Neurological Flashcards

1
Q

What is a TIA?

A

A transient ischaemic attack is a similar presentation to a stroke, but it resolves in 24hrs.

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2
Q

How common is stroke?

How common is TIA?

A

150,000 people have a stroke in UK each year

20,000 people have TIA in UK each year

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3
Q

Who does stroke/TIA affect?

A

Can affect anyone

Most cases in people aged >65

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4
Q

What causes a stroke/TIA?

A
Infarction due to ischaemia (80%)
Intracerebral haemorrhage (20%)

Caused by:

  • small vessel occlusion it thrombosis in situ
  • cardiac emboli
  • Atherothromboembolism
  • CNS bleeds
  • other: sudden⬇️ in BP as in sepsis watershed stroke; carotid artery dissection; vasculitis; subarachnoid haemorrhage
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5
Q

What are the risk factors for stroke/TIA?

A
Hypertension
Smoking
Diabetes
⬆️ Lipids
Family history

Cardiac risk factors: AF; valve disease; peripheral vascular disease, previous stroke

Ethnicity - higher risk in blacks and Asians

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6
Q

What are the symptoms of stroke/TIA?

A

Weakness of arm/leg/both- ranging from total paralysis of one side of body to mere clumsiness of one hand

Weakness and twisting of one side of the face- can cause drooling

Problems with balance coordination, vision, speech, communication, or swallowing

Dizziness or unsteadiness
Numbness in a part of the body
Headache
Confusion
Loss of consciousness
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7
Q

What are the signs of a stroke on examination?

A
Bleeding = meningism, headache, coma
Ischaemia = carotid bruit, AF, IHD, past TIA

Dysphasia affects large proportion of stroke patients

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8
Q

What are the 3 different areas mainly affected by infarcts and how do they present?

A

Cerebral Hemisphere infarcts (50%) = contralateral hemiplegia which is initially flaccid (floppy limb falls like a dead weight when lifted) and then becomes spastic, contralateral sensory loss, homonymous hemianopia, dysphagia.

Brainstem Infarction (25%) = a wider range of effects which include quadriplegia, disturbances of gaze and vision, locked-in syndrome, later medullary syndrome from vertebrobasilar occlusion

Lacunar infarcts (25%) = small infarcts around the basal ganglia, internal capsule, thalamus and pons, may cause pure motor, pure sensory, mixed motor and sensory signs, or ataxia, intact cognition and consciousness.

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9
Q

What are the possible differential diagnoses of stroke/TIA?

A
Head injury
⬆️/⬇️ glucose
Space occupying lesion
Hemiplegic migraine
Todd's palsy
Infections: encephalitis; abscesses, HIV
Drugs: opiate overdose
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10
Q

What investigations are necessary to diagnose a stroke/TIA?

A

Pulse (AF), BP, ECG
Blood glucose (hypo/hyperglycaemia)
Urgent CT
Blood tests: FBC, ESR, sylhilis test

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11
Q

What are the treatments for stroke/TIA?

A

Stroke- Thrombolysis if onset was less than 4.5 hours ago

  • NBM if unsafe swallow
  • Antiplatelet agents - only when haemorrhagic stroke excluded

TIA - control CV risk factors
- start Antiplatelet drugs, clopidogrel/aspirin, consider warfarin and consider carotid endarterectomy

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12
Q

What is a subarachnoid haemorrhage?

A

Spontaneous bleeding into the subarachnoid space

Can be caused by berry aneurysm
Popular sites: junction of posterior communicating and internal carotid artery, junction of anterior communicating and anterior cerebral or bifurcation of middle cerebral artery

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13
Q

How common is subarachnoid haemorrhage?

A

9/100000/year

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14
Q

Who does it affect?

A

Typical age 35-65

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15
Q

What causes a subarachnoid haemorrhage?

A

Rupture of saccular aneurysms (80%)
Arteriovenous malformations (15%)
No cause found

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16
Q

What are the risk factors for subarachnoid haemorrhage?

A
Smoking
Alcohol misuse
Hypertension
Bleeding disorders
Micotic aneurysms
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17
Q

What are the symptoms of a subarachnoid haemorrhage?

A
Sudden thunderclap headache
Vomiting
Collapse
Seizures
Coma may follow
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18
Q

What are the signs of a subarachnoid haemorrhage on examination?

