Care of MSK Disorders Flashcards
collaborative care for scleroderma
- PT and OT
- protect hands and feet from cold and injury (want warm moist heat)
- small frequent meals
- drug therapy
healing stages of fracture
- hematoma (within 72 hours)
- granulation tissue (3-14 days)
- callus formation (2 weeks)
- ossification (3 weeks to 6 months) -> usually when cast comes off
- consolidation -> when bony union is formed (up to 1 year)
- remodeling
collaborative care for osteoporosis
- exercise (low impact)
- fall and fracture prevention
- Ca and vitamin D supplements
- Drug therapy
diffuse scleroderma sxs
CREST
- calcinosis: painful calcium deposits in SQ tissue
- Raynaud’s phenomenon: restricted extremity blood flow in response to cold/stress
- esophageal dysfunction: scarring leads to strictures
- scelrodactyly: tightening of skin on fingers and toes; shiny and taut; facial skin appears tight and mask like
- telangiectasia: red spots on hands/palms, forearms, face and lips
collaborative care for gout
- hot/cold therapy
- joint immobilization
- steroid injections
- avoid purine rich food
- medication
- adequate fluid intake
2 types of traction for fractures
- skin traction (Buck’s traction): used commonly for hip fractures
- skeletal traction: surgically placed pins that place traction as they heal
medications used for gout
- colchicine
- allopurinol
- NSAIDs
- prednisone
other clinical manifestations of RA (damage to other systems)
- sjogren’s syndrome
- lymphadenopathy
- pericarditis/myocarditis
- pleuritis/interstitial fibrosis
- amyloidosis
- myositis/tenosynovitis
- Raynaud’s phenomenon
- peripheral edema/neuropathy
characteristics of SLE
- more common in women
- higher incidence in African Americans, Hispanics, and Native Americans
- genetic predisposition
- risk factors include hormones, environmental triggers (sunburn), infections, and certain meds
diagnostic testing for fractures
- physical exam
- Xray
- CT
- MRI
characteristics of scleroderma
- systemic sclerosis
- more common in African Americans
- usual onset at age 30-50
- more common in women
- unknown cause
how to care for a cast
- neuromuscular assessments
- evaluate extremity
- ROM exercises on other extremities
- if itching -> use hair dryer on cool setting
- thoroughly dry cast w/ hair dryer if wet
- report signs of complications
diagnostic tests for scleroderma
- anticentromere antibody (80%)
- UA (proteinuria)
- elevated creatinine
- CXR, PFTs, and EKG
types of fracture immobilization
- casts or splint
- external fixation (when multiple procedures needed)
- internal fixation (rods, pins, screws, and plates)
collaborative care for fractures
- fracture reduction
- traction: improves bone alignment and blood flow to extremity
- fracture immobilization
- care for open fractures
- adequate nutrition and fluid intake
- neuromuscular assessments
describe pain/stiffness of OA
- pain worsens w/ activity or use of joint
- stiffness worse after resting (after sleeping)
- pain as barometric pressure decreases (rain storms)
- may have referred pain
collaborative care for SLE
- manage exacerbations
- drug therapy
medication used for osteoporosis
- Bisphosphonates - alendronate (Fosamax) once a week
- should be taken with a full glass of water and 30 minutes before eating or or taking other meds
how to prevent dislocation after hip fracture surgery
- don’t allow legs to cross over midline
- no more than 90 degree flexion of hip
- pillows or abductor pillow between legs when turning
- towel rolls or pillows placed on lateral sides of legs
- avoid turning pt on affected side until approved by surgeon
- keep hip in neutral, straight position
specific sxs of RA
- involvement of all joints and cervical spine
- stiffness/pain
- limited ROM
- signs of inflammation
- joint stiffness w/ inactivity
- joint deformities of bilateral hands/feet
- contractures
- rheumatoid nodules
goals for treatment of scleroderma
prevent and treat secondary complications
T/F: OA is an inflammatory process
False
diagnostic tests for OA
- Xray
- CT/MRI
- bone scan
describe chronic gout
- multiple joint involvement
- tophi (visible sodium urate crystal deposits)
- joint deformity
- nephrolithiasis
clinical manifestations of scleroderma
- tightening of skin and organs due to sclerosis/thickening
- limited to cutaneous (80%)
- includes face, hands, lower arms, feet and lower legs
- diffuse progresses to trunk (includes lung, heart, and renal disease)
types of fractures
- transverse: horizontal fracture
- spiral: caused by twisting motion (possible abuse in peds)
- greenstick: stress causes bending/splintering (common in peds)
- comminuted: crushed bone fragments
- oblique
- pathologic (osteoporosis and cancer)
- stress: commonly occurs in feet
clinical manifestations of SLE
- vague sxs: fever, weight loss, and fatigue
- butterfly rash
- photosensitivity
- alopecia
- polyarthrialgia and morning stiffness
- endocarditis, pericarditis, and pleural effusion
- antiphospholipid syndrome
- lupus nephritis
- seizures, headache, and neuropathy
- depression and psychosis
- anemia, leukemia, and thrombocytopenia
- increased risk of infection (common cause of death)
collaborative care of patients with OA
- balance rest/activity
- avoid long periods of standing, kneeling, or squatting
- ice (acute) and heat (chronic) -> caution if pt has neuropathy
- weight management
- exercise and ROM
- mediations
- surgery (remove bone spurs and replacing joints)
pt teaching for prevention of OA
- avoid trauma
- use safety measures to avoid injury
- avoid smoking
- maintain healthy weight
- exercise
diagnostic testing for osteoporosis
- bone scan (assess bone density)
- gold standard is dual-energy Xray absorptiometry (DXA)
- quantitative US