PSYCHIATRY Flashcards

1
Q

Describe the aetiology of ADHD.

A

ADHD is most likely caused by a complex interplay of factors:
neurobiologic (neuroanatomical and neurochemical)
genetic influences
environmental/psychosocial factors
CNS insults (such as perinatal factors, CNS infections, FAS or premature.)
Research repeatedly demonstrates that ADHD runs in families

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2
Q

What are the 3 core behaviours of ADHD?

A
  1. Hyperactivity.
  2. Inattention.
  3. Impulsivity.
    (HII)

These symptoms occur in every child from time to time but when they are persistent and impact on daily functions, more investigation is needed

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3
Q

ADHD core behaviours: give 3 signs of impulsivity.

A
  1. Blurts out answers.
  2. Interrupts.
  3. Difficulty waiting turns.
  4. When older, pregnancy and drug use.
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4
Q

ADHD core behaviours: give 3 signs of inattention.

A
  1. Easily distracted.
  2. Not listening.
  3. Mind wandering.
  4. Struggling at school.
  5. Forgetful.
  6. Organisational problems.

Does not appear to be listening when spokento directly
Makes careless mistakes
Looses important items

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5
Q

What is the diagnostic criteria for ADHD? According to DSM-5 (Diagnostic and Statistical Manual of Mental Disorders)

A

ADHD definition <17 Years

6/9 inattentive symptoms and 6/9 hyperactivity/impulsivity.

Present before 12 years
Developmentally inappropriate
Several symptoms in 2 or more settings
Clear evidence symptoms interfere/reduce the quality of social/academic/occupational function
.

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6
Q

What are some differentials of ADHD?

A

Age-appropriate behaviour in active children;
attachment disorder; hearing impairment; learning difficulty; a high IQ child
insufficiently stimulated/challenged in mainstream school; behavioural
disorder; anxiety disorder; medication side-effects (e.g. antihistamines).

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7
Q

What tools can be used in order to diagnose ADHD?

A
  1. Clinical interview - are there any RF’s for ADHD?
  2. ADHD nurse classroom observation.
  3. Questionnaires (SNAP), Conor’s questionaire
  4. Quantitative behavioural (QB) analysis.

Brown attention deficit disorder scale
WHO adult ADHD self-report scale

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8
Q

Describe the nn pharmalogical treatment for ADHD.

A
  1. Education.
  2. Parenting programmes and school support.
    Behavioural interventions, e.g. encouraging realistic expectations, positive reinforcement of desired behaviours (small immediate rewards), consistent contingency management across home and
    school, break down tasks, reduce distraction.

Implementing Routines
Evidence base for fish oils in diet
Learning support

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9
Q

What are some medicine for ADHD?

A

Methylphenidate (ritalin, concerta, Equasym)
Atomoxetine (Strattera®) A non-stimulant NE reuptake inhibitor licensed for the treatment of ADHD.

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10
Q

What are some things you need to consider/ SE of ADHD medication?

A

headache, insomnia, loss of appetite, stomach ache, dry mouth, nausea

Can stunt growth
Need to Monitor weight, height and BP
Methyphenidate is Not recommended to take during pregnancy

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11
Q

What are the 3 main features of the deficits seen in ASD?

A

They can be categorised as deficits in social interaction, communication and behaviour

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12
Q

Outline some social interaction issues often seen in those with ASD

A

NO DESIRE TO INTERACT WITH OTHERS
BEING INTERESTED IN OTHERS TO HAVE NEEDS MET
LACK OF MOTIVATION TO PLEASE OTHERS
AFFECTIONATE ON OWN TERMS

Touches inappropriately
Poor Eye contact
Plays alone
Finds it stressful to be with other people

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13
Q

Outline some communication issues often seen in those with ASD

A

Repetitive use of words or phrases
Delay, absence in language development
Lack of appropriate non-verbal communication such as smiling, eye contact, responding to others, and sharing interest
Lack of desire to communicate at all
PEDANTIC LANGUAGE, VERY LITERAL, POOR OR NO UNDERSTANDING OF IDIOMS AND JOKES

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14
Q

Outline some behavioural issues seen in Autism

A

USING TOYS AS OBJECTS
INABILITY TO PLAY OR WRITE IMAGINATIVELY
RESISTING CHANGE
PLAYING SAME GAME OVER AND OVER
OBSESSIONS/RITUALS
There may be self-stimulating movements that are used to comfort themselves, such as hand-flapping or rocking.
Extremely restricted food preferences

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15
Q

Describe the treatment for ASD.

A
  • Education and games to encourage social communication.
  • Visual aids and timetables.
  • Parenting workshops and school liaison.
    Manage Comorbidity

There are no medications available for ASD

Diagnosis should be made by a specialist in autism. This may be a paediatric psychiatrist or paediatrician with an interest in development and behaviour. A diagnosis can be made before the age of 3 years. It involves a detailed history and assessment of the child’s behaviour and communication..

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16
Q

Outline some of the people within the MDT for dealing with ASD.

A

Child psychology and child and adolescent psychiatry (CAMHS)
Speech and language specialists
Dietician
Paediatrician
Social workers
Specially trained educators and special school environments
Charities such as the national autistic society

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17
Q

What are some risk factors for depression?

A

Prior depression
Family Hx depression
Female
Hx abuse
Drug and alcohol use
Low socioeconomic status
Recent bereavement, stress or medical illness, traumatic life event
Co-existing medical conditions (chronic disease)

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18
Q

What are the 3 key symptoms of depression?

A

Low mood
Loss of energy (anergia)
Anhedonia (loss of enjoyment of formerly pleasurable activities)

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19
Q

What are some things you may find on consulation/examination/investigations for depression?

A

Carry out mental state examination
- Appearance may be normal, or evidence of self beglect. substnace abuse, tearfulllness, anxious, fidegty

Speach may be monotonic and slow - patient may appear distracted

Psychotic features - eg auditory hallucinations, loss of insight

Baseline tests for FBC and TFT may be useful for ruling out anaemia and hypothyroidism, that can lead to depression

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20
Q

What is the name of the questionaire used in depression?

A

The Patient Health Questionnaire-9 (scored out of 27) is used to grade depression

– It asks patients to report over the last 2 weeks how often they have been experiencing symptoms

– Made of 9 items which is scored from 0-3

– Mild = 5-9 – Moderate = 10-14 – Moderate/Severe = 15-19 – Severe = >19

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21
Q

What is the non pharmalogical measurements for mild depression?

A

Mild depression
* Watchful waiting (GP monitoring progress post diagnosis)
* Guided self-help: workbook/online course + therapy support
* Exercise
* Talking therapies - CBT, interpersonal therapy (IPT), psychodynamic psychotherapy
○ CBT:
§ Aim to help understand thoughts/behaviour + how they affect you
§ Recognises events in past but concentrates on how can change thinking/feeling/behaviour in present
§ Available on NHS for depression/mental health problems
○ IPT:
§ Focus on relationships with others and problems within them
§ E.g. issues with communication, coping with bereavement

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22
Q

What is the treatment for moderate/severe depression?

A

Moderate/severe depression
* Antidepressants (SSRIs, TCAs) - continued for 6+ mths after Sx stop
* Combination therapy e.g. meds + talking therapy

SSRI - Selective serotonin reuptake inhibitors eg Sertraline, paroxetine, fluoxetine, citalopram
Fluoxetine 1L in children

TCAs (Tricyclic antidepressants):
Imipramine, amitriptyline

SNRIs (Serotonin-noradrenaline reuptake inhibitors):
Venlafaxine, duloxetine, Mirtazapine

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23
Q

What is some treatment for very severe depression

A

Resistant depression Tx w/ combo of antidepressants +
Lithium
Atypical antipsychotic
Another antidepressant

ECT very effective in severe cases (Electroconvulsive Therapy)

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24
Q

Outline what bipolar disorder consists of - what is the ICD-10 definition

A

Bipolar affective disorder - recurrent episodes of altered mood and activity

Involving upswings and downswings (hypomania/mania + depression)

Hx of 2 mood disorders, at least one:
Hypomania < 4d
Mania >7 d

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25
Q

What are some of the causes/risk factors for bipolar disorder?

A

Genetic links + environmental stressors/triggers -> mood disorder

A number of studies have reported abnormalities in the hypothalamic-pituitary-adrenal (HPA) axis in bipolar disorder which
are consistent with reduced HPA axis feedback

Prolonged psychosocial stressors during childhood, such as neglect or abuse, are associated with HPA axis dysfunction in later life, which may result in hypersensitivity to stress.

People with a history of childhood sexual or physical abuse appear to be more at risk and to have a worse prognosis

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26
Q

types of bipolar, according to DSM-5 - outline what is seen in bipolar I disorder, and bipolar II disorder

A

Bipolar 1 - mania & depression, sometimes more episodes of mania
Bipolar 2 - more episodes of depression and only mild hypomania (easy to miss, always ask Sx of mania in person presenting w/ typical depression Sx)

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27
Q

Types of bipolar - outline what is seen in cyclothymia -

What differentiates mania from hypomania?

A

Cyclothymia - chronic mood fluctuations over 2+ yrs, episodes of depression and hypomania (not mania). Rapid cycling, episodes only lasting few days

**presence of psychotic Sx e.g. auditory hallucinations/grandiose delusions differentiates mania from hypomania

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28
Q

What are some things you might see in an episode of hypomania? How long do these tend to last?

A

Lasts about 4 days

Elevated mood
Increased energy, talkativeness
Poor concentration
Mild reckless behaviour (overspending)
Sociability/overfamiliarity
Increased libido/sexual disinhibition
Increased confidence
Decreased need to sleep
Change in appetite

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29
Q

What are some things you might see in an episode of mania? How long do these tend to last?

