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
incomplete dislocation of the hip
subluxation
26
femoral head loses contact with the acetabulum, hip rests in a dislocated position
dislocation
27
DDH assessment
- 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
DDH clinical manifestations of infants
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
DDH clinical manifestations of toddlers/older children
Waddling gait Marked lordosis when standing Affected leg shorter than other leg Presence of Trendelenburg sign
30
diagnostics of DDH
* *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