Exam 3: Mobility Flashcards

1
Q

Causes of alterations in mobility

A

Neurologic insult (trauma or hypoxia to brain or spinal cord)

Genetic dysfunction or structural abnormality

Can be present at birth but not identified until later

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

When is myelination complete?

A

By 2 years old

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Why are adolescents at in increased risk for injury?

A

They have increased muscle growth which leads to increased clumsiness

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Common mobility treatments

A

Goal: Immobilization and reduction; prevent treatment complications (compartment syndrome, osteomyelitis)

RICE
Splinting
Bracing
Casting
Traction (skin vs. skeletal)
Surgery (internal vs. external fixation)
Pain management

Prevent

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Developmental Dysplasia of the Hip (DDH)

A

Improper alignment of the femoral head and the acetabulum creating instability in the hip

Etiology: Genetic predisposition, fetal development, breech positions, oligohydramnios, laxity of ligaments in hip

Patho: Hip instability, subluxation, complete dislocation

If untreated, can lead to osteoarthritis and pain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

How does the hip develop normally?

A

The hip can only develop normally if the femoral head is properly maintained within the acetabulum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Complications of DDH (if continued dislocation or subluxation)

A

Avascular necrosis of femoral head
Hip instability
Limited ROM
Palsy of femoral nerve
Early onset of osteoarthritis (painful)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Clinical manifestations of DDH

A

Limited abduction
Asymmetry of gluteal and thigh folds

Diagnostic testing: Allis/Galeazzi sign (limb length discrepancy), Barlow (aDduction = hip instability) and Ortolani (aBduction = hip dislocation) 8-12 weeks, ultrasound <6 months, x-ray > 6 months

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is the goal of DDH treatment?

A

To maintain the hip joint in reduction allowing the femoral head and acetabulum to develop properly`

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Pavlik Harness

A

Newborn - 6 months

Prevents extension and aDduction

Priority nursing considerations:
Safety: Positioning, no swaddling, car safety, strap adjustments ONLY by specialist
Growth: Move legs and arms freely, encourage developmentally appropriate play, tummy time
Skin integrity: Assess skin under straps, onesie, knee/thigh socks, diaper under harness, assess skin folds, keep skin clean and dry
Perfusion: NV checks

Family education: Keep on for prescribed time, straps adjusted by specialist Q1-2 weeks, adherence and follow up appointments

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Bryant Traction

A

6 months - 2 years

May be used first to stretch soft tissue

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Spica Cast

A

> 2 years or failed previous therapy

Closed reduction (no cutting) and spica cast worn for 12 weeks

Pain control: Acetaminophen (1st day), ibuprofen (> 6 months)
Elimination: Diaper under the cast, change diaper frequently
Perfusion: NV checks
Safety: Car seat, injury prevention
Skin: Cast care: petal/soft edges, handle with palms of hand, nothing in cast, keep skin clean and dry, ensure no skin breakdown especially in perineal area
Developmental: Tummy time, age appropriate play

Family education: Pain control, elimination patterns, cast and skin care

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Abductor brace

A

Worn for approximately 2 months after spica cast removed

Support and ensure healing

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Scoliosis

A

Complex deformity of spine

Lateral S or C curvature >10°

Etiology: Idiopathic (occurs most often during adolescence), congenital (anomalous vertebrae development), neuromuscular (cerebral palsy, muscular atrophy)

Patho: Structural changes occur as a result of curvature, ribs on concave side forced together while ribs on convex side separate, narrowing on vertebral canal

Concern: Over time if not repaired will cause damage to CV and respiratory systems

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Clinical manifestations of scoliosis

A

Uneven shoulder height
Prominent scapula
One-sided rib hump
Truncal asymmetry
Pain not a normal finding for idiopathic scoliosis
Unequal hips - often present with uneven hemline

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Diagnostic testing of scoliosis

A

Inspection = Adam’s test (forward bending)
Scoliometer
X-ray most definitive
Screenings every 6-9 months
Early detection lessens deformity

Goal: Stop progression of curve

17
Q

Clinical therapy for scoliosis

A

Mild = Curvatures of 10-20°: Exercise, strengthening, follow-up evaluations

Moderate = Curvatures of 20-40º: Prevents further curvature, Boston Brace, biggest issue is ADHERENCE

Severe = Curvatures > 45º: Surgery (Spinal fusion, Harrington rod), purpose: stabilize spine. If PT has not reached puberty yet they are NOT a candidate for surgery because they could still grow

18
Q
A