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Internal illnesses. Rheumatoid arthritis (lecture notes) Directory / Lecture notes, cheat sheets Table of contents (expand) LECTURE No. 44. Rheumatoid arthritis Rheumatoid arthritis is a chronic systemic connective tissue disease with a progressive lesion of predominantly peripheral (synovial) joints, similar to erosive-destructive polyarthritis. Classification. When making a diagnosis, a division is made: 1) according to clinical characteristics: poly-, oligo-, monoarthritis, the presence of visceritis, combination with other rheumatic diseases; 2) by the presence of rheumatoid factor: seropositive, seronegative; 3) according to the degree of activity: minimal I, moderate II, maximum III, remission; 4) according to the x-ray stage: I - osteoporosis, II - narrowing of the joint spaces, III - erosion, IV - ankylosis; 5) by functional insufficiency: I degree - professional ability is preserved, II degree - is lost, III degree - the ability to self-service is lost. Clinic. The main syndromes are articular (damage mainly to small joints of the hands and feet, ulceration of the cartilage of the surface of the joints, deformity, ankylosing, morning stiffness syndrome), cardiac (myocarditis, endocarditis with the formation of a superficial heart disease, pericarditis), pulmonary (adhesive pleurisy, fibrosing pneumonitis) , renal (chronic glomerulonephritis, amyloidosis), trophic disorders (rheumatoid nodules in the periarticular tissues of the affected joints), vascular (digital arteritis in the nail phalanges), asthenovegetative (fever, weight loss), anemic (secondary iron deficiency anemia). The main clinical forms are articular (the main form of manifestation of the disease - in 80% of cases), benign, articular-visceral, Felty's syndrome (1% of cases - pancytopenia, enlargement of the spleen and peripheral lymph nodes), malignant, rapidly progressive form, Sjögren's syndrome (involvement parenchyma of the salivary and lacrimal glands with subsequent atrophy). The basis of diagnosis are major and minor criteria. К big criteria include the following: 1) morning stiffness; 2) pain during movement or soreness of at least one joint; 3) joint swelling; 4) swelling of at least one more joint (established with an interval of no more than 3 months); 5) symmetry of swelling of the joints; 6) subcutaneous nodules; 7) typical radiological changes in the joints with the inclusion of periarticular osteoporosis; 8) rheumatoid factor in the blood; 9) characteristic changes in synovial fluid; 10) characteristic histological changes in the synovial membrane; 11) characteristic histology of rheumatoid nodules. In the presence of seven criteria, the diagnosis is considered reliable, less than seven criteria - probable. Small Criteria: 1) subcutaneous rheumatoid nodules; 2) medium or high titers of rheumatoid factor; 3) characteristic radiological changes in the joints; 4) the presence of a symptom of morning stiffness (at least 30 minutes); 5) the presence of a rheumatoid hand (ulnar deviation, "walrus flipper"). If these signs are present, a diagnosis of rheumatoid arthritis can be made. Additional diagnostic study. The examination algorithm corresponds to that adopted for systemic connective tissue diseases. High titers of rheumatoid factor are found, with x-ray studies - narrowing of the interarticular gaps, erosion, ankylosis. Complications. Complications are subluxations, ankylosing, bursitis, cysts, secondary iron deficiency anemia, amyloidosis, neurocirculatory dystonia of mixed origin, recurrent iridocyclitis, atrophic changes in regional muscles, secondary infections. Differential diagnostics. Should be carried out with acute rheumatism, reactive polyarthritis, systemic lupus erythematosus, rheumatoid-like syndromes (Bekhterev's disease, Sjögren's, Reiter's disease, psoriatic arthropathy), deforming osteoarthritis, gout. Treatment. Non-steroidal anti-inflammatory drugs are prescribed (butadione, indomethacin, voltaren, ortofen, brufen, naproxen, ketoprofen, ponstan, etc.), preference is given to long-acting drugs. Hormone therapy is carried out (corticosteroids, with the ineffectiveness of non-steroidal anti-inflammatory drugs and the ongoing activity of the process - 15-20 mg with a slow decrease and the addition of non-steroidal anti-inflammatory drugs in increasing doses). Cytostatic immunosuppressants are administered (decrease in the formation of immune complexes and rheumatoid factor) - azathioprine pr 50 mg 2-3 times a day, chlorbutin 2 mg 2-3 times a day; D-penicillinamine, cuprenil 0,15-0,3 g 2-3 times a day for 4-5 months, delagil. Basic therapy is carried out with gold preparations (krizanol 2 ml intramuscularly once a week for 1-7 months), aminoquinoline preparations are used: rezoquin, plaquenil 8-0,12 g, 0,25 tablet at night for 1-10 months. Plasmapheresis, hemosorption (to remove immune complexes) is also carried out. Physiotherapy treatment, physiotherapy exercises, sanatorium treatment, surgical methods of correction are shown - to restore the function of the joints. Flow. The course of the disease depends on the form: with articular - slowly progressive with gradual deformation of the joints (10-15 years), with articular-visceral - rapidly progressive (2-3 years). Forecast. With the articular form, the prognosis is favorable, with the articular-visceral form - unfavorable. Prevention. To prevent the development of relapses of the disease, long-term use of basic drugs, non-steroidal anti-inflammatory drugs is carried out. Author: Myshkina A.A. << Back: Nodular periarteritis >> Forward: Allergy We recommend interesting articles Section Lecture notes, cheat sheets: ▪ Theory and methodology of education. Lecture notes ▪ The budget system of the Russian Federation. Crib See other articles Section Lecture notes, cheat sheets. Read and write useful comments on this article. Latest news of science and technology, new electronics: The existence of an entropy rule for quantum entanglement has been proven
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