Psychiatry Flashcards

1
Q

What is Autism Spectrum Disorder?

A

A neuro-developmental disorder characterised by abnormal social interaction, communication and restricted, repetitive behaviours. ASD is four times more prevalent in boys than girls.

Risk increased if a sibling has ASD and increases chance of having ADHD and/or learning difficulties

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2
Q

What is the aetiology of ASD?

A

Not completely understood but it is believed there are genetic factors due to risk increased in twins and siblings. Commonly associated with some genetic syndromes e.g. fragile X, tuberous sclerosis, Down’s etc

Others: increased maternal age, prenatal infections, obstetric complications, exposure to toxins or teratogens

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3
Q

What are the clinical features of ASD?

A

Presentation is highly variable

  1. Social:
    Lack of response to other people’s emotions
    Unable to interpret social cues
    Inability to form social attachments
  2. Communication:
    Usually delayed or minimal expressive speech
    Impairment in make-believe or fantasy play
    Lack of social gestures
    Conversational skills tend to be one-way (monologues, endless questions etc…)
  3. Repetitive Restrictive Behaviours & Interests:
    Resist change with a rigid daily routine
    Preoccupations with specific interests like dates or timetables
    Inability to adapt to new environments
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4
Q

How is ASD diagnosed?

A

Full developmental history
Screening tools - MCHAT, CARS, CAST etc
Diagnostic tools - ADI-R, DISCO, ADOS, etc

For a formal diagnosis, must impair daily function and be present in the early developmental period and can’t be better better explained by learning disability or global developmental delay.

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5
Q

What other Ix may be needed when a diagnosis of ASD is made?

A

Genetic testing
Metabolic testing
Neuroimaging (e.g. MRI brain)
Electroencephalogram

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6
Q

How is ASD managed?

A

Very individualised to achieve as much functional independence as possible and improve the quality of life for the patient.

  • Early diagnosis + special educational programmes
  • Occupational therapy
  • Speech therapy
  • Clinical psychology
  • Sleep hygiene
  • Family support
  • Medications should not be used routinely to treat the core features of ASD. They may be used to treat concurrent medical or psychiatric co-morbidities but in conjunction with behavioural interventions
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7
Q

What is ADHD?

A

A neurodevelopmental condition characterised by an abnormally high activity level and an inability to concentrate.

More common in boys, usually presents before 7 but can be diagnosed at any age in 2 or more important settings

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8
Q

What are the RF for ADHD?

A

FHx
Prematurity
Low birth weight
Low paternal education
Prenatal smoking
Maternal depression
Maternal nicotine+alcohol
Psychosocial adversity

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9
Q

What are the clinical features of ADHD?

A

Inattention, Hyperactivity and Impulsivity having an adverse effect on QoL in 2 or more settings
e.g. short attention span, quickly losing interest in tasks, constantly fidgeting or unable to sit still, impulsive behaviour, described as disruptive, poor organisational skills, acting without thinking

Many patients will have co-morbidities like learning difficulties, dyspraxia, Tourette’s, mood disorders, anxiety etc

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10
Q

How is ADHD diagnosed?

A

Clinical diagnosis - Can use “strengths and difficulties questionnaire” or the “Conners’ rating scale”. In adults, assessment can be aided by the Diagnostic Interview for ADHD in Adults (DIVA) questionnaire. Can also use DSM-5 criteria (under 16= 6 or more in each, 17+= 5 or more in each. Categories = inattention + hyperactivity & impulsivity)

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11
Q

How is ADHD managed?

A

10 week watch and wait, if symptoms persist then refer
Management will depend on age and severity
1. Parent ADHD support programme
2. Methylphenidate + CBT

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12
Q

What are the RF for GAD?

A

Female sex
Family history
Childhood abuse and neglect
Environmental stress (e.g. redundancy, divorce)
Emotional trauma
Substance abuse

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13
Q

What is the DSM-V criteria for GAD?

A
  • Excessive anxiety and worrying (more days than not for six months or longer)
  • The worry and anxiety is difficult to control
  • Three of the following have been present (more days than not for six months):
    Restlessness
    Easily fatigued
    Sleep disturbance
    Irritability
    Muscle tension
    Trouble concentrating

In addition, the following must be present:
Symptoms cause significant distress and impair normal function
Symptoms or episode not caused by another condition of substance
Episode not better explained by other mental health illnesses

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14
Q

What are the differentials for anxiety?

A

Social phobia
Panic disorder
Obsessive-compulsive disorder
Post-traumatic stress disorder
Acute stress disorder
Thyroid/endocrine
AF
Pheochromocytoma
Alcohol and drugs

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15
Q

What tool is used to assess the severity of GAD?

A

GAD-7 is a self-reported questionnaire that can act as a screening tool and measure of severity for GAD.

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16
Q

What are the processes thought to drive the spiral of anxiety?

A

Avoidance, anxious rumination and attentional + cognitive biases are all linked to evolution
Low self worth and poor sleep also feed into it.

Avoidance - perpetuates anxiety because it makes it hard to unlearn your fear of stimulus
Ruminations - Keep thinking through catastrophic outcomes so may propogate anxiety
Attentional and cognitive bias - primes you to pay attention to threats which is useful in flight or fight but not in situations where you can’t escape your fear e.g. school

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17
Q

What is GAD?

A

Persistent “free-floating” anxiety (not restricted to/predominant in any specific circumstances), or excessive worry focused on multiple everyday events.

Common features of generalised anxiety disorder include:
Subjective experience of nervousness
Difficulty maintaining concentration
Muscular tension or motor restlessness
Sympathetic autonomic over-activity
Irritability
Sleep disturbance.

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18
Q

What are phobic anxiety disorders?

A

Abnormal state anxiety evoked only/predominantly by a specific external situation/object which is not currently dangerous. The key feature is the avoidance of that situation.

Types of phobic anxiety disorders include:
Agoraphobia (crowds, public places, leaving home ♀>♂)
Social phobia (associated with low self-esteem and fear of criticism. ♂=♀)
Specific phobias (e.g. claustrophobia, animal phobias, etc.)

Characteristic features include:
Anticipatory anxiety (about exposure to precipitant, and about anxiety itself)
Somatic symptoms (e.g. palpitations, sweating, trembling, dyspnoea, chest pain, dizziness, chills, hot flushes)

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19
Q

What is panic disorder?

