised thought
  • Always distinguish between hallucinations (perceptions without external stimulus) and delusions (fixed false beliefs not amenable to contrary evidence)

Substance Use History

Systematic substance use assessment should cover all major substance classes:

Substance Screening Questions Australian Context
Alcohol AUDIT-C; quantity/frequency; withdrawal history; previous detox Most common substance of misuse in Australia; ~1 in 4 exceed NHMRC guidelines
Cannabis Frequency; method of use; psychosis association; dependence features Most commonly used illicit drug; strong association with first-episode psychosis in young people
Methamphetamine Route (smoked vs. IV); frequency; psychotic features; violence risk Crystal methamphetamine (ice) a major public health concern; high rates in rural/regional Australia
Opioids Prescription vs. illicit; naloxone history; overdose history; opioid substitution therapy Prescription opioid misuse exceeds heroin; rising opioid-related deaths
Benzodiazepines Source; daily use; withdrawal seizures; co-prescribing concerns High prescribing rates; often obtained from multiple prescribers
Nicotine Smoking status; pack-years; cessation attempts; nicotine dependence (FagerstrΓΆm) Smoking prevalence ~10% general population; significantly higher in ATSI communities and psychiatric populations

Personal and Social History

A comprehensive personal and social history provides the biographical context essential for understanding the patient's presentation:

  • Developmental history: Birth complications, developmental milestones, childhood behavioural problems, learning difficulties
  • Educational history: Level of education, academic performance, school exclusions or truancy
  • Relationship history: Marital/relationship status, domestic violence, sexual history
  • Occupational history: Current employment, occupational functioning, history of job losses
  • Forensic history: Criminal charges, incarceration, violence history
  • Family psychiatric history: Mental illness in first-degree relatives (especially mood disorders, psychotic disorders, suicide)
  • Abuse and trauma history: Childhood abuse (physical, sexual, emotional), neglect, adult trauma, PTSD screening
  • Social supports: Living situation, social network, cultural and spiritual supports
  • Current medications: Psychiatric and non-psychiatric, including over-the-counter and complementary medicines
  • Allergies: Medication allergies and previous adverse drug reactions
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Collateral history: Always attempt to obtain collateral information from family members, carers, GPs, and previous treating teams (with appropriate consent). Collateral history frequently reveals information the patient may minimise, omit, or lack insight into β€” particularly regarding substance use, psychosis, and risk.

Psychiatric Disorders Overview

The following overview covers the major psychiatric disorder categories encountered in Australian clinical practice. Diagnosis is based on DSM-5-TR (American Psychiatric Association, 2022) or ICD-11 (World Health Organization, 2019) criteria, applied within the context of a thorough psychiatric history and mental state examination.

Mood Disorders

Major Depressive Disorder (MDD)

Characterised by discrete episodes of depressed mood and/or loss of interest or pleasure, lasting at least two weeks, with associated neurovegetative symptoms (sleep, appetite, energy, concentration, psychomotor changes) and functional impairment. Prevalence in Australia: approximately 8–10% lifetime risk.

  • Diagnostic criteria (DSM-5): β‰₯5 of 9 symptoms for β‰₯2 weeks, including at least depressed mood or anhedonia
  • Severity: Mild (5–6 symptoms, minimal impairment), Moderate (symptoms and functional impact between mild and severe), Severe (most symptoms, marked impairment, possible psychotic features)
  • Key differentials: Bipolar disorder (screen for prior mania/hypomania), hypothyroidism, medication-induced (beta-blockers, corticosteroids, interferon), adjustment disorder

Bipolar Disorder

Characterised by episodes of mania (Bipolar I) or hypomania (Bipolar II) alternating with depressive episodes. Lifetime prevalence approximately 1–2% in Australia. Misdiagnosis as unipolar depression is common β€” always screen for prior manic or hypomanic episodes.

  • Mania: β‰₯7 days of elevated/irritable mood with β‰₯3 associated symptoms (grandiosity, decreased sleep, pressured speech, flight of ideas, distractibility, increased goal-directed activity, excessive involvement in risky activities); may require hospitalisation
  • Hypomania: β‰₯4 days, same symptoms but less severe, no hospitalisation required, no psychosis, no marked functional impairment

Anxiety Disorders

Anxiety disorders are the most prevalent class of mental illness in Australia (12-month prevalence ~15–17%). The anxiety disorders include:

Disorder Key Features Australian Prevalence (12-month)
Generalised Anxiety Disorder (GAD) Excessive, uncontrollable worry about multiple domains for β‰₯6 months; restlessness, fatigue, muscle tension, sleep disturbance ~3–4%
Social Anxiety Disorder Marked fear of social situations involving scrutiny; avoidance of social interactions ~3–5%
Panic Disorder Recurrent unexpected panic attacks with persistent concern about future attacks; may include agoraphobia ~2–3%
Specific Phobias Excessive fear of specific objects/situations (e.g., heights, animals, blood-injection-injury) ~5–8%
Post-Traumatic Stress Disorder (PTSD) Re-experiencing, avoidance, hyperarousal, negative cognitions after trauma exposure; β‰₯1 month duration ~4–5% (higher in veterans, ATSI communities)
Obsessive-Compulsive Disorder (OCD) Intrusive obsessions and/or compulsions that are time-consuming (>1 hour/day) or cause distress ~2%

Psychotic Disorders

Psychotic disorders are characterised by disruptions to thinking and perception that impair the individual's sense of reality. The lifetime prevalence of psychotic disorders in Australia is approximately 3%.

