Multiple Sclerosis Student Version
Multiple Sclerosis Student Version
Multiple Sclerosis
April 2018
Aetiology
• A chronic (usually progressive) inflammatory demyelinating condition
involving the immune system.
• When MS is active, activated T-cells (lymphocytes) cross the blood-
brain barrier and attack myelin and oligodendrocytes causing
demyelination and inflammatory response.
• Axonal conduction/nerve transmission becomes distorted.
• Inflammation dies down in the plaque and healing mechanisms follow,
forming a scar – gliosis.
• Further episodes of acute inflammatory process can damage axons
(usually later in the disease).
Epidemiology and Incidence
• Most common disabling neurological disorder among young people.
• Most commonly diagnosed between the ages of 20 and 40; slightly
more common in women.
• Between three and seven people per 100,000 population are
diagnosed with MS each year.
• About 100 to 120 people per 100,000 population have MS.
• It is estimated that in England and Wales about 1800 to 3400 people
are newly diagnosed with MS each year and that 52,000 to 62,000
people have MS.
(NICE guidelines, 2003)
Diagnosis
• Clinical history and examination (McDonald Criteria)
• MRI scanning (MRI scans confirm a diagnosis in over 90 per cent of
people with MS.)
• Evoked potentials
• Lumbar puncture
Risk factors
• Minor gender bias ( female: male)
• Minor familial trait
• Geographical distribution
• Possible viral ‘trigger’ –link with Epstein Barr virus
• Low levels of Vitamin D
• Lifestyle factors
Global prevalence of MS (per
100,000 population)
Patterns of Disease Progression
Signs and Symptoms
• Depends on site and extent of lesion(s)
• Cerebral hemisphere- memory, processing, emotions, selective
movement, altered sensation.
• Spinal cord- weakness, spasticity, tingling, numbness, L’hermitte’s
sign, altered bladder and sexual function.
• Optic nerves- Impaired vision and eye pain
• Medulla and pons- Dysarthria, double vision, vertigo, nystagmus,
oscillopsia
• Cerebellar white matter- Dysarthria, nystagmus, oscillopsia, intention
tremor, ataxia
Primary Clinical Problems
• Weakness
• Spasticity/spasms
• Sensory loss/alteration
• Pain
• Ataxia/tremor
• Swallowing difficulty
• Speech problems
• Visual problems
• Fatigue
• Cognitive deficits
• Depression
• Emotionalism
• Bladder, bowel dysfunction
• Sexual dysfunction
Secondary Clinical Problems
• Contractures
• Muscle atrophy
• Osteoporosis
• Urinary tract infections
• Skin breakdown
• Reduced Cardio Vascular fitness
Tertiary Problems
• Income
• Status
• Social isolation
• Depression
• Anxiety
• Relationships
Multiple Sclerosis -NICE guidelines
Interventions
• Lifestyle changes
• Disease modifying therapies Interferons
• Symptom management ( pharmaceutical)
• Symptom management ( physical )
• Symptom management ( other MDT members )
• Encourage person centred care and facilitate self management and
agency
Outcome Measures
• MS clinical study measures : https://
www.nationalmssociety.org/For-Professionals/Researchers/Resources
-for-Researchers/Clinical-Study-Measures
Overarching:
• Functional Systems Score (FSS) and Expanded Disability Status Scale
(EDSS)
• Multiple Sclerosis Functional Composite (MSFC)
Specific
• 9 hole peg test
• Timed 25 foot walk; Ambulation Index
Supporting guidelines
• NICE pathways and guidelines (October 2014) https://
www.nice.org.uk/guidance/cg186
• Physiotherapy (2008)
https://
www.mssociety.org.uk/sites/default/files/Documents/Professionals/Ph
ysios/Translating_NICE_and_NSF_a%20guide%20for%20physios.pdf
References
• Marieb, E.N. & Hoehn, K. (2010). “Human anatomy & physiology”. 8th edn. San Francisco: Pearson
Benjamin Cummings
• Stokes, M. (2004). "Physical Management in Neurological Rehabilitation. 2nd edition". Elsevier
Mosby.