MS 1 Flashcards

1
Q

when do the sutures of the cranium close fully

A

Sutures of the cranium do not fuse completely until age 18 months

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2
Q

how long does growth at the epiphyseal plate occur

A

Growth occurs at the epiphyseal plate until adult height is reached (stimulated by pituitary GH)

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3
Q

what is important to know about the bones and muscles of children compared to adults

A
  • Bones are more pliable & porous in children resulting in bend or buckle (esp infants)
  • Soft tissues are more resilient & bone healing is more rapid in children than in adults
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4
Q

when should you investigate for child abuse

A

if infant/young child has a broken bone, possibly investigate for child abuse (should not be very easy to break) have bendy bones

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5
Q

why do children recover from bone injuries quickly

A

d/t very vascular bones and children tend to have a lot of calcium in their diet

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6
Q

what diagnostic tests can be used for evaluating MS

A
X-ray
Ultrasound
Arthrography (local anesthesia)
Bone scan (sedation)
CT (sedation)
MRI (sedation)
Arthroscopy (local or general anesthesia)
Joint aspiration (local anesthesia)
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7
Q

what is imperative to assess for in MS physical exam

A

Five P’s of vascular impairment

1) Pain & joint tenderness
2) Pallor
3) Pulselessness distal to the fracture site
4) Paresthesia distal to the fracture site
5) Paralysis

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8
Q

why are we so concerned about the pt having one of the 5 Ps

A

Very concerned about 5 Ps because can lead to possible paralysis, permanent injury to the nerves, and compartment syndrome

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9
Q

what is the purpose of casting

A

to immobilize the fracture site & involve joints above & below the fracture

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10
Q

what are the types of casting

A

Plaster of paris (drying takes 24-48 hours)

Synthetic

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11
Q

cast care

A
  • A wet cast should be handled by the palms of the hands to prevent indenting the cast & creating pressure areas
  • No hot spots should be felt; nothing inside cast
  • Check for swelling in first 6-8 hours; Elevate; protect from water & urine
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12
Q

why do you not IMMEDIATELY put a cast on after injury

A
  • d/t initial swelling and tissue damage (have swelling under control BEFORE cast is put on)
  • still have risk once cast is on, that some swelling may occur (educate to ensure elevated extremity above heart for 72 hrs after casted)
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13
Q

10 yr old complaining about toes or fingers feel odd (tingly, feels like they are asleep) what should mom do?

A
  • mom goes ahead and calls provider, talks to nurse who triages with mom and tells her to ELEVATE it and get swelling decreased)
  • eventually will need to come in and see provider to prevent compartment syndrome
  • IF has one of the 5 Ps??, (cannot extend fingers ex) is an EMERGENCY d/t potential for nerve damage
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14
Q

which type of cast is used more often now

A

synthetic

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15
Q

describe clubfoot

A
  • A common deformity in which the foot is twisted out of its normal shape or position
  • Unilateral clubfoot is more common than bilateral
  • May occur as an isolated defect or more be in association with other disorders or syndromes
  • Cause is unknown(familial, more common in boys)
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16
Q

an inversion or bending inward

A

Talipes varus (clubfoot)

17
Q

an eversion or bending outward

A

Talipes Valgus (clubfoot)

18
Q

*most common – plantar flexion in which the toes are lower than the heel

A

Talipes equinus (clubfoot)

19
Q

dorsiflexion, in which the toes are higher than the heel

A

Talipes calcaneus (clubfoot)

20
Q

treatment of clubfoot

A
  • Correction of the deformity (if not, may affect gait eventually)
  • Maintenance of the correction until normal muscle balance is regained
  • Follow-up observation to avert possible recurrence of the deformity
  • Casting is begun immediately after birth
  • Surgery is usually performed between ages 4 months to 1 year
21
Q

with surgery or casting what is always a potential risk

A

-With surgery or casting always risk you will impact extremity involved: may end up with one leg that is shorter or muscle that is smaller

22
Q

describe Developmental Dysplasia of the Hip (DDH)

A
  • Occurs in 1 – 3% of newborns
  • Left hip affected more often than right hip
  • Increased incidence with breech presentation and among siblings of affected children
  • More commonly seen in females – four times as often as boys
23
Q

three degrees of DDH

A

Acetabular dysplasia
Dislocation
Subluxation

24
Q

mildest form, no subluxation or dislocation

A

Acetabular dysplasia

25
Q

incomplete dislocation of the hip

A

subluxation

26
Q

femoral head loses contact with the acetabulum, hip rests in a dislocated position

A

dislocation

27
Q

DDH assessment

A
  • Diagnosis should be made during the neonatal period, treatment initiated before 2 months of age is most successful
  • Hip examination needs to be included as part of the health examination until the child begins to walk (until 24 mos)
28
Q

DDH clinical manifestations of infants

A

Shortening of the limb on the affected side
Unequal gluteal folds (prone position)
Restricted abduction of hip on affected side
Positive Ortolani test
Positive Barlow test

29
Q

DDH clinical manifestations of toddlers/older children

A

Waddling gait
Marked lordosis when standing
Affected leg shorter than other leg
Presence of Trendelenburg sign

30
Q

diagnostics of DDH

A
  • *Ultrasound is the BEST way to determine DDH, identify before 3 months as it is easier to identify earlier and implement measures ASAP
  • As a provider*** do it before 3 months ultrasound, can pick it up better when younger (according to dr. Comeaux)
  • Radiographic examination – infants older than 4 months