  • Schizophrenia: β‰₯6 months of characteristic symptoms (delusions, hallucinations, disorganised speech, negative symptoms, grossly disorganised/catatonic behaviour); significant functional decline. Peak onset: males 18–25, females 25–35.
  • Schizoaffective disorder: Concurrent mood episodes and schizophrenic symptoms; both present for majority of illness duration
  • Brief psychotic disorder: Psychotic symptoms lasting 1 day to 1 month with full return to premorbid functioning
  • Delusional disorder: Non-bizarre delusions for β‰₯1 month without other prominent psychotic symptoms
  • First-episode psychosis: A psychiatric emergency in Australia β€” early intervention services (e.g., EPPIC in Victoria) aim for assessment within 72 hours of referral
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Safety alert β€” First-episode psychosis: All individuals presenting with a first episode of psychosis should be referred urgently to an early psychosis intervention service or acute mental health team. Duration of untreated psychosis (DUP) correlates directly with long-term outcomes. Every week of delay in treatment worsens prognosis.

Somatic Symptom and Related Disorders

Previously termed "somatoform disorders," these conditions are characterised by prominent somatic symptoms associated with disproportionate thoughts, feelings, and behaviours:

  • Somatic symptom disorder: One or more distressing somatic symptoms with excessive health-related anxiety, disproportionate time/energy devoted to symptoms, persisting for >6 months
  • Conversion disorder (functional neurological symptom disorder): Neurological symptoms (weakness, tremor, gait disturbance, seizures, sensory loss) not explained by neurological disease
  • Illness anxiety disorder: Preoccupation with having or acquiring a serious illness; minimal somatic symptoms; excessive health-related behaviours
  • Factitious disorder: Intentional production of symptoms motivated by assumption of the sick role

Organic Brain Disorders

Organic (secondary) psychiatric conditions arise from identifiable medical or substance-related aetiologies and must always be excluded:

Condition Key Features Common Causes
Delirium Acute onset, fluctuating course, altered consciousness, disorientation, inattention, perceptual disturbances, psychomotor disturbance Infection, medications (anticholinergics, opioids, benzodiazepines), metabolic derangement, hypoxia, withdrawal states
Dementia Insidious cognitive decline affecting β‰₯2 domains (memory, language, executive function, visuospatial, personality); progressive course Alzheimer's disease (60–70%), vascular dementia, Lewy body dementia, frontotemporal dementia
Substance-induced Psychiatric symptoms temporally related to substance use or withdrawal; resolve with abstinence Alcohol, cannabis, methamphetamine, synthetic cannabinoids, corticosteroids, anticholinergics
Medical conditions Psychiatric symptoms as manifestation of underlying medical disease Thyroid disease, Cushing's syndrome, autoimmune encephalitis, HIV, syphilis, Wilson's disease, temporal lobe epilepsy

Substance Misuse Disorders

Substance use disorders are defined by DSM-5-TR as a pattern of use leading to clinically significant impairment or distress, manifested by at least 2 of 11 criteria within a 12-month period. Severity is classified as mild (2–3 criteria), moderate (4–5), or severe (β‰₯6).

  • Dual diagnosis: The co-occurrence of a substance use disorder and another psychiatric disorder is the norm rather than the exception. Approximately 60–80% of individuals with a substance use disorder have a comorbid mental health condition, and vice versa.
  • Assessment: Use validated screening tools β€” AUDIT (alcohol), DAST-10 (drugs), ASSIST (WHO Assist β€” all substances)
  • Treatment: Integrated treatment of both conditions simultaneously is the gold standard in Australia, as outlined by the RANZCP and the Australian Government's National Drug Strategy

Mental State Examination

The Mental State Examination (MSE) is the systematic observation and documentation of the patient's current psychiatric state at the time of assessment. It is the psychiatric equivalent of the physical examination. The MSE should be recorded using standardised terminology that is understood by all mental health professionals in Australia.

1
Appearance
General appearance, age, dress, grooming, hygiene, nutrition, distinguishing features, psychomotor state (agitation, retardation, abnormal movements, catatonia)
2
Behaviour
Eye contact, rapport, cooperation, social behaviour, mannerisms, tics, gestures, posture, gait, response to examination
3
Speech
Rate (slow, normal, pressured), volume (quiet, normal, loud), tone, rhythm, spontaneity, coherence, latency of response
4
Mood and Affect
Mood (patient's self-reported emotional state); Affect (clinician-observed emotional expression): range, reactivity, congruence, lability, intensity
5
Thought Form and Content
Form: flight of ideas, tangentiality, circumstantiality, loose associations, neologisms, word salad, thought blocking. Content: delusions, overvalued ideas, obsessions, phobias, suicidal/homicidal ideation
6
Perception
Hallucinations (auditory, visual, tactile, olfactory, gustatory), illusions, depersonalisation, derealisation
7
Cognition
Orientation (time, place, person), attention, memory (short-term, long-term), concentration, general knowledge β€” formal testing (MMSE, MoCA) if indicated
8
Insight and Judgement
Awareness of illness, understanding of need for treatment, appreciation of consequences of actions, capacity for informed decision-making