A

Sx mania (lasting atleast 1wk, more extreme than hypomania)
Uncontrollable elation
Overactivity
Pressure of speech (words can’t get out fast enough)
Impaired judgement
Extreme risk-taking behaviour
Social disinhibition
Inflated self-esteem, grandiosity
Psychotic Sx can occur
Insight often absent during episodes

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30
Q

What are some differentials that you need to rule out in bipolar disorder?

A

Substance abuse (amphetamines, cocaine)
Endocrine disease - Cushing’s, steroid-induced psychosis
Schizophrenia
Schizoaffective disorder - Dx when affective and first rank schizophrenic Sx equally prominent
Personality disorders - emotionally unstable, histrionic
ADHD in younger people

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31
Q

What is the first management of bipolar disorder, for episodes of mania

A

First ensure that the patient stops taking any antidepressant, then treat with antipsychotics

– 1st line is antipsychotic: Haloperidol or Olanzapine or Risperidone

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32
Q

What is the 2nd line management for episodes of mania seen in bipolar, and what cna be used in v acute attacks that are severe

A

Lithium (slower onset) or valproate 2nd line

Benzodiazepines may be used in the short term for acute behavioural disturbance. Lorazepam and antipsychotics may be useful
for rapid tranquillisation

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33
Q

What is the treatment of bipolar, for a depressive episode?

A

– For depression –> Treat with antipsychotics alone or in combination with SSRI’s

– 1st line is Olanzapine, Lamotrigine or Quetiapine and Fluoxetine

– Do not just prescribe SSRIs by themselves as they can precipitate mania

If a patient is taking an antidepressant at the onset of an acute manic episode, the antidepressant should be stopped.

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34
Q

What are some side effects of lithium

A

L - leukocytosis
I - insipidus diabetes (nephrogenic)
T - tremors (if coarse, think toxicity)
H - hydration (easily dehydrates, need to drink lots, is renally cleared)
I - increased GI motility
U - underactive thyroid
M - metallic taste (warning of toxicity), mums beware - teratogenic

Lithium + diuretics -> dehydration

Lithium + NSAIDs -> kidney damage

& weight gain, hypothyroidism

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35
Q

What are some other conditions you would want to do to rule out other causes of symptoms seen in GAD?

A

depression and obsessive compulsive disorder

Hyperthyroidism - do TFTs
Pheochromocytoma
Lung disease - excessive salbutamol use
Congestive HF - heart meds -> anxiety
Hypoglycaemia
Do Bloods, and BP

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36
Q

What are some risk factors/causes of developing GAD?

A

Family Hx anxiety
Physical/emotional stress
Financial, bereavement etc
Hx physical/sexual/emotional trauma (in childhood)
Excessively pushy parents in childhood
Other anxiety disorder - coexisting depression
Chronic physical health condition
Worries about physical health
Female 2:1 Male

Environmental triggers/contributors: family relationships, friendships, bullies, school pressures, alcohol and drug use e.g. benzodiazepines

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37
Q

Outline some neuropathology that is thought to be linked to GAD

A

Low levels of GABA, contribute to anxiety.
Been seen that frontal cortex and amygdala
undergo structural remodelling induced by the stress of maternal separation and isolation, which alters behavioural and physiological responses in adulthood.

  • Heightened amygdala activation occurs in response to disorder-relevant stimuli in post-traumatic stress disorder, social phobia and specific phobia

Basically overfiring/activation of the amygdala

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38
Q

What is the non pharmalogical management of GAD?

A

Mild anxiety can be managed with watchful waiting and advice about self-help strategies (e.g. meditation), diet, exercise and avoiding alcohol, caffeine and drugs.

Moderate to severe anxiety can be referred to CAMHS services to initiate:

Counselling
Cognitive behavioural therapy

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39
Q

What is the pharmacological management of GAD?

A

SSRI (sertraline is first-line SSRI)
– Be careful in young people as the SSRI increases anxiety initially and can lead to suicidal thoughts
Pre-gabalin

– If acutely anxious –> Benzodiazepine (but not for > 4 weeks)

Beta blockers e.g. bisoprolol for physical Sx

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40
Q

OCD - Define what is meant by Obsessions, and give some examples of some

A

Obsessions = unwanted/uncontrolled thoughts and intrusive images, pt finds difficult to ignore

aggressive impulses e.g. - images of hurting a child or parent
contamination e.g. – becoming contaminated by shaking hands with another person
need for order e.g. – intense distress when objects are disordered or asymmetric
religious e.g. – blasphemous thoughts, concerns about unknowingly sinning
repeated doubts e.g. – wonder if a door was left unlock

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41
Q

OCD - Define what is meant by Compulsions

A

repetitive actions pt feels they must do, generating anxiety if not done - often way to handle the obsessions

checking e .g. – repeatedly checking locks, alarms, appliances
cleaning e.g. – hand washing
hoarding e.g. – saving trash or unnecessary items
mental acts e.g. – praying, counting, repeating words silently

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42
Q

What are some causes/Risk factors for developing OCD?

A

Genetic predisposition (twins, especially monozygotic)
Developmental factors
Emotional/physical/sexual abuse
Neglect
Social isolation
Teasing, bullying
Parental over protection
Psychological factors
Over-inflated sense of responsibility
Intolerance of uncertainty
Belief in controllability of intrusive thoughts
Stressors
Pregnancy
Postnatal period

Family Hx
Stressful life events
Environmental factors

Rarely
In adults: neurological conditions e.g. brain tumour, Huntington’s chorea, frontotemporal dementia, complication of brain injury to frontal lobe/basal skull

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43
Q

What is the non pharmalogical treatment for OCD?

A

Mild functional impairment Offer short CBT (<10h), including
exposure-response prevention (ERP) or group therapy
* Moderate functional impairment Offer more intensive CBT (>10h)

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44
Q

What is the pharmacological treatment of OCD?

A

or drug therapy (SSRI, e.g. fluoxetine 20–40mg od)
* Severe functional impairment Offer psychological therapy + drug treatment.

If inadequate response at 12wk, offer a different SSRI or
clomipramine (a TCA that also acts as a serotonin reuptake inhibtior).

Refer if symptoms persist

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45
Q

What are some causes/risk factors for developing phobias?

A

animals (spides, snakes, worms)
Blood/injection/injury
Situational (lifts, flying, enclosed space)
Natural environment (storms, heights, water)
Other: choking, vomiting, clowns

Amygdala, anterior cingulate cortex and insula hyperactivity involved in underlying mechanism of action

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46
Q

What are the 3 types of Phobias?

A

Simple phobia Inappropriate anxiety in the presence of ≥1 object/situation, e.g. flying, enclosed spaces, spiders

Social phobia Intense/persistent fear of being scrutinized or negatively
evaluated by others leads to fear and avoidance of social situations (e.g. using a telephone, speaking in front of a group).

Agoraphobia fear of fainting and/or loss of control are
experienced in crowds, away from home, or in situations from which escape is difficult. Avoidance results in patients remaining within their
homes where they know symptoms will not occur.

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47
Q

What are the general treatments for phobias?

A

For simple phobias - Treatment is only needed if symptoms are frequent, intrusive, or prevent necessary activities. Exposure therapy is effective.

For social and agoraphobia -
drug therapy SSRIs, and TCAs eg Clomipramine
Psychological therapies CBT (cognitive restructuring) +/- exposure

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48
Q

What is meant by baby blues? How long does it last for?

A

a period of low mood and irritability, which normally starts three to four days after birth, and lasts for 1-2 weeks.

Symptoms are usually mild, only last a few days and resolve within two weeks of delivery. No treatment is required.

Happens in over 50% of mothers

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49
Q

What is seen in Postnatal depression? How long must symptoms be going on before a diagnosis can be made?

A

a depressive episode within the first twelve months postpartum, peak incidence is 2 months after birth

Postnatal depression is similar to depression that occurs outside of pregnancy, with the classic triad of:

Low mood
Anhedonia (lack of pleasure in activities)
Low energy

Symptoms should last at least two weeks before postnatal depression is diagnosed.

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50
Q

What is some of the treatment for post natal depression? What would be the medication of choice

A

self-help strategies and non-directive counselling (‘listening visits’ by a health visitor).

Moderate to severe depression usually requires treatment with antidepressant medication and/or psychotherapy (CBT).

Breast-feeding is not a contraindication for antidepressant treatment, but drugs with low excretion in breastmilk, such as sertraline, are preferred.

High levels of Fluoxetine can transfer in breast milk

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51
Q

What is seen in postpartum psychosis?

A

Postpartum psychosis – 1-2:1000
Depression
Mania
Psychosis

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52
Q

What is the treatment of puerperal psychosis?

A

Admission to the mother and baby unit
Cognitive behavioural therapy
Medications
Electroconvulsive therapy (ECT)

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53
Q

What is the problem with SSRIs in pregnancy?

A

Can lead to neonatal abstinence syndrome (also known as neonatal adaptation syndrome).

It presents in the first few days after birth with symptoms such as irritability and poor feeding.

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54
Q

Define PTSD

A

Post traumatic stress disorder
Develop (immediately/delayed) post exposure to stressful event/threatening, catastrophic situation

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55
Q

What are some common causes of PTSD?

A

Serious accident e.g. RTA
Witness of violence - school, domestic, torture, terrorist attack, rape
Combat exposure
Natural disaster
Sudden death of loved one
Multiple major life stressors

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56
Q

What are the clinical feautres of PTSD? How long must they be present for?

