36912752 rheumatoid arthritis ppt

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    RHEUMATOID ARTHRITIS

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    What is RA?A Chronic,

    systemic inflammatory disease,

    characterised by symmetrical

    joint involvement which is

    typically erosive/destructive.

    hallmark feature: persistentsymmetric polyarthritis (synovitis)

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    Recap on the anatomy and physiology

    Function of JOINTS:

    To allow articulation between twoor more bones and

    secondarily to permit movementby contraction of opposing

    muscles.

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    Unknown

    Genetic

    Auto immune

    Etiology

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    Pathophysiology

    Antigen

    Environmental agent, infectious agent

    Activates CD4 helper

    T cells and probably

    B lymphocytes

    T cells stimulatessynovial macrophage

    and fibroblast

    Activates

    B lymphocytes

    Genetic

    Susceptibility

    HLA-DR4HLA-DQ

    HLA- DPCytokines

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    Pathophysiology

    Pannus formation

    Joint destruction

    Cartilage fibrosis

    Ankylosis

    Joint injury

    RANKL

    Activatesosteoclast

    Formation of

    rheumatoid

    factor

    Formation ofautoimmune complexes

    and probable deposition

    in the joint

    Cytokines

    Fibroblast

    Chondrocytes

    Synovial cells

    Enzymes release

    (collagenase, streptomelysin,

    elactase, PGE2 and matrix

    metalloproteinases, others)

    T cells stimulates

    synovial macrophage

    and fibroblast

    Activates B lymphocytes

    Proliferation

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    INTERLEUKIN 1

    IL-1 is a potent stimulator of synoviocytes,

    chondrocytes and osteoblasts (Figure 1).

    IL-1 is a proinflammatory cytokine that amplifies

    and perpetuates the disease process in RA

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    1. arth rit is

    Clinical Manifestations

    Associated with

    low fever

    Fatigue

    Morning stiffness

    Joint soft, warm to

    touch

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    Clinical Manifestations

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    2. extra-articu lar featu res

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    3. Associated syndromes(possib le compl icat ion s)

    Clinical Manifestations

    (a) Sjgrens syndrome-salivary gland

    inflammation and keratoconjunctivitis

    (b) Feltys syndrome-profound neutropenia,

    thrombocytopenia and splenomegaly

    (C) Pulmonary involvement-(pleuritis, interstitial

    pneumonitis, alveolitis and intrapulmonaryrheumatoid nodules)

    (d) Cardiac involvement-pericarditis

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    ns

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    Diagnnostic criteria1. Morning stiffness lasting more than

    1 hour

    2. Arthritis of 3 or more joint areas.

    3. Arthritis of the hand joints

    4. Symetric arthritis

    5. Rheumatoid nodules over extensor

    surface or bony prominences.

    6. Serum rheumatoid factor.7. Radiologic changes.

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    o l igoart icu lar JIA

    Polyart icu lar J IA

    System ic J IA

    Types of JIA

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    1. Acute Pain r/t inflammation & swelling

    2. Fatigue r/t increased metabolic rate

    3. Impaired physical mobility r/t decreasedrange of motion

    4. Disturbed body image r/t physical &

    psychological changes

    Nursing Diagnosis:

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    THANK

    YOU

    FOR

    LISTENING!