Test 3: CIDP and Post-Polio Flashcards

1
Q

things that are different with CIDP compared to AIDP

A

can have multiple plateaus
can have relapses
complete remission rare
slower progression
need long term meds
less likely to be ventilated
posterior column symptoms

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2
Q

diagnosis of CIDP

A

look for infection markers, HIV, hepatitis, lyme’s disease

serum IgG, IgM, IgA

LP to check CSF

nn conduction tests

1/3 have been incorrectly diagnosed

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3
Q

what characteristics indicate good or poor prognosis

A

decreased comorbidities, absence of monoclonal protins, elevated CSF proteins = good prognosis

predominant distal weakness = poor

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4
Q

immunotherapy effects

A

77% ambulate after 6 months; 82% at a year

children respond best

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5
Q

etiology and incidence of CIDP

A

1-7 cases in 100000

underreported

men more than women

older then 50 = more likely

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6
Q

risk factors for CIDP

A

no clear risk factors, just possible associations:
- autoimmune
- DM
- HTN
- antecedent infection

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7
Q

main S&S of AIDP

A

fatigue
pain
impaired physical function

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8
Q

other side effects of CIDP

A

depression
lower QOL
cognition not affected

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9
Q

medical management of CIDP

A

long term meds common

oral prednisone; pts responds well but significant side effects

IVIG = helpful but can damage vein access overtime

subcutaneous IG = alternative if IV admin not feasible

plasmapheresis = for those who don’t respond to IVIG or corticosteroids

immunosuppressants coupled with IVIG

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10
Q

PT exam components for CIDP

A

absent DTRs
weak MMT
sensory testing
balance
gait
hx recurrence
depression screen
functional mobility
rule out UMN S&S
screen endurance/fatigue
evaluate pain

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11
Q

PT intervention for CIDP

A

aerobic (3x/wk for 12 wks) = increase VO2Max; 70% max was target HR

resistance (3x/wk for 112 wks) = increase in isokinetic mm strength in pts; 3 sets 12 reps of 12 rep max weight

functional task training

gait

balance

etc

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12
Q

things to keep in mind given CIDP presents similar as MS

A

monitor fatigue throughout (RPE and HR)

non-pharm management for pain

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13
Q

what is polio

A

viral infection (enterovirus)

transmission = droplet or contact with fecal matter

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14
Q

types of severity with polio

A

1 = virtually asymptomatic
2 = GI, flu like, mm pain
3 = flu like that progresses to paralysis
- 10% of those paralyzed died
- some require mechanical vent

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15
Q

pathophysiology of polio

A

anterior horn cells in SC are targeted

these can die and lead to damage of axons interacting with the anterior horn cells (called Wallerian degeneration process)

mm atrophy is result

LMN S&S

usually asymmetric

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16
Q

hx of polio

A

common 1950-70s

initially thought to be static disease but then post polio was discovered

in 50s vaccine was developed; largely eradicated in US

17
Q

what is post polio syndrome

A

new mm S&S that occur decades after primary polio infection

avg = 25 years later

18
Q

incidence/etiology of post polio

A

1.6 million polio survivors in US at risk of developing; about 25-50% will develop

women more likely

more serious polio case = more likely to develop

pts who have post polio are likely 70+ bc of when the vaccine came out

19
Q

pathophysiology of post polio

A

after initial infection axons go through process of collateral sprouting to regain functional ability

surviving axons increase innervation ratio (i.e. instead of innervating 3000 mm fibers, now one axon innervates 5000)

eventually axon cannot take this increased stress and new denervation occurs

20
Q

S&S of post polio

A

mm weakness
atrophy
fatigue
mm/jt pain

weakness can also affect axial mm and impair breathing

weakness is worse with cold and increased PA

weakness slowly progresses over time

21
Q

diagnosis of post polio

A

EMG

mm biopsy; how innervated are mm fibers

rule out other neuro disorder

22
Q

medical management of post polio

A

fatigue management with anticholinergics (not largely effective)

non pharm pain management

can do tendon transfer sx for impaired foot posture

23
Q

PT exam/eval for post polio

A

LMN signs
strength
functional ability
rule out UMN signs

fatigue/endurance (do not push past fatigue lvl)

pain scales
gait
balance

** similar training to ALS; do not want to over fatigue

24
Q

PT treatment fro post polio

A

be careful with exercise and conventional strengthening
- mm and nerves have exhausted all collateral sprouting ability; of you tax too much there may be irreparable damage

lifestyle modification

compensation (lightweight bracing as needed)

energy conservation

never exercise to fatigue

only do non-exhaustive exercise and track vitals and RPE

may have jt deformities from uneven strain of mm on joint; consider this when picking intervention (may need orthoses or sx)