Psychiatry Flashcards

1
Q

Schizophrenia - define, clinical features, dx & management

A

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

Most common form of psychosis with an onset typically early in life (15 to 35). Chronic condition characterised by acute episodes of psychosis

Hallucinations - ‘‘perceptions in absence of stimuli’’
○ Most commonly auditory
Delusions - fixed false belief
Thought & speech disorders
Negative symptoms
○ alogia (poverty of speech), emotional blunting, social isolation, self-neglect and avolition (lack of self-will).

Clinical dx - investigate to r/o infection, metabolic abnormalities & organic brain disease
• Particular interest in autoimmune encephalitis (esp anti-NMDA R)

Pharmacological
• Atypical antipsychotics - 6 to 8 week trial
○ Olanzapine, quetiapine
• Treatment resistant schizophrenia (not responding to 2+ antipsychotics)
○ Clozapine
• Depot Antipsychotic - IM injection every 2-4wks

Psychological
	• Education & support 
	• CBT
	• Family interventions
Art therapy
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2
Q

Schizoaffective Disorder - define

A

Characterised by symptoms of schizophrenia & a mood disorder (depression or mania) in the same episode of illness

Mood symptoms should meet the criteria for either a depressive illness or a manic episode together with one or two typical symptoms of schizophrenia

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3
Q

Post Natal Depression - define, RFs, S&S & management

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DEFINITION: Low mood in the post-natal period, occurs in about 1 in 10 women, with a peak around 3mths after birth

Often starts within 1-2mths of giving birth but can start several months after having the baby

Aetiology & Risk factors:
Possible causes/reasons why:
• Environmental/situational circumstances e.g. recent stressful situations, domestic violence in the past,
• Previous mental health problems, including depression
• Depression or anxiety during pregnancy
• Poor support from partner, family or friends – or marital difficulties

Risk Factors:
	• Pre-existing mental illness
	• Family history
	• Depression in pregnancy
	• Significant social stressors
	• Physical health – anaemia/ hypothyroid
Presentation/Clinical Features:
Classical triad of: low mood, anhedonia & low energy
	• Persistent low mood
	• Insomnia
	• Loss of appetite
	• Loss of energy/drive
	• Reduced motivation/self care
	• Feelings of inadequacy as a mother
	• Suicidal thoughts
	• Thoughts of harm to baby & psychotic symptoms in severe cases --> Puerperal Psychosis

Management:
• Support – various dependent on severity
• Severe cases may require specialist support or admission to MBU
• Self help for mild/moderate cases
• Talking Therapies
• Medication

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4
Q

Puerperal Psychosis - define, risk factors, S&S & management

A

DEFINITION: A psychiatric emergency - psychosis which develops shortly after giving birth

Rare but serious condition, which approx. 1 in 1000 women develop & typically occurs 2-3weeks after delivery

Aetiology & Risk factors:
• Previous post-natal psychosis
• Women w/ past history of bipolar or schizoaffective disorders

Cause is unknown but may have genetic factors & the hormonal changes and sleep deprivation which occurs in new mums may be a factor

Presentation/Clinical Features:
Symptoms can vary & change rapidly - within hours
	• High mood
	• Depression
	• Confusion
	• Hallucinations 
	• Delusions
	• Changes in personality 
Management:
Preventative support
	• Mum's who may be at risk should have preconception counselling
	• Specialist support during pregnancy
	• Pre-birth planning care plan
Treatment
	• Urgent assessment & diagnosis
	• Transfer to mother & baby unit
	• Pharmacological options inc: antipsychotics, mood stabilisers 
	• CBT

Prognosis
Most severe symptoms 2-12 weeks & a full recovery can take 6-12mths (most women do make full recovery)

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5
Q

Depression - define, RF, S&S, investigations & management

A

DEFINITION: An affective mood disorder characterised by persistent low mood, loss of pleasure and/or lack of energy accompanied by emotional, cognitive & biological symptoms

Pathophysiology & Aetiology
• Genetic x Environment model; multi-factorial & influenced by number of bio-psychosocial factors
• Twin studies estimate hereditability of depression as 40-50%, multiple genes likely involved
• Monoamine hypothesis - deficiencies causing depression
• HPA overactivity
• Psychosocial factors can increase the likelihood of developing depression
○ .e.g. personality type, stressful life events and failure of effective stress control mechanisms

