Psychiatry Matrix

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Last updated 12:33 AM on 7/6/26
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165 Terms

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Psychosis

Impaired perception of reality through one or more of:

  1. Hallucinations (sensory abnormalities w no stimuli)

  2. Delusions (fixed false beliefs inconsistent to cultural/social norms)

  3. Disorganised thinking, speech or behaviour

Primary Psychosis: results from psychiatric disorder (e.g. Schizophrenia)

Secondary Psychosis: results from general medical condition and/or the effect of a substance (inf., endocrine, neurological = stroke/tumour, autoimmune = SLE, B12 def.)

Psychotic Disorder: disease/condition producing psychosis

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Schizophrenia Dx (R1)

Pos, Neg and Cognitive signs/sx of Psychosis persist for >6m, PLUS Social and Functional decline:

  • A) 2+ for >1m of:

    • 1) Delusions, 2) Hallucinations, 3) Disorganised Speech

    • PLUS

    • 4) Grossly Disorganised or Catatonic Behaviour, 5) Neg. Sx (dec. emotions)

  • B) Severe impact on function ability (work, care etc)

  • C) Duration persists >6m (Criteria A = >1m)

  • D) Ruled out Schizoaffective, Depressive or Bipolar

  • E) Ruled out attribution to effects of substances

RF: Genetics, Substances, Environmental/Psychosocial

  • Men = 18-25

  • Women = 25-35 (menarch) + >40 (menopause)

    • Late Onset Schizophrenia: >40-60, W>M, fewer neg. sx

Screening Tools:

  • PANSS (Pos + Neg Sx Scale)

  • BPRS (Bried Psychiatric Rating Scale)

  • Screen for organic cause (CRP, TSH, Urine)

MSE: A/B: poor, disorganised; M: abnorm; S: abnorm, delusions; C: low/distracted; R: __; I: impaired; J: impaired; P: hallucinations

<p>Pos, Neg and Cognitive signs/sx of Psychosis persist for <strong>&gt;6m</strong>, PLUS Social and Functional decline:</p><ul><li><p>A) 2+ for &gt;1m of: </p><ul><li><p>1) Delusions, 2) Hallucinations, 3) Disorganised Speech</p></li><li><p>PLUS </p></li><li><p>4) Grossly Disorganised or Catatonic Behaviour, 5) Neg. Sx (dec. emotions)</p></li></ul></li><li><p>B) Severe impact on function ability (work, care etc)</p></li><li><p>C) Duration persists &gt;6m (Criteria A = &gt;1m)</p></li><li><p>D) Ruled out Schizoaffective, Depressive or Bipolar</p></li><li><p>E) Ruled out attribution to effects of substances</p></li></ul><p><strong><u>RF</u></strong>: Genetics, Substances, Environmental/Psychosocial</p><ul><li><p>Men = 18-25</p></li><li><p>Women = 25-35 (menarch) + &gt;40 (menopause)</p><ul><li><p><strong><em>Late Onset Schizophrenia</em></strong>: &gt;40-60, W&gt;M, fewer neg. sx</p></li></ul></li></ul><p><strong><u>Screening Tools</u></strong>:</p><ul><li><p>PANSS (Pos + Neg Sx Scale)</p></li><li><p>BPRS (Bried Psychiatric Rating Scale)</p></li><li><p>Screen for organic cause (CRP, TSH, Urine)</p></li></ul><p><strong>MSE</strong>: A/B: poor, disorganised; M: abnorm; S: abnorm, delusions; C: low/distracted; R: __; I: impaired; J: impaired; P: hallucinations</p>
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Substance‑Induced Psychosis (R1)

Psychosis must be a direct consequence of substance USE or WITHDRAWAL

Sx development is related to the time the substance was last ingested, and sx duration is usually brief

Causes:

  1. Recreational: Alcohol, Hallucinogens, Cocaine, Cannabis, Amphetamines

  2. Medications: Analgesics (Opioids), Antihistamines, Sedatives/Hypnotics, Antidepressants (SSRIs), Benzo, Antiparkinsons (dopaminergics), Corticosteroids

Substance-Induced Psychotic Disorder: when sx outlast expected intoxication/withdrawal duration

  • However, >4wks indicates other psychotic disorder

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Schizoaffective Disorder (R2)

Mix of Schizophrenia and Bipolar Disorder (Psychosis AND Mania) for >2wks

  • A) Period of either:

    • 1) Major Depressive Eps

    • 2) Manic Ep

    • 3) Mixed Ep with Schizophrenia sx of Criteria A

  • B) Delusions or Hallucinations for >2wks in SAME period of illness as Criteria A WITHOUT Mood Sx

  • C) Sx of Mood Ep. for majority of illness period

  • D) Ruled out attribution to effects of substances

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Schizophreniform Disorder (R2)

Schizophrenic sx/psychosis for a shorter duration of 1-6m

2/3 Pts develop Schizophrenia or Schizoaffective dis.

Criteria:

  • A) 2+ for >1m of:

    • 1) Delusions

    • 2) Hallucinations

    • 3) Disorganised Speech

  • PLUS

    • 4) Grossly Disorganised or Catatonic Behaviour

    • 5) Neg. Sx (dec. emotions)

  • B) Severe impact on function ability (work, care etc)

  • C) Duration persists 1-6m

  • D) Ruled out Schizoaffective, Depressive or Bipolar

  • E) Ruled out attribution to effects of substances

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Delusional Disorder (R3)

At least 1 delusion

No other prominent psychotic sx (hallucinations, disorganised speech, negative sx)

  • A) Nonbizarre delusions >1m (i.e., involving situations that occur in real life, such as being followed, poisoned, infected, loved at a distance, or deceived by spouse or lover, or having a disease)

  • B) Criterion A for Schizophrenia has never been met

  • C) Functioning/Behaviour not impaired apart from the ramifications of the particular delusion

  • D) Any assoc. Mood Eps. have been comparatively brief

  • E) Ruled out attribution to effects of substances

Nonbizzare Del: can be true +/or consistent w cultural/social norms

Bizzarre Del: canNOT be true +/or inconsistent w cultural/social norms

Grandiose Del: insists special powers/importance

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Brief Psychotic Disorder/Episode (R3)

Psychosis for <1m

  • A) Presence of >1 of:

    • 1) Delusions

    • 2) Hallucinations

    • 3) Disorganised Speech

    • 4) Disorganised/Catatonic Behaviour

  • B) Duration is >1d BUT <1m with FULL functional return

  • C) Have Ruled out Mood Disorder With Psychotic Features, Schizoaffective Disorder, Schizophrenia or Substance Effects

RF: Stressful life event

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Psychotic Disorders Mx

Screen for: past Dx of Psychosis, onset (sudden = 2°), head trauma, meds/drug hx, PMHx (Cushings, autoim, THYROID DISEASE!), Life Stressors, FHx

Ix: TFT, BMP, CBC, LFTs, ESR, ANA, Vit B12, Thiamine, HIV/Syphilis, Preg., Urine Tox, MRI/CT Head, EEG

Mx:

Psychosocial Intervs: better for neg/cog sx (CBTp)

Antipsychotic Medications:

  • 1st Line:

    • SGAs: Aripiprazole, Risperidone, Olanzapine, Quetiapine

    • FGAs: Haloperidol, Chlorpromazine

  • Tx Resistant: Clozapine

    • Following failure of TWO different antipsychotics each for ≥ 6wks

    • Requires CBC for neutropenia risk monitoring

    • Must be titrated (cannot start/restart at full dose), abrupt cessation = rapid relapse

    • AEs = CONSTIPATION! → toxic megacolon (gastric hypomotility), myocard., Agranulocytosis (Severe Neutropenia → rare)

SGA > FGA

1st Gens (FGA) = dopamine receptors (muscular sx)

2nd Gens (SGA) = dopamine + serotonin (metabolic sx => monitor lipids, weight and BGLs)

  • Ari = young pts/ASD, acathesia (restlessness)

  • Risp = young pts/ASD, hyperprolactinaemia/galactorrhea

  • Olanz = weight gain/metabolic issues (O = wide)

  • Quet = sedating (Quet = Quiet)

  • Halo = Dystonia + NMS risk, EPSEs, hyperprolact., QT risk

  • Chlor = anticholinergic effects, photosens., HYPOtension

<p><strong>Screen for</strong>: past Dx of Psychosis, onset (sudden = 2°), head trauma, meds/drug hx, PMHx (Cushings, autoim, THYROID DISEASE!), Life Stressors, FHx</p><p><strong>Ix</strong>: TFT, BMP, CBC, LFTs, ESR, ANA, Vit B12, Thiamine, HIV/Syphilis, Preg., Urine Tox, MRI/CT Head, EEG</p><p><strong><u>Mx</u></strong><u>:</u></p><p><strong>Psychosocial Intervs</strong>: better for neg/cog sx (CBTp)</p><p><strong>Antipsychotic Medications:</strong></p><ul><li><p>1st Line:</p><ul><li><p><u>SGAs</u>: <em>Aripiprazole, Risperidone, Olanzapine, Quetiapine</em></p></li><li><p><u>FGAs</u>: <em>Haloperidol, Chlorpromazine</em></p></li></ul></li><li><p>Tx Resistant: <em>Clozapine</em></p><ul><li><p>Following failure of TWO different antipsychotics each for ≥ 6wks</p></li><li><p>Requires CBC for neutropenia risk monitoring</p></li><li><p>Must be titrated (cannot start/restart at full dose), abrupt cessation = rapid relapse</p></li><li><p>AEs = CONSTIPATION! → toxic megacolon (gastric hypomotility), myocard., Agranulocytosis (Severe Neutropenia → rare)</p></li></ul></li></ul><p><u>SGA &gt; FGA</u></p><p><strong>1st Gens (FGA)</strong> = dopamine receptors (muscular sx)</p><p><strong>2nd Gens (SGA)</strong> = dopamine + serotonin (metabolic sx =&gt; monitor lipids, weight and BGLs)</p><ul><li><p><em>Ari </em>= young pts/ASD, acathesia (restlessness)</p></li><li><p><em>Risp </em>= young pts/ASD, hyperprolactinaemia/galactorrhea</p></li><li><p><em>Olanz </em>= weight gain/metabolic issues (O = wide)</p></li><li><p><em>Quet </em>= sedating (Quet = Quiet)</p></li><li><p><em>Halo </em>= Dystonia + NMS risk, EPSEs, hyperprolact., QT risk</p></li><li><p><em>Chlor </em>= anticholinergic effects, photosens., HYPOtension</p></li></ul><p></p>
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Bipolar I Disorder (R1)

