Neuro Flashcards

1
Q

Causes of olfactory nerve problems

A

COVID
Trauma to nose which disrupts cribriform plate
Frontal and temporal lobe tumours
Kallmans syndrome

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2
Q

If problem with visual acuity what is first thing do

A

Assess with pinhole occluder to see if refractive errors

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3
Q

What does impaired colour vision suggest

A

Problem with the optic nerve

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4
Q

CN7 tests

A

Smile
Raise eyebrows
Close eyes and then try to oppose opening

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5
Q

If notice impaired hearing on crude assesment what do

A

Otoscopy
Webers and rinnes

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6
Q

How assess CN9-10

A

Look for NG tube/PEG
Ask to repeat phrases to assess speech- british constitution, red lorry, yellow lorry
Look at uvula and say ahhh
Offer gag reflex

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7
Q

How assess CN12

A

Look at tongue
Ask to poke out tongue

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8
Q

What looking for in inspection of limb exams

A

Involuntary movements
Wasting
Fasiculations
Scars
Trauma damage

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9
Q

Spasticity vs rigidity

A

Spasticity- increases as move the limb
Rigidity- tense throughout

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10
Q

Potential sites of neuro lesions

A

Brain
Spine
Spinal root
Peripheral nerve
Neuromuscular junction

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11
Q

Acute stroke management

A

A-E approach initially- low GCS requiring intubation or identifying AF etc
Examination-assessing dysfunction with NIHSS
CT scan to exclude haemorrhage and identify if proximal cerebral artery occlusion, could then do CTPA and MRI to identify ischaemic penumbra if
Management then could involve thrombolysis, thrombectomy or 300mg aspirin depending on duration of symptoms

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12
Q

Post stroke management

A

Swallow assessment and feeding- SALT within 24 hours
Glycaemic control
BP control
Fluid balance
Rehab assessed using barthel index

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13
Q

What is the mcdonald criteria

A

Used to diagnose MS
Gold standard is 2 clinical attacks disseminated in time with 2 objective lesions on MRI
Other options include
- 2 clinical attacks with evidence of 1 lesion but then require additional evidence such as CSF oligoclonal bands or another attack

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14
Q

UMN differentials

A

Stroke
Tumour
Infection- encephalitis, abscess
Motor neurone disease
Spinal pathology- traumatic transection, ischaema, infection

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15
Q

Cerebellar differential causes

A

MS
Stroke
Tumour
Infection
Drug induced- alcohol, anti-epileptics like phenytoin, carbamazepine
B12 deficiency
Wernickes
Cerebral palsy
Genetic- friedrichs ataxia, ataxia telengiectasia, episodic ataxia
Paraneoplastic syndromes

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16
Q

MS management

A

MDT approach led by neurology team including physios, occupational therapists, opthalmologist, SALT, psychologists
Managing exacerbations- oral or IV methylprednisolone depending on severity
Preventing progression with immunological agents such as natalizumab, peg interferon b and alemtuzumab
Managing complications
- spasticity with gabapentin, benzos, baclofen
- erectile dysfunction with sildenafil
- tiredness- amantadine and CBT
- incontinence- intermittent catheterisation or oxybutynin
- depression- amitryptyline

17
Q

Causes of horners

A

Split into central, preganglionic and post ganglionic
Central- MS, stroke
Pre ganglionic- cervical rib, trauma, thyroidectomy
Post- carotid artery dissection and

18
Q

Causes of motor neuropathy

A

Acquired
- GBS
- Lead poisoning
- Diphteria
Hereditary
- porphyria
- hereditary sensorimotor neuropathy

19
Q

Sensory predominant peripheral neuropathy

A

Metabolic
- uraemia
- B12
- hypothyroid
- alcohol
- uraemia
Infective
- leprosy
Systemic diseases
- Amyloidosis
- vasculitis

20
Q

Charcot marie tooth presentation

A

Pes cavus
Wine shaped leg
Foot drop
Hyporeflexia
Weakness in foot

21
Q

Charcot marie tooth management

A

MDT approach led by neurology
- physiotherapy which encourages exercise
- occupational therapy
- bracing
- orthopaedics to correct foot

22
Q

Nerve conduction studies findings

A

Demyelination- reduced speed
Axonal injury- reduced amplitude

23
Q

Investigations for charcot marie tooth disease

A

Nerve conduction studies- depends on the subtype
- CMT 1 is axonal loss
- CMT 2 is demyelination

24
Q

Causes of peripherla demyelination

A

GBS
Chronic inflammatory demyelination polyradiculoneuropathy
CMT type 2

25
Q

Central demyelination conditions

A

MS
JC virus causing progressive multifocal leukoencephalopathy

26
Q

Parkinsons management

A

MDT approach led by neurology
- include physio, OT, SALT
- medication includes- levodopa, dopamine agonists, monoamine oxidase B inhibitors
- first line depends if interruption of daily life, if so then levodopa with peripheral decarboxylase inhibitor like carbidopa

27
Q

Differentials for parkinsons

A

Drug induced
Essential tremor
Lewy body dementia

28
Q

Investigations for parksinsons

A

Clinical diagnosis but if diagnostic uncertainty could do DAT scan which will show reduced dopamine uptake in substantia nigra

29
Q

Proximal muscles weakness

A

Endocrine- cushings, steroids, thyrotoxicosis
Muscular dystrophy
Osteomalacia
Inflam- myositis, polymyalgia rheumatica
Neuromuscular disorders- MG, LEMs

30
Q

Bilateral upper motor neurone signs

A

MS
Myelopathy
MND

31
Q

Myelopathy damage areas and main findings

A

Central transection- spinothalamic+UL>LL
Anterior transection- bilateral below lost, dorsal preserved
Posterior transection- dorsal column
Brown sequard

32
Q

Causes of central spinal transection

A

Syringiomyelia