Paediatric Conditions Flashcards

1
Q

What is a salter-harris fracture?

A

One which involves the epiphysea plate or growth plate of a bone. It is a common injury found in children and occurs in 15% of all childhood fractures.

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2
Q

What are the five main levels of Salter-Harris fracture?

A
Type 1 - Slipped
Type 2 - Above
Type 3 - Lower
Type 4 - Through or Transverse
Type 5 - Rammed or Ruined
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3
Q

What is the mnemonic for remembering?

A

SALTR

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4
Q

Give seven causes of limp

A
  • Femoral Fracture
  • Slipped Capital Femoral Epiphysis
  • Perthe’s disease
  • Distal tibial buckle fracture
  • Transient synovitis
  • Developmental Dysplasia of the Hip
  • Septic Arthritis
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5
Q

What is a slipped capital femoral epiphysis?

A

Instability of the proximal femoral growth plate, and is one of the most common adolescent hip disorders.

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6
Q

What occurs in a slipped capital femoral epiphysis?

A

the femoral shaft rolls into external rotation and the femoral neck is displaced forwards while the epiphysis remains in the acetabulum.

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7
Q

Give two overall ways in which you can categorise slipped capital femoral epiphysis

A

Type of slip

Stable vs unstable

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8
Q

Give four ways in which you can categorise a type of slip

A

Pre-slip – Wide epiphyseal line without slipping
Acute form – Slippage occurs spontaneously
Acute on chronic – Slippage occurs when there is an already exisiting chronic slip
Chronic slip – Steadily progressive slippage

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9
Q

Outline the aeitology of slipped capital femoral epiphysis

A

The slip usually occurs through the hypertrophic zone of the cartaliginous growth plate Many patients are either fat and sexually immature or excessively tall and thin. This could mean that there is an imbalance between pituitary hormone activity, which stimulate rapid growth and increased physeal hypertrophy, and gonadal hormones which influence physeal maturation and epiphyseal fusion.
A disparity may result in the physis being unable to resist the shearing stresses imposed by an increase in body weight.

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10
Q

What is the epidemiology of slipped capital femoral epiphysis

A

Most commonly in boys age 10-17, with peak age being 11.5 for girls, 13 for boys. Left hip more commonly affected than the right. Three times as common in boys.

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11
Q

Give four overall risk factors for slipped capital femoral epiphysis

A

Mechanical: Local trauma, obesity
Inflammatory conditions: Neglected septic arthritis
Metabolic conditions: Hypothyroidism, hypopituitarism, growth hormone deficiency
Radiaiton of the pelvis: Chemotherapu, renal osteodystrophy induced bone dysplasia

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12
Q

What is the usual presentation of the slipped capital femoral epiphysis

A

Often has a protracted history of minor episodes of pain – an “acute on chronic” slip. Patient is usually around puberty, overweight or very tall and thin.
Discomfort in the hip, groin, medial thigh and knee during walking. Pain accentuated by running/jumping/pivoting.
Pain in hip, external rotation and sometimes leg shortening (especially in chronic cases). Flexion, abduction and medial rotation are limited.

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13
Q

What occurs on x-ray in slipped capital femoral epiphysis

A

Tretowan’s sign, which occurs when klines line does not intersect with the femoral head.

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14
Q

Give four differenital diagnosis for slipped capital femoral epiphysis

A
  • Perthe’s disease
  • Acute hip fracture
  • Septic Arthritis
  • Acute transient synovitis
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15
Q

What should be used to investigate slipped capital femoral epiphysis

A

AP and lateral x-rays show widening of the epiphyseal line or displacement of the femoral head.

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16
Q

Outline the management of SCFE

A

Analgesia and immediate orthopaedic referral if the diagnosis is suspected – make sure leg is immobilised, either verbally or with a restrictor.

Surgical management is the definitive treatment, with screws inserted percutaneously. Corrective osteotomy for deformities after patient has stopped growing.

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17
Q

What are the complications of SCFE

A
  • Chondrolysis

- Avascular necrosis of the epiphysis (occurs in 10-25% of cases)

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18
Q

What is the prognosis for SCFE?

A

Depends on the initial degree of slippage and prompt recognition by a general practicioner. End result is good to excellent in 95% of cases if fragments are displaced by less than 1/3 of the diameter of the femoral neck.