Manic episodes >1wk OR causing hospitalisation NOT due to an organic/substance related cause

RF: FHx!!!, Age (18-30)

VERY High Risk of Suicide: Do Risk Assessment

Manic Eps

Distinct periods of abnormally and persistently elevated, expansive, or irritable mood, PLUS abnormally and persistently increased energy or activity

3+ sx of DIGFAST:

  1. Distractibility: attention draws easily to irrelevant stimuli

  2. Impulsivity/High-Risk Behavior: excessive activities with painful consequences (e.g., buying sprees, sexual indiscretions)

  3. Grandiosity: Inflated self-esteem

  4. Flight of Ideas/Racing Thoughts

  5. Activity Increase/Goal-Directed Activity: increased energy at work, school, or socially, +/- psychomotor agitation

  6. Sleep Def/Decreased Sleep: feeling rested after only a few hours

  7. Talkativeness: pressured speech

<p>Manic episodes &gt;1wk OR causing hospitalisation NOT due to an organic/substance related cause</p><p><strong>RF:</strong> FHx!!!, Age (18-30)</p><p>VERY High Risk of Suicide:<em> Do Risk Assessment</em></p><p><strong><u>Manic Eps</u></strong> </p><p>Distinct periods of abnormally and persistently elevated, expansive, or irritable mood, PLUS abnormally and persistently increased energy or activity</p><p>3+ sx of <strong><em>DIGFAST</em></strong>:</p><ol><li><p><strong>D</strong>istractibility: attention draws easily to irrelevant stimuli</p></li><li><p><strong>I</strong>mpulsivity/High-Risk Behavior: excessive activities with painful consequences (e.g., buying sprees, sexual indiscretions)</p></li><li><p><strong>G</strong>randiosity: Inflated self-esteem</p></li><li><p><strong>F</strong>light of Ideas/Racing Thoughts</p></li><li><p><strong>A</strong>ctivity Increase/Goal-Directed Activity: increased energy at work, school, or socially, +/- psychomotor agitation</p></li><li><p><strong>S</strong>leep Def/Decreased Sleep: feeling rested after only a few hours</p></li><li><p><strong>T</strong>alkativeness: pressured speech</p></li></ol><p></p>
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Bipolar II Disorder (R2)

  1. Hypomanic (low levels of mania) >4d

PLUS

  1. Major Depressive episode >2wks

WITHOUT

  1. Full manic episode/Major functional impairment

<ol><li><p>Hypomanic (low levels of mania) &gt;4d</p></li></ol><p><em>PLUS</em></p><ol start="2"><li><p>Major Depressive episode &gt;2wks</p></li></ol><p><em>WITHOUT </em></p><ol start="3"><li><p>Full manic episode/Major functional impairment</p></li></ol><p></p>
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Drug‑Induced Mania (R3)

Mania distinct from a primary bipolar disorder (non-substance-induced)

Sx preceding the substance use, or persisting for a SIGNIFICANT TIME (>1m) after cessation

Substance Abuse: Usually cocaine and amphetamines, can be caused by ETOH, cannabis, opioids etc

Medications: antiparkinsonian drugs, corticosteroids, thyroxine

Suspicious for pts with mania age >35yrs

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Cyclothymic Disorder (R3)

Episodes of hypomania and depression that:

  1. Do not meet the full DSM‑5 diagnostic criteria for hypomania or major depressive disorder

  2. Present at least half the time during a 2‑year period with ≤ 2 months of symptom remission

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Bipolar and Related Disorders Mx

Consider ceasing antidepressants which can cause mania, should only use (SSRIs preferred) WITH Mood Stabilisers

Address triggers (sleep dep,. substance use)

Electroconvulsive Therapy (ECT) for sev./med intolerant

Medications: Combination Therapy (1 + 2) for Mod-Sev.

  1. Mood Stabilisers:

    • Lithium (1st line)

    • Valproate (Avoid in Preg.)

    • Lamotrigine (ONLY for depressive eps/depres-prominent)*

  2. Antipsychotics: SGAs preferred (Aripip, Risp, Olanz, Quet)

  3. Benzodiazepines: Lorazepam (for SHORT TERM and SEVERE: agitation, insomnia, behavioural disturbances)

Antidepressants: not usually used (may cause abnormal mood states/switching) but may be necessary for bipolar depression (Venlafaxine/strong antidepressants should be avoided)

Bipolar Depression: Quetiapine monotherapy, Lithium, Lamotrigine (more for prevention, slower onset), Lurasidone (often with lithium or valproate)

*Do NOT give high dose of Lamotrigine or Lam + Val due to high risk of SJS/TENS (skin burns)

<p>Consider ceasing antidepressants which can cause mania, should only use (SSRIs preferred) WITH Mood Stabilisers</p><p>Address triggers (sleep dep,. substance use)</p><p>Electroconvulsive Therapy (ECT) for sev./med intolerant</p><p><strong><u>Medications</u></strong>: <em>Combination Therapy (1 + 2) for Mod-Sev.</em></p><ol><li><p><strong>Mood Stabilisers</strong>:</p><ul><li><p><em>Lithium </em>(1st line)</p></li><li><p><em>Valproate </em>(Avoid in Preg.)</p></li><li><p>Lamotrigine (ONLY for depressive eps/depres-prominent)<strong>*</strong></p></li></ul></li><li><p><strong>Antipsychotics</strong>: SGAs preferred (<em>Aripip, Risp, Olanz, Quet</em>)</p></li><li><p><strong>Benzodiazepines</strong>: <em>Lorazepam </em>(for SHORT TERM and SEVERE: agitation, insomnia, behavioural disturbances)</p></li></ol><p><strong>Antidepressants</strong>: not usually used (may cause abnormal mood states/switching) but may be necessary for <u>bipolar depression</u> (<em>Venlafaxine</em>/strong antidepressants should be avoided)</p><p><strong><u>Bipolar Depression</u></strong>: <em>Quetiapine </em>monotherapy, <em>Lithium</em>, <em>Lamotrigine </em>(more for prevention, slower onset), <em>Lurasidone </em>(often with lithium or valproate)</p><p><strong>*</strong>Do NOT give high dose of Lamotrigine or Lam + Val due to high risk of SJS/TENS (skin burns)</p>
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Major Depressive Disorder (R1)

>5 sx from the 9 Sx Domains for >2wks including at least one of:

  1. Depressed mood

  2. Loss of interest or pleasure (anhedonia)

PLUS Functional Impact/Distress (Social, Occup. etc)

NOT attributable to a substance or medical condition

NO Hx of Mania/Hypomania Eps (rule out Bipolar)

The 9 symptom domains:

  1. Depressed mood most of the day, nearly every day

  2. Markedly reduced interest or pleasure in most activities

  3. Significant weight loss or gain, or appetite change

  4. Insomnia or hypersomnia

  5. Psychomotor agitation or retardation (observable by others)

  6. Fatigue or loss of energy

  7. Feel worthless or excessive/inappropriate guilt

  8. Reduced concentration or indecisiveness

  9. Recurrent thoughts of death, suicidal ideation, or suicide attempt

<p>&gt;5 sx from the 9 Sx Domains for &gt;2wks including at least one of:</p><ol><li><p>Depressed mood</p></li><li><p>Loss of interest or pleasure (anhedonia)</p></li></ol><p><em>PLUS </em>Functional Impact/Distress (Social, Occup. etc)</p><p><em>NOT </em>attributable to a substance or medical condition</p><p><em>NO </em>Hx of Mania/Hypomania Eps (rule out Bipolar)</p><p><strong><u>The 9 symptom domains:</u></strong></p><ol><li><p>Depressed mood most of the day, nearly every day</p></li><li><p>Markedly reduced interest or pleasure in most activities</p></li><li><p>Significant weight loss or gain, or appetite change</p></li><li><p>Insomnia or hypersomnia</p></li><li><p>Psychomotor agitation or retardation (observable by others)</p></li><li><p>Fatigue or loss of energy</p></li><li><p>Feel worthless or excessive/inappropriate guilt</p></li><li><p>Reduced concentration or indecisiveness</p></li><li><p>Recurrent thoughts of death, suicidal ideation, or suicide attempt</p></li></ol><p></p>
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Substance‑Induced Depressive Disorder (R3)

Clinically significant depressive syndrome that:

  1. Develops during or soon after substance intoxication, withdrawal, or medication exposure

  2. Is attributable to that substance

  3. Is not better explained by a primary depressive disorder

Substance/Med is capable of causing depressive sx

  • E.g. ETOH, Opioids, Sedatives/Hypnotics, Stimulant Withdrawal, Other Prescribed Meds

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Persistent Depressive Disorder/Dysthymia (R3)

Chronic depressive condition characterised by:

  1. Depressed mood for most days for >2yrs

    • >1yr for children/adolescents (will be irritable > sad)

  2. >2 additional depressive sx

  3. No prolonged symptom‑free periods (not >2m)

  4. No history of mania or hypomania

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Disruptive Mood Dysregulation Disorder/DMDD (R3)

Childhood disorder characterised by severe, chronic irritability, rather than episodic mood elevation

  • A) Frequent Severe Temper Outbursts (Verbal/Behav)

  • B) Persistent Irritable Mood/Anger (close to 24/7)

  • C) Frequency of Temper Outbursts >3 times/wk

  • D) Duration >12m, No sx-free period >3m (consec.)

