Orthopaedics unit 3 orthopaedic conditions in childhood - deck 1 Flashcards

1
Q

During normal development we expect children to reach a certain milestone at a certain age. What is the average age that a child wil reach each of the following milestones:

  1. Sits independently
  2. Stands
  3. Walks
A
  1. Sit independently - 9 months
  2. Stand - 12 months
  3. Walk - 20 months

Note that there is a lot of variation in normal development and failure to reach a certain milestone is usually not a sinister sign

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2
Q

When children start to walk their gait takes many months to mature and so minor variations are to be expected.

List the 4 main common, but minor, abnormalities that we should know about which can cause an abnormal gait in a child

A
  1. Knock knees and bow legs (valgus and varus knees)
  2. In-toeing
  3. Flat feet
  4. Curly toes.
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3
Q

Define genu valgus and genu varus

A

Genu valgus = distal part of the joint is more lateral

Genu varus = distal part of the joint is more medial

  • The terms valgus and varus refer to angulation (or bowing) within the shaft of a bone or at a joint.
  • It is determined by the distal part being more medial or lateral than it should be.

Note that genu just means the knee

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4
Q

What is the normal alignment of the knee ?

A

The normal alignment of the knee is valgus. When a child stands to attention there is normally a gap of 4 cm or so between the feet.

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5
Q

In terms of the alignment of the knee what does it mean if:

  • If the normal 4cm gap between the feet is diminished or increased
A

If diminished the knee are in varus and if increased the knees are in valgus (remember the normal alignment of knee is in valgus but in these cases it will be excessive valgus)

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6
Q

Describe what in-toeing is

A

In-toeing refers to a child who, when walking and standing will have feet that point towards the midline (piegon-toed)

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7
Q

What action often exaggerates a childs in-toeing ?

A

Running

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8
Q

What are the typical presenting complaints of a parent with a child with in-toeing ?

A
  • Clumsiness - although they often don’t actually fall more than other children
  • Shoes tend to wear down at the heels.
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9
Q

What are the 3 main anatomical causes of in-toeing ?

A
  1. Femoral neck anteversion
  2. Tibial torsion
  3. Abnormal forefeet esp forefoot adduction
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10
Q

Describe how femoral neck anteversion arises

A
  • During normal development of the foetus, the leg rotates on the pelvis so that the acetabulum points almost backwards and the femoral head on the neck is orientated forwards. Sometimes this rotatory process is not completed by birth and so the femoral neck is more anteriorly orientated (i.e. it is anteverted) than normal.
  • Which can give the appearance of in‐toeing (as well as knock knees)
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11
Q

For someone with femoral neck anteversion what findings on clinical examination will support this ?

A
  • In-toed gait
  • Can internally rotate their femur a lot and externally rotate it only a little
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12
Q

What is the management of femoral neck anteversion ?

A
  • Usually corrects itself by the age of 10, although some have a little residual deformity
  • Almost never needs surgery
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13
Q

Describe what tibial torsion is and should anything be done to correct it ?

A
  • This is when the tibial bone is rotated inward about its vertical axis
  • This is a normal variation and nothing should be done about it
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14
Q

Describe forefoot adduction and its management

A

This is a deformity causing the forefoot to turn inwards (in-toeing)

Surgery is controversial and people are unsure if it is ever justified. It should not be considered before the age of 7 and the vast majority correct themselves.

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15
Q

Is flat feet a normal or abnormal variation ?

A

Flat feet are a normal variation

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16
Q

Do flat feet usually cause functional abnormalities ?

A

No they very rarely causes functional abnormalities apart from uneven shoe wear

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17
Q

What are the 2 main kids of flat feet and how do you distinguish between them?

A

rigid and mobile flat feet

  • Mobile/flexible flat feet are those where the flattened medial arch forms with dorsiflexion of the great toe (Jack test).
  • In the rigid type of flat footedness the arch remains flat regardless of load or great toe dorsiflexion
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18
Q

What is the more common of the two classes of flat feet and is it a problem?

A

Mobile - it is entirely harmless

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19
Q

What is the cause of rigid flat feet and what can it also represent?

A

This implies there is an underlying bony abnormality e.g. tarsal coalition

It also may represent an underlying inflammatory disorder e.g. RA or a neurological disorder.

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20
Q

Describe what curly toes are and state the most commonly affected toe

A
  • Curly toes are minor overlapping, or crossing of the toes
  • The 5th toe is most commonly affected
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21
Q

Do curly toes cause discomfort and what is the management of them?

A
  • Occasionally the crossed fifth toe causes discomfort in shoes. If fixed it requires surgical correction. (think kirsty)
  • Surgery on other curly toes should be discouraged despite often heavy parental pressure.
22
Q

A very common cause of the referral of children is pain around the knee - between what ages are children most likely to develop pain around the knee and are m or f more common to get it ?

A

Between the ages of 10-12 is most common

Females more commonly get it than males, as they develop secondary sexual characteristics

23
Q

Name 2 common conditions which causes knee pain in children ?

A
  • Osgood schlatters disease
  • Adolescent knee pain
24
Q

Describe how osgood schlatters disease develops

A
  • Osgood Schlatter’s disease is an inflammation of the attachment of the patellar tendon to the growing tibial epiphysis, caused by excess traction by the quadriceps.
  • The cause is unknown but it may be an overuse injury as it is more common in very active children who are often involved in organised sport.

