Children's Orthopaedics Flashcards

1
Q

How many standard deviations are considered within normal limits

A

2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

How does angular profile vary between newborns and children aged 4-6 years

A

Newborns = Genu valgus
1.5 - 2 years = Normal angular profile
2 - 2.5 years = Genu varum
4-6 years = Normal angular profile

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Give examples of abnormal features in toddlers which correct themselves with age

A

Overlapping toes
Internally rotated feet
Flat feet

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

If a deformity is asymmetrical/unilateral, it is less likely to be pathological. TRUE/FALSE?

A

FALSE

a deformity is more likely to be pathological if it is only present on one side

e.g. Blouts disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Describe the two ways in which bones can grow during development

A

Longitudinal/vertically from the growth plate (epiphysis) by enchondral ossification

Circumferential (bone gets wider)
from the periosteum by appositional growth

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

When do humans begin to lose bone mass, and do males or females lose it quicker?

A

Post-menopause OR after age of 50

Men start with a higher bone mass BUT both genders lose it at the same rate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Give an example of a dangerous recreational activity for young children which can damage their epiphyseal growth plate

A

Trampolining

damages blood vessels and growing bone in this region

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How many children have a short stature as a result of a pathological condition?

A

1 in 5 children

remember to check parents height

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What factors can affect the growth plate?

A
Diet / Nutrition
Sunshine, Vitamins (Vit D & A)
Injury
Illness
Hormones (GH)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

When a child is growing, they are more likely to fracture the shaft of a bone. TRUE/FALSE

A

FALSE

more likely to fracture developing growth plates

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

At what age do children develop each of their integral physical movements (crawling, walking, jumping etc)?

A
6-9 months - Sits alone, crawls
8-12 months – stands
14-17 months walks
24 months jumps
3 years manages stairs alone
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

At what age do children develop the ability to move their head, speak, feed themself and become potty trained?

A

1-6 months Loss of primitive reflexes – grasp , stepping
2 months head control
9-12 months few words
14 months feeds self, uses spoon
18 months stacks 4 blocks, understands 200 words
3 years potty trained

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Why should you be concious to not over-review children with undetermined conditions?

A

Overtreatment and over-investigation = fear of doctors, feelings of stigmatisation and psychologic distress

both experienced by parent and child

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Persisting mild genu varum can run in families. TRUE/FALSE?

A

TRUE => reassure families that this is normal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

When may genu varum be considered abnormal?

A
  • unilateral (asymmetry >5°)
  • severe >2SD/16° from mean
  • short stature >2SD
  • Painful
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What pathological conditions can cause genu varum?

A
Skeletal Dysplasia
Rickets – deficiency vitamin D
Tumour e.g. enchondroma
Blounts disease
Trauma => physeal injury
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What is Blount’s disease?

A

The outside of the growth plate continues to grow whilst the inside slows down

=> causing an angular deformity

typical Beak-like protrusion on xray

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What surgical intervention can be undertaken on a child with Blount’s disease?

A

Debridement of growth plate to get rid of dead material and encourage further growth

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

When does Genu Valgum usually peak?

A

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

When should a child with Genu Valgum be referred or considered for surgery?

A

Refer if asymmetric, painful, severe (>2SD)

> 8cm intermalleolar distance at age 11
=> consider surgery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

How is intoeing often tested clinically in children

A

Often accentuated when running

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

What 3 deformities can cause intoeing?

A

femoral neck anteversion
Internal Tibial Torsion
metatarsus adductus

or combination

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

How do children with femoral neck anteversion usually like to sit?

A

In the W position

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Describe the pathogenesis of femoral neck anteversion

A

Femoral neck usually sits at 40 degrees anteriorly

when you get older this regresses to 10-15 degrees

some children have a condition where the femoral neck does not regress as quickly

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

At what age are children usually affected by internal tibial torsion?

A

Usually seen in toddlers (1-3 yrs)

vast majority resolve by 6 yrs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

What treatment is used for internal tibial torsion

A

Bracing & orthotics = ineffective and not required

Surgery very rare for severe cases!

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

Is metatarsus adductus usually a serious presentation?

A

No it is Common and Benign and usually Resolves

If not passively correctable then serial casting may help age 6-12 months

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

How common is flat feet in adults?

A

1 in 5 adults have this condition

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

Are babies born with flat or arched feet?

A

FLAT => develop medial arch once walking as tibialis posterior strengthens

30
Q

What can cause flexible flat feet?

A

generalised ligamentous laxity

tightness gastrocsoleus complex

31
Q

What test is used if there is suspicion of a tight gastrocsoleous complex in flat feet?

A

Calf tightness assessment

=> need to relax gastrocs by flexing knee

32
Q

What scoring system is used to test hypermobility?

A

Beighton Score 9/9

33
Q

What can cause rigid flat foot?

A

underlying bony connection known as tarsal coalition

May benefit from surgery if painful

34
Q

What toes are most affected by curling and when does this condition usually resolve?

A

Most 3rd or 4th toes

Vast majority resolve by 6 years

35
Q

What age group and gender are most likely to develop anterior knee pain

A

Females>males

Adolescent

36
Q

What other symptoms often occur with anterior knee pain

A

Localised patellar tenderness

pain on walking up Stairs/ doing squats

37
Q

What should be analysed in the radiology of a patient with anterior knee pain?

A

ALWAYS THE HIP

can be a result of arthritis or fracture

38
Q

What are the main congenital conditions which present in a paediatric orthopaedic clinic?

A
  • Clubfoot (CTEV)
  • Rocker bottom foot (CVT)
  • Neurofibromatosis
  • Skeletal dysplasia
39
Q

What neuromuscular conditions are commonly seen in patients presenting to a paediatric orthopaedic clinic?