  • E) Sx in >2 settings (sev. in >1): home, school, w peers

  • F) Dx age only bw 6-18yrs (onset sx before 10yrs)

  • G) Exclusion of Mania/Not Better Explained by Another Dx/Disorder or Substances/Med. Condition

Disruptive mood dysregulation disorder is a childhood condition characterised by severe, recurrent temper outbursts and persistent irritability lasting at least 12 months across multiple settings, with onset before age 10 and no history of manic or hypomanic episodes

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Depressive/Mood Disorders Mx

Antidepressants:

  1. SSRIs

  2. SNRIs/Other ()

SSRIs:

  • Sertriline: all-rounder, 1st line, min AEs,

  • Fluoxetine: min AEs, more activating than Sert (gives energy)

<p><strong><u>Antidepressants:</u></strong></p><ol><li><p>SSRIs</p></li><li><p>SNRIs/Other ()</p></li></ol><p><strong>SSRIs:</strong></p><ul><li><p><em>Sertriline</em>: all-rounder, 1st line, min AEs,</p></li><li><p><em>Fluoxetine</em>: min AEs, more activating than <em>Sert </em>(gives energy)</p></li></ul><p></p>
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Generalised Anxiety Disorder/GAD (R1)

>6m of Excessive Worry about Everyday Issues that:

  1. Is disproportionate to any inherent risk

  2. Causes distress or impairment

  3. Is hard to control

>3 sx are present most of the time: SICK FT

  1. Sleep disturbance

  2. Irritability

  3. Concentration poor

  4. Keyed Up/Restlessness or nervousness

  5. Fatigued easily

  6. Tension (in muscles)

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Panic Disorder (R2)

Recurring unexpected panic attacks over >1m

Patient remains persistently concerned/anxious about having another attack

Not Due to Subs/Med Conds/Other Mental Disorders

At least one panic attack is followed by ≥1 month of one or both of:

  1. Persistent concern/worry about panic attacks or their consequences

  2. Persistent concern or worry about

Panic Attacks: sudden onset of intense physical and cognitive symptoms of anxiety that may be triggered by specific cues or occur unexpectedly

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Agoraphobia (R2)

  • A) Marked fear or anxiety for >6m regarding >2 of:

    1. Using public transport (e.g. buses, trains, planes)

    2. Being in open spaces (e.g. car parks, marketplaces)

    3. Being in enclosed spaces (e.g. shops, cinemas)

    4. Standing in line or being in a crowd

    5. Being outside the home alone

  • B) Reason for fear is hard to escape/get help

  • C) Situations are avoided/endured w distress/need a companion due to provoking fear/anxiety

  • D) Fear is out of proportion to posed danger

  • E) Functional Impairment (social, occupational etc)

  • F) Not better explained by another disorder

Can be diagnosed with/without panic disorder

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Specific Phobias (R2)

Intense fears of SPECIFIC OBJECTS or SITUATIONS persistent for >6m that are triggered upon actual or anticipated exposure to phobic stimuli

  • Exposure to the phobic stimulus almost always provokes immediate fear or anxiety

  • Situations w phobic cues are avoided/endured with intense anxiety

  • Excessive fears can cause functional impairments or lifestyle disruptions and is out of proportion

Mx: Exposure Therapy/CBT, Benzos for infrequent sx

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Anxiety Disorders Mx

First Line: SSRIs

Buspirone

  • Short-term mx of anxiety sx (not for panic attacks)

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Obsessive‑Compulsive Disorder (R1)

Presence of one or both of:

  1. Obsessions: recurrent/persistent thoughts, urges or images that are intrusive/unwanted causing anxiety or distress (attempt to ignore/neutralise)

  2. Compulsions: repetitive behaviours/mental acts in response to an obsession aiming to prevent/reduce anxiety or distress that pt feels driven to perform

Obsessions/Compulsions are Time Consuming (>1hr/d) or cause distress/impaired functioning

Not better explained by sub./condition/disorder

Mx = Pharm + CBT/ERP

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Body Dysmorphic Disorder/BDD (R3)

  • A) Preoccupation with appearance: >1 perceived flaws or defects not observable/apparent to others

  • B) Repetitive Behaviours/Mental Acts (skin pick etc)

  • C) Clinically Significant Distress or Impairment

  • D) Not Better Explained by an Eating Disorder

Muscle Dysmorphia Specifier: Preoccupation that the body is too small or insufficiently muscular (M > F)

Mx = Pharm + ERP

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Hoarding Disorder (R3)

  • A) Persistent Difficulty Discarding Possessions (value regardless, perceived need to save items)

  • B) Accumulation/Clutter due to difficulty discarding

  • C) Clinically Significant Distress or Impairment

  • D) Not better explained by sub./condition/disorder

Mx = CBT

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Trichotillomania (R3)

  • A) Recurrent pulling out of hair, resulting in hair loss

  • B) Repeated Attempts to Stop

  • C) Clinically Significant Distress or Impairment

  • D) Not better explained by sub./condition/disorder

Mx = HRT

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Excoriation Disorder (R3)

  • A) Recurrent skin picking, resulting in skin lesions

  • B) Repeated Attempts to Stop

  • C) Clinically Significant Distress or Impairment

  • D) Not better explained by sub./condition/disorder

Mx = Pharm + HRT

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Obsessive‑Compulsive & Related Disorders Mx

Non-Pharm: CBT/ERP!/HRT

Pharm: SSRIs +/- Tricyclic Antis (Clomipramine)

  • Do not give citalopram to BDD

  • Clomipramine: Seratonin-Specific, Less Tolerated than SSRIs

ERP (Exp + Response Prev): systematic exposure to feared stimuli while preventing compulsive behaviours to reduce anxiety

HRT (Habit Revers Train): identifies triggers and substitutes behaviors

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Post Traumatic Stress Disorder - PTSD (R1)

All 4 Groups of sx for >1m following exp. to trauma:

  1. Intrusion symptoms ≥1 (memories, reactions, etc)

  2. Avoidance ≥1 (memories, reminders/places etc)

  3. Negative alterations in cognition and mood ≥2 (e.g. inhibited memory, blame, neg. beliefs/emotions)

  4. Alterations in arousal and reactivity ≥2 (irritable, reckless, sleep disturbance, dec. concentration etc)

Sx cause functional impairment

Mx: Prazosin is effective for PTSD nightmares

Trauma: actual/threatened death, serious injury, or sexual violence through direct experience, witnessing, of learning of from close family/friend

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Acute Stress Disorder (R2)

Sx for 3d-1m, within 4wks following exp. to trauma

  1. Intrusion symptoms ≥1 (memories, reactions, etc)

  2. Avoidance ≥1 (memories, reminders/places etc)

  3. Negative alterations in cognition and mood ≥2 (e.g. inhibited memory, blame, neg. beliefs/emotions)

  4. Alterations in arousal and reactivity ≥2 (irritable, reckless, sleep disturbance, dec. concentration etc)

Sx cause functional impairment

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Adjustment Disorders (R2)

  • A) Emotional or behavioural sx within 3m of an identifiable stressor

  • B) Causes disproportionate distress or functional impairment

  • C) Not better explained by substance/condition/disorder

  • D) Resolves within 6m of the stressor ending

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Trauma & Stress‑Related Disorders Mx

Mild/Mod Sx <3m: active monitoring, supportive

Severe <3m or Sx ≥3: Psych Therapy, Pharm

  • Trauma-focused cognitive behavioural therapy (TFCBT)

  • Eye movement desensitisation and reprocessing (EMDR)

Pharm:

  • 1st Line: SSRIs, SNRIs (Venlafaxine, monitor BP), Mirtazapine (for insomnia), Prazosin ( PTSD nightmares)

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Dissociative Identity Disorder (R3)

  • A) Presence of >2 distinct identities (alters) that control a person's behavior, often caused by severe, chronic childhood trauma

  • B) Causes recurrent amnesia/gaps in recall

  • C) Clinically Significant Distress or Impairment

  • D) Not a Normal Cultural or Religious Practice

  • E) Not Due to Substances or Medical Conditions

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Dissociative Amnesia (R3)

  • A) Inability to Recall Important Information, usually following trauma/stress and is inconsistent with ordinary forgetting

  • B) Clinically Significant Distress or Impairment

  • C) Not better explained by sub./condition/disorder

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Depersonalisation/Derealisation Disorder (R3)

  • A) Persistent or Recurrent Experiences of One or Both of:

    1. Depersonalisation (robotic)

    2. Derealisation (detachment)

  • B) Reality Testing Remains Intact

  • C) Clinically Significant Distress or Impairment

  • D) Not better explained by sub./condition/disorder

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Dissociative Disorder Mx

Psychotherapy, CBT

Psychoeducation

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Borderline Personality Disorder/BPD (R1) - Cluster B

Personality and Emotional Regulation Disorder

Pervasive pattern of instability in affect, self‑image, and interpersonal relationships with marked impulsivity

>5 of IMPULSIVE:

  1. Impulsivity in >2 potentially self‑damaging areas (e.g. sex, money, substances)

  2. Moodiness

  3. Paranoia: Transient, stress‑related paranoid ideation or severe dissociative symptoms

  4. Unstable self image/Identity disturbance

  5. Labile intensive relationships: Unstable and intense interpersonal relationships

  6. Suicidal: Recurrent suicidal behaviour, gestures, threats, or self‑mutilating behaviour

  7. Inappropriate/intense anger or difficulty controlling anger

  8. Vulnerability or abandonment

  9. Emptiness: Chronic feelings of emptiness

Mood fluctuations over the course of the DAY/short periods (Bipolar = over longer periods/episodic/wks)

