MUSCULOSKELETAL Flashcards

1
Q

What difference in childrens bones makes them stronger than adults?

A

Periosteum

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2
Q

Ligament characterisitcs

A

links bones
provide stability
lack elasticity & blood supply

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3
Q

tendon characteristics

A

muscles to bones
little blood supply –> long healing time

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4
Q

Main Cast complication?

A

Compartment syndrome

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5
Q

what is compartment syndrome?

A

Pressure in fascial compartment causing inflammation –> decreases blood flow leading to ischemia & necrosis

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6
Q

5 P’s of compartment syndrome?

A

Pain unrelieved by narcotics
Pallor
Pulselessness
Paraesthesia (numbness/tingling)
Poikilothermia: Cold

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7
Q

what should you assess in neurovas assessment for compartment synd?

A

Pain
Sensation
Temperature (cool = poor circulation)
cap refill
color
pulse (distal)

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8
Q

for a spica hip cast what are key interventions?

A

Turn every 2 hours
protect proximal edges of leg cast from soiling (bivalving cast)

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9
Q

what is a bivalve procedure?

A

Cut down one or both sides to relieve pressure

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10
Q

what position helps a child in Spica cast feed independently?

A

Prone on floor

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11
Q

what is a complication of being in spica cast?

A

cast synd: Duodenum is compressed
- causes V, abdominal distention & bowel obstruction

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12
Q

prevention of cast syndrome?

A
  • Frequent repositioning
  • Fluids&increased fiber in childs diet
  • “belly hole” to allow expansion
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13
Q

in skin traction, how must the patient be positioned?

A

Parallel to weight/traction

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14
Q

what are appropriate interventions for a child in a long leg cast after an open reduction?

A
  • Handle cast carefully when wet to prevent dents
  • Elevate leg & apply ice for short periods
  • Ensure proximal edge of cast stays clean
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15
Q

What is the appropriate timing for ice?

A

first 48 hours for 15 min

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16
Q

after a scoliosis spinal fusion, how must the patient be turned?

A

by logrolling

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17
Q

besides logrolling what are other appropriate interventions for a spinal fusion?

A
  • Incentive spirometer Qhr
  • Monitor chest tube for leak/drainage
  • Assess neuro status & V/S Qhr
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18
Q

Osgood-Schlatter disease is characterized by what?

A

Pain below knee cap
Worse by activity & better with rest

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19
Q

what is the priority nursing diagnosis for a patient with a brace treating scoliosis?

A

no redness/breakdown under brace

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20
Q

what lab values would be low with Rickets?

A

Calcium (under 8.5) & phosphorus (under 3)

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21
Q

do children’s bones heal quicker than adults? & why?

A

Yes
& bc bones are still growing

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22
Q

how would you describe a spiral fracture?

A

diagonal line that coils around the bone

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23
Q

In legg-calve-perthes diesease, what would a priority be for someone on bed rest?

A

Ensuring full ROM in all joints
(to prevent immobility complications)

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24
Q

what type of trait is Duchenne’s? & what does that mean about the disease?

A

Sex linked recessive
Its highly likely to only effect males

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25
Q

what s/sx would occur in Rickets?

A
  • Bone pain (Arms, legs, pelvis or spine)
  • Short stature
  • Bone deformities
  • Dental problems
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26
Q

what conditions can Bryant’s traction (skin tract) be used for & what are the limitation/position put in?

A
  • Developmental dysplasia (hip) or femur fractures
  • Must weight less than 26.4 lbs
  • Laying supine with thighs flexed & hips slighly off bed
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27
Q

what is skin traction?

A

Pulling force applied to material directly attached to limb
Only used for short perids

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28
Q

important parent teaching for bryant’s traction?

A

Diapering needs to be modified
- Small diaper placed in perineal area w/ all edges of cast outside of diaper

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29
Q

when should you do neuromuscular assessments for affected limbs (skin traction)?

A
  • Q4hr
    • check for numbness in finger/toes = poss compartment synd
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30
Q

what should you assess Q2-4 hr for skin traction?

A
  • circulation
  • sensation
  • pain
  • pallor/cyanosis
  • pulse (distal)
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31
Q

how often should skin traction be removed/reapplied?

A

Q4 hr
Remove body oils with rubbing alcohol

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32
Q

when is skeletal traction used?

A
  • Rarely, for when traction weight >5lb+
  • Long periods of time until bone is ready for open reduction.
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33
Q

can the weights be removed in skeletal traction?

A

No
- pin is placed distally to the fracture

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34
Q

Pin care uses what?

A

Cleaning would with normal saline gauze
(abx if ordered)

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35
Q

for skeletal traction how often are neurovascular status checks preformed?

A

Q1-2 hr for first 48 hour –> Q4hr

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36
Q

how often should pin sites be assessed & specifically for what?

A
  • Q8hr
  • Osteomyelitis
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37
Q

what is recommended pain management with skeletal traction?

