11 rheumatoid athritis
TRANSCRIPT
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Age Mostly in 30-40 yrs Increasing in older patients
US Health Examination (1960-62)0.3% age< 35 th
10.0% age> 60 th Sex
Women : Man (2,5 :1) Another factors
Social status, education, & Psycho-stress
EPIDEMIOLOGY
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Unclear Suggested
Genetic factor, HLA DR-4
Environment
Arthritogenic agents (bacteria, virus)
ETIOLOGIC FACTOR
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Genetic Arthritogenicfactors (Bacteri,virus) (HLA DR4)
AutoimmuneHumoral immunity (RF)
Cellular immunityInflamatory mediators, cytokines
SYNOVITIS
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AntigenB lymphocyteSynovium
Ig G Production(abnormal)
FR Production
Immune complex
Complemen activation
Synovium inflammation
Ag 1 Ab 1 / Ag 2
Ab 2
(Ag2 + Ab2)
Arthriti s
Humoral Immunity (RF) in RA
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An auto antibody to antibody An Ab that bind to Fc portion of IgG
molecule 75-80 % in RA High titer in severe case of RA
May be present in other disesas 3% in normal population
Rheumatoid Factor (RF)
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Phatologic Inflammation of RA
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Synovium inflammation (synovitis)with hypertropic, and villi proliferation
tumor-like proliferation (pannus)
to damage cartilage, bone and tendon
PATHOLOGIC
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History : pain, swelling and morningstiffness of small peripheral joint
Often with general symptom ,(generalfatigue,
Symmetrical arthritis in small peripheral joint
Extra articuler manifestation : rare
CLINICAL MANIFESTATION OF RA
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Early sign : tenderness andswelling mono articular andasymmetric
Within a week or few monthsymmetrical arthritis (warm, pain,tender, without local heat)Joints : wrist, MCP, PIP,small joint s of the feet, etc
Late stage : joint deformitySwan neck deformity
Arthritis in small peripheral joints
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Early onset of RA Late stage of RA
Rheumatoid Arthritis of hand
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Skin Rheumathoid nodul in pressure areas (rare in
Indonesia) Vasculitis (purpura, echimosis, necrosis of nail,
ulcer or gangren) Eye
Kerato- conjungtivitis sicca (Sjogrens Syndrome) Scleritis, episcleritis
EXTRA ARTICULAR MANIFESTATION OF RA
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Lung
Instertitial Pnemonitis
Pleural effusions, fibrosis
Cardiovascular
Pericarditis , myocarditis
Nodul reumathoid in myocard atau palve
Hematology
Mild Anaemia (on chronic disease)Feltys Syndrome (granulocytopenia,splenomegaly &
recurrent infection)
EXTRA ARTICULAR MANIFESTATION OF RA(cont)
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Rheumatoid nodule
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Laboratory Test Anemia (nn) ESR or CR (Good indication of inflamation)
Lymphocyteosis Rheumatoid Factor positip (85%) Electrophoresis (increasing of Ig) )
DIAGNOSTIC INVESTIGATIONS
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Imaging / X Ray Normal (in early onset) Soft tissue swelling Periarticular osteopenia Marginal or central erossion and cysts
DIAGNOSTIC INVESTIGATIONS
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CRITERIA of RHEUMATOID ARTHRITIS(The American Rheumatism Associations, 1987 revised criteria)
1. Morning stiffness ( 1 jam)2. Arthritis of 3 joints or more
3. Arthritis of hand joints
4. Symetrical Arthritis
5. Rhematoid nodule
6. Serum Rheumatoid Factor
7. Typical radiologic changes of RA
Rheumatoid Arthritis : 4 criterias or more,Note : Criteria 1 through 4 must have been present for at least 6 weeks
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Early Diagnosis and early treatment The goal : to achive the remission
Patient Education and motivation To suppress the inflamations To perform maximal joint function To protect joint damage
The tool : Education Physical rehabilitation Medications Surgical therapy Other : alternatif treatmant
By the teams (Ruematologist/Internist, Orthopedist,Physioterapist, Psychiater, Social worker and Family)
MANAGEMENT OF RA
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Simptomatis NSAID
Glucocorticoid Antiinflammatory dan immunosupressive effect Without disease modifying effect
DMARDs (Disease Modifying Anti Rheumatic Drugs)
Biologic response modifiers TNF alfa=antagonist, IL1-Ra
MEDICINAL THERAPY
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Traditional methode (Pyramida sytem)
Combination of Multiple drugs :
Step-do w n B r idge
Start with multiple drugs (oral Steroid, methotrexate,Sulfasalazine, Chloroqiun, etc)
Start with multiple drugs (step by step, stop the mostdangerous drug and the last, chloroquin)
Continuous until several month-years.
The choice of DMARDs
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DMARD FOR RHEUMATOID ARTHRITIS THERAPYDrugs Onset Dose Side effects
Hydroxychloroquine 2-4mont
200 mg;2x/day
Rash, diarrhea, retina toxicity
Sulfazalacine 1-2mont
1000 mg;2-3x/day
Rash, myelosuppression, GIintolerance
Methotrexate 1-2mont
7,5-17,5mg/wk
GI symptoms, stomatitis, rash ,alopesia, myelosuppression, liverand lung impairment
Azatioprine 2-3mont
50-150mg/day
Mielosuppression, liver impairment,flu-like illness, GI symptoms
D-penisillamine 3-6mont
250-750mg/hr
Myelosuppression. stomatitis,dyspepsia, proteinuria,autoimmune disorder, rash
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