Appearance

Document the patient's general appearance upon first meeting. Key descriptors include:

  • Physical: Apparent age vs. chronological age, height, weight (BMI), nutritional status, signs of self-harm (scars, burns), signs of substance use (track marks, nasal septum perforation, dental erosion)
  • Dress and grooming: Appropriateness for context, cleanliness, grooming, cosmetics, unusual or eccentric clothing
  • Psychomotor activity: Retardation (depression, parkinsonism), agitation (anxiety, akathisia, mania, psychosis), catatonia (immobility, posturing, waxy flexibility, mutism, stereotypies, echolalia/echopraxia)

Behaviour

Behaviour is observed throughout the interview. Key observations include:

  • Rapport: Quality of therapeutic relationship; cooperative, guarded, hostile, evasive, overly familiar
  • Eye contact: Normal, reduced (depression, anxiety, autism), intense (mania, paranoia)
  • Non-verbal communication: Gestures, facial expressions, body language, mirroring
  • Response to examination: Compliance, resistance, suspiciousness

Speech

Speech is assessed both through content and form:

  • Rate: Slow (depression, sedation, parkinsonism), normal, rapid/pressured (mania, anxiety, stimulant use)
  • Volume: Quiet/whispered (depression, auditory hallucinations), normal, loud (mania, hearing impairment)
  • Spontaneity and latency: Spontaneous, responsive, minimal spontaneous speech; increased response latency (depression, cognitive impairment)
  • Rhythm and prosody: Monotone (depression, negative symptoms of schizophrenia, autism), dysprosodic (Parkinson's disease, right hemisphere lesions)

Mood and Affect

This is one of the most commonly confused domains of the MSE:

Mood
  • The patient's self-reported emotional state
  • Asking: "How have you been feeling in yourself?"
  • Documented in the patient's own words (e.g., "I feel flat," "I feel on top of the world")
  • Stable, enduring emotional tone over hours to days
Affect
  • The clinician's observed emotional expression during the interview
  • Described by: range (full, constricted, flat), reactivity (normal, blunted), congruence (congruent vs. incongruent with mood/stated content), intensity (normal, heightened), lability (normal, labile)
  • Moment-to-moment emotional expression

Thought Form and Content

Thought Form (the "how" of thinking)

Disturbances in the form of thought include:

  • Flight of ideas: Rapidly shifting between topics with loose connections β€” mania, anxiety
  • Tangentiality: Responses diverge from the question and never return
  • Circumstantiality: Responses include excessive unnecessary detail but eventually return to the point
  • Loose associations: Shifts between unrelated topics without logical connection β€” schizophrenia
  • Neologisms: Made-up words with personal meaning β€” schizophrenia, aphasia
  • Thought blocking: Sudden cessation of speech mid-sentence β€” schizophrenia
  • Perseveration: Repetition of words or ideas β€” organic brain disorders, severe depression
  • Word salad: Incoherent, jumbled speech with no discernible meaning β€” severe schizophrenia

Thought Content (the "what" of thinking)

  • Delusions: Fixed, false beliefs not amenable to contrary evidence. Types: persecutory, grandiose, referential, erotomanic, somatic, nihilistic, jealous, control/passivity
  • Overvalued ideas: Unreasonable beliefs held with less intensity than delusions, but influencing behaviour (e.g., anorexia nervosa, body dysmorphic disorder)
  • Obsessions: Intrusive, repetitive, ego-dystonic thoughts (e.g., contamination, harm, symmetry)
  • Suicidal and homicidal ideation: Must be assessed directly in every MSE (see Suicide Risk Assessment below)
  • Preoccupations: Recurrent themes of concern (health, finances, relationships)

Perception

Disturbances of perception are divided into:

  • Hallucinations: Perceptions without an external stimulus. Categorised by modality:
    • Auditory β€” most common in schizophrenia; voices commenting, conversing, commanding; may be ego-syntonic or ego-dystonic
    • Visual β€” more common in organic states, delirium, substance use, Lewy body dementia
    • Tactile β€” formication (insects crawling under skin β€” "cocaine bugs"), somatic sensations
    • Olfactory/Gustatory β€” temporal lobe epilepsy, organic states
  • Illusions: Misinterpretations of real external stimuli (e.g., shadows perceived as figures)
  • Depersonalisation: Feeling of detachment from one's self or body
  • Derealisation: Feeling that the external environment is unreal or dreamlike
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Assessment technique: When screening for hallucinations, begin with normalising questions such as: "Sometimes when people are under a lot of stress, they experience things that others don't β€” like hearing voices or seeing things. Has anything like that happened to you?" Avoid leading or dismissive questions.

Cognition

Cognitive assessment is covered in detail in the section below. At minimum, document:

  • Orientation: Time (date, day, month, year, season), place (building, city, state, country), person (own name, names of others)
  • Attention and concentration: Serial 7s, WORLD backwards, digit span
  • Memory: Immediate recall (3 words), short-term (5 minutes), long-term (remote events)
  • General knowledge: Current and past prime ministers, state capital

Insight and Judgement

Insight is a multidimensional concept. Assess on a spectrum:

Good Insight
Full Awareness
Patient recognises they are unwell, understands the nature of their illness, and accepts the need for treatment
Partial Insight
Limited Awareness
Patient acknowledges some symptoms but minimises severity; may accept treatment reluctantly; partial understanding of consequences
Poor/No Insight
Absent Awareness
Patient denies any illness; attributes symptoms to external causes; refuses treatment; impaired capacity for informed decisions

Judgement refers to the patient's ability to make reasonable decisions about their behaviour and wellbeing. It is closely related to insight and is assessed by exploring the patient's understanding of the consequences of their actions and their ability to make safe, informed decisions. Impaired judgement may indicate the need for assessment of capacity under relevant state and territory mental health legislation (e.g., Mental Health Act 2014 in Victoria, Mental Health Act 2007 in NSW).

