4.4 - Pediatric Examination Flashcards

Week 4, Thursday

1
Q

Describe each of the following motor development theories

Neuromaturation Theory
Cognitive Theory

A

Neuromaturation Theory
- Motor skills develop as the nervous system develops
- “Hierarchic” maturation of neural control
- Biases NATURE

Cognitive Theory
- Environment drives development
Biases NURTURE

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2
Q

Describe the stages of motor learning

A

1) Cognitive - “understanding the goal”
2) Associative - “fine tuning”
3) Autonomic - “automatic”

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3
Q

Describe each of the following developmental principles

Cephalocaudal
Proximodistal
Reflexive to voluntary
General to specific

A

Cephalocaudal - develop head & neck control > trunk control > extremities

Proximodistal - develop proximal control before distal control

Reflexive to voluntary - movements start initially as reflexes then progress to voluntary control

General to specific - just like it sounds lol

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4
Q

Describe the developmental spiral / developmental regression

A

Children “spiral down” to a previous developmental position in order to perform a higher gross motor task

Ex: Child can obtain quadruped position, but must regress back to prone to reach for a toy (a progressive skill)

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5
Q

Describe each of the following reflexes & when they should be integrated by

ATNR
STNR
Tonic Labyrinthine
Galant
Rooting
Step
Landau

A

ATNR - turn head to side, ipsilateral arm extends, contralateral arm bends (“fencing posture”); 6 mos

STNR - head extends –> arms extend & legs flex (quadruped position); head flexes –> UEs flex, LEs extend (downward dog); onset 4-6 mos, integration by 12 mos

Tonic Labyrinthine - prone –> flexor tone; supine –> extensor tone; birth to 6 mos

Galant - stroke on side of back –> ipsilateral sidebend; 9 mos

Rooting - 6 mos

Step - 4 mos

Landau - “superman pose”; occurs around 5 mos

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6
Q

Describe the gross motor milestones through infancy

A

3 months: prone prop, hands to midline
4-6 months: rolling (often prone to supine first)
5 months: hands to feet
6 months: sit independently
8-9 mos: creeping
9-10 mos: pull to stand
10-11 mos: cruising
12-15 mos: independent standing & walking
18-24 mos: running & jumping
2-3 yo: start to stand on one foot, kick ball
4-5 yo: hopping on one foot, gallop
6 yo: skip

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7
Q

Describe some common red flags in the pediatric population

A

Night pain
Pain after activity only
Limp
“can’t keep up with peers”
Gower’s sign
Nystagmus
Primitive reflexes after it should be integrated
Change in function

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8
Q

What is a VP shunt?

A

A ventriculoperitoneal shunt

Drains excess CSF from the brain to treat hydrocephalus

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9
Q

Describe s/sx of a VP shunt failure

What should be done if this is suspected?

A

SUNSETTING EYES

Change in function
Flu like symptoms
Swelling / redness along shunt tract

Medical emergency!

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10
Q

What is a tethered spinal cord?

Describe the s/sx
What should be done if this is supsected?

A

Caudal end of spinal cord becomes stuck & begins to stretch out as the child grows

S/Sx:
- Common around puberty / growth spurt
- Rapid scoliosis
- Changes in urological function
- Back pain that worsens w/ activity

Medical emergency!

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11
Q

What is Legg-Calve-Perthes?

Describe the typical presentation
What should be done if this is suspected?

A

AVN of the femoral head

Clinical Presentation:
- 4-8 yos - really YOUNG
- M > F
- Limp
- Pain w/ activity - groin, anterior / lateral hip, knee
- Painful / limited hip abd & IR

Radiograph of femoral head

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12
Q

What is slipped capital femoral epiphysis (SCFE)?

Clinical Presentation
What should be done if this is supsected?

A

Superior slippage of the femur on the femoral epiphysis

Clinical Presentation:
- 9-16 yo (“SCFE = skipping = older children”)
- M > F
- Limp
- Limited hip flx, abd, IR
- Pain - groin, hip, knee, thigh
- Risk Factor: OBESITY

A/P and frog-leg radiograph

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13
Q

What is hip dysplasia?

Clinical Presentation
What should be done if this is suspected?

A

Flattening of the femoral acetabulum

Clinical Presentation
- (+) Ortolani test
- (+) Barlow test

Ultrasound of hip (typically under 6 mos)
A/P hip radiograph (older children)

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14
Q

Describe the Barlow & Ortolani tests

A

https://med.stanford.edu/newborns/clinical-rotations/residents/residents-newborn-exam/barlow-and-ortalani-manuevers.html

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15
Q

Describe a spondylolisthesis

Clinical Presentation
What should be done if this is suspected?

A

BIL pars interarticularis fracture with anterior slippage of one vertebral body on another

Clinical Presentation:
- 10-15 yo
- Hypermobile females (gymnastics, cheerleaders)
- Step deformity
- Back pain w/ EXTENSION

Oblique radiograph (scotty dog sign)

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16
Q

Describe Duchenne Muscular Dystrophy

Clinical Presentation
What to do if you are suspecting this?

A

A progressive neuromuscular degenerative disorder
- Only occurs in males (x-linked recessive trait)
- Mutation in the dystrophin gene –> lack of dystrophin protein –> allows for damage w/in the sarcolemma w/ contraction of the muscle
- Fat and connective tissue begin to replace the damaged muscle
- progresses rapidly w/ death typically occurring by the time they are a teenager

Clinical Presentation:
- Typically presents between 2-5 years of age
- GOWER’s SIGN
- “Can’t keep up with peers”
- Pseudohyertrophy of calves
- Lordosis
- Tight hip flexors & gastroc, weak hip extensors

Refer to pediatrician, neuro, and genetics

17
Q

Juvenile Arthritis

Clinical Presentation
What to do if suspecting this?

A

Clinical Presentation:
- Joint pain & swelling
- Morning stiffness
- Weakness
- Limp
- “Not able to keep up with peers”
- Delayed milestones

Refer to rheumatology

18
Q

What standardized assessment is typically used for children w/ CP?

A

Gross motor function measure (GMFM)
Gross motor functional classification system (GMFCS)

Evaluates changes in gross motor function in kids w/ CP (5 mos - 16 yrs)

19
Q

What does the Peabody assess? What age groups?

A

Total motor development (fine and gross)
0-5/6 yo

20
Q

What does the AIMS assess? What age groups?

A

Gross motor milestones
0-18 months