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Abstracts tagged "DMARDs"

  • Abstract Number: 1713 • 2013 ACR/ARHP Annual Meeting

    Disparity In Biologic Therapy In Ethnic Minorities With Rheumatoid Arthritis: Can It All Be Due To Lack Of Access To Drug?

    Gail S. Kerr1, Ted R. Mikuls2, Christopher J. Swearingen3, Chunqiao Luo4 and Yusuf Yazici5, 1Rheumatology, Washington DC VAMC, Georgetown and Howard University, Washington, DC, 2Omaha VA Medical Center and University of Nebraska Medical Center, Omaha, NE, 3Pediatric Biostatistics, University of Arkansas for Medical Sciences, Little Rock, AR, 4Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, AR, 5Department of Medicine, Division of Rheumatology, New York University School of Medicine, New York, NY

    Background/Purpose: Ethnic disparities in the administration of DMARDs exist, but the impact of differing health care systems on access in ethnic minorities treated by rheumatologists,…
  • Abstract Number: 442 • 2013 ACR/ARHP Annual Meeting

    Tolerability and Non-Serious Adverse Events In Rheumatoid Arthritis Patients Treated With Tofacitinib As Monotherapy Or In Combination Therapy

    A. Dikranian1, K. Soma2, R. Riese2, D. Gruben2 and T. V. Jones3, 1San Diego Arthritis Medical Clinic, San Diego, CA, 2Pfizer Inc, Groton, CT, 3Pfizer Inc, Collegeville, PA

    Background/Purpose: Tofacitinib is a novel, oral Janus kinase (JAK) inhibitor for the treatment of rheumatoid arthritis (RA). Tolerability remains an ill-defined construct in clinical trials.…
  • Abstract Number: 1693 • 2013 ACR/ARHP Annual Meeting

    Initial Triple DMARD Therapy Is More Efficient Than Methotrexate Monotherapy In Recent Onset Rheumatoid Arthritis; 1-Year Data Of a Randomized Clinical Trial (tREACH)

    P.H.P. de Jong1, J.M.W. Hazes2, K.H. Han3, A.M. Huisman4, D. van Zeben5, P.A. van der Lubbe6, A.H. Gerards6, B. van Schaeybroeck7, P.B. de Sonnaville8, M.V. Krugten9, J.J. Luime2 and A.E.A.M. Weel3, 1Department of Rheumatology, Erasmus University Medical Center, Rotterdam, Netherlands, 2Rheumatology, Erasmus University Medical Center, Rotterdam, Netherlands, 3Rheumatology, Maasstad Hospital, Rotterdam, Netherlands, 4Rheumatology, Sint Franciscus Gasthuis, Rotterdam, Netherlands, 5Department of Rheumatology, Sint Franciscus Gasthuis, Rotterdam, Netherlands, 6Department of Rheumatology, Vlietland Hospital, Schiedam, Netherlands, 7Rheumatology, Albert Schweitzer Hospital, Dordrecht, Netherlands, 8Department of Rheumatology, Admiraal de Ruyter hospital, Goes, Netherlands, 9Department of Rheumatology, Admiraal de Ruyter Hospital, Vlissingen, Netherlands

    Background/Purpose: Recommended treatment for DMARD naïve patients is methotrexate (MTX) with or without glucocorticoids (GCs). Triple DMARD therapy however is not recommended, because well proven…
  • Abstract Number: 443 • 2013 ACR/ARHP Annual Meeting

    Efficacy and Safety Analyses Of Tofacitinib From Pooled Phase 2, Phase 3 and Long-Term Extension Rheumatoid Arthritis Studies: US Compared With Non-US Populations

    S. B. Cohen1, Roy Fleischmann1, J. M. Kremer2, A. Koenig3, K. Kwok4, L. Wang5, C. a. Mebus5, R. Riese5 and T. Robinson3, 1Metroplex Clinical Research Center, Dallas, TX, 2Albany Medical College and The Center for Rheumatology, Albany, NY, 3Pfizer Inc, Collegeville, PA, 4Pfizer Inc, New York, NY, 5Pfizer Inc, Groton, CT

    Background/Purpose: Tofacitinib is an oral Janus kinase inhibitor approved in the US for the treatment of rheumatoid arthritis at 5 mg BID. Phase (P) 3…
  • Abstract Number: 1458 • 2013 ACR/ARHP Annual Meeting

    Rates Of Switching and Healthcare Costs Associated With Switching Biologic Disease-Modifying Antirheumatic Drugs In a Commercial Population: Evidence From Real-World Observational Studies

    A Nadkarni, F Lobo and T Juday, Bristol-Myers Squibb, Plainsboro, NJ

    Background/Purpose: Several biologic disease-modifying antirheumatic drugs (bDMARDs) are approved for the treatment of moderate-to-severe RA. Switching between bDMARD therapies is common in real-world settings, and…
  • Abstract Number: 437 • 2013 ACR/ARHP Annual Meeting

