Muskuloskeletal Flashcards

1
Q

Developmental considerations for kids

A
  • reach skeletal maturity (ossification) by 17Y in males, 2Y after menarche in F
  • epiphysis/epiphyseal plate fine unless fracture occurs on plate–may not grow to normal length
  • porous bone–incomplete bone break may occur in kids
  • thicker periosteum
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2
Q

Casts

A

Rigid device that immobilizes the affected body part while allowing other body parts to move
- made of plaster, fiberglass often, polyester-cotton
- used for arm, leg, brace, body

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3
Q

NC for patient in cast

A
  • handle cast with palms if wet
  • turn cast every 2 hours until dry; can take 24-48h if plaster, fiberglass w/i minutes; don’t use heat or dryers
  • don’t give ibuprofen bc can impede bone healing but may need other pain meds incl narcotics and NSAIDs
  • ice over cast can help with itch and dec swelling
  • elevate extremity
  • infx in cast will be warm to touch–can drill a small hole and look
  • watch for skin b/d—edges can get pokey—may need to put moleskin there
  • don’t stick things down to itch besides fingers to test tightness
  • good assessment—5 Ps—pain, pallor, pulse, paralysis, paresthesia
  • exercise non-affected side
  • isometric exercises for affected side—prevent foot drop by keeping foot at 90 degree angle and having them lay on stomach
  • good diet, lots of fluids
  • assess tightness of cast
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4
Q

Potential complications of cast

A
  • keep heel off mattress
  • feel for hot spots, tingling of skin by pt (cast might be too tight)
  • notify MD at once of wound drainage
  • skin b/d—petal edges
  • watch pressure areas esp (elbow, knee, ankle)
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5
Q

NC for cast removal

A
  • loud noise of cutter may be scary
  • cast cutter works by vibration so it won’t cut the child
  • explain procedures, demonstrate on yourself, provide distraction, provide headphones, restrain child as needed, reward child after
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6
Q

Traction

A

Application of a pulling force to the body to provide reduction, alignment, and rest at that site
- includes skin, skeletal, and manual traction
- used to get bones back in place

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7
Q

NC for traction

A
  • maintain correct balance btwn traction pull and counter traction force
  • care of weights–make sure correct ones are not ordered
  • make sure feet are not at end of bed
  • skin inspection
  • pin care
  • assessment of neurovascular status
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8
Q

Assessment for traction

A

Temperature—extremity and infection
Ropes hang freely
Alignment
Circulation check (5 Ps)
Type and location of fracture
Inc fluid intake
Overhead trapeze
No weights on bed or floor

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9
Q

5 Ps of circulatory check

A

Pain, pulse–use cap refill if cast covers pulse, paresthesia, paralysis, pallor

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10
Q

Developmental dysplasia of the Hip (DDH)

A
  • spectrum of disorders related to abnormal development of the hip
  • caused by lag in development or the way the baby lays in utero
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11
Q

Risk factors for DDH

A
  • breech birth
  • big baby
  • female
  • C/S
  • twin
  • swaddled with legs out
  • positive FH
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12
Q

Dysplasia

A

Ball is slightly out of socket; least severe

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13
Q

Dislocated DDH

A

Ball is completely out of the socket at rest

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14
Q

Subluxation DDH

A

In resting position, the ball is not located normally in the socket; rests partway out of socket

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15
Q

CM for DDH (infant and older child)

A
  • Infant—asymmetry of gluteal or thigh fold, limited abduction, affected leg looks longer, Galleazzi sign (short femur), ortolani test (hip click during rotation)
  • Walking child—Positive Trendelenburg sign (when standing on one leg, hip drop occurs in the leg that you are standing on), waddling gait or limp
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16
Q

DDH tx by age

A
  • early identification and tx (before 6M)
  • positioning the hip in flex, abducted positions to deepen the hip socket
  • 0-6M—Pavlik harness (not thick diapering)
  • 6-18M—preop skin traction (3W)—Buck or Russell, closed or open reduction under general anesthesia, hip spica cast (2-4M until hip stable)
  • Older child—surgical reduction—osteotomy of acetabulum
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17
Q

