Psychiatry - Investigations Flashcards

1
Q

Investigations to rule out other organic causes of depression

A
FBC (low levels cause fatigue)
Blood glucose (DM causes fatigue)
TFTs (exclude hypothyroidism)
Ca levels (hyperparathyroidism can cause depression)
Vitamin D+B12 (low levels cause fatigue)
HIV/syphilis serology, drug screening

Imaging: CT or MRI – if presentation or examination is atypical or where there are features suspicious of an intracranial lesion e.g. unexplained headache or personality change

Cognitive assessment: where dementia/pseudodementia are differentials

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2
Q

Schizophrenia ix

A

full physical work up
to exclude organic causes (neurological system)
to pick up comorbid physical health problems (cardiovascular system incl weight + BP)
to ensure baseline tests have been done before starting an anti-psychotic

  • Full physical examination and vital signs
  • Collateral history
  • Blood tests – FBC, U+Es, LFTs, TFTs, ESR, CRP, CBG, lipid profile, HIV testing, syphilis serology
  • Urinary drug screen – can identify common illicit substances (e.g. cannabis, amphetamine) but many drugs, esp NPS can’t be detected
  • Baseline ECG – ideal before starting an antipsychotic

Additional investigations if clinical presentation suggests organic pathology
• CT/MRI brain – older patients, pt w a hx of head injury or focal neurological signs
• EEG – when investigating TLE or post-ictal symptoms (can get psychosis in the post-ictal state)
• Anti-NMDA + voltage-gated potassium channel (VGKC) antibodies – if autoimmune encephalitis is suspected
• LP – for suspected encephalitis
• Social investigation – Medication free period of inpatient observation may clarify the diagnosis if someone develops psychosis while using drugs

Risk assessment
• Risk to self – suicide, self-neglect, social decline, victimisation by others
• Risk from others
• Risk to others – aggression (might be a direct response to persecutory delusions or command hallucinations).
Other factors that increase the risk of violence – substance misuse, medication non-concordance, specific threats of violence, hx of aggression

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3
Q

Baseline investigations before starting antipsychotics

A
weight
waist circumference
pulse, BP
fasting blood glucose, HBA1c
blood lipid profile
prolactin levels
assessment of any movement disorders
assessment of nutritional status
diet and level of physical activity
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4
Q

What should be monitored in schizophrenic patients who are on atni-psychotics?

A
o	Response to treatment + SE
o	Adherence
o	Emergence of movement disorders
o	Waist circumference 
o	BMI
o	Overall physical health
o	FBC, LFT, U&Es, lipid profile, CBG (followed by a glucose tolerance test and HbA1c if abnormal) 
o	Weight
	Weekly for 6 weeks
	At 12 weeks
	At 1 year
	Annually thereafter

o Pulse + BP
 At 12 weeks
 1 year
 Annually thereafter

o some people need monitoring of
 prolactin levels – if hyperprolactinaemia is suspected or likely (e.g. risperidone)
 ECGs – important in older people + those on high-dose antipsychotics or clozapine – to monitor the QTc interval;

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5
Q

Neuroimaging in schizophrenia might show

A

Neuroimaging not carried out to d schizophrenia but in patients there might be:
• Increased size of lateral ventricles
• Reduced brain size (usually temporal lobes)
• Negative symptoms – correlated with decreased blood flow + other abnormalities in the frontal cortex
• EEG - decreased connections between different brain areas

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6
Q

Neuroleptic malignant syndrome NMS - ix + results

A
  • Increased CK (hallmark)
  • increased WCC
  • Increased LFTs
  • Decreased renal function
  • Metabolic acidosis
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7
Q

GAD ix

A

• Rule out a medical condition
o FBC, fasting glucose, fasting lipid profiles, U+Es, LFTs, serum bilirubin, serum creatinine, urinalysis, urine toxicology, TSH
o ECG

• Screening tools:
o GAD-7
o BAI (Beck Anxiety Inventory)

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8
Q

PTSD ix

A

• As clinically indicated
• Screening and rating scales
o CAPS-5 – Clinician-Administered PTSD Scale for DSM-5
o PCL-5 – PTSD checklist for DSM-V

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9
Q

OCD ix

A

• Rating scales
o Y-BOCS – Yale-Brown Obsessive Compulsive Scale
o FOCI – Florida Obsessive Compulsive Inventory

• Anti-streptolysin O (ASO)

• anti-DNAse B titres
o Patients suspected of having a recent group A (Beta-hemolytic) streptococcus bacteria infection, from Streptococcus pyogenes.
o Should be ordered if there is an acute or dramatic onset, or exacerbation of symptoms

o Some evidence that streptococcal throat infections increase risk for mental disorders, particularly OCD + tics

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10
Q

Panic disorder ix

A
  • Panic disorder severity scale
  • NICE – there is insufficient evidence on which screening instrument to use in the diagnosed process – therefore consultation skills should be relied upon to elicit all necessary information

