lecture 4: guillain barre syndrome and CNS tumors Flashcards

1
Q

what is another name for guillain barre syndrome

A

Acute Inflammatory Demyelinating Polyradiculoneuropathy (AIDP)

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2
Q

guillain barre syndrome is an immune mediated ____ that affects ____ ___ and ____ nerves , leading to ____ neuropathy and flaccid paralysis with possible sensory and ANS effects

A

polyneuropathy
nerve roots
peripheral
motor

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3
Q

guillain barre syndrome usually follows an ____

A

infection

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4
Q

what kind of onset is guillain barre syndrome

A

rapid

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5
Q

is Guillain-Barré Syndrome/ a UMN or LMN disorder

A

lower
schwann cells make up the myelin

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6
Q

what age and sex does Guillain-Barré Syndrome/ usually affect

A

males
any ages but usually > 50

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7
Q

what is usually the first symptoms of someone with Guillain-Barré Syndrome/

A

weakness and tingling/loss of sensation in the hands and feet , ascending the limbs

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8
Q

how are the motor symptoms in Guillain-Barré Syndrome/

A

goes distal to proximal (ascending paralysis)
rapid and progressive
relative symmetrical motor involvement

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9
Q

how is the sensory loss in Guillain-Barré Syndrome/

A

glove adn stocking

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10
Q

how are the relaxes in Guillain-Barré Syndrome/

A

decreased

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11
Q

what cranial nerve involvement is in Guillain-Barré Syndrome/

A

CN 7,9, 10 , 11 , 12

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12
Q

what is present in up to 50% if pts with Guillain-Barré Syndrome/

A

dysautonomia

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13
Q

1/3 patients required assisted ___ due to paralysis and weakness in diaphragm, intercostals , accessory inspiratory musculature

A

ventilation

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14
Q

is the single breath count test is < ___ then they might require mechanical ventilation for Guillain-Barré Syndrome/

A

19

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15
Q

what Guillain-Barré Syndrome disability scale is used as a outcome measure what score is it if that patient is

confined to bed or chair
requiring assisted ventilation
dead

A

4,5,6

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16
Q

when is the acute stage of GBS

A

1-10 days

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17
Q

when is the peak of motor sysmtoms for GBS

A

2-8 weeks post onset

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18
Q

when is the plateau periods for GBS

A

2-8 weeks

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19
Q

when can improvement begin for GBS

A

2-3 months post onset

20
Q

what does it mean when most patients have a fulminating course of GBS

A

disease develops rapidly and severely

21
Q

when is max paralysis for GBS

A

1-2 days of onset

22
Q

most GBS patients will reach their peak at how many weeks

23
Q

what factor of GBS are associated with poor prognosis

A

Severity of muscle weakness (especially tetraplegia)
• If respiratory support required
• Cranial nerve involvement associated with loss of eye movement, swallowing
• Rapid rate of progression from onset
• Length of time to nadir
• Older age at onset
• History of GI illness
• Recent cytomegalovirus

24
Q

what kind of deficit do GBS patients have and what is the primary movement dysfucntion

A

force production and weakness

25
Q

during the ascending phase of GBS is PT invovled

A

maybe or maybe not

education is important durign this stage and gentle PROM , AAROM and AROM

26
Q

what kind of ROM is being done during the plateau stage of GBS

A

AAROM and AROM

27
Q

when do u Encourage multi-joint and cross-plane work without forgetting need for
single joint and/or gravity minimized positions for GBS patients

A

during the plateau stage

28
Q

what considerations should u have during the descending phase of GBS

A

• Eccentric contractions
• Fast-twitch fibers
• Pain
• Fatigue
• Vitals

29
Q

when should u avoid exercise for GBS patients

A

in acute and progressive stages , limited to ROM (AROM or AAROM)

30
Q

when can u do Limited repetition low resistance activities can be commenced once strength
begins to return

A

after plateau

31
Q

when should u avoid eccentric contr4actions from GBS

A

if less then or equal to 3/5 strength

32
Q

what are the two distinct groups that CNS tumors are presents in

A

childeren 0-14 and adults 40-70

white , male

33
Q

what is teh difference between primary and secondary tumor presentation

A

primary: originate in the CNS

secondary: metastatic tumors that spring to the CNS from systemic cancer sits out of the brain

34
Q

what is the Most common cause of cancer death in children and adolescent 0-19 years

A

primary CNS tumors

35
Q

how does secondary tumors usually spread

A

through arterial circulation

36
Q

what determines the impairment the patient with a tumor will have

37
Q

what is the most common type of non malignant brain tumor

A

meningioma

38
Q

what is the most common type of malignant brain tumor

A

glioblastoma

39
Q

what sign and symptoms is present in 50% of patients with CNS tumor

40
Q

what are the signs and symptoms of a CNS tumor

A

headache
seizures
altered mental status
papilledema

41
Q

what are focal neurological signs of CNS tumor

A

weakness,
numbness, loss of coordination, vision
problems, speech difficulties, seizures,
altered mental state (memory loss, confusion,
change in personality)

42
Q

what is the frontal and parietal lobe responsible for

A

frontal: personality , movement , sense of smell

parietal lobe: identification of objects , sense of pain and touch , spatial position

43
Q

what is the temporal and occipital lobe responsible for

A

temp: mem, speech, musical rhythm

occ: vision

44
Q

what does the pons and medulla control

A

pons: eye and face movement

medulla: heart and lungs

45
Q

when is a headache a red flag

A
  • interrupts sleep or is worse on waking and improves thru the day
  • elicited by postural changes, coughing , or exercise
  • recent onset is more severe

-new onset of headaches in older poeple

  • associated with nausea, commit , papilledema or focal neurological sings
46
Q

has exercise been found to provide positive benefits to cancer survivors