1. Past Papers Flashcards

(88 cards)

1
Q

what is the main overview to your approach to management of a violent patient?

A

examine first and then take a history

ABC of management

restraint and tranuilisation

continuously monitor the patient

refer

differentials

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2
Q

Main: what is your approach to the management of a violent patient?

A
  1. examine first and then take a history
    - observe and examine the situation
    - de-escalate the situation
    - take collateral
    - examine patient when patient is retrained
  2. ABC of management
    - Assessment: look for signs of the cause (this stage is completed once the patient is sedated)
    - Back up: staff/ resources to ensure no harm to people or property
    - Containment: pharm or non-pharm.
    (5 C’s of containment = be calm, take control, confidently manage staff, contain the patient with reassurances, constraint if needed in the situation)
  3. restraint and tranuilisation
    - 4 point immobilisation = 4 preassigned staff - each take a hip and shoulder of the patient and then the doctor or nurse in charge sedates the patient immediately
    - administration of drugs: PO takes longer to work; IM needs monitoring; IV works rapidly but requires back up/ resus
  • drug options:
    benzodiazepines (Lorazepam 2-4mg SL/PO/IM or in severe cases, Diazepam)

Antipsychotic agents: haloperidol 5-10mg PO/IM/IV +- Lorazepam or Risperidone 1-2mg PO or olanzepine 10mg PO/IM/IV

For 4 point immobilisation: Inject 2-4mg Lorazepam and 5-10mg Haloperidol IM which can be repeated twice in 30-60min interval

  1. continuously monitor the patient
    - look for EPSEs
    - treat the underlying cause
  2. refer
    - if unable to establish cause
    - hospitalisation is required
    - initial strategies to manage persistence violence fails
  3. differentials
    - criminal behavior
    - antisocial personality disorder
    - substance use disorders
    - acute psychotic episode
    - mania
    - depression
    - dementia
    - anxiety
    - delirium
    - epilepsy
    - cerebral infarctions/ bleeds/ TB
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3
Q

In managing a violent patient, what are the 5 C’s of containment?

A

5 C’s of containment =

be calm
take control
confidently manage staff
contain the patient with reassurances
constraint if needed in the situation

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4
Q

In managing a violent patient, what happens in the 3rd step of restraint and tranuilisation

A
  1. restraint and tranuilisation
    - 4 point immobilisation = 4 preassigned staff - each take a hip and shoulder of the patient and then the doctor or nurse in charge sedates the patient immediately
    - administration of drugs: PO takes longer to work; IM needs monitoring; IV works rapidly but requires back up/ resus
  • drug options:
    benzodiazepines (Lorazepam 2-4mg SL/PO/IM or in severe cases, Diazepam)

Antipsychotic agents: haloperidol 5-10mg PO/IM/IV +- Lorazepam or Risperidone 1-2mg PO or olanzepine 10mg PO/IM/IV

For 4 point immobilisation: Inject 2-4mg Lorazepam and 5-10mg Haloperidol IM which can be repeated twice in 30-60min interval

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5
Q

In managing a violent patient, what are your drug options?

A
  • drug options:
    benzodiazepines (Lorazepam 2-4mg SL/PO/IM or in severe cases, Diazepam)

Antipsychotic agents: haloperidol 5-10mg PO/IM/IV +- Lorazepam or Risperidone 1-2mg PO or olanzepine 10mg PO/IM/IV

For 4 point immobilisation: Inject 2-4mg Lorazepam and 5-10mg Haloperidol IM which can be repeated twice in 30-60min interval

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6
Q

In managing a violent patient, what happens in the 2nd step of the ABCs of management

A
  1. ABC of management
    - Assessment: look for signs of the cause (this stage is completed once the patient is sedated)
    - Back up: staff/ resources to ensure no harm to people or property
    - Containment: pharm or non-pharm.
    (5 C’s of containment = be calm, take control, confidently manage staff, contain the patient with reassurances, constraint if needed in the situation)
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7
Q

In managing a violent patient, what are the differentials

what could be wrong with this patient?

A
  1. differentials
    - criminal behavior
    - antisocial personality disorder
    - substance use disorders
    - acute psychotic episode
    - mania
    - depression
    - dementia
    - **delirium **
    - anxiety
    - epilepsy
    - cerebral infarctions/ bleeds/ TB
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8
Q

In managing a violent patient, what medication do you use to sedate the patient?

A

For 4 point immobilisation: Inject 2-4mg Lorazepam and 5-10mg Haloperidol IM which can be repeated twice in 30-60min interval

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9
Q

Discuss the mood stabiliser lithium in terms of monitoring and therapeutic levels

A

Monitoring: Measure trough levels after 5 days, then monthly, then 3 monthly once stabilised therapeutic serum level

Narrow therapeutic index: 0.6-1mmol/l [0.4-0.7 for geriatric patients]

If it is required, the dose can be increased in increments and trough levels can be
repeated after 5 days

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10
Q

Discuss the mood stabiliser lithium in terms of the clinical presentation of toxicity

A

Mild toxicity reached at = 1.5-2.5mmol/l
moderate = 2.5-3.5mmol/l
severe > 3.5mmol/l

o Seen a lot in **chronic treatment ** or if there is decreased excretion due to drug
interactions, dehydration or renal impairment

o Features: nausea and vomiting, dehydration
renal dysfunction, electrolyte imbalance,
restlessness, tremor/fasciculations,
confusion/apathy, dysarthria, ataxia,
hyperreflexia, muscle weakness,
flat or inverted T waves, arrhythmias,
hypotension, convulsions and coma

o Management: gastric lavage within 1-2hrs; monitor fluids and electrolytes/serum
lithium level/cardiac functions, haemodialysis for moderate-severe toxicity

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11
Q

Discuss the mood stabiliser lithium in terms of the use in women of child bearing age

A

o Increase risk of Ebstein’s anomaly due to T1 exposure and T2 and T3 problems Ā
polyhydramnios, PTL, thyroid abnormalities, floppy baby syndrome

So if mother has:

o Mild stable bipolar disorder: taper down and stop lithium pre-pregnancy

o Moderate risk of relapse: taper and discontinue during T1

o Severe BPD: maintain lithium during pregnancy Ā informed consent, counsel,
detailed USS and echo at 16-18 weeks

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12
Q

Discuss the mood stabiliser lithium in terms of definition

A

Lithium is mood stabiliser, gold standard for treating bipolar mood disorder

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13
Q

Discuss the mood stabiliser lithium in terms of the indications

A
  • acute manic episodes
  • prophylaxis for manic episodes
  • augmentation of antidepressants in resistant/recurrent depression
  • aggressive or self-mutilating behavior
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14
Q

Discuss the mood stabiliser lithium in terms of the contraindications

A
  • cardiac disease
  • renal impairment
  • T1 pregnancy
  • epilepsy
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15
Q

Discuss the mood stabiliser lithium in terms of what investigations you would do before you start the mood stabiliser

A
  • ECG
  • renal function
  • pregnancy test
  • TSH
  • Ca
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16
Q

Discuss the mood stabiliser lithium in terms of the starting dose

A
  • 400-600mg at night
  • increased weekly depending on serum levels** to 2g**
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17
Q

Discuss the mood stabiliser lithium in terms of the side effects

A

Head and neck
2. dry mouth,
4. alopecia, folliculitis, rash, leukocytosis
3. goitre,
4.Hypothyroidism,

GIT
6. Upset GI: N&V, diarrhoea
7. Increased weight,

Limbs
3. tremors and teratogen,

Other
1. Leucocytosis,
2. Insipidus diabetes,
7. Miscellaneous (ECG changes, acne)

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18
Q

what is the management of lithium toxicity?