A

Recurrent unpredictable episodes of severe acute anxiety, which are not restricted to particular stimuli or situations.

Characteristic features include:
A crescendo of anxiety, usually resulting in exit from the situation
Somatic symptoms (e.g. palpitations, sweating, trembling, dyspnoea, chest pain, dizziness, chills, hot flushes)
Secondary fear of dying/losing control (often related to the somatic symptoms)

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20
Q

How is GAD managed?

A
  1. Psychoeducation, sleep hygiene, and self-guided cognitive-based therapy (CBT)/ relaxation techniques.
  2. CBT - may use exposure therapy and applied relaxation.
  3. Pharmacological (equal 1st line with CBT). SSRI, SNRI or atypical antidepressant depending on side-effect profile.

Also, Busipirone (5HT1A agonist) is suitable for short term management (Delayed onset of action, diminished efficacy in previous benzo users, SE = dizziness, headache and nausea, minimal sedation)
B-blockers effective in patients with somatic anxiety symptoms
Low-dose antipsychotics or Pregabalin may also be of use

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21
Q

Which drug should be avoided in chronic anxiety?

A

Avoid benzodiazepines (e.g. diazepam) for chronic anxiety. because they have such an immediate effect, this group of drugs is highly addictive. Tolerance develops rapidly, so after a month or two of benzodiazepines, your patient will be back to the same level of anxiety but also addicted to benzodiazepines.

They can be used for transient causes of anxiety (ie. fear of flying) or in crisis only, maximum of 2 weeks prescription advised.

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22
Q

What is depression?

A

Depression is a mood (affective) disorder characterised by persistent low mood, low energy and loss of interest/enjoyment in everyday activities (anhedonia). It can be unipolar (first occurrence or recurrent) or bipolar (with occurrences of mania and depression).

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23
Q

What are the RF for depression?

A

Chronic conditions
History of depression or other mental health illness
FHx
Substance misuse
Female sex
Medication (e.g. corticosteroids)
Older age
Recent childbirth
Psychosocial issues (e.g. unemployment, homelessness)
Separated/Divorced
Grief
History of childhood abuse
History of head trauma

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24
Q

What is the DSM-V criteria for depression?

A

defined by DSM-V as the presence of five of the following symptoms, for at least two weeks, one of which should be low mood or loss of interest/pleasure:

Low mood
Loss of interest or pleasure
Significant weight change
Insomnia or hypersomnia (sleep disturbance)
Psychomotor agitation or retardation
Fatigue
Feelings of worthlessness
Diminished concentration
Recurrent thoughts of death or suicide

In addition, the following must be present:

Symptoms cause significant distress and impair normal function
Symptoms or episode not caused by another condition of substance
Episode no better explained by other mental health illnesses
No episodes of mania or hypomania

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25
Q

What are the 3 core symptoms of depression?

A

Low mood
Anhedonia: low interest or pleasure in most activities of the day
Lack of energy (anergia)

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26
Q

What are the other symptoms of depression other than the core 3?

A

Weight change: exclusion of intentional dieting
Disturbed sleep: insomnia or hypersomnia
Psychomotor retardation (slowed down actions) or psychomotor agitation (increased restlessness)
Reduced libido
Worthlessness or guilt feelings
Decreased concentration
Recurring thoughts of harm, death or suicide: nihilistic thoughts

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27
Q

What are the somatic symptoms of depression?

A

Anhedonia
Loss of emotional reactivity
Diurnal mood changes: mood often worse in the morning
Early morning wakening: typically 2-3 hours earlier than usual
Psychomotor retardation or psychomotor agitation
Appetite loss
Weight loss

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28
Q

What are the psychotic symptoms of depression?

A

if present, these are usually mood-congruent and may include:

Delusions: often revolving around guilt and personal inadequacy
Hallucinations: can be auditory, olfactory or visual

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29
Q

What are DDx for depression?

A

Substance/medication use
Bipolar affective disorder
Premenstrual dysphoric disorder
Bereavement
Anxiety disorders
Alcohol-use disorder
Physical health illness or organic illness differentials include:
- Hypothyroidism
- Cushing’s disease or syndrome
- Vitamin B12 deficiency

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30
Q

What are the Ix for depression?

A

Screening tool = PHQ-9
Risk assessment to self, others and from others

Exclude organic causes if indicated:
- Full blood count: anaemia
- Thyroid function test: hypothyroidism (elevated thyroid stimulating hormone)
- Vitamin B12: vitamin b12 deficiency
- Imaging and other investigations (e.g. a CT head) may be performed in patients with atypical features and signs indicative of an organic pathology

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31
Q

What is the short term management for mild depression?

A

First-line management should involve initiating primarily low-intensity psychosocial interventions.

Antidepressants should not be routinely offered unless that is the patient’s preference. Exceptional cases to consider starting on biological therapy (i.e. antidepressants) include:
Past history of moderate or severe depression
Presence of mild depression that has been present for at least 2 years
Presence of mild depressive symptoms after other interventions

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32
Q

What is the long term management of mild depression?

A

Risk assessment
Ongoing review: response to low-intensity psychosocial intervention, compliance and symptoms. An SSRI antidepressant should provide benefit within 4-6 weeks.
Measurement scales to assess response to treatment and quality of life
Relapse prevention plan
Assess for social support, and review previous issues flagged up during consultations
If taking antidepressant therapy review compliance, side effects and adjust doses if appropriate

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33
Q

What is the short term management of moderate or severe depression?

A

may include a combination of antidepressant therapy (biological treatment) and high-intensity psychosocial interventions.

Combination of individual CBT and an antidepressant (e.g. SSRI)
Individual CBT
Individual behavioural activation
Antidepressants (e.g. SSRI) alone
Individual problem-solving
Counselling
Short-term psychodynamic psychotherapy
Interpersonal psychotherapy
Guided self-help
Group exercise

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34
Q

In severe depression what additional treatments may be considered?

A

If presenting with psychotic symptoms, then treatment should be augmented with an antipsychotic (quetiapine or olanzapine).

Electroconvulsive therapy (ECT) should be considered in severe cases of depression where:

The patient has a strong preference for ECT: this usually applies when patients have responded to ECT well before
Rapid treatment of the patient is needed: cases of life-threatening depression where the patient is not eating or drinking
Multiple other treatments have been trialled unsuccessfully

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35
Q

Generally which antidepressant medications are offered as first line?

