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10 Cards in this Set

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Rheumatoid Arthritis

Chronic systemic inflammatory autoimmune disorder characterized by symmetrical inflammation of multiple joints


Extra articular manifestations


rheumatoid nodules, vasculitis, eye inflammation , neurological dysfunction, cardiopulmonary disease, lymphadenopathy, splenomegaly


Progressive damage to soft tissue, cartilage, and bone without treatment

RA pathophysiology

Chronic inflammation of the synovial tissue lining the joint capsule results in proliferation of the tissue.


-PTO inflammatory cytokines, tumor necrosis factor and interleukin -1


-activated T cells and B cells


- most patients have antibodies called rheumatoid factors


The inflamed synovium invades thé cartilage and bone surface producing erosions of bone and cartilage leading to destruction of joint

Goals of therapy with RA

Minimize disease activity and joint damage


Enhance physical function and quality of life


Maximize duration of remission


Disease remission

Médications for RA

NSAIDS and other medications:


Do not prevent or slow joint destruction —non selective NSAIDS, COX 2 selective inhibitors, steroids

Médications for RA

NSAIDS and other medications:


Do not prevent or slow joint destruction —non selective NSAIDS, COX 2 selective inhibitors, steroids

Disease Modifying AntiRheumatic Drugs (DMARDS)

MTX


Hydroxychloroquine


Sulfasalazine


Leflunomide


Biological modifiers


Gold


Azathioprine


Cyclosporine


Cyclophosphamamide


Penicillamine

DMARDs

- should initiate within the first 3 months of symptom onset


- given to reduce mortality and prevent progresssion of RA


-onset: delayed weeks to months before benefit seen—no direct analgesic or anti-inflammatory effect


-narrow range of effectiveness


Unique adverse event profile: use often limited by toxicities


Consists of nonbiologic and biologic agents

MTX

First line DMARD for all patients


Onset 2-3wks (max 4-6wks)


Low cost: oral or SQ


Administer once weekly

MTX mechanism

Folic acid antagonist, immunosuppressant, inhibits T lymphocytes proliferation and cytokine production

Hydroxychloroquine

Limited ability to prevent joint damage when used as mono therapy


Mechanism- unknown


Has some inflammatory properties