Common Orthopedic Problems of Children Congenital Acquired Bones Neuromuscular 1.

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Common Orthopedic Problems of Children • Congenital • Acquired • Bones Neuromuscular 1

Transcript of Common Orthopedic Problems of Children Congenital Acquired Bones Neuromuscular 1.

Page 1: Common Orthopedic Problems of Children Congenital Acquired Bones Neuromuscular 1.

Common Orthopedic Problems of Children

• Congenital• Acquired• Bones

• Neuromuscular

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General Nursing Considerationsany musculoskeletal condition

• Prevent neurovascular injury

• Prevent/monitor for infection

• Prevent injury r/t falls, etc

• Comfort

Manage nutrition Anxiety Knowledge deficit

(child & parent) re: disease process and treatment

Manage effects of immobilization

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Effects of Immobilization

PHYSICAL effects on muscular system– Significant loss of muscle strength,

endurance, and muscle mass–Bone demineralization– Loss of joint mobility; contractures

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Physical effects on other systems

• Pulmonary • Cardiac• Skin integrity• Elimination – GI– GU

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Effects of Immobilization

EMOTIONAL• Removes outlet for expressing anxiety• Decreases environmental stimuli– Risk for delayed development

• Provide appropriate diversional activities

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Anatomy

• Ossification • Diaphysis• Epiphysis • Epiphyseal

plate• Periosteum

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Bone characteristics in children

• Long bones porous• Thicker periosteum: more rapid

healing• Remodeling

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Pediatric Fractures

• r/t trauma or bone disease– w/trauma, always look for other injuries.

• Complications:– Emboli–Hemorrhage– Fat emboli– Infection

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Fractures: Infants

• Rare• Birth trauma• Child abuse• Osteogenesis imperfecta

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Fractures:

younger children

• Clavicle• Forearm • Hip fractures rare–MVI

School Age

• Bike – auto• Skateboard• Scooter• Sports

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Pediatric Fractures

• “simple” fx: no break in skin• Children’s bones are more flexible – can bend

or buckle.• Greenstick: break occurs through the

periosteum on one side of the bone while only bowing or buckling on the other side. Seen most frequently in forearm.

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Fig. 50-UF04a, p. 1410

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Physeal Growth Plate Fracture:Salter-Harris Classification

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Common Treatments

• Immobilization–Cast– Traction–Bedrest–Brace

• Surgery

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Care of child in a cast

• CMS• No small toys • No baby powder• Developmental teaching, play

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The Five P's of Vascular Impairment

• Pain• Pallor• Pulselessness• Paresthesia• Paralysis

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Compartment Syndrome

• Muscles & nerves enclosed in a compartment of inelastic fascia.

• swelling compromises circulation.• Result: necrosis of tissue• Sx: worsening pain – rest of 5 P’s• Tx: bivalve the cast; fasciotomy • Prevention • Early Detection: CMS checks• A Medical Emergency !!!

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Traction:

Purpose • Fatigue the involved

muscle (reduce spasm)

• Realign bone pieces• Immobilize fracture

site until casting can be done

Guidelines for care• Understand therapy• Maintain traction• Maintain alignment• Proper care: skin,

skeletal• Prevent complications

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Developmental Dysplasia of Hip

• Definition: the head of the femur is improperly seated in the acetabulum of the pelvis.

• Congenital or developmental• Varying in degree

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Treatment Goals

• Prevent:–Weakness of hip muscles– Stiffness, ROM–Arthritis

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DDH

• Routine infant screening–Asymmetry of gluteal skin folds– Limited ROM–Asymmetric abduction–Positive Allis’ sign–Ortolani- Barlow maneuvers

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Therapeutic management DDH:

newborn to 6 months• Pavlik Harness –Maintain flexion, abduction, external

rotation• Worn continuously 23 hrs/day (usually 3-6 mo).

– Skin integrity– Lower extremity tissue perfusion

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Parental Teaching

1.Neuro vascular (CMS checks)2.Requires modification in car seat, feeding, holding

in general3.Skin integrity – diaper over harness, but t-shirt

under harness4.Remember developmental task of infant – needs

stimulation: talking singing, things at eye level, encourage upper extremity movement.

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Therapeutic management: DDH: 6-18 mo

• Traction followed by cast immobilization• Open reductions

–post-op spica cast

• Braces 23

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Therapeutic management DDH: Older child

• Tx more difficult; operative reduction• Successful reduction– very difficult >4 yrs old

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Other Musculoskeletal Alterations Involving Hip

• Legg-Calve-Perthes Disease– 4-8 yr old

• Slipped capital femoral epiphysis– adolescents

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Osteomyelitis

• Infection of bone• Antibiotics• Surgery • Immobilization–Bedrest– Splint, Cast

• I & D

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Bone Cancers: Osteosarcoma

• Osteogenic sarcoma • Usually presents in

adolescent boys.• Often metastasize when

discovered • CM’s: progressive pain

@ tumor site, palpable mass; limping (if leg involved); fracture

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Treatment: Osteosarcoma

• Surgery• Chemotherapy• Amputation (less now)• Radiation therapy (palliative)

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Ewing’s Sarcoma

• Tumor arises in nerve tissue; bone marrow & soft tissue

• Metastasize approx 1/3• Sx: pain, swelling, fractures• Tx: same as osteo– More responsive to radiation.

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Spinal Abnormalities

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Fig. 50-8, p. 1423

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Scoliosis

• Def: curvature of spine 10 degrees or more on x-ray

• Causes: – congenital– neuromuscular disease– idiopathic

Treatment• Watchful waiting

• Bracing

• Surgery

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Post op Spinal surgery

• ROM• Log Roll• C&DB• NPO/NG tube• Neurovascular checks (CSM)• Monitor Hct• Pain

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Muscular Dystrophy

• Group of muscular diseases - 5 types• Similarities

• Genetic component• Progressive, degenerative• weakness, atrophy, & deformity

• DIFFER:• Age• Which muscle groups affected

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Duchenne (pseudohypertophic)

• Most common type• Meet motor developmental milestones• Manifests after walking (age 3-7)– Waddling gait, difficulty climbing stairs, riding bike, running

• More progression: Gower’s sign• Wheelchair by age 9-12• Death by age 20 in 75%

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Outcomes

• Maintain function @ optimal level–PT– Even when ill: get OOB

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Outcomes• Maintain Skin integrity• Prevent obesity (pt. will maintain weight w/in

[parameters])• Respiratory support (pt. will maintain O2 sat >

___ )• Emotional support family & patient• Financial support

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