A

SSRIs like citalopram will be offered first line. Sertraline may be used in co-morbid patients as it has fewer drug-drug interactions

Fluoxetine is first line in kids

General rule is that antidepressants should be continued for 6 months minimum unless there are adverse effects. When stopping, they need to be tapered off.

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36
Q

Which medications need to be avoided in patients with high suicide risk or a history of overdose?

A

avoid certain antidepressants in patients with suicide risk or a history of overdose (e.g. tricyclics, venlafaxine).

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37
Q

What is bipolar disorder?

A

Bipolar disorder is a cyclical mood disorder that fluctuates between episodes of mania/hypomania and depression.

Bimodal incidence, peaks from 15-24 and 45-54. Same incidence in men and women. Likely to be comorbid with other mental health issues and increases risk of physical conditions such as CV disease.

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38
Q

What are the etiological factors of bipolar?

A

Genetic - Having a 1st degree relative with bipolar increases your risk of depression, bipolar and schizoaffective disorders. Heritability is around 60% in monozygotic twins and around 20% in dizygotic twins.

Environmental - nothing specific just the same predisposers of all mental health conditions. Negative life events can trigger an episode in someone with bipolar.

Neurobiological - Increased dopaminergic signalling, disturbance of the HPA axis leading to higher cortisol and corticosteroid use all linked to mania

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39
Q

What are some risk factors for bipolar?

A

Genetic factors
Prenatal exposure to Toxoplasma gondii (the parasite that causes toxoplasmosis)
Premature birth <32 weeks gestation
Childhood maltreatment
Postpartum period
Cannabis use

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40
Q

What are bipolar I and II?

A

In bipolar I, the person has experienced at least one episode of mania
In bipolar II, the person has experienced at least one episode of hypomania, but never an episode of mania. They must have also experienced at least one episode of major depression.

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41
Q

What are the clinical features of mania?

A

Elevated mood
Increased energy resulting in overactivity, pressure of speech, and a decreased need for sleep
Inability to maintain attention, often with marked distractibility
Self-esteem which is often inflated with grandiosity and increased confidence
Loss of normal social inhibitions
Mood congruent psychotic symptoms

The manic episode should last for at least seven days and have a significant negative functional effect on work and social activities

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42
Q

What are the clinical features of hypomania?

A

Persistent, mild elevation of mood
Increased energy and activity, usually with marked feelings of wellbeing
Increased sociability, talkativeness, over-familiarly, increased sexual energy and a decreased need for sleep
Irritability may be present
Absence of psychotic features

Should last for at least 4 days

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43
Q

What is cyclothmyia?

A

Refers to chronic mood disturbance with depression and hypomania symptoms that do not meet the criteria for a full episode

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44
Q

What are the DDx for bipolar?

A
  • Mental health disorders: schizophrenia, unipolar depression, personality disorder or anxiety disorder.
  • Substance misuse: cocaine, ecstasy or amphetamines
  • ‘Organic’ causes: thyroid disorder, multiple sclerosis, Cushing’s, Addison’s, cerebrovascular disease, dementia, epilepsy, SLE, encephalitis.
  • Iatrogenic causes: antidepressants, corticosteroids, levodopa or dopamine agonists.
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45
Q

What is the acute management for mania?

A

Trial of oral antipsychotics:
Haloperidol
Olanzapine
Quetiapine
Risperidone

If on antidepressant medication, this should be tapered off and discontinued.

Benzodiazepines may be used as an adjunct to manage symptoms of increased activity and allow for better sleep.

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46
Q

What is the management of depression in bipolar?

A

Antidepressants can induce mania or rapid cycling so different to the manangement in unipolar derpression.

Fluoxetine + olanzapine
Quetiapine alone
Olanzapine alone
Lamotrigine alone

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47
Q

After an acute episode of bipolar has passed, what is the long term management?

A

Mood stabilising medication such as lithium. If lithium is not effective, sodium valproate may be added but this is highly teratogenic.

Structured psychotherapy is also important.

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48
Q

What is OCD?

A

Obsessive compulsive disorder is characterised by the presence of obsessions and/or compulsions.

Obsessions: intrusive thoughts, urges and images that cause anxiety and distress.
Compulsions: repetitive behaviours that one feels compelled to perform, these may be observable or occur in the mind (e.g. repeating a phrase).

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49
Q

How can OCD present?

A
  • intrusive unwanted anxiogenic thoughts
  • patients typically recognise these are irrational thoughts
  • repetitive behavioural or mental acts to neutralise anxiety caused by obsessions
  • compulsions give brief relief and are self-enforcing
  • higher frequency of compulsions related to treatment resistance
  • concomitant schizotypal personality disorder and Tic disorder related to worse outcomes
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50
Q

Which disorders are related to OCD?

A

Body dysmorphic disorder (BDD)
Body-focused repetitive behaviour disorders (ie. trichotillomania, dermatillomania)
Hypochondriasis (health anxiety disorder)
Hoarding disorder

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51
Q

What questions can you ask when diagnosing someone with OCD?

A

Do you wash or clean a lot?
Do you check things a lot?
Is there any thought that keeps bothering you that you would like to get rid of, but cannot?
Do your daily activities take a long time to finish? Interference of over an hour a day
Are you concerned about putting things in a special order, or are you upset by mess?
Do these problems trouble you?

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52
Q

How is OCD managed?

A

Do risk assessment and screen for other MHx

Mild - refer for low-intensity CBT with Exposure and Response Prevention (ERP) is commonly offered.

Moderate - offer intensive CBT with ERP or an SSRI. Clomipramine may be used as second-line therapy.

Severe - refer for specialist input. Consider an SSRI (e.g escitalopram) combined with CBT in the interim. Clomipramine may be used as second-line therapy.

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53
Q

What is the most commonly used measure of OCD?

A

Yale Brown Obsessive Compulsive Scale
Should be used on patients about to start treatment for OCD and then every 6 months after that to track

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54
Q

What is PTSD?

A

A disorder that may develop following exposure to a stressful event or a situation of exceptionally threatening or catastrophic nature. It is thought to result from impaired memory consolidation of experiences too traumatic to be processed normally, which leads to a chronic hyperarousal of fear circuits.

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55
Q

What are RF for developing PTSD?