A

Symptoms – These must be present >1 month

– Persistent intrusive thoughts and re-experiencing –> flashbacks, nightmares and intrusive images

– Autonomic hyperarousal –> persistent activation gives startle, hypervigilance, insomnia

– Avoidance –> patient avoids situations and stimuli associated with the event

– Emotional detachment –> feeling detached from people and lack of ability to experience feelings

– Higher risk of depression, substance misuse, unexplained physical symptoms

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57
Q

What are some non pharmalogical managements for PTSD

A

CBT - eg education about the nature of PTSD, selfmonitoring of symptoms, anxiety management, breathing techniques

Eye movement desensitization and reprocessing (EMDR): Using voluntary multi-saccadic eye movements to reduce anxiety associated with disturbing thoughts

Stress management
Hypnotherapy

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58
Q

What are some pharmaogical managments for PTSD

A

SSRIs (e.g. paroxetine 20–40mg/day; sertraline 50–200mg/day) are licensed for PTSD,

It may be helpful to target specific symptoms:
* Sleep disturbance (including nightmares): may be improved by mirtazapine (45mg/day),

  • Anxiety symptoms/hyperarousal: consider use of BDZs (e.g. clonazepam 4–5mg/day), buspirone, antidepressants, propranolol.
  • Intrusive thoughts/hostility/impulsiveness: some evidence for use of carbamazepine, valproate, or lithium.
  • Psychotic symptoms/severe aggression or agitation: may warrant use of an antipsychotic (some evidence for olanzapine, risperidone etc)
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59
Q

What are some primary causes of insomia?

A

Fear/anxiety about falling asleep
Change of environment (adjustment disorder) Inadequate sleep hygiene
Idiopathic insomnia (rare, lifelong inability to sleep)
Behavioural insomnia of childhood

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60
Q

What are some secondary causes of insomia?

A

Sleep-related breathing disorder e.g. sleep apnoea
Circadian rhythm disorders
Shift work

REM behavioural disorder e.g. Lewy body dementia, PD

Medication conditions causing pain -> awake

Psychiatric disorders - depression (early morning waking), anxiety (early/middle insomnia)

Drugs/alcohol - steroids, antidepressants, stimulants

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61
Q

What are some nonpharmacological management options for insomnia?

A

Encourage good sleep hygiene, routines
Remove noise, light, and distractions
Wind down before bed
Avoid caffeine/stimulation
Sleep restriction
Prevent naps during day to promote sleeping @ night

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62
Q

What are some pharmalogical management options for insomnia?

A

Medication (once good sleep hygiene proved unsuccessful)
Z drugs 1L - zopiclone, zolpidem, zapeplon
Sedating antidepressants - mirtazepine

Melatonin

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63
Q

What is paraphrenia?

A

psychotic illness characterized by delusions and hallucinations, without changes in affect (although there may be reactive anxiety), a form of
thought, or personality.

it’s the most common form of psychosis in old age - aka late-onset schizophrenia

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64
Q

What are some things you’d see in paraphrenia?

A

*no evidence of dementia w/ later onset cases - no memory problems

Delusions, hallucinations - often about neighbours
Paranoid - often re. neighbours spying, taking things
can also be misidentification, hypochondraical, religious
Partition delusion - believe people/objects can go through walls
Less -ve Sx (blunting/apathy) and formal thought disorder compared to early onset

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65
Q

What is the treatment steps in paraphrenia?

A

Relieve isolation and sensory deficits.
Low-dose atypical antipsychotics preferred as elderly are very sensitive
to side-effects, but non-compliance secondary to lack of insight is often
an issue.

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66
Q

Broadly speaking, what is seen in a cognitive impairment?

A

Minor problems w/ cognition - mental abilities: memory, thinking
Not severe enough to interfere w/ everyday life
Mild cognitive impairment = pre-dementia condition in some people

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67
Q

What are some causes of a cognitive decline, particulary in the elderly?

A

Depression, anxiety, stress
Sleep apnoea and other sleep disorders
Physical illness (constipation, infection)
Poor eyesight/hearing
Vitamin/thyroid deficiencies e.g. Vit B12
SE of medication: CCBs, anticholinergics, benzodiazepines
Drug/alcohol abuse

Uncontrolled health conditions like high BP, high cholesterol, diabetes, obesity

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68
Q

What are teh symptoms of cognitive decline?

A

Not severe enough to interfere w/ daily life -> not defined as dementia
(dementia Dx = 2/more of problems with: memory, reasoning, language, coordination, mood, behaviour)

Memory - forgetting recent events/repeating same question
Reasoning, planning, problem solving - struggling to think things through
Attention - v easily distracted
Language - taking longer than usual to find right word for something
Visual depth perception - struggling to interpret 3D object, judge distances, navigate stairs

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69
Q

What are some investigations for a cognitive decline

A

Take a thorough, collateral history

Review of medications
MSE
Input from family/collateral Hx
Bloods/urine if suspect infection/another clinical cause

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70
Q

What is the management for a cognitive impairment>

A

Prophylaxis/Mx of precipitative Sx:
Poorly controlled heart condition/diabetes/strokes -> ^ risk MCI
So control e.g. prevent high BP

Medication management of depression/anxiety
Good sleep hygiene

Preparation for the future when memory may get worse
Power of attorney etc

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71
Q

What are some causes of delirium?

A

Infection - UTI, pneumonia, septicaemia
Toxicity - substance misuse, intoxication withdrawal (d.tremens), opioids
Vascular - CVA (stroke), haemorrhage, head trauma
Epileptic
Metabolic - hyper/othyroidism, hyper/oglycaemia, hypoxia, hypercortisolaemia
Medications - anticholinergics, parkinson’s meds, benzodiazepines, drug accumulation, polypharmacy, postsurgery, steroids
Nutritional/dehydration - thiamine B1 deficiency, B12 deficiency, folate deficiency

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72
Q

What are some causes of Psychosis, that can be differentials to schizophrenia?

A

Bipolar disorder – often may present with symptoms of schizophrenia
Psychotic Depression
Alcohol hallucinations, due to withdrawal
Drugs - especially Cannabis, Cocaine, LSD, magic Mushrooms (Psilocybin)
Dopamine Agonists, like Levo Dopa in Parkinsons

Other health conditions, like
Encephalitis
Epilspeys (temporal lobe seizure,)
Dementia, and Parkinsons
B12 def,
hypoglycaemia,
Trauma
Brief Psychotic disorder – symptoms are present for less than a month, then disappear.

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73
Q

Outline what schizophrenia is - what are the 4 main things seen in it, as well as in psychosis in general?

A

Schizophrenia, a form of psychosis, is characterised by distortion to thinking and perception and inappropriate or blunted affect.

See Hallucinations, and delusions, Thought and speech disorders and negative symptoms

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74
Q

Schizophrenia and psychosis - define hallucinations

A

Hallucinations: hallucinations can be defined as perceptions in the absence of stimuli. Most commonly auditory but may be visual or affect smell, taste, or tactile senses.

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75
Q

Schizophrenia and psychosis - define delusions

A

Delusions: a fixed, false belief not in keeping with cultural and educational background.

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76
Q

Outlien what is thought to be some of the pathogenesis behind schizophrenia

A

increased size of the ventricles and reduced whole-brain volume, in those with Schizophrenia

Increased activity of dopamine in the mesolimbic region is associated with symptoms of psychosis.

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77
Q

what are some risk factors for developing schizophrenia?

A

fHx/genetic link
Affected brain development in early life (trauma, epilepsy, developmental delay, perinatal infection)
Smoking cannabis in adolescence
Severe childhood bullying/physical abuse
Socioeconomic deprivation
Adverse life events
Social isolation
Typical age onset 20-30s

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78
Q

What are some general things you may see in schizophrenia, and how may they be categorized?

A

Positive:
- Delusions, Hallucinations, Disorganised speech and behaviour, and Catatony

Negative:
- Less emotions, Loss of interest, Poverty/decreased speech, less motivation

Cognitive
- Decline in cognition, memory, learning

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79
Q

How may a diagnosis of schizophrenia be made? in line with the ICD-10

A

ICD-10 Diagnosis of schizophrenia made when:

  • At least 1 first-rank Sx
  • Or at least 2 second-rank Sx

For 1+ months

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80
Q

What are the first rank symptoms for schizophrenia, according to Schneider, in line with the ICD-10 Diagnosis

A

First rank Sx:
Delusional preceptions

3rd person auditory hallucinations (running commentary, hears people talking about them, not to them)

Thought disorder/alienation (broadcast, withdrawal, insertion, deletion)

Passivity phenomena (made to do/feel things against their will - someone controlling thoughts, feelings, actions)

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81
Q

What are the second rank symptoms of schizophrenia, according to Schneider, in line with the ICD-10 Diagnosis

A

Any other type of hallucination, not third person auditory
Formal thought disorder (words come out wrong, thoughts muddled)
Catatonic behaviour - excitement, posturing or waxy flexibility, negativism, mutism and stupor.
Negative symptoms - marked apathy, paucity of speech, and blunting or incongruity of emotional responses (it must be clear that these are not due to depression or to neuroleptic medication).

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82
Q

What are some tests you would do on someone w schizophrenia?

A

Bloods for organic causes psychosis - brain tumours, cysts, PD, Huntington’s, brain injury, severe systemic infection
FBC
LFT
TFT
Syphillis serology
Bloodborne Virus screen

Autoimmune causes -anti–NMDA receptor antibodies for autoimmune encephalitis,ANA, anti-DS DNA for Lupus

Collateral Hx from someone else

Blood, hair or urinary screens may be used for illicit drugs and alcohol, particularly in those presenting with acute psychosis of unknown cause.
MSE, risk assessment

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83
Q

What are some atypical anti psycotics, and how do they work?