• Clinician should be alert to the common clinical situation of comorbidities
o Panic disorder with depression
o Panic disorder with substance misuse

• Cardiac, respiratory and abdominal examination should be performed according to the clinical presentation to rule out an organic cause

• Bloods
o FBC
o U&Es
o LFTs, serum bilirubin, serum creatinine
o Fasting glucose, fasting lipid profiles
o TFT
o Urinalysis, urine toxicology for substance use

• ECG
o To assess for signs of ventricular preexcitation (short PR, delta wave)
o Short or long QT interval for patient with palpitations
o Ischaemia, infarction, pericarditis in patients with chest pain

•	Work-up for phaeochromocytoma
o	Plasma metanephrines
o	24-hour urinary metanephrines 
o	Abdominal MRI
o	Scintigraphy 
o	Abdominal CT 

• If panic attacks are acute, associated with cardiac symptoms + persistent vital sign changes  consider PE work-up  order a D-dimer

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11
Q

Alzheimer’s disease ix

A
•	CSF
o	 levels of CSF Aβ42 
o	Increased total tau 
o	Increased phosphorylated tau
•	PET – can visualise amyloid plaques
•	FDG PET scans 
o	Hypometabolism in: bilateral tempoparietal regions, posterior cingulate cortex, increased amyloid tracer retention 
•	MRI
o	Atrophy with a characteristic pattern involving the medial temporal lobes, hippocampus, paralimbic and/or tempoparietal cortex
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12
Q

Lewy body dementia investigations

A

SPECT (single photon emission computed tomography) /PET – low striatal dopamine transporter uptake
MRI – generalized atrophy, sparring of the medial temporal lobes
Cognitive testing – MMSE, MoCA – deficits in attention, executive function, visual processing, spatial and perceptual difficulties occur early, memory and object naming tend to be less affected

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13
Q

Approach to a patient with non-rapidly progressive dementia

A

• Rule out delirium
o Delirium – acute onset, fluctuating course, inattention, disorganize thinking, altered level of consciousness
o UTIs in the elderly can cause delirium
o Negative culture does not mean that there is no UTI
o Asymptomatic bacteriuria should not be treated with antibiotic – adverse risks e.g. C. diff
• Rule out depression
o “pseudodmentia”
o Can cause atypical presentations – anxiety, irritability, unexplained physical complaints, worsening cognition
o Once depression is treated, the dementia symptoms go away
• Rule out substance use disorders
o UDS, HIV
• Rule out any reversible causes
o FBC (anaemia), TSH (hypo/hyperthyroidism), Cr (assess renal function and ability to clear medications), U+Es (hyponatraemia), Ca (hypercalcaemia), glucose (hyperglycemia), ferritin/iron, vitamin B12, LFTs (alcohol misuse, SDHs, alcohol related dementia, Korsakoff’s syndrome), ESR (rule out inflammatory conditions)
o Neuroimaging
o Screen for syphilis
o ECG, CXR, MSU
o Medication induced dementia
 Polypharmacy
 Anticholinergic medications
 Other medications that could cause cognitive issues – steroid dementia syndrome related to glucocorticoid use
 Other neurological disorders e.g. normal pressure hydrocephalus
• Is it dementia, mild cognitive impairment (MCI) or normal aging?
o Dementia (major neurocognitive disorder) – objective findings of cognitive loss with impairment of ADLs
o Mild cognitive impairment – objective findings of cognitive loss without impairment of ADLs
o Normal cognitive aging – no objective findings of cognitive loss

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14
Q

• Further tests for
AD

LBD

Frontotemporal dementia

Vascular dementia

A

• Further tests for
AD
o FDG-PET or perfusion SPECT (if FDG-PET is unavailable) or
o Examine CSF for
 Either total tau or total tau + phosphorylated-tau 181 and
 Either amyloid beta 1-42 or amyloid beta 1-42 and amyloid beta 1-40
o The older the person is, the more likely they are to get a false positive with CSF examination

LBD
o 123I-FP-CIT SPECT
o 123I-MIBG cardiac scintigraphy if first test unavailable

Frontotemporal dementia
o FDG-PET or
o Perfusion SPECT

Vascular dementia
o MRI
o CT if MRI unavailable/contraindicated

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15
Q

Which investigations differentiate delirium from dementia

A

• Delirium vs Dementia
o People in hospital with cognitive impairment of an unknow cause – consider one of th following to find out if they have delirium or delirium superimposed on dementia compared with dementia alone
 Long confusion assessment method (CAM)
 Observational Scale of level of arousal (OSLA)
o If it’s not possible to tell if person has delirium or dementia – treat delirium first

