Muscular System
Decreased muscle size, strength, and endurance
Muscle atrophy (wasting) occurs due to disuse, leading to a significant loss of muscle mass over time.
Loss of joint mobility can result in contractures, which are permanent tightening of muscles and tendons that restrict the range of motion.
Weak abdominal and back muscles lead to decreased core stability, significantly impacting overall balance and posture.
Nursing considerations
use antiembolism stockings or intermittent compression devices to promote venous return (monitor circulatory and neurovascular status of extremities when such devices are used)
plan play activities to use the uninvolved extremities
place in upright posture when possible
have pt perform ROM, active, passive, and teaching exercises
Maintain correct body alignment
use joint splints as indicated to prevent further deformity
maintain ROM
Maintain body alignment
see nursing considerations for the respiratory system
Skeletal System
Bone demineralization can occur, increasing the risk of fractures due to weakened bone structure.
A negative calcium balance results from immobilization, as insufficient load on bones diminishes calcium retention.
Patients may experience increased risk of osteoporosis, particularly in individuals with prolonged immobilization, as the lack of mechanical stress on bones fails to stimulate bone remodeling.
Nursing consideration
with paralysis, use an upright posture on a tilt table
handle extremities carefully when turning and positioning
Administer calcium-mobilizing drugs (diphosphonates) and normal saline infusions if ordered
ensure adequate intake of fluid; monitor output
acidify urine
Promptly treat urinary tract infections
monitor serum calcium levels
provide electrolyte replacement as indicated
Metabolism
Decreased metabolic rate contributes to weight gain and, if energy intake is not adequately monitored, may lead to obesity over time.
Negative nitrogen balance can occur, indicating that muscle breakdown exceeds muscle synthesis, leading to overall muscle wasting.
Hypercalcemia, a potentially dangerous condition, may develop as bone resorption releases excess calcium into the bloodstream.
Decreased production of stress hormones, such as cortisol, may alter metabolic functions and immune responses.
nursing consideration
Mobilize as soon as possible
have pt perform active and passive resistance exercises and deep-breathing exercises
ensure adequate food intake
provide a high-protein, high-fiber diet
Encourage small, frequent feedings with protein and preferred foods
prevent pressure areas
Implement appropriate interventions to lower physical and psychosocial stresses
Cardiovascular System
Decreased efficiency of orthostatic neurovascular reflexes can lead to orthostatic hypotension, characterized by faintness or dizziness upon standing.
Diminished vasopressor mechanisms increase the risk of inadequate blood pressure regulation.
There is the altered distribution of blood volume, which can lead to reduced perfusion of vital organs.
Increased risk of venous stasis may ultimately lead to thrombus formation, creating a significant risk of deep vein thrombosis (DVT).
Dependent edema, a swelling caused by the accumulation of fluid in tissues, can complicate the management of immobilized patients.
nursing consideration
monitor peripheral pulses and skin temp changes,
use antiembolism stockings or intermittent compression devices to decrease pooling when upright
provide abdominal support
in severe cases, use antigravitational pants
position horizontally
monitor hydration, blood pressure, and urinary output.
elevate extremities without knee flexion
monitor for signs of pulmonary embolism-sudden dyspnea, chest pain, respiratory arrest.
promptly intervene to maintain adequate oxygenation if S/S of pulmonary emboli are noted
Respiratory System
Decreased activity levels reduce the overall need for oxygen, which can lead to complications such as hypoxia if not monitored.
Diminished vital capacity—measured by decreased lung capacity—affects breathing efficiency and can predispose individuals to respiratory infections.
Poor abdominal tone can hinder respiratory function and lead to complications such as atelectasis, where parts of the lung collapse.