A
  • Cerebral palsy
  • Tip toe walking
  • Duchenne muscular dystrophy
  • High arch (cavus) foot
40
Q

What are the main features of clubfoot?

A

– C cavus
– A adductus
– V varus
– E equinus (ballerina feet - constantly pointed, cant bring foot to anterior leg)

41
Q

What is the clinical term for Clubfoot?

A

Congenital talipes equinovarus (CTEV)

42
Q

What gender usually gets Clubfoot and how many of these cases are bilateral?

A

2:1 boys

50% cases are bilateral

43
Q

What causes Clubfoot?

A

Most = Idiopathic
OR

Assoc. with conditions such as:

  • Myelomeningocoele (spina bifida)
  • Diastrophic dwarfism
  • Tibial hemimelia (short/absent tibia)
44
Q

What is Postural Talipes and how do you differentiate it from Clubfoot?

A
  • tightness in muscles around ankle
  • due to position of baby in womb
  • not caused by problems with bones in foot and
  • will not cause any problems with walking
  • diagnosed by examining the baby’s feet
  • Pt can dorsiflex their foot to neutral or further in postural talipes NOT clubfoot
45
Q

How is Clubfoot treated?

A

Ponseti Method
Casting for 4-6 weeks

+/- achilles tenotomy to allow ankle to straighten
(achilles tendon heals undamaged due to childrens ability to heal)

46
Q

What is “Rocker Bottom” Feet?

A

• Irreducible dislocation of talus on navicular

47
Q

What is the clinical term for Rocker Bottom Feet?

A

Congenital Vertical Talus (CVT)

48
Q

What are the signs of Rocker Bottom Feet?

A

– Round plantar surface

– Equinus hindfoot

49
Q

What other conditions can predispose to Rocker Bottom Feet?

A
Myelomeningocoele (Spina Bifida)
Arthrogryposis (curved joints)
Spinal muscular atrophy
Neurofibromatosis
Trisomies
50
Q

Where does neurofibromatosis commonly affect?

A

–Extremities
–Spine (scoliosis) >10%
–Skin (neurofibromas)

51
Q

What Type of Neurofibromatosis is most common?

A

NF1 => Type 1

52
Q

Neurofibromatosis is an Autosomal Dominant condition. TRUE/FALSE?

A

TRUE

NF1 gene mutation (neurofibromin) found on Chromosome 17

53
Q

What is the diagnostic criteria for neurofibromatosis?

A
2/7 of the following:
• >6 café au lait spots
• ≥2 neurofibromas / plexiform neurofibroma
• Freckling axilla / inguinal region
• Optic glioma
• ≥2 Lisch nodules
• Cortical thinning / pseudoarthrosis
• First degree relative affected
54
Q

What is skeletal dysplasia?

A

abnormal development of cartilage and bone

55
Q

What clinical signs are apparent in skeletal dysplasia?

A

–Shortening of involved bone
–Short stature (usually) <2SD from normal

Can be Proportionate / disproportionate
=> e.g. trunk much longer than legs

56
Q

What is the genetic mutation involved in achondroplasia?

A

Fibroblast growth factor receptor 3 (FGFR3)

  • Autosomal dominant
  • 80% spontaneous mutations
57
Q

What features are usually seen in achondroplasia

A
– Normal trunk / short limbs
– Frontal bossing
– Genu varum
– Normal intelligence
– Motor delay
58
Q

What is cerebral palsy?

A

Non-progressive neuromuscular disorder:

• Injury to immature brain (<2 years)
– Prematurity
– Perinatal (infection / anoxic (birth) injuries / meningitis)

59
Q

What are the common features of cerebral palsy?

A

– Upper Motor Neurone disease > muscle weakness / spasticity
– Early: abnormal muscle forces > dynamic deformity
– Late: contractures / fixed deformity / dislocation

60
Q

What is the “clasp knife spasticity” concept?

A

Testing muscles shows tightness then sudden relaxation

61
Q

How are Cerebral Palsy conditions classified?

A

classified by how much patient is able to walk

62
Q

What methods are used to treat Cerebral palsy?

A

MEDICINES:

  • Benzodiazepines
  • Baclofen

SURGERY:

  • identifies over-firing nerves and cuts them
  • non-reversible

BOTOX:
- injected to relax muscles

63
Q

What X-Linked neuromuscular condition presents with progressive muscle weakness?

A

Duchenne Muscular Dystrophy (DMD)

64
Q

What is the pathophysiology of DMD?

A

– Absence dystrophin protein

– replacement of muscle with fibrofatty tissue

65
Q

When do patients with DMD usually present?

A

2-5 years of age

66
Q

Describe the age progression of DMD

A
2-5 = diagnosis
10 = need walking assistance
15 = wheelchair
20 = Pts often pass away
67
Q

What features are present in Duchenne Muscular Dystrophy?

A

– Muscle weakness (prox > distal)
– Clumsy walking
– Positive Gowers sign (walks hands up knees to get up)
– Scoliosis

68
Q

What is Cavus feet?

A
Pes cavus (high arched foot)
• Elevated longitudinal arch &amp; varus hindfoot
69
Q

What causes Cavus Feet?

A

– Idiopathic / familial

– 2/3 due to neurological disorder:

  • polio,
  • cerebral palsy
  • myelomeningocoele (spina bifida)
  • Spinal Cord Injury

– Charcot Marie Tooth
- peripheral nerve disease

70
Q

What is the management for Cavus Foot?

A

Management:
– conservative

Surgery:
– Soft tissue surgery
– Bony (osteotomies)