Paediatric Orthopaedics Flashcards

1
Q

What is Perthe’s disease? Who does it most commonly affect?

A

Disruption of the blood flow to the femoral head - leads to avascular necrosis

Boys aged 4-8

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2
Q

What is the long-term affect of Perthe’s disease?

A

Over time, re-vascularisation of the femoral head leads to early hip osteoarthritis

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3
Q

How does Perthe’s disease present?

A

Gradual onset of…

Pain in the hip/groin

Limping

Restricted hip movement

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4
Q

How is Perthe’s disease diagnosed?

A

XR may be normal but can show sclerosis and fragmentation
May also show widening of joint space and decreased femoral head size

If XR is normal can do an MRI

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5
Q

How is Perthe’s disease managed?

A

If less than 50% of the femoral head is affected - conservative management

If more than 50% affected - plaster cast

May need surgical management

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6
Q

What is developmental hip dysplasia?

A

Structural abnormality of the hips

Caused by abnormal development of fetal bones during pregnancy

Tendency for dislocation

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7
Q

What are risk factors for developmental hip dysplasia?

A

1st degree family history

Breech presentation from 36 weeks

Breech presentation at birth

Multiple pregnancy

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8
Q

What 2 special tests can be used to diagnose developmental hip dysplasia?

A

Ortolani test

Barlow test

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9
Q

How is developmental hip dysplasia managed?

A

<6 months = Pavlik harness

> 6 months = surgery

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10
Q

What is Rickets?

A

Defective bone mineralisation caused by a deficiency of vitamin D or calcium, leading to soft/deformed bones due to secondary hyperparathyroidism

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11
Q

What are risk factors for Rickets?

A

Dark skin

Colder climate

Spend a lot of time indoors

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12
Q

What are symptoms of Rickets?

A

Lethargy

Bone pain

Bone deformity

Poor growth

may be symptoms of high serum calcium - stones

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13
Q

What bone deformities are seen in Rickets?

A

Bowing of legs

Knock knees

Rachitic rosary

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14
Q

What blood tests should be conducted in suspected Rickets?

A

Serum 25-hydroxyvitamin D

Low calcium

Low phosphate

Increased ALP

Increased PTH

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15
Q

How is Rickets managed?

A

Vitamin D supplementation

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16
Q

What is Achondroplasia? What is the hereditary pattern?

A

Most common cause of dwarfism

Autosomal dominant

17
Q

What are features of Achondroplasia?

A

Short limbs + short digits

Normal trunk length

Large head

Flattened mid-face + nasal bridge

Foramen magnum stenosis

18
Q

What is osteogenesis imperfecta? How does it present?

A

A genetic condition causing brittle bones which are prone to fracture

Recurrent inappropriate fractures

Blue/grey sclera

Hypermobility

Deafness

Dental imperfections

19
Q

What is slipped upper femoral epiphysis? How does it present?

A

When the head of femur slips along the growth plate

More common in obese children

May be some trauma that triggered onset of symptoms

Pain is disproportionate to severity of trauma

Restricted range of movement - Loss of internal rotation

Painful limp

20
Q

How is slipped capital femoral epiphysis diagnosed?

A

AP and lateral Xrays

21
Q

How is slipped capital femoral epiphysis managed?

A

Internal fixation with a single cannulated screw

22
Q

What is transient synovitis? How does it present?

A

Acue hip pain following a recent viral infection

Limp/inability to weight bear
Groin/hip pain
Low grade fever

Self-limiting

23
Q

When might you consider septic arthritis over transient synovitis?

A

High grade fever warrants investigation for septic arthritis