Interference with diaphragmatic excursion
Mechanical or biochemical retention of secretions increases the risk of developing pneumonia, bacterial and viral pneumonia, and atelectasis.
hypostatic pneumonia
Loss of respiratory muscle strength (poor cough)
nursing consideration
Supply torso support to promote chest expansion
carry out chest percussion, vibration, drainage (or suctioning) as necessary
use an incentive spirometer
Support the chest wall by splinting with a pillow when pt coughs
administer immunizations as necessary (pneumoccal, meningoccal)
Gastrointestinal System
Distention of the abdomen may occur due to poor abdominal tone, impacting digestion and potentially leading to discomfort.
monitor bowel sounds
Difficulty feeding in a prone position may hinder nutrition intake, leading to further health complications.
encourage small, frequent feedings
Anorexia and constipation become common due to immobility, necessitating dietary modifications to encourage regular bowel movements.
have pt sit upright position in the bedside chair if possible,
carry out bowel training program with hydration, stool softeners, increased fiber intake, mild laxatives if necessary
stimulate appetite with favored foods
Urinary System
Altered gravitational force can cause urinary retention, increasing the risk of urinary tract infections (UTIs).
position as upright as possible to void
Difficulty voiding while supine may lead to an over-distended bladder in immobilized patients.
Catheterize only for severe urinary retention,
stimulate bladder emptying with warm running water as necessary
Impaired ureteral peristalsis can complicate the urinary drainage pathway, resulting in urinary stasis.
Administer antibiotics as indicated
Integumentary System
Decreased circulation and pressure in skin areas due to immobility lead to reduced healing capacity and a heightened risk of skin breakdown and pressure sores, particularly in bony prominences.
turn and reposition at least every 2-4 h
Frequently inspect the total skin surface
eliminate mechanical factors causing pressure, friction, moisture, or irritation
place on a pressure-reduction mattress
Assess the ability to perform self-care and assist with bathing, grooming, and toileting as needed
encourage self-care to potential ability
ensure adequate intake of proteins, vitamins, and minerals
Decreased environmental stimuli can lead to altered perception of self and the environment, affecting mental health.
Increased feelings of frustration, helplessness, and anxiety may arise as natural routines are disrupted.
Risk of developing depression, anger, and aggressive behaviors becomes significant, particularly in children and adolescents.
Possible developmental regression in skills can occur due to loss of mobility and social interaction.
Effects on Family
Disruption in family function is common due to the child's immobilization, leading to emotional strain among family members.
Extended periods of immobilization complicate logistics, necessitating adjustments in daily routines for family management.
Family support systems and home care assistance become essential to provide adequate care and relief for affected children.
Development of coping skills through individual counseling and support groups can aid families in managing stress and emotional needs.
Nursing Care during Immobilization
Implement interventions to minimize complications associated with prolonged immobility:
Use antiembolism stockings or intermittent compression devices to enhance blood circulation and prevent venous stasis.
Position the patient upright to promote better airway clearance and lung function.
Encourage range of motion (ROM) exercises and maintain proper body alignment to prevent musculoskeletal complications.
Monitor intake/output (I&O), recommending a high-protein, high-fiber diet to support nutritional needs and gastrointestinal health.
Regularly change position every 2 hours to prevent the development of pressure ulcers.
Soft Tissue Injuries
Common causes of soft tissue injuries include mishaps during play and sports, highlighting the importance of precautionary measures.
Types of Soft Tissue Injuries:
Contusion:(bruise)
Results from direct impact, causing larger, painful, swollen areas.
Immediate ice application is recommended to reduce swelling.
ecchymosis, black and blue discoloration
Dislocation:
Stress on joint ligaments leads to excessive pain and abnormal joint positioning.
A common injury in young kids is subluxation or partial dislocation( pulled elbow or nursemaid’s elbow)
Treatment is determined by the severity of the injury
Usually, no anesthetic is required
Sprain:
Characterized by a snap, tear, or pop sensation, often accompanied by rapid swelling and bruising.
Guarding the joint
pain joint is too loose
Common sprain sites include ankles and knees
Strain:
Slow injury tendency is typically followed by overloading or excessive exertion on muscles or tendons.
Management includes Rest, Ice, Compression, Elevation (RICE) techniques.
1st 12 to 24 hrs are the most critical period
Soft-tissue injuries should be iced immediately ( ice should never be applied for more than 30 min at a time)
point of injury should be kept several inches above the level of the heart for therapy to be effective
Common injury in children
methods of treatment are different in kids than in adults
Because childhood is a time of rapid bone growth, treatment doesn’t require a long period of immobilization
Rare in infants, warrants investigation
Injuries need to be investigated if they are at various stages of healing.
distal forearm: the most frequently broken bone in childhood
school age: bike-related, sports injuries
transverse
crosswise at right angles to the long axis of the bone
Oblique
slanting but straight between a horizontal and a perpendicular direction
spiral
slanting and circular, twisting around the bone shaft
Growth Plate Injuries
weakest point of long bones: the cartilage growth plate (epiphyseal plate)
These are frequent injury sites in children that can affect future bone growth and development.