DDH NC

A
  • always put undershirt on child under chest straps and put knee socks under feet and leg straps
  • check skin for redness 2-3x/day
  • gently massage skin under straps daily to increase circulation
  • avoid lotions and powder
  • teach how to hold child with harness on
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18
Q

Congenital clubfoot

A

Talipes equinovarus; true bone deformity and malposition with soft tissue contracture (can’t be manipulated straight unlike many newborns)

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19
Q

Positional clubfoot

A

Occurs from intrauterine crowding and responds to simple stretching and casting

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20
Q

Syndromic clubfoot

A

Assoc with other congenital abnormalities and often resistant to treatment

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21
Q

Congenital clubfoot tx

A

true/idiopathic clubfoot which usually required surgical correction

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22
Q

Therapeutic management of congenital clubfoot

A
  • serial casting–gradual manipulation where a new cast is put on every 1-1.5 weeks for 8-12W and feet are gradually stretched; surgical, outpatient, can leave when pt wakes up and eats
  • Surgery with pins and lasts 2-3M if serial casting doesn’t work
  • child will wear splint or brace to maintain correction
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23
Q

NC for congenital clubfoot tx

A
  • potential for injury r/t cast (N/V impairment)
  • assess 5 Ps; apply ice for swelling and elevate cast
  • risk of altered family process
24
Q

Osteogenesis imperfecta

A

Brittle bone disease; inherited disease of connective tissue (abnormal pre-collagen but normal calcium and phosphorous)
- infants can be born with fractures
- conn tissue and bone defects

25
Q

OI CM

A
  • weak bones
  • bone fragility–break over 100 bones in life
  • poor growth
  • bruising and recurrent epistaxis
  • blue sclerae
  • pre-senile hearing loss (20-30Y)
  • thin skin bc thin collagen
  • excess diaphoresis and teeth discoloration
  • mild hyperpyrexia
  • normal intelligence
  • fewer fractures in adolescence
26
Q

Osteogenesis imperfecta therapeutic management

A
  • lightweight braces & splints to straighten bones
  • simple exercise and/or P.T. (swimming, non-contact)
  • surgery to correct deformity or rod to stabilize bone
  • Pamidronate disodium (IV) – aids bone healing and slows bone
    resorption (calcium regulator); Calcitonin; Biphosphonates
27
Q

OI NC

A

Careful handling to prevent fractures (don’t pull on them, BP cuff can break)
* teaching r/t limitations and activity for optimal G&D
* Family support
* OI Foundation
* OT
* Genetic Counseling

28
Q

Legg-Calve-Perthes Disease and sx

A

self-limiting aseptic necrosis of the femoral head; head loses circulation and becomes necrotic, grows back flat, causing deformity
- limp or pain esp at middle or end of day
- + T sign
- hx trauma
- dec joint ROM

29
Q

LCP tx

A
  • Keep the head of the femur (abduction) contained in the acetabulum to preserve its spherical shape & prevent flattening
  • Initial non-weight-bearing period to dec inflammation and restore motion (deformity occurs early in the disease)
  • Containment devices (head of femur in acetabulum)
  • Weight-bearing and non-weight-bearing devices (e.g., abduction, brace, leg cast, Bucks traction- to stretch tight adductor muscles)
  • Surgical reconstruction and containment
  • ROM - P.T
30
Q

LCP NC

A
  • educate
  • diversional activities
  • encourage return to school
  • pt adhere to tx
31
Q

Scoliosis

A

Complex spinal deformity (lateral, spinal rotation, thoracic kyphosis)

32
Q

Functional scoliosis

A

Occur from something happening to it like uneven leg legnth

33
Q

Structural scoliosis

A

true scoliosis; nothing causing it to be shaped a certain way

34
Q

Scoliosis CM

A
  • nonpainful lateral curve of spine
  • asymmetry of hips and shoulders
  • unequal scapula
  • unequal rib prominences
  • asymmetry of ab skinfolds
35
Q

Scoliosis assessment

A

Bend over and touch toes and see curve of spine; screen during well-child exam

36
Q

Scoliosis tx

A
  • MILD (<20 degree curve): observation, eval q 3-12
    months
  • MODERATE (20-40 degree curve): bracing until cessation of bone growth.
  • SEVERE (> 40 degree curve): surgical spinal fusion with instrumentation (Harrington or Luque rod; Dwyer cable)
37
Q