Cognitive Assessment & Suicide Risk Assessment

Cognitive Assessment

Cognitive assessment is a critical component of psychiatric evaluation, particularly when organic brain disorders (delirium, dementia) are suspected. Bedside cognitive testing should be performed whenever there is clinical concern about cognitive function. The following tools are widely used in Australian clinical practice:

Mini-Mental State Examination (MMSE)

The MMSE (Folstein, Folstein & McHugh, 1975) is the most widely used bedside cognitive screening tool globally. It assesses five cognitive domains and yields a score out of 30:

Domain Tasks Maximum Score
Orientation Date (5), Place (5) 10
Registration Name 3 objects; repeat them immediately 3
Attention and Calculation Serial 7s from 100 (or spell WORLD backwards) 5
Recall Recall the 3 objects (after 5 minutes) 3
Language Name objects (2), repeat phrase, follow 3-stage command, read/write sentence, copy intersecting pentagons 9
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Interpretation: Score β‰₯24/30: normal range (adjust for age and education). 18–23: mild cognitive impairment. <17: moderate to severe impairment. The MMSE has limited sensitivity for mild cognitive impairment β€” consider the Montreal Cognitive Assessment (MoCA) for this purpose. Copyright restrictions apply to the MMSE; alternative freely available tools include the MoCA, ACE-III, and Rowland Universal Dementia Assessment Scale (RUDAS) β€” the latter is particularly validated for use in culturally and linguistically diverse populations in Australia.

Frontal Lobe Assessment

The MMSE has limited sensitivity for frontal lobe/executive dysfunction. Supplementary bedside tests include:

Essential
Clock Drawing Test
Draw a clock face showing a specific time (e.g., "10 past 11"). Tests visuospatial ability, executive function, and planning. Errors include poor number spacing, incorrect hands, perseveration, left-sided neglect. Scored on multiple systems (Shulman, Sunderland, etc.)
Essential
Verbal Fluency
Name as many animals (or words beginning with a specific letter β€” F, A, S) as possible in 60 seconds. Normal: β‰₯15 animals in 60 seconds (adjust for age/education). Reduced fluency: frontal lobe dysfunction, depression, early dementia
Available
Luria Hand Sequences
Fist–edge–palm sequence: patient taps table with fist, then edge of hand, then palm. Repeat 3 times. Tests motor programming and perseveration. Inability to perform after 3 attempts suggests frontal lobe dysfunction
Available
Go/No-Go Test
Patient taps once when examiner taps once, but does NOT tap when examiner taps twice. Tests impulse control and response inhibition. Failure suggests disinhibition (frontal lobe, mania)
Available
Trail Making Test
Part A: connect numbers 1β†’25 in order. Part B: alternate between numbers and letters (1β†’Aβ†’2β†’B…). Tests attention, processing speed, cognitive flexibility. Part B particularly sensitive to executive dysfunction
Available
Abstraction
Proverb interpretation (e.g., "People in glass houses shouldn't throw stones" β€” what does that mean?) and similarities (e.g., "How are a watch and a ruler alike?"). Concrete responses suggest frontal lobe dysfunction or psychosis

Suicide Risk Assessment

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Critical safety principle: Suicide risk assessment is a mandatory component of every psychiatric evaluation. You must ask directly about suicidal ideation, intent, plan, and means. Asking about suicide does not increase risk β€” it is an essential, life-saving clinical intervention.

The assessment of suicide risk should be systematic, thorough, and documented. Use a structured approach while maintaining a compassionate, non-judgemental clinical stance.

Systematic Risk Assessment Framework

1
Ideation
"Have you had thoughts that life is not worth living?" "Have you wished you were dead?" "Have you thought about harming yourself or ending your life?" β€” Frequency, intensity, duration, controllability
2
Intent
"Have you thought about acting on these feelings?" β€” Sense of resolve, reasons for living, ambivalence, future orientation
3
Plan
"Have you thought about how you would do it?" β€” Specificity, lethality, availability of means, rehearsed?
4
Means and Access
"Do you have access to [identified means]?" β€” Firearms, medications (stockpiling), bridges, ligatures. Lethality of means is a critical determinant of risk
5
Protective Factors
Reasons for living (children, partner, faith, future plans), social support, engagement with treatment, previous help-seeking behaviour, therapeutic alliance

