Musculoskeletal - Conditions Flashcards

1
Q

Rheumatoid Arthritis

A
  • chronic, systemic inflammatory disease, characterised by persistent synovitis of multiple joints
  • autoimmune response to an antigen triggering the formation of an abnormal immunoglobulin G
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2
Q

RA - Risk Factors

A
  • gender - women more likely to get RA
  • age - most common 35-50
  • family history
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3
Q

RA - Clinical Manifestations

A
  • sudden or insidious onset
  • tender, warm, swollen joints
  • polyarticular (affects numerous joints)
  • symmetrical
  • joint inflammation
  • fever / fatigue
  • pain and stiffness
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4
Q

RA - Deformities

A
  • Boutonniere deformity
    • hyperextension of the distal interphalangal joint (bends opposite direction to usual)
  • hallux valgus deformity
    • lateral deviation of the thumb (away from midline)
  • swan neck deformity
    • hyperextension of the proximal interphalangal joint & flexion of the DIP
  • ulnar drift deformity
    • fingers drift towards ulnar (outwards)
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5
Q

RA - Diagnosis

A
  • morning stiffness that lasts 1 hour and persists over 6 weeks
  • arthritis with swelling / effusions in over 3 joints
  • arthritis of hand joints
  • symmetrical arthritis
  • rheumatoid nodules
  • positive serum rheumatoid factor
  • x-ray changes
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6
Q

RA - Complications

A
  • joint destruction
  • deformities
  • cataracts
  • skin ulceration
  • cardiopulmonary effects
    • pleurisy
    • pleural effusion
    • pericarditis
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7
Q

RA - Nursing Management

A
  • relieve pain & reduce inflammation
  • medication regieme
    • PQRST
    • anti-inflammatory drugs
    • encourage decreased activity / increased rest
    • supportive splints
  • reduce fatigue
    • encourage sleep routine
    • plan morning activity (improve condition & alleviate pain)
    • rest periods & prioritize activities
    • reduce stressors
  • physical mobility & self care
  • preserve joint function
    • discuss limitations with patient, individualise care
    • OT/physio referral
    • devices to assist with ADL’s (frames, walkers, canes)
    • exercise programs, including hydrotherapy
  • surgical interventions if required
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8
Q

Osteoarthritis

A
  • degenerative joint disease characterised by degeneration & loss of articular cartliage in synovial joints
  • idopathic
    • no known precipitating factors
    • most common type
  • secondary
    • identifiable cause (ie - joint trauma, inflammation, skeletal disorder)
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9
Q

OA - Risk Factors

A
  • older age
  • gender (women more likely)
  • obesity
  • physical inactivity
  • joint damage / trauma
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10
Q

OA - Clinical Manifestations

A
  • progressive loss of articular cartilage and synovitis
  • joint pain & stiffness (does not have to be just morning stiffness)
  • pain worsens during day, is relieved by rest
  • stiffness after rising & inactivity
  • limitation of movement
  • functional impairment
  • joint instability / disformity
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11
Q

OA - Joint Specific Clinical Manifestations

A
  • hands
    • heberden’s & bouchard’s nodes
  • spine
    • pain & stiffness, limited ROM
    • muscle spasms, nerve root compression
  • hips
    • referred pain to groin, buttock, thigh or knee
    • loss of internal rotation, limited extension, adduction & flexion
  • knees
    • pain & bony enlargement
    • effusions (synovial fluid build up)
    • crepitus (grinding sensation)
    • instability & deformity
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12
Q

OA - Deformities

A
  • Heberden’s nodes
    • nodes on distal interphalangal joints (DIP)
  • Bouchard’s nodes
    • nodes on proximal interphalangal joints (PIP)
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13
Q

OA - Diagnosis

A
  • no specific test available
  • need to rule out other conditions
  • MRI - joint degeneration (late feature)
  • synovial fluid analysis
  • arthroscopy
  • x-ray (evidence of joint narrowing, osteophytes)
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14
Q

OA - Nursing Management

A
  • pain control
    • analgesia, anti-inflammatories (NSAIDs, DMARDs)
    • non-pharmacological - heat
  • prevention of progression
    • preventative measures:
    • weight reduction
    • decrease load on joints
    • rest, splints & braces
    • exercises
  • restoration of joint function
    • surgical interventions:
    • osteotomy - cutting into the bone
    • arthrodesis - fusing / fixing the joint
    • joint replacement
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15
Q

Osteoporosis

A
  • decrease in bone mass & density
  • dependent partly on how much bone mass you attain in your youth
  • occurs with age due to rate of bone reabsorption is greater than the rate of bone formation
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16
Q

Osteoporosis - Risk Factors

A
  • modifiable
    • diet (calcium, vitamin D)
    • high alcohol intake
    • smoking
    • physical inactivity
    • medications: steroids, heparin, antacids
    • oestrogen deficiency
  • un-modifiable
    • genetics / body type
    • gender (equal till after menopause)
    • premature menopause
    • amenorrhoea
    • caucasion
17
Q

Osteoporosis - Clinical Manifestations

A
  • most people unaware until fracture occurs
  • fractures (wrist, spine & hip most common)
  • pain, weakness, stiffness, unsteady gait
  • loss of height
  • khyphosis forming
18
Q

Osteoporosis - Diagnosis

A
  • bone mass density testing (BMD testing)
    • usual sites, hips, spine, wrist or whole body
    • T score & Z score: normal = +1 to -1, osteoporosis = -2.5
  • x-ray - fracture detection
  • serum calcium, phosphorus & alkaline phosphorus levels
  • dexa scan - duel energy xray absorbtiometry: two types of energy measuring the rate of absorbtion
19
Q

Osteoporosis - Nursing Management

A
  • management aimed at:
    • preventing bone loss
    • reducing risk of fractures
  • Hormone Replacement Therapy
    • prevents bone loss during & after menopause
    • use for less than 5 years, long term use associated with heart disease, DVT, breast cancer
  • nursing aims:
    • education
    • managing pain
    • physiotherapy
    • dietary & vitamin supplements
    • exercise
    • avoid smoking & alcohol
    • getting support
20
Q

Paget’s Disease

A
  • disorder of bone remodelling, leads to thickened and enlarged bones, structurally abnormal & brittle
  • localised increase in osteoclast formation leads to bone reabsorption, formation increases, osteoblasts deposit bone chaotically leading to poor quality bone without lamellar structure
  • leads to pain, fractures & deformity, higher risk of developing bone cancer
21
Q

Paget’s Disease - Manifestations & Management

A
  • insidious onset
  • pain in affected bone
  • on x-ray bone may appear enlarged & bowed
  • overlying skin warm, but not tender
  • bowed legs & kyphosis noticed over time
  • drug therapy: bisphosphonates (reduce bone turnover), calcitonin (inhibit osteoclast activity), NSAIDs, analgesia
  • exercise programs
22
Q

Rickets & Osteomalacia

A
  • known as Rickets in children, & osteomalacia in adults
  • vitamin D deficiency
  • leads to softening of bones, bones become deformed
23
Q

Rickets - Causes

A
  • insufficient calcium absorption from the gut due to a lack of dietary calcium or resistance to vitamin D
  • lack of exposure to sunlight (vitamin D deficiency)
  • phosphate deficiency due to altered elimination by the kidney or decreased intestinal absorption
24
Q

Rickets - Treatment

A
  • improved diet, including calcium & vitamin D
  • large doses of vitamin D
  • treatment for any underlying disorder
  • surgery to correct bone deformities