Neurology Flashcards

1
Q
  1. Functions of the brain stem?
  2. Affects on the brain stem during stroke?
A
  1. BP, breathing, HR, swallowing
  2. Dysphasia, vertigo, insomnia, difficulty organising/ understanding the environment, inability to coordinate balance and movement
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2
Q
  1. Functions of the cerebellum?
  2. Effects on the cerebellum during stroke?
A
  1. Balance and coordination, fine muscle control
  2. Inability to coordinate fine movements, walk, grab/ reach out to objects, make rapid movements, vertigo/ tremors, slurred speech,
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3
Q
  1. Occipital lobe functions?
  2. Effects on the occipital lobe during stroke?
A
  1. Vision
  2. Colour and movement agnosia, difficulty reading/ writing, VF defects, difficulty locating objects, hallucinations, inability to recognise words and seeing objects inaccurately
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4
Q
  1. Parietal lobe functions?
  2. Effects on the parietal lobe during a stroke?
A
  1. Language, reading, coordination, sensation, intelligence, reading
  2. Anomia, agraphia, alexia, dyscalculia, apraxia, inability to focus visual attention
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5
Q
  1. Temporal lobe functions?
  2. Effects on the temporal lobe during a stroke?
A
  1. Speech, behaviour, memory, emotions, vision, hearing
  2. Wernicke’s aphasia, difficulty IDing and naming objects, aggressive behaviour, short-term memory loss, hypersexuality,
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6
Q
  1. Functions of the frontal lobe?
  2. Effects on the frontal lobe during a stroke?
A
  1. Locomotion, mood, intelligence, judgment, logic, decision-making, behaviour, personality, planning, inhibition, memory
  2. Loss of simple body movements, Broca’s aphasia, loss of flexible thinking, sequencing, interaction, inability to focus, problem-solving difficulties, changes in mood, behaviour, personality
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7
Q

Essential problem with ischaemic VS haemorrhagic strokes?

What is the % proportion for each?

A

Ischaemic: Blockage in the blood vessel stops blood flow- 85%

Haemorrhagic: Blood vessel bursts leading to reduction in blood flow- 15%

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8
Q

Subtypes for ischaemic/ haemorrhagic stroke?

A

Ischaemic:
Thrombotic (thrombus from large vessel- carotids)
Embolic (blood clot, fat, air or clumps of bacteria)
AF

Haemorrhagic:
Intracerebral haemorrhage (bleeding within brain)
Subarachnoid haemorrhage (bleeding on surface of brain)

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9
Q

Risk factors for ischaemic/ haemorrhagic stroke?

A

Ischaemic:
General risk factors for cardiovascular disease
age
hypertension
smoking
hyperlipidaemia
diabetes mellitus

Haemorrhagic:
age
hypertension
arteriovenous malformation
anticoagulation therapy

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10
Q

Contraindications for thrombolysis?

A

Previous intracranial haemorrhage

Seizure at onset of stroke

Intracranial neoplasm

Suspected SAH

Stroke or traumatic brain injury in preceding 3 months

Lumbar puncture in preceding 7 days

Gastrointestinal haemorrhage in preceding 3 weeks

Active bleeding

Oesophageal varices

Uncontrolled hypertension >200/120mmHg

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11
Q

Management for meningitis in adults?

A
  1. IV Ceftriaxone (amoxicillin should be given as well if immunocompromised, elderly, neonate)

Chloramphenicol if severe penicillin allergy

  1. IV Dexamethasone given to all >3 months
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12
Q

Management for meningitis in children?

A

Antibiotics
< 3 months: IV amoxicillin (or ampicillin) + IV cefotaxime

> 3 months: IV cefotaxime (or ceftriaxone)

Steroids: >3 months

Fluids
Cerebral monitoring
Public health notification

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13
Q

Management for cluster headache?

A

Acute:
-100% oxygen (80% response rate within 15 minutes)
-subcutaneous triptan (75% response rate within 15 minutes)

Prophylaxis:
-verapamil is the drug of choice

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14
Q

Headaches red flags?

