Pediatric Rehab MSK Flashcards

1
Q

What is Sprengel’s deformity?

A

Failure of scapula to descend from its cervical region overlying the 1st through 5th ribs (instead of 2nd to 8th).

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2
Q

Clinical presentation of Sprengel’s deformity

A

1- Shortened neckline, 2-Lack of normalscapulothoracic motion, 3-malposition of the glenoid limiting forward flexion and abduction, and 4- Presence of an omovertebral bar (connects scapula to cervical spine)

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3
Q

Clinical presentation of Klippel-Feil Syndrome

A

Short neck, low hairline, restricted neck movement.

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4
Q

Sports contraindicated in Klippel-Feil Syndrome

A

Contact sports

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5
Q

Atlantodens Interval (ADI) up to __mm is accepted

A

5mm

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6
Q

Rigid pes planus is associated with other anomalies in 50% of cases. These are….

A

Tarsal coalition:

  • Talocalcaneal coalitions (8-12 years)
  • calcaneonavicular coalition (12-16 years)
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7
Q

Diagnosis of tarsal coalition

A

CT

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8
Q

Differential diagnosis of pes cavus

A

CMT, spinal dysraphysm, Friedrich’s ataxia, spinal tumor

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9
Q

Rocker bottom foot

A

Congenital vertical talus

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10
Q

congenital vertical talus is associated with

A

neuromuscular and genetic disorder including trisomy 13, 14, 15 and 18.

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11
Q

Larsen syndrome clinical signs

A

-flat facies, -multiple congenital dislocations, -ligamentous laxity, -cervical spine instability

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12
Q

Arthrogryposis multiple congenita. Before therapy needs to rule out….

A

Fractures. The birth can be complicated with the contracture are results in fracture. Therapy should not be initiated until such fractures are ruled out.

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13
Q

Risk of surgical correction of knee flexion contractures…

A

Neurovascular overstretching

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14
Q

Indicators of poor outcome in Juvenile Idiopathic Arthritis

A
  • greater severity or extension of arthritis at onset
  • symmetrical disease
  • early wrist or hip involvement
  • presence fo RF
  • persistent active disease
  • Early radiographic changes (erosion or joint space narrowing)
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15
Q

Drug scalation in oligoarthritis JIA

A

NSAIDs-> IA steroid -> methotrexate -> TNF alpha inhibitors.

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16
Q

Septic arthritis organism

  • in all age group
  • in neonates and infants
A
  • all age group: Gram positive aerobe (s.aureus 60%)

- neonates and infants: S. aureus and gram neg anaerobes.

17
Q

Reactive arthritis

A

Autoimmune response triggered by antigen deposit in the joint space.
Preceding infections: Chlamydia
Yersinia and Campylobacter (can be associated with HLAB-27)

18
Q

Treatment of Reactive arthritis

A

Antibiotics if organism still present. Analgesics, steroids and immunosupressants.

19
Q

Hemophilia treatment /rehab

A
  • Main treatment is injections of cryoprecipitate.
  • Joint immobilization for 48 hours. Once pain and swelling subside start PROM.
  • Analgesics, anti-inflammatory and aspiration of blood from the joint if skin is tense.
  • Aquatherapy
  • Contact sports are generally contraindicated.
20
Q

Legg-Calve-Perthes disease

  • What is?
  • Age of presentation
A
  • Osteonecrosis of the capital femoral epiphysis

- 4-10 years

21
Q

Physical findings in Legg-Calve-Perthes

A
  • Limitation in internal rotation, extension and abduction of the affected hip
  • Shortening of the leg
  • hip or knee pain
22
Q

Treatment of Legg-Calve-Perthes

A
  • Disease process is self-limited, but may last for 2-4 years.
  • Goal is to reduce pain and stiffness
  • NSAIDs
  • Non-weight bearing with crutches (if significant pain)
  • Hip abduction (40-45 degrees ) orthosis. Full time, until subchondral ossification is demonstrated on Xray, although controversial
  • Surgery if Caterall classification III or IV.
23
Q

Most common type of hip pain in children

A

Acute Transient Synovitis of the hip

24
Q

Peak age for transient synovitis of the hip

25
Age at presentation of Slipped Capital Femoral Epiphysis
-12-16 years for boys, 10-14 for girls
26
Conditions associated with SCFE
Endocrine - Hypothyroidism, hypopituitarism, hypogonadism, excessive growth hormone. - Specially when presentation is outside of the usual age.
27
Presentation of SCFE
External rotation of the leg, leg shortening, Trendelenburg's gait, hip pain
28
SCFE, diagnosis and treatment
-Diagnosis with lateral hip xray showing displacement, using Klein's line -Treatment- Non weightbearing -> In situ pinning. Weightbearing avoided for at least 6 weeks.
29
Highest risk factors for Developmental Dysplasia of the Hip
``` First-born female presenting with breech position. Other risk factors: -Caucasian -Hip swaddling in extension -Family history -Primiparity -Ligamentous laxity -Birth weight >4,000gm -Torticollis -Metatarsus adductus -Oligohydramnios -Hip asymmetry -Congenital knee dislocation/recurvatum ```
30
Treatment of Developemental Dysplasia of the hip if - Positive Barlow's but negative Ultrasound - Positive imaging (ultrasound or xray)
-Positive Barlow's but negative Ultrasound- Serial CLINICAL examination until reaches walking age. -Positive imaging (ultrasound or xray)- Pavlik harness with monthly ultrasound if less than 6 months. Then xray through growing years. Hip abduction orthosis if more than 6 months of age. If Pavlik fails in children under 18 months-> closed reduction with spica cast. If the previous fails, surgical reduction is required after 18 months.
31
What is Nursemaid's elbow? Mechanism of action?
Radial head subluxation from a upward pull on the extended pronated arm.
32
Nursemaid's elbow clinical presentation and treatment
The child will hold the arm in felxed and pronated position. | Treatment: closed reduction with the patient under sedation.