A

Neck stiffness
Kernigs sign
Retinal/subhyloid/vitreous bleeds

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19
Q

What are the possible differential diagnoses of subarachnoid haemorrhage?

A

Meningitis
Migraine
Intracerebral bleed
Cortical vein thrombosis

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20
Q

What investigations are necessary to diagnose subarachnoid haemorrhage?

A

CT within 48hrs
LP if CT is negative and >12h headache onset
- CSF in subarachnoid haemorrhage is bloody early on and then xanthochromic (yellow) after several hours due to bilirubin

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21
Q

What are the treatments of subarachnoid haemorrhage?

A

Refer to neurosurgery immediately
Maintain cerebral perfusion by keeping well hydrated
Nimodipine (ca2+ antagonist that reduces vasospasms)
Pain relief
Anticonvulsants and antiemetics

Surgery- endovascular coiling or neurosurgical clipping

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22
Q

What is peripheral neuropathy?

A

Damage to one or more of your peripheral nerves meaning impulses traveling from CNS to PNS are disrupted

Symptoms depend on which nerves affected (sensory, motor or autonomic)

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23
Q

How common is peripheral neuropathy?

A

2/100 people

Increases with age

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24
Q

Who does peripheral neuropathy affect?

A

Can affect anyone

Most commonly diabetics

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25
Q

What are the causes and risk factors of peripheral neuropathy?

A

Hyperglycaemia - in poorly controlled diabetes
Dietary deficiencies - B12 or folate
Medicines - chemotherapy and HIV therapy
Toxins - insecticides or solvents
Cancers
Alcohol excess
CKD- poorly functioning kidneys leads to salts and chemicals imbalance in bloodstream➡️PN
Injuries- broken bones and compression injuries can put direct pressure on PNs
Infections - eg Guillain-Barré syndrome
Connective tissue diseases
Inflammatory conditions

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26
Q

What are the symptoms of peripheral neuropathy?

A

Sensory neuropathy:

  • tingling and numbness
  • loss of sensation to pain, temperature
  • loss of coordination
  • burning/shooting pains
  • feet and hands often affected first

Motor neuropathy:

  • muscle weakness (can lead to falling, breathing & swallowing problems)
  • muscle wasting
  • muscle twitching (fasiculations) and cramps
  • muscle paralysis

Autonomic Neuropathy:

  • dizziness&fainting (lack of BP control➡️lowBP)
  • reduced ability to sweat ➡️ inability to tolerate heat
  • urinary incontinence - loss of bladder control
  • bloating, constipation/diarrhoea
  • impotence
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27
Q

What investigations are necessary to diagnose peripheral neuropathy?

A
Nerve conduction tests
Electromyography- tests electrical activity of muscles
Nerve biopsy
Skin biopsy
X-Ray/CT for underlying cause
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28
Q

What is the treatment for peripheral neuropathy?

A

Depends on underlying cause

Diabetes - controlling blood sugars
Vitamin deficiencies - consuming more vitamins

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29
Q

What is epilepsy?

A

Epilepsy is the recurrent tendency to have spontaneous, intermittent, abnormal electrical activity in part of the brain, manifesting in seizure

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30
Q

How common is epilepsy?

A

1% of population

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31
Q

Who does epilepsy affect?

A

Most commonly starts in children/over 60’s
More common in people with learning disability
Feature of >200 genetic disorders

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32
Q

What causes epilepsy?

A
Most idiopathic
Cerebrovascular disease
Head injury
Cranial surgery
CNS infections - meningitis/encephalitis
Neurogenerative diseases
Autoimmune diseases
Brain neoplasm
Genetic diseases
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33
Q

What are the risk factors for epilepsy?

A

Stress
Poor sleep
Alcohol misuse

All these lower seizure threshold

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34
Q

What are the symptoms of epilepsy?

A
Sudden falls
Involuntary jerky movements of limbs whilst awake
Blank spells
Olfactory, gustatory, visual, auditory hallucinations
Unexplained urinary incontinence
simple partial seizures
Epigastric fullness sensation
Deja vu
Premonition 
Extreme emotions
Inability to understand or express language
Loss of memory
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35
Q

What are the signs of epilepsy on examination?

A

Usually unremarkable

Check for neurological/cerebrovascular signs

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36
Q

What are the possible differential diagnoses of epilepsy?