A
  • gastric lavage within 1-2hrs
  • monitor:
    fluids and electrolytes
    serum lithium level
    cardiac functions
  • haemodialysis for moderate-severe toxicity
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19
Q

what are the features of lithium toxicity?

A

Brain
- confusion/apathy, dysarthria, ataxia
- convulsions and coma

Muscles
- hyperreflexia, muscle weakness
- restlessness
- tremor/fasciculations,

Heart muscle and blood
- flat or inverted T waves, arrhythmias,
- hypotension

GIT
- nausea and vomiting,
- dehydration
- renal dysfunction
- electrolyte imbalance,

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20
Q

what are the toxicity levels of lithium toxicity?

A

Mild toxicity = 1.5-2.5mmol/l
moderate = 2.5-3.5mmol/l
severe > 3.5mmol/l

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21
Q

what is the teratogenicity for lithium toxicity?

A

o Increase risk of **Ebstein’s anomaly **due to T1 exposure and T2 and T3 problems Ā
polyhydramnios, PTL, thyroid abnormalities, floppy baby syndrome

So if the patient has:

o Mild stable bipolar disorder: taper down and stop lithium pre-pregnancy

o Moderate risk of relapse: taper and discontinue during T1

o Severe BPD: maintain lithium during pregnancy Ā informed consent, counsel,
detailed USS and echo at 16-18 weeks

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22
Q

Main: Discuss the mood stabiliser lithium in terms of:

monitoring and therapeutic level
side effects
clinical presentation of toxicity
the use in women of child-bearing age

A

Lithium is mood stabiliser, gold standard for treating bipolar mood disorder

Indications:

  • acute manic episodes
  • prophylaxis for manic episodes
  • augmentation of antidepressants in resistant/recurrent depression
  • aggressive or self-mutilating behavior

**Contraindications:
**
- cardiac disease
- renal impairment
- epilepsy
- T1 pregnancy

**Before initiation:
**
- pregnancy test
- renal function
- TSH
- Ca
- ECG

**Starting dose:
**
- 400-600mg at night,
- increased weekly depending on serum levels to 2g

**Side effects:
**Leucocytosis, Insipidus diabetes, tremors and teratogen, Hypothyroidism,
Increased weight, Upset GI, Miscellaneous (ECG changes, acne)

weight gain, nausea and vomiting, diarrhoea, anorexia, dry mouth, goitre, hypothyroidism,
diabetes insipidus, alopecia, folliculitis, rash, leukocytosis

Monitoring and therapeutic level:
Not much difference between toxic and therapeutic levels

Narrow therapeutic index: 0.6-1mmol/l [0.4-0.7 for geriatric patients]

Measure trough levels after 5 days, then monthly, then 3 monthly once stabilised
therapeutic serum level

If it is required, the dose can be increased in increments and trough levels can be
repeated after 5 days

**Toxicity:
**o Mild = 1.5-2.5mmol/l, moderate = 2.5-3.5mmol/l, severe > 3.5mmol/l

o Occurs in chronic treatment or if there is decreased excretion due to drug
interactions, dehydration or renal impairment

o Features - nausea and vomiting, dehydration, renal dysfunction, electrolyte
imbalance, restlessness, tremor/fasciculations, confusion/apathy, dysarthria, ataxia,
hyperreflexia, muscle weakness, flat or inverted T waves, arrhythmias, hypotension, convulsions and coma

o Management - gastric lavage within 1-2hrs; monitor fluids and electrolytes/serum
lithium level/cardiac functions, haemodialysis for moderate-severe toxicity

**Teratogenicity:
** o Increase risk of Ebstein’s anomaly due to T1 exposure and T2 and T3 problems Ā
polyhydramnios, PTL, thyroid abnormalities, floppy baby syndrome

o Mild stable bipolar disorder: taper down and stop lithium pre-pregnancy

o Moderate risk of relapse: taper and discontinue during T1

o Severe BPD: maintain lithium during pregnancy Ā informed consent, counsel,
detailed USS and echo at 16-18 weeks

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23
Q

Main: what is the side effect profile of 1st generation anti-psychotics

A
  • Typicals/First gen: Chlorpromazine [phenothiazine], Haloperidol [Butyrophenone]
  • Atypicals/Second gen: Clozapine, Olanzapine, Risperidone

EPSEs

  • acute dystonia typically in sternocleidomastoid and tongue but can be widespread
  • akathisia [feeling of inner restlessness],
  • parkinsonism
  • NMS - neuroleptic malignant syndrome [rigidity/fluctuating consciousness/pyrexia]
  • late TDS - tardive dyskinesia [continuous slow writhing movements] more common with typicals, caused by D2-R blockade in corpus striatum
  • orphenadrine co-administration reduces EPSEs

**Anticholinergic side effects:
**
- dry mouth
- blurred vision
- glaucoma
- dysuria
- urinary retention
- constipation
- ileus

Anti-adrenergic: postural hypotension, sexual dysfunction

Anti-histamininc: sedation and weight gain

Other side effects: raised prolactin and cardiac conduction abnormalities from prolonged QT syndrome

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24
Q

In the side effect profile of 1st generation anti-psychotics, what are the EPSEs?