    Patterns Of Use Of Oral and Subcutaneous Methotrexate Use In Rheumatoid Arthritis Patients Enrolled In The U.S. Medicare Program

    Jeffrey R. Curtis1, Fenglong Xie2, Jie Zhang1, Lang Chen3, Huifeng Yun4, Michael H. Schiff5, David Mackey6 and Seth Ginsberg7, 1Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 2Rheumatology & Immunology, University of Alabama at Birmingham, Birmingham, AL, 3Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 4Epidemiology, University of Alabama at Birmingham, Birmingham, AL, 5Rheumatology Division, University of Colorado, Denver, CO, 6Clinical Immunology/Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 7Creaky Joints, New York, NY

    Background/Purpose: Although methotrexate (MTX) is the cornerstone of RA treatment, use of oral and subcutaneous (SC) preparations in real-world settings is not well characterized. Methods:…
  • Abstract Number: 1418 • 2013 ACR/ARHP Annual Meeting

    Effects Of Smoking Status On Response To Treatment With Tofacitinib In Patients With Rheumatoid Arthritis

    J. M. Kremer1, J. D. Greenberg2, C. Turesson3, D. Gruben4, C. A. Mebus4, E. Bananis5 and T. Robinson6, 1Albany Medical College and The Center for Rheumatology, Albany, NY, 2Rheumatology, NYU Hospital for Joint Diseases, New York, NY, 3Lund University, Malmö, Sweden, 4Pfizer Inc, Groton, CT, 5Specialty Care, Pfizer Inc, Collegeville, PA, 6Pfizer Inc, Collegeville, PA

    Background/Purpose: Cigarette smoking is a known risk factor for developing rheumatoid arthritis (RA).1 Several recent observational studies suggest that cigarette smoking may be associated with…
  • Abstract Number: 361 • 2013 ACR/ARHP Annual Meeting

    Risk Of Venous Thromboembolism and Use Of Disease-Modifying Antirheumatic Drugs For Rheumatoid Arthritis

    Seoyoung C. Kim1, Daniel H. Solomon2,3, Jun Liu4, Jessica M. Franklin5, Robert J. Glynn6 and Sebastian Schneeweiss7, 1Div. of Pharmacoepidemiology and Pharmacoeconomics, Div. of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, MA, 2Division of Pharmacoepidemiology, Harvard Medical School, Brigham and Women's Hospital, Division of Rheumatology, Division of Pharmacoepidemiology, Boston, MA, 3Division of Rheumatology, Brigham and Women's Hospital, Boston, MA, 4Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital, Harvard Medical School, Boston, Boston, MA, 5Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital, Boston, MA, 6Brigham and Women's Hospital, Boston, MA, 7Division of Pharmacoepidemiology, Brigham and Women's Hospital, Boston, MA

    Background/Purpose: Recent research suggests that rheumatoid arthritis (RA), an autoimmune systemic inflammatory disease, increases the risk of venous thromboembolism (VTE) including pulmonary embolism and deep…
  • Abstract Number: 198 • 2013 ACR/ARHP Annual Meeting

    Accuracy Of International Classification Of Diseases (Ninth Revision) Coding For Rheumatoid Arthritis In The Primary Care Setting

    Sheena Ogando1, Karolina M. Weiss1 and Harry D. Fischer2, 1Department of Medicine, Albert Einstein College of Medicine at Beth Israel Medical Center, New York, NY, 2Division of Rheumatology, Albert Einstein College of Medicine at Beth Israel Medical Center, New York, NY

    Background/Purpose: Current quality measures are diagnosis driven and focus on management.  For rheumatoid arthritis (RA), the Physician Quality Reporting System requires that a disease modifying…
  • Abstract Number: 1355 • 2013 ACR/ARHP Annual Meeting

    Subcutaneous Administration Of Methotrexate With a Prefilled Autoinjector Pen Results In a Higher Relative Bioavailability Compared To Oral Administration Of Methotrexate

    Uwe Pichlmeier and Kay-Uwe Heuer, medac GmbH, Wedel, Germany

    Background/Purpose: Methotrexate (MTX) is commonly used in the treatment of RA, psoriasis, and psoriatic arthritis. Subcutaneously administered MTX is well absorbed and appears to overcome…
  • Abstract Number: 378 • 2013 ACR/ARHP Annual Meeting

    HBV Reactivation and Consequent Hepatitis In Rheumatoid Arthritis Patients With Different HBV Carring State: A Clinical Observation Follow-Up

    Lie Dai, An Qi Liang, Ying Qian Mo, Jian Da Ma, Le Feng Chen, Dong Hui Zheng and Lang Jing Zhu, Division of Rheumatology, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, China