Milwaukee brace

A

Pushes hips down and apply pressure around neck; rarely used

38
Q

Boston brace

A

Can be camoed under clothes some, can be very hard on self-image

39
Q

Scoliosis NC

A
  • self-image for brace
  • adherence is big problem
  • need to wear for 23h/day
40
Q

Scoliosis NC pre-op

A
  • may be hospitalized for halo traction before surg (makes spine straighter)
  • lots of xrays and lab work
  • teaching on log roll, PCA pump, IS use
  • delayed for acne on back
41
Q

Scoliosis NC post-op

A
  • monitor VS (esp watch for hypoT), wound assess on back, circ, 5 Ps
  • often in hospital 5-7 days after
  • IS q2
  • keep flat for day
  • pain relief (PCA)
  • many post-op complications like spinal/neuro injury, SIADH, atelectasis, pneumothorax, ileus
  • start PT early
  • take ownership of care
42
Q

Juvenile Idiopathic arthritis (formerly juv rheumatoid arthritis)

A

Chronic inflam of synovial fluid

43
Q

Systemic JIA

A

fever, rash, pericarditis/other organs are affected

44
Q

Pauciarticular JIA

A

affects under 5 joints, can lead to blindness (uveitis) so need check ups q6M

45
Q

Polyarticular JIA

A

affects at least 5 joints; spinal and hip involvement (crippling)

46
Q

CM of JIA

A
  • spiking fever
  • skin rash
  • pericarditis
  • morning stiffness–hallmark sign
  • swelling of joint
  • warm joints
  • joint pain
  • malaise
  • anorexia
  • wt loss
  • loss of motion
  • eye probs
47
Q

Management of JIA

A

Goals:
- get inflammation under control and then ROM with heat & exercise (a.m.)
swim, play (need to wiggle; lie prone watching TV)
- prevent deformity – PT & OT; ROM
- relieve symptoms (pain) – NSAIDs (Ibuprofen; Naprosyn)
Severe: methotrexate
Corticosteroids short term; many S/E
Around the clock pain meds work well so pain stays under control

48
Q

Drugs for JIA

A
  • NSAIDs (ibuprofen and Naprosyn)
  • Methotrexate for severe cases
  • Corticosteroids for short-term (many SE)
  • ATC work well
  • Biologic modifier–monthly injection, affect things at the genetic level
49
Q

JIA NC

A
  • pain, impaired mobility
  • warm bath to loosen joints
  • good nutrition to avoid extra wt on joints
  • exercise to relieve stiffness
50
Q

Osteomyelitis

A

Infx of bones caused by staph or hemophilus flu; endogenous or exogenous cause

51
Q

Patho of osteomyelitis

A
  • bacterial infection carried to bone (spreads laterally)
  • abscess formation & local bone destruction dead bone forms sequestrum (necrotic)
  • bone may become honeycombed with sinuses that retain infective material
  • chronic site for exacerbations
52
Q

Most common bones in osteomyelitis

A

femur and tibia

53
Q

Osteomyelitis CM

A
  • child appears very ill
  • abrupt bone pain (tenderness, edema, erythema)
  • unwilling to move limb or bear weight
  • fever
  • irritability
  • malaise – will not feel like participating in age-appropriate activities
  • poor appetite
54
Q

Therapeutic management of osteomyelitis

A
  • IV abx for 3-4W, then orally
  • Penicillin G, methicillin, oxacilllin
  • heat
  • bedrest
  • surgical I&D of abscess (sequestrectomy)
55
Q

Complications of osteomyelitis

A

Pathologic fractures and chronic osteomyelitis

56
Q

NC for osteomyelitis

A
  • supportive (high risk for injury r/t NV
    impairment)
  • pain management
  • maintenance of IV access (PICC line)
  • cast care (sometimes used for immobilization when kids won’t stop walking)
  • nutrition: high calorie drinks & protein for tissue
  • repair and to prevent negative N balance
  • diversional activity: quiet play on bedrest
57
Q

Where should weight be placed on crutches?

A

the hands