A
Syncope
Cardiac arrhythmia 
TIA
Migraine
Non- epileptic seizures
Paroxysmal vertigo
Acute encephalopathy 
Sleep disorders
Hyperventilation
Panic attacks
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37
Q

What are the 3 diagnostic questions?

A

Are they really seizures?
What type of seizures are they?
Are there any triggers?

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38
Q

What investigations an be done to diagnose epilepsy?

A
Neuroimaging (MRI) 
Electroencephalograph (EEG) to confirm diagnosis
Blood tests
ECG
Neuropsychological assessment
39
Q

What are the possible treatments of epilepsy?

A

Drug choice depends on type of seizure
Generalised tonic-clonic seizures and tonic, atonic, myoclonic seizures - sodium valproate/lamotrigine, 2nd line carbamazepine
Absence seizures- sodium valproate, lamotrigine

If drugs don’t work then neurological resection or vagaries nerve stimulation

40
Q

What are the classification of epileptic seizures?

A

1) focal (partial seizures)

2) primary generalised seizures

41
Q

What are focal (partial) seizures?

A

60% of people with epilepsy have
Can be unsubtle or unnoticeable
Simple partial seizures - awareness unimpaired with no post octal symptoms
Complex partial seizures - awareness impaired, mainly temporal lobe
Partial seizure with secondary generalisation - electrical disturbance spreads widely, typically convulsive

42
Q

What are primary generalised seizures?

A

Simultaneous onset of electrical discharge throughout cortex - because of this, consciousness is lost at the onset of the seizure

43
Q

What are the types of primary generalised seizures?

A
  • absence- brief, less then 10secs, presents in childhood
  • tonic-clonic - loss of consciousness, limbs stiffen (tonic) then jerk (clonic) with post ictal confusion and drowsiness
  • myoclonic - sudden jerk of limb, face or trunk
  • atonic - no loss of consciousness, sudden loss of muscle tone causing a fall
  • infantile spasms - associated with tuberous sclerosis
44
Q

What is meningitis?

A

An inflammation of the leptomeninges and underlying subarachnoid cerebrospinal fluid.

The inflammation can be caused by infection with viruses or bacteria or micro-organisms, or non-infective causes.

45
Q

How common is meningitis?

A

~3,200 cases of bacterial meningitis in UK per year.

46
Q

Who does meningitis affect?

A

More common in infants, young children and elderly.

47
Q

What causes meningitis?

A

Neonates: group B streptococci, listeria monocytogenes, E. coli

Infants: H. Influenzae type b (

48
Q

What are the risk factors for meningitis?

A

Pts with CSF shunts or dural defects
Pts having spinal procedures

Bacterial endocarditis, diabetes, alcoholism and cirrhosis, IVDUs

Splenectomy and sickle cell disease

Crowding

49
Q

What are the symptoms of meningitis?

A
Fever
Headache
Stiff neck
Back rigidity
Photophobia
Opisthotonos if severe
Unconscious 
Seizures
50
Q

What are the signs of meningitis on examination?

A
Kernig's sign
Non- blanching rash
Brudzinski's sign 
Focal neurological defects
Shock - tachycardia and/or hypotension, respiratory distress, altered mental state and ⬇️ urine output 
Bulging fontanelle
51
Q

What are the possible differential diagnoses of meningitis?

A

Intracranial abscess
Encephalitis
Subarachnoid Haemorrhage
Brain tumour

52
Q

What investigations are necessary to diagnose meningitis?

A

Lumbar puncture (provided no signs of ⬆️ICP)
Renal function tests
Coagulation profile
Chest X-Ray for lung abscess
Urine cultures, nasal swabs and stool virology
MRI

53
Q

What is the treatment of meningitis?

A

Supportive therapy (fluids, antipyretics, antiemetics, analgesia and nutritional support)
Treatment of causative organism (antibiotics)
Treatment of any complications (seizures/⬆️ICP)

54
Q

How are migraines classified?

A

Episodic or Chronic

Migraine without aura
Migraine with aura
Migraine aura without headache

55
Q

How common is migraine?

A

Affects 6% of men and 18% of women

56
Q

What causes migraine?