A

Traumatic events, DV, bullying, natural disaster, torture, terrorism, combat, traumatic brain injury, sudden death of loved one, sexual assault, multiple major stressors, lack of social support, history of substance abuse or mental health disorders

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56
Q

How does PTSD present?

A

HARD:
- Hyperarousal: persistently heightened perception of current threat (may include enhanced startle reaction)
- Avoidance of situations/activities reminiscent of the events, or of thoughts/memories of the events
- Re-experiencing the traumatic events (vivid intrusive memories, flashbacks, or nightmares).
- Distress: strong/overwhelming fear and physical sensations when re-experiencing

Also, impaired memory of event, anhedonia, detachment from others, irritable/outbursts, reckless behaviour, exaggerated startle response, depression and anxiety, substance misuse

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57
Q

What differentiates PTSD from an acute stress reaction?

A

ASR is usually less than a month after an event

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58
Q

How is PTSD diagnosed?

A

PTSD checklist DSM-V, there are military, civillian or specific ones

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59
Q

How is PTSD managed?

A

Mild/moderate = ACS active monitoring

Severe =
1) Trauma-focused CBT OR Eye-Movement Desensitization and Reprocessing (EMDR) therapy with SSRI OR venlafaxine (possible adjunctive antipsychotic)

Plus psychoeducation/sleep hygiene/ relaxation etc. as above.

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60
Q

What is personality disorder?

A

Personality disorder (PD) is an umbrella term that covers a number of variations of maladaptive personality traits that are lifelong, persistent, deeply ingrained maladaptive behaviours that characterises an individual, deviate markedly from culturally expected or accepted ‘normal’ range and have an onset in late childhood or early adolescence

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61
Q

What are the subtypes of personality disorders?

A

Cluster A - Odd/Eccentric
Cluster B - Dramatic/Emotional
Cluster C - Fearful/Anxious

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62
Q

Which personality disorders are in Class A?

A

Odd and Eccentric
- Paranoid
- Schizoid
- Schizotypal

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63
Q

How does paranoid personality disorder present?

A

Suspicious of others
Unforgiving
Spouse Infidelity
Perceives attack
Envious
Cold affect/Criticism poorly taken
Trust in others reduced

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64
Q

How does schizoid personality disorder present?

A

Characterised by a lack of interest in others, apathy and a lack emotional breadth.
They tend to have few friends and do not form relationships, preferring solitary activities.
Flattened affect, indifferent, low sex drive, little pleasure taken in activities

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65
Q

How does schizotypal PD present?

A

Characterised by a pattern of extreme difficulty interacting socially, bizarre or magical thinking and distorted perceptions.
Inappropriate behaviour and strange speech and affect can cause others to perceive them as strange.
They share some features with schizophrenics, but maintain a better grasp on reality.

66
Q

What are the subtypes of Class B personality disorders?

A

Dramatic/Emotional
- Antisocial
- Borderline
- Histrionic
- Narcissistic

67
Q

How does antisocial PD present?

A

Characterised by a patterns of disregard and violation of the rights of other’s. Individuals lack empathy and are often manipulative and impulsive.
Aggressive and unremorseful
Consistently irresponsible with failure to obey laws and social norms

68
Q

How does borderline personality disorder present?

A

Pattern of abrupt mood swings, unstable and intense relationships and instability in self-image
Self harm is common, recurrent suicidal feelings
Relationships alternate between idealization and devaluation (splitting)
Inability to control temper and general affect
Chronic feeling of emptiness

69
Q

How does histrionic PD present?

A

Characterised by provocative/attention seeking behaviours and excessive displays of emotions
Often sexually inappropriate
Vain/Shallow and self-dramatising
Relationships are considered to be more intimate than they really are
Easily influenced

70
Q

How does narcissistic PD present?

A

Involves a pattern of grandiosity, need for admiration of others and a lack of empathy
Has a sense of entitlement and will take advantages of others to achieve their own wants
Arrogant and preoccupied by their own fantasies and desires

71
Q

How does avoidant PD present?

A

Involves strong feelings of inadequacy and fear of social situations where they may be criticised
Patients are extremely sensitive to criticism
Often self impose isolation while craving acceptance and social contact

72
Q

How does dependent PD present?

A

Characterised by an intense psychological need to be cared for by others
Lack initiative and need others to make decisions on their behalf
Urgently search for new relationships as soon as one ends to provide care and support

73
Q

What is obsessive compulsive PD?

A

A personality disorder in which the individual is occupied with control, it is NOT associated with recurrent, intrusive thoughts unlike the classical “OCD”
Signs include: strict cleaniness, perfectionism
It is often at the detriment of social/leisure activities
Symptoms are often persistent and without distress

74
Q

How is personality disorder diagnosed?

A

Has to be over 18
Standardised Assessment of Personality Abbreviated Scale (SAPAS)
Millon Clinical Multiaxial Inventory III - MCMI-III
Suicide Risk
MRI/CT, urine and bloods

  • Pattern manifests in 2 or more areas:
    Cognition, Affectivity, Interpersonal Functioning, Impulse Control
  • The enduring pattern is inflexible and pervasive across a broad range of personal/social situations AND causes significant distress or impairment in social, occupational or other important areas of functioning
75
Q

How are personality disorders managed?

A
  • Cognitive behavioural therapy (CBT) and psychoeducation is the key management option of choice.
  • Dialectical behaviour therapy for EUPD
  • Psychodynamic psychotherapy
  • Supportive care can be provided during crises to help keep the patient safe.
  • There are no medical treatments recommended for personality disorders
76
Q

What screening questionnaire is often used for eating disorders?

A

S – Do you make yourself SICK because you feel uncomfortably full?
C – Do you worry you have lost CONTROL over how much you eat
O – Have you recently lost more than ONE STONE (6kgs) in a three month period
F – Do you believe yourself to be FAT when other say you are thin?
F – Would you say FOOD dominates your life?

77
Q

What is anorexia nervosa?

A

Anorexia Nervosa is a disorder characterised by deliberate weight loss, induced and sustained by the patient. There must be clear concerns from the individual regarding their weight and shape, with a fear of becoming fat as an intrusive overvalued idea. Patients may have weight or calorie goals in mind and are often determined to achieve this no matter what, and regardless of the impact on their physical health.

78
Q

What are the RF for anorexia nervosa?