Risk factors - ‘FF, AA, PP & SS’
• Female & family hx
• Alcohol/adverse events
• Past depression/physical co-morbidities
• Lack of social support/socioeconomic status

Presentation/Clinical Features:
Symptoms can be divided into: core, cognitive, biological & psychotic

Core
• Anhedonia
• Low mood
• Lack of energy

Cognitive 
	• Lack of concentration 
	• Negative thoughts 
	• Excessive guilt 
	• Suicidal ideation 

Mild depression = 2 core symptoms + 2 other symptoms
Moderate depression = 2 core symptoms + 3–4 other symptoms
Severe depression = 3 core symptoms + ≥4 other symptoms
Severe depression with psychosis = 3 core symptoms + ≥4 other symptoms + psychosis

Biological
	• Diurnal variation in mood
	• Early morning waking 
	• Loss of libido
	• Psychomotor retardation
	• Weight loss/LOA

Psychotic
• Hallucinations
• Delusions

Differentials - BPD, thyroid dysfunction, r/o organic illness, substance abuse, normal bereavement

Investigations & Diagnosis:
• Thorough hx & full risk assessment if actively feeling suicidal
○ Diagnostic questionnaires e.g. PHQ-9, HADS
• Bloods
○ FBC - Hb (anaemia)
○ TFTs - hypothyroidism
○ U&Es, LFTs, Ca
○ Glucose
• Imaging
○ MRI or CT if atypical i.e. unexplained headache or personality change

Management:
Mild-Moderate Depression 
	• Watchful waiting; lifestyle, self help & reassess in 2wks
	• Antidepressants 
	• Exercise 
	• Self-help programmes
	• CBT 

Moderate-Severe Depression
• Full suicide risk assessment
• Psychiatry referral if:
○ Suicide risk is high, or depression is severe, recurrent depression, or unresponsive to treatment
• Antidepressants
○ 1st line: SSRIs e.g. sertraline, citalopram
○ Others inc TCAs, SNRIs, MAOI
• Psychotherapy
○ Refer for CBT and interpersonal therapy (IPT).
• Social support:
○ Engaging with activities in the community that the individual is avoiding or attending social support groups with others.

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6
Q

Bipolar Disorder - define, RFs, S&S, inx & management

A

DEFINITION: Chronic episodic mood disorder, characterised by at least one episode of mania/hypomania & a further episode of mania or depression

Mean age onset 19yrs of age, M=F at 1:1

Risk factors:
• Age - early 20s
• Anxiety Disorders
• After depression

* Strong family hx
* Substance misuse
* Stressful life events
Presentation/Clinical Features:
Manic Symptoms
	• Irritability
	• Distractibility
	• Disinhibited e.g. spending, social, sexual 
	• Grandiose delusions 
	• Flight of ideas
* Activity
* Increased appetite 
* Sleep decreased 
* Talkative
* Elevated mood/energy 
* Reduced concentration

Differentials - remember to always screen for mania in depressed patients, as may not necessary reveal this

Investigations & Diagnosis:
• Thorough history - screen for clinical features
○ ‘Have you had any new interests or exciting ideas lately?’ (delusions/overvalued ideas).
○ ‘Do you have any special abilities that are unique to you?’ (grandiose delusions).
○ ‘Are you afraid that someone is trying to harm you?’ (persecutory delusions).
○ Also ask about family history of bipolar affective disorder and substance misuse.
• Self-rating scales
○ Mood disorder questionnaire
• Bloods
○ FBC (routine), TFTs (both hyper/hypothyroidism are differentials), U&Es (baseline renal function with view to starting lithium), LFTs (baseline hepatic function with view to starting mood stabilizers), glucose, calcium (biochemical disturbances can cause mood symptoms).
• Urine drug test
○ Illicit drugs can cause manic symptoms
• CT head - r/o SOL