A

Atypical anti-psychotics – work by blocking dopamine and serotonin:

Quetiapine
Olanzapine
Risperidone
Clozapine
Aripiprazole

Atypical are first line now (other than clozapine)

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84
Q

What are some typical anti-psychotics, and how do they work?

When should they be tried?

A

Typical anti-psychotics – work by dopamine blockade (D2 receptors):
Haloperidol
Chlorpromazine

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85
Q

When should you trail clozapine as an antipsychotic? What do you need to do with it?

A

If two other anti-psychotics have not been effective, then clozapine should be considered.

Second line – Clozapine – atypical antipsychotic – this is not included as a first line treatment, as requires close monitoring as it has a tendency to cause aplastic anaemia, which can be fatal. If two other anti-psychotics have not been effective, then clozapine should be considered.

CPMS – Clozepine monitoring system. A national service in the UK, that gives advice on the drug dosage to use, depeninding on the blood test results you send to them. Compulsory for anyone on clozepine. Only consultant psychiatrists can prescribe clozapine

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86
Q

What checks need to be done regulary for people on antipsychotic medications?

A

ECG – as QTC prolongation can occur

Glucose and lipids – antipsychotics can lead to diabetes and metabolic syndrome

If on CLOZAPINE – regular FBCs to check for AGRANULOCYTOSIS

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87
Q

What are some other side effects of antipsyhcots?

A

Diabetes/insulin resistance and dyslipidaemia
QT segment changes on ECG
Agranulocytosis – clozapine
Extra-pyramidal side effects due to the dopamine blockade -
Urinary retention
Blurred vision
Dry mouth
Weight gain
Hyperprolactinaemia (due to dopamine blockade and dopamine down regulates prolactin)

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88
Q

What are some extra pyrimidial side effects of antipsycotics, and how can they be treated?

A

Acute dystonic reaction (hours)
Muscle spasm, acute torticolis, eyes rolling back

Parkinsonism (days)
Tremor, bradykinesia

Akathisia (days to weeks)
“inner restlessness, pacing and agitated, often intolerable. They literally can’t stop moving e.g. shaking legs, touching table
Massive RF for suicide in young males with schizophrenia

Tardive dyskinesia (months to years)
Grimacing, tounge protrusion, lipsmacking
Very difficult/impossible to treat as you’ve upregulated all the D2 receptors
These side effects are worse and more common in the older antipsychotics

Treat with Procyclidine, an anticholinergic drug

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89
Q

What are some non pharmacological treatments of schizophrenia?

A

Individual CBT: normally consists of at least 16 one-on-one sessions. It helps patients create links between their thoughts, feelings and actions with their experience of schizophrenia.

Family intervention: should include the patient suffering from schizophrenia if possible as well as their main carer. Normally consists of 10 sessions over 3 months - 1 year.

Art therapies can be particularly helpful for negative symptoms.
Self-help groups and forums (e.g. Hearing Voices groups) enable people with psychosis to share experiences and ways to cope with symptoms

This should be done alongisde antipyscotic

90
Q

Outline some differential diagnosis for medically unexplainable symptoms

A

Factitious, symptoms are fabricated and not experienced as real by the patient

Somatoform disorder - Symptoms are unconsciously generated by the mind, but experienced as real by patient

Undiagnosed - symptoms are arising from a physical cause that hasn’t been identified yet

91
Q

What is a somatisation disorder? How is it classified?

A

Characterised in ICD-10 by at least two years of multiple physical symptoms with no physical explanation (symptoms are felt as real by pt)

patients persistently refuse to accept the advice of doctors that there is no physical explanation, and their social and family functioning is impaired as a result of the illness

92
Q

What are some causes/risk factors for somatisation disorder?

A

MC in women
Hx sexual or physical abuse
Adverse childhood events
Hx trauma related disorders

?psychological stress
Physical injury
Surgery
Another neurological disorder

93
Q

What are some clinical signs of a somatisation disorder, and what are the most common symptoms?

A

Speech disturbance
Swallowing disturbance
Distractable Sx e.g. tremor that stops when pt asked to walk/perform cognitive task

Often GI/skin complaints
Cognitive complaints - forgetfulness, short term memory problems
Refusing to believe no organic cause

94
Q

What is the management of a somatisation disorder?

A

Treatment should begin by ruling out all organic illnesses.

Acknowledge symptom severity and experience of distress as real but emphasize negative investigations
and lack of structural abnormality. Reassure patient of continuing care

Some evidence for the effectiveness of patient education in symptom
re-attribution, brief contact psychotherapy, group therapy, or CBT if the
patient can be engaged in this.

95
Q

What is seen in a conversion disorder?

A

Physical signs!

Presents with neurological SIGNS (rather than symptoms)
But the examination is inconsistent
The patient is not faking it consciously, but there is no evidence of underlying pathology

96
Q

What are some signs seen in conversion disorders?

A

paralysis
Loss of speech
Sensory loss
Seizures
Amnesia

Examination and investigations are inconsistent

97
Q

What is the management of conversion disorders?

A

Management:

– First exclude organic cause –> then therapies like hypnosis, psychotherapy, stress management

treating any underlying mood disorder and exploring with the patient and the family any ‘secondary gain’ (such as sympathy or avoidance of family conflict) that might be maintaining symptoms.

98
Q

Whats the difference between somatisation and conversion disorders?

A

Dissociative disorders differ from somatisation in that they more often present with signs rather than only symptoms and are often acute in their presentation.

99
Q

Outline what is seen in hypochondrial disorder

Where is it most common in?

A

This is a disorder where patients believe they have a serious underlying disease e.g. cancer, HIV, AIDS

– Similarly, to before, there is no physical or organic explanation

– Patients don’t accept negative test results and instead feel great distress and worry

– It is more common in men and people who have more contact with disease (e.g. health workers)

100
Q

What is hypochondrial disorder also asscoated with ?

A

Dysmorphophobia is related to hypochondriacal disorder. It is an excessive preoccupation with imagined or barely noticeable defects in physical appearance. For example, patients may
become preoccupied by the size of their nose, believing an objectively normal nose to be ugly and deformed

Many think it is on a spectrum with obsessive–compulsive
disorder.

101
Q

what is the management of hypochondrial disorder?

A

Allow patient time to ventilate their illness anxiet-ies. Clarify that symptoms with no structural basis are real and severe.

Explain negative tests and resist the temptation to
be drawn into further exploration

Uncontrolled trials demonstrate antidepressant
benefit, even in the absence of depressive symptoms. Try fluoxetine 20mg,

and CBT

102
Q

What are dissociative disorders? What is seen in the,

A

(PSYCHIATRIC SIGNS)
This is a group of conditions that involve disruptions or breakdowns in memory, awareness, identity or perception.

– In these disorders, psychiatric symptoms occur in the absence of pathology and these are more common in women

– According to the psychoanalytic view of psychiatry, painful memories are “cut-off” from conscious self and instead “converted” into more bearable

– It is seen as a way to cope with previous emotional trauma

103
Q

Give some different types of dissociative disorders

A

Dissociative amnesia – A condition where the patient has no recollection of upsetting and personal information

Dissociative fugue – A form of dissociative amnesia in which the patient flees away from their home
– They display amnesia for their identity, memories, personality and this can last hours to days

Dissociative identity disorder –It is a condition where the patient develops multiple personalities which can take over.
– It is strongly linked to early childhood trauma e.g. sexual abuse
– Patient has amnesia for when the different personalities take over, but maybe aware of their existence

104
Q

What is the management fo disassociative disorder?

A

First involves checking if there is an organic cause

– Psychotherapy (e.g. hypnosis) is main line to explore trauma and recall true identity

105
Q

Other delusional disorders - Outline what is seen in Cortards syndrome

A

holds the delusional belief that they are dead, do not exist, are putrefying, or have lost their blood or internal organs

106
Q

What is Charles - Bonnet Syndrome? What conditions are known to cause it

A

Complex visual hallucinations in a person with partial or severe blindness

(macular degeneration, diabetic retinopathy)

Patients understand that the hallucinations are not really and often have insight compared to other disorders

For those experiencing CBS, knowing that they have this syndrome and not a mental illness seems to be the most comforting treatment so far, as it improves their ability to cope with the hallucinations.

107
Q

Outline what is seen in Muchausens syndrome

A

This is a condition where patients will produce physical or psychological symptoms to attain a patient’s role

– Patients can feign the symptoms, exaggerate them or deliberately hurt themselves to produce symptoms

– Typically, patients take hallucinogens, inject faeces to make abscesses and contaminate urine samples.

108
Q

Outline what is seen in malingering

A

Malingering (FINANCIAL GAIN)
This is when a patient feigns or exaggerates their symptoms purely for a financial reward or other gain.

– Unlike Munchanhausen syndrome, it is not to play a patient’s role but to receive compensation, personal damages or get off work

– It is not a medical diagnosis, but can lead to a large economic burden on health care systems

109
Q

Give some other types of delusional disorders

A

Erotomanic - believe another person (often famous/important) is in love with them, may attempt to contact/stalking behaviour
Grandiose - overinflated sense self worth, power, identity, believe have talent/made important discovery
Jealous - spouse/sexual partner unfaithful without any concrete evidence
Persecutory - believe someone/something is mistreating/spying on/attempting to harm them, may repeatedly contact legal authorities
Somatic - physical issue/medical problem e.g. parasite, bad odour

110
Q

Give the definition of personality

A

The characteristics and relatively
permanent sets of behaviours, cognitions,
and emotional patterns that evolve from
biological and environmental factors

‘Characteristic lifestyle and mode of relating
to others’ (ICD – International
Classification of Diagnosis)

111
Q

What is a personality disorder?