A

Cause not clear

Theory: blood vessels in part of the brain go into spasm (which accounts for the aura) then dilate (which accounts for the headache)

Some things trigger migraines:
Diet (certain foods)
Environmental (smoking, glaring light, loud noises, strong smells)
Psychological (depression, anxiety, anger, tiredness, stress, sudden relaxation)
Medicines (HRT)
Other (periods, menopause)

57
Q

What are the risk factors for migraine?

A

Family history
Age (most people experience their first at adolescence)
Gender (women 3x more likely)

58
Q

What are the symptoms of migraine?

A

Migraine without aura:

  • headache: usually on one side, pain moderate or severe throbbing or pulsating
  • other migraine symptoms that are common: nausea/vomiting/photophobia
  • other symptoms that sometimes occur: being off food/blurred vision/poor concentration/hunger/diarrhoea

Migraine with aura

  • symptoms same but include an aura before headache
  • visual most common (temp loss of vision, flashing lights etc)
  • numbness and pins and needles
  • speech problems
  • smells
59
Q

What are the phases of a migraine attack?

A

Premonitory phase
Aura phase
Headache phase
Resolution phase

60
Q

What are the differential diagnoses of migraines?

A
Cluster headache
Tension headache
Increased BP
Intracranial pathology
TIA
61
Q

What investigations are necessary to diagnose migraine?

A
Optic fundoscopy
BP
Head and neck exam
Head circumference
Neurological exam
62
Q

What are the possible treatments for migraine?

A

Non- pharmacological = warm or cold packs to head, rebreathe no into paper bag

Pharmacological =

  • NSAIDs
  • 5HT agonists (triptans)- cause constriction of blood vessels in brain which dilate in migraines
  • antiemetics
63
Q

How common are tension headaches?

A

Lifetime prevalence 30-80%

64
Q

Who do tension headaches affect?

A

More common in women

Most common in young adults

65
Q

What causes tension headaches?

A
Anxiety
Depression
Poor posture
Poor sleep
Stress
Muscular tightness
66
Q

What are the risk factors for tension headaches?

A

Being a young adult

Being female

67
Q

How can tension headaches be classified?

A

EPISODIC:

  • fewer than 15 days each month
  • can evolve into chronic

CHRONIC:

  • occurs on more than 15 days each month
  • more likely to be medication induced
  • more likely to be associated with comorbidity such as depression
68
Q

What are the symptoms of a tension headache?

A

30 minutes- 7days duration

Pain is mild to moderate in intensity
- described as “fullness/tightness/squeezing/pressure/like a skull cap/like a band or vice

Pain bilateral, occipito-nuchal or bi frontal

Associated symptoms:

  • muscular tightness/stiffness in neck
  • difficulty concentrating
  • stress & anxiety
69
Q

What are the possible differential diagnoses of tension headaches?

A
Migraine
Giant cell arteritis
Trigeminal neuralgia
Subarachnoid haemorrhage
Sinusitis
70
Q

What investigations are necessary in tension headaches?

A

No real investigations
Examine head and neck
BP
Optic fundi

71
Q

What are the possible treatments of tension headaches?

A

Non pharmacological:
Treat stress, anxiety or depression
Exercise and posture

Pharmacological:
NSAIDs
Aspirin
Tricyclic antidepressants - amytriptyline

72
Q

How common is Parkinson’s Disease?

A

Prevalence 65.6-125/100,000

>60s = 5/1000
>80s = 40/1000
73
Q

Who does Parkinson’s Disease affect?

A

More common with increasing age
Mainly >50s
Slightly more common in Males

74
Q

What causes Parkinson’s Disease?

A

Mitochondrial DNA dysfunction causes degeneration of dopaminergic neurones in the substantia nigra pars compacta which is associated with Lewy bodies.
This causes a decrease in striatal dopamine levels

75
Q

What are the risk factors for Parkinson’s disease?

A

Increasing age
Male
Pesticide exposure

76
Q

What are the symptoms of Parkinson’s Disease?

A

Bradykinesia or hypokinesia with one or more of:

  • resting tremor
  • postural instability
  • muscular rigidity
77
Q

What are the signs of Parkinson’s disease on examination?

A

Reduced facial expression
Reduced blinking
Slow monotonous speech

78
Q

What are the possible differential diagnoses of Parkinson’s disease?

A
Benign essential tremor - tremor worse on movement
Drug induced Parkinsonism
Huntingtons
Multi infarct dementia
Lewy body dementia
79
Q

What investigations are necessary to diagnose Parkinson’s disease?

