Module 12.1 - Multiple Sclerosis Flashcards Preview

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Flashcards in Module 12.1 - Multiple Sclerosis Deck (9)
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1
Q

What is multiple sclerosis?

A

An immune-mediated inflammatory demyelinating disease of the central nervous system (CNS) which is characterized pathologically by multifocal areas of demyelination

2
Q

Describe the etiology of multiple sclerosis

A
  • Highly variable progression and many atypical forms
  • Diagnosed primarily clinically
  • Women have a 2 – 3 times higher incidence than men.
  • Onset of disease is earlier in women than men.
  • Caucasians have higher incidence than African Americans.
  • Onset occurs in 20s-40s for up to 80% of patients
  • No clear etiology, but thought to be multifactorial in cause
    • Viral infection as precursor
    • No clear genetic association
3
Q

What are the 5 types of multiple sclerosis?

A

A. Relapsing-Remitting (RRMS) – 85-90% of cases at onset; characterized by clearly defined relapses with full recovery, or with residual deficit upon recovery. Minimal disease progression during periods between relapses; most individuals will eventually enter a secondary progressive phase

B. Secondary Progressive (SPMS) – occurs 10-20 years after disease onset; characterized by initial RRMS course followed by gradual worsening with or without occasional relapses

C. Primary Progressive (PPMS) – represents about 10% of cases at disease onset; characterized by progressive accumulation of disability from disease onset with occasional plateaus, and relapses

D. Malignant MS – occurs in approx. 6% of patients; usually older at diagnosis; aggressive, rapid progressive course leading to significant disability in a relatively short amount of time after disease onset

E. Benign MS – occurs in about 15% of patients; a retrospective diagnosis made when the individual remains fully functional 10-15 years after disease onset; a single demyelinating event followed by no relapse

4
Q

What are some subjective findings associated with multiple sclerosis?

A
  • Motor weakness, spasticity or stiffness
  • Sensory alterations – numbness, burning, tingling in 1 or more limbs, facial numbness
  • Brain stem symptoms- double vision, dysphasia, vertigo
  • Visual deficits- decreased acuity, impaired color perception, field deficits, double vision/blurred vision
  • Cerebellar symptoms- gait ataxia, tremor, uncoordinated movements
  • Cognitive dysfunction – short term memory, slowed processing, difficulty in higher level problem solving
  • Fatigue – 90% Of patients
  • Sleep Disorders
  • Bladder, bowel and sexual dysfunction
  • Seizure
  • Tonic spasms
5
Q

What are some physical exam findings associated with multiple sclerosis?

A
  • Sensory disturbances 20-50% Of patients
  • Decreased vibratory sense, position sense, pinprick perception and temperature sensation
  • Reflexes- abnormal DTRs, positive Babinski and Hoffman, spastic limb weakness
  • Brain Stem disorders – nystagmus, hearing loss, tinnitus
  • Cerebellar disorders – ataxia, tremor, lack of coordination
  • Visual disorders- 25% of patients initially present with optic neuritis; visual field defect, trigeminal neuralgia
  • Frontal Lobe – cognitive dysfunction, emotional lability
6
Q

What lab/diagnostic tests are used to diagnose multiple sclerosis?

A

A. Complete neurological exam with noted deficits

B. MRI Findings: white matter lesions in brain, lesions in spinal cord, T2 weighted lesions in periventricular white matter of brain and spinal cord, cerebral atrophy

C. CSF Findings: elevated IgG with oligoclonal bands in CSF but not serum; 70% of patients with bands in CSF (not conclusive)

D. Evoked Potentials: slowed conduction or prolonged evoked response, not conclusive

E. McDonald Diagnostic Criteria: developed in 2001, latest revision 2010; core requirement of the diagnosis is the objective demonstration of dissemination of CNS lesions in both space and time, either clinically alone or a combination of clinical and MRI findings.

  • Dissemination in space: MRI shows 1 or more T2 lesions in at least 2 of 4 MS typical regions of the CNS OR by the clinical development of attack of a different CNS site
  • Dissemination in time: MRI shows the simultaneous presence of asymptomatic gadolinium enhancing and non-enhancing lesions at any time or a new T2 or gadolinium enhancing lesion on follow-up MRI irrespective of its timing with reference to baseline scan. OR the development of a second clinical attack.

F. Other

  • No other explanation for MRI findings, CSF findings, or abnormal evoked potentials
7
Q

How do you manage a patient with multiple sclerosis?

A

A. Neurology consult

B. Mild acute exacerbations- not always requiring treatment if no functional decline present

C. Acute intervention for relapse:

  • Glucocorticoids, oral of IV: High dose (500-1000mg/day) ;usually Methylprednisolone; duration dependent on clinical response
8
Q

What is the role of Disease modification medications in multiple sclerosis?

A

Reduces relapse rate, delays disability; initiate early in course of disease to slow progression of disease

  • Fingolimod (Gilenya)- 0.5mg po daily; observe for bradycardia
  • Interferon beta-1b: Betaseron or Extavia used in relapsing form of MS; SQ administration every other day; watch for depression/suicidality; injection site necrosis
  • Interferon beta-1a : Avonex- used in relapsing MS; IM weekly dosage; watch for flu like symptoms, fatigue depression, myalgias
9
Q

What are important symptoms to control in patients with multiple sclerosis?

A

Spasticity, fatigue, mood disorders, immobility, seizures, incontinence, cognitive effects, gait disturbances, sexual dysfunction