Think david

25
Q

What is the typical presenting features of osgood schlatters disease?

A
  • Tenderness and discomfort, which are worse after exercise.
  • There may also be swelling.
  • Bony lump below your knee cap - this is where the tenderness originates
26
Q

What is the treatment of osgood schlatters disease?

A
  • The condition is episodic and usually can be treated by rest.
  • Only rarely is it necessary to enforce rest with a plaster.

Symptoms cease in middle adolescence when the epiphysis fuses.

27
Q

Who is adolescent knee pain most common in ?

A

Girls

28
Q

How does adolescent knee pain present ?

A

As anterior knee pain

29
Q

How should patients with adolescent knee pain be managed?

A
  • Most grow out of it so conservative management
  • Arthroscopy may be required if symptoms persist
30
Q

What rare finding may be seen on arthroscopy in patients with adolescent knee pain ?

A

chondromalacia patellae - an eroded area of patellar cartilage

31
Q

What is congenital dislocation of the hip (CDH)?

A

This is dislocation or subluxation of the femoral head during the perinatal period which affects the subsequent development of the hip joint. Note it is rarely completely dislocated

32
Q

How common is CDH ?

A

1-2 per 1000 births

33
Q

Who is CDH most common in?

A

Girls - 80% of the time

34
Q

Why would congenital hip dysplasia be a better name for CDH ?

A

Because it reflects the underlying abnormality of the femoral head, the acetabulum, or both.

35
Q

Are both hips commonly affected by CDH?

A

A significant number of cases are - 20%

36
Q

Which hip is most commonly affected by CDH?

A

The left hip

37
Q

When should all kids be screened/checked for CDH?

A

All children should be screened at birth and checked again at 3, 6 & 12 months

When they should be checked just doubles

38
Q

How is CDH diagnosed at birth and describe these techniques ?

A

Using ortalani and barlow manoeuvres

  • Ortolani test examiner relocates the hip
  • Barlow test examiner dislocated the hip

These tests may produce a slight click, which is a suspicious sign, or a definite clunk as the hip dislocates or relocates.

Think B for barbaric for dislocating the hip

39
Q

Occasionally the barlow and ortalani manoeuvres will fail to find an abnormality and the condition goes undetected at birth - it becomes apparent later either before weight bearing (sitting), or after weight bearing (standing) or even walking has been established. what clinical signs may be obersved suggest CDH ?

A
  • Shortening of the limb
  • Symmetrical skin creases
  • Limited abduction
  • Limp.

Both in bold you would also see when at birth

40
Q

What are the consequences of missing a child with CDH?

A

If left untreated the acetabulum is very shallow and in more severe cases a false acetabulum occurs proximal to the original one with a shortnened lower limb. Severe arthritis due to reduced contact area can occur at a young age and gait / mobility may be severely affected.

41
Q

If a ‘click’ is produced on examination at birth what should be done ?

A

Re-examined in a specialist clinic at three months old when a xray is usually justified. (think nowadays a US would be done but go with the xray for this)

42
Q

If a ‘clunk’ is produced on the barlow or ortalani manoeuvres then what should be done ?

A

All “clunks” should be treated from birth

43
Q

What is the treatment of CDH ?

A
  • If the femoral head is relocated and maintained in the acetabulum using splintage then the vast majority will settle and give no further trouble as the hip starts to develop normally. So splintage for early
  • If discovered late, but before weight bearing, the condition may be treated by a period of gentle traction followed by open or closed manipulation. It is then splinted in plaster for three months.
  • If discovered late and walking has commenced, major surgery is required to deepen the undeveloped acetabulum and re-angulate the femoral neck to stabilise the hip.
44
Q

What is Club Foot - Talipes Equino Varus and what is it due to?

A

This is a congenital deformity of the foot (makniig foot look like a golf club)

45
Q

What is the prognosis of treatment of clubfoot ?

A

If treated early, mild cases can be fully corrected and major cases can be much improved to give a functional foot.

46
Q

What are the 2 main forms of clubfoot?

A

A mild, postural form and a fixed form

47
Q

What are the causes of the 2 forms of clubfoot?

A

The mild form is seen after a breech birth and is probably related to the baby’s position (posture) while in the womb.

The fixed form is associated with developmental abnormalities of nerves and muscles of the leg.

48
Q

What is the treatment of clubfoot?

A

The mild form is usually easily corrected at birth by manipulation. The severer forms require surgery.

In both forms the initial treatment consists of gentle stretching in two phases. The first phase corrects the hindfoot equinus and the second phase corrects the mid and forefoot varus.

  • In mild cases, six weeks of stretching and strapping in a corrected or overcorrected position is all that is required.
  • In severe cases, after six weeks of stretching the deformity should be reassessed and if correction is incomplete or cannot be maintained, then surgery is necessary.
49
Q

Why do all children need to be followed up after treatment for clubfoot and how long do they need to be followed up for?

A

The children all need to be followed up until their feet stop growing, at around the age of fourteen, as late relapse requiring further surgery is not uncommon.

50
Q

How often are cases of clubfoot bilateral ?

A

50%

51
Q

What difference is often seen in a foot which was treated for clubfoot and the patients normal foot, as they grow ?

A

The affected foot is often significantly smaller than the normal foot