Rhemathoid arthritis RA
Upcoming SlideShare
Loading in...5
×
 

Rhemathoid arthritis RA

on

  • 707 views

 

Statistics

Views

Total Views
707
Views on SlideShare
707
Embed Views
0

Actions

Likes
1
Downloads
78
Comments
0

0 Embeds 0

No embeds

Accessibility

Upload Details

Uploaded via as Microsoft PowerPoint

Usage Rights

© All Rights Reserved

Report content

Flagged as inappropriate Flag as inappropriate
Flag as inappropriate

Select your reason for flagging this presentation as inappropriate.

Cancel
  • Full Name Full Name Comment goes here.
    Are you sure you want to
    Your message goes here
    Processing…
Post Comment
Edit your comment

    Rhemathoid arthritis RA Rhemathoid arthritis RA Presentation Transcript

    • Overview 1 2 3 4 5
    • There are three types of joints – fibrous, fibrocartilaginous and synovial. Synovial joints These include the ball-and-socket joints (e.g. hip) and the hinge joints (e.g. interphalangeal). They possess a cavity and permit the opposed cartilaginous articular surfaces to move painlessly over each other. Movement is restricted to a required range, and stability is maintained during use. The load is distributed across the surface, thus preventing damage by overloading or disuse. 3
    • Synovium and synovial fluid . The joint capsule, which is connected to the periosteum, is lined with synovium which is a few cells thick and vascular. Its surface is smooth and nonadherent and is permeable to proteins and crystalloids. As there are no macroscopic gaps, it is able to retain normal joint fluid even under pressure. Macrophages and fibroblastlike synoviocytes form the synovial layer by cell-to-cell interactions mediated by cadherin-II. The synoviocytes release hyaluronan into the joint space, which helps to retain fluid in the joint. Synovial fluid is a highly viscous fluid secreted by the synovial cells and has a similar consistency to plasma. Glycoproteins ensure a low coefficient of friction between the cartilaginous surfaces. Tendon sheaths and bursae are also lined by synovium. 4
    • • Rheumatoid Arthritis (RA) is a chronic, autoimmune, inflammatory systemic disease of unknown etiology characterized by persistent joint inflammation(chronic symmetrical polyarthritis) that results in progressive joint destruction, joint deformity, and physical disability. RA may affect other organs and may also result in an increased risk for premature death. The average life expectancy of RA patients is decreased by 3 to 18 years compared to age and gender matched controls. Because it can affect multiple organs of the body, rheumatoid arthritis is referred to as a systemic illness and is sometimes called rheumatoid disease.
    • Rheumatoid arthritis is a chronic disease, characterized by periods of disease flares and remissions. The cause of rheumatoid arthritis is not known. In rheumatoid arthritis, multiple joints are usually, but not always, affected in a symmetrical pattern. Rheumatoid arthritis can affect people of all ages. Damage to joints can occur early and does not correlate with the severity of symptoms. The "rheumatoid factor" is an antibody that can be found in the blood of 80% of people with rheumatoid arthritis.
    • A joint is where two bones meet to allow movement of body parts. Arthritis means joint inflammation. The joint inflammation of rheumatoid arthritis causes swelling, pain, stiffness, and redness in the joints. The inflammation of rheumatoid disease can also occur in tissues around the joints, such as the tendons, ligaments, and muscles. In some people with rheumatoid arthritis, chronic inflammation leads to the destruction of the cartilage, bone, and ligaments, causing deformity of the joints. Damage to the joints can occur early in the disease and be progressive. Moreover, studies have shown that the progressive damage to the joints does not necessarily correlate with the degree of pain, stiffness, or swelling present in the joints.
    • Rheumatoid arthritis is a common rheumatic disease, affecting approximately 1.3 million people in the United States, according to current census data. The disease is three times more common in women as in men. The prevalence is high in the Pima Indian population and low in black Africans and Chinese people. The disease can begin at any age, but it most often starts after age 40 and before 60. In some families, multiple members can be affected, suggesting a genetic basis for the disorder.
    • The cause of rheumatoid arthritis is unknown.. It is believed that the tendency to develop rheumatoid arthritis may be genetically inherited (hereditary). It is suspected that certain infections or factors in the environment might trigger the immune system to attack the body's own tissues; resulting in inflammation in various organs of the body such as the lungs or eyes. Environmental factors also seem to play some role in causing rheumatoid arthritis. For example, scientists have reported that smoking tobacco increases the risk of developing rheumatoid arthritis.
    • Genetic and environmental factors play a part. Gender. Women before the menopause are affected three times more often than men. After the menopause the frequency of onset is similar between the sexes, suggesting an etiological role for sex hormones. The use of the oral contraceptive pill has shown no affect on RA overall, as previously thought, but it may delay the onset of disease. Familial. The disease is familial with an increased incidence in first degree relatives and a high concordance amongst monozygotic twins (up to 15%) and dizygotic twins (3.5%). In occasional families it affects several generations.
    • Genetic factors are estimated to account for up to 60% of disease susceptibility. There is a strong association between susceptibility to RA and certain HLA haplotypes. HLA-DR4, which occurs in 50–75% of patients, correlates with a poor prognosis, as does HLA-DRB1 Individuals with HLA-DRB1 combined with a positive rheumatoid factor are13 times greater risk for developing bone erosions in early disease. 11