Treatment: may include open reduction and internal fixation to prevent growth disturbances
Salter-Harris classification system
Healing Process
Healing occurs at different rates depending on age group:
Neonatal period: 2-3 weeks for rapid recovery.
Early childhood: Approximately 4 weeks as growth factors are significant.
Later childhood: Healing takes about 6-8 weeks due to increased bone density.
Adolescence: Healing averages 8-12 weeks as bone maturation advances.
Diagnosis and Management of Fractures
Tools for diagnosis include radiographs and comprehensive history-taking to evaluate injury extent.
Suspicion of fractures in a young child who refuses to walk or bear weight
Nursing care
assesses the neurovascular status of injured extremities
position the kids in supine position for injuries to the distal arms, pelvis, lower extremities
position the child in a sitting position for injuries to the shoulder or upper arm
provide splinting at the joint above and below the injured area
elevate the affected extremity and apply ice packs
Goals of fracture management involve:
Proper reduction and immobilization to ensure alignment and healing.
Restoration of function through rehabilitation strategies.
Prevention of deformity through monitoring and timely interventions.
Symptoms of Fractures (The Six P’s):
Pain and point tenderness: Sharp localized pain experienced at the fracture site.
Pallor: Skin color changes indicating possible reduced blood flow.
Pulselessness: Observed in severe cases, signifying compromised circulation.
Paresthesia: Unusual sensations in distal areas, potentially indicating nerve involvement.
Paralysis: Loss of movement or control distal to the fracture suggests critical injury.
Pressure: Swelling around the fracture site can suggest local inflammation.
Cast application typically involves Plaster of Paris or synthetic materials, ensuring an appropriate fit for immobilization.
Plaster of Paris casts are heavy, not water-resistant, and can take 10 to 72 hr to dry
Synthetic fiberglass casts are light, water-resistant ,and dry quickly (5 to 20)
Home care management is crucial and includes:
Monitor cast tightness for signs of swelling or decreased blood flow.
Providing skin care assistance to prevent irritation or breakdown during cast wear.
elevate the casted area by using pillows during the 1st 24 to 48 hrs to prevent swelling
turn and position every 2hr so that dry air circulates around and under the cast
notify provider immediately of any soft spots on the cast, changes in sensation or increased pain
Types of Casts
Long leg cast: Provides extensive immobilization for fractures in the leg.
Short leg cast: Used for lower leg and ankle injuries in pediatric patients.
Spica cast: Special cast for hip immobilization, requiring specific handling.
Arm casts: Fractures in the upper extremities require careful assessment and monitoring.
Used primarily for: (the most fractured bone is the femur in children)
Providing physiologic stability to affected regions.
Assisting in the alignment and evaluation of injuries.
Relieving muscle fatigue and immobilizing the site effectively for healing.
position of distal and proximal bone ends
prevent deformity
reduce muscle spasms
skin traction: (Buck, Russell, Bryant traction)
uses a pulling force that is applied by weight.
Nursing actions
Maintain body alignment
provides management for muscle spasms
Routinely monitor skin integrity and document findings
Consult the provider for an overbed trapeze to assist the child to move in bed
Common among young athletes who exceed their body's limits, leading to stress fractures.
at risk for recurrent upper respiratory infections, sleep and mood disturbances, loss of appetite, decreased interest in training nad competition and inability to concentrate.
Stress fractures are a consequence of repetitive, excessive stress on the bone that causes microfractures within the bone
symptoms:
sharp, persistent, progressive pain or deep, persistent dull ache located over the bone
pain on impact (heel strike)
most clinical sign is pain over the involved bony surface
DX: MRI
Treatmnets
rest is the primary therapy, usually interpreted as reduced activity and the use of alternative exercise
physical therapy
cryotherapy, cold whirlpool baths
taping or bracing
Medication
NSAIDS
give 1 hr before the activity
describes a spectrum of disorders related to the abnormal development of the hip that may occur.
formerly called “congenital hip dysplasia” or “congenital dislocation of the hip”
girls are more commonly affected, and a positive family history increases a child’s risk of having DDH
Signs of DDH
Asymmetry of gluteal and thigh folds
Limited hip abduction is seen in flexion
apparent shortening of the femur indicated by the level of knees in flexion (Galeazzi sign)
Ortolani maneuver with clunk elicited
and barlow tests are most reliable from birth to 4 wks of age. with test, the thigh is abducted and light pressure is applied to see if the femoral head can be felt to slip posteriorly out of the acetabulum.
