lecture 4: guillain barre syndrome and CNS tumors Flashcards

(46 cards)

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 (bc it is a LMN disorder)

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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

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

A

19

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15
Q

The Guillain-Barré Syndrome disability scale is used as a outcome measure for function/acitvity, what score is it if that patient is

able to walk without support of a stick bu incaoable of manual work
confined to bed or chair
requiring assisted ventilation
dead
able to walk with a AD

A

2, 4,5,6, 3

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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
during the **ascending** phase of GBS is PT invovled
maybe or maybe not education is important durign this stage and gentle PROM , AAROM and AROM
26
what kind of ROM is being done during the **plateau** stage of GBS
AAROM and AROM
27
when do u Encourage multi-joint and cross-plane work without forgetting need for single joint and/or gravity minimized positions for GBS patients
during the plateau stage
28
what considerations should u have during the **descending** phase of GBS
* Eccentric contractions * Fast-twitch fibers * Pain * Fatigue * Vitals
29
when should u avoid exercise for GBS patients
in acute and progressive stages , limited to ROM (AROM or AAROM)
30
when can u do **Limited repetition low resistance activities** can be commenced once strength begins to return
after plateau
31
when should u avoid **eccentric contr4actions** from GBS
if less then or equal to 3/5 strength
32
what are the two distinct groups that CNS tumors are presents in
childeren 0-14 and adults 40-70 white , male
33
what is teh difference between primary and secondary tumor presentation
primary: originate in the CNS secondary: metastatic tumors that spring to the CNS from systemic cancer sits out of the brain
34
what is the **Most common** cause of cancer death in **children and adolescent 0-19 years**
primary CNS tumors
35
how does **secondary** tumors usually **spread**
through arterial circulation
36
what determines the **impairment** the patient with a **tumor** will have
location
37
what is the **most common** type of **non malignant brain tumor**
meningioma
38
what is the **most** **common** type of **malignant brain tumor**
glioblastoma
39
what **sign and symptoms** is present in **50**% of patients with **CNS tumor**
headache
40
what are the signs and symptoms of a CNS tumor
headache seizures altered mental status papilledema
41
what are **focal neurological signs** of CNS tumor
* weakness, * numbness, loss of coordination, vision * problems, speech difficulties, seizures, * altered mental state (memory loss, confusion, change in personality)
42
what is the **frontal** and **parietal** lobe responsible for
frontal: personality , movement , sense of smell parietal lobe: identification of objects , sense of pain and touch , spatial position
43
what is the **temporal** and **occipital** lobe responsible for
temp: mem, speech, musical rhythm occ: vision
44
what does the **pons** and **medulla** control
pons: eye and face movement medulla: heart and lungs
45
when is a headache a red flag
- 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
has exercise been found to provide positive benefits to cancer survivors
yes