paediatric orthopaedics Flashcards

1
Q

talipes equino varus

A

clubfoot
foot points downards and inwards
can be corrected by splintage or is neurological or skeletal so cant
series of casts
percutaneous tenotomy of achilles tendon- 90% will need this

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2
Q

MSK issues that cause concern

A

in toed gait
bow legs
flat feet
curly toes
late walkers

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3
Q

how to check in toeing

A

gait angle
forefoot alignment
thigh foot angle (lies on front and look arial view when bent knee)
hip rotation
86% reassured at first visit, never operate before 10 years

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4
Q

internal tibial torsion

A

increased thigh foot angle
90% resolve
no role for splints or physio etc

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5
Q

metatarsus adductus

A

90% resolve by 1 year
5% persist to adulthood
toes point in

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6
Q

normal physiological shape of legs

A

babies start off varus legs
then straight
then valgus
then straight
people concerned but reassure normal

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7
Q

flat feet

A

normal at birth diminishes with age
jacks test lift toe up heel turns into varus
insoles no benefit

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8
Q

curly toes

A

strong fam history
tightness in flexor tendons
mostly cosmetic problem
if functional problem consider flexor tenotomy if over 6 years

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9
Q

walking age mean

A

12 months. 50% take longer than mean. beyond 18 months refer

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10
Q

developmental dysplasia of hip

A

structural abnormality in the hips caused by abnormal development of the fetal bones during pregnancy
instability in the hips and a tendency or potential for subluxation or dislocation
can persist into adulthood

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11
Q

the big 3

A

developmental dysplasia of hip DDH
slipped upper femoral epiphysis SUFE
perthes disease

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12
Q

DDH signs

A

picked up during the newborn examinations or later when the child presents with hip asymmetry
Ortolani test
Barlow test
clunking
reduced range of movement in the hip
limp.
short femur
hamstring test

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13
Q

DDH epidemiology

A

common in inuits
eastern europe
not african
commoner in girls
left hip commoner

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14
Q

risk factors DDh

A

first born
breech
family history
increased weight

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15
Q

DDH investiagtions

A

ultrasound gold standard
xrays also

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16
Q

management DDH

A

pavlik harness if less than 3 months. permanent for 6-8 weeks
surgery if fail or if post 3 months of age then hip spica cast to immobilise
over age 6 and bilateral leave alone.
over aged 10 and unilateral leave alone
older child the poorer the results

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17
Q

perthes disease

A

idiopathic disruption of blood flow to the femoral head, causing avascular necrosis of the bone. affects the epiphyses of the femur
children aged 4-12 years
more common in boys

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18
Q

presentation perthes disease

A

short stature
pain in hip or groin
limp (random and sudden)
knee pain on exercise (referred)
stiff hip joint
systemically well
no history of trauma
familial tendency

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19
Q

investigations

A

xray
blood tests normal
technitium bone scan

20
Q

prognosis perthes

A

younger do better
proportion of head involved- herring A B and C shows level of collapse, C being worst

21
Q

treatment perthes

A

maintain hip motion with physio
analgesia
restrict painful activities
regular x rays to assess
supervised neglect- improve in 2-3 years
osteotomy in selected groups of older children
if bilateral consider other conditions but 10% can be

22
Q

slipped upper femoral epiphysis

A

head of the femur is displaced (“slips”) along the growth plate
more common in boys
aged 8 – 15 years
more common in obese children.

23
Q

presentation SUFE

A

adolescent, obese male undergoing a growth spurt
may be a history of minor trauma trigger
pain disproportionate to the severity of the trauma
relieved on rest
painful to weight bear

vague symptoms- hip, groin, thigh, knee, painful limp, restricted movement in hip
hip in external rotation
reduced internal rotation esp in flexion painful to try
plain x rays- trethowans sign helps to show. ice cream falling off its cone

24
Q

classification of SUFE

A

acute- 3 weeks
chronic- beyond
magnitude of slip
stable v unstable - weight bearing

25
Q

management in SUFE

A

surgery to return femoral head to correct position and fix it in place to prevent slipping further
stable- usually pinned in situ
unstable- open reduction but avascular necrosis risk

26
Q

limping infant 1-3 years common causes

A

septic arthritis
fracture
DDH

27
Q

limping child 4-10 years common causes

A

transient synovitis
perthes
JIA

28
Q

limping child more than 10 common causes

A

SUFE
spondylolisthesis
overuse

29
Q

gowers sign positive

A

check creatinine kinase as muscular dystrophy

30
Q

infection- limp

A

SA wont walk
OM can
TS will walk
pain in SA and OM
recent URTI /ear infection- TS
general malaise- OM SM

31
Q

septic arthritis

A

> 38degrees
no weight bearing
12000/ml WBC
40mm/hr
CRP >30
surgery is treatment
empirical antibiotics

32
Q

transient synovitis

A

diagnosis of exclusion
spectrum of severity
history of viral infection
low CRP and normal WBC excludes sepsis
not that unwell
limping

33
Q

complex exceptional needs defined

A

severe impairment in at least 4 categories with enteral or parenteral feeding
or
severe impairment in at least 2 categories and ventilation/CPAP
AND
sustained for more then 6 months and ongoing

34
Q

examples of complex needs

A

spina bifida
syndromes
cerebral palsy
muscular dystrophy
neurofibromatosis

35
Q

Cerebral palsy

A

permanent and non progressive motor disorder due to brain damage before birth or during first 2 years of life
causes can be prenatal, perinatal or postnatal
can be spastic, athetoid, ataxia, mixed

36
Q

gross motor function classification system

A

1- walks without limits
2- walk with limits
3- walks using hand held mobility device
4- may use powered mobility themselves
5- transported in manual wheelchair

37
Q

problems in CP

A

spasticity
lack of voluntary limb control
impaired senses
weakness
poor coordination
hip displacement- early surgical intervention

38
Q

orthopaedic priorities in CP

A

spine, hip, feet
maintain sitting balance
improve standing posture
gait

39
Q

management non surgical CP

A

diazepam, baclofen
botulinum toxin, baclofen intra thecal pump
antiepileptics
glycopyronium bromide for excessive drooling
physio
OT
SALT
dieticians

40
Q

surgeries CP

A

soft tissue release
bony relaignment- osteotomy
risks and benefits need to be weighed up

41
Q

scoliosis

A

deviation in coronal plane
>10 degree deviation is clinically significant
non structural- due to extrinsic cause
structural - abnormal rotation of vertebrae

42
Q

high risk progression scoliosis

A

premenarchal
<12yo at presentation
size of curve at presentation
neuromuscular causes eg CP and muscular dystrophy

43
Q

types of scoliosis

A

congenital
idiopathic (most common)
neuromuscular

44
Q

examination of scoliosis

A

inspect posterior torso in forward flexion
abnormal neurology or pain should be noted as not normally a feature

45
Q

investigations in scoliosis

A

AP erect whole spine
MRI to show cause