Lecutre 8: Pediatric Orthotic Problme Solving Flashcards

(62 cards)

1
Q

What is midfoot break associated with

A

Ankle DF movement

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2
Q

What is the SVA (shank to vertical angle) angle affected by

A

What type of shoe the pt is wearing

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3
Q

What is teh PTG

A

Patient
Task
Goal

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4
Q

What is the difference between R1 vs R2

A

R1- is the catch during ROM
R2- full ROM

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5
Q

Can the ankle AFO angle be set at neutral if the patient does not have the ROM range

A

No

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6
Q

PTG means patient , task and goasl can it can also mean what

A

Prioritize the goals

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7
Q

What are the task for the non ambulatory AFO

A
  1. Contracture Management
  2. Wound heeling, protection, or prevention
  3. Positioning
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8
Q

What are the therapeutic benefit of the force application from a orthosis

A

▪Resist motion
▪Assist motion
▪Transfer force
▪Protect a body part

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9
Q

What is the major element in during comfort for a othrosis

A

Minimizing pressure by maximizing the area

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10
Q

The greater the portion of the body that the orthosis cover then what happens

A

The lower the unit pressure

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11
Q

The amount of ____ and the area of the ___ subjected to the force influences the comfort of the corthosis

A

Force

Body

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12
Q

What is the most common basic pressure system for most orthoses

A

3 point force system

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13
Q

What does the 3 point force system consist of

A

Principle force acting in one direction and two counterforces acting in the opposite direction

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14
Q

What point pressure system is parapodium

A

4

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15
Q

How many groups of classfication is there for the Winters Gait

A

4 groups

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16
Q

What is group 1 characterized by for winters gait classification

A
  • foot drop during swing
  • flat foot or forefoot contact during IC
  • excessive hip and knee flexion drug in swing
  • adequate DF during stance
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17
Q

What is group 2 characterized by in the winters gait classification

A

More constant PF throughout gait

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18
Q

What is group 3 characterized by in the winters gait classification

A

Progressing to knee hyperextension and increased lumbar lordosis

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19
Q

What is group 4 characterized by in the winters gait classification

A

Most severe pattern

Limited hip movement and significantly increased lumbar lordosis

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20
Q

What are common compensations in the gait of children with hemiplegia (case 4)

A
  • hemi pelvic retraction
  • increased push off on unaffected side
  • early firing of fibularis longus
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21
Q

What outcome measures are discussed in case 4 (hemiplegic)

A
  • Gait Deviation Index (GDI)
  • Salfort Gait Tool (SF-GT)
  • Visual Gait Assessment
  • GMFM
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22
Q

What is a supramallelar orthoses

A

Type of AFO that crosses the ankle

does not help at the knee

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23
Q

Who is the sure step SMO designed for

A

Children with Down syndrome

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24
Q

What is the difference between a typical SMO and a surestep SMO

A

Shorter toe plate and trim lines for the surestep

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25
What is the surestep SMO designed to promote/imporove
High level activities such as jumping and hoping by improving sub talar joint alignment
26
What kind of disorder is Down syndrome and what is the reason
Genetic disorder Trisomy 21 (additional chromosome)
27
What is **Down syndrome** characterized by (5)
▪ Hypotonia ▪ Ligament Laxity ▪ Flatfeet ▪ Cognitive limitations ▪ Delayed Milestones
28
What kind of instability is present in approx 15% of all people with DS
Atlantoaxial instability
29
When shoudl xray be taken for a person with DS
Between ages 3 and 5 years
30
What kind of **hip** issues can a kid with **DS** have
▪ DHD ▪ Acetabular dysplasia
31
who is a **SMO with PLS extension** designed for
Clients that have **sagittal** plane talocrual joint issues in addition to **coronal** subtalar joint issues
32
What are 2 examples of clients that would benefit from a S**MO with PLS extension**
▪ITW ▪Spastic Hemiplegic CP functioning at a GMFCS level II
33
Who are **ground floor reaction AFO** designed for
Pateints with duchenne mm dystrophy
34
What does the **ground floor reaction AFO** provide
Knee extension moment during ambulation
35
What is the most common inherited muscular dystrophy and mm diseae of childhood
Duchenne muscular dystrophy
36
What is a Fatal disease of progressive weakness of skeletal and respiratory muscles
Ducheene
37
What is the typical life expectancy for **Duchenne Muscular Dystrophy**
20 and 30 years
38
For **Duchenne Muscular Dystrophy** there is a **protein** present where
Skeletal mm, smooth mm and in the brain
39
What is **absent** in Duchenne Muscular Dystrophy
Dystorphin ## Footnote whihc is critical for mm fiber stability
40
How does **boys** with **Duchenne Muscular Dystrophy** usually present
* clumsy * may walk up on their toes * show gross motor regression
41
What are the **gait characteristics** for duchenne’s
* wide BODY * lumbar lordosis * knee hyperextension * toe walking
42
there will be ___ of the calf mm and a (+) ___ sign for **duchenne**
▪Pseudohypertrophy ▪Gower
43
When do **cortiosteriods** improve mm mass, strength and function for **duchenne**
First 6 months
44
When is **ambulation** for **duchenne** usually **lost** by
12 y/o
45
What affects about **75-90%** of **non ambulatory** children with **DMD**
Scoliosis
46
When is **sx intervention** for **scoliosis** considered for kids with DMD
When the curve reaches approx 30° .. especially if the child is under 14 years of age
47
What **delays** the **development** of **scoliosis** for kids with DMD
Prolonged walking and standing
48
What is the **primary impairment** causing activity limitation from DMD
Mm weakness
49
What is the **predictable pattern** of invovlment for **DMD**
Proximal to distal Starts early in neck flexors and abdominal mm and then progresses to pelvic girdle and knee extensors and then down to limbs
50
**Spinal muscular atrophy** is a ___ ____ disorder
Autosomal recesssive
51
What is a Gene disruption characterized by degeneration of **anterior horn cells** of the spinal cord, muscle atrophy, wide spread muscle weakness, and **absent deep tendon reflexe**
Spinal muscular atrophy
52
What is the **most severe classification** for SMA
Type 1
53
When is **type 1 SMA** manifested before
6 month
54
When does **type 2** onset occur fro SMA
Between 7 to 18 months
55
When is the onset of **type 3** SMA
Onset after 18 months
56
What is the mildest form of SMA
Type 3
57
All 3 types of SMA are characterized by what 4 things
- limb and trunk weakness - mm atrophy - hypotonia and areflexia - progressive MSK issues
58
If a pateint has a **tight gastroc** will they pronate or supinate
Pronate
59
Resting or non ambulatory AFO is preventing what
Contracture
60
When would u use a **articulating AF0**
whne a joint allows to much motion and we need to control it
61
What are the **most common types of joints** used for a articulating AFO
◦ Overlapping ◦ Oklahoma ◦ Tamarack
62