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16
Q

Neuroimaging indications for someone presenting with symptoms of dementia

A

o Onset of cognitive signs/symptoms within the past 2 years, regardless of the rate of progression
o Unexpected and unexplained decline in cognition and/or functional status in a patient already known to have dementia
o Recent and significant head trauma
o Unexplained neurological manifestations (new onset severe headache, seizures, Babinski sign etc) at onset or during evolution (this also incl. gait disturbances)
o History of cancer, in particular if at risk for brain metastases
o Risk for intracranial bleeding
o Symptoms suggestive of normal pressure hydrocephalus
o Significant vascular risk factors
o Unusual or atypical cognitive symptoms or presentation e.g. progressive aphasia

17
Q

neuroimaging in someone presenting with symptoms of dementia

A

• MRI > CT
o Exclude other pathologies (SOL, SDH, NPL, vascular disease), establish subtype
• HMPAO SPECT
o To differentiate AD, VD, FTD if dx is in doubt
o LBD SPECT (single photon emission computed tomography) /PET – low striatal dopamine transporter uptake
o FTD SPECT/PET Frontal and/or anterior temporal hypoperfusion or hypometabolism
• FDG PET
o 2nd line ix if SPECT unavailable
• CSF examination
o Inflammatory, infective, malignant causes of dementia
o In cases where dementia is rapidly progressive, the presentation is unusual or if the person is 55 years of age, CJD
• EEG
o If dx of delirium, FTD, CJD is suspected
o Assessment of seizure disorder in people with dementia

18
Q

When is brain biopsy indicated in someone presenting with symptoms of dementia?

A

• Brain biopsy
o In highly selected people whose dementia is thought to be due to potentially reversible condition (e.g. cerebral vasculitis) that cannot be diagnosed in another way

19
Q

Delirum ix

A

• CAM – Confusion Assessment Method
• History
o Patient history + collateral history
o Medical + psychiatric history (acute + chronic)
 Sensory impairments (hearing/vision)
 Elimination patterns (urinary and bowel frequency)
o Recent surgeries
o Medication history (prescription, OTC)
o Substance use history (esp. alcohol)
o Previous cognitive functioning, ADLs, IADLs
o Hx of presenting illness
 Onset + course of confusion
 Hx of previous episodes of delirium (+ treatment response)
 Sleep patterns
o Social hx
• Routine investigations
o FBC, U+Es, BUN/Cr, extended electrolytes (Ca, Mg, PO43-), CK, ESR, CRP
o LFTs, lipase, albumin, troponin
o Random glucose, B12, TSH, free T3/T4, O2 sats or ABGs, CXR, CT head, ECG
o Infectious aetiology work up – HIV, lactate
o Urinalysis (cultures), urine drug screen, urine/serum toxicology screen
• Baseline ECG

20
Q

Anorexia nervosa ix

A

• Squat test
o Difficulty standing up from squatting without help

Screening and rating scales
• EDDS – eating disorder diagnostic scale
• The SCOFF questionnaire – PACES
o 5-question screening questionnaire for AN and BN
o 2 or more positive answers should raise your index of suspicion of a case  take a more detailed history
 S – do you ever make yourself sick because you feel uncomfortably full?
 C – do you worry you have lost control over how much you eat?
 O – have you recently lost more than one stone (14 pounds/6.4 kg) in a 3-month period?
 F – do you believe yourself to be fat when others say you are too thin?
 F – would you say food dominates your life?
Lab findings
• If amenorrhoea  pregnancy test in women of childbearing age
• Urinalysis
o Low specific gravity – consumption of large quantities of free water
o Ketonuria - starvation
• Serum pH and ketones if DKA suspected
• FBC
o Leukopenia
o  lymphocytes
o Anaemia (normocytic + normochromic)
o Thrombocytopenia
• ESR – N or low (to rule out organic cause of weight loss)
• Electrolytes are typically decreased
o  Na, PO4, Mg, K, Ca, Zn
o Urea
o Self-induced vomiting – may lead to metabolic alkalosis ( serum bicarbonate, losing H+ from stomach), Cl, K
o Laxative abuse – mild metabolic acidosis (losing HCO3- through diarrhoea) , Na, K
o High urea – if dehydration
• Endocrine
o N/ T4
o  T3
o  rT3 (reverse T3)
o  serum oestrogen levels
o  serum testosterone
o  GH
o  cortisol
o  GnRH
o  leptin
• Estradiol (F), testosterone (M)
• Hypercholesterolaemia
•  LFTs (ALT/AST, ALP (osteopenia))
•  serum amylase
• most things low
• G’s and C’s raised: growth hormone, glucose (leading to impaired glucose tolerance), salivary glands, cortisol, cholesterol, carotinaemia

ECG
• Sinus bradycardia (common)
• Arrhythmias (rare)
• Significant prolongation of QTc (>450ms) seen in some individuals

Bone mineral density scan/DEXA scan
• After 1 year of underweight in children + young people
• After 2 years of underweight in adults
• Or earlier if bone pain or recurrent fractures