A

Female gender
Age (most commonly affects adolescents and young people)
Family history of eating disorders, depression, or substance abuse
Previous criticism of eating habits and weight
Increased pressures to be slim (e.g. ballet dancers, models, athletes)
History of sexual abuse
Low self-esteem
Obsessive personality
Emotionally unstable personality disorder

79
Q

What are the clinical features of anorexia nervosa?

A

Excessive weight loss
Amenorrhoea
Lanugo hair is fine, soft hair across most of the body
Hypokalaemia
Hypotension
Hypothermia
Changes in mood, anxiety and depression
Solitude
Cardiac complications include arrhythmia, cardiac atrophy and sudden cardiac death.

80
Q

What are the typical biochemistry results for anorexia patients?

A

Hypokalaemia
Low sex hormone levels (FSH, LH, oestrogen and testosterone)
Raised growth hormone and cortisol levels
Hypercholesterolaemia

81
Q

What assessments are used to assess patients with eating disorders?

A

MEEDs- Medical Emergencies in Eating Disorders
MARSIPAN is outdated

82
Q

What ECG changes should you look for in a patient with anorexia nervosa?

A

reduce energy expenditure with minimal calorie intake, bradycardia and hypotension are commonly seen, as well as a prolonged QT interval. A prolonged QT interval increases the risk of a fatal arrhythmia such as Ventricular Fibrillation.

83
Q

What are the DSM 5 criteria for anorexia nervosa?

A

Restriction of energy intake relative to requirements leading to a significantly low weight in the context of age, sex, developmental trajectory, and physical health

Intense fear of gaining weight or persistent behaviour that interferes with weight gain, even though at a significantly low weight

Disturbance in the way in which one’s body weight or shape is experienced, undue influence of bodyweight or shape in self-evaluation, or persistent lack of the recognition of the seriousness of the current body weight.

84
Q

How would you classify BMI in anorexia nervosa according to DSM V?

A

Mild: BMI ≥17 kg/m²
Moderate: BMI 16-16.99 kg/m²
Severe: BMI 15-15.99 kg/m²
Extreme: BMI <15 kg/m².

85
Q

What investigations would you order in a patient with AN?

A

FBC - shows neutropenia before anaemia
U+E - metabolic changes
TFT - Thyroxine abuse
ESR - Exclude infection
Hormones

86
Q

What are indications for inpatient treatment for AN?

A

Rapid weight loss, failure of outpatient treatment, marked change in mental status, psychosis, hight risk of suicide or serious physiological change such as:
T<36
BPM<40
Hypotension
Raised LFTs

87
Q

How is AN managed?

A

Encourage weight gain
Psychoeducation and therapy:
SSCM, MANTRA or CBT-E

88
Q

What is bulimia nervosa?

A
  • Eating must be in a discrete period of time and must be of an amount of food that is definitely larger than most people would eat during a similar period of time and under similar circumstances.
  • There must be a sense of lack of control over the eating during the episode.
  • There is recurrent inappropriate compensatory behaviour to prevent weight gain, such as self-induced vomiting; misuse of laxatives, diuretics, enemas, or other medications; fasting; excessive exercise.
  • The binge eating and inappropriate compensatory behaviours both occur, on average, at least once a week for 3 months.
  • Self-evaluation is unduly influenced by body shape and weight.
  • The disturbance does not occur exclusively during episodes of anorexia nervosa.
89
Q

What are the clinical features for bulimia nervosa?

A

Alkalosis, due to vomiting hydrochloric acid from the stomach
Hypokalaemia
Erosion of teeth
Swollen salivary glands
Mouth ulcers
Gastro-oesophageal reflux and irritation
Calluses on the knuckles where they have been scraped across the teeth. This is called Russell’s sign.

90
Q

What investigations would you order for a patient with bulimia?

A

Same as AN
ECG - look for tall P, flat T - hypoK

91
Q

How is Bulimia managed?

A

CBT + Fluoxetine, interpersonal psychotherapy, family therapy if under 18

92
Q

What is binge eating disorder?

A

Binge eating disorder is characterised by episodes where the person excessively overeats, often as an expression of underlying psychological distress. This is not a restrictive condition like anorexia or bulimia, and patients are likely to be overweight.

Binges may involve:
- A planned binge involving “binge foods”
- Eating very quickly
- Unrelated to whether they are hungry or not
- Becoming uncomfortably full
- Eating in a “dazed state”

93
Q

What is refeeding syndrome?

A

Refeeding syndrome occurs in people that have been in a severe nutritional deficit for an extended period, when they start to eat again. Patients are at higher risk if they have a BMI below 20 and have had little to eat for the past 5 days. The lower the BMI and the longer the period of malnutrition, the higher the risk.

As the starved cells start to process glucose, protein and fats again they use up magnesium, potassium and phosphorus. This shift in nutrients from extracellular to intracellular causes Hypomagnesaemia, Hypokalaemia,
Hypophosphataemia

These patients are also at risk of cardiac arrhythmias, heart failure and fluid overload.

94
Q

How is refeeding syndrome managed?

A
  • Slowly reintroducing food with restricted calories
  • Magnesium, potassium, phosphate and glucose monitoring along with other routine bloods
  • Fluid balance monitoring
  • ECG monitoring
  • Supplementation with electrolytes and vitamins, particularly B vitamins and thiamine
95
Q

What is delirium?

A

Delirium refers to an acute confusional state that causes disturbed consciousness, attention, cognition & perception.

Delirium is characterised by:
- Acute onset (hour to days)
- Fluctuating symptoms (alters throughout the day)
- Disturbance in awareness and attention (reduced awareness, distractible)
- Disturbance in cognition (e.g. memory, language, disorientation)
- Evidence of an organic cause (e.g. medical condition, medication, intoxication)

96
Q

How is delirium classified?

A

Hyperactive delirium: characterised by inappropriate behaviour, agitation or hallucinations. Wandering and restlessness are common

Hypoactive delirium: characterised by reduced activity. Patients may appear quiet, lethargic, withdrawn and have reduced concentration

Mixed delirium: characterised by the presence of both hypoactive and hyperactive features

97
Q

What does PINCH ME stand for in delirium?

A

Pain, Infection, Nutrition, Constipation, Hydration, Medication, Environment

98
Q

How does delirium present?