A

-compromised immunity, caused, for example, by HIV or immunosuppressive drugs

-age under 20 years and a history of malignancy
a history of malignancy known to metastasise to the brain

-vomiting without other obvious cause

worsening headache with fever

-sudden-onset headache reaching maximum intensity within 5 minutes - ‘thunderclap’

-new-onset neurological deficit

-new-onset cognitive dysfunction
(change in personality, impaired level of consciousness)

-recent (typically within the past 3 months) head trauma

-headache triggered by cough, valsalva (trying to breathe out with nose and mouth blocked), sneeze or exercise

-orthostatic headache (headache that changes with posture)

-symptoms suggestive of giant cell arteritis or acute narrow-angle glaucoma

-a substantial change in the characteristics of their headache

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15
Q
  1. How does peripheral neuropathy caused by diabetes present?
  2. Management for peripheral neuropathy?
A
  1. Sensory loss in a ‘glove and stocking’ distribution affecting lower legs first
  2. First-line treatment: amitriptyline, duloxetine, gabapentin or pregabalin

If the first-line drug treatment does not work, try one of the other 3 drugs

Tramadol may be used as ‘rescue therapy’ for exacerbations of neuropathic pain

topical capsaicin may be used for localised neuropathic pain

Pain management clinics may be useful in patients with resistant problems

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16
Q

What additional investigations can be done in a young person with a stroke?

A

‘Young’ stroke blood tests include thrombophilia and autoimmune screening - performed in those under 55 with no obvious cause of a stroke

ANA
APL
ACL
LA
ESR
Syphilis serology

17
Q

Symptoms of carpal tunnel?
Examination for carpal tunnel?
Causes?
Management?

A

History
-pain/pins and needles in thumb, index, middle finger
-unusually the symptoms may ‘ascend’ proximally
-weakness of thumb abduction
-wasting of thenar eminence (NOT hypothenar)
-Tinel’s sign: tapping causes paraesthesia
-Phalen’s sign: flexion of wrist causes symptoms

Causes
idiopathic
pregnancy
oedema- heart failure
lunate fracture
rheumatoid arthritis

Management:
trial of wrist splint +/- steroid injections
if fails -> surgical decompression

18
Q

Management for lower back pain?

A

Lower back pain without sciatic symptoms:

NSAIDs +/- PPIs
If sx persist for 4-6 weeks -> referral for MRI

19
Q

What is the definition of Parkinson’s?

Classical triad of sx?

A

Neurodegenerative condition caused by degeneration of dopaminergic neurons in the substantia nigra.
The reduction in dopaminergic output results in a classical triad of features:

Bradykinesia-> poverty of movement, shuffling gait, difficulty in initiating movement

Tremor-> mostly at rest, pill-rolling tremor, worse when stressed or tired

Rigidity- lead-pipe and cogwheel rigidity

20
Q

Other characteristic features of Parkinson’s?

A

Other characteristic features:

mask-like facies
flexed posture
micrographia
drooling of saliva
psychiatric features: depression is the most common feature (affects about 40%); dementia, psychosis and sleep disturbances may also occur
impaired olfaction
REM sleep behaviour disorder
fatigue
autonomic dysfunction:
postural hypotension

21
Q
  1. What is Myasthenia Gravis?
A

-Autoimmune condition resulting in insufficient functioning acetylcholine receptors.

-Antibodies to acetylcholine receptors are seen in 85-90% of cases. (MuSK, LRP4)

-Abs bind ACh-recepotors and blocks these receptors and prevents ACh from stimulating and triggering muscle contraction

-Associated with Thymoma (thymus cancer)

Women <40
Men >60

Muscle weakness-> affects proximal muscles
Worse with activity
Improves with rest

22
Q

Myasthenia Gravis symptoms?

How to elicit symptoms?

A

-extraocular muscle weakness: diplopia
-proximal muscle weakness: face, neck, limb girdle
-ptosis
-dysphagia
-fatigue in jaw
-slurred speech

Repeated blinking -> ptosis
Upward gazing -> diplopia
Repeated abduction-> unilateral weakness

Thymectomy scar following thymoma treatment

23
Q

Investigations for Myasthenia Gravis?

