Multiple Sclerosis Presentation PDF

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NavigableJadeite1784

Uploaded by NavigableJadeite1784

University of the West of England

Lois Stevens

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multiple sclerosis neurological disease medical presentation

Summary

This presentation provides an overview of multiple sclerosis (MS), covering various aspects such as epidemiology, causes, pathology, diagnosis, and treatments. The presentation highlights the prevalence of MS, particularly among young adults, and the different types of MS, with a focus on the progressive nature of the disease. The presentation also discusses potential treatment options, encompassing pharmacological and other considerations.

Full Transcript

Presentation by Lois Stevens Multiple Sclerosis Senior Lecturer MULTIPLE SCLEROSIS Most common disabling neurological disease amongst young adults. Approx 85,000 people in the UK, though recent mapping has shown this to be more likely nearer 100’000.  2,500,000 worldwide. ...

Presentation by Lois Stevens Multiple Sclerosis Senior Lecturer MULTIPLE SCLEROSIS Most common disabling neurological disease amongst young adults. Approx 85,000 people in the UK, though recent mapping has shown this to be more likely nearer 100’000.  2,500,000 worldwide. Women more likely then men (2:1) Diagnosis usually between 20 and 40 years. Epidemiology Prevalence increases as you move away from the equator. Race Certain ethnic groups have a lower prevalence (i.e. Maoris in New Zealand) Migration Moving as an adult from an area of low risk to an area of high risk you retain the risk from the original area. Moving as a child you obtain the local risk. CAUSES Genetics Infection Lack of sunlight Diet Environment CHANCE Pathology Pathology Pathology Progressive autoimmune inflammatory disorder affecting CNS myelin Demyelinating plaques appear in the white matter as seen in radiographic images Preponderance of lesions in the peri- ventricular white matter, within the optic nerves and in the long tracts of the spinal cord Pathology Acute lesion: marked inflammatory reaction, destruction of myelin and degeneration of oligodendrocytes – relative sparing of the cell body and axon Older lesion: infiltration with macrophages, proliferation of astrocytes, laying down of fibrous tissue Ultimately leaves a fibrous scar with no potential for recovery Pathology Axonal damage in late stages of the disease Probably responsible for the more progressive and chronic forms of the disease Shows on MRI as brain atrophy, degeneration of the ascending and descending tracts and ventricular dilation MRI DIAGNOSIS CLINICAL SIGNS MRI LUMBAR PUNCTURE VISUAL EVOKED POTENTIALS Site of damage Spinal cord. Brain Stem. Optic Nerve Cerebellum. Areas involved with thought and emotion. Non specific area. Clinical signs will reflect the site and severity of lesions. Cerebellar Signs Ataxic gait – wide base/poorly co-ordinated limb placement Intention tremor – only during volitional movement, not seen at rest Dysmetria – overshooting/undershooting Dysdiadochokinesia Slurred speech - rhythm and flow disrupted Balance difficulties Impairments Spasticity and spasm Weakness Fatigue Pain Gait impairments https://youtu.be/W8nCWxMbSDU TYPES OF MS TYPES OF MS TYPES OF MS TYPES OF MS TREATMENTS - PHARMALOGICAL Disease modifying drugs Beta Interferon 1a (Avonex, Rebif) Beta Interferon 1B (Betaferon) Glatiramer acetate (Copaxone) Can reduce the relapse rate for people with RRMS by about one third over a two year period. TREATMENTS - PHARMALOGICAL STEROIDS Methylpredinisolone Helps to reduce inflammation Year 2 Treatments Research Outcome Measures

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