A
  • Abnormal consciousness: Reduced level of awareness and focus, drowsy or semicomatose, hyperactive
  • Abnormal cognition: Memory loss, disorientation (e.g. to place, person or time), poor language (e.g. loss ability to speak a second language), poor speech
  • Abnormal thinking: Distractible and inattention (e.g. unable to follow commands), disorganised thinking (e.g. poor flow of ideas, disorganised speech, unable to express their needs)
  • Abnormal perception: Visual or auditory hallucinations, paranoid delusions, misperception
  • Other features: Labile changes in mood (e.g. irritable, paranoid, fear, depression), agitation, sleep-cycle disturbances, hypersensitive (light/sound)
99
Q

What can be used to do a cognitive assessment in a delirious patient?

A

Confusion Assessment Method (CAM)
The 4A’s test (4AT)
Abbreviated mental test (AMT)

100
Q

What are the differences between dementia and delirium?

A

Features supportive of dementia: changes are slowly progressive with limited fluctuation. Attention is usually in tact and very early memories may be preserved (i.e. short term memory more affected).

Features supportive of delirium: changes are acute, transient and usually reversible. There is often an associated acute illness.

101
Q

What investigations would you order to investigate delirium?

A
  • Bedside: Observations, ECG, Cultures: sputum, urine, stool, Capillary blood glucose
  • Bloods: FBC, U+E, LFT, Bone profile, Ca2+, HbA1c, B12, Folate, TFT, CRP, ESR, Drugs, Syphilis
  • Imaging: CXR, CT head, Echo
102
Q

How is delirium managed?

A
  • Mental Capacity Act
  • Treat underlying cause/co-morbidities
  • Environmental management
  • Minimise sensory deficits - glasses/hearing aids
  • Agitation can be managed with haloperidol (0.5-1.0mg PO) or lorazepam (0.5-1.0mg PO), however, they should be avoided as they may worsen or prolong delirium.
103
Q

What is the most common and 2nd most common type of dementia?

A

Alzheimer’s
Vascular

104
Q

What is Alzheimer’s and what is the pathophysiology?

A

Alzheimer’s disease (AD) is a progressive neurodegenerative disorder that causes significant deterioration in mental performance. This leads to impairment in normal social and occupational function.

It’s caused by a build up of amyloid protein deposits around brain cells and tau protein tangles within brain cells.

105
Q

How does Alzheimer’s present?

A
  • Cognitive impairment: poor memory, disorientation, language problems
  • Behavioural and psychological symptoms of dementia (BPSD): agitation, depression, sleep cycle disturbance, motor disturbance
  • AD is characterised by early impairment of memory. This manifests as short-term memory loss and difficulty learning new information
  • Activities of daily living: an increasing reliance on others for assistance, problems with high-level functioning (e.g. work, finance), problems with basic personal care
106
Q

What is the pharmacological management of Alzheimer’s?

A

Mild-to-moderate AD: acetylcholinesterase inhibitors (e.g. donepezil, rivastigmine).

Moderate-to-severe AD: N-methyl-D-aspartic acid receptor antagonist (e.g. memantine). May be used in combination with acetylcholinesterase inhibitors.

107
Q

What other management needs to be considered in Alzheimer’s in addition to medications?

A
  • Assess capacity
  • Advanced care planning
  • Treat concurrent mood disorders
  • Inform DVLA
  • Programmes to improve/maintain cognitive function (e.g. structured group cognitive stimulation programmes). Also exercise, aromatherapy, therapeutic use of music/dancing, massage.
  • End of life care
108
Q

What is vascular dementia?

A

Vascular dementia is a result of multiple infarcts in the brain tends to present with sudden onset cognitive decline and stepwise deterioration in someone with previous cardiovascular illness or events, as a result of the developing infarcts.

Any condition that affects the brain parenchyma by impairing cerebral blood flow (i.e. ischaemia) or causing haemorrhage can lead to vascular cognitive impairment, and therefore, VD.

109
Q

How does vascular dementia present?

A
  • Can be Post-stroke or Vascular dementia without recent stroke:
  • Cognitive impairment: poor memory, disorientation, language problems
  • Behavioural and psychological symptoms of dementia (BPSD): agitation, depression, sleep cycle disturbance, motor disturbance
  • VD is characterised by a ‘stepwise’ decline in function. There are predominant gait abnormalities, attention, and personality changes. May have focal neurological signs (e.g. due to previous stroke)
  • Activities of daily living compromised
110
Q

What Ix would you order for VD?

A

Routine bloods, MRI Head, other tests if indicated:
ECG
Virology (e.g. HIV)
ECHO (e.g. if suspected heart failure or coronary artery disease)
Syphilis testing
CXR

111
Q

What is Lewy Body Dementia?

A

Lewy body dementia, is a common subtype of dementia that is characterised by the histopathological findings of intracytoplasmic inclusions known as Lewy bodies that contain alpha-synuclein.

3rd most common, M>F

112
Q

What is the difference between LBD and Parkinson’s Disease Dementia?

A

Parkinson’s disease dementia: dementia occurring in the setting of established Parkinson’s disease. This is defined as having Parkinson’s disease for more than one year before the onset of dementia.

Dementia with Lewy body: development of dementia and Parkinsonism concurrently. This is defined as developing dementia within one year of Parkinsonism features

113
Q

What are the clinical features of LBD?

A

DLB is characterised by:
- Fluctuating cognition with pronounced variations in attention and alertness
- Recurrent visual hallucinations that are typically well formed and detailed
- REM sleep behaviour disorder, which may precede cognitive decline
- One or more spontaneous cardinal features of parkinsonism (e.g. bradykinesia, rest tremor, rigidity)

Severe sensitivity to antipsychotic agents
Postural instability and repeated falls
Syncope or other transient episodes of unresponsiveness
Severe autonomic dysfunction (eg, constipation, orthostatic hypotension, urinary incontinence)
Hypersomnia (i.e. excessive daytime sleepiness)
Hyposmia (i.e. decreased sense of smell)
Other symptoms are the same as other dementias

114
Q

How is LBD managed?

A
  • Cholinesterase inhibitors (e.g. Rivastigmine, Donepezil): generally offered as first-line treatments
  • Memantine: often used in severe AD or VD but limited efficacy in DLB
  • Anti-psychotics (e.g. Quetiapine) generally reserved for severe, refractory behavioural symptoms
  • Melatonin: may be used in refractory REM sleep disorders
  • Levodopa: this is an antiparkinson medication that may be used for severe, disabling Parkinsonism features
115
Q

What is frontotemporal dementia?