A

EPSEs

  • acute dystonia typically in sternocleidomastoid and tongue but can be widespread
  • akathisia [feeling of inner restlessness],
  • parkinsonism
  • NMS - neuroleptic malignant syndrome [rigidity/fluctuating consciousness/pyrexia]
  • late TDS - tardive dyskinesia [continuous slow writhing movements] more common with typicals, caused by D2-R blockade in corpus striatum
  • orphenadrine co-administration reduces EPSEs
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25
In the side effect profile of 1st generation anti-psychotics, what are the anticholinergic side effects?
Anticholinergic side effects: - **dry** **mouth** - **blurred** **vision** - glaucoma - **dysuria** - urinary **retention** - constipation - ileus
26
In the side effect profile of 1st generation anti-psychotics, what are the anti-adrenergic side effects?
postural **hypotension**, **sexual** dysfunction
27
In the side effect profile of 1st generation anti-psychotics, what are the anti-histaminic side effects?
Anti-histamininc: **sedation** and **weight** gain
28
In the side effect profile of 1st generation anti-psychotics, what are the categories of side effects?
EPSEs Anticholinergic Antiadrenergic Antihistaminic Other side effects
29
Main: How do you assess a depressed patient who you suspect might be suicidal in casualty?
1. Determine whether they're high or low **risk** by looking at the risk **factors**: Look at risk factors: **SADPERSONS** *5-6: medium risk,* 7 or more: high risk ● S: Male **sex** ● A: **Age** (<19 or >45 years) ● D: **Depression** ● P: Previous attempt ● E: Excess **alcohol** or substance use ● R: **Rational** thinking loss ● S: **Social** supports lacking ● O: Organized **plan** ● N: No **spouse** ● S: **Sickness** (GMC) + general risk factors (family history, non-compliance, feelings of hopelessness, unemployment) 2. Then determine **ideation**, intention, plan - **ideation**: **content** and **duration** of thoughts - **intention**: **self-harm** vs suicide - **plan**: **detail**, **lethality**, concealment and **preparation** 3. Then **examine** and **assess** them ● Assessment steps: o Ensure **physical** condition is **stabilised** o Physical **examination** for **medical** **illness**/drug intoxication o **Collateral** interviews from family, colleagues, friends o Psych exam: Hx, **MSE** o Current **presentation of suicidality: lethality** of method, level of intent, steps enacted, feelings of hopelessness o **Psychiatric** illness and **history** thereof o History of **previous** suicide **attempts** o **Psychosocial** situation o Individual **strength** and **vulnerabilities** – **coping** mechanisms, **personality** traits, past response to **stressors** 4. Then do a **post assessment** ● Post-assessment: Likely **risk** of further self-harm, is there a **treatable** mental illness, **psychosocial** problems that need to be addressed, **intervention** and support required to reduce risk 5. Look out for the **warning signs **of suicide = o **Talk**: self-criticism, talking about killing themselves, joke about suicide, having no reason to live, being a burden to others, feeling trapped o **Behaviour**: increased substance use, looking for a way to kill themselves, reckless, *change* in *personality*, *withdrawal* from activities, loss of interest in appearance, *sleeping* too much/too little, calling people to say bye, preparing for death by *giving away* possessions o **Mood**: depression,* loss of interest*, *rage*, irritability, humiliation, anxiety, excessive feelings of guilt
30
In the assessment fo a depressed/ suicidal patient, what are the warning signs of suicide?
5. Look out for the warning signs of suicide = o **TALK**: self-**criticism**, talking about **killing** themselves, **joke** about suicide, having no reason to live, being a **burden** to others, feeling **trapped** o **BEHAVIOUR**: increased **substance** use, looking for a **way** to kill themselves, **reckless**, change in **personality**, **withdrawal** from activities, loss of interest in **appearance**, **sleeping** too much/too little, calling people to say bye, preparing for death by giving away **possessions** o MOOD: **depression**, loss of **interest**, **rage**, **irritability**, humiliation, **anxiety**, excessive feelings of guilt
31
In the assessment of a depressed/ suicidal patient, what are the main risk factors and how do you score them?
1. Determine whether they're high or low risk by looking at the risk factors: Look at risk factors: SADPERSONS 5-6: medium risk, 7 or more: high risk ● S: Male **sex** ● A: **Age** (<19 or >45 years) ● D: **Depression** ● P: Previous **attempt** ● E: Excess **alcohol** or substance use ● R: Rational **thinking** loss ● S: Social **supports** lacking ● O: Organized **plan** ● N: No **spouse** ● S: **Sickness** (GMC) + general risk factors (family history, non-compliance, feelings of hopelessness, unemployment)
32
In the assessment fo a depressed/ suicidal patient, in step 2, what do you need to determine? (IIP)
**Ideation** **Intention** **Plan** - ideation: **content** and duration of thoughts - intention: **self-harm** vs suicide - plan: **detail**, **lethality**, concealment and **preparation**
33
In the assessment of a depressed/ suicidal patient, how do you assess and examine the patient?
4. ● Assessment steps: o Ensure **physical** condition is **stabilised** o Physical **examination** for **medical** illness/drug intoxication o **Collateral** interviews from family, colleagues, friends o Psych exam: Hx, **MSE** o Current **presentation of suicidality: lethality** of method, level of **intent**, steps enacted, feelings of **hopelessness** o **Psychiatric** illness and **history** thereof o History of **previous** suicide **attempts** o **Psychosocial** situation o Individual **strength** and **vulnerabilities** – **coping** mechanisms, **personality** traits, past response to stressors
34
In the assessment of a depressed/ suicidal patient, what do you do post-assessment?
Post-assessment: Likely **risk** of further self-harm, is there a **treatable** mental illness, **psychosocial** problems that need to be addressed, **intervention** and **support** required to reduce risk
35
Main: what is the clinical presentation of PTSD?
● Presence of Severe **psychological** **disturbance** following a **traumatic** event characterised by **involuntary** **re-experiencing** of elements of the event with symptoms of **hyperarousal**, **avoidance** and emotional numbing ● Symptoms and signs: o **Within 6 MONTHS** of traumatic event, **present** for at least **1 month **with clinically significant **distress** or **impairment** in social, occupational or other important areas of **functioning** o **EXPOSURE**: **directly** **experiencing**, witnessing, events happening to close person, **repeated**/extreme **exposure** to details of traumatic events o **ONE OR MORE:** **recurrent**/intrusive **memories** of event, recurrent **dreams**, **dissociative** **reactions** where it feels **like events** are **recurring**, **intense**/prolonged **distress** to **cues** that symbolise/resemble event o **AVOIDANCE** OF STIMULI associated with event – efforts to **avoid** distressing **memories** or **external** **reminders** of those distressing memories o **NEGATIVE** **ALTERATIONS** in cognition and **mood** – **inability** to **remember** aspects, **negative** **beliefs** about **oneself**, **distorted** **cognition** about cause and **consequence** of **event**, **negative** **emotional** state, **diminished** **interest** in activities, **detachment**/estrangement from others, **inability** to experience **positive** **emotions** o **INCREASED** **PHYSIOLOGICAL** SENSITIVITY and arousal: **sleep** disturbance, **irritability** or **outbursts** of anger, difficulty **concentrating**, **hypervigilance**, **exaggerated startle response**, reckless/**self-destructive**
