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1.
Autoimmun Rev ; 6(8): 511-4, 2007 Sep.
Article in English | MEDLINE | ID: mdl-17854740

ABSTRACT

Psoriatic arthritis (PsA) is a common unique form of inflammatory arthritis associated with psoriasis. Its exact prevalence is unknown but 5-30% of the 2-3% of subjects of the general population affected with psoriasis are developing PsA. Typically PsA presents as an oligoarticular asymmetrical arthritis with predominant distal finger joint pattern, presence of spinal involvement enthesitis and dactylitis. There is evidence that T-cells play a key role in the immunopathology of PsA as well as Psoriasis. Leflunomide, a selective pyrimidine synthesis inhibitor with the property to inhibit T-cell activation and proliferation has been shown to improve both joint and skin symptoms in patients with PsA. Significant response rates have been observed for Psoriatic Arthritis Response Criteria (PsARC), modified ACR20 and PASI 50 after 24 weeks of treatment with 20 mg/d Leflunomide orally in a randomised, placebo controlled multicenter trial (TOPAS Study). Leflunomide treatment also improved quality of life and showed a favourable safety profile. It is therefore concluded that Leflunomide offers an efficacious, well tolerated, safe, and relatively inexpensive therapeutic option for the treatment of actively inflamed joints and psoriatic skin lesions in patients with PsA.


Subject(s)
Arthritis, Psoriatic/drug therapy , Isoxazoles/therapeutic use , Anti-Inflammatory Agents, Non-Steroidal/adverse effects , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Antirheumatic Agents/adverse effects , Antirheumatic Agents/therapeutic use , Arthritis, Psoriatic/immunology , Humans , Isoxazoles/adverse effects , Leflunomide
2.
Rheumatol Int ; 28(1): 21-6, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17571266

ABSTRACT

We evaluated a combined physician and patient questionnaire designed for identifying early rheumatoid arthritis (RA) and spondyloarthritis (SpA) in a cohort of 220 patients supposed for admission to an early arthritis clinic (EAC). The documents including personal and basis demographic data, referral diagnosis, questions related to RA and SpA classification criteria, functional limitations and previous diagnostic and therapeutic attempts were fax-transmitted to referring practices and returned before first EAC appointment. 125 referrals before introduction of the questionnaire served as controls. We found that a functional impairment of the hands provided more accurate prediction of RA than reports on morning stiffness or joint swelling. No clinical data proved predictive for SpA. We observed an unintended increase in the prescription of analgesics/NSAID and corticosteroids. In conclusion, questionnaires as designed here may provide substantial information for diagnosis of RA, but also imply the risk of unmeant therapeutic attempts.


Subject(s)
Ambulatory Care Facilities , Arthritis, Rheumatoid/diagnosis , Patients , Physicians , Surveys and Questionnaires , Cohort Studies , Germany , Humans , Outpatient Clinics, Hospital
4.
Z Arztl Fortbild Qualitatssich ; 97(6): 377-81, 2003.
Article in German | MEDLINE | ID: mdl-14524052

ABSTRACT

Continuing medical education is essential to improve the quality of health care delivery. The efficacy of postgraduate medical education generally improves when participants feel that their specific needs are met by a particular educational activity. Audit circles of general practitioners allow for a discussion of relevant issues. The present paper describes a novel concept for delivering knowledge and skills in arthritis and rheumatic conditions to general practitioners. A well-designed paper case was used for discussion in established audit circles of general practitioners, and a specially trained expert rheumatologist participated as an external expert to answer all those questions that could not be solved by the other participants. The participation of such as an expert-on-demand was found extremely helpful, as an evaluation during pilot sessions in 6 pre-existing audit circles of general practitioners revealed.


Subject(s)
Education, Medical, Continuing/methods , Physicians, Family/education , Rheumatic Diseases/therapy , Rheumatology/standards , Humans , Quality Assurance, Health Care
5.
Arthritis Res ; 4(2): 139-44, 2002.
Article in English | MEDLINE | ID: mdl-11879550

ABSTRACT

An excess of the proinflammatory substance IL-18 is present in joints of patients with rheumatoid arthritis (RA), and expression of IL-18 receptor (IL-18R) regulates IL-18 bioactivity in various cell types. We examined the expression of IL-18R alpha-chain and beta-chain and the biologic effects of IL-18 in fibroblast-like synoviocytes (FLS) after long-term culture. The presence of both IL-18R chains was a prerequisite for IL-18 signal transduction in FLS. However, all FLS cultures studied were either resistant or barely responsive to IL-18 stimulation as regards cell proliferation, expression of adhesion molecules ICAM-1 and vascular cell adhesion molecule (VCAM)-1, and the release of interstitial collagenase and stromelysin, IL-6 and IL-8, prostaglandin E2, or nitric oxide. We conclude that the presence of macrophages or IL-18R+ T cells that can respond directly to IL-18 is essential for the proinflammatory effects of IL-18 in synovitis in RA.


Subject(s)
Receptors, Interleukin/metabolism , Synovial Membrane/metabolism , Arthritis, Rheumatoid/immunology , Arthritis, Rheumatoid/metabolism , Cell Division/drug effects , Cells, Cultured , Collagenases/metabolism , Culture Media, Conditioned/metabolism , Dinoprostone/metabolism , Fibroblasts/drug effects , Fibroblasts/metabolism , Fibroblasts/pathology , Humans , Intercellular Adhesion Molecule-1/metabolism , Interleukin-18/metabolism , Interleukin-18/pharmacology , Interleukin-18 Receptor alpha Subunit , Interleukin-6/metabolism , Interleukin-8/metabolism , Matrix Metalloproteinase 3/metabolism , Nitric Oxide/metabolism , RNA, Messenger/metabolism , Receptors, Interleukin/genetics , Receptors, Interleukin-18 , Signal Transduction , Synovial Membrane/drug effects , Synovial Membrane/pathology , U937 Cells/drug effects , U937 Cells/metabolism , U937 Cells/pathology , Vascular Cell Adhesion Molecule-1/metabolism
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