A

Fronto-temporal dementia presents with cognitive impairment, personality change and disinbition, in keeping with the frontal area of the brain which is affected. Atrophy of the frontal and temporal lobes is seen.

FTD shows a strong genetic predisposition. In 10-25% of cases, there is an autosomal dominant pattern of inheritance. In up to 40% of cases there is a family history of dementia or neuropsychiatric conditions without a clear inheritance pattern.

116
Q

What are the clinical features of frontotemporal dementia?

A

Disinhibition (e.g. socially inappropriate behaviour)
Loss of empathy
Apathy (losing interest and/or motivation)
Hyperorality (e.g. dietary changes, attempt to consume non-edible products, eat beyond satiety)
Compulsive behaviour (e.g. cleaning, checking, hoarding)

117
Q

How does primary progressive aphasia present?

A

Effortful speech
Halting speech
Speech-sound errors
Speech apraxia (i.e. difficulty in articulation)
Word-finding difficulty
Surface dyslexia or dysgraphia: mispronouncing difficult words (e.g. yacht)

118
Q

How is frontotemporal dementia managed?

A
  • No disease modifying drugs
  • Might use SSRIs or atypical antipsychotics
  • Financial advice/lasting power of attorney
  • Supervision particularly if behaviour is problematic
  • Exercise and Mobility
  • Speech and language: assessment by a speech and language therapist is important with communication aids and swallow assessment in later stages of disease
  • Behavioural modification: variety of methods effective, keeping a behaviour chart can be useful and ensuring carers get respite.
119
Q

What is schizophrenia?

A

A psychotic disorder characterised with delusions, hallucinations and thought disorder.

Incidence is roughly the same in men and women but men tend to get it early (before 25) and women get it before 35.

Pathophysiology and aetiology are poorly understood. Strong genetic links, stress diathesis model, obstetric complications, adverse childhood events, use of hallucinogens

120
Q

What risk does a patient have of developing schizophrenia:
- General population
- Sibling
- Parent
- Both parents
- Identical twin

A

General risk – 1%
If sibling has condition – 9%
If parent has condition – 13%
If both parents have condition – 48%
If monozygotic twin has it - 50%
If dizygotic twin has it - 15%

121
Q

What brain changes might be seen in someone with schizophrenia?

A

Enlarged ventricles, small amounts of grey matter loss and smaller, lighter brains.

122
Q

What are the 6 types of schizophrenia?

A

Paranoid schizophrenia
Hebephrenic schizophrenia
Catatonic schizophrenia
Undifferentiated schizophrenia
Residual schizophrenia
Simple schizophrenia

123
Q

What features are needed for a diagnosis of schizophrenia according to ICD-10?

A

A psychotic episode lasting at least a month with 1 of these:
- Thought echo, thought insertion or withdrawal, or thought broadcasting.
- Delusions of control, influence or passivity, clearly referred to body or limb movements or specific thoughts, actions, or sensations; delusional perception.
- Hallucinatory voices 3rd party, running commentary on the patient’s behaviour, or discussing or coming from some part of the body.
- Persistent delusions of other kinds that are culturally inappropriate and completely impossible

Or a psychotic episode lasting at least a month with 2:
- Persistent hallucinations in any modality, when occurring every day for at least one month accompanied by delusions
- Neologisms, breaks or interpolations in the train of thought, resulting in incoherence or irrelevant speech.
- Catatonic behaviour
- “Negative” symptoms

124
Q

What are the positive symptoms of schizophrenia?

A

Thought echo (hearing your own thoughts out loud)*
Thought insertion or withdrawal*
Thought broadcasting*
3rd person auditory hallucinations*
Delusional perception *
Passivity and somatic passivity*
Odd behaviour
Thought disorder
Lack of insight

125
Q

What are the negative symptoms of schizophrenia?

A

Blunted affect
Apathy
Social isolation
Poverty of speech
Poor self-care

126
Q

What types of auditory hallucinations can a patient experience?

A
  • Third person – talking about the individual who hears them. May be single or multiple voices. These are the most common type of auditory hallucination in schizophrenia.
  • Thought echo – the individual hears their thoughts spoken aloud, either simultaneously (as thinking the thought) or just afterwards.
  • Second person – talking to the individual – can still occur in schizophrenia, but also present in lots of other mental disorders.
127
Q

What is passivity?

A

The patient believes that their movements, emotions or will is being altered in a similar way to the thought issues, for examples, they believe their movements are being controlled.

128
Q

What is incongruity of affect?

A

The patient may burst out laughing or become very angry for no apparent reason, or they may have inappropriate emotional reactions – e.g. laughing at bad news.

129
Q

What is:
- Catatonia
- Stupor
- Strange posture
- Negativism
- Automatic obedience
- Wavy flexibility

A
  • A state where the person may not respond to stimuli and exhibits strange physical behaviour. Can be associated with any mental health condition. Includes:
  • Stupor – the patient is unable to move or speak except for moving their eyes.
  • Strange postures – that are normally very difficult to hold
  • Negativism – the patient does the exact opposite of what they are asked
  • Automatic obedience
  • Waxy flexibility – the patient has strange muscle tone that allows the doctor to put the patient into physical position that would otherwise be very difficult and/or painful.
130
Q

What investigations would you order for someone with suspected schizophrenia?

A

FBC, TFTs, U&Es, LFTs, CRP and a fasting glucose
Urine culture: to rule out urinary tract infection causing delirium
Urine drug screen: to rule out drug intoxication
HIV testing if applicable
Syphilis serology if applicable
Serum lipids: before starting antipsychotics
CT head: if an organic neurological cause is suspected

131
Q

What care is given to someone with suspected schizophrenia?

A

There are four stages to a CPA:
Assessing health and social needs
Creating a care plan
Appointing a key worker to be the first point of contact
Reviewing treatment

132
Q

What blood tests do you do before commencing antipsychotic therapy?

A

Fasting blood glucose
HbA1c
Blood lipid profile
Prolactin levels

133
Q

When would you consider the use of clozapine?

A

NICE does advise the use of clozapine if the patient has failed to respond adequately to 2 different antipsychotics (one of which is an atypical antipsychotic that is not clozapine).

134
Q

How do typical/first gen antipsychotics typically work?

