paediatrics ortho Flashcards

1
Q

“limping child” main ortho problems in children 9

A
fracutre
Hip DDH
perthes
SCFE
Septic 
transient synovitis
osteomyelitis
malignancy 
NAI
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2
Q

what anatomical feature of children’s bones make it different to adults

A

physis
periosteum thick
ossification centres

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3
Q

how are paediatric fractures different to adults

A
heal quicker
less morbidity
tolerate bed rest beter
more closed reductions ie MUA than open
thick periosteum aids conservative management
physeal
ability to remodel with time
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4
Q

treatment option for paediatric forearm#

A

MUA
k wires and nails
remodelling

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5
Q

Treatment for femoral #

A

bed traction
flexible nails
physeal consider

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6
Q

what considerations are there for the physis

A

risk of growth problems
partial/ complete arrest
articular involvemnet

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7
Q

age of physis fusion

A

12-14

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8
Q

salter harris classification and treatment

A
straight=conservative
above=conservative
lower=operate
through=operate
physis= crush injury so might need to fuse other leg
I-V
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9
Q

what ages do
DDH
perthes
and SCFE present at

A

DDH=toddler
perthes=younger 3-5
SCFE=9-15

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10
Q

What is DDH

A

-disorder of abnormal development acetabular dysplasia
-capsular laxity
ie hip not in socket

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11
Q

meaning of dysplasia

A

a hip that can be provoked to dislocate or is subluxed

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12
Q

3 tests to dx of DDH and when should it be diagnosed

A

positive ortolani sign: abducts the hip while applying ant force= reduces hip joint from dislocate
Positive barlow sign= adducts the hip while applying post force= hip will dislocate from reduced
within first 3 months of life
also use USS

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13
Q

incidence of DDH

A

most common MSK

1: 000 dislocated
1: 100 dysplasia

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14
Q

most common presetnation of DDH 4

A

unilateral 80%
mostly left hip
limited hip abduction
leg length difference

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15
Q

risk factors for DDH 6

A
first born 
female 6:1
breech position
FHX
oligohydramnios: less amniotic fluid
congential abnormalities
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16
Q

Treatment of DDH by age of dx

A

6-18 months= spica cast
>18 months: open reduction and cast
>24 months: femoral/ pelvic osteotomy

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17
Q

what is perthes

A

idiopathic avascular necrosis of proximal femoral epiphysis

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18
Q

incidence of perthes

A

1 in 1000

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19
Q

age of perthes

A

4-10

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20
Q

perthes bilateral or unilateral

A

more common unilateral 88%

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21
Q

male to female ratio perthes

A

5:1 male to female

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22
Q

risk factors for perthes

A

fhx
low birth weight
second hand smoke
lower SES

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23
Q

2 main theories behind perthes

A

temporary interruption of blood supply to head get increased bone density and impaired physis growth
and
environmental influence: smoke, trauma

24
Q

pathoanatomy of perthes

A

disruption in vascular supply
bone collapses and subsequent remodel
abnormal response to minor trauma

25
perthes worse prognosis factors
age >6 female sex decreased hip range of motion-stiff hip
26
clinical features of perthes
Tredelenburg gait pain loss of IR and abduction leg length diff
27
perthes treatment
observation as self-limiting | surgery in minority
28
when is a pelvic/ femoral osteotomy indicated for Perthes
older children >8 | more severe disease and femoral head collapse
29
What is SCFE and what happens to the femoral neck
Disorder of the proximal femoral physis leads to slippage of physis relative to femoral neck posterior and internal rotation of femoral neck
30
incidence of scfe
10 per 100,000
31
risk factors for scfe 4
obese children males 3:2 african americans pacific islanders
32
average age for boys and girls
8-15 boys=13.4 girls=12.2 assoc. to puberty
33
clinical presentation scfe
``` 8-15 obese endocrinopathy short ER hip loss of IR and abduction of hip can't bear weight no trauma hx ```
34
management scfe
all require operative pinned in situ- no reduction in edinburgh prophylactic fixation of other hip
35
risk of contralateral side slip for scfe in one year
50%
36
complications of SCFE
chondrolysis avn secondary OA
37
what is the line called in scfe where the femoral neck misses the femoral head
klein line
38
septic arthritis commonest form of spread
haematogenous
39
commonest age of septic arthritis in kids
50% under age of 2
40
pathogens for septic arthritis
neonates: staphylocci, streptococci s.aureus h.influenzae drug user: e.coli and pseudonomas sti; neisseria gonorrhoea
41
routes of septic arthritis
haematogenous extension from adjacent bone direct inoculation from trauma/ surgery
42
kochers criteria for septic arthritis
``` must have 3/4 for a 90% certainty wbc >12,000 inability to weight bear fever >38.5 esr >40 or crp >20 ```
43
poor prognostic indicators for septic arthritis
age <6 months osteomyelitis hip versus knee delay >4 days till presentation
44
sepsis 6
``` give oxygen aspirate joint/ culture empirical antibiotics fluids measure lactate measure urine output ```
45
what is transient synovitis
looks like septic arthritis but less severe | inflammatory secondary to reactive arthritis in children
46
clinical presentation of TS
may have fever and raised CRP can be well and no pus often follows a URTI aspirate no culture
47
management TS
self-limiting | analgesia
48
what is osteomyleitis
infection of bone
49
why are children at risk of osteomyelitis
rich metaphyseal blood supply and immature immune system
50
usual osteomyelitis spread
from haematogenous
51
clinical presentation osteom
pain inability to weight bear fever maybe x-ray often normal first 2 weeks
52
causes of osteom
rare TB and kingella causes
53
red flags for malignancy in a child
constant night pain systemic symptoms swelling
54
what is NAI
inconsistent history or delay seeking medical attention | ie child abuse
55
what specific injuries might be an NAI
long bone fracture <2 posterior rib# metaphyseal corner