Multiple Sclerosis Flashcards

1
Q

Describe some features of multiple sclerosis

A

Disease of young people, has variable severity, diverse presentation and the prognosis is uncertain

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1
Q

What is multiple sclerosis?

A

A central nervous system disease affecting the white matter
Demyelination (inflammation) causing focal disturbance of function
Most patients develop progressive disability

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2
Q

Describe the prevalence of multiple sclerosis

A

190 per 100000 in Scotland
50-60 cases per year in Aberdeen

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3
Q

What is the average age of onset for multiple sclerosis?

A

Around 20-30

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4
Q

Describe the pathogenesis of multiple sclerosis

A

Complex genetic inheritance and has association to autoimmune disease - more females to males
Commoner in temperate climate

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5
Q

What is the initial presentation of multiple sclerosis?

A

Relapse - demyelination
Inflammation which has gradual onset over days and stabilises days to weeks
Gradual resolution - partial or complete recovery

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6
Q

What are some symptoms of a relapse in multiple sclerosis?

A

Optic neuritis, sensory symptoms, limb weakness, brainstem - diplopia, vertigo/ataxia, spinal cord - bilateral motor and sensory symptoms and bladder involvement

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7
Q

Describe optic/ retrobulbar neuritis

A

Subacute visual loss, pain on moving eye, colour vision impaired, resolves over weeks/ months
Initial optic disc swelling, optic atrophy and relative afferent pupillary defect

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8
Q

What is a relative afferent pupillary defect?

A

Dark room, shin torch into eye and constriction
As swing to affected eye then they dilate
Swing light and they constrict

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9
Q

Describe a brainstem relapse

A

CN involvement
Pons - internuclear ophthalmoplegia
Cerebellum - vertigo, nystagmus and ataxia
UMN signs in limbs
Sensory involvement

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10
Q

What is left internuclear ophthalmoplegia?

A

Normal gaze to left
Gaze to right causes left eye to not abduct and nystagmus in right eye

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11
Q

What does a spinal cord lesion cause?

A

Partial or transverse (complete) myelitis
Sensory level is often with band of hyperaesthesia
Weakness/ UMN changes below demyelination
Bladder and bowel involvement

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12
Q

What is the process of demyelination?

A

Autoimmune process - activated T cells cross blood brain barrier causing demyelination
Acute inflammation of myelin sheath causing loss of function

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13
Q

Can demyelination repair?

A

Yes and can have recovery of function
Post inflammatory gliosis may be functional deficit

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14
Q

What is clinically isolated syndrome (CIS)?

A

When no further episodes of demyelination as MS is episodes of demyelination in space and time

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15
Q

Describe further relapes in MS

A

May occur within months or years of first episode
Variable site and severity
Is underlying infection in some
Fewer relapses in pregnancy

16
Q

What does progression of MS cause?

A

Axonal loss - which contributes to persistent disability
Can see black holes on MRI
Later seen as cerebral atrophy

17
Q

What are some progressive phase symptoms and signs?

A

Fatigue, temp. sensitivity, dysesthesia, stiffness or spasm, balance and slurred speech, bladder and bowel, diplopia/ visual loss, dysphagia and cognitive memory affected

18
Q

What can be seen on examination of progressive MS?

A

Afferent pupillary defect, nystagmus, cerebellar signs, weakness, spasticity, hyperreflexia and plantars extensor

19
Q

What are the types of MS?

A

Relapsing remitting (RRMS) 85%
Secondary progressive (SPMS)
Primary progressive (PPMS) 10-15%

20
Q

Describe primary progressive MS

A

Often presents in 5th or 6th decade, no relapses, spinal and bladder symptoms
Prognosis is poor

21
Q

How is MS diagnosed?

A

Evidence of demyelination separated in time and space
Can be clinical or MRI based
Posers criteria - clinical

22
Q

How are active lesions seen on MRI?

A

Add Gadolinium to show active lesions - demyelination

23
Q

What are some other investigations used in MS?

A

Lumbar puncture - normal CSF and protein but few WCC and oligoclonal bands present
CXR, Bloods, visual evoked response

24
What are some differential diagnosis for MS?
Acute disseminated encephalomyelitis, autoimmune condition, demyelination conditions, sarcoidosis, vasculitis, infection and adrenoleukodystrophy
25
What are come differential diagnosis of optic neuritis?
Neuromyelitis optica, sarcoid, ischaemic optic neuropathy, B12 deficiency, Wegener's granulomatosis, local compression, infection
26
What are some differential diagnosis for myelitis?
Inflammation - sarcoid, SLE, neuromyelitis optica Infection or post-infection Tumour, paraneoplastic process, stroke
27
What is the treatment for MS?
Treatment for relapse, disease modifying treatment, health and diet, symptomatic control and MDT approach
28
What is the treatment for an acute relpase?
Look for underlying infection Oral prednisolone - IV, rehabilitation and symptomatic treatment
29
What is included in symptomatic treatment of MS?
Spasticity muscle relaxants/ antispasmodics, physio Dysesthesia-amitriptyline, gabapentin urinary anticholinergic Rx, bladder stimulator Constipation - laxatives Sexual dysfunction - sildenafil
30
What are some other symptomatic treatments?
Fatigue graded exercise, Depression - CBT and medication, cognitive memory aids, tremor aids, vision - carbamazepine, speech - SALT
31
Who is included in the MDT for MS?
MS nurse, physiotherapy, occupational therapy, speech and language therapy, dietician, rehab specialists, continence advisor and psychiatry
32
What are the 2st line treatments for disease modifying treatments?
SC or IM injections - beta-interferons and glatiramer acetate Oral - teriflunomide and dimethyl fumarate
33
What are the 2nd line agents used for treatment?
natalizumab, Fingolimod, Cladribine and Ocrelizumab Alemtuzumab
34
Describe disease modifying treatment
Not a cure, reduces relapse rate, does not slow the progression and has side effects
35
What can immunosuppression cause?
Progressive multifocal leukoencephalopathy (PML)