A

single fibre electromyography: high sensitivity (92-100%)

Abs:
ACh-Abs
MuSK-Abs
LRP4-Abs

CT/ MRI thorax of thymus gland-> check for thymoma

Tensilon test: IV edrophonium

24
Q

Management for Myasthenia Gravis?

A

ACh-inhibitors: pyridostigmine is first-line

Immunosuppression is usually not started at diagnosis, but the majority of patients eventually require it in addition to long-acting acetylcholinesterase inhibitors:
prednisolone initially
azathioprine, cyclosporine, mycophenolate mofetil may also be used

Thymectomy

25
What are the UMN signs? 'everything up'
Affects brain and spinal cord Positive Babinski sign Increased reflexes Poor coordination Pyramidal muscle weakness Increased muscle tone (spasticity) Positive clonus
26
What are the LMN signs? 'everything down'
Affects anterior horn cell, motor nerve roots or peripheral motor nerve Marked atrophy Fasciculations Reduced tone Variable patterns of weakness Reduced or absent reflexes Down going plantars or absent response- Negative Babinski Foot drop
27
1. Causes of Guillain-Barre syndrome? Diagnosis?
1. Campylobacter jejuni-> following gastroenteritis 4 weeks prior CMV EBV 2. Mainly clinical Nerve-conduction studies -> reduced signal LP-> raised protein, normal cell count and glucose
28
1. Symptoms of Guillian-Barre? 2. Management?
1. Acute, symmetrical, ascending weakness Starts in feet Peripheral loss of sensation and neuropathic pain Can affect CN-> facial weakness Urinary retention, ileus and arrhythmias 2.Supportive care VTE/ PE prophylaxis IVIG -> first-line Intubation/ ventilation/ ICU if resp failure
29
1. Diagnosis for MS? 2. Management for MS?
1. History and exam MRI Oligoclonal bands in CSF Visual evoked potentials (VEPs) 2. Oral or IV methylprednisolone- acute DMARDs
30
1. What are the causes of SAH? 2. Symptoms?
1. Traumatic head injury- most common Spontaneous cause: -Berry aneurysm (85%) -AVM -Mycotic infective aneurysm 2. Sudden-onset thunder-clap headache Meningism symptoms N&V Seizures Coma
31
1. Investigations for SAH? 2. Management for SAH?
1. CT-head LP -> xanthochromia CT-intracranial angiogram 2. Bed rest, analgesia, VTE prophylaxis Nimodipine -> prevent vasospasm Surgical coil repair -> if aneurysm at risk of bleeding
32
What ophthalmology condition is associated with MS?
Optic neuritis- central scotoma, painful eye movements, MOST COMMON PRESENTING FEATURE IN MS Optic atrophy- pale optic disc
33
MOA of Pyridostigmine?
Long-acting acetylcholinesterase inhibitor Reduces the breakdown of acetylcholine in the neuromuscular junction, temporarily improving symptoms of myasthenia gravis
34
Management of myasthenic crisis?
Intravenous immunoglobulin, plasmapheresis
35
Imaging modality for MS?
MRI brain and spine with contrast
36
37
List Predominately sensory loss causes of peripheral neuropathy
diabetes uraemia leprosy alcoholism vitamin B12 deficiency amyloidosis
38
List Predominately motor loss causes of peripheral neuropathy
Guillain-Barre syndrome porphyria lead poisoning hereditary sensorimotor neuropathies (HSMN) - Charcot-Marie-Tooth chronic inflammatory demyelinating polyneuropathy (CIDP) diphtheria
39
List 2 other types of peripheral neuropathy other than motor and sensory loss
Alcoholic neuropathy secondary to both direct toxic effects and reduced absorption of B vitamins sensory symptoms typically present prior to motor symptoms Vitamin B12 deficiency subacute combined degeneration of spinal cord dorsal column usually affected first (joint position, vibration) prior to distal paraesthesia