Rheumatoid Arthritis Pre-lecture Flashcards

1
Q

Rheumatoid arthritis

A

chronic disease
symmetrical joint involvement
most common systemic inflammatory disease

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2
Q

Epidemiology

A

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

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3
Q

MHC

A

major histocompatibility complex
HLA: hyman lymphocyte antigen typing: HLA-DR4 and HLA-DR1
consider possibility of a genetic etiology/redisposition

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4
Q

Pathogenesis of RA

A

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

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5
Q

RA progression

A

inflammation might decline but disability increases

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6
Q

Clinical presentation - prodromal effects

A

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

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7
Q

Diagnostic criteria

A

joint involvement
serology
duration of sx
acute phase reactants
diagnosed with RA if score is 6 or more

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8
Q

Joint involvement

A

most common joints: hands, wrists, feet
may involve: elbows, shoulders, hip, knees, ankles

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9
Q

Joint involvement in hands

A

wrist, metacarpal, proximal interphalangeal

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10
Q

Extraarticular manifestations

A

rheumatoid nodules, vasculitis, pulmonary, ocular, cardiac, felty’s, other

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11
Q

Rheumatoid nodules

A

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

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12
Q

Vasculitis

A

inflammation of small, superficial blood vessels
depends upon duration of disease
stasis ulcers
infarction –> necrosis

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13
Q

Pulmonary

A

pleural effusions
pulmonary fibrosis
nodules
rare: interstitial pneumonitis or arteritis

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14
Q

Ocular

A

keratoconjunctivitis sicca: itchy dry eyes + inflammation; sjogrens syndrome (KS + RA)
inflammation: sclera, espisclera, cornea
nodules

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15
Q

Cardiac

A

increased risk of CV mortality
pericarditis
conduction abnormalities
rare: myocarditis

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16
Q

Felty’s

A

have all 3: splenomegaly, neutropenia, RA

17
Q

Other

A

lympadenopathy, renal disease, thrombocytosis, anemia

18
Q

Laboratory indicators

A

help diagnose + assess disease progression
anemia, thrombocytosis, ESR, CRP, RF, anti-CCP/ACPA, ANA, joint aspirations, radiographic findings

19
Q

Erythrocyte sedimentation rate (ESR)

A

non-specific (diagnostic indicator)
normal: 0-20 mm/hr
elevated in RA > 20

20
Q

C-reactive protein (CRP)

A

normal 0-0.5 mg/dL
+ –> > 0.5 mg/dL
> 10 mg/dL can indicate bacterial infection

21
Q

Rheumatoid factor

A

hallmark diagnostic criteria!
antibody specific for IgM
not all pts with RA diagnosis are RF+
60-70% are RF+
higher the titer –> poorer the prognosis

22
Q

Anti-CCP/ACPA

A

auto-antibody presence test
high specificity, present earlier in disease, predictive value for erosive disease, marker of poor prognosis

23
Q

Antinuclear antibodies (ANA)

A

elevated titers suggest autoimmune disease, more indicative of SLE (less specific for RA), reported as a titer

24
Q

Joint aspiration

A

turbid, WBC 5,000-50,000/mm^3, glucose: normal to low compared to serum

25
Q

Radiographic changes

A

joint space narrowing
erosions of bone

26
Q

Poor prognosis - social factors

A

low socioeconomic status, lack of formal education, psychological stress, poor health assessment questionnaire scores

27
Q

Poor prognosis - physical factors

A

extra-articular manifestations, elevated ESR and CRP, high titers of RF, elevated anti-CCP/ACPA, erosions on x-ray, duration of disease, swelling of >20 joints

28
Q

Treatment goals

A

improve/increase QOL, reduce morbidity and mortality
alleviate s/sx of disease, preserve fx, prevent structural damage and deformity, control/avoid extra-articular manifestations

29
Q

Early treatment of RA

A

goal of preventing long-term disability
early, more aggressive tx helps prevent long-term disability
can improve fx and decrease inflammation with earlier treatment

30
Q

Nonpharmacologic treatment

A

education, emotional support, rest, weight reduction, physical/occupational therapy, heat, splints/prosthetics, surgery
should NOT be used as monotherapy

31
Q

Pharmacologic treatment

A

NSAIDs, corticosteroids, DMARDs, biologic agents anti-TNF and non-TNF, monoclonal antibodies, targeted synthetic DMARDs