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39 Cards in this Set

  • Front
  • Back
Is Inflammation the Primary Pathological Process in Arthritis?
No
Secondary Factors
- trauma
- repetitive use
- obesity
- developmental diseases
Diagnostic Method of OA
- x-rays
- no changes in synovium, urine, or blood noted
Early Features of Degenerative Joint Disease/OA
- cartilage degenerates
- focal swelling/softening of cartilage
- loss of proteoglycans
Late Features of Degenerative Joint Disease/OA
- fibrillations in the surface of deepen into fissures
- subchondral bony ebernation
- margins of the cartilage develop spurs
What Does OA Normally Affect?
- affects weight bearing joints
- particularly 1st carpometacarpal and MP joints
- Heberden's Nodes
- generally affects one side at a time - not systemic
- causes a decreased shock absorption affect
What are Heberden's Nodes?
where OA affect the distal IP joints
Symptoms of OA
- may be bilateral
- pain
- ROM limited to extreme positions such as IR with hip flexion
- muscle weakness, atrophy, and fatigue
- joint instability is NOT seen in OA
Non-surgical Options in OA
- combinations of NSAIDS, weight reduction, exercise for strength, joint protection, and flexibility
- assistive devices for weight bearing
Surgical Options in OA
- joint arthroplasties
- total joint replacements
- cartilage repairs
- muscle transfers are NOT a suitable rx option
Spondylosis
narrowing of the intervertebral space, degenerative joint disease typically in cervical spine
Charcot's Joint
- any of the tarsal joints loss of sensory modalities due to repetitive micro-fractures of tarsal bones = loss of nocioceptors - has an inflammatory component
Incidence of RA
- affects 1% of the population = 2.1 million Americans
- mostly women
- occurs middle age with sometimes happening in the 20s/30s
RA Factor and 6 Criteria for Dx
occurs in approximately 75% of the population in the adult form
1. >1 hr morning stiffness
2. 3 or more joints involved (wrist jts, PIP, MP)
3. joint swelling
4. RA Nodules
5. ulnar drift
6. Serum RA+ Factor
Pain Patterns in RA
- periods of pain remissions possible
- bilateral upper and lower joint symptoms
- systemic in contrast to OA
- Felty's Syndrome
Symptoms of Felty's Syndrome
- Anemia
- Thrombocytopenis
- Neutropenia
Causes of RA
- process triggered when synovial vascular lining cells are activated by some process not yet understood
- cells proliferate developing a "pannus"
- erosion of bone and cartilage
- muscles and ligaments rupture in response
Lab & Imaging Studies
- elevated ESR
- anemia
- joint swelling
- bone resorption in later stages
- high titer of RA factor
What Are Some of the Clinical Manifestations of RA?
- severe inflammation joints
- more likely to be systemic
- juvenile and adult forms
- small joints/ generally bilateral and symmetrical
- excaberations and remissions
Classifications of RA
- class I: completely able to perform usual ADLs
- class II: able to perform usual self-care and vocational activities, but limited in avocational activities
- class III: able to perform usual self-care activities, but limited in vocational and avocational activities
- class IV: limited in ability to perform usual self-care, vocational, and avocational activities
Additional Forms of RA
- Ankylosing Spondylitis
- Psoriatic Arthritis
- Juvenile RA
- Systemic Lupus
- Gout
Symptoms of Psoriatic Arthritis
- dry skin lesions and finger nail bed changes identified
- distal IP joints of fingers most commonly affected
Epidemiology of Psoriatic Arthritis
- 1/3 of patients with psoriasis have arthritis with delay of joint involvement for as long as 20 years
- both sexes affected equally
- SI joint commonly involved
Juvenile RA: Forms and Twin Peaks of Age For Onset?
Forms:
- Systemic
- Polyarticular
- Pauciacticular (most common)
Peaks:
- between 1-3 and again at 8-12
- females affected 2x more then males
Lab Findings for JRA
- leukocytosis in systemic and polyarticular forms
- increase WBC levels
- 50% of cases have + antinuclear antibodies
- imaging studies show joint erosion, pannus (soft tissue swelling)
Disease Progressions for JRA For the 3 Forms
systemic
- episodic high fevers, rashes, lymphadenopathy, slenomegaly
- 1/2 of cases resolve in adolescence/teenage years
polyarticular
- lower grade fevers, synovitis in 4 or more joints
pauciarticular
- no systemic signs
- increased incidence of iridocyclitis
What is Lupus?
- inflammatory connective tissue disorder of unknown etiology occurring predominately in women
Symptoms of Lupus
- butterfly rash
- episodic fever & malaise
- utericarial plaques (blisters)
- thrombocytopenia
- increased antinuclear antibodies
Progression of Lupus
- intermittent arthalgias leading to acute polyarthritis
- pneumonitis and pleurisy
- diffuse myocarditis - congestive heart failure
- splenomegaly
- renal involvement
Gout
metabolic disease in which deposition of monosodium urate crystals in the joints produce inflammatory changes
- affects 1st MP joint of the foot
- also seen in ankle, wrist, fingers, and elbows
Gout Incidence
- hereditary incidence of 6-18%
- serum urate concentration likely controlled by multiple genes
- differential diagnosis is the presence of urate crystals in the WBC in synovial fluid
Tophi
- actual calcified crystals in the joint spaces
Exercises for Prevention and Wellness
- maintain proper body weight
- sustain good postural alignment
- use joints for ADLs
Goals of Rx For OA
- decrease inflammation
- restore flexibility
- educate on proper body mechanics
Goals of Rx for RA
- energy conservation
- joint protection
- maintenance of cardiovascular levels
- decrease inflammation
Methods For Protecting the Joints
- using a straight cane
- viscoelastic insoles and foot orthosis to decrease impact vibration and disperse weight
- aquatic therapy
Restoring Muscle Balance
- isometric exercises
- stretching muscles
- resistive exercises of joints
- joint mobilization
Restoring Functional Activities
- closed kinetic chain exercises (in midrange)
- balance and equilibrium exercises
- energy conservation education
To Normalize Specific Joint Movement Patterns
use splints and braces