Positive Trendelenburg sign (if child is weight bearing)
Or talipes equinovarus (TEV) is a complex deformity of the ankle and foot that includes forefoot adduction, midfoot supination, hindfoot varus, and ankle equinus.
The foot is pointed downward (plantarflexed) and inward in varying degree of severity.
Talipes Varus: inversion or bending inward
Talipes valgus: eversion or bending out
talipes equinus: plantar flexion with toes lower than the heel (horse feet)
Talipes calcaneus: dorsiflexion with toes higher than the heel.
therapeutic management
3 stages
Correction of the deformity
Start early with serial casting
gentle manipulation and stretching
cast care
rapid growth
Maintenance of the correction until normal muscle balance is regained
followed-up to avert possible recurrence
Ponseti method (serial casting)
series of castings applied during the 1st month of life and continuing until max correction is accomplished (5 to 8 wks)
weekly manipulation of the foot to stretch the muscles, with subsequent placement of a long-leg cast
following casting, a heel cord tenotomy is usually performed, followed by application of long leg cast for 3 wks
after casting is complete, a Denis Browne bar and specialized sandals (abduction brace) are applied to maintain alignment and prevent recurrence
abduction brace is worn at bedtime for 3 to 5 yrs
An inherited connective tissue condition that results in bone fractures and deformity, along with restricted growth.
several types of osteogenesis imperfecta (OI). Type 1 is a mild and common form
assessment
multiple bone fractures (fragile bones and deformities)
blue sclera
early hearing loss
small, discolored teeth
DX: bone biopsy
Pt-centred care
med: bisphosphonate therapy (pamidronate)
increase bone density, prevent fractures
occupational therapy and genetic therapy
screen small children with fractures for this disorder
impaired circulation to the femoral head that results in aseptic necrosis
condition can be unilateral or bilateral, with insidious onset.
stages: synovitis, necrotic, fragmentation, reconstruction
Risk factors
age: 2-12 but more common between 4 to 8 yrs
trauma, decreased circulation, and inflammation to the femoral head
finding
intermittent painless limp, hip stiffness, limited ROM,
hip, thigh, knee pain
shortening of the affected leg
DX: radiograph of the hip and pelvis, MRI
surgery: osteotomy of the hip or femur
goal is to keep the head of the femur in the acetabulum
containment with various appliances and devices
rest, no weight bearing initially
NSAIDs
Home traction in some cases
most common spinal deformity
complex spinal deformity in 3 planes
lateral curvature
spinal rotation, causing rib asymmetry
thoracic hypokyphosis
may be congenital or develop during childhood
multiple potential causes; most cases idiopathic
generally becomes noticeable after preadolescent growth spurt
clothes: may be ‘ill-fitting’
mostly seen in females
expected findings
asymmetry in scapula, ribs, flanks, shoulders, and hips
improperly fitting clothing (one leg shorter than the other)
diagnostic procedures
observe the child, who should be wearing only underwear, from the back
have the child bend over at the waist with arms hanging down and observe for asymmetry of ribs and flank
measure spinal curvature with a scoliometer
Radiography
use the cobb technique to determine the degree of curvature
risser scale to determine the skeletal maturity
MRI and CT
lung capacity: pulmonary function studies, chest x-ray
in addition to primary curve, compensatory curve often present to align head with gluteal cleft
Therapeutic management of spinal curvature
team approach to treatment
bracing (Boston and Wilmington)
wear brace for 23 hrs per day only remove to shower
exercise
surgical intervention for severe curvatures (spinal fusion with rod placement)
Harrington rods
luque rods
Care mangegemnt of spinal curvatures
concerns of body image
the therapy program and the nature of the device must be explained thoroughly to both the child and the parent so they will understand the anticipated results, how the appliance corrects the defect.