Risk Factors for Suicide

Static / Historical Risk Factors
  • Previous suicide attempt (strongest predictor)
  • Male sex (3:1 male-to-female ratio for completed suicide)
  • Age >65 years (highest completed suicide rate)
  • Family history of suicide
  • History of childhood abuse/trauma
  • Chronic physical illness (chronic pain, cancer, HIV)
  • History of psychiatric illness
Dynamic / Modifiable Risk Factors
  • Current suicidal ideation, intent, and plan
  • Hopelessness (stronger predictor than depression alone)
  • Active psychosis (command hallucinations)
  • Substance intoxication or withdrawal
  • Recent discharge from psychiatric inpatient unit (first 7 days)
  • Relationship breakdown, financial crisis, legal problems
  • Social isolation and lack of supports
  • Access to lethal means
  • Agitation, insomnia, anhedonia

SAD PERSONS Scale

The SAD PERSONS scale is a mnemonic screening tool used in Australian emergency and primary care settings. Each factor scores 1 point:

Letter Risk Factor Score
SSex β€” male1
AAge <19 or >451
DDepression / hopelessness1
PPrevious attempt1
EExcessive alcohol or substance use1
RRational thinking loss (psychosis)1
SSeparated, divorced, widowed1
OOrganised or serious plan1
NNo social supports1
SStated future intent ("I will do it")1
Score 0–3
Low Risk
Consider outpatient follow-up with GP, counselling, safety planning
Setting: Community / GP follow-up
Score 4–6
Moderate Risk
Psychiatric assessment recommended; consider crisis team, short-stay unit, or emergency mental health review
Setting: ED / Crisis team / Mental health triage
Score 7–10
High Risk
Urgent psychiatric assessment required; strong consideration for involuntary admission under state Mental Health Act; do not leave patient unattended
Setting: ED / Inpatient admission
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Important: Risk scales (including SAD PERSONS) are screening aids only and must never replace comprehensive clinical assessment and formulation. The predictive value of any single scale for completed suicide is limited. Clinical judgement, thorough history, and formulation remain the gold standard. Always document your clinical reasoning and risk formulation.

Safety Planning

A safety plan (Stanley & Brown model) should be collaboratively developed with every patient identified as at risk. The plan includes:

  1. Warning signs that a crisis may be developing
  2. Internal coping strategies (things the patient can do on their own)
  3. Social contacts and settings that provide distraction
  4. People to contact for help (family, friends, supports)
  5. Professionals and agencies to contact in a crisis (Lifeline 13 11 14, Beyond Blue 1300 22 4636, Suicide Call Back Service 1300 659 467, 000 for emergency)
  6. Making the environment safe (means restriction)

Mandatory Reporting and Duty of Care

Under Australian common law and state/territory mental health legislation, clinicians have a duty of care to act on identified suicide risk. This includes:

  • Assessing and documenting risk at every contact
  • Implementing least restrictive interventions consistent with safety
  • Communicating risk to the treating team and relevant stakeholders
  • Considering involuntary assessment or admission under state/territory Mental Health Act when indicated
  • Notifying relevant authorities as required by mandatory reporting obligations (e.g., child protection, elder abuse)

Special Populations

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Pregnancy and Perinatal

Perinatal depression and anxiety: Affects 1 in 5 women in Australia. Edinburgh Postnatal Depression Scale (EPDS) is the standard screening tool. Score β‰₯13 warrants further assessment.
Postpartum psychosis: Psychiatric emergency occurring in 1–2 per 1,000 births; onset typically within first 2 weeks postpartum. Requires immediate psychiatric admission (often with baby).
Teratogenic considerations: Valproate is absolutely contraindicated in pregnancy (fetal valproate syndrome). Lithium carries Ebstein's anomaly risk (slight). SSRIs are generally continued if benefits outweigh risks. Clozapine, benzodiazepines, and antipsychotics require careful risk-benefit analysis.
Screening: The Edinburgh Postnatal Depression Scale (EPDS) and Antenatal Risk Questionnaire (ANRQ) are recommended at antenatal booking, third trimester, and 6–12 weeks postpartum (perinatal mental health guidelines).
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Paediatric and Adolescent

Assessment modifications: Developmental stage must be considered. Use age-appropriate language. Involve parents/caregivers as informants, but also interview the child/young person alone (mandatory for adolescents).
Common presentations: Anxiety disorders, ADHD, ASD, behavioural disorders, depression, eating disorders, self-harm (non-suicidal self-injury is common in adolescents).
Suicide risk: Suicide is the leading cause of death in Australians aged 15–24 years. Assessment requires sensitivity and direct questioning. Headspace and Kids Helpline (1800 55 1800) are key Australian resources.
Consent and confidentiality: Gillick competence applies in Australia. Mature minors may consent to psychiatric assessment and treatment without parental consent. Balance confidentiality with duty of care.
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Older Adults

Delirium vs. dementia vs. depression: The "3 Ds" are the most important differential diagnoses in geriatric psychiatry. Delirium is acute and fluctuating; dementia is chronic and progressive; depression is characterised by pervasive low mood with cognitive features ("pseudodementia").
Cognitive screening: The Rowland Universal Dementia Assessment Scale (RUDAS) is validated in Australia for use across culturally and linguistically diverse populations. The MMSE and MoCA remain widely used.
Late-life suicide: Older adults (especially males >80 years) have the highest suicide rate in Australia. Depression is the most common psychiatric risk factor; often presents with somatic complaints, irritability, and cognitive complaints rather than sadness.
Medication considerations: Increased sensitivity to anticholinergic effects, benzodiazepines, and antipsychotics. The Beers Criteria (American Geriatrics Society) guide potentially inappropriate medication use. Start low, go slow.
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Renal Impairment

