Guillain-Barre Syndrome Flashcards

1
Q

what is GBS

A

acute generalized weakness
broad group of demyelinating inflammatory polyradiculoneuropathies

  • nerve roots and epripheral nerves are affected-
  • LMN disorder

results in flaccid paralysis

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2
Q

pathophysiology

A

involves autoimmune reactions-> cross-reaction with neural tissue

Myelin is destroyed-> inflammation occurs

acute inflammatory lesions are present within several days of onset of sysmptom

Never conduction is slowed and may be blocked completely

Schwann cells are destroyed by AXONS are left in tack

**Schwann cells do begin to regrow after 2-3 weeks of demylennation and inflammation subsides

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3
Q

clinical features

A

rapid and progressive over 3-7 days

loss of motor function occurs: distally and then progresses to proximal

*distal extremity paraesthesia=pins and needles

dysesthesia= abnormal burning and pain sensation

pain reported as musculature=myalgia

DTR’s are absent from demyelination of peripheral nerves

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4
Q

Postpolio Snydrome

A

-late effects of poliomyelitis

viral infection which attacks some of the anterior horn cells in spinal cord=muscular paralysis

due to increased metabolic demands by giant motor units

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5
Q

GIANT MOTOR UNITS-PPS

A

formed during recovery process from the original viral infection

polio destroyed anterior horn cells

muscle fibers innervated by ant. cells that were destroyed were taken up by reinnervating them anterior horn cells not destroyed which causes giant motor units

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6
Q

clinical features of PPS

A
fatigue
new weakness
pain
cold intolerance
decreased function
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7
Q

Symptoms of GB

A

rapid 3-7 days
symmetrical extremity weakness with hyporeflexia

initially proximally, then distally

initially LE then UE and face if effected

respiration and swallowing muscles effected

neuropathic or radicular pain

tachycardia-cardiac irregularities

facial flushing

abnormalities of sweating, pulmonary dysfunction and impaired sphincter control

fever

nausea

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8
Q

medical management for GB

A

plasmapheresis w/ respiratory dysfunction

IV immunoglobulin

ICU w/ ventilator if rapid progressiveness

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9
Q

Rehab for GB in acute phase

A

pulmonary rehab
skin management
PROM with orthotics to prevent contractions

ther ex/ mobility training upon fair to good muscle grade

pain management w/ TENS

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10
Q

Sub acute Rehab with GB

A

Ther EX: ARROM within pt. tolerance, avoid overuse to prevent pain

functional mobility training

  • orthotics
  • ambulation devices

continue with pain management

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11
Q

REHABILITATION PHASE GB

A

continue to progress resistive exercise as tolerated

cont. functional mobility training

adaptive equipment
pain management

gradual aerobic training

OT:

  • UE strength
  • ADL training and adaptive equp.
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12
Q

Prognosis with rehabilitation phase

A

20% permanent physical limitation
-ankle DF

within 6 months-85% ambulatory

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13
Q

Bulbar palsy

A

facial nerve CN7 involved with bilateral facial weakness

double vision from eye muscle weakness -CN 3,4,6

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14
Q

what is plasmapheresis with GB

A

remove blood from body and seperate red and white blood cells from plasma and only blood cells are returned to patient

  • body makes more plasma to replace
  • it elminates some of the immune factors responsible for disease progression
  • reduces length of illness
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15
Q

3 phases of GB

A
  1. acute
    - 4 weeks
    - 100% core symptoms occur
  2. Plateau
    - stabilization of symptoms
    - no longer progressing
    - can last 4 weeks
  3. recovery
    - patient begins to improve
    - 80% of pts. recover within a year but some have residual deficits
    - can last several months to years
    - poor outcome for those who needed ventilation and had rapid progression of demyelination
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