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Abstracts tagged "Adverse events"

  • Abstract Number: 2479 • 2012 ACR/ARHP Annual Meeting

    Rheumatoid Arthritis Does Not Increase Risk of Short Term Total Knee Replacement (TKR) Adverse Events (AE)

    Zachary J. LoVerde1, Lisa A. Mandl2, Beverly K. Johnson2, Mark P. Figgie3, Friedrich Boettner4 and Susan M. Goodman2, 1New York Medical College, Valhalla, NY, 2Rheumatology, Hospital for Special Surgery, New York, NY, 3Orthopedics, Hospital for Special Surgery, New York, NY, 4Orthopaedics, Hospital for Special Surgery, New York, NY

    Background/Purpose: TKR is commonly performed for rheumatoid arthritis (RA) and osteoarthritis (OA). Historically, RA patients were at higher risk of post-operative AEs. The purpose of…
  • Abstract Number: 2483 • 2012 ACR/ARHP Annual Meeting

    Folic Acid Pathway Single Neucelotide Polymorphisms Associated with Methotrexate-Related Significant Adverse Events

    Lisa A. Davis1, Brooke Ivan Polk2, Alyse D. Mann3, Roger K. Wolff4, Gail S. Kerr5, Andreas M. Reimold6, Grant W. Cannon7, Ted R. Mikuls8 and Liron Caplan9, 1Div of Rheumatology, Univ of Colorado School of Med, Aurora, CO, 2University of Colorado Medical School, Aurora, CO, 3Research, Denver VA Medical Center, Denver, CO, 4University of Utah, Salt Lake City, UT, 5Rheumatology, Washington DC VAMC, Georgetown and Howard University, Washington, DC, 6Rheumatology, Dallas VA and University of Texas Southwestern, Dallas, TX, 7Division of Rheumatology, George E. Wahlen VA Medical Center, Salt Lake City, UT, 8Omaha VA Medical Center and University of Nebraska Medical Center, Omaha, NE, 9Div of Rheumatology, Denver VA and University of Colorado School of Medicine, Aurora, CO

      Background/Purpose: Methotrexate (MTX) is the cornerstone medication in the treatment of rheumatoid arthritis (RA). While MTX has been associated with a number of adverse…
  • Abstract Number: 2169 • 2012 ACR/ARHP Annual Meeting

    Short to Medium Term Safety of Glucocorticoid Therapy in Rheumatoid Arthritis: A Systematic Review and Dose-Response Analysis of Randomized Controlled Trials

    Simon Tarp1, Daniel Furst2, John R. Kirwan3, Maarten Boers4, Henning Bliddal5, Thasia Woodworth6, Else Marie Bartels7, Bente Danneskiold-Samsoe5, Lars Erik Kristensen8, Steffen Thirstrup9, Mette Rasmussen9, Marian Kaldas10 and Robin Christensen1, 1Musculoskeletal Statistics Unit, The Parker Institute, Department of Rheumatology, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Denmark, 2Div of Rheumatology, UCLA Medical School, Los Angeles, CA, 3Academic Rheumatology Unit, Bristol Royal Infirmary, Bristol, United Kingdom, 4Epidemiology & Biostatistics, VU University Medical Center, Amsterdam, Netherlands, 5Department of Rheumatology, The Parker Institute, Copenhagen University Hospital at Frederiksberg, Copenhagen F, Denmark, 6Leading Edge Clinical Research LLC, Florida, FL, 7Department of Rheumatology, The Parker Institute, Copenhagen University Hospital at Bispebjerg and Frederiksberg, Copenhagen F, Denmark, 8Rheumatology, Skåen University Hospital, Lund University, Lund, Sweden, 9Institute for Pharmacology and Pharmacotherapy, University of Copenhagen, Copenhagen, Denmark, 10David Geffen School of Medicine, University of California in Los Angeles, Los Angeles, CA

