MS/MND/spinal cord/muscular disorders Flashcards
Proportion of patients with relapsing-remitting MS who go on to develop secondary progressive?
65%
Management of MS? (2)
Disease-modifying drugs e.g. Interferon beta, fingolimod
MePred 0.5g daily for flares
What does MND never involve? (2)
Eye movements
Sensory nerves
Prognosis of MND?
Death from ventilatory failure usually within 3-5 years after diagnosis
Only disease-modifying drug licensed for MND?
Riluzole- confers a survival benefit/delays time to mechanical ventilation
Symptom control in MND: cramps
Quinine (1st line)
Symptom control in MND: spasticity
Baclofen, tizanidine, dantrolene, gabapentin
Symptom control in MND: drooling
Propantheline, glycopyrronium bromide, amitriptyline, botox
Symptom control in MND; dysphagia
Discuss parenteral feeding e.g. PEG
Three forms of CJD?
Sporadic (“classical”)
Variant- (from ingestion of nervous tissue in beef with bovine spongiform encephalitis)
Familail prion disease
Injury to the spinal cord above T1 causes?
Quadriplegia/tetraplegia
Injury to the spinal cord below T1 causes?
Paraplegia
Ipsilateral movement loss with contralateral pain and sensation loss?
Brown-Sequard syndrome
Wasting + weakness of hands and arms, with loss of temperature + pain sensation in a “cape” distribution
Syringomyelia
Inflammation of the spinal cord at a single level
Transverse myelitis