Updated consensus statement on biological agents for the treatment of rheumatic diseases, 2006
Additional information has come to light in the past year, both corroborating the major positive effect these drugs have had in rheumatoid arthritis (RA), psoriatic arthritis (PsA), ankylosing spondylitis (AS), and other rheumatic diseases, and further documenting adverse events. [...]an update of t...
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Published in | Annals of the rheumatic diseases Vol. 65; no. suppl 3; pp. iii2 - iii15 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article Conference Proceeding |
Language | English |
Published |
London
BMJ Publishing Group Ltd and European League Against Rheumatism
01.11.2006
BMJ Elsevier Limited BMJ Group |
Subjects | |
Online Access | Get full text |
ISSN | 0003-4967 1468-2060 |
DOI | 10.1136/ard.2006.061937 |
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Abstract | Additional information has come to light in the past year, both corroborating the major positive effect these drugs have had in rheumatoid arthritis (RA), psoriatic arthritis (PsA), ankylosing spondylitis (AS), and other rheumatic diseases, and further documenting adverse events. [...]an update of the previous consensus statement is appropriate. 1 The consensus statement is annotated to document the credibility of the data supporting it as much as possible. Because these agents are not free of toxicity, patients or their representatives should be provided with information about potential risks and benefits so that they may give informed consent for treatment. |
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AbstractList | Additional information has come to light in the past year, both corroborating the major positive effect these drugs have had in rheumatoid arthritis (RA), psoriatic arthritis (PsA), ankylosing spondylitis (AS), and other rheumatic diseases, and further documenting adverse events. [...]an update of the previous consensus statement is appropriate. 1 The consensus statement is annotated to document the credibility of the data supporting it as much as possible. Because these agents are not free of toxicity, patients or their representatives should be provided with information about potential risks and benefits so that they may give informed consent for treatment. |
Author | Breedveld, F C Smolen, J S Burmester, G R Emery, P Keystone, E C Schiff, M H Weinblatt, M E Weisman, M H Furst, D E Kalden, J R van Riel, P L C M |
AuthorAffiliation | G R Burmester , Department of Rheumatology, and Clinical Immunology, Charité Hospital, Berlin, Germany P L C M van Riel , University Nijmegen Medical Centre, Nijmegen, the Netherlands J R Kalden , Department of Internal Medicine III, Institut for Clinical Immunology, University of Erlangen‐Nuremberg, Erlangen Germany J S Smolen , Institute of Rheumatology, Clinic for Internal Medicine III, Vienna General Hospital, Vienna, Austria M E Weinblatt , Brigham and Women's Hospital, Boston, MA, USA P Emery , Leeds University, Department of Rheumatology, Leeds General Infirmary, Leeds, UK M H Weisman , Cedar Sinai Hospital, Los Angeles, CA, USA E C Keystone , Department of Rheumatology, Mount Sinai Hospitial, Toronto, Canada D E Furst , David Geffen School of Medicine, Los Angeles, CA, USA F C Breedveld , Department of Rheumatology, Leiden University Medical Centre, Leiden, the Netherlands M H Schiff , Denver Arthritis Clinic, Denver, CO, USA |
AuthorAffiliation_xml | – name: M H Schiff , Denver Arthritis Clinic, Denver, CO, USA – name: G R Burmester , Department of Rheumatology, and Clinical Immunology, Charité Hospital, Berlin, Germany – name: D E Furst , David Geffen School of Medicine, Los Angeles, CA, USA – name: F C Breedveld , Department of Rheumatology, Leiden University Medical Centre, Leiden, the Netherlands – name: M H Weisman , Cedar Sinai Hospital, Los Angeles, CA, USA – name: P Emery , Leeds University, Department of Rheumatology, Leeds General Infirmary, Leeds, UK – name: P L C M van Riel , University Nijmegen Medical Centre, Nijmegen, the Netherlands – name: J S Smolen , Institute of Rheumatology, Clinic for Internal Medicine III, Vienna General Hospital, Vienna, Austria – name: E C Keystone , Department of Rheumatology, Mount Sinai Hospitial, Toronto, Canada – name: M E Weinblatt , Brigham and Women's Hospital, Boston, MA, USA – name: J R Kalden , Department of Internal Medicine III, Institut for Clinical Immunology, University of Erlangen‐Nuremberg, Erlangen Germany |