36
Someone comes in w PTSD, how are they presenting?
● Symptoms and signs: o Within **6 MONTHS of** traumatic **event**, present for **at least 1 month** with clinically significant **distress** or **impairment** in social, occupational or other important areas of **functioning** o **EXPOSURE**: **directly** **experiencing**, witnessing, events happening to close person, **repeated**/extreme **exposure** to details of traumatic events o **ONE OR MORE**: **recurrent**/intrusive **memories** of event, recurrent **dreams**, **dissociative** **reactions** where it feels like events are recurring, **intense**/prolonged **distress** to **cues** that symbolise/resemble event o **AVOIDANCE OF STIMULI** associated with event – efforts to **avoid** distressing **memories** **or **external **reminders** of those distressing memories o **NEGATIVE ALTERATIONS** in cognition and mood – **inability to remember** aspects, **negative** beliefs about **oneself**, **distorted** **cognition** about cause and **consequence** of event, **negative** **emotional** state, **diminished** **interest** in activities, **detachment**/estrangement from **others**, **inability** to experience **positive** **emotions** o **INCREASED PHYSIOLOGICAL SENSITIVITY** and arousal: **sleep** disturbance, **irritability** or outbursts of **anger**, difficulty **concentrating**, **hypervigilance**, exaggerated startle response, reckless/self-destructive
37
Your friend asks, so what is PTSD?
Severe **psychological** **disturbance** **following** a **traumatic** event **characterised** by **involuntary** **re**-**experiencing** of elements of the event with **symptoms** of **hyperarousal**, **avoidance** and emotional **numbing**
38
Main: what is the clinical presentation of borderline personality disorder?
● Mnemonic –** AM SUICIDE** need 5: - **abandonment** - mood **instability** [unpredictable affect/labile] - **unstable** and intense relationships - **suicidal** behaviour/self-harm - **impulsivity** - **control** of **anger** is **poor** - identity disturbance [**unclear** **identity**] - **dissociative** symptoms - **emptiness**
39
someone comes in with borderline personality disorder, how are they presenting?
● Mnemonic –** AM SUICIDE** need 5: - **abandonment** - mood **instability** [unpredictable affect/labile] - **unstable** and intense relationships - **suicidal** behaviour/self-harm - **impulsivity** - **control** of **anger** is **poor** - identity disturbance [**unclear** **identity**] - **dissociative** symptoms - **emptiness**
40
Main: what are the differences between delirium and dementia?
Delirium/ Dementia 1. **Onset**: *Acute* [hours to days] Gradual // step-wise decline 2. **Duration**: *Days to weeks* // Months to years 3. **Course**: *Fluctuating* // Progressive 4. **Level** **OC**: *Clouded, fluctuating *// Alert 5. **Orientation**: *Impaired* // Initially intact, impaired later 6. **Attention**: *Decreased* // Not initially affected 7. **Sleep**: *Reversal of sleep wake cycle* // Occasional night-time confusion 8. **Restlessness**: *Worse at night* // Worse in the day 9. **Psychomotor** **activity**: *Agitated or slowed* // Initially unchanged, impaired later 10. **Mood** and **affect**: *Anxious, irritable, fluctuating *// Labile but not anxious 11. **Perceptions**: *Visual hallucinations *//Variable 12. **Reversibility**: *Reversible* // Irreversible
41
how do you know it's delirium and not dementia?
Delirium/ Dementia 1. **Onset**: *Acute* [hours to days] Gradual // step-wise decline 2. **Duration**: *Days to weeks* // Months to years 3. **Course**: *Fluctuating* // Progressive 4. **Level** **OC**: *Clouded, fluctuating *// Alert 5. **Orientation**: *Impaired* // Initially intact, impaired later 6. **Attention**: *Decreased* // Not initially affected 7. **Sleep**: *Reversal of sleep wake cycle* // Occasional night-time confusion 8. **Restlessness**: *Worse at night* // Worse in the day 9. **Psychomotor** **activity**: *Agitated or slowed* // Initially unchanged, impaired later 10. **Mood** and **affect**: *Anxious, irritable, fluctuating *// Labile but not anxious 11. **Perceptions**: *Visual hallucinations *//Variable 12. **Reversibility**: *Reversible* // Irreversible
42
In delirium and dementia, what are the categories that are used to compare the 2?
Delirium/ Dementia 1. Onset: 2. Duration: 3. Course: 4. Level OC: 5. Orientation: 6. Attention: 7. Sleep: 8. Restlessness: 9. Psychomotor activity: 10. Mood and affect: 11. Perceptions: 12. Reversibility: DOC LOA SRP MRP
43
# Primary, assess, educate, organic, urotherapy, techniues, infro, biofeed Main: what is your approach to the management of an 8 year old presenting with eneuresis (bed wetting)?
● Majority can be managed in **primary** **care** or by **specialist** **enuresis** **clinics**, referral to **psychiatry** only when there is wider disturbance of **emotions** and behaviour ● Careful **assessment** – includes thorough medical **history** and **examination** with **investigations** ● **Psychoeducation** of child and parents on **diagnosis** and **treatment** options ● Treat **organic** causes: **structural** abnormalities or **infection** of the Genito-urinary tract ● **Urotherapy**: **increase** bladder **capacity**, **decrease** **night**-time **urine** output, sensitise to unconsciousness awareness of bladder filling o **Techniques**: daily increase in fluid intake, **reduced** **nightly** **intake**, **regular** bladder **emptying**, **pre**-**bedtime** **voiding**, daily bowel action, **avoid** **caffeine** and high **sugar** containing drinks o **Information**, instruction, **life**-**style** advice, registration of symptoms and voiding habits, **support** with the caregiver o **Biofeedback**: pelvic floor **muscle** retraining o **Alarm** therapy: device that gives acoustic signal after episode of incontinence. Bell and Pad method o **Reward** systems [**star**-charts] ● **Medication**: **desmopressin**, **imipramine**, **oxybutynin**
44
So a child comes in with eneuresis, what techniques can you use under urotherapy?
o **Techniques**: daily increase in fluid intake, **reduced** **nightly** **intake**, **regular** bladder **emptying**, **pre**-**bedtime** **voiding**, daily bowel action, **avoid** **caffeine** and high **sugar** containing drinks o **Information**, instruction, life-style advice, registration of symptoms and voiding habits, support with the caregiver o **Biofeedback**: pelvic floor muscle retraining o **Alarm** therapy: device that gives acoustic signal after episode of incontinence. Bell and Pad method o **Reward** systems [star-charts]
45
So a child comes in with eneuresis, if urotherapy fails, what medication can you give them?
Medication: **desmopressin**, **imipramine**, **oxybutynin**
46
So a child comes in with eneuresis, how would you explain to the mum the goals of urotherapy?