A

Deeply ingrained, repetitive patterns of behaviour abnormal in a particular culture
Increase distress and risk to self/others
Decrease function

typically apparent by the time of
adolescence
Causes long-term difficulties in personal relationships or in functioning in society”

112
Q

What are the 3 clusters of personality disorders?

A

Split into cluster A, B, C - Mad, Bad and Sad

Split into cluster A, B, C
Cluster A - mad - paranoid, schizoid, schizotypal
Cluster B - bad - borderline (emotionally unstable), histrionic (centre of attention, making everything a drama), narcissist, antisocial
Cluster C - sad - avoidant/anxious, dependant, anankastic (obsessive compulsive)

113
Q

What are some risk factors/aeitology for personality disorders?

A

Childhood sexual abuse - strong link to borderline PD
Adverse events during pregnancy/birth/neonatal period
Poor parenting and adverse childhood
Conduct disorder as a child

Cognitive theory suggests that people with PDs developed ways of coping with early life adversity (e.g. turning anger against oneself rather than expressing it if this could result in parental violence) that manifest as maladaptive traits later in life (e.g. problems in interpersonal relationships).

114
Q

What are some features of symptoms seen in personality disorders?

A

Persistent:
o Starts in Childhood
o Present for at least;2 years

Problematic:
o Leads to significant personal distress that may only become apparent at a later stage
o Associated with significant difficulties with social relationships

Pervasive:
o Applies to various personal and social situations
o Significant distress or impairment must occur across ALL settings

115
Q

Give some specific persoanility disorders group in Cluster A personalty disorder

A

Paranoid
Schizoid
Schizotypal

116
Q

Define paranoid personality disorder and list some of its features (A)

A

unwarranted tendency to interpret the actions of others as demeaning or threatening

Thinks the world is – a conspiracy
Think people are – devious
Acts as if – always on guard, suspicious

117
Q

Define schizoid personality disorder and list some of its features (A)

A

pervasive pattern of indifference to social relationships and a restricted range of emotional experience and expression aloof

Thinks the world is – uncaring
Thinks people are – pointless, replaceable
Thinks they are the only person they can depend on
Commonest behaviour – withdrawal
Least likely to be – emotionally available and close

SchizoiD - = Distant

118
Q

deifne schizotypal personality disorder and list some of its features (A)

A

pervasive pattern of deficits in interpersonal relatedness and peculiarities of ideation, experience, appearance and behaviour

Strong desire to have relationships, unable to maintain them - poor at gauging others perception of them

SchizoTypical -

magical thinking

119
Q

What are some similarities and differences between cluster A personality disorder and schizophrenia?

A

Similarities - can have paranoia, and will experience the negative symptoms - of flat affect, and blunted emotions

indeed, maybe a genetic link between the two? ask about FH of one in relatives when taking a history for the other*

Differences - Paranoia is more intense in schizophrenia, and in schizophrenia, you have delusions, as well as positive symptoms like hallucinations and racing thoughts

120
Q

What are the personality disorders grouped together in Cluster B?

A

Bad

borderline (emotioanlly unstable)
antisocial,
histrionic
narcissist,

BAHN

121
Q

Define borderline personality disorder and list some of its features

A

Aka emotionally unstable - intense joy <–> rage
Most common type
Definition = pervasive pattern of instability of mood, interpersonal relationships and self-image

  • Self-damaging impulsivity (spending, sex,
    substance abuse, reckless driving, binge-eating)

Thinks people are – untrustworthy
Ashamed of themselves
Commonest behaviour – self-harm
Terrified of abandonment - might do extreme things to keep from leaving
Least likely to be – able to show self-compassion

Charlotte from Strike?

122
Q

Define antisocial personality disorder and list some of its features

A
  • Gross irresponsibility
  • Incapacity for maintaining relationships
  • Irritability
  • Disregard for moral values,
  • manipulative
  • Often charming
  • Low threshold for frustration and aggression
  • Incapacity for experiencing guilt
  • Deceitfulness
  • Disregard for personal safety

Have to be over 18 to get the diagnosis of this, with a history of conduct disorder
Overrepresented in the prison population

123
Q

Define histrionic personality disorder and list some of its features

A

Definition = pervasive pattern of excessive emotionality and attention seeking
Thinks the world is – their audience
Thinks people are – in competition for attention
Thinks they are vivacious (attractively lively and animated)
Commonest behaviour – exhibitionism
Least likely to be – able to listen to others

Few meaningful relationships, v superficial

124
Q

Define narcissistic personality disorder and list some of its features

A

pervasive pattern of grandiosity, lack of empathy and hypersensitivity to the evaluation of others
Thinks the world is – a competition
Thinks people are – inferior
Thinks they are – special
Commonest behaviour – competitiveness
Least likely to be – humble

125
Q

Name some other conditions that are thought to have a genetic link with personality disorders seen in Cluster B?

A

Depression
Bipolar
Substance abuse disorder

126
Q

What personality disorders can be seen in Cluster C?

A

Obsessive-Compulsive Personality Disorder (ICD), or Anankastic (DSM)
Anxious (ICD) or Avoidant (DSM)
Dependant PD

OAD

127
Q

Define anankastic/obsessive compulsive personality disorder and list some of its features

How can it be distinguished from OCD (obsessive compulsive disorder)

A

pervasive pattern of perfectionism and inflexibility

  • Excessive doubt, caution, rigidity and stubbornness
  • Preoccupation with details, rules, lists, order
  • Perfectionism interfering with task completion
128
Q

Define avoidant/anxious personality disorder and list some of its features

How is it different to social phobia

A

pervasive pattern of social discomfort, fear of negative evaluation and timidity

Persistent feelings of tension and inadequacy
* Social inhibitions
* Unwillingness to become involved with people unless
certain of being liked
* Restriction in lifestyle to maintain physical security

Social phobia is ansiexty related to specific things, like crowded spaces, public speaking etc - but Anxious persoanality disorder is more general and widespread

129
Q

Define dependant personality disorder and list some of its features

A

Definition = pervasive pattern of dependent and submissive behaviour
Thinks the world is – overwhelming
Thinks people are – stronger and more competent than themselves, wants people to make decisions for them
They are - needy
Commonest behaviour – clinging

V vunverable to getting in abuse, controlling relationships,

130
Q

Outline some of the management optiosn seen in helping those with personality disorders

A

Structure, consistency and clear boundaries (i.e. agreement of behaviour that is acceptable and unacceptable)

help with housing and other social
matters

Drugs are sometimes used to treat specific PD traits, e.g. mood stabilisers for impulsivity (not generally recommended because of lack of evidence).

Continuity of care very important – changes in doctors etc. may invoke strong emotional reactions

131
Q

What is some additional treatment you can give for treatment for an boarderline personality disorder?

A

Medications – mood stabilisers, sedatives during borderline PD crises

Mood stabilising medication
Topiramate
Lithium
Valproate
Lamotrigine

Adapted CBT for borderline PD

132
Q

Outline some different examples of SSRIs

A

Sertraline
Citalopram
Fluoxetine

133
Q

Outline the method of action for SSRIs

A

SSRIs inhibit the reuptake of serotonin. As a result, the serotonin stays in the synaptic gap longer than it normally would, and may repeatedly stimulate the receptors of the recipient cell

134
Q

What are some side effects of SSRIs?

A

Nausea, indigestion
Worsening of sexual dysfunction
Weight gain
Suicidal thoughts in younger people
Serotonin syndrome

135
Q

What are some drugs that SSRIs interact with, that you would need to provide w PPI cover?

A

NSAIDs, Aspirin and Heparin - give a PPI cover

NB - fluoxetine and paroextine have higher risk of interaction, as particulary good at inhibiting Liver enzymes

136
Q

What are some drugs that can precipitate serotonin syndrome in people with SSRIs?

A

Linezolid
Monoamine oxidase inhibitors (MAOIs)
Lithium
MDMA
Tramadol
St. John’s wort
Tricyclic antidepressants (TCAs)
Serotonin-norepinephrine reuptake inhibitors (SNRIs)

NB - fluoxetine and paroextine have a higher risk of interaction, as particularly good at inhibiting Liver enzymes

137
Q

Give some roles of Serotonin in the brain

A

CNS
Modulates thermoregulation, behaviour and attention

PNS
Regulates GI motility, vasoconstriction, bronchoconstriction, uterine contraction

Other
Promotes platelet aggregation (combined use with antiplatelet can increase bleeding risk

138
Q

What is serotonin syndrome?

A

Serotonin syndrome (SS) is a group of symptoms that may occur with the use of certain serotonergic medications or drugs.

Diagnosis is based on a person’s symptoms and history of medication use. Other conditions that can produce similar symptoms such as neuroleptic malignant syndrome, malignant hyperthermia, anticholinergic toxicity, heat stroke, and meningitis should be ruled out

139
Q

What are some symptoms of serotonin syndrome

A

The symptoms are often present as a clinical triad of abnormalities:

Cognitive effects: headache, agitation, mental confusion, hallucinations, coma

Autonomic effects: shivering, sweating, hyperthermia, vasoconstriction, tachycardia, nausea, diarrhea.

Neuromuscular hyperactivity : myoclonus (muscle twitching), hyperreflexia (manifested by clonus), tremor.

140
Q

What is the management of serotonin syndrome?

A

IV fluids, cooling measures
Benzodiazepines
Stop offending agent
If Sx persist after stimulus removed, consider cyproheptadine (serotonin antagonist)

141
Q

Outline examples of SNRIs

A

Venlafaxine
Duloxetine

142
Q

What is the MOA of SNRIs?

A

Leads increased concentration of norepinephrine in the synaptic cleft. - Inhibits 5HT reuptake pumps and NAd transporter

At low doses, they act like an SSRI - noradrenaline changes don’t occur much at low doses

143
Q

What are some side effects of SNRIs?