    Background/Purpose: Concerns regarding Adverse Effects (AEs) often dominate decisions on applying Glucocorticoid (GC) therapy. Evidence of AEs is mainly based on observational data without proper…
  • Abstract Number: 2158 • 2012 ACR/ARHP Annual Meeting

    Baseline Folate Related Biomarkers in Serum and erythrocytes Are Not Associated with Methotrexate Response and Adverse Events in Rheumatoid Arthritis

    Maurits C.F.J. De Rotte1, Saskia M.F. Pluijm2, Maja Bulatovic3, Johanna M.W. Hazes4 and Robert De Jonge1, 1Clinical Chemistry, Erasmus Medical Center, Rotterdam, Netherlands, 2Public Health, Erasmus Medical center, Rotterdam, Netherlands, 3Department of Paediatric Immunology, University Medical Centre Utrecht, Netherlands, 4Rheumatology, Erasmus MC, Rotterdam, Netherlands

    Background/Purpose: Methotrexate (MTX) is the most commonly used drug in rheumatoid arthritis (RA). 30% of patients fail to respond to the drug or suffer from…
  • Abstract Number: 2161 • 2012 ACR/ARHP Annual Meeting

    Methotrexate Polyglutamate Concentrations in Erythrocytes Are a Potential Tool for Therapeutic Drug Monitoring of Methotrexate Response in Rheumatoid Arthritis

    Maurits C.F.J. De Rotte1, Ethan den Boer2, Maja Bulatovic3, Saskia M.F. Pluijm4, Johanna M.W. Hazes5 and Robert De Jonge1, 1Clinical Chemistry, Erasmus Medical Center, Rotterdam, Netherlands, 2Clinical Chemistry, Erasmus University Hospital, Rotterdam, Netherlands, 3Department of Paediatric Immunology, University Medical Centre Utrecht, Netherlands, 4Public Health, Erasmus Medical center, Rotterdam, Netherlands, 5Rheumatology, Erasmus MC, Rotterdam, Netherlands

    Background/Purpose: Methotrexate (MTX) is the most commonly used drug in rheumatoid arthritis (RA). 30% of patients fail to respond to the drug or suffer from…
  • Abstract Number: 1853 • 2012 ACR/ARHP Annual Meeting

    Rheumatoid Arthritis Patients’ Experiences of Medication Side Effects and Subsequent Decision Making about Medications

    Yomei Shaw1, Ilinca D. Metes2, Susan L. Zickmund3, Dawn McBride2, Kelly A. Reckley2, Stephen R. Wisniewski4, Larry W. Moreland2, Mark S. Roberts1 and Marc C. Levesque2, 1Department of Health Policy and Management, University of Pittsburgh Graduate School of Public Health, Pittsburgh, PA, 2Division of Rheumatology and Clinical Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, 3Division of General Internal Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, 4Epidemiology, University of Pittsburgh, Graduate School of Public Health, Pittsburgh, PA

    Background/Purpose:  Medication adherence in rheumatoid arthritis (RA) patients can be influenced by their previous experiences with medication side effects.  Negative experiences may lead patients to…
  • Abstract Number: 1854 • 2012 ACR/ARHP Annual Meeting

    The Safety of Anti-TNF Biologic Agents in Rheumatoid Arthritis – A Meta-Analysis of 35 RCTs

    Tzuyu Lin1, Tatyana Shamliyan1, Hyon Choi2, Young Hee Rho3 and Karen Kuntz1, 1Division of Health Policy and Management, School of Public Health, University of Minnesota, Minneapolis, MN, 2Section of Rheumatology and the Clinical Epidemiology Unit, Boston University School of Medicine, Boston, MA, 3Clinical Epidemiology Unit, Boston University School of Medicine, Boston, MA

    Background/Purpose: The objectives of this systematic review were to study and update the safety of anti-TNF agents. We examined whether etanercept (ETN), compared to the…
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Embargo Policy

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM CT on October 25. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

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