Maternal-Child Nursing Care Optimizing Outcomes for Mothers, Children, & Families Chapter 30 Caring for the Child with a Musculoskeletal Condition Susan Ward Shelton Hisley A & P Review Bones Ligaments and tendons Muscles Immobilizing Devices Casts A cast is applied to the affected extremity to keep it immobile while healing. Casts Four categories (fiberglass or plaster casts) Upper extremity Lower extremity Spinal or cervical Total body Cast complications Compartment syndrome (accumulation of fluid in the fascia) Cast syndrome (portion of the duodenum is compressed between the superior and mesenteric artery and the aorta) Clinical Alert: Complication of the Child with a Fracture The classic sign of compartment syndrome is unrelenting pain that is unrelieved by narcotics. The nurse must notify the physician immediately. The priority intervention for compartment syndrome is prevention. Prevention is achieved by elevating the extremity to prevent excessive swelling and conducting frequent neurovascular checks. Critical Nursing Action: Cast Syndrome Cast syndrome can be prevented by three nursing interventions Reposition frequently Increase fluids and fiber in the child’s diet Cut a “belly hole” or a window in the cast to allow for abdominal expansion Casts: Nursing Care Five “Ps”—pain, pulse, pallor, paresthesia, and paralysis Elevate the affected extremity Give good hygiene (bathing and perineal care) Prevent constipation Educate parents about itching, small objects in cast, and cast removal) Assess child’s emotions Principles of Traction Skin Traction Types Bryant’s traction Russell’s traction Balanced suspension Nursing Care Neuromuscular assessments Q 4 hours Traction weights checked, hanging free Traction removed and reapplied Q 4 hours Perform skin care Q 4 hours Provide diversional activities Skeletal Traction Types Crutchfield tongs 90/90 femoral traction Dunlop traction Performing the Neurovascular Assessment Pain—Does the child complain of pain in the affected limb? Is it relieved by narcotic medication? Does it become worse when fingers or toes are flexed? If yes, notify the physician immediately (compartment syndrome). Sensation—Can the child feel touch on the extremity? Is two-point discrimination decreased? If yes, notify the physician immediately (compartment syndrome). Motion—Can the child move fingers or toes? Lack of movement may indicate nerve damage. Temperature—Does the affected limb feel warm? Does it feel cool? A cool extremity may change to feeling warm if a blanket is placed over it and the extremity is elevated. If the extremity is still cool after these interventions, there is poor circulation. Performing the Neurovascular Assessment Capillary refill time (CRT)—Apply brief pressure to the nail bed and note how quickly pink color returns to the nail bed. CRT of less than 3 seconds is the norm. If CRT is greater than 3 seconds, circulation is poor. Performing the Neurovascular Assessment Color—Note the color of the affected limb. Compare it to the color of the unaffected limb. Pink is the norm. If the color is paler than the unaffected limb, circulation is poor. Pulses—Check pulses distal to the injury or cast. If the pulse is difficult to locate, assess with a Doppler and mark the spot with an “X.” If the cast covers the foot or hand, it may not be possible to check the pulse, but the other neurovascular assessment can be implemented. Nursing Care for Skeletal Traction Neuromuscular assessments Q 4 hours Know signs of compartment syndrome and report them to the physician immediately Maintain traction Prevent skin breakdown Assess pin sites Q 8 hours of s/s of infection Manage pain Maintain good nutrition and elimination Assess for complications (osteomyelitis, pneumonia, circulatory compromise, ischemia, and disuse) Prepare family for discharge Provide psychosocial support Complications of Skeletal Traction Osteomyelitis Compartment syndrome Common Musculoskeletal Conditions Found in Children Club Foot Signs and symptoms Foot is plantar-flexed with an inverted heel Adducted forefoot Nursing care Provide cast care, neurovascular assessments Manage pain Educate family Legg-Calvé-Perthes Disease Signs and symptoms Hip or knee soreness or stiffness Painful limp, quadriceps muscle atrophy Nursing care Monitor non–weight-bearing Assess range of motion, pain, and neurovascular status; educate family Slipped Femoral Capital Epiphysis Signs and symptoms Pain in hip and knees, limping Externally rotating the leg Nursing care Maintain non–weight-bearing Ensure no range of motion Postoperative care Fractures (Bone Undergoes More Stress Than It Can Absorb) Characterized as open or closed Treatment Closed or open reduction Complications Compartment syndrome Shock, fat emboli, deep vein thrombosis Pulmonary embolism, infection Fractures Nursing care Obtain history Immobilize the bone (splints, braces, cases, external fixators, or