Feel unsafe in relationships, threat of abandonment

RF = genetics, trauma, difficult relationships

Usually emerges in adolescence or early adulthood

Is REVERSIBLE with Mx

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Antisocial Personality Disorder (R2) - Cluster B

Pervasive pattern of disregard for and violation of the rights of others

Sx occur since age 15yrs, with dx made in adulthood

  • A) Pervasive Pattern of Antisocial Behaviour (failure to conform, impulsive, deceitful, reckless)

  • B) Age Requirement >18rs (must be an adult)

  • C) Evidence of Conduct Disorder Before Age 15

  • D) Exclusion Criteria: Antisocial behaviour does not occur exclusively during schizo/bipolar/mania

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Narcissistic Personality Disorder (R2) - Cluster B

Pervasive pattern of grandiosity, need for admiration, and lack of empathy, beginning by early adulthood

>5 of:

  1. Grandiose sense of self‑importance

  2. Preoccupation with fantasies (success, power etc)

  3. Belief of being "special" and unique

  4. Requires excessive admiration

  5. Sense of entitlement

  6. Interpersonally exploitative behaviour

  7. Lack of empathy

  8. Envy of others/belief others envy them

  9. Arrogant, haughty behaviours or attitudes

Traits are Pervasive, Inflexible, Maladaptive

Not better explained by Mood disorders (e.g. mania), Substance use or Cultural/Occupational norms

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Obsessive‑Compulsive Personality Disorder (R2) - Cluster C

Pervasive pattern of preoccupation with orderliness, perfectionism, and control

>4 of:

  1. Preoccupation with details, rules, lists, order, organisation, or schedules

  2. Perfectionism that interferes with task completion

  3. Excessive devotion to work and productivity (not explained by financial necessity)

  4. Overconscientiousness, scrupulousness, and inflexibility about morality, ethics, or values

  5. Inability to discard worn‑out/worthless objects, even with no sentimental value

  6. Reluctance to delegate tasks or work with others

  7. Miserly spending style toward self/others (hoards)

  8. Rigidity and Stubbornness

Diagnosed in adulthood

Personality trait rather than anxiety disorder (OCD)

Limited insight but usually no obsession/compulsions

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Paranoid Personality Disorder (R3) - Cluster A

Pervasive pattern of distrust and suspicion of others

>4 of:

  1. Suspects, without sufficient basis, that others are exploiting, harming, or deceiving them

  2. Preoccupied with unjustified doubts about the loyalty or trustworthiness of friends or associates

  3. Reluctant to confide in others

  4. Reads hidden demeaning or threatening meanings into benign remarks or events

  5. Persistently bears grudges (unforgiving of insults, injuries, slights)

  6. Perceives attacks on character or reputation

  7. Recurrent suspicions, without justification, of the fidelity of a spouse/sexual partner

Disturbance does not occur exclusively during: Schizophrenia, Bipolar/Mania, Other Psych Disorder

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Schizoid Personality Disorder (R3) - Cluster A

Pervasive pattern of detachment from social relationships and a restricted range of emotional expression

> 4 of:

  1. Neither desires nor enjoys close relationships, including being part of a family

  2. Almost always chooses solitary activities

  3. Min-No interest in sexual experiences with another

  4. Takes pleasure in few/any activities

  5. Lacks close friends/confidants, except 1st‑degree relatives

  6. Appears indifferent to praise/criticism from others

  7. Shows emotional coldness, detachment, or flattened affectivity

Disturbance does not occur exclusively during: Schizophrenia, Bipolar/Mania, Other Psych Disorder

NOT Attributable to ASD or Medical/Neuro Condition

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Schizotypal Personality Disorder (R3) - Cluster A

Pervasive pattern of social and interpersonal deficits, marked by: acute discomfort with close relationships, cognitive/perceptual distortions, eccentric behaviour

> 5 of:

  1. Ideas of reference (exclude fixed delusions)

  2. Odd beliefs or magical thinking (e.g. superstitions, clairvoyance, belief in special powers)

  3. Unusual perceptual exp. (incl. bodily illusions)

  4. Odd thinking/speech (e.g. vague, circumstantial, metaphorical, or over‑elaborate)

  5. Suspiciousness or paranoid ideation

  6. Inappropriate or constricted affect

  7. Behaviour/appearance that is odd, eccentric, or peculiar

  8. Lacks close friends/confidants, except 1st‑degree relatives

  9. Excessive social anxiety (familiarity does not dec.)

Disturbance does not occur exclusively during: Schizophrenia, Bipolar/Mania, Other Psych Disorder

NOT Attributable to ASD or Medical/Neuro Condition

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Histrionic Personality Disorder (R3) - Cluster B

Pervasive pattern of excessive emotionality and attention‑seeking

> 5 of:

  1. Uncomfortable when not the centre of attention

  2. Interactive behaviour with others is often inappropriate, sexually seductive or provocative

  3. Rapidly shifting/shallow expression of emotions

  4. Consistently uses physical appearance to draw attention to self

  5. Style of speech is excessively impressionistic and lacking in detail

  6. Self‑dramatisation, theatricality, and exaggerated expression of emotion

  7. Suggestibility: easily influenced by others or circumstances

  8. Considers relationships to be more intimate than they actually are

Traits must not occur exclusively during: Mood Disorders (e.g. mania) or Substance Intoxication

Must be pervasive and enduring, not situational

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Avoidant Personality Disorder (R3) - Cluster C

Pervasive pattern of social inhibition, feelings of inadequacy, and hypersensitivity to negative evaluation

> 4 of:

  1. Avoids occupational activities that involve significant interpersonal contact (due to fears of criticism, disapproval, or rejection)

  2. Unwilling to get involved with people

  3. Shows restraint within intimate relationships

  4. Preoccupied with being criticised or rejected in social situations

  5. Inhibited in new interpersonal situations

  6. Views self as socially inept, personally unappealing, or inferior to others

  7. Unusually reluctant to take personal risks/engage in new activities

Must not be better explained by: Social anxiety disorder alone, ASD, Mood disorders

Must be pervasive and enduring, not situational

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Dependent Personality Disorder (R3) - Cluster C

Pervasive and excessive need to be taken care of, leading to submissive and clinging behaviour and fears of separation

> 5 of:

  1. Difficulty making everyday decisions without excessive advice and reassurance from others

  2. Needs others to assume responsibility

  3. Difficulty expressing disagreement

  4. Difficulty initiating projects or doing things independently

  5. Goes to excessive lengths to obtain nurturance and support

  6. Feels uncomfortable or helpless when alone

  7. Urgently seeks another relationship when one ends

  8. Unrealistic preoccupation with fears of being left to take care of themselves

Traits must not be better explained by: Major depressive dis, Anxiety dis, Medical illness

Must be pervasive and enduring, not situational

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Personality Disorder Mx

Psychotherapy = 1st line!

Create Crisis/Risk Management Plan

Adjunct Pharmacotherapy for Comorbidites (SSRIs for Depression/Anxiety etc)

Cluster Subtypes:

  • Cluster A: odd or eccentric

  • Cluster B: dramatic, emotional and erratic

  • Cluster C: anxious or fearful

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Anorexia Nervosa (R1)

Restriction of caloric intake relative to requirements leading to:

  1. Low body weight for age, height, gender and developmental status

  2. An intense fear of gaining weight

  3. A body image disturbance/Overvaluation of weight or shape as an expression of self-worth

Two Subtypes:

  1. Restrictive: no binging, limiting food intake, compulsive exercise

  2. Binge Eating and Purging: recurrent episodes of binge eating (uncontrolled overeating) and purging (eg self-induced vomiting, laxative or diuretic misuse)

Often have medical and psychological comorbidities (eg osteopenia, pancreatitis, depression, anxiety)

Hospitalise when BMI <15, BP <80 systolic, dec. vitals

  • Life-threatening Weight Loss: BMI <15 in adults, <75% of median BMI for age + sex in children/adolescents

  • Precipitous Weight Loss: LOW >1kg for two consecutive weeks

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Bulimia Nervosa (R1)

Severe preoccupation about weight and body shape

  1. Recurrent episodes of binge eating, loss of control over eating

  2. Compensatory mechanisms to prevent weight gain (self-induced vomiting, fasting, excessive exercise)

  3. Body weight in the adequate to obese range

Binge eating and compensatory behaviours occur at least once weekly for >3m

RF: women in 20s/30s, trauma hx

Common Signs: Parotid Hypertrophy, Tooth Erosion

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Feeding & Eating Disorder Mx

CBT/Psychotherapy

Nutritional replenishment/Re-feeding

Dietitian Referral

Pharm:

  • AN: No evidence for pharmacological mx

  • BN: SSRIs (1st = Fluoxetine, Citalopram, Fluvoxamine, Sertraline) - for young adults

Mx comorbidities (depression etc) and beware of pregnancy

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Alzheimer's Disease (R1)

Chronic, progressive neurodegenerative disorder with global, non-reversible impairment in cerebral functioning

  • A) Neurocognitive Decline + Memory Impairment

  • B) Insidious onset with gradual, steady decline

Deteriorating course over up to 8-10yrs

Brain lesions: neurofibrillary tangles, senile plaques, neuronal loss, brain atrophy, acetylcholine synth defects

Most common dementia but can coexist with others

RF = Age, FHx, Genetics, Down's Syn., Hyperlipidaemia, Cerebrovascular disease, Drugs, Unfinished School

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Vascular Dementia (R1)

Chronic progressive impairment of cognitive function caused by loss of brain parenchyma

  • Predominantly from cerebrovascular causes (infarction, haemorrhage, small-vessel changes)

  • Damage to grey and white matter

Signs:

  • Loss of Executive Functions (planning etc) > Memory

  • Motor and mood changes are often seen early

RF: age >60, obesity, HTN, smoking, DM

IX: MRI Brain, Ix causes of cog decline (UEC, BGL, B12)

Treat early and aggressively to prevent further cerebrovascular disease/address causes

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Frontotemporal Dementia (R2)

Neurodegenerative Dementia causing disruption in personality and social conduct ± primary language disorder (2nd most common after AD)

Sx: Parkinsonism (50% of pts), Language Impairment, Personality/Social Behaviour Decline, Altered Eating Habits, Inattentiveness, Impulsivity

Note: does not usually present w memory loss

RF: Age 45-65 (mid-life), FHx, Genetics

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Lewy Body Dementia (R2)

Neurodegenerative disorder with Lewy Bodies characterised by:

  1. Parkinsonism (Bradykinesia, Tremor, Rigidity)

  2. Progressive cognitive decline (with fluctuations)

  3. Prominent executive dysfunction

  4. Behavioural and sleep disturbances (REM disorder)

  5. Visuospatial impairment

Ix: Pathology shows presence of Lewy Bodies (Autopsy?), CT/MRI Head, Screening

Mx:

  • Behavioural = Cholinesterase Inhibitors (Donepezil and Rivastigmine are best for behavioural sx without motor sx exacerbation)

  • REM Disorder = Clonazepam/Melatonin

  • Motor Sx = Levodopa/Carbidopa

Lewy Bodies: toxic clumps formed by damaged alpha-synuclein proteins folding into irregular shapes (linked to progressive dopamine loss in the brain)

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Dementia due to Parkinson's Disease (R3)

Significant cognitive decline after >1yr of motor sx due to Parkinson’s Disease

Often overlap with Lewy Body Dementia (cognitive decline and motor sx begin and progress together)

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Dementia due to Prion Disease (R3)

Very rapidly progressive fatal dementias due to prions

Disease is spontaneous, genetic or acquired

Sx: Behavioural/psychiatric changes, memory impairment, visual disturbances, myoclonus, ataxia, language/hearing issues, movement dysfunction

RF: genetics, prion-contaminated surgical instruments, blood products/transfusions, UK Beef 1980-1996

Ix: pathology = definitive, MRI B

No cure - only palliative management (mortality = 1yr)

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Dementia due to Huntington's Disease (R3)

Autosomal dominant slow-progressing neurodegenerative disorder often presenting mid-life

Sx: chorea, incoordination, cognitive decline, personality changes, psychiatric sx (resulting in immobility, mutism, and inanition)

Prognosis: 20yrs from dx

RF: genetics/FHx (pre-test genetic counselling/testing is recommended)

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Dementia due to HIV (R3)

HIV-Associated Neurocognitive Disorder (HAND)

Rare neurodegenerative disorder resulting from HIV infection (virus attacks brain cells causing inflammation and damage)

  • Does not directly infect neurons but indirectly causes cognitive damage → subcortical dementia

More common in the later stages of HIV infection (7% of pts), but rare due to antiviral treatments (ART)

Severity levels:

  1. Asymptomatic Neurocognitive Impairment (ANI)

  2. Mild Neurocognitive Disorder (MND)

  3. HIV‑Associated Dementia (HAD) = severe form

Signs and Sx:

  • Cognitive Features

    • Bradyphrenia (slowed thinking), Impaired attention/concentration, Executive dysfunction (planning/decisions), Memory retrieval problems (rather than storage)

  • Motor Features

    • Gait instability, Poor coordination, Slowed movements, Tremor

  • Behavioral / Psychiatric Features

    • Apathy, Depression, Irritability, Social withdrawal

Unlike Alzheimer’s disease, language and visuospatial skills are preserved

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Neurocognitive Disorder Mx (Dementia)

  • Supportive: Exercise/Physical Activity, Memory Aids, CBT

  • End of life care

Pharmacological:

  1. Acetylcholinesterase Inhibitors: (Donepezil, Galantamine Rivastigmine)

    • Transdermal patch > oral

    • Improve/stabilise cognition, alertness and function (Good for Mild to Severe)

    • AEs: GIT sx, Brady, Neuro/Insomnia/Vivid dreams

  2. NMDA Receptor Antagonists: (Memantine)

    • SHORT-TERM improve/stabilisation in cognition/function

    • Good for Moderate to Severe

Supportive Pharm:

  1. SSRIs: comorbid depression, agitation/aggression

  2. Trazodone/Melatonin: insomnia

Vascular Prevention: Antiplatelets (Aspirin), Anticoagulants (Apixiban, Rivaroxaban)

Lewy Body Motor Sx = Levodopa/Carbidopa

Antipsychotics for acute mx of behavioural disturbance in dementia should be avoided increased risk of AEs/mortality

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Delirium (R1)

Disturbance in attention and awareness developing over a short period of time, is a change from baseline and fluctuates throughout the day (

Acute deterioration of mental state characterised by fluctuating sx of impaired attention, cognition and consciousness, typically developing over hours to days

Three Main Types:

  1. Hyperactive (agitation, restless, delusions, hallucinations)

  2. Hypoactive (quiet, withdrawn) - most common

  3. Mixed (alternates b/w hyper and hypo)

Ix: identify cause (bloods, BGL, ECG, temp, urine)

Mx: reverse causes, low stimuli environment

  • Avoid physical/chemical restraints (meds can worsen delirium)

  • IV Thiamine 3-5d if alcohol withdrawal

  • Antipsychotics if severe distress/hyperactive

    • Haloperidol, Olanzapine, Risperidol = Non Parkinson’s/Lewy Body Dementia

    • Quetiapine = Parkinson’s/LB Dementia

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Demoralisation (R1)

Clinical/dysphoric state of existential distress characterized by:

  • Helplessness

  • ± Hopelessness

  • ± Subjective incompetence/Loss of meaning or purpose

Often arising from chronic illness, severe stress, or perceived failure to cope

Unlike depression, focus is on subjective incompetence rather than anhedonia (pervasive loss of interest)

Mx: psychotherapy, supportive care

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Suicidality/Suicide Attempt (R1)

Two Types:

  1. Impulsive: short time between idea and action

  2. Planned: long time between idea and action (stages include idea, plan/research, prep etc)

RF: static (fixed, historic), dynamic (fluctuates in duration and intensity)

Mx: safety planning, psycotherapy, verbal de-escalation, consider involuntary tx, limit access to toxic drugs (overdose)

<p><strong><u>Two Types:</u></strong></p><ol><li><p><span>Impulsive: short time between idea and action</span></p></li><li><p><span>Planned: long time between idea and action (stages include idea, plan/research, prep etc)</span></p></li></ol><p><strong>RF</strong>: static (fixed, historic), dynamic (fluctuates in duration and intensity)</p><p><strong>Mx</strong>: safety planning, psycotherapy, verbal de-escalation, consider involuntary tx, limit access to toxic drugs (overdose)</p>
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Somatic Symptom Disorder (R2)

Neuropsychiatric condition causing somatic sx associated with significant distress or impairment

  • Distressing physical sx (pain, fatigue, GI symptoms, etc.) that disrupt daily life, with/out medical explanation

  • Excessive and persistent psychological responses

  • Sx for >6m

Underlying cause not understood, psychological stressors may be a RF

Mx: CBT, Physiotherapy

<p>Neuropsychiatric condition causing somatic sx associated with significant distress or impairment</p><ul><li><p>Distressing <strong>physical </strong>sx (pain, fatigue, GI symptoms, etc.) that disrupt daily life, with/out medical explanation</p></li><li><p>Excessive and persistent <em>psychological responses</em></p></li><li><p>Sx for &gt;6m</p></li></ul><p>Underlying cause not understood, psychological stressors may be a RF</p><p><strong>Mx</strong>: CBT, Physiotherapy</p>
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Functional Neurological/Conversion Disorder (R2)

Neuropsychiatric condition causing somatic sx associated with significant distress or impairment

  • Specific neurological (motor/sensory) signs and functional impairment

  • Problems with movement or sensation (e.g. weakness, tremor, numbness, non‑epileptic seizures, speech/gait problems) that look like neurological disease (inconsistent findings)

Underlying cause not understood, psychological stressors may be a RF

Dx: ‘rule in’ features on neuro exam

  • Sx improve with distraction

  • Inconsistency on exam

  • Patterns not matching known neuroanatomy

Mx: CBT, Physiotherapy, SSRIs etc (comorbid anx/dep)

<p>Neuropsychiatric condition causing somatic sx associated with significant distress or impairment</p><ul><li><p>Specific <strong><em>neurological </em></strong><em>(motor/sensory)</em> <em>signs</em> and functional impairment</p></li><li><p>Problems with movement or sensation (e.g. weakness, tremor, numbness, non‑epileptic seizures, speech/gait problems) that look like neurological disease (inconsistent findings)</p></li></ul><p>Underlying cause not understood, psychological stressors may be a RF</p><p><strong>Dx</strong>: ‘rule in’ features on neuro exam</p><ul><li><p>Sx improve with distraction</p></li><li><p>Inconsistency on exam</p></li><li><p>Patterns not matching known neuroanatomy</p></li></ul><p><strong>Mx</strong>: CBT, Physiotherapy, SSRIs etc (comorbid anx/dep)</p>
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Illness Anxiety Disorder (R2)

Disorder of health-related fear

Persistent fear/belief of having/developing a serious illness

  • Excessive fear of illness with minimal to no physical/somatic sx

  • Preoccupation with illness lasts ≥ 6m

  • Behaviours include: Repeated reassurance-seeking, Excessive internet searching, Frequent doctor visits or avoidance of medical care

Mx: CBT, Anxiety Mx (SSRIs etc)

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Psychological Factors Affecting Medical Conditions (R2)

  • A) Medical condition/symptom is present

  • B) Psychological/behavioural factors adversely affect the medical condition in one of:

    1. Influence the course of medical illness (e.g. cause exacerbation or trigger)

    2. Interfere with tx (e.g. poor adherence)

    3. Factors constitute additional well established health risks for the individual

    4. Influence the underlying pathophysiology, precipitating or exacerbating sx

  • C) Not better explained by another mental disorder

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Factitious Disorder (R3)

Patient consciously pretends to have physical sx without a clear secondary gain

  • A) Falscification of physical or psychological signs/sx or induction of injury or disease, associated with identified deception

  • B) The individual presents themself as unwell, injured or impaired

  • C) The deceptive behaviour is evident even in the absence of obvious external rewards

  • D) The behaviour is not better explained by another mental disorder e.g. delusional disorder

Can be Factitious disorder imposed on another (by proxy)

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Malingering (R3)

Patient consciously pretends to have physical sx with a clear secondary gain

  • A) Falscification of physical or psychological signs/sx or induction of injury or disease, associated with identified deception

  • B) The individual presents themself as unwell, injured or impaired

  • C) The deceptive behaviour is evident even in the presence of obvious external rewards

  • D) The behaviour is not better explained by another mental disorder e.g. delusional disorder

Can be Factitious disorder imposed on another (by proxy)

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MedicationInduced Symptoms (R1)

Corticosteroids:

  • Psychiatric AEs = euphoria, hypomania, depression, disturbances of mood, cognition, sleep and behaviour

  • Delirium/psychosis are less common

Yasmin (OCP), Beta Blockers:

  • Increased risk of depression

Ketamine

  • Dissociation associated with confusion, fear or euphoria

Levodopa (Dopamine Agonist):

  • AEs = depression, psychotic sx, impulse control disorders (e.g. gambling, hyper-sexuality, overspending, binge eating, inappropriate internet use)

Isotretinoin (Roaccutane - Acne):

  • Dry skin & mucus membranes, depression

Levetiracetam (Keppra - Anticonvulsant):

  • Behavioural changes (e.g. agitation, irritability, depressed mood, anxiety)

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EndocrineInduced Symptoms (R1)

Pheochromocytoma:

  • Classic triad of episodic headaches, tachycardia and sweating

  • Can cause anxiety symptoms (e.g. panic attacks)

Cushing's Syndrome:

  • Central obesity, proximal muscle wasting & hypertension

  • Can cause depression, mania and psychosis

Polycycstic Ovarian Syndrome:

  • Dx requires >2 of: Oligo/anovulation, Clinical or biochemical evidence of hyperandrogenism & polycystic ovaries

Hyperparathyroidism

  • ‘Bones, stones, abdominal moans and psychic groans’

  • Sx: renal stones and decreased bone density, fatigue, depressed mood, psychosis, cognitive dysfunction

Hyperthyroidism:

  • Palpitations, heat intolerance, weight loss & sweating

  • Anxiety, insomnia, depression, mania, psychosis

Hypothyroidism:

  • Bradycardia, weight gain, cold intolerance, hair loss, fatigue, depression

Addison’s Disease:

  • Fatigue, weight loss, salt craving, hyperpigmentation & hypotension

  • Depression, psychosis, anxiety, mania (less common)

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Encephalopathy (R2)

Diffuse disease of the brain (infection or inflammation) altering brain function or structure

Causes: Infections, Autoimmune Reactions, Metabolic Dysfunction (hepatic enceph), Toxins, Raised Intracranial Pressure, Chronic Progressive Trauma, Poor Nutrition, Hypoxia

Autoimmune Encephalitis: enceph. associated w abs against neuronal cell surface/synaptic proteins (tumours etc)

  • First Manifestation of Auto Enceph. is psychiatric/psychotic sx (acute/subacute changes to mood, behaviour, personality, cognition, consc. state)

  • Red Flag = Enceph sx + Psychiatric Sx

Mx: immunosuppression, address cause (tumours etc), psychiatric meds for sx

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Brain Tumours (R2)

Sx: generalised sx (headache, seizure), raised intracranial pressure (headache, N/V), focal neurological deficits (weakness, sensory loss), cognitive deficits (memory, mood)

Sx can often be mistaken for depression

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Acquired Brain Injury (R2)

Any injury to the brain occurring after birth

  • Traumatic (TBI): head-strike, concussion, shear forces (damage axons, not seen on imaging)

  • Non-Traumatic: encephalitis, meningitis, stroke, substance abuse, brain tumour, hypoxia (MI, overdose etc)

Sx: depend on type and location of injury

  • Physical: Motor/speech/sensory changes, amnesia, epilepsy

  • Cognitive: memory, impulse control, planning, judgement, concentration, abstract thought, attention

  • Mental Health: mood/substance use disorders, anxiety, sleep disturbance, psychosis, aggression

  • Psychosocial: loss of identity, relationship breakdown, financial stressors, social isolation

  • Neurocognitive Disorders: Alzheimer's, Parkinson's

Mx: reduce stimulation, avoid triggers, pain mx, pharm

  • Pharmacological: Psychotropics (start low go slow), Antipsychotics, Benzos; Consider BB, Valproate, Carbamazepine

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HIV-Related Sequelae (R3)

Long-term health complications resulting from HIV infection, including opportunistic infections (e.g., tuberculosis, pneumonia) and mental disorders

Common comorbid mental disorders with HIV disease:

  • Delirium

  • Minor cognitive-motor disorder (MCMD)

  • HIV-associated dementia

  • Major depression

  • Bipolar disorder (including AIDS mania)

  • Schizophrenia (increased risk with HIV)

  • Substance abuse/dependence

  • Post-traumatic stress disorder (PTSD)

  • Personality Disorder

  • Increased suicide risk

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Post-Partum Depression (R1)

Onset of a depressive episode/illness within 4 weeks of childbirth

  • Episodes of postnatal depression last 3-6m (may be m-yrs)

Psychiatric emergency requiring prompt referral

Sx: depressed mood, anhedonia, weight changes, sleep disturbance, psychomotor problems, low energy, excessive guilt, loss of confidence or self-esteem, poor concentration, or suicidal ideation

Exclude postnatal psychosis and bipolar disorder in all pts

RF: minimal social support, antenatal anxiety, PMHx depression or pregnancy loss, preterm birth

<p>Onset of a depressive episode/illness within 4 weeks of childbirth</p><ul><li><p>Episodes of postnatal depression last 3-6m (may be m-yrs)</p></li></ul><p>Psychiatric emergency requiring prompt referral</p><p><strong>Sx</strong>: depressed mood, anhedonia, weight changes, sleep disturbance, psychomotor problems, low energy, excessive guilt, loss of confidence or self-esteem, poor concentration, or suicidal ideation</p><p>Exclude postnatal psychosis and bipolar disorder in all pts</p><p><strong>RF</strong>: minimal social support, antenatal anxiety, PMHx depression or pregnancy loss, preterm birth</p>
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Post-Partum Psychosis (R1)

Psychiatric emergency! (Inc. risk of suicide/infanticide, abuse)

  • Arrange immediate psychiatric evaluation/safety assessment

Presents within 4wks of delivery

  • Sudden change in mental status, agitation, confusion, or insomnia, accompanied by mood features such as anxiety, mania, irritability, or depression

  • Pt typically does not recognise their behaviours/thoughts as abnormal

Sx: delusions, hallucinations, bizarre behaviour, depressed mood, mania, mood liability, insomnia

RF: bipolar disorder, prior eps, FHx, primiparity, sleep dep.

Mx: Psychotropics + ECT

  • Tx/monitoring should continue for at least 6-12m following remission given the high risk and dangers of relapse

<p>Psychiatric emergency! (Inc. risk of suicide/infanticide, abuse)</p><ul><li><p><span>Arrange immediate psychiatric evaluation/safety assessment</span></p></li></ul><p>Presents within 4wks of delivery</p><ul><li><p><span>Sudden change in mental status, agitation, confusion, or insomnia, accompanied by mood features such as anxiety, mania, irritability, or depression</span></p></li><li><p><span>Pt typically does not recognise their behaviours/thoughts as abnormal</span></p></li></ul><p><strong>Sx</strong>: delusions, hallucinations, bizarre behaviour, depressed mood, mania, mood liability, insomnia</p><p><strong>RF</strong>: bipolar disorder, prior eps, FHx, primiparity, sleep dep.</p><p><strong>Mx</strong>: Psychotropics + ECT</p><ul><li><p><span>Tx/monitoring should continue for at least 6-12m following remission given the high risk and dangers of relapse</span></p></li></ul><p></p>
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Baby Blues (R2)

Mild lowered mood/tearfulness in the days post-partum (3-5d after birth)

  • Cause unknown but believed to be due to rapid hormone changes

  • Affects up to 80% of women

  • Often coincides with onset of lactation (1-2d post-partum)

  • Should shift within 3-7d and is not usually an emergency presentation (caution for developing anxiety or depression)

Sx: mood swings, teariness, feeling overwhelmed and/or anxious

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Perinatal Obsessive-Compulsive Disorder (R3)

Egodystonic intrusive images of harming the baby

  • 'Infant-focused' obsessions without compulsions

  • Often associated with avoidance behaviours

  • Obsessions are often of ego-dystonic aggressive thoughts towards the child or of some misfortune coming to the child

  • Obsessions about accidental harm to the infant and other infant-focused obsessions, checking compulsions, self-reassurance and seeking reassurance from other

Onset and exacerbation of pre-existing OCD both linked to post-partum period

Increased risk of harm to self (not usually to child) and secondary depression

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Perinatal Psychiatry Mx

Psychotherapy including relationship therapy

Pharm:

SSRIs

  • Usually first-line for depression, including during breastfeeding

Avoid some Anti-Depressants such as paroxetine

Psychiatric Referral

  • May be necessary for patients who do not respond to treatment

Urgent psychiatric assessment is warranted if:

  • There is a risk of self-harm or harm to the child at any time

  • A postnatal psychosis, manic or mixed ep. is suspected

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Intellectual Disability (R1)

Onset during developmental period and includes both intellectual and adaptive functioning deficits PLUS the following criteria:

  • A) Deficits in intellectual functioning confirmed by clinical assessment and standardized intelligence testing

  • B) Deficits in adaptive functioning leading to failure to meet developmental and sociocultural standards for personal independence and social responsibility

    • Without support, deficits limit functioning in >1 activity of daily living (e.g. communication, socialising, independent living) across multiple environments

  • C) Onset of deficits during developmental period

RF: Genetic (Klinefelter’s, Down’s, Fragile X), Perinatal (maternal DM, inf. prematurity), Malnutrition, Trauma

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Autism Spectrum Disorder/ASD (R1)

  • A) Persistent deficits in social communication and social interaction across multiple contexts

    • Deficits in social-emotional reciprocity

    • Deficits in nonverbal communicative behaviors used for social interaction

    • Deficits in developing, maintaining, and understand relationships

  • B) Restricted, repetitive patterns of behavior, interests, or activities with >2 of:

    • Stereotyped or repetitive motor movements, use of objects, or speech

    • Insistence on sameness, inflexible adherence to routines, or ritualized patterns of verbal or nonverbal behavior (e.g., extreme distress at small changes, difficulties with transitions, rigid thinking patterns)

    • Highly restricted, fixated interests that are abnormal in intensity or focus

    • Hyper/hyporeactivity to sensory input or unusual interest in sensory aspects of the environment (e.g. apparent indifference to pain/temperature, adverse response to specific sensations)

  • C) Sx must be present in the early developmental period

  • D) Sx cause clinically significant impairment in social, occupational, or other important areas of current functioning

  • E) Disturbances are not better explained by intellectual disability (intellectual developmental disorder) or global developmental delay

    • Intellectual disability and autism spectrum disorder frequently co-occur

    • To make comorbid diagnoses of ASD and intellectual disability, social communication should be below that expected for general developmental level

Must also rule out causes of speech delay (e.g. deafness)

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AttentionDeficit and Hyperactivity Disorder/ADHD (R2)

Persistent pattern of inattention and/or hyperactivity–impulsivity that interferes with functioning or development:

  1. Inattention:

    • >6 sx of inattention in <16rs, >5 sx for >17yrs/adults

    • Sx of inattention have been present for >6m

    • Sx are inappropriate for developmental level

  2. Hyperactivity and Impulsivity:

    • >6 sx of hyperactivity-impulsivity <16rs, >5 sx for >17yrs/adults

    • Sx of hyperactivity-impulsivity have been present for >6m

    • Sx are disruptive and inappropriate for the person’s developmental level

Additional Criteria:

  • Several inattentive or hyperactive-impulsive sx were present before age 12

  • Several sx are present in >2 settings (e.g. home, school or work; w friends/relatives)

  • Clear evidence that the sx interfere with/reduce quality of social, school, or work functioning

  • Sx are not better explained by another mental disorder and do not happen only during the course of schizophrenia or another psychotic disorder

Three Main Types:

  1. Combined

  2. Predominantly Inattentive

  3. Predominantly Hyperactive-Impulsive

RF: prematurity, FHx, substance use hx, epilepsy/ABI

Mx: Stimulants - Meth/Dex/Lis (1st), Atomoxetine, Guanfacine, Clonidine

<p>Persistent pattern of&nbsp;inattention&nbsp;and/or&nbsp;hyperactivity–impulsivity&nbsp;that interferes with functioning or development:</p><ol><li><p><strong>Inattention</strong>:</p><ul><li><p>&gt;6 sx of inattention in &lt;16rs, &gt;5 sx for &gt;17yrs/adults</p></li><li><p>Sx of inattention have been present for &gt;6m</p></li><li><p>Sx are inappropriate for developmental level</p></li></ul></li><li><p><strong>Hyperactivity </strong>and <strong>Impulsivity</strong>:</p><ul><li><p>&gt;6 sx of hyperactivity-impulsivity &lt;16rs, &gt;5 sx for &gt;17yrs/adults</p></li><li><p>Sx of hyperactivity-impulsivity have been present for &gt;6m</p></li><li><p>Sx are disruptive and inappropriate for the person’s developmental level</p></li></ul></li></ol><p><strong><u>Additional Criteria:</u></strong></p><ul><li><p>Several inattentive or hyperactive-impulsive sx were present <em>before </em>age 12</p></li><li><p>Several sx are present in &gt;2 settings (e.g. home, school or work; w friends/relatives)</p></li><li><p>Clear evidence that the sx interfere with/reduce quality of social, school, or work functioning</p></li><li><p>Sx are not better explained by another mental disorder and do not happen only during the course of schizophrenia or another psychotic disorder</p></li></ul><p><strong><u>Three Main Types</u></strong>:</p><ol><li><p>Combined</p></li><li><p>Predominantly Inattentive</p></li><li><p>Predominantly Hyperactive-Impulsive</p></li></ol><p><strong>RF</strong>: prematurity, FHx, substance use hx, epilepsy/ABI</p><p><strong>Mx:</strong> Stimulants - <em>Meth/Dex/Lis </em>(1st), <em>Atomoxetine, Guanfacine, Clonidine</em></p>
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Global Developmental Delay (R3)

Children under the age of 5yrs old, who fail to meet developmental milestones across a range of intellectual functioning

  • Pts are too young to partake in standardised intellectual testing

  • Will require reassessment as the child grows older

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Specific Learning Disorder (R3)

  • A) Difficulties in learning and using academic skills, with >1 of:

    • Inaccurate, slow of effortful reading

    • Difficulty understanding the meaning of what is read

    • Spelling difficulties

    • Expression (grammar) difficulties when writing

    • Difficulties with numbers or calculation

    • Difficulties with mathematical reasoning

  • B) Substantially below what is expected for individual's age

  • C) Learning difficulty begins in school-age years

  • D) Not better explained by another condition or sensory disability

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Developmental Coordination Disorder (R3)

  • A) Learning and execution of coordinated motor skills is below expected level for age, given opportunity for skill learning

  • B) Motor skill difficulties significantly interfere with activities of daily living and impact academic/school productivity, prevocational and vocational activities, leisure and play

  • C) Onset is in the early developmental period

  • D) Motor skill difficulties are not better explained by intellectual delay, visual impairment or other neurological conditions that affect movement

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Communication Disorders (R3)

Group of disorders characterised by deficits in speech, language and/or communication

  • Speech: expressive production of sounds

  • Language: form, function and use of conventional system of symbols in rule governed form of communication

  • Communication: any verbal or nonverbal behaviour/expression (intentional or unintentional) that influences the behaviour, attitudes or ideas of another person

Types of Communication Disorders:

  • Language Disorders: difficulties in the acquisition and use of language

  • Speech Sound Disorder: disorder of speech sound production

  • Childhood-Onset Fluency Disorder (Stuttering): disturbance in the normal fluency and time patterning of speech

  • Social (Pragmatic) Communication Disorder: difficulties in the social use of verbal and nonverbal communication

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Tic Disorder (R3)

Tourette's Disorder:

  • A) BOTH multiple motor AND >1 vocal tics have been present at some time during the illness

  • B) Tics may wax and wane but have persisted for >1yr

  • C) Onset before age 18

  • D) Not attributable to another condition/substance

Persistent (Chronic) Motor or Vocal Tic Disorder:

  • As above except:

    • Single/multiple motor

  • OR

    • Vocal tics (not both)

Provisional Tic Disorder:

  • A) Single/multiple motor &/or vocal tics

  • B) Present for <1year

  • C) Onset before age 18

  • D) Not attributable to another condition/substance

  • E) Criteria for above 2 disorders have never been met

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Stereotypic Movement Disorder (R3)

  • A) Repetitive, seemingly driven, and apparently purposeless motor behaviour

  • B) Interferes with social, academic or other activities and may cause self-injury

  • C) Onset in early developmental period

  • D) Not attributable to another condition

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Neurodevelopmental Disorder Mx

Psychotherapy: Social Skills Training, Occupational Therapy, Counselling

Pharm:

ASD: for severe behavioural issues

  • Risperidone: calms aggressive behaviours etc

ADHD: Stimulants are first line!

