Pediatric Orthotic Problem solving Flashcards

1
Q

Typical guidelines for bracing state that we should brace to which one: R1 or R2?

A

R1, within spasticity free ROM

However, Dr. Bickley states that she braces to R2

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2
Q

When should you evaluate the effects of an AFO?

A

Wait a week or two for the patient to get used to it

don’t make immediate judgements on how effective it is as soon as they put it on and walk for the first time

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3
Q

What are the 3 ways an AFO can help with non-ambulatory needs

A

Contracture managment

Wound healing, protection/prevention

positioning

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4
Q

What should we keep in mind about orthotic comfort?

A

Orthotic MUST be comfortable

especially a night time AFO, it cannot interfere with pt sleep

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5
Q

What are the two methods of making an orthotic more comfortable

A

Minimize pressure by maximizing area covered

Provide sufficient leverage by increasing the longitudinal segments of the orthotic

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6
Q

the most basic pressure system for an orthotic is the _______

A

3 point pressure system

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7
Q

how does a surestep SMO compare to a regular SMO?

A

shorter toe plate and trimlines

designed to promote higher level activities like running and jumping

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8
Q

What issues are associated w/ downsyndrome

A

Atlantoaxial instability
-Present in 15% of pt with DS
-Take radiographs between 3-5yo

Cardiac issues

Thyroid Issues

Hip Issues
-DHD
-Acetabular Dysplasia

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9
Q

T or F: a SMO w/ a PLS extension is good for crouch gait

A

F

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10
Q

Idiopathic toe walking and Spastic CP at a GMFCS level II can benefit from what kind of orthotic

A

SMO with PLS extension

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11
Q

What planes does the SMO with PLS extension control

A

Controls sagittal plane talocrural issues (with the PLS extension)

Coronal plane Subtalar joint issues (with the SMO)

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12
Q

What kind of orthotic is best for Duchenne’s Ms Dystrophy

A

GRF AFO

Unless they’re non-ambulatory!

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13
Q

Signs of duchennes muscular dystrophy?

A

Clumsy, may walk on toes, show motor REGRESSION

GOWERS SIGN!!!!

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14
Q

T or F: Prolonged walking and standing delay the development of scoliosis in Duchenne muscular dystrophy

A

T

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15
Q

What MSK problem is associated w/ Duchenne’s muscular dystrophy

A

Scoliosis

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16
Q

What type of medication often improves muscle mass and function in the first 6 months of treatment for Duchenne’s

A

Corticosteroids

17
Q

Surgical intervention for scoliosis is typically considered when the curve reaches approximately ______, especially when the child is under ______

18
Q

What is the pattern of weakness in Duchenne’s muscular dystrophy

A

Proximal to distal

not all muscles affected equally

early in neck flexors and abdominal muscles

19
Q

how do you differentiate duchennes muscular dystrophy from idiopathic toe walking

A

they just now started walking on toes at 5-6 y/o and are now clumsy

20
Q

Gait prognosis for Duchenne

A

gait typically lost by age of 12

21
Q

What is the most severe classification of Spinal Muscular Atrophy

A

Type 1- Manifests before age of 6 months

death by 2 years old

most common

22
Q

What is the mildest form of Spinal Muscular Atrophy

A

Type 3,

Onset after 18 months

Children may walk independently or with AD into late adolescence and early adulthood

23
Q

When does each type of Spinal Muscular Atrophy appear?

A

Type 1- Appears before 6 months

Type 2- Onset between 7 months and 18 months

Type 3- onset after 18 months

24
Q

What is the prognosis for each type of SMA?

A

Type 1- Death at age of 2

Type 2- may live into adulthood w/ proper treatment and monitoring of pulmonary function

Type 3- normal life expectancy, may require AD to walk

25
Q

How are all 3 types of SMA characterized?

A

Significant limb and trunk weakness

Atrophy pronounced more proximally and in LE

Hypotonia and Areflexia

Progressive musculoskeletal issues

26
Q

What is the cause of Duchenne?

A

Progressive neuromuscular disorder

Genetic mutation causes: Absence of dystrophin, a protein normally present in muscles and in the brain –> causes muscle cells to be easily damaged

27
Q

Duchennes typically affects what gender

28
Q

Differences between duchenne and SMA?

A

DMD- Later onset, may not have family history, psuedo hypertrophy of calve muscles

SMA- Inhereted, Earlier onset, Affects reflexes( Areflexia), Affects limbs more than DMD

29
Q

What kind of shoes do we want and not want for orthotic use?

A

Removable inserts

Extra depth

Laces or velcro

NOT: Canvas shoes or sandals/slip-ons

30
Q

What are 3 common compensations in gait for children w/ hemiplegia

A

Hemi-pelvis retraction

increased pushoff w/ unaffected side

early firing of fibularis longus

31
Q

how do we delay the development of scoliosis in children with DMD?

A

Prolonged walking and standing