#82 - Vascular/Mechanical Dysfunction of bones - Hip disorders. Flashcards

1
Q

What is DDH?

A

Developmental Dysplasia of the hip. It is an abnormal formation of one or both hips during the gestational period (in utero).

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2
Q

What are the 5 risk factors (5F’s) for DDH?

Which is the most important

A
  • Female (joint laxity)
  • First born (small uterus)
  • Family history - (maternal pelvis shape)
  • Frank Breech
  • Foot deformities and other packaging issues (torticollis, etc.)
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3
Q

What is the barlow test?

A
  • Test for DDH.
  • Sublux the hip –> hip gets popped out of the acetabulum with this maneuver

Pneumonic - BAR = We are going out tonight! = hip gets popped out.

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4
Q

What is the ortolani test?

A

Test for DDH, done after the barlow test dislocates the hip.
-Reduces the hip back into it’s position after the barlow test.

B before O, after going out, time to go home.

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5
Q

What is the galeazzi test?

A

test for knee height difference in newborns - will detect possible DDH. Affected hip will be shorter. It is useful from 3 to 12 months.

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6
Q

Which two newborn tests are only useful in the first 3 months of life?

A

Barlow and ortolani.

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7
Q

Which tests for DDH are useful after 12 months?

A

Tredelenburg sign is seen (gluteus medius lurch)

  • short leg limp.
  • stiff legs.
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8
Q

Positive Barlow/ Ortolani. How do you confirm DDH?

A

Ultrasound used to confirm in newborns.

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9
Q

Positive galeazzi on a newborn 9 months old

A

X ray. X ray needed to confirm if older than 6 months (Structures no longer cartilaginous, ultrasound no good)

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10
Q

Treatment for DDH in young vs. older children vs. adult

A

Young: Pavlik harness (presses hip into acetabulum)

Older: open/closed reduction in the OR

Adult: hip replacement.

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11
Q

10 month female walks with her toes on the left. She has dislocated hip on x ray and DDH. What is her prognosis?

A

With open reduction, very good. There is excellent remodeling potential at this age.

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12
Q

What is the natural history of DDH, left untreated?

A

-Eventually, the person will develop pseudoacetabulum in a different part of the hip. This will cause severe degenerative changes, and they will need an early joint replacement.

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13
Q

What is Legg-Calve-Perthes disease, aka Perthes?

A

It is an idiopathic avascular necrosis of the femoral head.

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14
Q

Who gets Perthes?

A

males, age 4-10

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15
Q

What will an x-ray look like of a boy with Perthes?

A

The hip may be in one of 3 stages. If both hips are affected (10-15%) of cases, The two hips will ALWAYS be in different stages. If they are in the same stage think something different.

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16
Q

3 stages of disease in Perthes.

A

Avascular necrosis –> Fragmentation/resorption –> re-ossification

17
Q

Goal of treatment in Perthes.

A

They cannot stop the stages from happening. The goal is to maintain a round head and joint during remodeling.

18
Q

What is the treatment for Perthes?

A

no agreed upon treatment - Huge variability. (traction beds, etc have been used in the past.

19
Q

If a child is in this age range at the time of presentation with Perthes,, they may receive intervention (surgery)

A

6-8 years old.

Under 6 do really well, above 8 do very poorly w/ or w/o treatment.

20
Q

If younger than 6 at presentation with Perthes, prognosis is (good/bad)

A

good - nearly all make it to 50 without treatment

21
Q

If older than 8 at presentation with Perthes, prognosis is (good/bad)

A

bad - nearly all get degenerative joint disease before age 40

22
Q

What is SCFE?

A

Slipped Capital Femoral Epiphysis. “Ice cream slipped off the cone” It is a displacement of the proximal femoral metaphysis through the growth plate. Common in obese males nearing the end of skeletal maturity.

23
Q

What is the cause of a SCFE?

A

it is due to an abnormally wide zone of hypertrophy?

24
Q

Which moves in SCFE: the femoral head, or the metaphysis (long bone)

A

the metaphysis moves, while the head stays put.hence the name (Slipped Capital Femoral Epiphysis.) is a misnomer

25
Q

Who is at risk for SCFE?

A

-obese (50% of patients are >95% for weight)

-females 10-14
males 10-16.
more males.
minorities

26
Q

T/F SCFE is related to endocrine changes

A

True. 80% occur during growth spurt.

27
Q

How is SCFE diagnosed?

A

Pt has pain in one leg standing
CAN BE KNEE PAIN(referred)
-limping gait
-lack of hip internal rotation compared to other side
-“obligate” external rotation with hip flexion.

28
Q

Which SCFE patients are good candidates for a prphylactic screw in the non-affected hip?

A

Those who present really young (10 years old) - high risk to get it in the other hip..

29
Q

What is the treatment for SCFE?

A

If mild/moderate, screw to prevent the head from slipping any further. If more than 2/3 slipped, you can do an open reduction, but it’s risky.

30
Q

What is a stable vs. unstable SCFE?

A

stable = patient is able to walk with (or without) crutches

unstable = patient unable to walk even without crutches.

31
Q

T/F SCFE Is a surgical emergency.

A

True

32
Q

T/F SCFE patients should undergo a period of physical therapy before surgery.

A

NO! Do not let the child walk. Weight bearing can worsen the slippage!!

33
Q

Natural history of SCFE

A

avascular necrosis of the femoral head–> degenerative joint changes necessitating joint replacement.