Pediatric Musculoskeletal Disorders NUR 2310 Flashcards

1
Q

Unilateral or bilateral (41%)
Affected foot points downward, toes turn inward, and bottom of foot twisted inward
May affect bones and ankle joints, as well as tendon and ligaments.

A

Clubfoot, a congenital disorder. (3:1) in males Cause is unknown
Increased incidence if 1st degree relative had clubfoot
Seen with other anomalies like cerebral palsy

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2
Q

the parents of a new born son with clubfoot asks about how they can get their son to live a normal life without surgery. what does the nurse say

A

Treatment includes serial casting, Denis-Browne Bar or braces and in extreme cases surgical intervention may be required

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3
Q

clubfoot diagnose

A

Diagnosis
Visual inspection
X-ray and MRI

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4
Q

the nurse hears the infant crying. the nurse assesses the cast feet and notice capillary refill is 1, and cooler than usual, what should the nurse do

A

the child’s foot circulation is being cut off therefore increASING THE RISK FOR AMPUTATION. call doctor. Remember the 5 P’s for cast care[pain, paralysis, paresthesia, pallor,]

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5
Q

upon new born examination the nurse notice the female infant has Unequal gluteal folds when prone what disorder does the nurse speculate

A

Developmental Dysplasia of The Hip-
Shortened limb on affected side
Restricted abduction of hip on affected side
Unequal gluteal folds when infant prone
Positive Ortolani test
Positive Barlow test

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6
Q

If Developmental Dysplasia of The Hip
(DDH) goes uncorrected, what manifestations will develop

A

Affected leg shorter than the other
Telescoping or piston mobility of joint
Marked lordosis if bilateral dislocations
Waddling gait if bilateral dislocations

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7
Q

the parent ask if there is a way to treat their child nonsurgical, what will the nurse say

A

The Pavlik harness (shown on the slide) is a commonly used abduction device that allows for the head of the femur to sit in the acetabulum. It should be worn 24 hours a day for 3-4 months. For children greater than 6 months skin traction or surgery may be required if the abduction device doesn’t work. A significant risk factor for both surgical and non-surgical treatments for DDH is avascular necrosis of the femoral head.

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8
Q

is a Pavlik harness a good recommendation for a toddler of 2 yrs

A

spica casting is a better option since 2 yr old are constantly moving but excess movement is contraindicated for DDH

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9
Q

this is is a group of progressive, degenerative, inherited diseases causing wasting of the muscles.

A

Muscular Dystrophy; The absence of dystrophin results in degeneration of skeletal or voluntary muscles that control movement. Fat & connective tissue replace degenerated muscle.

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10
Q

Nursing Management and Family Teaching
DDH

A

Assessment of child
Child will learn maximum mobility in harness, cast, or brace
Skin evaluation for pressure points/ulcers
Cast care for family
Harness application or when to return to Dr. for adjustment

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11
Q

during a health check-up the nurse notice the 4 yr old has a waddling gait, lordosis, and have very big calf muscles for his age. what condition the nurse suspects the child to have

A

Muscular Dystrophy (MD)
Clinical Manifestations
Onset between ages 2 & 4 years
Progressive muscle weakness, wasting, and contractures
Waddling gait, frequent falls
Lordosis

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12
Q

the doctor orders a diagnostic test, what test is most likely to be ordered

A

muscle biopsy will reveal that fatty and connective tissue has replaced normal muscle tissue.
electromyogram (EMG)
nerve conduction velocity (NCV) , blood enzyme test
Serum creatine kinase (CK)

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13
Q

the mother ask how her son has Muscular Dystrophy (MD)
when her other two daughters are fine. she said she was very healthy when carrying her son. what is the nurse’s respones

A

this disease is X-linked recessive disease, meaning that she has/ carries this gene and her son got it. it only affects boys

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14
Q

the mother feels guilty about his MD and ask is there any treatment for him. what does the nurse say

A

ROM, Bracing, Performance of ADLs, Surgical release of contractures (as needed), Physical therapy and Occupational therapy can slow down the progression but this is a lifelong disease

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15
Q

MD things to know

A

There is no cure for muscular dystrophy. As the nurse it is important to ensure that supportive care is provided and complications are prevented. The primary goal is to maintain function in the unaffected muscles as long as possible and keep the child as active as possible. Survival may be prolonged through the use of cough augmentation, non-invasive ventilator support and steroid use.

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16
Q

the child is likely to die from cardiac or respiratory complications, why is this the case

A

the heart muscle and the diaphragm and intercostal muscles will all be affected because of the missing protein dystrophin

17
Q

cerebral palsy signs and symptoms

A

motor impairments including abnormal motor patterns including spasticity, muscle weakness, and ataxia; abnormal brain function is not progressive

18
Q

Medical Management of cerebral palsy

A

Medications to reduce spasticity include baclofen, dantrolene sodium, and diazepam
Medications to decrease abnormal movements and control drooling include scopolamine

19
Q

during a school health check, the nurse noticed the 13 yr old girl has a lateral curve of 26 deg. of the spine, what does she document

A

the child has scoliosis and needs a follow up with her guardian to discus treatment with a brace

20
Q

Scoliosis Pathophysiology

A

Lateral curvature of spine
Spinal rotation causing rib asymmetry
Thoracic hypokyphosis resulting in respiratory problems

21
Q

Scoliosis Pathophysiology plus more

A

A lateral curvature between 25-40 degrees requires the child to wear a brace. A lateral curvature greater than 40 degrees requires surgical intervention. As the spine and ribs rotate towards the convex portion of the lateral curve, the muscles and ligaments in the convex side become thin and atrophied, while the muscles and ligaments on the concave side become contracted and thickened. The thoracic cavity becomes asymmetrical resulting in respiratory difficulties.

22
Q

Scoliosis
Diagnosis

A

Screenings by pediatrician
Standing radiographs to determine degree of curvature
Asymmetry of shoulder height, scapular or flank shape, or hip height
Often have primary curve and compensatory curve to align head with gluteal cleft

23
Q

treatment of scoliosis

A

Treatment for scoliosis is required when the curvature of spine is greater than 10-11 degrees and varies depending on the severity of the curvature. Monitoring is the preferred treatment option if the curve does not progress and remains below 40 degrees. Bracing is used to prevent further progression of moderate curve. There are three types of braces used: the Boston, Milwaukee and Charleston bending brace. Surgical intervention is required for children with curves greater than 40 degrees and includes autogenous spinal fusion and the placement of rods that provide support for the spinal column. Harrington rods support the spinal fusion using hooks but causes “flat-back syndrome”. The Cortel-Dubousset rod corrects the curve and rotation of the spinal column. Complications from back surgery include: nerve damage, spinal cord damage and lung problems.