  1. Stimulants: Methylphenidate (short or long acting - Ritalin), Dexamfetamine, Lisdexamfetamine

    • Improve attention and impulses

    • Should not be given to pts <6yrs

  2. Atomoxetine, Guanfacine, Clonidine (for aggression)

  3. Bupropion, Clonidine, Modafinil, Reboxetine, Venlafaxine

  4. Lamotrigine, Aripiprazole, Agomelatine, Armodafanil, Desvenlafaxine

Methylphenidate: Ritalin = SA or LA, Concerta = Extended Release (less potential abuse, only use if responsive to immediate-release MPH)

Dexamfetamine: No response to MPH, higher risk of AEs, Lisdexamfetamine (Vyvanse) = LA

Atomoxetine: Strattera (Noradr. Reup. Inh.), cannot combine w other stimulants, only if stimulants not tolerated, good for co-morbid anxiety/psychosis/tics, AEs = prolonged QT + stunt growth, low risk of misuse

Guanfacine: Intuniv (Alpha-Adrenergic Rec. Ag), if Stimulants or Atomoxetine not tolerated, if tic disorder, Adjunct w Stimulants if poor response, AEs = Hypotens/Bradyc/Sedation

Clonidine: Catapres, good for aggression and sleep disturbance, not good for inattention, shorter half life than guanfacine (similar role), AEs = Hypotens

Must monitor ADHD sx, Height/Weight, BP/HR, AEs etc

<p><strong><u>Psychotherapy</u></strong>: Social Skills Training, Occupational Therapy, Counselling</p><p><strong><u>Pharm</u></strong>:</p><p><strong>ASD:</strong><em> for severe behavioural issues</em></p><ul><li><p><em>Risperidone</em>: calms aggressive behaviours etc</p></li></ul><p><strong>ADHD:</strong> <em>Stimulants are first line!</em></p><ol><li><p>Stimulants: <em>Methylphenidate </em>(short or long acting - Ritalin), <em>Dexamfetamine, Lisdexamfetamine</em></p><ul><li><p>Improve attention and impulses</p></li><li><p>Should not be given to pts &lt;6yrs</p></li></ul></li><li><p><em>Atomoxetine, Guanfacine, Clonidine </em>(for aggression) </p></li><li><p><em>Bupropion, Clonidine, Modafinil, Reboxetine, Venlafaxine</em></p></li><li><p><em>Lamotrigine, Aripiprazole, Agomelatine, Armodafanil, Desvenlafaxine</em></p></li></ol><p><strong><em>Methylphenidate</em></strong>: <u>Ritalin</u> = SA or LA, <u>Concerta</u> = Extended Release (less potential abuse, only use if responsive to immediate-release MPH)</p><p><strong><em>Dexamfetamine</em></strong>: No response to MPH, higher risk of AEs, <span><strong><em>Lisdexamfetamine </em></strong>(<u>Vyvanse</u>) = LA</span></p><p><span><strong><em>Atomoxetine</em></strong>: <u>Strattera</u> (Noradr. Reup. Inh.), <em>cannot</em> combine w other stimulants, only if stimulants not tolerated, good for co-morbid anxiety/psychosis/tics, AEs = prolonged QT + stunt growth, low risk of misuse</span></p><p><span><strong><em>Guanfacine</em></strong>: <u>Intuniv</u> </span>(Alpha-Adrenergic Rec. Ag), if Stimulants or Atomoxetine not tolerated, if tic disorder, Adjunct w Stimulants if poor response, <span>AEs = Hypotens/Bradyc/Sedation</span></p><p><strong><em>Clonidine</em></strong>: <u>Catapres</u>, good for aggression and sleep disturbance, not good for inattention, shorter half life than guanfacine (similar role), AEs = Hypotens</p><p><em>Must monitor ADHD sx, Height/Weight, BP/HR, AEs etc</em></p>
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Anorexia/Bulimia Nervosa in Paediatrics/<12yrs (R1)

AN: Developmental Emergency! (Affect growth/development)

Weight Assessment uses Growth Charts more than BMI

BN: weight is usually near-normal, binges may be smaller/chaotic/poorly defined, compensatory behaviours may be less extreme/inconsistent

Differences in Presentations:

2/3 have similar psychological sx to adult patients

Key differences:

  • Limited Insight

  • Less likely to report fear of weight gain or being fat

  • Less likely to understand the seriousness of their illness

  • More likely to present with non-specific somatic symptoms

  • More likely to have unspecified eating disorder (or ARFID)

  • Less likely to use vomiting or laxatives

  • Lose weight more rapidly

  • More likely to have a lower percentage of ideal weight

  • Increased proportion of boys in this age group

Cx: Growth retardation, Osteoporosis, Infertility/Amenorrhoea, Alterations in brain development/cognitive impairment, Depression/Anxiety/OCD

Mx: FBT (Family-Based Tx), Nutritional/Fluid Resus

Higher focus on weight restoration before insight

Refeeding Syndrome:

  • Potentially fatal shifts in fluids and electrolytes that may occur in undernourished children/adolescents being re-fed

  • Hallmark biochemical feature is hypophosphataemia

  • Risk in Nutritional and Fluid resus/re-introduction

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Avoidant-Restrictive Food Intake Disorder/ARFID (R3)

Pattern of food avoidance or restriction that is not associated with excess concern about body image and results in at least one of:

  1. Significant weight loss in adults

  2. Failure to meet developmental height and weight targets in children or adolescents

  3. Significant nutrient deficiency

  4. Dependence on enteral feeding or oral nutrition supplements

  5. Marked interference with psychosocial functioning

Mx: behavioural refeeding, graded food exposure, cognitive therapies

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Pica (R3)

Persistent craving and consumption of non-food item (e.g. dirt, paint chips, ice, hair) with no nutritional value for >1m

Often occurs in children, pregnant women, or individuals with developmental disabilities

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Rumination Disorder (R3)

Presence of persistent or recurrent regurgitation of recently ingested nonacidic gastric contents, which are subsequently swallowed (most often) or spat out, for at least 6m

  • Pressurisation of the abdominal cavity caused by contraction of the abdominal muscles, overcoming the lower oesophageal sphincter.

  • Causes regurgitation of gastric contents into the oesophagus and pharynx

Regurgitation may appear as vomiting, but there is an absence of nausea and retching

Distinguished from GORD if regurgitation ceases if gastric contents become acidic, and if sx do not respond to PPIs

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Enuresis (R3)

  • A) Repeated voiding of urine into bed/clothes - whether involuntary or intentional

  • B) Clinically significant either based on frequency, significant distress &/or impairment in functioning

  • C) At least 5 years old (or equivalent developmental level)

  • D) Not attributable to a substance or another medical condition.

Can be either nocturnal, diurnal or both

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Encopresis (R3)

  • A) Repeated passage of stool into inappropriate places (e.g. clothing/floor - whether involuntary or intentional)

  • B) Clinically significant either based on frequency, significant distress &/or impairment in functioning

  • C) At least 4 years old (or equivalent developmental level)

  • D) Not attributable to a substance or another medical condition (unless this is constipation overflow)

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Oppositional Defiant Disorder (R3)

  • A) Pattern of angry/irritable mood, argumentative/defiant behavior, or vindictiveness >6m with >4 sx from any of the following categories, and exhibited during interaction with at least one individual who is not a sibling.

    1. Angry/Irritable Mood: Often loses temper, touchy/easily annoyed, angry/resentful

    2. Argumentative/Defiant Behavior: Often argues with authority figures/adults, actively defies/refuses to comply, deliberately annoys others, blames others

    3. Vindictiveness: Has been spiteful or vindictive at least twice within the 6m

  • B) Disturbance in behavior is associated with distress in the individual/others in his or her immediate social context (e.g., family, peer group, work colleagues), or it impacts negatively on social, educational, occupational, or other important areas of functioning

  • C) The behaviors do not occur exclusively during the course of a psychotic, substance use, depressive, or bipolar disorder

    • Also, the criteria are not met for disruptive mood dysregulation disorder. 

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Conduct Disorder (R3)

  • A) A repetitive and persistent pattern of behavior in which the basic rights of others or major age appropriate societal norms or rules are violated, as manifested by the presence of at least three of the following 15 criteria in the past 12 months from any of the categories below, with at least one criterion present in the past 6 months:

    1. Aggression to People and Animals: Often bullies, threatens, intimidates others, initiates physical fights. Has used a weapon, been physically cruel to people/animals, stolen, forced someone into sexual activity

    2. Destruction of Property: Has deliberately engaged in fire setting with the intention of causing serious damage, deliberately destroyed others’ property

    3. Deceitfulness or Theft: Has broken into another’s house/building/car, often lies to obtain goods/favors/avoid obligations, stolen items without confronting a victim

    4. Serious Violations of Rules: Often stays out at night before age 13, truant from schoo before age 13, has run away from home overnight at least twice

  • B) The disturbance in behavior causes clinically significant impairment in social, academic, or occupational functioning.

  • C) If the individual is age 18 years or older, criteria are not met for antisocial personality disorder

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Reactive Attachment Disorder (R3)

Attachment trauma causing extreme withdrawal and rarely seeks comfort/support from primary caregivers

  • A) Consistent pattern of inhibited, emotionally withdrawn behaviour towards adult caregivers, manifested by both:

    1. Rarely seeks comfort when distressed

    2. Rarely/minimally responds to comfort when distressed

  • B) A persistent social & emotional disturbance characterised by at >2 of:

    1. Minimal social/emotional responsiveness to others

    2. Limited positive affect

    3. Episodes of unexplained irritability, sadness/tearfulness (even in non-threatening interactions with adult caregivers)

  • C) The child has experienced a pattern of extremes of insufficient care, including at least one of:

    1. Social neglect/deprivation with persistent lack of basic emotional needs being met (e.g. comfort, stimulation and affection)

    2. Repeated changes of primary caregivers that limit opportunity to form stable attachments

    3. Rearing in an unusual setting that limit opportunity to form selective attachments (e.g. institutions)

  • D) The care described in criterion C is assumed to be the reason for symptoms in criterion A & B

  • E) Does not meet criteria for ASD

  • F) The disturbance is evidence <5 years old

  • G) Developmental age is at least 9 months old

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Disinhibited Social Engagement Disorder (R3)

Attachment trauma leading to an overfamiliarity with people

  • A) Pattern of behaviour where child actively approaches and interacts with unfamiliar adults, exhibiting at >2 of:

    1. Reduced or absence reticence in approaching and interacting with unfamiliar adults

    2. Overly familiar verbal/physical behaviour

    3. Diminished checking back with adult caregiver when venturing away (even in unfamiliar circumstances)

    4. Willingness to go off with unfamiliar adults with minimal hesitation

  • B) Criterion A behaviours are not limited to impulsivity

  • C) The child has experienced a pattern of extremes of insufficient care, including at >1 of:

    1. Social neglect/deprivation with persistent lack of basic emotional needs being met (e.g. comfort, stimulation and affection)

    2. Repeated changes of primary caregivers that limit opportunity to form stable attachments

    3. Rearing in an unusual setting that limit opportunity to form selective attachments (e.g. institutions)

  • D) The care described in criterion C is assumed to be the reason for symptoms in criterion A & B

  • E) Developmental age is at least 9 months old