Urotherapy: increase **bladder** **capacity**, **decrease** **night**-time **urine** output, **sensitise** to **unconsciousness** awareness of bladder **filling**
47
Main: what is the clinical presentation and management of neuroleptic malignant syndrome?
Definition: A **rare**, life-threatening **reaction** to **anti**-**psychotic** and other medication characterised by **fever**, muscular **rigidity**, altered **mental** status and **autonomic** dysfunction Symptoms/ signs: **hyperthermia** >38, muscular **rigidity**, **confusion**/agitation/**altered** **LOC**, **tachycardia**, **tachypnoea**, hyper/**hypotension**, diaphoresis, tremor, **incontinence**/retention/obstruction, creatinine kinase/urinary myoglobin, **leukocytosis**, **metabolic** **acidosis** Management: o **Benzos** for acute **behavioural** disturbance [restraint and IM may alter CK levels] o **Stop** any possible **causative** agents [anti-psychotics] and restart anti-Parkinsonian symptoms o **Supportive**: oxygen, **correct** hypotension with **fluids**, reduce **temp** with **cooling** blankets/**anti-pyretics**/cooled IVI fluids/ice packs/ice-water enema o **Rhabdomyolysis**: vigorous **hydration** and alkalinisation of urine using IVI **sodium** **bicarbonate** to **prevent** renal **failure** o **Pharmacotherapy** to reduce **rigidity**: **Dantrolene** 0.8-2.5mg/kg IV qds, up to 500mg **Lorazepam**, 2nd line bromocriptine or amantadine, 3rd line **Nifedipine**, consider **ECT** o **Follow** **up**: **monitor** closely, once settled **allow 2+ weeks** before restarting **medication** [use low dose/low- potency/**atypicals**] and consider **prophylactic** **bromocriptine**
48
People are out here talking about neuroleptic malignant syndrome, what is it?
A **rare**, **life**-**threatening** reaction to anti-psychotic and other medication characterised by **fever**, muscular **rigidity**, altered **mental** status and **autonomic** dysfunction
49
Someone comes in with neuroleptic malignant syndrome, how are they presenting?
- hyperthermia >38 ~ - muscular rigidity ~ - confusion/agitation/altered LOC ~ - tachycardia - tachypnoea - hyper/hypotension - diaphoresis, tremor, incontinence/retention/obstruction ~ - creatinine kinase/urinary myoglobin - leukocytosis - metabolic acidosis
50
Someone comes in with neuroleptic malignant syndrome, how are you going to manage them?
o **Benzos** for acute behavioural disturbance [restraint and IM may alter CK levels] o **Stop** any possible **causative** agents [anti-psychotics] and restart anti-Parkinsonian symptoms o **Supportive**: **oxygen**, correct hypotension with **fluids**, reduce temp with cooling blankets/**anti**-**pyretics**/cooled IVI fluids/ice packs/ice-water enema o **Rhabdomyolysis**: vigorous hydration and alkalinisation of urine using IVI **sodium** **bicarbonate** to prevent renal failure o **Pharmacotherapy** to reduce **rigidity**: **Dantrolene** 0.8-2.5mg/kg IV qds, up to 500mg **Lorazepam**, 2nd line bromocriptine or amantadine, 3rd line **Nifedipine**, consider ECT o **Follow** **up**: **monitor** closely, once settled allow **2+ weeks** before restarting **medication** [use low dose/low- potency/**atypicals**] and consider prophylactic bromocriptine
51
Someone comes in with neuroleptic malignant syndrome, what is the medical management to reduce the rigidity?
o **Pharmacotherapy** to reduce rigidity: - **Dantrolene** 0.8-2.5mg/kg IV qds - up to 500mg **Lorazepam** - 2nd line **bromocriptine** or amantadine, - 3rd line **Nifedipine** - consider **ECT**
52
Main: what is the role of the mental health review board?
● **Independent**, partially **JUDICIAL** BODIES that derive **authority** from the **Mental** **Healthcare** **Act** ● Functions: - **considering** **appeals** against decisions of head of health establishment, - making **decisions** with regards to assisted and **involuntary** care, treatment and rehab **services**, - considering reviews and making **decisions** on **transfer** of patient to **max** **security** facilities - periodic reports of the mental health status of mentally ill prisoners ● Ensure **STEPS FOLLOWED **according to **MHCA** ● Provide **LEGAL ASSISTANCE** to patient if requested ● **CHECKS FORMS** completed correctly: ensure legitimacy of process and accuracy of forms (they have to **fill in a form 13** to say that the hospital does have grounds to do the 72 hour assessment and hold the patient during this time) ● Ensure no one is **DETAINED ERRONEOUSLY** ● **ENSURE PROCEDURES** are followed ● **REVIEWS CASE** if patient sends **form 15 (for an appeal)**; MHCB needs to give notice of receiving application within 7 days and see patient within 30 days Members: o **Mental** healthcare **practitioner**: **medical** practitioner, **psychiatrist**, psych **nurse**, **psychologist**, **OT**, **social** **worker** o Legal: **magistrate**, attorney or advocate o **Community** member: good understanding of mental health and referral systems in SA
53
With the MHR board, who are the peops behind the mental health review board?
Members: o **Mental** healthcare **practitioner**: **medical** **practitioner**, **psychiatrist**, psych **nurse**, **psychologist**, **OT**, **social worker** o **Legal**: **magistrate**, attorney or advocate o **Community** member: good understanding of mental health and referral systems in SA
54
Main: what are the side effects of SSRIs?
Head and neck - headache, - dry mouth - excessive sweating [diaphoresis] GIT - Nausea and GI upset [diarrhoea], Vibes - restlessness/agitation/nervousness, - insomnia, - rash, - anxiety, - weight gain, - sexual dysfunction
55
Main: Compare the side effect profile of first generation antipsychotics vs. second generation antipsychotics
● First generation: Eg: **Haloperidol** [high potency] and **Chlorpromazine** [low potency] - **EPSEs**: dystonia, parkinsonism, akathisia [unpleasant inner restlessness and strong compulsion to move], tardive dyskinesia - Postural hypotension - **alpha-adrenergic blockade** - Sedation and weight gain - **histamine blockade** - Dry mouth, blurred vision, constipation, urinary retention, glaucoma, ileus - **anticholinergic effect** - Hyperprolactinemia, skin photosensitivity, arrhythmias, sexual dysfunction, NMS ● 2nd generation: Eg: **Clozapine**, Olanzapine, **Risperidone**, Amisulpride, Quetiapine, - **QT prolongation**, arrhythmia, Torsade, impaired glucose tolerance, diabetes, weight gain, dyslipidaemia [metabolic syndrome] and sexual dysfunction ~ - **Clozapine**: For treatment-resistant schizophrenia, intolerable EPSE, negative psychotic features - *Side effects*: **agranulocytosis**, **myocarditis**, **toxic** **megacolon**, seizures, sedation, weight gain, **hypersalivation** - **Neutrophils < 1.5x109 – Stop Clozapine** - Monitoring: WCC – prior to starting treatment then weekly for 18 weeks then every 2 weeks for 6 months then monthly
56
With 1st gen antipsychotics, You give a patient a 1st gen antipsychotic, what side effects might they experience?
● First generation: Eg: **Haloperidol** [high potency] and **Chlorpromazine** [low potency] - **EPSEs**: dystonia, parkinsonism, akathisia [unpleasant inner restlessness and strong compulsion to move], tardive dyskinesia - Postural hypotension - **alpha-adrenergic blockade** - Sedation and weight gain - **histamine blockade** - Dry mouth, blurred vision, constipation, urinary retention, glaucoma, ileus - **anticholinergic effect** - Hyperprolactinemia, skin photosensitivity, arrhythmias, sexual dysfunction, NMS
