Rheumatoid Arthritis Pre-lecture Flashcards
Rheumatoid arthritis
chronic disease
symmetrical joint involvement
most common systemic inflammatory disease
Epidemiology
prevalence: 2.1 mil (1-2% of pop)
age: any age, onset usually 30-50 yrs, shortens lifespan by 3-18 yrs
sex: female > male
race: no discrimination
MHC
major histocompatibility complex
HLA: hyman lymphocyte antigen typing: HLA-DR4 and HLA-DR1
consider possibility of a genetic etiology/redisposition
Pathogenesis of RA
synovial space is infiltrated with inflammatory cells: macrophage, T cells, plasma cells –> development of pannus - inflamed proliferating synovia invades into healthy cartilage + bone –> erosions, destroys joint
the release of cytokines, mediators of the immune/inflammatory response, leads to cell proliferation + death
RA progression
inflammation might decline but disability increases
Clinical presentation - prodromal effects
non-specific sx found early in presence of RA; difficult to link these sx to RA
fatigue, weakness, loss of appetite, joint pain, low grade fever, stiffness + muscle ache –> joint swelling
Diagnostic criteria
joint involvement
serology
duration of sx
acute phase reactants
diagnosed with RA if score is 6 or more
Joint involvement
most common joints: hands, wrists, feet
may involve: elbows, shoulders, hip, knees, ankles
Joint involvement in hands
wrist, metacarpal, proximal interphalangeal
Extraarticular manifestations
rheumatoid nodules, vasculitis, pulmonary, ocular, cardiac, felty’s, other
Rheumatoid nodules
common: hands, elbows, forearms (pressure points)
more common in erosive disease (happes longer the pt has the disease or the less control the pt has over the disease)
20% of pts affected
asymptomatic = 0 intervention
Vasculitis
inflammation of small, superficial blood vessels
depends upon duration of disease
stasis ulcers
infarction –> necrosis
Pulmonary
pleural effusions
pulmonary fibrosis
nodules
rare: interstitial pneumonitis or arteritis
Ocular
keratoconjunctivitis sicca: itchy dry eyes + inflammation; sjogrens syndrome (KS + RA)
inflammation: sclera, espisclera, cornea
nodules
Cardiac
increased risk of CV mortality
pericarditis
conduction abnormalities
rare: myocarditis