A

CT or MRI brain scan
- if pt fails to respond to therapeutic dose of L-dopa for 12 weeks

PET scan
- scanning with fluorodopa can localise dopamine deficiency in the basal ganglia

Transcranial sonography
- differentiate PD from atypical and secondary parkinsonian disorders

80
Q

What are the possible treatments for Parkinson’s disease?

A

Currently no cure but treatments help relieve symptoms and maintain quality of life

Medicines:
Levodopa - body converts to dopamine. Always given with another medicine (benserazide or carbidopa) to prevent levodopa being converted into dopamine in the blood
Dopamine agonists - act as substitute for dopamine (ropinerole, pramioexole)

81
Q

What is a Parkinsonism?

A
A condition that mimics the main characteristics of Parkinson's disease:
Tremor
Rigidity
Postural instability
Bradykinesia
82
Q

How can Parkinson’s disease be differentiated from a Parkinsonism?

A

Parkinson’s disease symptoms will go away with dopamine replacement therapy

83
Q

What are the main types of Parkinsonism?

A

Corticobasal degeneration
Dementia with Lewy bodies
Drug induced Parkinsonism
Vascular Parkinsonism

84
Q

What is proximal Myopathy?

A

Muscular disease in which muscle fibres do not function for one of many reasons, resulting in muscular weakness.

It usually affects muscles without involving the nervous system or any disorder of the neuromuscular junction

85
Q

What are the most common proximal myopathies?

A

The muscular dystrophies are the most common of such disorders.

Duchenne muscular dystrophy is the most common muscular dystrophy

86
Q

What is the difference between neuropathy and myopathy?

A

MYOPATHY:

  • gradual onset
  • symmetrical proximal weakness
  • dystrophies usually affect specific muscle groups
  • preserved tendon reflexes

NEUROPATHY:

  • paraesthesia, bladder problems
  • distal weakness
87
Q

What is multiple sclerosis?

A

MS is a disease where patches of inflammation occur in parts of the brain and/or spinal cord.

This can cause damage to parts of the brain and lead to various symptoms

88
Q

What causes MS?

A

Multiple areas of scar tissue (sclerosis) form along the neurons.
This slows or blocks transmission of impulses to and from brain and spinal cord.
In this way movement and sensation may be impaired

89
Q

What are the different patterns of MS?

A

Relapsing/remitting MS:
remission and relapsing of symptoms

Secondary progressive MS:
Follows on from relapsing/remitting
Gradually more or worsening symptoms with fewer remissions

Primary progressive MS:
From beginning symptoms gradually develop and worsen over time

Benign MS

90
Q

What are the symptoms of MS?

A

Visual - demyelination of optic nerve, optic neuritis is common presenting symptom of MS
Eye movements - double vision, nystagmus
Facial weakness - Bell’s palsy, trigeminal neuralgia
Hearing and balance - deafness, demyelination in brain stem can cause severe positional vertigo
Cognitive symptoms
Psychological symptoms
Taste and smell
Unpleasant sensations - tightness, burning, twisting, tearing and pulling sensations due to damage to dorsal column
Paraesthesia and numbness

91
Q

What investigations are necessary to diagnose MS?

A

Exclude differentials by checking:
- FBC, CRP, U&Es, LFT, TFT, glucose calcium and B12

Electrophysiology can detect demyelination in apparently unaffected pathways with characteristic delays

MRI scan: 95% of pets have periventricular lesions and over 90% show discrete white master abnormalities

92
Q

What are the treatments of MS?

A

Medicines that aim to modify disease process:

  • immunomodulatory agents (interferon beta-1a/b)
  • reduce number of relapses
  • small effect on slowing down progression

Steroid medication to treat relapse:

  • given if relapse causes disability
  • reduces inflammation
  • course of steroids shorten relapse duration. It do not affect progression of disease

Other medications to help ease symptoms:

  • anti-spasm drugs
  • painkillers for neuropathic pain
  • medicines for urinary problems
  • antidepressants
  • medicines for erectile problems

Other treatments therapies and support
- eg physio, speech therapy, counselling

93
Q

What is a stroke?

A

Cerebrovascular event is caused by disruption of blood supply to the brain.
It is characterised by rapidly developing signs of focal or global disturbance or cerebral functions lasting for more than 24hrs or leading to death.