    • Rheumatoid arthritis is typified by widespread persisting synovitis (inflammation of the synovial lining of joints, tendon sheaths or bursae). The cause of this is unclear, but the production of rheumatoid factors (RFs) by plasma cells in the synovium and the local formation of immune complexes play a part. The synoviocytes play a central role in synovial inflammation. In RA the synovium becomes greatly thickened to the extent that it is palpable as a ‘boggy’ swelling around the joints and tendons. There is proliferation of the synovium into folds and fronds, and it is infiltrated by a variety of inflammatory cells, including polymorphs, and lymphocytes and plasma cells. There are disorganized lymphoid follicles. The normally sparse surface layer of lining cells becomes hyperplastic and thickened. There is marked vascular proliferation. Increased permeability of blood vessels and the synovial lining layer leads to joint effusions that contain lymphocytes and dying polymorphs. 12
    • 13
    • Hands and wrists Shoulders Elbows Feet Knees Hips Cervical spine 14
    • 15
    • Typically :symmetrical swollen , painful, and stiffness of small joint of hands & feet that worse in the morning. This can fluctuate ,and large joint may become involve. Less common : sudden onset ,widespread arthritis .Systemic illness with extra -articular symptom; fatigue, low-grade fever, wight loss, lack of appetite , pericarditis and pleurisy, recurrent soft tissue problem ,polymyalgia onset-vague limb aches. 16
    • When only one joint is involved, the arthritis can mimic the joint inflammation caused by other forms of arthritis, such as gout or joint infection. Chronic inflammation can cause damage to body tissues, including cartilage and bone. This leads to a loss of cartilage and erosion and weakness of the bones as well as the muscles, resulting in joint deformity, destruction, and loss of function. Rarely, rheumatoid arthritis can affect the cricoarytenoid joint. When this joint is inflamed, it can cause hoarseness of the voice. 17
    • Finger deformities •intrinsic plus deformity •swan neck deformity •boutonniere deformity •mallet deformity •ulnar deviation (towards the little finger) of the fingers Thumb deformities •Type 1 is a boutonniere deformity; it is most common •Type 2 is a flexion deformity of metacarpo-phalangeal with extension of inter-phalangeal joint •Type 3 is a swan neck deformity; second most common •Type 4 is abduction of the proximal-phalanx and adduction of the metacarpal. Wrist deformities •dorsal (backward) dislocation of the ulna bone •ulnar shifting of the wrist bones •tendon rupture •radial shifting (towards the index finger) of the metacarpals 18
    • Caused by the tightness of the intrinsic muscles (interossei and lumbrical muscles) of the hand. When the metacarpo-phalangeal joint is extended it is not possible to flex the proximal inter- phalangeal joint. 19
    • Swan neck deformity is a condition in which the distal joint (behind the nail) of the finger goes into flexion and the proximal joint goes into extension. 20
    • Is caused by the stretching of the collateral ligaments of the metacarpo-phalangeal joints stretching of the accessory ligaments causing the ulnar drifting of the flexor tendons contracture of the intrinsic muscles of hand ulnar deviation or rupture of the extensor tendons. 21
    • Boutonniere deformity is a condition in which the proximal joint (away from the knuckle joint) of the finger goes into flexion and the distal joint goes into extension. 22
    • Since rheumatoid arthritis is a systemic disease, its inflammation can affect organs and areas of the body other than the joints. Examples of other areas that may be affected include: Sjogren's syndrome is inflammation of the glands of the eyes and mouth and causes dryness of these areas. Rheumatoid inflammation of the lung lining (pleuritis) causes chest pain with deep breathing or coughing. Tissue inflammation surrounding the heart, called pericarditis, can cause chest pain that typically changes in intensity when lying down or leaning forward.
    • Rheumatoid disease can reduce the number of red blood cells (anemia) and white blood cells. Decreased white cells can be associated with an enlarged spleen (Felty's syndrome) and can increase the risk of infections. Firm lumps under the skin (rheumatoid nodules) can occur around the elbows and fingers where there is frequent pressure. A rare and serious complication is blood-vessel inflammation (vasculitis). Vasculitis can impair blood supply to tissues and lead to tissue death. This is most often initially visible as tiny black areas around the nail beds or as leg ulcers. 24
    • Complications of the condition oRuptured tendons oRuptured joints (Baker’s cysts) oJoint infection oSpinal cord compression (atlantoaxial or upper cervical ospine) oAmyloidosis (rare) oSide-effects of therapy Septic arthritis This is a serious complication with significant morbidity and mortality. Affected joints are hot and inflamed with accompanying fever and a neutrophil leucocytosis in the blood. However, these signs are often absent, and any effusion, particularly of sudden onset, should be aspirated. Staphylococcus aureus is the most common organism. Blood cultures are often positive. Treatment is with systemic antibiotics and drainage. 25
    • Complications of the condition Amyloidosis Amyloidosis is found in a very small number of people with severe rheumatoid arthritis. RA is the most common cause of secondary AA amyloidosis. AL amyloidosis causes a polyarthritis that resembles RA in distribution and is also often associated with carpal tunnel syndrome and subcutaneous nodules. AA amyloidosis is secondary amyloidosis AL amyloidosis primary amyloidosis ATTR amyloidosis the most common form of familial amyloidosis, associated with mutations of the gene encoding transthyretin. 26