A
  • Epidural w/ bupivacaine (Marcaine) + narcotic morphine sulfate
  • Hydromorphone
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38
Q

what is plagiocephalyl?

A
  • Cranial sutures overriding & can impede brain growth
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39
Q

normal ages for fontanelles to close?

A

3 months = posterior
12/18 months = posterior

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40
Q

s/sx of PLAGIOCEPHALY

A
  • full/bulging fontanelle
  • bony ridges along sutures
  • bulging brows/uneven cheekbones/eye sockets
  • prominent blood vessels in scalp
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41
Q

treatment for PLAGIOCEPHALY

A
  • corrective helmet
  • molded helmet if not improved w/in 4 months
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42
Q

how long do you wear a corrective helmet?

A

23hr/day for 3-6 months

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43
Q

what position should be encouraged when a child is wearing a helmet?

A

Tummy time (varying head position is important)

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44
Q

what is CRANIOSYNOSTOSIS? & what can is cause?

A
  • premature fusion of 1 or more cranial sutures
  • incomplete brain development –> seizures, mental delay, visual/breathing problems
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45
Q

what are s/sx of CRANIOSYNOSTOSIS?

A
  • Sleepiness (or less alert than usual)
  • Increased irritability
  • High pitched cry
  • Changes in head circumference
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46
Q

treatment options for CRANIOSYNOSTOSIS?

A
  • head shape normal = molded helmet
  • surgery is primary treatment (craniotomy)
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47
Q

what is torticollis?

A

“twisted neck” lateral flexion of cervical spine
- fibrosis of sternocleidomastoid muscle

48
Q

what can be hindered with torticollis?

A
  • Developmental milestone bc of unable to turn head (can’t see/hear/touch)
49
Q

classic s/sx of toricollis?

A
  • Twisted neck
  • Spasmodic torticollis
50
Q

nursing care for torticollis?

A
  • PT w/ botox to inhibit muscle spasms
  • tummy time to strengthen muscles
51
Q

what is clubfoot?

A

-Hindfoot & forefoot rotated inwards w/ arched midfoot (when pointed down)

52
Q

what can cause clubfoot?

A
  • maternal obesity/smoking
  • amniocentesis before 20 weeks
  • position of fetus in utero
53
Q

what are the 4 types of clubfoot?

A
  • Postural: Resolves with stretching & casting
  • Idiopathic: True congenital w/ varied severity
  • Neurogenic: Usually r/t spina bifida
  • Syndromic: Associated with rigid feet & other anomalies
54
Q

S/Sx fo clubfoot?

A
  • Plantar flexed foot
  • Inverted heel
  • Adducted forefoot
  • CAN’T be manipulated into a neutral position
55
Q

when/how is clubfoot diagnosed?

A
  • @ birth w/ physical exam
  • 20 week ultrasound
56
Q

what is the treatment for clubfoot?

A
  • Serial casting
  • Brown cast
  • Tenotomy
57
Q

edu about serial casting?

A

Q 1-2 weeks recasting moving into a more neutral position

58
Q

what is Brown’s split? education about it?

A
  • Splint molded around heel while forefoot is abducted & knee flexed @ 90.
  • Changed weekly & worn 23 hours/day till 3 y
59
Q

what is a tenotomy?

A

Cutting & repositioning tendon (achilles for length)

60
Q

what is metatarsus adductus (varus)?

A

Front part of foot (toes area) point inward (medial)
“pigeon toes”

61
Q

s/sx of metatarsus adductus?

A
  • High arch
  • Separated big toe
  • Bean shaped foot (forefoot turned inward)
62
Q

best treatment for metatarsus adductus?

A
  • wearing shoes on opposite foot
63
Q

what is legg calve perthes?

A

Hip disorder where femur head temp loses blood supply

64
Q

who is most commonly affected by LCP?

A

3-12yr
- Caucasians & Asians

65
Q

s/sx of legg-clave-perthes (LCP)?

A
  • Hip/knee soreness or stiff
  • Limping (especially after activity or late in day)
  • Quad muscle atrophy
66
Q

how would you diagnose LCP?

A

radiograph then MRI shows osteonecrosis

66
Q

what is the goal when caring for LCP?

A

keep femoral head in acetabulum

66
Q

best way to achieve treatment goal of LCP?

A

bedrest to reduce inflammation & restore joint ROM

67
Q

discharge info for LCP?

A

Avoid weight bearing activities

68
Q

what is polydactyly & syndactyly?

A

P: One/both hands 6+ finger/toes
S: 2+ phalanges of fingers/toes are fused together

69
Q

which is more complicated syndactyly or polydactyly?

A

Syn
- Separate nerves, tendons/ligaments and blood vessels.

70
Q

surgical care for syndactyly?

A

osteotomy & place a distractor
- pin placed in bones and 1/4 turn of allen wrench 2x week

71
Q

s/sx of sprain?

A
  • Pain
  • Swelling
  • Bruising
  • INSTABILITY
  • LOSS of joint mvmt
72
Q

s/sx of strain?