Lithium: Narrow therapeutic index; renally excreted. Requires dose adjustment in renal impairment. Monitor lithium levels, eGFR, calcium, and thyroid function regularly. Toxicity risk increases significantly when eGFR <60 mL/min.
Dose adjustment: Many psychotropics require dose reduction in CKD (gabapentin, pregabalin, lithium, certain SSRIs). Consult renal dosing guidelines.
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Hepatic Impairment

Drug metabolism: Most psychotropics are hepatically metabolised. Dose reduction is generally required in significant hepatic impairment (Child-Pugh B or C). Monitor LFTs at baseline and periodically.
Sodium valproate: Hepatotoxicity risk; contraindicated in severe hepatic impairment. Monitor LFTs, especially in first 6 months.
Clozapine: Can cause hepatotoxicity; monitor LFTs. Hepatic impairment may require dose reduction and slower titration.
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Immunocompromised

Clozapine: Can cause agranulocytosis (risk ~0.8%). Regular FBC monitoring is mandatory under the Australian Clozapine Patient Register. Dose modification with immunosuppressive medications.
HIV-positive patients: Higher rates of depression, anxiety, psychosis, and cognitive impairment. Drug-drug interactions between antiretrovirals and psychotropics (especially P450 interactions). Refer to HIV-psychiatry guidelines.

Aboriginal and Torres Strait Islander Health Considerations

Aboriginal and Torres Strait Islander Health

Aboriginal and Torres Strait Islander Australians experience significantly higher rates of psychological distress, mental illness, and suicide compared to non-Indigenous Australians. This disparity reflects the profound and ongoing impacts of colonisation, intergenerational trauma, forced removal of children (Stolen Generations), systemic racism, socioeconomic disadvantage, and disconnection from Country, culture, and community.

The social and emotional wellbeing (SEWB) framework, developed by the Australian Government in partnership with Aboriginal and Torres Strait Islander communities, recognises that mental health is inseparable from connection to land, culture, spirituality, ancestry, family, and community. Psychiatric assessment of Aboriginal and Torres Strait Islander people must be conducted within this broader conceptual framework.

Epidemiology
Aboriginal and Torres Strait Islander Australians experience psychological distress at 2.5–3 times the rate of non-Indigenous Australians. Suicide rates are approximately twice the national rate, with the highest rates in remote and very remote areas. The suicide rate for Indigenous young people (15–24 years) is approximately 4 times that of non-Indigenous young people.
Culturally Safe Assessment
Use culturally appropriate communication styles β€” allow more time, use plain language, avoid direct questioning where culturally inappropriate, and recognise that eye contact may have different cultural significance. Ask about connection to Country, culture, family, and community as part of the assessment. Use the SEWB framework rather than imposing a purely Western diagnostic model. Involve Aboriginal and Torres Strait Islander health workers and liaison officers where available.
Yarning and Narrative Approaches
"Yarning" is a culturally embedded communication style that builds trust and rapport. Clinical yarning (developed by Lin et al., 2016) integrates medical information-gathering within a yarning framework. Allow silences β€” they are culturally appropriate and may indicate reflection, not avoidance.
Intergenerational Trauma
The legacy of the Stolen Generations, forced removal, institutionalisation, and cultural suppression directly impacts mental health across generations. Trauma-informed care is essential. Recognise that historical trauma may manifest as distrust of institutions, reluctance to engage with services, and avoidance of authority figures including clinicians.
Remote and Rural Access
Specialist psychiatric services are limited in remote and very remote Australia. Aboriginal Community Controlled Health Organisations (ACCHOs) provide primary mental health care. Telepsychiatry (via platforms such as the Royal Flying Doctor Service and state telehealth services) is increasingly used. The Access to Allied Psychological Services (ATAPS) and Better Access programmes have specific Indigenous components.
Substance Use and Solvent Abuse
Substance use, including alcohol, cannabis, and petrol/sniffing (particularly in remote NT and WA communities), is a significant contributor to psychiatric morbidity. Culturally specific treatment programmes (e.g., through NACCHO member services) are preferred over mainstream approaches. Mandatory reporting of child abuse/neglect (including substance-affected parenting) applies in all Australian jurisdictions.
Screening Tools
The Kessler Psychological Distress Scales (K5 and K10) are widely used and validated for Aboriginal and Torres Strait Islander populations. The Westerman Aboriginal Symptoms Checklist (WASC) is specifically designed for Indigenous Australian populations and covers emotional, social, and behavioural wellbeing.
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Key resources: The Royal Australian and New Zealand College of Psychiatrists (RANZCP) Position Statement on Aboriginal and Torres Strait Islander Mental Health (2021) provides guidance for culturally responsive psychiatric practice. The Australian Indigenous HealthInfoNet (healthinfonet.ecu.edu.au) is a comprehensive resource for evidence-based information on Indigenous health. Always consider referral to an Aboriginal health worker or Aboriginal mental health worker for support with assessment and management.

