Developmental & Congenital Orthopaedics -Dr. Hood Flashcards

1
Q

*What is idiopathic scoliosis?

A

Fixed lateral curvature measuring > 10° in coronal plane

common right thoracic

more common and severe in females

*< 10 degrees=spinal asymmetry

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2
Q

What are the 3 classifications of idiopathic scoliosis?

A

Infantile (0-3)
Juvenile (3-10)
Adolescent (>10)

based off age

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3
Q

*What are the 3 types of scoliosis?

A

idiopathic

congenital: Abnormal Vertebrae (failure of formation or failure of segmentation)
neuromuscular: Accompanying Syndromes

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4
Q

*What is peak growth velocity? When does this take place in females? When is it likely that pts will require surgery?

A

Is the best predictor of curve progression

In females it occurs justbefore menarcheandbefore Risser 1 (girls usually reach skeletal maturity 1.5 yrs after menarche)–> when the curve progresses most rapidly

*If curve is >30° before peak height velocity there is a strong likelihood of the need for surgery because it will progress much worse

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5
Q

What is the Cobb angle?

A

measure the curve based off the vertebrae that is most tilted on either end draw line out cobb angle

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6
Q

What is the Risser staging a measurement of?

A

Ossification of iliac crest apophysis

Lateral to medial

Estimates skeletal maturity

maturity=5

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7
Q

*When is surgery indicated for scoliosis ?

A

> 55 degree curvature

absolutely

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8
Q

What is the goal of bracing of scoliosis?

A

doesn’t correct curve, but keep from progressing

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9
Q

What is the goal of scoliosis surgery?

A

a well-balanced spine, not necessarily a straight spine

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10
Q

*What is the genetic component for Achondroplasia?

A

FGFR-3 gene

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11
Q

What is achondroplasia?

A

Error in Endochondral Ossification (in long bones)

especially in the physis (growth plate) in the proliferative zone

trident hand –> cannot appose long and ring fingers

Flat bones are NOT affected –> normal head and trunk with dysmorphic limbs

excessive lumbar lordosis and shortened pedicles–> spinal stenosis

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12
Q

*What are the ortho concerns for achondroplasia patients (2)?

A

spinal stenosis (especially lumbar) from short pedicles

and can have cervical foramen stenosis –> can present with apnea –> dissipates with growth

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13
Q

What is the most important part of the PE for a kiddo with in-toeing?

A

rotational profile

Gait: determine foot progression angles

  1. Assess hip rotation
  2. Assess tibial rotation
  3. Determine the alignment of the foot

Gait is controlled by CNS and affected by lower limb alignment

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14
Q

What position will kids with femoral anteversion sit in? What are some other symptoms of femoral ante version?

A

“W”

Usually 3-5 yo girls
Sits in the “W”
“Kissing patellae”
“Egg-beater” run
Severe if > 90°
Resolves with growth - no association with osteoarthritis
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15
Q

*What is the best thing to do for most in-toeing?

A

observation and reassurance

most rotational issues will resolve on their own

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16
Q

What is talipes equinovarus?

A

club foot

17
Q

how is idiopathic club foot treated? What about secondary?

A

idiopathic (CTEV) : serial casting

acquired: often needs surgery

18
Q

What are the 3 main principles with Congenital Talipes Equino-Varus (CTEV)?

A

Abnormal Intertarsal Relationships

Congenital Subluxations –>Talo Calcaneo Navicular Joint

Soft Tissue Contractures

–> early detection is key! and make sure to exclude other diagnoses

19
Q

What is the goal of treatment for CTEV?

A

functional, painless and stable foot –> want it to be plantigrade

cosmetics is a secondary goal

20
Q

*What is the gold standard treatment for club foot?

A

early detection and SERIAL CASTING (plaster casts)- –> then brace (2nd phase)

success rate is 85-90%

<1/3 require tendon transfer to maintain after casting

NOT surgery (2nd line treatment)

21
Q

What is the most reliable exam finding for hip dysplasia in kids > 3 months?

A

limited hip abduction

22
Q

*What imaging study should be used on kids 1-2 months of age? > 3 months? Why?

A

US=1-2 months

xray=3+ months

femoral head not ossified in younger kids –> can’t see

23
Q

What is goal of treatment for DDH? How is it treated in babies 0-6 months

A

containment of the hip

0-6 months: pavlik harness
–> if unsuccessful–> spica cast

24
Q

What is the end stage treatment for kids with DDH over the age of 2?

A

pelvic or femoral osteotomy (cut and reposition the hip)