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Rheumatoid Arthritis

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Title: Rheumatoid Arthritis


1
Rheumatoid Arthritis
  • Anand Lal, M.D.

2
Rheumatoid Arthritis
  • Chronic systemic inflammatory disease of unknown
    etiology
  • Affects the Synovial Membranes of multiple joints
  • Prevalence 1-2
  • Female Male ratio 31
  • Usual age of onset 20-40 years though individuals
    of any age group may be affected

3
Rheumatoid Arthritis
  • Pathologic finding chronic synovitis with pannus
    formation. The pannus erodes cartilage, bone,
    ligament and tendons. In the acute phase effusion
    and other manifestations of inflammation are
    evident in the later stages ankylosis of the
    joint may set in. In both the acute and chronic
    phase, there may be widespread inflammation of
    the tissues around the joint that can lead to
    significant joint destruction.

4
Rheumatoid Arthritis
  • Clinical presentation
  • usually presents insidiously
  • prodromal syndrome of malaise, weight loss and
    vague periarticular pain and stiffness may be
    seen
  • less commonly, the onset is acute, triggered by a
    stressful situation such as infection, trauma,
    emotional strain or in the postpartum period.
  • the joint involvement is characteristically
    symmetric with associated stiffness, warmth
    tenderness and pain

5
Rheumatoid Arthritis
  • Clinical Features
  • the stiffness is characteristically worse in the
    morning and improves during the day its duration
    is a useful indicator of the activity of the
    disease. The stiffness may recur especially after
    strenuous activity.
  • the usual joints affected by rheumatoid arthritis
    are the metacarpophalangeal jts, the PIP jts, the
    wrists, knees, ankles and toes.
  • Entrapment syndromes may occur especially carpal
    tunnel syndrome

6
Rheumatoid Arthritis
  • 20 of patients with rheumatoid arthritis will
    have subcutaneous nodules, usually seen over bony
    prominences but also observed in bursa and tendon
    sheaths these nearly always occur in
    seropositive patients as do most other
    extra-articular manifestations
  • splenomegaly and lymphadenopathy can occur
  • low grade fever, anorexia, weight loss, fatigue
    and weakness can occur

7
Rheumatoid Arthritis
  • After months to years, deformities can occur the
    most common are
  • ulnar deviation of the fingers
  • swan neck deformity, which is hyperextension of
    the distal interphalangeal joint and flexion of
    the proximal interphalangeal joint
  • boutonniere deformity, which is flexion of the
    distal interphalangeal joint and extension of the
    proximal interphalangeal joint
  • valgus deformity of the knee

8
Rheumatoid Arthritis
  • Dryness of the eyes, mouth and other mucus
    membranes is found, especially in advanced
    disease
  • Pericarditis and pleuritis can occur but are
    usually clinically silent
  • aortitis can occur as a late complication,
    usually associated with vasculitis rupture of
    the aorta can lead to aortic regurgitation

9
Rheumatoid Arthritis
  • Labs
  • Rheumatoid factor, an IgM antibody is seen in the
    sera of 75 of patients with rheumatoid
    arthritis. High titers of rheumatoid factor are
    associated with severe disease.
  • Rheumatoid factor is also found in other diseases
    like syphilis, sarcoidosis, infective
    endocarditis, TB, leprosy, parasitic infections
    in advanced age and in asymptomatic relatives of
    patients with rheumatoid disease.
  • Antinuclear antibody are seen in 20 of patients
    with rheumatoid arthritis, though their titer is
    lower than in SLE

10
Rheumatoid Arthritis
  • Labs
  • The ESR is elevated both in the acute and chronic
    phases of the disease
  • a moderate anemia is often present which is
    usually hypochromic normocytic
  • the white count is normal or slightly increased
    but leukopenia may occur, often in presence of
    splenomegaly (e.g., Feltys syndrome)
  • the platelet count is often elevated in
    proportion to the degree of joint inflammation

11
Rheumatoid Arthritis
  • Labs
  • joint fluid examination is valuable. The fluid is
    translucent to opaque and has between 3000 and
    50,000 WBCs /microL. There are 50 or more
    polymorphonuclear leukocytes. The culture is
    negative.
  • X-ray
  • of all the laboratory tests, x-ray changes are
    most specific for rheumatoid arthritis. However,
    they are not sensitive and usually are negative
    during the first 6 months of the disease

12
Rheumatoid Arthritis
  • X-rays
  • the earliest changes occur in the wrist or feet
    and consist of soft tissue swelling and
    juxta-articular demineralization. Later,
    diagnostic changes consisting of joint space
    narrowing and erosions develop. The erosions are
    first seen at the ulnar styloid and at the
    juxta-articular margin, where the bony surface is
    not protected by cartilage. Diagnostic changes
    also occur in the cervical spine with C1-2
    subluxation, but this can take several years to
    develop.