57
With 2nd gen antipsychotics, You give a patient a 2nd gen antipsychotic, what side effects might they experience?
● 2nd generation: o Clozapine, Olanzapine, Risperidone, Amisulpride, Quetiapine, - **QT prolongation** - arrhythmia - Torsade, - impaired glucose tolerance, - diabetes, - weight gain, - dyslipidaemia [metabolic syndrome] and sexual dysfunction
58
With 2nd gen antipsychotics, clozapine, what do you choose to give clozapine?
For treatment-resistant schizophrenia, intolerable EPSE, negative psychotic features
59
With 2nd gen antipsychotics, you give a patient clozapine, what are the side effects you're expecting?
▪ Side effects: - agranulocytosis, - myocarditis, - toxic megacolon, - seizures, - sedation, - weight gain, - hypersalivation
60
With 2nd gen antipsychotics, you give your patient clozapine, what monitoring do you need to do?
▪ Monitoring: WCC – prior to starting treatment - then weekly for 18 weeks - then every 2 weeks for 6 months - then monthly
61
With 2nd gen antipsychotics, you give your patient clozapine, when do you decide to stop?
▪ Neutrophils < 1.5x10^9 – Stop Clozapine
62
Main: Discuss approach to unruly and disruptive child in the classroom [ADHD] and mention the differentials
Aetiology: **parent** with **alcohol** dependence, **antisocial**, **ADHD**, conduct disorder and **schizophrenia** OR **sibling** with **disruptive** behaviour **disorder** ● **See** family and the child, **support** the parent, **screen** for high risk families ● Obtain a full **history** with **collateral** from **school**, social worker and **legal** system ● Assess for **comorbidities** and make a diagnosis ● **Formulate** the **problems** and establish **management** plan ● **Address** **child** **protection** concerns ● Treat **comorbidity** ● **Medical** treatment: **antipsychotics** to manage acute and chronic aggression, stimulants such as **Methylphenidate** [Concerta or **Ritalin**] ● **Psychological**: o **Parent** **management** **training**: **education** programmes – provide with **info** of **normal** vs concerning **behaviours**, emphasise a **parenting** **style** that recognises strengths of child/**positive** **reinforcement**/non-punitive punishment, importance of their behaviour model [psychoeducational] o **Child** interventions: **CBT**, social skills, problem-solving, **anger** **management**, **confidence** building o **Functional** **family** therapy o **Multi**-**systemic** therapy: family-based, including school and community ● **Social**: community/**school** interventions, **NGOs** ● **Differential**: **ADHD**, **adjustment** disorder, **autism** spectrum disorder, normal child but parents/teachers have unrealistic expectations, oppositional defiant disorder, **learning** **disability**, **PTSD**, **anxiety** disorder, depression, learning difficulty, **psychosis**, deviance
63
A child comes in with ADHD, what could have caused it?
- **parent** with **alcohol** dependence, - **antisocial**, - **ADHD**, - conduct disorder and **schizophrenia** - **sibling** with **disruptive** behaviour disorder
64
A child comes in with ADHD, what is the medical management?
**antipsychotics** to manage acute and chronic aggression, **stimulants** such as Methylphenidate [Concerta or **Ritalin**]
65
# Parent, child, family, multisystemic A child comes in with ADHD, what is the psychological management
o **Parent** management training: - education programmes – provide with info of normal vs concerning behaviours, - emphasise a parenting style that recognises strengths of child/positive reinforcement/non-punitive punishment, - importance of their behaviour model [psychoeducational] o **Child** interventions: - CBT, - social skills, - problem-solving, - anger management, - confidence building o Functional **family** therapy o **Multi**-**systemic** therapy: family-based, including school and community
66
A child comes in with ADHD, how can you help them through social management
community/school interventions, NGOs
67
A child comes in with ADHD, what differentials are you thinking about?
Differential: - **ADHD** - **adjustment** disorder - **autism** spectrum disorder, normal child but parents/teachers have unrealistic expectations, - oppositional defiant disorder, learning disability, - **PTSD** - **anxiety** disorder - **depression** - **learning** **difficulty** - **psychosis** - deviance
68
# antidepressant, anticholinergic, adrenergic, serotonin antagonism, antih Main: what are the side effects of TCAs?
● Serotonin/noradrenaline reuptake inhibition: **antidepressant** effects ● **Anticholinergic**: dry mouth, blurred vision, constipation, urinary retention, confusion/memory problems, palpitations/tachycardia ● **Adrenergic** antagonism: postural hypotension, sexual dysfunction ● **5-HT2 (serotonin) antagonism**: anxiolytic, reduced sexual function, sedation ● **Anti-histamine**: drowsiness and weight gain
69
Main: what is the presentation and management of delirium
● **Clinical** features: - impaired ability to direct/**sustain** and shift **attention**, - global **impairment** of **cognition** with disorientation and impairment of recent **memory** and **abstract** **thinking**, - **disturbance** in sleep-wake **cycle** with nocturnal worsening, - **psychomotor** **agitation**, - **emotional** **lability**, - **perceptual** **distortions**, - **speech** may be rambling or **incoherent** and **thought** **disordered**, - poorly developed **paranoid** **delusions**, - **rapid** onset with **fluctuations** in severity over minutes and hours ● **Hyperactive** delirium: **- psychomotor agitation, **- increased **arousal**, - **inappropriate** behaviour, - **delusions** and **hallucinations** ● **Hypoactive** delirium: **- psychomotor retardation, **- **lethargy**, - excess **somnolence** ● Management: o Identify and **treat** precipitating **cause**/exacerbating factors: - **DIMTOP**, (drugs, infrctions, metabolic, trauma, oxygen deficient, psychological) - optimise condition of patient with attention to **hydration**, - **nutrition**, - input and output and **pain** **control** ~ o Provide environmental and **supportive** measures: - **education** to those who interact with patient, - make environment **safe**, - create environment which **optimises** **stimulation** [adequate lighting, reduce noise, mobilise when possible and correct sensory impairment], - reality **orientation** techniques [clear communication, same staff members, clocks and calendars] ~ o Avoid **sedation** unless severely agitated or needed to minimise unnecessary risk - use single medication and start at low dose - Oral **haloperidol** 0.5-1mg daily, - oral **lorazepam** 0.5-1mg daily - oral **risperidone** 1-4mg daily. - Consider antipsychotics first as benzos tend to worsen delirium. - If caused by **alcohol** withdrawal, give **benzos** and thiamine ~ o Regular clinical review and **follow** **up**: - **MMSEs** useful for monitoring cognitive improvement at follow up
70
Main: what is the presentation and management of EtOH withdrawal?