traction) Prevent infection Perform neurovascular assessment Manage pain Provide pin care (if applicable) Prevent complications Restore function Educate family (nutrition) Provide emotional support Soft Tissue Injuries (Sprains and Strains) Signs and symptoms Pain, swelling, and ecchymosis Nursing care RICE Immobilize the joint Collaborate with the physical therapist Provide home care education Sports Injuries Signs and symptoms (knee and elbow injury) Pain Tenderness in joint Loss of full extension of the joint Nursing care Manage pain Immobilize the joint RICE Teach parents about prevention Osgood-Schlatter Disease Signs and symptoms Pain below the kneecap Pain aggravated by activity and relieved by rest Nursing care Manage pain Ice knee after exercising Maintain limited activity Collaborate with physical therapist Osteomyelitis Signs and symptoms Localized tenderness, redness, warmth Pain on palpation Nursing care Administer intravenous antibiotics Promote rest and manage pain Provide good nutrition and diversional activities Teach parents about antibiotic compliance Juvenile Arthritis Signs and symptoms Joints are swollen, tender, and warm to touch Limited range of motion of joints Nursing care Medications Prevent injuries and identify exacerbations Teach family about disease and proper care Collaborate with physical therapist Provide age-appropriate activities Include the child in decision making Muscular Dystrophies Muscular Dystrophies A group of muscle disorders that cause the gradual wasting of symmetrical groups of skeletal muscle Muscular Dystrophies Types Congenital myotonic dystrophy Facioscapulohumeral muscular dystrophy Pseudohypertrophic muscular dystrophy (Duchenne) Muscular Dystrophies Signs and symptoms Progressive symmetrical muscle wasting Muscle weakness without loss of sensation Gower maneuver Nursing care Help patient maintain independent living for as long as possible Prevent respiratory infections Monitor skin Ensure good nutrition Assess mobility Foster independence and self-care Provide emotional support Scoliosis Signs and symptoms Unequal shoulder heights Scapulae prominences Waist angles, rib prominences, and chest asymmetry Leg length discrepancy Scoliosis Nursing care Perform scoliosis screening Discuss bracing and exercise Assess body image and maintain orthotic brace compliance Surgery when pulmonary function becomes compromised Preoperative care (explain to child and parents what to expect, tour ICU, and teach ROM exercises) Postoperative care (VS, neurological status, fluid balance, pain control, NG tube, advance diet, chest tube, s/s infection, logrolling, prevent constipation, discharge teaching, community resources, and encourage adolescent to be as active as possible) Kyphosis Signs and symptoms Uneven shoulder heights Pain in the thoracic region Nursing care Perform kyphosis screening Maintain orthotic brace compliance Surgery may be necessary (pre- and postoperative care same as scoliosis) Lordosis Signs and symptoms “Swayback” Excessive backward cavity of the spine Nursing care Perform lordosis screening Reduce predisposing factors; obesity Teach about postural exercises Discuss support garments Spinal Fusion Nursing care Pre- and postoperative care similar to scoliosis Monitor fluid balance (monitor for Syndrome of Inappropriate Antidiuretic Hormone [SIADH]) Assess circulation Manage pain Begin ambulation after __ days (follow medical doctor’s order) Provide good nutrition Collaborate with the physical therapist Arrange for home care (durable medical equipment) Tetanus (Lockjaw) Signs and symptoms Progressive stiffness and tenderness of the muscles in the neck and jaw Trismus (difficulty opening the mouth) Risus sardonicus (a peculiar grin) Opisthotonus posturing Laryngospasm of the respiratory muscles Tetanus prophylaxis through immunization is the key to preventing tetanus. Nursing care Give tetanus immune globulin (TIG) and antibiotics Closely monitor and maintain respiratory support Monitor fluids and electrolytes and caloric intake Give NG feedings or TPN Assist with ET intubation (laryngospasms) Eliminate stimulation Conduct frequent neurological assessments Assess O2 saturation and blood gasses Perform oropharyngeal suctioning Give medications Maintain hydration Collaborate with other health team members Osteogenesis Imperfecta (OI) Signs and symptoms Lax joints Small and weak muscles Numerous fractures Bone deformities (bowing) Growth pattern disturbances Nursing care Give medication (Reclast) Rule out child abuse Postoperative care VS, neurovascular assessments, pain management, and hydration Coordinate play and physical therapy Encourage genetic counseling Provide family education Osteoporosis A condition where the bones lose density and calcium and become brittle Signs and symptoms Osteopenia, fractures Nursing care Facilitate nutritional counseling Provide family education