13
Rheumatoid Arthritis
  • 1987 American College of Rheumatology Revised
    criteria for the diagnosis of Rheumatoid
    Arthritis
  • At least four of the following
  • Morning stiffness gt 1hour
  • Synovitis in three joints simultaneously
  • Synovitis in wrist or hand MCP or PIP joints
  • Symmetrical arthritis (some joint areas on both
    sides of the body)
  • Rheumatoid nodules
  • Serum rheumatoid factor
  • Radiographic changes typical of Rheumatoid
    Arthritis

14
Rheumatoid Arthritis
  • Differential Diagnosis
  • Rheumatic fever migratory arthritis, elevated
    ASO and dramatic response to Aspirin
  • Systemic Lupus Erythematosus Butterfly rash,
    discoid lupus erythematous, photosensitivity,
    alopecia, high titers of Anti Ds-DNA, renal and
    CNS disease
  • Osteoarthritis no constitutional manifestations
    and no evidence of joint inflammation
  • Gouty Arthritis usually monoarticular initially
    but can become polyarticular in the later years

15
Rheumatoid Arthritis
  • Differential Diagnosis
  • Pyogenic arthritis usually monoarticular, fever
    and chills, abnormal joint fluid
  • Chronic Lyme disease commonly monoarticular and
    associated with positive titers
  • Human Parvovirus infection arthralgia more
    common than arthritis, rash may be present,
    serologic evidence of parvovirus B19 infection
  • Polymyalgia rheumatica is associated with
    proximal muscle weakness and stiffness

16
Rheumatoid Arthritis
  • Differential Diagnosis
  • several cancers produce paraneoplastic syndromes
    including polyarthritis e.g., hypertrophic
    pulmonary osteoarthropathy produced by lung and
    gastrointestinal cancers. Diffuse swelling of the
    palmar fascia has been associated with several
    cancers including ovarian cancer.

17
Rheumatoid Arthritis
  • Treatment
  • goal of treatment
  • reduce inflammation and pain,
  • preservation of function, and
  • prevention of deformity.

18
Rheumatoid Arthritis
  • Treatment
  • Nonpharmacologic treatment
  • Education and emotional factors
  • Physical and occupational therapies
  • Systemic and articular rest
  • Exercise
  • Heat and cold
  • Assistive devices like splints, canes, raised
    toilet seat and/or crutches or walker
  • Weight loss

19
Rheumatoid Arthritis
  • Treatment
  • Nonsteroidal Anti-inflammatory agents like
    aspirin usually given in a dose of 1 gram three
    to four times per day. If patients develop
    tinnitus, a common side effect, the dose should
    be reduced by .6-.9 grams every 3 days until the
    patient improves. Enteric coated aspirin and
    nonacetylated forms of aspirin like salsalate may
    be associated with less GI distress. GI
    irritation may also be reduced by taking the
    aspirin with meals or antacids.

20
Rheumatoid Arthritis
  • Treatment
  • Other NSAIDs Ibuprofen, naproxen, sulindac and
    other NSAIDs may also be effective though they
    are associated with a number of side effects
    including
  • GI irritation and peptic ulcers (misoprostol can
    reduce the incidence of peptic ulcers associated
    with NSAIDs)
  • Kidney damage
  • Liver damage

21
Rheumatoid Arthritis
  • Treatment (Disease Modifying Agents (DMARDs)
  • Methotrexate considered by many to be the drug
    of choice for RA. It produces a beneficial effect
    in 2-6 weeks and is given once weekly. The usual
    dose is 7.5-15 mg once a week. The most common
    side effect is gastric irritation and stomatitis.
    Other side effects are hepatotoxicity,
    pancytopenia and interstitial pneumonitis.

22
Rheumatoid Arthritis
  • Treatment
  • Antimalarials such as hydroxychloroquine sulfate
    is effective in 25-50 of patients and in most
    cases after 3-6 months of therapy. It is reserved
    for mild disease.
  • Gold salts are used, especially in cases where
    patients are not responding to Methotrexate or in
    case of erosive disease.
  • Corticosteroids produce immediate and dramatic
    anti-inflammatory benefit but are limited by
    their many side effects

23
Rheumatoid Arthritis
  • Treatment
  • Sulfasalazine is a good second line agent for
    rheumatoid arthritis with an efficacy similar to
    gold and penicillamine. Side effects include
    neutropenia and thrombocytopenia.
  • Azathioprine is an antimetabolite which is
    reserved for use in case of severe cases.
  • Penicillamine

24
Rheumatoid Arthritis
  • Prognosis
  • Patients can follow two divergent courses 50-75
    experience remission in 2 years (these patients
    are negative for rheumatoid factor and have good
    functional status even during disease activity).
    Conservative therapy is advised for this group.
    Patients who have severe disease have a worse
    prognosis, and on an average die 10-15 years
    earlier than people without RA. Since most of the
    joint damage occurs in the first two years, these
    patients should be started on a disease modifying
    agent early.

25
Rheumatoid Arthritis
  • Juvenile chronic arthritis is similar to
    rheumatoid arthritis but is seen in children.
    Synovitis persisting for 6 weeks is essential to
    making this diagnosis. Four forms are recognized
  • polyarticular form resembles adult RA
  • oligoarticular form affects young girls during
    peak ages of 2-4
  • systemic onset disease or Stills disease is
    characterized by fever and rash
  • a juvenile form of ankylosing spondilitis
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