Musculoskeletal System Flashcards

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1
Q

Disorder where a disruption of blood flow to the femoral head leads to necrosis

A

Legg-Calve Perthes

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2
Q

S/S of legg-calve perthes

A

Painless limp, hip/pain stiffness that increases with activity, reduced ROM of hip, can cause affected leg to become shorter

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3
Q

Legg-calve perthes treatment

A
  • non-surgical: activity restriction and limited weight-bearing, NSAIDs, PT
  • surgical: osteotomy — femur is cut, repositioned, and secured in hip socket using plates and screws
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4
Q

Genetic disorder that causes deformity of the foot

A

Clubfoot

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5
Q

S/S of clubfoot

A

Affected foot turned inward sharply, calf muscle on affected leg may be smaller

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6
Q

Gold standard treatment for clubfoot

A

Serial casting followed by bracing (children will need between 5-10 casts, and then once the foot is in the proper position they will need to wear a brace)

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7
Q

Clubfoot family teaching

A

Compliance with bracing to prevent recurrence**, wear brace 24 hr/day for 3 months (after that, children will still need to wear brace at night and during naps for several years)

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8
Q

Asymmetry of the cranium of skull caused by prolonged pressure on one side of the skill that causes it to flatten over time

A

Positional plagiocephaly

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9
Q

Signs of positional plagiocephaly

A

Misshapen skull, bald spot, facial asymmetry

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10
Q

Main risk factor for positional plagiocephaly

A

Putting babies to sleep on back at night (make sure to reposition baby’s head during sleep)

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11
Q

Positional plagiocephaly treatment

A

Helmet therapy for 23 hours/day lasting for about 3 months

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12
Q

Positional plagiocephaly family education

A

Provide tummy time for baby (at least 3x/day for 10-15 min), avoid having baby spend prolonged time in car seat or swing

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13
Q

S/S of scoliosis

A

Asymmetry of child’s shoulder, scapular shape, or hip height, change in posture causing clothes to not lay or fit correctly

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14
Q

Screening for scoliosis

A

Adam’s forward bend test — shows asymmetry of ribs/flanks. Scoliometer measures degree of truncal rotation. Definitive diagnosis through x-ray

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15
Q

Scoliosis treatment

A
  • Non-surgical: Bracing (worn at all times except during showering or swimming); educate family that thin t-shirt or tank top should be worn beneath the brace to protect skin
  • Surgical: spinal fusion — nurse should perform neurologic assessments following surgery, turn patient by LOG-ROLLING to maintain alignment of spine, administer opioid analgesics on a schedule
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16
Q

Dislocation or instability of the hip joint

A

Developmental dysplasia of the hip (DDH)

17
Q

DDH risk factors

A

Females, breech position birth, family hx

18
Q

S/S of DDH

A

Affected leg appears shorter, asymmetric skin folds on the thighs or buttocks, limited ROM of the hip joint, asymmetric gait once the child is walking

19
Q

Screening for DDH

A

Barlow and Ortalani maneuver: provider will apply gentle pressure to infants thighs, move the femoral head in the acetabulum and listen for clicks, clunks, and pops — positive Barlow or ortalani sign indicate DDH. Ultrasound or x-ray confirms diagnosis

20
Q

DDH treatment

A

Pavlik harness — infants under 6 months
Surgery and hip spica cast — infants and children over 6 months

21
Q

Pavlik harness for DDH

A
  • keeps baby’s legs apart and legs turned outward
  • family education: harness should be worn 23 hrs/day and at least 6 weeks, assess skin several times a day, gently massage skin under straps, avoid lotions and powders, baby should wear undershirt and socks under harness, baby’s diaper should be placed under the straps, DO NOT adjust harness yourself (appointments with provider every 1-2 weeks for eval and adjustment of straps)
22
Q

Genetic disorder that causes issues with the synthesis of collagen, which is essential for making bones hard

A

Osteogenesis imperfecta

23
Q

S/S of osteogenesis imperfecta

A

extremely brittle bones resulting in bone deformities and fractures, blue sclera, hearing loss, short stature

24
Q

Osteogenesis imperfecta treatment

A

Supportive: bisphosphonates (Alendronate), bracing and splinting, surgical stabilization, PT, OT, assistive devices (wheelchairs, walkers)

25
Q

Disorder that causes bone loss due to vitamin D deficiency which impairs bone mineralization (bc calcium requires vitamin D for absorption)

A

Rickets

26
Q

Rickets risk factors

A

Insufficient sunlight exposure, insufficient dietary intake of vitamin D, disorders that impair production or absorption of vitamin D (celiac disease, CF)

27
Q

S/S of rickets

A

Bone deformities such as bow legs and knock knees, bone pain, fractures

28
Q

Labs associated with rickets

A

Increased alkaline phosphatase, decreased vitamin D

29
Q

Rickets treatment

A

Vitamin D supplementation, increased exposure to sunlight, increased intake of vitamin D rich foods (fish, eggs)

30
Q

Chronic autoimmune disorder where the child’s immune system attacks the joints causing inflammation and pain

A

Juvenile idiopathic arthritis

31
Q

S/S of juvenile idiopathic arthritis

A

Joint swelling, warmth, stiffness (especially in morning), decreased ROM in the joint
Note: there are several types of JIA. Some may cause rash, lymphadenopathy, enlarged liver and spleen, serositis (includes membranes that line heart and lungs)

32
Q

Labs associated with JIA

A

Elevated ESR and CRP, (+) ANA test

33
Q

Treatment of JIA

A

NSAIDs, corticosteroids, DMARDs (methotrexate), PT, OT, splinting of painful joints

34
Q

JIA family teaching

A

Encourage use of moist heat (warm shower) to relieve join stiffness, firm mattress recommended

35
Q

Neurovascular assessment are particularly important when caring for a patient with a fracture. What assessments are included in a neurovascular assessment?

A

Pain, sensation, skin temp, skin color, cap refill, pulses, movement

36
Q

Family education for hip spica cast

A

Monitor for constipation (d/t decreased mobility and pain meds), increase intake of fiber and fluid