Management:
	• Full risk assessment - suicide, ask about driving 
		○ Consider Mental Health Act
	• ''CALMER''
		○ Consider hospitalization/CBT 
		○ Antipsychotics (Atypical) 
		○ Lorazepam 
		○ Mood stabilizers (e.g. lithium) 
		○ Electroconvulsive therapy 
		○ Risk assessment
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7
Q

Management of Bipolar Affective Disorder - ‘‘CALMER’’

A
• ''CALMER''
		○ Consider hospitalization/CBT 
		○ Antipsychotics (Atypical) 
		○ Lorazepam 
		○ Mood stabilizers (e.g. lithium) 
		○ Electroconvulsive therapy 
		○ Risk assessment
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8
Q

Emotionally Unstable Personality Disorder - S&S & management

A
• Abandonment feared
	• Mood instability
	• Suicidal behaviour
	• Unstable relationships
Intense relationships
• Control of anger poor
• Impulsivity 
• Disturbed sense of self (identity)  Emptiness (chronic)

• Full review & assessment of patient
	○ Co-morbid psychiatric illness and substance misuse are common in patients with PD. 
		§ recognition and treatment are essential. 
	○ Risk assessment is crucial
		§ Potential stressors that induce crises should be identified and reduced. 

• Pharmacological management will not resolve the PD, but may be used to control symptoms. 
	○ Low-dose antipsychotics for ideas of reference, impulsivity and intense anger
	○ Antidepressants may be useful in emotionally unstable personality disorder.
	○ Mood stabilizers can also be given (i.e. quetiapine) 

• Safety Netting 
	○ Give the patient a written crisis plan. At times of crisis, if dangerous and violent or if there is a suicide risk consider the Crisis Resolution Team and detention under the Mental Health Act.
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9
Q

Generalised Anxiety Disorder - define, aetiology, risk factors, clinical features, differentials, investigations & management

A

Syndrome of ongoing, uncontrollable, widespread worry about many events or thoughts that the patient recognises as excessive & inappropriate. Symptoms must be present on most days for at least 6mths duration

Aetiology of GAD can be divided into biological (genetic & neurophysiological) & environmental causes
• Biological
○ Genetic; twins & family hx (5x increase in 1st degree relatives)
○ Neurophysiological; theories around dysfunction in hippocampus & amygdala. Alterations in GABA, serotonin & noradrenaline
• Environmental
○ Stressful life events; hx of child abuse, problems w/ relationships, personal illness, employment of finances
○ Substance dependence or exposure to organic solvents

Risk Factors
Pre-disposing 
	• Genetics, childhood upbringing, personality type & demands for high achievement 
	• Being divorced
	• Living alone or as a single parent 
	• Low socioeconomic status 

Precipitating
• Stressful life events; domestic violence, unemployment, relationship problems
• Personal illness e.g. chronic pain, arthritis, COPD

Maintaining
• Continuing stressful events, martial status, living alone & ways of thinking which perpetuate anxiety

Presentation/Clinical Features:
‘‘WATCHES’’ (specific to GAD)
• Worry - excessive & uncontrollable
• Autonomic hyperactivity - sweating, increase in pupil, tachycardia
• Tension in muscles & tremor
• Concentration difficulty & chronic aches
• Headache/hyperventilation
• Energy loss
• Restlessness
• Startled easily & sleep disturbances - difficulty getting to sleep then intermittent awakening and nightmares

Differentials - depression, schizophrenia, personality disorders, excessive caffeine or alcohol consumption, withdrawal from drugs, organic (anaemia, hyperthyroidism, pheochromocytoma, hypoglycaemia)

Investigations & Diagnosis:
Bloods
	• FBC - infection & anaemia 
	• TFTs - hyperthyroidism 
	• Glucose - hypoglycaemia 

Questionnaires
• GAD-2 or GAD-7
• Hospital Anxiety & Depression Scale
• Beck’s Anxiety Inventory

Management - bio-psychosocial model
• Biological; first line is SSRI (sertraline is recommended)
○ SNRIs can also be used
○ Medication should be continued for at least 1yr
• Psychological; low vs high intensity
○ Low intensity form - psychoeducational groups
○ High intensity form - cognitive behavioural therapy & applied relaxation
• Social;
○ Includes self-help methods & support groups
○ Exercise - encouraged & may benefit

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