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19
Q

What is a synonym for developmental dysplasia of the hip?

A

Congenital dislocation of hip

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20
Q

What does a DDH entail?

A

Developmental dysplasia of the hip refers to a spectrum of severity ranging from mild acetabular dysplasia with a stable hip, to more severe forms of dysplasia with neonatal hip instability, to established hip dysplasia with or without later subluxation or dislocation.

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21
Q

Give four factors which play a role in the genesis of DDH

A

Genetic factors
Hormonal factors
Intrauterine malposition
Post-natal factors

22
Q

What are the epidemiological features of DDH?

A

Developmental dysplasia of the hip effects 1-3% of new borns and is responsible for 30% of hip replacements in those under 60 years of age. The left hip is dislocated more often than the right, and it is more common in cultures with swaddling.

23
Q

What are three risk factors for DDH?

A
  • Having a sibling with hip dysplasia
  • Being a girl
  • Vaginal delivery of children in breech positions
24
Q

How does screening for DDH work?

A

Screening for DDH is part of the physical examination of newborn and 6-8 week old babies. Sometimes Ultrasound is used, if there is a family history or if the child was delivered breech.

25
Q

What are two tests done for DDH on under 6 month olds?

A

Ortolani test

Barlow test

26
Q

What is the ortolani test?

A

The examiner applies forward pressure to each femoral head in turn, in an attempt to move a posteriorly dislocated femoral head forwards into the acetabulum. Palpable movement suggests that the hip is dislocated or subluxed, but reducible.

27
Q

What is the Barlow test?

A

backward pressure is applied to the head of each femur in turn, and a subluxable hip is suspected on the basis of palpable partial or complete displacement

28
Q

What is looked for in patietns >6 months

A
  • The child is examined lying supine with the hips and knees flexed to 90° and the height of each knee is compared.
  • A positive sign is that one leg appears shorter than the other.
  • This is usually due to dislocation of the hip; however, any discrepancy of limb length will produce a positive sign.
    Other physical signs for late dislocation include asymmetry of the gluteal thigh or labral skin folds, discrepancy in leg length, a widened perineum on the affected side, buttock flattening, and asymmetrical thigh skin folds, decreased abduction on the affected side, and standing or walking with external rotation of the affected leg.
29
Q

Give four investigations for DDH

A

Ultrasound, athrography, CT and MRI.

30
Q

How is DDH managed?

A

Bracing is used for children

31
Q

What is perthe’s disease/

A

Avascular necrosis of the femoral head in children. The precipitating cause is unknown but the cardinal step is ischaemia of the femoral hea1

32
Q

Outline the pathophys of perthe’s disease?

A

Up to the age of 4 months the femoral head is supplied by 1) metaphyseal vessels which penetrate the growth disc, 2) lateral epiphyseal vessels running in the retinacula and 3) some vessels running in the ligamentum teres. Between 4 and 7 years of age the metaphyseal vessels are gone and the ligamentum teres vessels are undeveloped, and thus blood supply comes soley from lateral epiphyseal vessels. These are vulnerable to effusion, stretching and pressure – such pressure could cause venous pressure, increasing intraosseous pressure and leading to infarction.

33
Q

What are the three stages of Perthe’s disease

A

Stage 1 – Ischaemia and bone death
Stage 2 – Revascularization and repair
Stage 3 – Distortion and remodelling

34
Q

What is a condition found in 50% of perthe’s sufferers?

A

Thrombophillia is reported in 50% of patients.

35
Q

What is the classification for Perthe’s?

A

Herring classification

36
Q

What is the epidemiology of perthe’s?

A
  • 4-8 years is most common age of presentation
  • Male to female ratio is 5:1
  • More commonly seen in urban populations versus rural
37
Q

What are the presenting features of perthe’s?

A
  • 4-8 years is most common age of presentation
  • Male to female ratio is 5:1
  • More commonly seen in urban populations versus rural
38
Q

What are the four main investigations for Perthe’s?

