Week 10 - Pediatric Orthopedic Conditions: OT Management Flashcards

1
Q

for peds, an OT should split a complex eval. into ___ ___.

A

multiple sessions

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2
Q

name 5 ways in which an OT can prevent and/or minimize anxiety during a peds eval.

A
  • play with child before eval.
  • role play with doll, sibling, or parent
  • leave child seated on parent’s lap
  • have parent provide instructions
  • save anything painful or scary for last
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3
Q

name 2 types of self-report evals. for peds.

A
  • semi-structured interviewing: parent and/or child

- pt.-reported outcome measures (proxy report)

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4
Q

name 2 types of pain evals. for peds.

A
  • observation - FLACC scale (2 months - 7 years)

- Wong-Baker FACES Pain Rating Scale (3+)

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5
Q

name 2 types ROM and strength evals. for peds.

A
  • observe during play, transitional movements, interactions with objects
  • over 3, can usually participate with goniometry and MMT
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6
Q

name 4 aspects of peds. interventions.

A
  • fun in-clinic and home programs: simple but novel, play and games, non-traditional (hippotherapy, aquatic therapy)
  • short sessions
  • family involvement
  • developmentally appropriate activities and teaching/learning - motor, cognitive, psychosocial
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7
Q

which physical agent modalities should be avoided for peds?

A

avoid ultrasound over growth plates

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8
Q
  • spine looks like S or C when viewed from rear
  • spinal changes in frontal, transverse, and/or sagittal planes
  • may be associated with lordosis or kyphosis
A

adolescent idiopathic scoliosis

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9
Q

what is the assessment for adolescent idiopathic scoliosis?

A

Adams forward bend test

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10
Q

name 3 types of management for adolescent idiopathic scoliosis.

A
  • observation
  • bracing
  • operative
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11
Q

what is the gold standard surgical technique for adolescent idiopathic scoliosis?

A

spinal fusion

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12
Q

what is the gold standard non-surgical technique for adolescent idiopathic scoliosis?

A

Schroth method

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13
Q
  • twisted neck
  • unilateral SCM contraction which leads to ipsilateral lateral flexion and contralateral rotation
  • limitations in ROM
  • more common in males
A

congenital muscular torticollis

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14
Q

name 3 secondary problems of congenital muscular torticollis.

A
  • positional plagiocephaly
  • facial asymmetry
  • perceptual and balance issues if chronic
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15
Q

congenital muscular torticollis treated ____ most often.

A

nonoperatively

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16
Q

congenital muscular torticollis treated ____ most often.

A

nonoperatively

17
Q

why do pts. with congenital muscular torticollis go to OT?

A
  • ROM deficits
  • functional limitations
  • developmental delays
18
Q
  • “clicky” hips, abnormal gait, asymmetrical LE skin folds, extreme external rotation so feet seem to point backwards
  • affects developmental milestones
  • ranging subluxation to dislocation
A

developmental hip dysplasia

19
Q

name 2 ways in which developmental hip dysplasia is managed.

A
  • bracing/casting: pavlik harness, hip spica cast, hip flexion and abduction
  • operative
20
Q

name 4 methods of OT treatment for developmental hip dysplasia.

A
  • seating
  • positioning for breastfeeding, sleep, etc.
  • ADL education (diapering, dressing, bathing)
  • with cast/brace removal, address transitional movements and weight bearing during functional activities.
21
Q
  • joint pain, redness, swelling, morning stiffness
  • joint deformities and instability
  • fatigue
A

juvenile idiopathic arthritis

22
Q

the onset of juvenile idiopathic arthritis is before what age?

23
Q

juvenile idiopathic arthritis must persist for at least how many weeks?

A

at least 6 weeks

24
Q

transverse arrest: amelia through aphalangia

longitudinal arrest: radial, ulnar, tibial, fibular, central, intersegmental deficiency

A

failure of formation

25
soft tissue or skeletal: arthrogryposis, syndactyly, campodactyly, thumb in palm, syntosis
failure of differentiation
26
whole limb through polydactyly
duplication
27
whole limb through macrodactyly
overgrowth
28
whole limb through brachydactyly
undergrowth
29
amniotic band syndrome (ABS)
constriction band syndrome
30
- average trunk, short arms, legs, and fingers, macrocephaly, limited elbow ROM, spinal problems - positioning to support head, neck, back - diet and low-impact exercise/recreation - assistive devices to access body and environment - social integration and emotional issues
achondroplasia
31
primary bone cancer
osteosarcoma or ewing sarcoma
32
primary bone cancer is most commonly diagnosed in which groups?
preteens/teens
33
primary bone cancer is most commonly diagnosed in which groups?
preteens/teens
34
primary bone cancer is more common where?
LE
35
name 4 peds-specific fracture conditions.
- growth plate (salter-harris classification) - torus/"buckle" and greenstick fractures - timeframes for healing - consider potential for child abuse
36
flattened portion of skill, can develop due to positioning but can be corrected with cranial orthoses
positional plagiocephaly
37
hip is loose
subluxation
38
hip joint is separated
dislocation
39
orthoses for children should align with which 2 stages?
their developmental stage and their cognitive stage