A

aise BP, contraindicated in heart disease
Similar to SSRIs

Similar to SSRI = Sweating

Dose-dependant hypertension

144
Q

Outline some examples of tricyclic antidepressants

A

Amitriptyline

Imipramine

Clomipramine

Dosulepin

Higher Dose depression, lower dose - used for pain

145
Q

Outlline the MOA of tricyclic antidepressants

A

Action on the presynaptic neurone - inhibit the uptake of monoamines at the presynaptic membrane (bind to ATPase monoamine pump)

Increase serotonin, noradrenaline

Decrease acetylcholine, histamine, sodium and calcium

146
Q

What are some side effects of tricyclic antidepressants?

A

Dangerous in overdose due to It affecting sodium and calcium - very cardiotoxic
CHECK ECG IF THE PATIENT IS ON THESE
Look for
- Wide QRS - more than 3 small squares
- Sinus tachycardia

Anticholinergic side effects:
Blurred vision - pupil dilation
Urinary retention
Dry mouth
Constipation
Confusion
agitation

147
Q

When would you consider using Monoamine Oxidase inhibitors?

A

MAOIs are seldom used, and then only in treatment -
resistant depression or atypical depression old fashioned

(depression with increased sleep, increased appetite, and phobic anxiety).

Basically, in atypical depression

148
Q

How do monoamine oxidase inhibitors work?

A

MAOIs inactivate monoamine oxidase enzymes that
oxidise the monoamine neurotransmitters, such as dopamine, noradrenaline, serotonin (5 - HT), and tyramine. - more of them in the CNS

149
Q

What are some side effects of Monoamine oxidase inhibitors?
Give some examples of them

A

Can cause v. v. high BP if taken with tyramine (aged cheese, cured meats, broad beans). Tyramine reaction crisis can lead to SAH

anticholinergic side - effects, weight gain, insomnia, postural hypotension, tremor, paraesthesia of the limbs, and peripheral oedema

eg Selegiline, Phenelzine

150
Q

Give some side effects of atypical antidepressants, like Mirtazapine

A

Drowsiness
Weight gain

151
Q

Define Phenomenology - how does it shape psychiatric practise?

A

the direct investigation and description of phenomena as consciously experienced by an individual, namely a patient

Pysch, emphasises that psychiatric symptoms should be diagnosed according to their form rather than according to their content.

This means, for example, that a delusion is a delusion not because it is deemed implausible by a person in a position of authority, such as a doctor, but because it
is ‘ an unshakeable belief held in the face of evidence to the contrary, and that cannot be explained by culture orreligion ’
<3 xxxx

152
Q

When would you perscribe lithium?

A

acute manic episodes and in the long-term prophylaxis of Bipolar affective disorder

Lithium should only be started if there is a clear inten
ion to continue it for at least three years, as poor complince and intermittent treatment may lead to rebound mania. The starting dose of lithium should be cautious

153
Q

What are some side effects of lithium at lower dose?

A

Side effects - at lower doses 0.4-1 mmol/L
* Nausea
* Fine tremor
* Weight gain
* Oedema
* Polydipsia and polyuria
* Hypothyroidism

154
Q

What are some side effects of lithium toxicity? Above 1.0 mmol/L

A

Above 1.0 mmol/L
Signs of toxicity
* Vomiting
* Diarrhoea
* Coarse tremor
* Slurred speech
* Ataxia
* Drowsiness and confusion

Lithium is Teratrogenic!!

155
Q

What pyschiatric disorder could you use sodium valporate and carbamazepine, and lamotrigeine for?

A

Bipolar, prophylactically

They are Teratrogenic!!

156
Q

What are some side effects of Sodium valporatte and lamotrigine ?

A

Lamotrigine
Skin reactions (including Stevens–
Johnson syndrome)
aseptic meningitis drowsiness
diplopia
leucopenia
insomnia

Sodium valpoarate
Nausea
Gastric itrartaion
diarrhoea
Weight gain

They are Teratrogenic!!

157
Q

Name 3 broad kinds of psychological therapies

A

1 Supportive therapy

Explorative pyschotherapies=
2 Cognitive and Behavioural therapies
3 Psychodynamic therapies

158
Q

Outline what is seen in supportive therapy - for what may it be used?

A

Explanation and reassurance

establishing rapport, facilitating emotional expression, reection, reassurance

  • Non-directive problem-solving,
    e.g. for adjustment disorders, stress, bereavement
  • Mild depression or anxiety

Counselling is similar to supportive therapy
in that it involves explanation, reassurance, and support.

159
Q

Outline what is seen in CBT

A

This is a therapy with works on the interplay between thoughts, emotions and behaviours. Its aim it to tackle both negative the cognitive thinking and behaviour in mental illness.

a) Cognitive –> Aim is to help people identify and challenge automatic negative thoughts and abnormal beliefs

b) Behaviour –> This is based on learning theory of operant condition (positive and negative reinforcement)

– If people have habitual wrong behaviours (e.g. avoidance in anxiety) it teaches people relaxation techniques and gradual exposure with positive reinforcement to change their behaviour.

160
Q

For what things can CBT be used to treat?

A

CBT is used to treat depression, anxiety, eating disorders and
some personality disorders. It can also be used to treat psychosis

161
Q

Outline what is seen in psychodynamic/pyshcoanalyitc therapies

A

psychoanalysis stems from the work of Sigmund Freud.

  • views human behaviour as determined by unconscious forces derived from primitive emotional needs.

Therapy aims to resolve longstanding underlying conflicts and unconscious defence mechanisms (e.g. denial, repression).

Helping the person to become more aware of the unconscious processes which are giving rise to
symptoms or to difficult repeating patterns

Helping the person construct a narrative of their life and give meaning to symptoms

162
Q

What is the general procedure seen in Psychodynamic therapies?

e. g. Psychoanalysis + Psychodynamic Psychotherapy

A

– The patient explores their subconscious by using free association (says whatever is on their mind)

– The therapist interprets these statements to link the patient’s past experience with their current life and their relationship with the therapist. This uses 2 skills:

– Transference –> when the patient re-experiences strong emotions from early relationships with the therapist

– Counter-transference –> When the therapist experiences strong emotions towards the patient

The relationship heals!!!!!!

163
Q

Outline what is seen in
Cognitive Analytic Therapy (CAT)

For what can it be used?

A

Short time, cheaper pyschological treatment

– It looks at the ways an individual think and feels and the events and relationships underlying experiences.

– They key of this therapy is reflection after – therapist writes a goodbye letter and asks patient to respond - gets patients to find new nad better ways of coping with established problems

Used in ‘Personality Disorder’, Eating disorders

164
Q

What is seen in Dialetcai ldehvaiour therapy? When may it be used?

A

similar to CBT and also provides group skills training to equip the individual with alternative coping strategies

Skills such as mindfulness (bringing one’s attention back to thepresent moment), which is derived from Buddhist meditation.

Used for those with Boarderline personality disorders, eating disorders

165
Q

Outline what is seen in Eye movement desensitization and reprocessing

A

– Patients then recall the disturbing events and the emotion they felt at the time (e.g. sexual abuse and feeling powerless

– They then work together to create a positive belief about the event (“I am stronger now and so not powerless”)

– The therapist then activates both sides of your brain using Dual Activation Stimulation (DAS) by making they do eye movements usually involves the therapist directing the patients’ lateral eye movements by asking them to look first one way then the other
(saccadic eye movements)

– This allows the brain to reprocess the upsetting memories by removing the old emotion and replacing it with the more positive, empowering emotion

– This means the memory is no longer experienced as a traumatic.

166
Q

What is seen in interpersonal psychotherapy, and for what may it be used for?

A

IPT is a talking treatment that helps people with depression identify and address problems in their relationships with family, partners and friends.

The idea is that poor relationships with people in your life can leave you feeling depressed, it gets the patient to view their emotions in terms of their interpersonal network e.g. a close member may have died (causing grief)
The rest of the session then involves work on how to cope and change their views of these events and transform their relationship into a positive one

used for moderate and severe depression

IPT is usually offered for 16 to 20 sessions.

167
Q

What is ECT? For what can it be used for?

A

Electroconvulsive Therapy - uses electrodes to induce a modified cerebral seizure

Severe depression
Prolonged or severe episode of mania that has not responded to treatment
Cataonia

ECT should be used to induce fast and short-term improvement of severe symptoms after all other treatment options have failed, or when the situation is thought to be life-threatening (because of high risk of suicide or not eating and drinking).

168
Q

How is ECT thought to work?

A

This is a treatment option which uses electrodes to induce a modified cerebral seizure in the brain

– This leads to massive amounts of neurotransmitter release, hormone secretion and a transient increase in blood brain barrier permeability.

– It is used to induce fast improvement after all other treatment options have failed

169
Q

When does English Mental Health Act permit
ECT to be given?

A

Patient gives informed consent
(before every treatment)

The patient lacks capacity, and it does not conflict with
advance decision
AND
It’s an emergency, and the independent consultant has
not yet assessed (Section 62 of Mental Health Act)
OR
An Independent Consultant (appointed by Mental Health Act Commission) agrees to it

IF A PATIENT HAS CAPACITY AND REFUSES, IT CANNOT BE GIVEN

170
Q

Outline the procedure of ECT

A

Procedure:

– Patient is nil-by-mouth for 4 hours before intervention

– Patient is given short-acting anaesthetic + muscle relaxant drug

– Preoxygenation is given to increase SpO2

– A shock is delivered to the scalp either bilaterally or unilaterally

– This evokes a 20-60s seizure within the brain

171
Q

What are some contraindications for ECT

A

– Raised intracranial pressure (absolute)

– Stroke and MI (relative contraindication

172
Q

What are some side effects of ECT?