A

Blockade of dopamine receptors (D2). Commonly used examples include haloperidol and chlorpromazine.

They can cause a number of significant side effects. Extrapyramidal side effects may occur resulting in dystonia and tremor. Tardive dyskinesia, which refers to uncontrolled repetitive movements such as smacking lips together, may develop with prolonged use.

135
Q

How do atypical antipsychotics work?

A

Block dopamine receptors (D2), and many act on serotonin receptors. Commonly used examples include clozapine and olanzapine. Extrapyramidal side-effects and tardive dyskinesia are less common, however, they are associated with significant weight gain and insulin resistance. Agranulocytosis and bone marrow suppression may occur.

136
Q

What is the recommended treatment for SAD?

A

2hrs 2500lux light in morning for 1-2 weeks
Maintenance 30 mins 2500lux every 1-2days

If light therapy does not help then trial an SSRI

137
Q

Othello Syndrome

A

Patients hold the delusional belief that their partner is cheating on them. Affects males more than females. They may be threatening towards their partner and stalk or have them followed.

138
Q

Cotard Syndrome

A

In this delusional disorder, patients believe that parts of their own body are dead or decaying. Typically associated with severe depression and suicidal tendency.

139
Q

Capgras Syndrome

A

Patients hold the delusional belief that a friend or relative (often their partner) has been replaced by an exact double.

140
Q

De Cleram​bault’s Syndrome

A

Classically effects women. Patients believe that another individual (often a celebrity) is deeply in love with them, and is incapable of living without them.

141
Q

Charles Bonnet Syndrome

A

Characterised by the subjective experience of visual hallucinations secondary to sight loss.

142
Q

What is used to assess postpartum depression?

A

Edinburgh Postnatal Depression Scale (EPDS)
PHQ9

143
Q

How is postpartum depression managed?

A

SSRI + CBT
Paroxetine, sertraline or citalopram - Lowest levels present in breast milk

144
Q

What is postpartum psychosis?

A

Postpartum psychosis is a severe mental health disorder that typically occurs within the first two weeks postpartum, characterised by symptoms including paranoia, delusions, hallucinations, mania, depression, and confusion.

145
Q

How is postpartum psychosis managed?

A

MBU admission
CBT
Antipsychotics
Mood stabiliser
Antidepressants
ECT

145
Q

What is postpartum psychosis?

A

Postpartum psychosis is a severe mental health disorder that typically occurs within the first two weeks postpartum, characterised by symptoms including paranoia, delusions, hallucinations, mania, depression, and confusion.

146
Q
A
146
Q

What is somatisation?

A

The presence of physical symptoms that cannot be explained by a medical condition, drug or other mental health disorder. It is an unconscious process. Common presenting symptoms are gastrointestinal symptoms and abdominal pain, fatigue, weakness and musculoskeletal symptoms.

Patients can present with inconsistent examination findings, strange neurological symptoms that don’t conform to myotome/dermatome distribution.

147
Q

What is conversion disorder?

A

A psychiatric condition that results in a presentation of neurological symptoms without any underlying neurological cause (e.g. paralysis, pseudoseizures, sensory changes). It is not an intentional process, and the symptoms are very much “real” to the patient. It is linked to emotional stress and usually after a precipitating event.

148
Q

What is hypochondriasis?

A

Patients have excessive concern that they will develop a serious illness despite a lack of evidence. Patients often demand unnecessary tests and investigations, and can be quite debilitated as a result of their constant worrying.

149
Q

What is postpartum psychosis?

A

Postpartum psychosis is a severe mental health disorder that typically occurs within the first two weeks postpartum, characterised by symptoms including paranoia, delusions, hallucinations, mania, depression, and confusion.

149
Q

What is the difference between hypochondriasis and somatoform disorder?

A

Patients with hypochondriasis typically have no or very few symptoms unlike Somatoform disorder where patients experience dramatic physical symptoms and experience a degree of disfunction.

150
Q

What is Munchausen’s Syndrome?

A

Patients intentionally fake signs and symptoms (e.g. adding blood to urine and complaining of pain) in order to adopt “the patient role”.

151
Q

What is Malingering?

A

Patients intentionally fake or induce illness for secondary gain; e.g. drug seeking, disability benefits, avoiding work or prison time. NOT a mental health problem.

152
Q

What is a learning disability?

A

A learning disability constitutes a condition which affects learning and intelligence across all areas of life. a learning difficulty constitutes a condition which creates an obstacle to a specific form of learning, but does not affect the overall IQ of an individual. E.g. Down’s Syndrome = disability, dyslexia = difficulty, depression = MH

e.g. Fragile X, Praeder Willi, Down’s

153
Q

How would someone intoxicated with opiates present?

A

Drowsiness
Confusion
Decreased respiratory rate
Decreased heart rate
Constricted pupils
Track marks

154
Q

Symptoms of cannabinoid intoxication?

A

drowsiness, impaired memory, slowed reflexes and motor skills, bloodshot eyes, increased appetite, dry mouth, increased heart rate and paranoia. Cannabis acts at cannabinoid receptors.

155
Q

Symptoms of LSD?

A

Labile mood
Hallucinations
Increased blood pressure
Increased heart rate
Increased temperature
Sweating
Insomnia
Dry mouth
LSD primarily acts at dopamine receptors.

156
Q

Symptoms of stimulant use?

A

Euphoria
Increased blood pressure
Increased heart rate
Increased temperature

Cocaine acts at dopamine receptors. Methamphetamine acts at TAAR1 (Trace Amine-Associated Receptor 1) receptors. Both increase the available amount of dopamine in the brain

157
Q

What are the features of opiate withdrawal?

A

Agitation
Anxiety and irritability
Muscle aches or cramps
Chills
Runny eyes
Runny nose
Sweating
Hypersalivation
Yawning
Insomnia
Gastrointestinal disturbance such as abdominal cramps, nausea, diarrhoea and vomiting
Dilated pupils
Piloerection
Increased heart rate and blood pressure

158
Q

What does Lofexidine do?

A

alpha 2 receptor agonist
Minimises symptoms of opiate withdrawl

160
Q

What is postpartum psychosis?

A

Postpartum psychosis is a severe mental health disorder that typically occurs within the first two weeks postpartum, characterised by symptoms including paranoia, delusions, hallucinations, mania, depression, and confusion.