πŸ“š References

  1. 1. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR). Washington, DC: APA; 2022.
  2. 2. World Health Organization. International Classification of Diseases, 11th Revision (ICD-11). Geneva: WHO; 2019.
  3. 3. Australian Bureau of Statistics. National Study of Mental Health and Wellbeing, 2020–2022. ABS cat. no. 4327.0. Canberra: ABS; 2023.
  4. 4. Royal Australian and New Zealand College of Psychiatrists. Position Statement 100: Aboriginal and Torres Strait Islander Mental Health. Melbourne: RANZCP; 2021.
  5. 5. Folstein MF, Folstein SE, McHugh PR. Mini-Mental State: a practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975;12(3):189–198.
  6. 6. Nasreddine ZS, Phillips NA, BΓ©dirian V, et al. The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment. J Am Geriatr Soc. 2005;53(4):695–699.
  7. 7. Storey JE, Rowland JT, Basic D, Conforti DA, Dickson HG. The Rowland Universal Dementia Assessment Scale (RUDAS): a multicultural cognitive assessment scale. Int Psychogeriatr. 2004;16(1):13–31.
  8. 8. Stanley B, Brown GK. Safety planning intervention: a brief intervention to mitigate suicide risk. Cogn Behav Pract. 2012;19(2):256–264.
  9. 9. Lin I, Green C, Bessarab D. 'Yarn with me': applying clinical yarning to improve clinician-patient communication in Aboriginal health care. Aust J Prim Health. 2016;22(5):377–382.
  10. 10. Productivity Commission. Mental Health, Inquiry Report No. 95. Canberra: Australian Government Productivity Commission; 2020.
  11. 11. Australian Institute of Health and Welfare. Suicide and self-harm monitoring. Canberra: AIHW; 2023. Available at: www.aihw.gov.au/suicide-self-harm-monitoring.
  12. 12. Royal Australian and New Zealand College of Psychiatrists. Practice Guideline 10: The Psychiatric Assessment of Adults. 3rd ed. Melbourne: RANZCP; 2020.
  13. 13. Beyondblue. Depression and Anxiety in the Perinatal Period: A Guide for GPs and Other Primary Care Providers. Melbourne: Beyondblue; 2017.
  14. 14. Patterson S, Hart J, McMullen L, et al. The Westerman Aboriginal Symptoms Checklist β€” Youth (WASC-Y): a measure of social and emotional wellbeing in Aboriginal young people. Aust Psychol. 2014;49(1):54–64.
  15. 15. Mann JJ, Apter A, Bertolote J, et al. Suicide prevention strategies: a systematic review. JAMA. 2005;294(16):2064–2074.
for PBS-listed medicines at participating pharmacies.
Cultural safety
Engagement with Aboriginal Community Controlled Health Organisations (ACCHOs) is essential. Cultural safety training for non-Indigenous clinicians, use of Aboriginal Health Workers and Liaison Officers, and incorporation of traditional healing practices alongside Western medicine improve treatment adherence and outcomes. Avoidance of eye contact, respect for gender-sensitive examination practices, and understanding of sorry business protocols are critical elements of culturally safe care.
Medication adherence
Complex DMARD regimens with frequent monitoring requirements present adherence challenges. Long-acting depot injections (e.g., methotrexate SC) may improve adherence compared to oral regimens. Community pharmacy partnerships through the Indigenous Pharmacy Programmes improve medication management.
Specific conditions
Rheumatic heart disease (RHD) requires secondary prophylaxis with benzathine penicillin G (BPG) 1.2 MU IM every 3–4 weeks for a minimum of 10 years or until age 21 (whichever is longer). RHD registers (e.g., NT RHD Register) facilitate recall and follow-up. The Australian RHD Endgame Strategy targets elimination by 2031.
Referral pathways
Referral through ACCHOs and Aboriginal Hospital Liaison Officers (AHLOs) improves engagement. The Specialist Outreach Assistance Programme provides funded specialist visits to remote communities. NT, WA, and QLD have specific rheumatology outreach programmes targeting Indigenous communities.

