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
Purpose of COPM
To identify goals in self care, productivity, leisure - family centered
26
What needs to be consider for ped Rx
the environment, the task activity, the instructions you give, and other things like breaks, choices and control
27
Tone assessment
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)