A
  • limited motion
  • muscle spasms
  • swelling
73
Q

What does RICE stand for?

A

R: Rest
I: ice - first 48 hr, 15 min intervals
C: compression, ACE wrap
E: Elevation

74
Q

how do you wrap a strain/sprain?

A

wrap area distally & work up to proximal area beyond injury

75
Q

consequences if there’s break on epiphyseal plate?

A

limb length differences, limb deformity and joint incongruity

76
Q

where does osteomylitis most often occur?

A

long bones in lower extremities

77
Q

what is the most common cause of osteomylitis?

A

Staphylococcus aureas

78
Q

s/sx of osteomylitis

A

pain in affected bone
- fever
- guarding of limb
- localized tenderness, redness/ warmth

79
Q

care for osteomylitis?

A
  • Broad spectrum antibiotics (after blood culture)
    eval 2 days after inital dose
80
Q

surgical care for osteomylitis?

A

K wire: Steel rod placed thru long bone w/ antibiotics implanted into bone cement

81
Q

what labs would you monitor for osteomylitis?

A

ESR (tell if infection is resolving)

82
Q

what is juvenile arthritis?

A

Autoimmune inflammatory response

83
Q

when is the peak onset and gender for juvenile arthritis

A

1-3 y & 8-12y
- females 2x likely as males

84
Q

juvenile arthritis causes what in children?

A

Leading cause of blindness & disability in children

85
Q

s/sx of juvenile arthritis?

A
  • Swollen, tender joint
  • limited ROM
  • Afternoon fever up to 105
  • Morning stiffness
86
Q

labs to monitor for juvenile arthritis?

87
Q

meds for juvenile arthritis?

A
  • NSAIDS: Ibuprofen, Naproxen
  • Methotrexate
  • Prednisone (steroid)
88
Q

what type of exercises are best for juvenile arthritis?

A

isometric exercises (planks, wall sits)

89
Q

what is scoliosis?

A

nonpainful lateral curve of spine (>/=110)

90
Q

what does S & C curve scoliosis look like?

A

S: Curve in 2 opposite directions
C: Curve laterally in one direction

91
Q

3 types of scoliosis

A
  • Nonstructural: Spine corrects itself
  • Structural: Curve can’t correct self
  • Congenital: Abnormal fetal development
92
Q

s/sx of scoliosis?

A
  • unequal shoulder heights (measure from floor to acromioclavicular joint)
  • Scapula/rib prominences
  • Cafe au lait spots
93
Q

what is Cobb’s angle?

A

Measurement of curvature of spine in degrees

94
Q

degrees of cobbs angle for scoliosis?

A

10-15: Mild, assess @ regular check up
15-40: Moderate, use back brace (23hr/day) & possible surgical correction

95
Q

spinal surgery pain management

A

PCA pain pumps or epidural
then 3 days post op –> PO

96
Q

how many days post op can the patient start ambulating

97
Q

how should a patient be positioned in bed with spinal fusion?

A
  • HOB no more than 30 degrees
    (may make eating difficult)
98
Q

discharge education for spinal fusion?

A

No twisting/bending or lifting heavy objects & no contact sports for 2 years

99
Q

first line of treatment for hip dysplasia?

A

pavlic harness
(don’t ever readjust)
(hip aduction - no leg extension)
(no baby poweder)

100
Q

when treating SCFE, when can full weight bearing be resumed?

A

1 week post op

101
Q

what is NOT true regarding SCFE?

A
  • affected limb may be longer than unaffected
  • ROM exercises should be done Q8hr
102
Q

what groups have the higher incidence of SCFE?

A
  • Male obese children
103
Q

S/SX of SCFE?

A
  • Pain in groin reffered to thigh,knee
  • Pain with internal rotation of hip
  • Limited abduction
  • Shorter effected leg
104
Q

what advice does the nurse give if a child is overly fussy after tylenol & toes seem cool?

105
Q

if a patient has a scoliosis curve of 35, what is the most likely next step?

106
Q

priority action after surgery/casting?

A
  • neurovascular check Qhr
107
Q

for a child in a spica cast, what is a modification made for the child?

A
  • Using a wagon instead of a stroller
108
Q

s/sx of hip dysplasia?

A

limited abduction of affected hip.

unequal gluteal folds

unequal leg lengths when bent (galeazzi)

postive tendelenburg (older)

109
Q

which position(s) is more likely to cause a baby to have hip dysplasia?

A

Breech

Intrauterine

110
Q

what movement does the Pavlik harness allow & what does it not?

A

Allow: Hip flexion/ aBduction

No: Hip extension/aDduction

111
Q

if a child presents with unequal gluteal folds, what would be a priority question to ask the parents?

A

has your child been limping? (LCP)

112
Q

if a child is given a neuromuscular block, what intervention would be a priority?

A

Providing ventilator care to prevent pneumonia

113
Q

what diagnostic testing would be ran for a child with a family hx of muscular dystrophy?

A

Muscle biopsy
Creatinine Kinase
Electromyelogram