Author_xml | – sequence: 1 givenname: D E surname: Furst fullname: Furst, D E organization: Cedar Sinai Hospital, Los Angeles, CA, USA – sequence: 2 givenname: F C surname: Breedveld fullname: Breedveld, F C organization: Cedar Sinai Hospital, Los Angeles, CA, USA – sequence: 3 givenname: J R surname: Kalden fullname: Kalden, J R organization: Cedar Sinai Hospital, Los Angeles, CA, USA – sequence: 4 givenname: J S surname: Smolen fullname: Smolen, J S organization: Cedar Sinai Hospital, Los Angeles, CA, USA – sequence: 5 givenname: G R surname: Burmester fullname: Burmester, G R organization: Cedar Sinai Hospital, Los Angeles, CA, USA – sequence: 6 givenname: P surname: Emery fullname: Emery, P organization: Cedar Sinai Hospital, Los Angeles, CA, USA – sequence: 7 givenname: E C surname: Keystone fullname: Keystone, E C organization: Cedar Sinai Hospital, Los Angeles, CA, USA – sequence: 8 givenname: M H surname: Schiff fullname: Schiff, M H organization: Cedar Sinai Hospital, Los Angeles, CA, USA – sequence: 9 givenname: P L C M surname: van Riel fullname: van Riel, P L C M organization: Cedar Sinai Hospital, Los Angeles, CA, USA – sequence: 10 givenname: M E surname: Weinblatt fullname: Weinblatt, M E organization: Cedar Sinai Hospital, Los Angeles, CA, USA – sequence: 11 givenname: M H surname: Weisman fullname: Weisman, M H organization: Cedar Sinai Hospital, Los Angeles, CA, USA |
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Keywords | Rheumatism Treatment Diseases of the osteoarticular system Biological agent |
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Snippet | Additional information has come to light in the past year, both corroborating the major positive effect these drugs have had in rheumatoid arthritis (RA),... |
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SubjectTerms | Abatacept ACR American College of Rheumatology ankylosing spondylitis Antirheumatic Agents - adverse effects Antirheumatic Agents - therapeutic use Arthritis, Psoriatic - drug therapy Arthritis, Rheumatoid - drug therapy Biological and medical sciences CHF Clinical medicine congestive heart failure Consensus Statement DAS Disease Disease Activity Score disease modifying antirheumatic drug Diseases of the osteoarticular system DMARD Drug dosages guideline HAQ-DI Health Assessment Questionnaire disability index Humans IL-1ra immunity Immunization Immunoconjugates - adverse effects Immunoconjugates - therapeutic use Immunologic Factors - adverse effects Immunologic Factors - therapeutic use Infections inflammation Interleukin 1 Receptor Antagonist Protein - adverse effects Interleukin 1 Receptor Antagonist Protein - therapeutic use Medical Outcome Survey Short Form 36 Medical sciences methotrexate Miscellaneous. Osteoarticular involvement in other diseases MTX Pain Patients Pharmaceutical industry PsA psoriatic arthritis Rheumatic diseases Rheumatic Diseases - drug therapy rheumatoid arthritis rituximab SF-36 Spondylitis, Ankylosing - drug therapy Studies TNF TNF blocking TNF inhibitors Tumor Necrosis Factor-alpha - antagonists & inhibitors Tumor necrosis factor-TNF tumour necrosis factor VAS visual analogue scale |
Title | Updated consensus statement on biological agents for the treatment of rheumatic diseases, 2006 |
URI | http://ard.bmj.com/content/65/suppl_3/iii2.full https://api.istex.fr/ark:/67375/NVC-X55P7VJQ-X/fulltext.pdf https://www.ncbi.nlm.nih.gov/pubmed/17038465 https://www.proquest.com/docview/1777852006 https://www.proquest.com/docview/68959068 https://pubmed.ncbi.nlm.nih.gov/PMC1798383 |
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