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?

A

16

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
Q

soft tissue or skeletal: arthrogryposis, syndactyly, campodactyly, thumb in palm, syntosis

A

failure of differentiation

26
Q

whole limb through polydactyly

A

duplication

27
Q

whole limb through macrodactyly

A

overgrowth

28
Q

whole limb through brachydactyly

A

undergrowth

29
Q

amniotic band syndrome (ABS)

A

constriction band syndrome

30
Q
  • 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
A

achondroplasia

31
Q

primary bone cancer

A

osteosarcoma or ewing sarcoma

32
Q

primary bone cancer is most commonly diagnosed in which groups?

A

preteens/teens

33
Q

primary bone cancer is most commonly diagnosed in which groups?

A

preteens/teens

34
Q

primary bone cancer is more common where?

A

LE

35
Q

name 4 peds-specific fracture conditions.

A
  • growth plate (salter-harris classification)
  • torus/”buckle” and greenstick fractures
  • timeframes for healing
  • consider potential for child abuse
36
Q

flattened portion of skill, can develop due to positioning but can be corrected with cranial orthoses

A

positional plagiocephaly

37
Q

hip is loose

A

subluxation

38
Q

hip joint is separated

A

dislocation

39
Q

orthoses for children should align with which 2 stages?

A

their developmental stage and their cognitive stage