Trigger - Misc Flashcards

1
Q

unsuccessful attempts at remyelination results in plaques and scaring

A

MS

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2
Q

Hypovitaminosis D predisposes you to what diagnosis

A

MS

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3
Q

symptoms worsen with increasing body temp

A

uthoff phenomenon in MS

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4
Q

Shock like sensation down legs

A

Lhermittes symptoms in MS

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5
Q

increased risk of optic neuritis and relative afferent pupil defect

A

eye problems in MS, theres alot more, i just put theswez

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6
Q

what cranial nerves are effected in MS

A

5,7,9

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7
Q

detrusor muscle hyperreflexia

A

MS

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8
Q

what is clinically isolated MS syndrome

A

first MS attack, must last 24 hrs. doesnt have to meet all criteria

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9
Q

what kind of tremor can present in MS

A

intention tremor

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10
Q

deterioration in function separate from attacks

A

secondary MS

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11
Q

steady decline in function from onset of disease. no remission or relapse

A

primary MS

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12
Q

waves of remission and relapse in functional status.

A

RRMS

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13
Q

marked delay in latency during evoked potential testing

A

diagnostic of MS even in asymptomatic patients

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14
Q

oligoclonal bands and intrathecal IgG on CSF analysis

A

diagnostic study for MS patients with Isolated syndrome or atypical presentation.

also may see mild WBC elevation

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15
Q

acute tx of MS meds

A

methylprednisolone

Plasma exchange if needed

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16
Q

what must ptts be tested for prior to being given disease modifying agents

A

hep A
hep B
hep C
VZV

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17
Q

what are indications for disease modifying drugs in MS? what are the modifying drugs

A

CIS w rilsent lesions or relapsing RRMS or SPMS

  • monoclonal abx (ocrevus)
  • oral therapies
  • platform injection therapies
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18
Q

BBW for irsk of progressive multifocal leukoencephalopathy. all pts MUST be tested for JC abx prior to therapy

A

Ocrevus (MAB) for MS

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19
Q

ampyra is used when

A

K+ channel blocker that is used in MS when LE weakness interferes with ambulation

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20
Q

magnesium, abx, corticosteroids are used as protective factors for what

A

cerebral palsy

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21
Q

leading cause of childhood disabiltiy

22
Q

hand preference before 12 months, gross motor delay in year 1.

A

Cerebral palsy

23
Q

imaging can be cranial US, MRI of brain, or CT

A

Cerebral palsy

only do MRI if baby is >3 weeks

24
Q

usually follows trauma and presents with patchy bone demineralization, skin changes.

A

complex regional pain syndrome

25
single limb prevented use via pain
Complex regional pain syndrome
26
pain made worse by loud noises, light touch, motion and stress
Chronic regional pain syndrome acute phase 3 months
27
when does cyanosis/pallor and atrophy of subcutaneous tissue present. Joint fibrosis also present here
subacute stage of chronic regional pain syndrome 9 months
28
edema resolves, skin is dry/pale/cool/shiny. joint stiffness progresses and osteoporosis can happen
chornic stage of chronic regional pain syndrome
29
budapest criteria
chronic regional pain syndrome
30
first line treatment is OT and PT
Chronic regional pain syndrome
31
Fatal neurodegenetaive disease of both upper and lower motor neurons characterized by progressive loss of motor function
amyotrophic lateral sclerosisis
32
what is the MC type of ALS
sporadic
33
what is hte MCC of death in ALS
pneumonia
34
Impaired astrocytes increase glutamate => increased Ca2+ uptake too much ca = mitochonrial oxidative stress
pathophys of ALS
35
drooling, amotional lability, involuntary laughing crying
bulbar dysfunction in ALS involuntary laughing/crying = psuedobulbar affect syndrome
36
EMG will show both acute and chronic denervation and reinnervation. Both upper and lower motor neuron lesion dysfunction
ALS
37
Only proven med that extends life in ALS patients
riluzole inhibits release of glutamate (ALS = excess glutamate)
38
Only used for pts with a SOD1 gene mutation
tofersen
39
MC caused by sepsis
toxic metabolic encephalopathy
40
diagnosis of exclusion
toxic metabolic encephalopathy
41
asterixias, brisk DTRs , exagerated physiologic tremors
toxic-metabolic encephalopathy
42
Cafe au lait spots
Neurofibromatosis
43
soft, pea sized lesions that are nonpainful or tender
neurofibromas found in neurofibromatosis
44
bowing of the lower legs scoliosis
NF type 1
45
compression of the pituitary, optic gliomas
NF type 1
46
ADHD common in this disorer
NF type 1
47
MCC of death in NF type 1
malignant tumor
48
MC lesion in NF type 2
Benign, slow-growing tumor of the vestibulocochlear nerve CN 8
49
gradual hearing loss, tinnitus, ataxia, HA
NF type 2
50
Multiple, non-cutaneous schwannomas without vestibular involvement
schwannomatosis
51
Focal pain of neuropathic and nocipceptive nature Focal numberness and weakness Muscle atrophy
schwannomatosis SOOOO PAINFULLLLLL