A

Patients have reported that ECT causes cognitive impairment.
Therefore cognitive function should be assessed prior to, during
and after a course of treatment. Assessment should include:
* orientation and time to reorientation after each treatment,
* new learning,
* retrograde amnesia,
* subjective memory impairment.
* dysrhythmias due to vagal stimulation,
postictal headache,
* confusion,
* retrograde and anterograde amnesia with difficulties in registration and recall that may persist for several weeks

173
Q

What is Neuroleptic malignant syndrome?

A

Psychiatric emergency caused by excess of neuroleptic medication (aka both typical and atypical antipsychotics) or acute withdrawal from Parkinson’s medication

Cocaine and ectasy can also cause it

174
Q

Why does Neuroleptic malignant syndrome happen? What are some symptoms of it?

A

NMS results from as dopaminergic hypothalamic spinal tracts are blocked, so they can’t tonically inhibit preganglionic sympathetic neurons as usual

Occurs over hrs-days (within 10d) - gradual
Hyperpyrexia
Hyporeflexia
Fluctuating consciousness
Diffuse rigidity
Raised CK - Rhabdomyolysis can occur

175
Q

What is the management of Neuroleptic malignant syndrome?

A

The mainstay of treatment involves stopping
the drug and supportive measures such as oxygen, IV fluids, and cooling blankets

Drugs - dantrolene and lorazepam may also be used to decrease muscle rigidity.

176
Q

What are some symptoms of opiate overdose

A

Acute presentation = drowsiness
Respiratory depression -> resp acidosis CO2 retention)
Hypotension
Tachycardia
Pinpoint pupils
Chronic = constipation

177
Q

What is the management of an opiate overdose?

A

ABCDE approach

  • Methadone (opioid agonist) or buprenorphine (opioid partial agonist) are first line; they are less euphoriant and have a
    relatively long half-life than opioids of abuse.
  • Lofexidine is sometimes used for short detoxification treatments or where abuse is mild or uncertainNaltrexone (opioid antagonist) blocks the euphoric effects and
    is occasionally used to help prevent relapse.
178
Q

What are some signs of opioid withdrawal?

A

Clinical features of withdrawals are mediated by noradrenaline overactivity:
* Dilated pupil
* Tachycardia + hypertension
* Insomnia, restlessness, anxiety, irritability,
tremor
* Abdo pain, nausea, vomiting, diarrhoea
* Watering eyes
* Muscle aches

Treatment Lofexidine

179
Q

In both ICD - 10 and DSM - IV the first step in diagnosis is to specify the substance or class of substance - what kind of substances are commonly involved in substance abuse?

A

ICD - 10
F10 Alcohol
F11 Opioids
F12 Cannabinoids
F13 Sedatives or hypnotics
F14 Cocaine
F15 Other stimulants, including caffeine
F16 Hallucinogens
F17 Tobacco
F18 Volatile solvents
F19 Multiple drug use and other

180
Q

The second step in diagnosis is to specify the type of
disorder involved, according to the ICD 10 - what types of substance abuse disorders are there?

A

ICD - 10
.0 Acute intoxication
.1 Harmful use
.2 Dependence syndrome
.3 Withdrawal state
.4 Withdrawal state with delirium
.5 Psychotic disorder
.6 Amnesic syndrome
.7 Residual and late-onset psychotic disorder
.8 Other mental and behavioural disorders

181
Q

Give some risk factors for a substance abuse disorder

A

Addiction liability - depends on:
How substance taken: orally, injection, inhaling
Rate substance crosses blood brain barrier and triggers reward pathway in brain
Time takes to feel effect of substance
Substance ability to induce tolerance ± withdrawal symptoms

Male
Aged ~ 18-25
Mental health conditions: ADHD, bipolar, depression, GAD, panic disorder, PTSD
Adverse childhood experiences: childhood abuse/neglect, witnessing domestic violence, family members with SUD

182
Q

How many g and ml is one unit of alchohol

A

One unit of alcohol is equivalent to 10ml or 8g of pure alcohol

183
Q

Outline some of the physiological effects that alcholol has on the body

A
  • Alcohol increases GABA function (GABA-A receptor activation)
  • GABA is the main inhibitory neurotransmitter in the brain - calming effect
  • Alcohol reduces glutamate function - inhibitory action at NMDA glutamate receptors
    ○ Glutamate is the major excitory neurotransmitter that is involved in brain processing such as learning and memory
    ○ Effects on glutamate lead to amnesia and sedation
184
Q

What are some signs of alchohol dependance?

A

CANT STOP
C - compulsion to drink
A - aware of harms but persists
N - neglect of other activities
T - tolerance to alcohol
S - stopping causes withdrawal
T - time preoccupied with alcohol
O - out of control use
P - persistent, futile wish to cut down

Withdrawal
Tremors
Anxiety
Nausea, vomiting
Headache
Tachycardia
Irritability, aggression
Delirium

185
Q

What are some investigations/questionaires to screen for alcohol dependency?

A

CAGE questionnaire screening
C - do you ever think about cutting down
A - do you get annoyed when others comment on drinking habit
G - ever feel guilty about drinking
E - ever drink in morning (eye-opener)

AUDIT questionnaire
Developed by WHO
Multiple choice for harmful alcohol use screen

186
Q

What are some blood tests results you would see in an alcoholic?

A

Bloods
Raised MCV
Raised ALT and AST (AST:ALT ratio above 1.5 suggests ALD)
Raised GGT
Raised ALP later in disease
Raised bilirubin in cirrhosis
Low albumin (reduced synthetic function of liver, reduced clotting factor production)
Deranged U&Es in hepatorenal syndrome

187
Q

What is the management for someone who is alcohol dependant?

A

Management – Patients are often referred to an alcohol dependence programme to help them quit.

– They can use a mixture of behavioural interventions (e.g. CBT) and pharmacological treatment

– Disulfiram –> this inhibits acetaldehyde dehydrogenase, so people feel hungover as soon as they drink alcohol (avoid in ischaemic heart disease)

– Acamprosate –> this is a weak NMDA antagonist which is used to reduce alcohol craving

188
Q

Outline the pathophysiology behind delirium tremens

A

Alcohol boosts GABA, which inhibits the brain and dampens excitatory glutamate receptors. Over time, the brain adapts, becoming more sensitive to excitatory signals.

When alcohol stops, the brain becomes overactive, causing symptoms like confusion and agitation.

189
Q

what are some symptoms of delerium tremens? What is the management?

A

Symptoms – Together they are called delirium tremens – Early on –> increased anxiety, with sweating and agitation

– After 24 hours –> Seizures with visual hallucinations

– From 48-72 hours –> Course tremors, agitation, delusions and severe visual hallucinations

Management – 1st line is benzodiazepine chlordiazepoxide

190
Q

What is the mangaement of alchohol withdrawal?

A

Pharmacological management of alcohol withdrawal and detoxification
* Chlordiazepoxide - benzodiazepine commonly used in the UK (long acting)
* Diazepam (long acting)
* Lorazepam (short acting) - can be considered when there is liver injury
Oxazepam (short acting)

191
Q

How can we gauge the severity of alcohol withdrawal?

A

The CIWA-Ar is used to guide the pharmacological management of alcohol withdrawal.

Clinicians add up scores for all ten criteria. The total CIWA score can be used to assess the presence and severity of alcohol withdrawal:

Absent or minimal withdrawal: score 0-9
Moderate withdrawal: score 10-19
Severe withdrawal: score > 20
The total CIWA score influences the frequency at which further observations are made:

Initial score is ≥ 8: repeat hourly for 8 hours. Then if stable 2-hourly for 8 hours. Then if stable 4-hourly.
Initial score < 8: assess 48-hourly for 72 hours and if score < 8 for 72 hours, discontinue assessment.
The total CIWA score guides clinicians with regards to the need for pharmacological management of alcohol withdrawal:

Symptom-triggered regimen (not prescribed regular withdrawal medication): give PRN medication when CIWA score is ≥ 8
Fixed-dose reducing regime with PRN medication (prescribed regular withdrawal medication): give additional PRN medication if CIWA score is ≥ 15

192
Q

Define Wernicke’s Encephalopathy

A

is a neurological emergency resulting from thiamine deficiency with varied neurocognitive manifestations.

193
Q

What is Korsakoff’s Syndrome? How is it related to Wernickes?

A

Hypothalamic damage & cerebral atrophy due to thiamine
(vitamin B1) deficiency (eg in alcoholics).

Wernicke’s encephalopathy is the acute, reversible stage of the syndrome, and if left untreated it can later lead to Korsakoff syndrome, which is chronic and irreversible.

194
Q

How can chronic alcoholism lead to a thiamine deficiency?

A

It block the phosphorylation of thiamine, stopping it from being converted into its active form

Ethanol reduces gene expression of Thiamine transporter, so can stop it getting absorbed in the duodenum.

Alcoholic tend to have a poor diet, relying on alcohol for calories so will not get enough Thiamine (b1) anyway

195
Q

How can a lack of thiamine (vit B1) affect the brain?

A
  • Thiamine deficiency impairs glucose metabolism and this leads to a decrease in cellular energy.
  • The brain is particularly vulnerable to impaired glucose metabolism since it utilises so much energy.
196
Q

What is the classical triad seen in Wernicke’s encephalopathy?

A

1 confusion
2 ataxia (wide-based gait; fig 2)

3 ophthalmoplegia (nystagmus,
lateral rectus or conjugate gaze palsies).

197
Q

What does Wernicke - Korsakoff syndrome predominantly target? What symptoms does this cause?