Withdrawal Presentation: - **Autonomic** hyperreactivity (high BP and Temp) - Hand **tremor** - **Insomnia** - N&V - Transient **hallucinations** - **Anxiety** - **Psychomotor** **agitation** - GTCS **Management** of acute withdrawal: - **Minor** symptoms above can be treated **supportively** - Can use **benzos**, **phenobarbital** or **Propofol** in status epilepticus Timelines: - **Hallucinations**: at 12-48 hours, usually **visual** - Withdrawal seizures are usual GTCS occur 12-48 hours after last drink - **Delirium** tremens: hallucination, disorientation, tachycardia, hyperthermia, agitation - Sweating typically starts 48-96 hours after last drink **Supportive** care: i. **Benzos** for agitation (IV **diazepam** best) ii. IV **fluid** iii. **Nutritional** support iv. Monitor **vitals** v. **Quite** protective environment vi. **Thiamine** and glucose (**prevent** **Wernicke**’s) vii. **Multivitamins** including **folate** ● **Management**: o **Detoxification** - which involves psychological support, - medication to relieve symptoms, - nutritional supplementation, - observation. - Can be in-patient or in community with support o **Detox**: - decide setting, - assess need for benzos, - consider need for other meds, - verbal and written advice, - inform GP of plans, - give patient a contact in case of emergency, - explicit follow-up o **Outpatient**: - for uncomplicated - if doubts about compliance see daily and breathalyse o **In-patient:** - history of complicated withdrawals, - symptoms of delirium, - comorbid physical/mental illness, - Wernicke’s, - severe n+v, - lack of stable home o **Benzo** **regimen** ▪ Helps with unpleasant withdrawal symptoms and reduces risk of withdrawal seizures ▪ **Diazepam** for in-patient use: faster acting, allows dose titration, can be given parenterally ▪ **Indications**: clinical symptoms of withdrawal, consumption > 10units/day over previous 10 days ▪ Not needed if: <10 units, no history of withdrawal, BAC =0 and no symptoms **o Thiamine – prevent Wernicke’s**
71
Main: what are the presenting symptoms and management of panic disorder?
**Symptoms**: o **Autonomic arousal**: tremor, tachycardia, tachypnoea, hypertension, sweating, GI upset. o **Concerns of death** from cardiac or resp problems leading to patients repeatedly presenting. Fear of death/losing control. o **Unexplained medical symptoms:** chest pain, back pain, GI symptoms, headache, fatigue, multiple symptoms o **Suicidal** [or homicidal] ideation, impulsive acts Symptoms: Abrupt **surge** of **fear** with** at least 4** of these present: - **SOB** - Dizziness - Hot **flushes** or chills - **Feeling** of choking - Palpitations - **Nausea**/ abdo discomfort - **Sweating** - Shaking - **Derealization** - Paresthesias - **Fear of dying**/losing control At least **1 attack** has been **followed** by a minimum period of **persistent** **worry** bout further attacks or significant **maladaptive** **change** related to attack ● **Pharmacological**: o **SSRIs**: initially increasing panic symptoms, start with lowest possible dose and gradually increase, may take up to 12 weeks to have beneficial effect. Citalopram 20-30mg, Sertraline 50-200mg o Alternative antidepressants: **SNRIs** [Venlafaxine], **TCA** o **Benzodiazepines**: not really recommended as there is potential for abuse and dependence. Effective for severe, incapacitating symptoms and can be used for 1-2 weeks in combination with antidepressant until the antidepressant becomes ‘effective’ o If rx successful: **continue for 12-18 months **before **trial of discontinuation** with gradual tapering of dose over 2-4 months. Do not confuse withdrawal effects with re-emergence of symptoms **Pharm** 1ST LINE= SSRI (**FLUOXETINE**?) Can **combine with CBT** ● **Psychological**: o **CBT**: treat phobic **avoidance** by **exposure**, **use of relaxation** and **control of hyperventilation**, teach about bodily responses associated with anxiety o **Psychodynamic** **psychotherapy**: ‘**emotion**-**focused**’ treatment where typical **fears** are **explored** **Psychosocial**: **CBT** has been found to be the **best** psychotherapy choice for **panic disorder**. It assists the patient in countering their anxious beliefs, being exposed to fear cues, changing their anxiety-maintaining behaviour. Does require highly motivated patient. And can be **resource intensive.** Psychoeducation is also of use with CBT.
72
Main: Discuss what is meant by facticious disorder
● When patients intentionally falsify their symptoms and past history and fabricate signs of physical or mental disorder with the aim of obtaining medical attention and treatment ● Diagnostic features: intentional and conscious production of signs and falsification or exaggeration of history ● Types: o Wandering: males who move from hospital to hospital, job to job, producing dramatic and fantastic stories. May be aggressive personality or dissocial PD o Non-wandering: female, stable lifestyle and less dramatic, paramedical professions. Chronic somatisation disorder or borderline PD o By proxy: mothers/carers/paramedical/nursing, simulate or prolong illness in their dependents
73
Main: what are the reasons why a patient remains psychotic after 3 months of treatment?
- **Defaulting** medication [many reasons for non-adherence], - drug **interactions** [inducers], - **incorrect** **dose**/dose not high enough, - **serum** **concentrations** not high enough, - ongoing **substance** use, - treatment **resistance**, - emotional **stressors**, - **incorrect** diagnosis, - **medical** **disease** of liver/kidneys impairing metabolism
74
Main: what is meant by pseudo-dementia?
● A presentation of **severe depression **in the **elderly** where the combination of **psychomotor retardation**, apparent **cognitive deficits** and **functional decline** cause diagnostic **confusion with dementia** ● **Features**: - previous history of depression, - depressed mood, - exaggerated symptoms, - poor effort on testing, - responds to antidepressants
75
Main: Discuss side effects of 3 classes of antidepressant in terms of SE profile and therapeutic uses
**● TCAs indications: **- possibly moderate/severe depressive disorders - moderate/severe anxiety states - nocturnal enuresis in child > 11 - neuropathic pain - migraine prophylaxis ● **SSRIs**: - moderate to severe depression, - anxiety but risk of agitation, - bulimia nervosa, - OCD - label for panic disorder, - GAD and some personality disorders **● SNRIs **o Venlafaxine – moderate and major depressive and anxiety disorders o Side effects: Anorexia, nausea, constipation, diarrhoea, hypertension, palpitations, dizziness, insomnia, drowsiness, nervousness, sweating
76
Main: what are the side effects of sodium valproate?
● **Indications**: acute **bipolar mania**, **maintenance** therapy for **BPD**, **epilepsy**, migraine prophylaxis ● **Dose-related side effects**: - anorexia, - nausea, - dyspepsia, - vomiting, - diarrhoea, - raised LFTs, - tremor, - sedation, - alopecia, - ataxia ● **Unpredictable**: - mild leukopenia and thrombocytopenia - increased appetite - weight gain ● **Rare**: - irreversible liver failure, - pancreatitis, - agranulocytosis, - PCOS/hyperandrogenism ● **Teratogenic**: NTD [ensure contraception and folate]
77
Main: what are the indications for ECT?
● Treatment for **depression** particularly if there is **psychotic** symptoms - **failure** of **drug** therapies - patient **preference** - high risk of **suicide** - high risk of medical morbidity and mortality - **catatonia** associated **with SCZ**/MDD/BPMD - treatment **resistant** **mania** - required therapies **contraindicated** in **pregnancy** - **post-natal** depression/psychosis - life-threatening nutritional compromise - **NMS** - neuroleptic malignant syndrome
