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19 Cards in this Set

  • Front
  • Back
RA
-AI disease
-chronic, systemic, inflamm
-primarily peripheral diarthrodial joints
-erosive, potentially destructive arthropathy
-unrelated to OA
prevalence
-onset 30-50
-2-3x more common in females
-potentially fatal
mechanisms of joint damage
-CHEMICAL, ENZYMATIC,
SYMMETRICAL LOSS OF CARTILAGE
-BONE LOSS DUE TO EROSION AND OSTEOPOROSIS
-bony swelling
-asymmetrical oligo or mono-arthritis
-DIP
ACR criteria
1. AM stiffness (longer)
2. 3 or more joints
3. hand involvement
4. symmetry
5. nodules
6. RF
7. radiographic changes
history
1. season of onset
2. AM stiffness
3. Gelling (when the move they feel better)
4. associated illnesses or exposures
physical exam
-symmetry
-soft tissue swelling
-PIPs, MCPs, Wrists
Labs
1. anemia
2. thrombocytosis
3. inc ESR, CRP
4. + Rf
5. + ANA
6. + Anti-CCP
rheumatoid factor
-never base dx solely on RF
-not diagnostic
-false positives (age, SBE, hep)
-false negatives
-RF positivity increases with disease duration
-high titer diagnosticaly more meaningful
-high titer wosre prognosis
Anti-CCP: CYCLIC CITRULLINATED PEPTIDE
-not essential for Dx
-more specific and more snesitive
-high titer worse prognosis
-helps localize the disease
synovial fluid
-imflamm fluid: WBC >1,000 and PMN >50%
-orders:
1. gram stain
2. cx
3. differential
4. crystal search
5. WBC count
radiology
-symmetrical joint space loss
-PIPs
-MCPs
-atlanto-axial subluxation
-corner erosions of small joints
-"windblown deformity"- knees
Extra-articular RA
-systemic sx
-wt loss
-anemia
-fever
-higher lever of RF and anti-CCP
extra-articular RA in lungs
-nodules
-pul interstitial fibrosis (may be the most impt b/c it can be difficult to distinguish from methotrexate pul toxicity)
-vasculitis
-pleuritis/pericarditis
-felty's syndrome
mgmt advanced
-early, aggressive interventiona improves outcome
-methotrexate
-bio agents
-combo therapy
worst prognosis
-hight anti-CCP
-high RF
-erosions
-high ESR or CRP
-extra-articular manifestations
oral steroid
-Pro:
1. tx flares
2. minimize or control dz activity
-Con:
1. higher dose or duration means more SE
2. difficult to stop
-most follow:
1. gluc
2. bone density
3. BP
methotrexate
-gold standard tx
-first line tx
-parenteral absorbed better than PO
-Toxicities: hematologic, rash, oral ulcers, inc LFTs, GI, folic acid def
-precautions: liver hx, alcohol mod
second line drugs
-Arava
-Imuran
-Remicade- IV Q2 months
-Abatacept
-Rituximab
when to refer to rheumatologist
-uncertain dx
-confusing lab rasults
-uncomfortable with DMARd or bio use
-pt not responding
-erosions or other radiographic changes
-SE