A

X-ray – May show some widening of the joint space and asymmetry of the ossific centres.
FBC and ESR
Hip aspiration – rule out septic arthritis

39
Q

What ius the management for Perthe’s for those

A

There is no consensus for the optimum treatment. The aim of treatment is to maintain the sphericity of the femoral head and the congruency of the femur-acetabulum relationship to prevent secondary degenerative arthritis. Early diagnosis and management can help prevent the collapse of the femoral head, progressive femoral head deformity, and impingement.
Children who have a skeletal age of 6.0 years or less at the onset of the disease do well without treatment. Operative treatment should be considered in children who are six years old or older and have over 50% femoral head necrosis when the diagnosis is made.

40
Q

How is physio used in perthe;s?

A

Physiotherapy using muscle strengthening and stretching exercises, produces significant improvement in articular range of motion, muscular strength and articular dysfunction, but these improvements are not seen on X-ray.

41
Q

What is the prognosis of perthe’s?

A

Physiotherapy using muscle strengthening and stretching exercises, produces significant improvement in articular range of motion, muscular strength and articular dysfunction, but these improvements are not seen on X-ray.
50% do well with no treatment, and patients less the 6 years of age the outcome is good regardless of treatment (this is due to higher remodelling potential). More than 80% have good outcome that persists into fourth decade of life, although many will require an artificial hip.

42
Q

What are the complications of Perthe’s?

A

Residual deformities may include coxa magna (broadening of the head and neck of the femur), coxa plana (osteochondritis of the femoral head), coxa breva (structural shortening of the neck of the femur) and hinged abduction (this occurs when an enlarged femoral head is pushed laterally and it impinges on the acetabular rim when the hip is abducted).

43
Q

What is the other name for club foot and what is it?

A

as talipes equinovarus, club foot is characterised by an excessively turned in foot and high medial longitundinal arch.

44
Q

What happens if club foot is left untreated?

A

If left untreated it can result in long-term disability, deformity and pain. Interventions can be conservative or surgical.

45
Q

What is the incidence of club foot?

A

The incidence of club foot is 1 in 1000 births. Males are more commonly affected than females and up to 50% of cases are bilateral.

46
Q

What is the pathology of club foot?

A

In 20% of cases club foot is associated with distal arthrogryposis (congenital joint contractures), myelomeningocele (spina bifida), amniotic band sequence, or other genetic syndrome such as trisomy 18 or cnromosome 22q11 deletion.
Maternal associations with club foot include teratogenic agents, oligohydraminios and congenital uterus constriction rings.

47
Q

What is presentation of a patient with club foot?

A
  • Calf muscle and the foot smaller than normal
  • Hindfoot is in rigid equinovarus (foot is turned inward and downward) and the forefoot is short, wide, adducted and supinated. The sole of the foot points mediall.
  • Heel is high and fibula prominent
48
Q

Give three conditions which are associated with club foot

A

Congenital hip dislocation, Spina Bifida, Cerebal Palsy, Arthrogryposis

49
Q

What imaging is used in club foot?

A

AP is taken with foot 30 degrees plantarflexed and the tube likewise angled 30 degrees perpendicular. Lines can be drawn through the long axis of the talus parallel to its medial border.
Lateral film I taken with foot in forced dorsiflexion.

50
Q

Wat is the scoring system for club foot?

A

Pirani Scoring system

51
Q

Outline the pirani scoring system

A

Pirani scoring system used to determine the likely success of treatment. It consists of 6 categories, three in the midfoot and three in the hindfoot, and each category is scored with 0, 0.5 and 1.
Categories
Mid-foot
Curvature of the lateral border
Medial crease
Uncovering of the lateral head of the talus
Hind-foot
Posterior crease
Emptiness of heel
Degree of dorsiflexion.
The scoring system (worst 6, best 0) can be used to identify severity of club foot and to monitor success of correction.

52
Q

What is the treatment for club foot?

A

Ponseti Method
Foot is reduced using weekly casts followed bya percutaneous tenotomy of the Achilles tendon to correct the equinus. Twenty four and then night-time splinting in abduction is the maintained for a period of 3-4 years.
When compared with surgical intervention, both the Ponseti method and surgery have a relatively high recurrence rate, but the ponseti method was associated with significantly less revision surgery.
Ponseti method (non-surgical correction) has an initial correction rate of 90% in idiopathic feet.
French functional method
Involves special physiotherapists and daily manipulation
Surgery
Soft-tissue responsible for shortening (tibialis posterior, abductor halluces and Achilles tendon) released. Complete soft tissue release performed between 6 and 12 months.