preopeartive care
pt is taught how to manage PCA
demonstrate log rolling that will be used after surgery
perform extensive preop teaching
Post op care
complications
breathing difficulties
lowered self-esteem
spinal cord or neurolgic injury
pneumothorax (decreased mobility)
hypotension (blood loss)
atelectasia (decreased mobility)
ileus (decreased mobility)
infection (wound)
SIADH
superior mesenteric artery syndrome: compression of the duodenum by the aorta and superior mesenteric artery that leads to an obstruction
emphasize the importance of physical therapy and proper positioning of the spine
encourage independence following surgery for the adolescent/child
chronic childhood arthritis
firmly known as “ juvenile rheumatoid arthritis”
also called “idiopathic arthritis of childhood”
possible causes
immunogenic trigger
environmental trigger
peak onset: 1 to 3 years of age
often undiagnosed
actually a heterogeneous group of disease
systemic onset (high fever, rash, hepatosplenomegaly, pericarditis, pleuritis, lymphadenopathy)
One to several joints effected
oligoarthritic (involves <4 joints)
polyarthritic (involves >5 joints)
psoriatic
affected kids: 90% have negative rheumatic factors
symptoms: may “burn ot” and become inactive
chronic inflammation of synovium with joint effusion, destruction of cartilage and ankylosis of joints as disease progresses
severe cases have uveitis
diagnostic evaluation of JIA
no definitive diagnostic tests
elevated ESR/CRP in some cases
antinuclear antibodies common, but not specific for JIA
leukocytosis during excerbations
diagnosis based on criteria of American college of rheumatology
Therapeutic management
no specific cure
goal of therapy:
control pain
preserve ROM and function
prevent deformities
promote normal growth and development
primarily outpatient care
exercising in pool
nighttime splinting
physical therapy, occupational therapy
Medication
NSAIDs (naproxen, ibuprofen, meloxicam, celecoxib)
DMARDs ( methotrexate and sulfasalazine)
biologic disease-modifying anti-rheumatic drugs
used with those who have poor prognosis and failed treatment with methotrexate
may cause malignancies
hold if febrile
Glucocoriticoids
life threathinign cases
short and taprer off
side effects
risk for infection, adrenal insufficiency, cushinggoid features, weight gain, mood or sleep changes, hypertension, diabetes and osteoporosis and avascular necrosis
Osteosarcoma and Ewing's sarcoma are among the most common types diagnosed in childhood,
they occur more commonly in boys; incidence is highest during accelerated growth rate of adolescence
peaks at 15 yrs of age
Diagnostic evaluation of bone tumors
rule out trauma or infection 1st
definitive diagnosis is findings on radiologic studies (computed tomography scans, bone scans) bone biopsy
MRI helps evaluate neurovascular and soft tissue extension
lab tests: alkaline phosphatase levels are elevated with some bone tumors
most frequent malignant bone tumor type in kids
peak: in the 2nd decade of life
most primary tumor sites: in diametaphyseal region of long bones
most cases: in distal femurs
other sites: humerus, tibia, pelvis, jaw
Therapeutic management
traditional approach; radical surgical resection or amputation of affected area
limb-salvage procedures: resection of bone with prosthetic replacement of affected area
chemotherapy accompanying surgical treatment
care management
preoop preparation (crucial)
support during adjustment to concept of amputation, surgical resection
body image concerns: issues of adolescents
pain managemnet
phantom limb pain characterized by sensations such as tingling, itching and more frequently, pain felt in the amputated limb.
pain and sensation is real and should be treated
primitive neuroectodermal turmor
second most common malignant bone tumor in kids and adolescents, rare after age 30 yrs
arise in marrow especially in
femur, tibia, ulna, humerus
vertebrae, pelvis, scapula, ribs, skull
therapeutic management
radiation: most common 1st approach
chemotherapy: adjunct to radiation
surgical resection in some cases: usually able to preserve affected limb
prognosis best if no metastasis at time of diagnosis; distal lesions have best potential for cure
care management
assisting family in dealing with diagnosis of malignancy
managing complications of radiation and chemotherapy
nutritional concerns throughout treatment regimen
protect radiation site from sunlight