78
Main: what are the good and poor prognostic factors of schizophrenia? ## Footnote Schizophrenia
● **Good**: - **female**, - **rapid** onset of symptoms - **older** age of first episode - predominantly **positive** symptoms - presence of **mood** symptoms - good **pre-illness functioning** ● **Poor**: - **genetic** factors - **substance** use - pregnancy and birth complications such as hypoxia and greater paternal age, - other prenatal/**perinatal issues like stress**, **infection**, **malnutrition** and maternal **diabetes**
79
Main: What are the side effects of carbamazepine ## Footnote Mood disorder; Medication
● **Antidiuretic** effects leading to hyponatraemia [can develops many months after initiation], - **decrease** in **thyroxine** levels, - **agranulocytosis**, - aplastic **anaemia**, - **hepatic** failure, - exfoliative dermatitis [**SJS**], - **pancreatitis**
80
Main: What is the specific managment of a phobia of mice?
● **Behavioural**: **exposure** is the treatment of choice which aims to reduce fear response – **Wolpe**’s systematic desensitisation ● **Cognitive**: **education**/anxiety **management**, **coping** skills, cognitive restructuring ● **Pharmacological**: generally not used unless severe then use **benzos** to **reduce** **fear**/avoidance and allow patient to engage in exposure but this may reduce efficacy of behaviour ● **Other techniques**: reciprocal inhibition, flooding
81
Main: Compare Schizophrenia and delusional disorder
**Delusional** disorder // *Schizophrenia* Presence of **delusions** for at least **1 month**, **criterion A** for schizophrenia **never met **// *Criterion A: 2+ of, for significant amount of time during 1 month period: delusions, hallucinations, disorganised speech, disorganised behaviour* **Function** **not** **markedly** **impaired** // *Level of social functioning in one or more major areas is below level prior to onset* **Manic**/**depressive** episodes **brief** **compared** to **delusional** periods // *No major depressive or manic episodes have occurred concurrently with active phase symptoms and if they have occurred, they have been present for a minority of the total duration* **Not** **attributable** to physiological effect of substance/other **medical** condition // *Not attributable to physiological effect of substance/other medical condition*
82
Main: What forms do you fill in for involuntary admissions?
● MHCA form **1** – **emergency** 24-hour admission ● Form **3** – **discharge** form ● Form **4** – application for **involuntary** admission filled in by **family** ● Form **5 x 2** – assessment by **2 physicians** ● Form **6** – **72-hour assessment** ● Form **7** – **admission**, filled in by **med manager** ● Form **8** – approval of **further** **involuntary** care ● Form **11** – **transfer** approval by med manager ● Form **15** – **patient** fills in when they **want to leave** How to do an involuntary admission. ● Fill in a **form 04**: an application in the head of the health establishment for the assessment of a user. Specify that it is as an involuntary patient. - Needs to be** filled out by**: **Someone** who **knows patient** well/sees daily, An associate, MHC practitioner if no one else (would have to specify why it is them filling it in, what efforts were made to find someone, and why you think they need to be admitted) - Everyone must be over 18! ● **Form 04** then needs to be **commissioned** ● Once this is filled in, the patient needs to present within 2 days of the form being filled out. ● **Next**, two separate doctors/MHC practitioners need to do **independent** **assessments** of the patient. At least one must be a doctor. ● They both fill out a **form 05**, which is a continued application to say that they believe the patient needs **further 72** hour assessment. ● If their **assessments** **agree**, a **form 07** is filled in, which is an application to the head of the health establishment to **detail the patient **for 72 hours** for further care** as a designated facility approved for this. When this is **signed by the head of establishment,** is when the 72 hours start. - During the **72 hours**, patient needs to be **seen daily **by a medical doctor and continuous notes must be made. ● **After** that time, **two form 06s** can be filled out (by two independent **MHC practitioners**, as least one is a doctor). ● **After** 72 hour assessment, **all forms submitted **to MHC **review board** who must **fill in a form 13** to say that the hospital has grounds to keep the patient in hospital. ● If the head of **head establishment** believes that the patient needs **further inpatient care after 72 hours,** (s)he fills in a **form 08.** ~ ● If need to be admitted as **emergency** patient: **form 01**. ● If **transferring** patient: **form 11.**
83
Main: What are the symptoms of atypical depression?
● Mood is depressed but remains reactive, hypersomnia, hyperphagia, leaden paralysis [heaviness in limbs], over-sensitivity to perceived rejection
84
Main: Define treatment resistant schizophrenia and treatment thereof
● Failure to respond to two or more antipsychotic medications given in therapeutic doses for 6 weeks or more ● Mx: o Clarify diagnosis: re-inspect to ensure correct diagnosis o Address comorbidity: substance use is common and worsens outcome o Non-compliance: psychoeducation, compliance therapy, family therapy o Pharmacological: Clozapine depot injection o Clozapine resistance: switching to untried 2nd gen or augmentation with benzamides and anti-epileptics o Rehab: maximise function/QoL and support those who remain symptomatic
85
Main: What is the management of a patient with social phobia?
● **Bio**: SSRI or SNRI as first line, - requires 4-6 weeks to work, - max effect at 12 weeks, - dose response effect, - may be prescribed on an as needed basis for performance only SAD ● **Psycho**: CBT group or individual, - maintenance sessions, - gradual desensitisation, - stress management and relaxation techniques ● **Social**: family psychoeducation, - assess how it affects job/relationships/family
86
Main: What are the Key clinical features needed to diagnose dementia
● Impairment in memory and one or more cognitive deficits, - cognitive decline from previous performance level, - interferes with independence of activities, - not exclusively in delirium setting, - not better explained by another illness ● Slow, - insidious onset with progressive course, - memory impairment, - normal attention and alertness, - usually intact orientation
87
Main: What is somatoform disorders?
● **Repeated** **presentation** with medically **unexplained** symptoms affecting **multiple** organ **systems**, first presenting before the age of 40 ● Non-specific and atypical symptoms ● Chronic ● Significant physiological distress and functional impairment and are at risk of iatrogenic harm
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Main: A child stabbed someone, probable diagnosis and management
● Probable diagnosis: oppositional **defiant** disorder, **conduct** disorder Management: ● **Antipsychotics**: **Risperidone** is the best one to use, treats acute and chronic aggression **● Same management principle as the ADHD question?