Children hip disorder Flashcards

1
Q

when does developmental dysplasia of the hip present

A

birth - 2 years

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2
Q

when does perthes present

A

4-8 years

peak age 6

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3
Q

when does SUFE present

A

10-16 years

peak age 12/13

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4
Q

development of the acetabulum

A

triradiate cartilage, ossifies over time so its fused and bony in adults
fused from ilium, ischium and pubis

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5
Q

why aren’t hip X-rays useful in younger patients

A

femoral head still cartilinagous so doesn’t show up

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6
Q

what is H line on Xray

A

runs between left and right triradiate cartilages

horizontal shows symmetry

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7
Q

what vertical line helps show whether hip is dysplased

A

to perpendicular lines to H line (the P line)

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8
Q

what is DDH

A

abnormal development resulting in dysplasia and possible subluxation or dislocation of hip

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9
Q

What are signs of DDH

A

dysplasia
shadow or underdeveloped acetabulum
subluxation
dislocation

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10
Q

what is the most common orthapaedic disorder in newborns

A

DDH

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11
Q

what factors allow hip to become dysplastic

A

capsular laxity and mechanical factors

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12
Q

what joint is it most common in

A
female (more laxity) 
left hip (way the baby lies in utero)
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13
Q

in what populations is DDH most commonly seen

A

native Americans
laplanders
due to the way they carry children in a papoose

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14
Q

what stimulates normal acetabular growth

A

correctly positions femoral head

absent in SSH, hip becomes sublaxed/dislocated

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15
Q

what is the pathophysiology of DDH

A

initial instability caused by maternal and fatal laxity, genetic laxity and intrauterine and post natal malpositioning

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16
Q

pathoanatomy of DDH

A

initial instability leads to dysplasia leading to gradual dislocation

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17
Q

why do DDH patients get trelenberg pathology

A

shortened leaver arm means that the abductors need to work harder

18
Q

risk factors for DDH

A
first borns 
6x more common in females 
breech presentations 
family history 
oligohydramnios
19
Q

patient presentation in DDH

A

abnormality on screening (early)
limping child (late)
pain later in life

20
Q

2 clinical tests that indicate DDH

A

Barlow test
-pushing backwards to try to dislocate hip
Ortolanis test
-abducting the hips to try and relocate them, fingers push femur forward into acetabulum

21
Q

what quadrant should the developing hip lie in (in relation to the H line)

A

medial inferior quadrant

22
Q

what is the early treatment for DDH

A
Pavlik harness 
23 hours a day for up to 12 weeks 
night time for a few more weeks 
puts the femoral head back into the acetabulum 
puts hit abducted and flexed
23
Q

what is the late presentation DDH treatment

A

surgery
closed reduction (put hip in the right position and cast that stays on for 3 months)
open reduction + osteotomies

24
Q

what is reactive synovitis

A

painful inflamed hip joint after a viral illness
pain present with pain referred to the knee
patient lies with flexed/externally rotated hip

25
Q

how is reactive synovitis diagnosed

A

kochers criteria
distinguished between reactive synovitis and septic arthritis
higher score - more likely to be septic arthritis

26
Q

Treatment for reactive synovitis

A

self limiting condition
analgesia/NSAIDS
repeat review/admission if concern

27
Q

septic arthritis of the hip presentation

A

short duration of symptoms
unable to weight bear and hip/groin pain
pyrexial, haemodynamically stable

28
Q

why is septic arthritis a surgical emergency

A

high bacterial load that causes sepsis
destruction of the joint due to proteolytic enzymes
potential for osteonecrosis of the hip due to increased pressure

29
Q

what causes septic arthritis

A

direct inoculation from trauma/surgery
hematogenous seeding
extension from adjacent bone
osteomyelitis

30
Q

most common causative organism for septic arthritis

A

staph aureus

neonates get strep
(Iv drug users get atypical)

31
Q

treatment for septic arthritis

A

open surgical wash out
samples prior to antibiotics
repeat wash out if not improving

32
Q

what is perthes disease

A

avascular necrosis of the hip (idiopathic)

most common in 4-8 y/o

33
Q

risk factors for perthes disease

A

family history
low birth weight
second hand smoke
asian, Inuit and Central European decent

34
Q

pathophysiology of perthes disease

A

osteonecrosis occurs secondary to femoral head blood supply disruption
revascularasation follows with sbsequent reabsorption and later collapse
leads to remodelling after collapse

35
Q

proposed mechanisms for perthes disease

A

possible association with clotting factors

repeated subclinical trauma and mechanical overload

36
Q

what are the stages of perthes disease

A

initial
fragmentation
reossification
remodelling

37
Q

is perthes disease unilateral

A

yes

38
Q

what is SUFE (slipped upper femoral epiphysis)

A

proximal femoral physic leads to slippage of the metaphysic relative to the epiphysis

39
Q

risk factors for SUFE

A
males
obesity 
age 10-16 
endocrine disorders 
rapid period of growth
40
Q

cause of SUFE

A

epiphysis can’t hold force of bodyweight (ice cream falls of cone)

41
Q

treatment for SUFE

A

surgery
percutaneous pinning of the hip
+/- pinning of other side because there is a risk of getting bilateral

open reduction if a very severe slip