Paediatric conditions 2.0 Flashcards

1
Q

What is osgood -schlatter syndrome? what is it caused by?

A

Activity related pain and swelling at insertion of patellar tendon on tibial tubercle - self-limiting

Caused by minor degree of separation of tibial tubercle, associated with patella alta

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2
Q

Osgood-schlatter syndrome S&S

A

acute severe pain - limp, low grade discomfort (exacerbated by running or playing sports)

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3
Q

Osgood-schlatter syndrome Rx

What is the time period for recover?

A
  • ice, rest, decrease activity, avoid squatting and jumping
  • brace, cast in severe cases
  • generally resolves in 6 weeks if following precautions, most cases within 3 months (tubercle fuses to tibia
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4
Q

What is osteochondritis dessicans? Where does it most commonly occur?

A

Lesion of subchondral bone and articular surface (distal femur most common - lateral surface of medial femoral condyle, also femoral capital epiphysis and talus)

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5
Q

What causes osteonchondritis dessicans?

A

Ischemic necrosis - exact cause of this unknown

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6
Q

Osteochondritis dessicans S&S

A
  • frequently asymptomatic, pain
  • swelling around knee
  • antalgic gait
  • locking (if fragment separates)
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7
Q

Osteochondritis dessicans Rx

A
  • most self-limiting, immobilization
  • graduated activity with quads strengthening
  • surgery if separation and intra-articular fragment (in skeletally immature
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8
Q

What is idiopathic toe walking?

A

Walking milestone normal but up on toes, child otherwise appears completely normal
Can often walk flatfooted if prompted

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9
Q

idiopathic toe walking S&S

A

child walks and runs on toes, variable degree of tightness in plantarflexors (restricts passive DF), always symmetrical

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10
Q

Idiopathic toe walking Rx

A
  • hard to treat, mainly cosmetic
  • AFO’s
  • PT (ROM, strength)
  • serial casting
  • botox
  • surgery controversial
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11
Q

What is congenital muscular torticollis? What may cause it?

A
  • Unilateral shortening or fibrosis of SCM at birth or shortly after

Causes:

  • birth trauma
  • intrauterine malposition
  • perinatal compartment syndrome
  • genetics
  • Increased risk with prolonged time on back
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12
Q

Congenital muscular torticollis associated conditions

A
  • plagiocephaly
  • facial asymmetry
  • hip dysplasia
  • MSK anomalies (ie. metatarsus adductus – uterine packing)
  • brachial plexus injury
  • TMJ dysfunction
  • developmental delay (during period of torticollis or longer)
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13
Q

3 types of torticollis

A

1) SCM “tumor” with palpable mass in SCM (not a neoplasm but scar tissue)
2) Muscular torticollis without palpable tumor but thickening and/or shortening of SCM
3) Postural torticollis where clinical features present without tumor or muscle tightness

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14
Q

5 “other” causes of torticollis

A
  • Boney malformations (ie. Klippel-Feil syndrome, cause child to adopt suboptimal postures)
  • Ocular torticollis (superior oblique muscle weakness, head tilt to correct double vision)
  • Space occupying lesion (ie. posterior fossa tumors)
  • Abnormal muscle tone (spasticity, dystonia, hypotonia, etc.)
  • Reflux (ie. Sandifer syndrome)
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15
Q

What would you include in a torticollis assessment

A
  • History – pregnancy/birth history, HPI, current health, feeding, treatments, etc.
  • Observation – resting posture (various positions), face/head shape, ocular alignment, movement quality, etc.
  • ROM – AROM/PROM c-spine flexion & rotation, hips & extremities, supine vs. prone, sitting vs. standing, etc.
  • Strength & tone – lateral head righting ( >4 months) symmetrical side to side, functional activities/gross motor skills, palpate for any masses/muscle tone
  • Development
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16
Q

Torticollis treatment

A
  • Stretching
  • Strengthening of weak neck & trunk muscles
  • Positioning (tummy time)
  • Environmental adaptations
  • Parental education
  • Other options include botox, T.O.T. collar, surgery, etc.
17
Q

What is plagiocephaly

A

The misshaping and flattening of an infant’s head through sustained external directional force

18
Q

4 components of pediatric examination

A

Hx
Systems Review
Intervention
Re-examination

19
Q

What is included in a peds History

A
  • prenatal
  • birth
  • general health
  • milestones
  • procedures/interventions
  • goals
20
Q

What is included in a peds systems review

A
  • cardiorespiratory
  • integumentary
  • MSK
  • neuro
  • communication/cognition/learning
  • level of consciousness
  • orientation
  • emotional/behavioral
21
Q

4 Peds outcome measures

A

FMS - Functional mobility scale
GMFCS - gross motor functional classification system
GMFM - Gross motor functional measure
COPM

22
Q

FMS (functional mobility scale) - population, scoring, purpose

A

age 4-18 with CP,
rates walking ability at 5, 50, 500 m (for home, school and community), questions not observation
N-6 want a high score
Used to figure out what device they will need

23
Q

GMFCS - Scoring, population, purpose

A

5 levels (I= high fxn, V= limited)

For kids with CP, based on self initiated movement

Good for communication between families and health care professionals and goal planning

24
Q

what if the GMFM (Gross motor functional measure)

A

standardized test for gross motor function for children with CP, all items that a 5 year old (normal development) would do, can measure over time to see change and set realistic goals

25
Q

Purpose of COPM

A

To identify goals in self care, productivity, leisure - family centered

26
Q

What needs to be consider for ped Rx

A

the environment, the task activity, the instructions you give, and other things like breaks, choices and control

27
Q

Tone assessment

A

muscle palpation, prom, quantifying tone, and primitive reflexes (clonus and Babinski), use modified Tardieu (assess rom at R1 (high velocity) and R2 (end of rom and slow speed), 0-5 (want a lower score)), or modified Ashworth (5 point scale, 0-4)