A
  • Mainly targets the limbic system, causing severe memory impairment:
    • Anterograde amnesia: inability to create new memories
    • Retrograde amnesia: inability to recall previous memories.
    • Confabulation: creating stories to fill in the gaps in their memory which they believe to be true.
    • Behavioural changes
198
Q

What investigations would you do in suspected Wernicke’s encephalopathy?

A
  • Diagnosis is typically made based on clinical presentation
  • Bloods including LFTs: measure thiamine levels, measure blood alcohol levels, liver function may be deranged in alcoholism
  • Red cell transketolase test: rarely done, thiamine is a co-enzyme to transketolases so transketolase activity will be low
  • MRI/CT: can confirm diagnosis by showing degeneration of the mammillary bodies

Lumbar puncture to rule out other causes of the symptoms of wernickes

199
Q

What is the management for Wernicke’s encephalopathy?

A

Urgent replacement to prevent irreversible Korsakoff’s syndrome (p718). Give thiamine (Pabrinex®)

Oral supplementation (100mg OD) should continue until no longer ‘at risk’, give other B vitamins as well

Correct Magnesium deficiency as well
If there is coexisting hypoglycaemia, correct it

200
Q

Why do you need to give Thiamine before you give glucose in a patient with Wernicke’s?

A

it’s important to normalise the thiamine levels first, because without thiamine pyrophosphate, most of the glucose will become lactic acid and that can lead to metabolic acidosis. (often the case in
this group of patients),

make sure thiamine is given before glucose, as Wernicke’s can be caused by glucose administration to a thiamine-deficient patient -

NOT GIVING THIAMINE AS YOU JUST THINK ITS HYPOGLYCAEMIA IS A COMMON MISTAKE DOCTORS MAKE

201
Q

How do cocaine and ampethamines work?

A

These drugs block the reuptake of dopamine and noradrenaline (and 5-HT) increasing transmission at synapses

202
Q

What are some signs of a cocaine/amphetmanie overdose?

A

Main effect – Increased energy and concentration, euphoria and hyperactivity

Side effects:

– Cardiovascular –> Increased pulse, blood pressure, hyperthermia, can lead to aortic dissection

– Heart –> QRS widening and QT prolongation

– GI –> Reduced appetite and ischaemic colitis

– Psychological –> Insomnia, agitation and hallucinations e.g. formication (sensation of ants under the skin)

– If you take a prolonged large dose, the euphoria can turn to depression and anxiety

– Can get psychosis –> delusions, visual and auditory hallucinations

203
Q

What is the management of a cocaine overdose?

A

– IV benzodiazepines + treat complications (heart attack, aortic dissections) + antipsychotics

204
Q

What are the 5 key principles you must consider when assessing mental capacity

A

i) A person is assumed to have capacity is assumed until it is established that the person lacks it

ii) A person should not be treated as unable to decide unless all practicable steps to help them have failed

iii) A person should not be treated as unable to decide just because it is unwise

iv) Decisions made on behalf of an incapable person must be in their best interests

v) Regard should be taken to find the solution which is least restrictive of the person’s rights and freedom of action

205
Q

Under the MCA, what are the 3 reasons why you may provide treatment for someone who does not have capacity?

A

– If a valid advanced decision to refuse treatment exists

– If a valid Lasting Power of Attorney for Health and Welfare exists

– If neither exists, the person providing treatment should act in the patient’s best interests.

206
Q

In order to section someone (forcibly admit someone to hospital/secure setting), for assessment what is grounds/personal is required and for how long? What part of the MHA?

A

Under section 2 of the mental health act

Need 2 Drs: one section 12 approved, one ideally previous contact w/ pt, and then approval from approved mental health professional (AMHP) to confirm the section.

Patient suffering from mental disorder to degree that warrants detention in hospital for assessment

Pt should be detained for own health/safety or the protection of others

Lasts 28 days, cannot be Cannot be renewed

207
Q

In order to section someone (forcibly admit someone to hospital/secure setting), for treatment what is grounds/personal is required and for how long? What part of the MHA?

A

Under section 3 of the mental health act

Again, Need 2 Drs: one section 12 approved, one ideally previous contact w/ pt, and then approval from approved mental health professional (AMHP) to confirm the section.

Patient suffering from mental disorder to degree that warrants detention in hospital for treatment.
Pt should be detained for own health/safety or the protection of others
The treatment needed cannot be effectively provided unless the patient is detained.
Appropriate medical treatment is available to them.

lasts 6 months, can be renewed

208
Q

What is outlined in section 4 of the MHA?

A

Patient suffering from mental disorder to degree that warrants detention in hospital for assessment
Pt detained for own safety/safety of others
Not enough time for 2nd Dr to attend i.e. due to risk

1 Dr (does not need to be section 12 approved)

Can only last 72 hours

209
Q

What is outline in section 5 of the mental health act, both in 5(2) and 5(4)

A

For pt already admitted (to psychiatric/general hospital) but wanting to leave

section 5(4) says Nurses can detain patients in hospital (this is their holding power until a Dr can attend,) for 6 hours

Section 5(2) says Doctors (this is their holding power until section 2/3 can be put in place)
NB - has to be Dr on a specific ward, cannot be done in A&E, for 72 hours

210
Q

What is outlined in section 135 of the mental health out

A

135 - allows police to enter house and mreove a patient to a place of safety

136 allows police to take someone to a place of safety for an assessment

Both can be done by a police, but the should try and confirm this with a doctor or nurse
Both for a duration of 72 hours

211
Q

If a patient has been detained under section 2,3,35,36 or 37, is consent required for treatment

A

Consent to Treatment
As a general rule, once a patient is detained under S2, 3, 35, 36 or 37 of the MHA, consent is not required for the administration of psychiatric treatment.

– The justification for treatment is provided by S63 which states that:

“The consent of a patient shall not be required for any medical treatment given to him for the mental disorder from which he is suffering”

Treatments are Covered by S63

All medical treatment for the mental disorder, including:

Treatments for the disorder itself (e.g. antipsychotics for schizophrenia)
Treatments for conditions causing the disorder (e.g. hypothyroidism causing depression)
Treatments for the physical consequences of the disorder (e.g. NG in anorexia)
Safe holds and physical control and restraint (when necessary)

212
Q

Define what self harm is - what are some reasons for it?

A

Intentional non-fatal self-inflicted harm

  • a desire to interrupt a sequence of events seen as inevitable and undesirable
  • a need for attention
  • an attempt to communicate/express themselves
  • a true wish to die

Used to express something hard to put into words, change emotional pain into physical pain, have a sense of being in control, punish themselves for feelings/experiences…

213
Q

What are some risk factors for self harm

A

Unlike completed suicide, DSH is more frequent in women,
the under-35s, lower socia l classes and the single or divorced.
* Like suicide, DSH is associated with psychiatric illness, particularly depression and personality disorder

214
Q

What are some clinical signs of self harm?

A

Cuts/scratches on arms/legs
Picking at skin
Burns
Bruising
Weight loss/weight gain
Hair loss (pulling at hair)

215
Q

When assessing self harm/suicide attempt, what are the 3 domains you should split factors into?

A

Before
During
After

216
Q

Suicide and self-harm risk assessment - what things should you try to find out about BEFORE they attempted suicide/self-harm?

A

Precipitants - specific event/build up?

Planned/impulsive?

Precautions taken against discovery? (left the house, turned off phone etc)

Alcohol/recreational drugs at time of event? - suggests more impulsive

217
Q

Suicide and self-harm risk assessment - what things should you try to find out about DURING they attempted suicide/self-harm?

A

Method (if drugs - what did they take, how much)
Was pt alone
Where was it - more remote = higher risk
What went through mind at the time
Did they think their self-harm would end their life?
What did they do straight after the self-harm?

218
Q

Suicide and self-harm risk assessment - what things should you try to find out about AFTER they attempted suicide/self-harm?

A

Did pt call anyone? Go to A&E?
Who were they found by
How they felt when help arrived
Current mood
Still feel suicidal? - would they attempt again

219
Q

What are some management options for self harm?

A

A good first step is to agree with patients what their problems
are and what immediate interventions are both feasible and
acceptable to them.
* Ensure that they know who they can turn to if suicidal intent
returns (e.g. A & E).
* Crisis Resolution Team referral may be necessary if suicidal
ideation is present.
* Think about reducing access to means of suicide if possible –
for example, by encouraging patients to dispose of unneeded tablets from the home, and by prescribing antidepressants of lower
lethality (e.g. SSRIs rather than tricyclics) and in small batches.
* Consider psychological therapy and encouraging engagement
in self-help and community social and support organisations.

220
Q

What are some risk factors for suicide?

A

SAD PERSONS

Sex (male)
Age <19 or >45
Depression

Previous suicide attempt
Excess alcohol or substance use
Rational thinking loss
Separated or single
Organised plan
No social support
Sickness

221
Q

What are some clinical signs of suicidal behaviour?

A

Warning signs:
* Obsessive thinking about death
* Feelings of hopelessness, worthlessness, helplessness
* Behaviours suggestive of absolute death wish:
○ Put financial affairs in order
○ Visiting people to say goodbye

in community, awareness of pts who:
Frequently, repeatedly attend
Disengaged w/ services
Prescribed several antidepressants
Heightened concern from family members

222
Q

what are some principles around suicide prevention?

A
  • Detect and treat psychiatric disorders.
  • Be alert to risk and respond appropriately to it.
  • Prescribe safely
  • Give urgent care at appropriate level of patients with suicide intent – refer to Crisis Resolution and Home Treatment Teams.
  • Can also admit for hospitalization (consider detention under the Mental Health Act) if patients considered unsafe outside hospital even with intensive support.

*Provide careful management of deliberate self-harm (DSH)

  • Act at the population level, tackling unemployment and reducing access to methods of self-harm.