πŸ“š References

  1. 1. Australian Institute of Health and Welfare (AIHW). Autoimmune disease in Australia. Cat. no. PHE 312. Canberra: AIHW; 2023.
  2. 2. Fraenkel L, Bathon JM, England BR, et al. 2021 American College of Rheumatology guideline for the treatment of rheumatoid arthritis. Arthritis Care Res. 2021;73(7):924–939.
  3. 3. Fanouriakis A, Kostopoulou M, Alber K, et al. 2019 update of the EULAR recommendations for the management of systemic lupus erythematosus. Ann Rheum Dis. 2019;78(6):736–745.
  4. 4. Chung SA, Langford CA, Maz M, et al. 2021 American College of Rheumatology/Vasculitis Foundation guideline for the management of antineutrophil cytoplasmic antibody-associated vasculitis. Arthritis Care Res. 2021;73(11):1583–1599.
  5. 5. Smolen JS, LandewΓ© RBM, Bijlsma JWJ, et al. EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2022 update. Ann Rheum Dis. 2023;82(1):3–18.
  6. 6. Australian Technical Advisory Group on Immunisation (ATAGI). Australian Immunisation Handbook. Australian Government Department of Health; 2024. Available from: immunisationhandbook.health.gov.au.
  7. 7. Rheumatic Heart Disease Australia (RHDAustralia). The 2020 Australian guideline for prevention, diagnosis, and management of acute rheumatic fever and rheumatic heart disease. 3rd ed. Darwin: Menzies School of Health Research; 2020.
  8. 8. Pharmaceutical Benefits Scheme (PBS). PBS Schedule. Australian Government Department of Health. Available from: pbs.gov.au. Accessed 2024.
  9. 9. Agarwal S, Cunnington J, Nossent J. Autoimmune disease in Indigenous Australians: a systematic review. Int J Rheum Dis. 2021;24(12):1487–1498.
  10. 10. Pisetsky DS. Antinuclear antibody testing β€” misunderstood or misused? Clin Immunol. 2023;255:109717.
  11. 11. Bertsias GK, Tektonidou M, Amoura Z, et al. Joint European League Against Rheumatism and European Renal Association–European Dialysis and Transplant Association (EULAR/ERA-EDTA) recommendations for the management of adult and paediatric lupus nephritis. Ann Rheum Dis. 2012;71(11):1771–1782.
  12. 12. Ledingham J, Deighton C; British Society for Rheumatology Standards, Audit and Guidelines Working Group. Update on the British Society for Rheumatology guidelines for prescribing TNFΞ± blockers in adults with rheumatoid arthritis. Rheumatology. 2005;44(2):155–158.
  13. 13. National Health and Medical Research Council (NHMRC). National statement on ethical conduct in human research. Canberra: NHMRC; 2023 (updated).
for PBS-listed medicines at participating pharmacies.
Cultural safety
Engagement with Aboriginal Community Controlled Health Organisations (ACCHOs) is essential. Cultural safety training for non-Indigenous clinicians, use of Aboriginal Health Workers and Liaison Officers, and incorporation of traditional healing practices alongside Western medicine improve treatment adherence and outcomes. Avoidance of eye contact, respect for gender-sensitive examination practices, and understanding of sorry business protocols are critical elements of culturally safe care.
Medication adherence
Complex DMARD regimens with frequent monitoring requirements present adherence challenges. Long-acting depot injections (e.g., methotrexate SC) may improve adherence compared to oral regimens. Community pharmacy partnerships through the Indigenous Pharmacy Programmes improve medication management.
Specific conditions
Rheumatic heart disease (RHD) requires secondary prophylaxis with benzathine penicillin G (BPG) 1.2 MU IM every 3–4 weeks for a minimum of 10 years or until age 21 (whichever is longer). RHD registers (e.g., NT RHD Register) facilitate recall and follow-up. The Australian RHD Endgame Strategy targets elimination by 2031.
Referral pathways
Referral through ACCHOs and Aboriginal Hospital Liaison Officers (AHLOs) improves engagement. The Specialist Outreach Assistance Programme provides funded specialist visits to remote communities. NT, WA, and QLD have specific rheumatology outreach programmes targeting Indigenous communities.

πŸ“š References

  1. 1. Australian Institute of Health and Welfare (AIHW). Autoimmune disease in Australia. Cat. no. PHE 312. Canberra: AIHW; 2023.
  2. 2. Fraenkel L, Bathon JM, England BR, et al. 2021 American College of Rheumatology guideline for the treatment of rheumatoid arthritis. Arthritis Care Res. 2021;73(7):924–939.
  3. 3. Fanouriakis A, Kostopoulou M, Alber K, et al. 2019 update of the EULAR recommendations for the management of systemic lupus erythematosus. Ann Rheum Dis. 2019;78(6):736–745.
  4. 4. Chung SA, Langford CA, Maz M, et al. 2021 American College of Rheumatology/Vasculitis Foundation guideline for the management of antineutrophil cytoplasmic antibody-associated vasculitis. Arthritis Care Res. 2021;73(11):1583–1599.
  5. 5. Smolen JS, LandewΓ© RBM, Bijlsma JWJ, et al. EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2022 update. Ann Rheum Dis. 2023;82(1):3–18.
  6. 6. Australian Technical Advisory Group on Immunisation (ATAGI). Australian Immunisation Handbook. Australian Government Department of Health; 2024. Available from: immunisationhandbook.health.gov.au.
  7. 7. Rheumatic Heart Disease Australia (RHDAustralia). The 2020 Australian guideline for prevention, diagnosis, and management of acute rheumatic fever and rheumatic heart disease. 3rd ed. Darwin: Menzies School of Health Research; 2020.
  8. 8. Pharmaceutical Benefits Scheme (PBS). PBS Schedule. Australian Government Department of Health. Available from: pbs.gov.au. Accessed 2024.
  9. 9. Agarwal S, Cunnington J, Nossent J. Autoimmune disease in Indigenous Australians: a systematic review. Int J Rheum Dis. 2021;24(12):1487–1498.
  10. 10. Pisetsky DS. Antinuclear antibody testing β€” misunderstood or misused? Clin Immunol. 2023;255:109717.
  11. 11. Bertsias GK, Tektonidou M, Amoura Z, et al. Joint European League Against Rheumatism and European Renal Association–European Dialysis and Transplant Association (EULAR/ERA-EDTA) recommendations for the management of adult and paediatric lupus nephritis. Ann Rheum Dis. 2012;71(11):1771–1782.
  12. 12. Ledingham J, Deighton C; British Society for Rheumatology Standards, Audit and Guidelines Working Group. Update on the British Society for Rheumatology guidelines for prescribing TNFΞ± blockers in adults with rheumatoid arthritis. Rheumatology. 2005;44(2):155–158.
  13. 13. National Health and Medical Research Council (NHMRC). National statement on ethical conduct in human research. Canberra: NHMRC; 2023 (updated).