    Background/Purpose: Approximate 7.2% Chinese were infected with hepatitis B virus (HBV), and the prevalence of concurrent HBV carriers in Chinese rheumatoid arthritis (RA) patients was…
  • Abstract Number: 173 • 2013 ACR/ARHP Annual Meeting

    HLA-DRB1*08:02 Is Associated With Bucillamine-Induced Proteinuria In Japanese Rheumatoid Arthritis Patients: A Case-Control Study

    Hiroshi Furukawa1, Shomi Oka1, Kota Shimada2, Shoji Sugii2, Atsushi Hashimoto3, Akiko Komiya1, Naoshi Fukui1, Taiichiro Miyashita4, Kiyoshi Migita4, Akiko Suda5, Shouhei Nagaoka6, Naoyuki Tsuchiya7 and Shigeto Tohma1, 1Clinical Research Center for Allergy and Rheumatology, Sagamihara Hospital, National Hospital Organization, Sagamihara, Japan, 2Department of Rheumatic Diseases, Tokyo Metropolitan Tama Medical Center, Tokyo, Japan, 3Department of Rheumatology, Sagamihara Hospital, National Hospital Organization, Sagamihara, Japan, 4Clinical Research Center, Nagasaki Medical Center, National Hospital Organization, Omura, Japan, 5Center for Rheumatic Diseases, Yokohama City University Medical Center, Yokohama, Japan, 6Department of Rheumatology, Yokohama Minami Kyousai Hospital, Yokohama, Japan, 7Molecular and Genetic Epidemiology Laboratory, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

    Background/Purpose: Bucillamine (Buc) is one of the commonly used disease-modifying anti-rheumatic drugs (DMARDs) in Japan. Drug-induced proteinuria can occur in rheumatoid arthritis (RA) patients treated…
  • Abstract Number: 1354 • 2013 ACR/ARHP Annual Meeting

    Successful Self-Administration Of Methotrexate In Rheumatoid Arthritis Patients Using a Prefilled Autoinjector Pen

    Jaime Pachon1, Alan Kivitz2, Kay-Uwe Heuer3 and Uwe Pichlmeier3, 1Arthritis and Rheumatic Care Center, Miami Research Associates, South Miami, FL, 2Altoona Center for Clinical Research, Duncansville, PA, 3medac GmbH, Wedel, Germany

    Background/Purpose:  Methotrexate (MTX) is the most commonly used and recommended DMARD for the treatment of RA. SC administered MTX is well absorbed and appears to…
  • Abstract Number: 349 • 2013 ACR/ARHP Annual Meeting

    Serum CTX-I Predicts Systemic Bone Loss At The Hip Over 1 Year In Patients With Early Psoriatic Arthritis

    Agnes Szentpetery1, Mark Kilbane2, Myra P. O'Keane2, Muhammad Haroon3, Phil Gallagher4, Susan van der Kamp5, Malachi McMenna6 and Oliver FitzGerald3, 1Rheumatology, Dublin Academic Medical Centre, St. Vincent's University Hospital, Dublin, Ireland, 2Metabolism Laboratory, Dublin Academic Medical Centre, St. Vincent's University Hospital, Dublin, Ireland, 3Department of Rheumatology, Dublin Academic Medical Centre, St. Vincent's University Hospital, Dublin, Ireland, 4Rheumatology, St. Vincent's University Hospital, Dublin, Ireland, 5DXA Unit, Dublin Academic Medical Centre, St. Vincent's University Hospital, Dublin, Ireland, 6Department of Endocrinology & Metabolic Bone Disease, Dublin Academic Medical Centre, St. Vincent's University Hospital, Dublin, Ireland

    Background/Purpose: There is a growing interest in bone and cartilage biomarkers that could be used predicting and assessing changes in structural damage in inflammatory arthritis.…
  • Abstract Number: 2683 • 2013 ACR/ARHP Annual Meeting

    Application Of a Multi-Biomarker Disease Activity (Vectra® DA) Score For Assessing Rheumatoid Arthritis Patients With Fibromyalgia Or Low C-Reactive Protein

    Yvonne C. Lee1, James Hackett2, Claire Alexander3, Michelle A. Frits1, Christine K. Iannaccone1, Nancy A. Shadick4, Michael E. Weinblatt5, Oscar Segurado6 and Eric H. Sasso6, 1Department of Medicine, Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, MA, 2Hackett & Associates, Inc., San Diego, CA, 3Clinical Operations, Crescendo Bioscience Inc., South San Francisco, CA, 4Rheumatology/Immunology, Brigham and Women's Hospital, Boston, MA, 5Division of Rheumatology & Immunology, Brigham and Women's Hospital, Boston, MA, 6Crescendo Bioscience Inc., South San Francisco, CA

    Background/Purpose: Clinical assessment of rheumatoid arthritis (RA) may be challenging if patients have fibromyalgia (FM) or if C-reactive protein (CRP) is low (£1 mg/dL). A…
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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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