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1.
Arthritis rheumatol ; 68(2)Feb. 2016.
Article in English | BIGG - GRADE guidelines | ID: biblio-964633

ABSTRACT

OBJECTIVE: To provide evidence-based recommendations for the treatment of patients with ankylosing spondylitis (AS) and nonradiographic axial spondyloarthritis (SpA). METHODS: A core group led the development of the recommendations, starting with the treatment questions. A literature review group conducted systematic literature reviews of studies that addressed 57 specific treatment questions, based on searches conducted in OVID Medline (1946-2014), PubMed (1966-2014), and the Cochrane Library. We assessed the quality of evidence using the Grading of Recommendations, Assessment, Development and Evaluation (GRADE) method. A separate voting group reviewed the evidence and voted on recommendations for each question using the GRADE framework. RESULTS: In patients with active AS, the strong recommendations included use of nonsteroidal antiinflammatory drugs (NSAIDs), use of tumor necrosis factor inhibitors (TNFi) when activity persists despite NSAID treatment, not to use systemic glucocorticoids, use of physical therapy, and use of hip arthroplasty for patients with advanced hip arthritis. Among the conditional recommendations was that no particular TNFi was preferred except in patients with concomitant inflammatory bowel disease or recurrent iritis, in whom TNFi monoclonal antibodies should be used. In patients with active nonradiographic axial SpA despite treatment with NSAIDs, we conditionally recommend treatment with TNFi. Other recommendations for patients with nonradiographic axial SpA were based on indirect evidence and were the same as for patients with AS. CONCLUSION: These recommendations provide guidance for the management of common clinical questions in AS and nonradiographic axial SpA. Additional research on optimal medication management over time, disease monitoring, and preventive care is needed to help establish best practices in these areas.(AU)


Subject(s)
Humans , Spondylitis, Ankylosing/drug therapy , Spondylitis, Ankylosing/therapy , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Antirheumatic Agents/therapeutic use , Spondylarthritis/drug therapy , Glucocorticoids/therapeutic use , Physical Therapy Modalities , Tumor Necrosis Factor-alpha/therapeutic use , Adalimumab/therapeutic use , Infliximab/therapeutic use , Etanercept/therapeutic use
2.
Ann Rheum Dis ; 61(11): 960-7, 2002 Nov.
Article in English | MEDLINE | ID: mdl-12379516

ABSTRACT

OBJECTIVE: To review publications relating to the blocking of interleukin 1 (IL1) as a strategy for treating human disease, ranging from rheumatoid arthritis (RA) to Alzheimer's disease. METHODS: The National Library of Medicine's PubMed database was searched for articles about pharmaceutical agents that reduce the biological actions of IL1. RESULTS: Fish oils and corticosteroids were identified as non-selective pharmacological interventions that reduce the activity of IL1, whereas a recombinant human IL1 receptor antagonist (anakinra) and a soluble recombinant type I IL1 receptor act selectively. To date, anakinra is the only selective intervention that has been shown in controlled clinical trials to be effective and well tolerated in the treatment of a specific human disorder, RA. In controlled clinical trials, anakinra provided significant clinical improvement and slowed radiographic disease progression in patients with active RA. Moreover, addition of anakinra to existing methotrexate treatment significantly reduced signs and symptoms of active disease. CONCLUSIONS: The clinical use of anakinra has been demonstrated in the management of RA, but blocking of IL1 in other human disorders, as well as the safety of the use of these blocking agents in chronic diseases, still needs to be defined by controlled clinical investigations.


Subject(s)
Antirheumatic Agents/therapeutic use , Arthritis, Rheumatoid/drug therapy , Interleukin-1/physiology , Receptors, Interleukin-1/antagonists & inhibitors , Sialoglycoproteins/therapeutic use , Animals , Disease Models, Animal , Humans , Interleukin 1 Receptor Antagonist Protein , Recombinant Proteins/therapeutic use
3.
Curr Pain Headache Rep ; 5(4): 313-9, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11403734

ABSTRACT

Patients with fibromyalgia have an altered quality of life that is hard to quantitate using existing indices. The principal legal issues associated with the syndrome are: Does fibromyalgia exist? Can it be caused by or flared by stress or trauma? Does disability apply to fibromyalgia and if so, how? These issues are critically reviewed.


Subject(s)
Disability Evaluation , Fibromyalgia/economics , Quality of Life/legislation & jurisprudence , Fibromyalgia/etiology , Humans , Stress, Psychological/complications , Wounds and Injuries/complications
4.
Curr Opin Rheumatol ; 12(5): 379-85, 2000 Sep.
Article in English | MEDLINE | ID: mdl-10990173

ABSTRACT

Systemic lupus erythematosus (SLE) can involve any part of the gastrointestinal tract. In this review, we list the gastrointestinal manifestations of SLE and analyze current approaches in investigating and treating these common conditions. Abdominal symptoms and signs may be due to SLE or due to medications used in the treatment of SLE. In patients with abdominal pain and active SLE, it is critical to diagnose vasculitis or thrombosis with appropriate scanning and institute early immunosuppressive or surgical treatment.


Subject(s)
Gastrointestinal Diseases/etiology , Lupus Erythematosus, Systemic/complications , Abdominal Pain/etiology , Humans , Oral Ulcer/etiology
5.
Lupus ; 9(3): 228-31, 2000.
Article in English | MEDLINE | ID: mdl-10805493

ABSTRACT

Basic science insights along with the assessment of risk factors so clearly documented by the Canadian and Hopkins cohorts in earlier papers of this special issue have clearly led to a change in the way rheumatologists manage SLE. This review will highlight specific ways it should alter our day to day treatment of lupus patients.


Subject(s)
Arteriosclerosis/etiology , Lupus Erythematosus, Systemic/complications , Lupus Erythematosus, Systemic/therapy , Antibodies, Antiphospholipid/metabolism , Arteriosclerosis/immunology , Coronary Disease/diagnosis , Coronary Disease/etiology , Homocysteine/blood , Humans , Hypolipidemic Agents/therapeutic use , Immunosuppressive Agents/therapeutic use , Lupus Erythematosus, Systemic/immunology , Risk Factors
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