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Abstracts tagged "comparative effectiveness"

  • Abstract Number: 1160 • ACR Convergence 2020

    Treatment Intensity and Impact on Bone Lesion Evolution and Distribution Patterns in Severe Chronic Recurrent Multifocal Osteomyelitis

    Aleksander Lenert1, T. Shawn Sato2, Sedat G Kandemirli1, Patrick Ten Eyck1 and Polly Ferguson3, 1University of Iowa, Iowa City, IA, 2University of Iowa, Iowa City, 3University of Iowa Carver College of Medicine, Iowa City, IA

    Background/Purpose: To compare bone lesion evolution and bone lesion distribution patterns identified by whole body magnetic resonance imaging (WB-MRI) by treatment intensity in patients with…
  • Abstract Number: 1241 • ACR Convergence 2020

    Patient-Reported Outcomes in Rheumatoid Arthritis Patients Treated with Tofacitinib or Biological DMARDs in Real Life Conditions in Two Latin America Countries

    Hugo Madariaga1, Juan Reyes2, Magda Gutierrez3, Dario Ponce de Leon4, Tatjana Lukic5 and Luisa Amador2, 1Centro Medico CEEN, Arequipa, Arequipa, Peru, 2Pfizer, Bogota, Cundinamarca, Colombia, 3Pfizer, Santiago, Region Metropolitana, Chile, 4PFIZER, LIMA, Peru, 5Pfizer Inc, New York, NY

    Background/Purpose: The objective of this study was to describe the efficacy, safety and patient reported outcomes in Latin-American patients with Rheumatoid Arthritis (RA) treated with…
  • Abstract Number: 1346 • ACR Convergence 2020

    Predicting Major Treatment Response to Tumor Necrosis Factor Inhibitorsin Patients with Ankylosing Spondylitis

    Runsheng Wang1, Abhijit Dasgupta2 and Michael Ward3, 1Columbia University Irving Medical Center, Division of Rheumatology, New York, NY, 2NIAMS, Bethesda, 3National Institutes of Health, Bethesda, MD

    Background/Purpose: The treatment response to tumor necrosis factor inhibitors (TNFi) in patients with active ankylosing spondylitis (AS) is heterogeneous.  In clinical practice, both patients and…
  • Abstract Number: 1351 • ACR Convergence 2020

    Efficacy of Ixekizumab versus Adalimumab in Psoriatic Arthritis (PsA) Patients with and Without Moderate-to-severe Psoriasis: 52-week Results from a Multicentre, Randomised Open-label Study

    Lars Erik Kristensen1, Masato Okada2, William Tillett3, Soyi Liu-Leage4, Celine El Baou5, Andrew Bradley5, Gabriella Meszaros4 and Kurt de Vlam6, 1The Parker Institute Copenhagen Denmark, Copenhagen, Denmark, Bispebjerg and Frederiksberg, Denmark, 2St. Luke's International University, Tokyo, Japan, Chuo-ku, Tokyo, Japan, 3Royal National Hospital for Rheumatic Diseases, Bath, UK; Department of Pharmacy and Pharmacology, University of Bath, Bath, UK, Bath, United Kingdom, 4Eli Lilly and Company, Indianapolis, IN, 5Eli Lilly and Company, Indianapolis, IN, USA, Indianapolis, IN, 6Department of Rheumatology, University of Leuven, Belgium, Leuven, Belgium

    Background/Purpose: Ixekizumab (IXE), a selective interleukin-17A antagonist, is approved for the treatment of active PsA, moderate-to-severe psoriasis (PsO), and radiographic/non-radiographic axial SpA in adults. The…
  • Abstract Number: 1492 • ACR Convergence 2020

    The Childhood Arthritis and Rheumatology Research Alliance Start Time Optimization of Biologic Therapy in Polyarticular JIA Study: Report of Primary Study Outcomes

    Yukiko Kimura1, George Tomlinson2, Laura Schanberg3, Mary Ellen Riordan4, Anne Dennos5, Vincent Del Gaizo6, Katherine Murphy7, Pamela F. Weiss8, Brian Feldman9 and Sarah Ringold10, 1Hackensack Meridian School of Medicine, Hackensack, NJ, 2Department of Medicine, University Hospital Network, Toronto, Toronto, ON, Canada, 3Duke University Medical Center, Durham, NC, 4Hackensack University Medical Center, Westwood, NJ, 5Duke University, Durham, NC, 6Childhood Arthritis & Rheumatology Research Alliance (CARRA), Whitehouse Station, NJ, 7Lousiana Department of Public Health, New Orleans, LA, 8Children's Hospital of Philadelphia, Philadelphia, 9The Hospital for Sick Children, Toronto, ON, Canada, 10Seattle Children's, Seattle, WA

    Background/Purpose: There is uncertainty regarding when to start biologic medications for polyarticular juvenile idiopathic arthritis (P-JIA). The Childhood Arthritis and Rheumatology Research Alliance (CARRA) developed…
  • Abstract Number: 2067 • 2019 ACR/ARP Annual Meeting

    Comparison of Medication New User Definitions in Multi-Specialty EMR Data

    Jeffrey Curtis1, Lang Chen 1, Narender Annapureddy 2, Cassie Clinton 1, Megan Clowse 3, Millie Long 4, W. Benjamin Nowell 5, Jim Oates 6, Rennie Rhee 7, Siddarth Singh 8, Fenglong Xie 9 and Timothy Beukelman 10, 1University of Alabama at Birmingham, Birmingham, AL, 2Vanderbilt University, Nashville, TN, 3Duke University, Durham, 4University of North Carolina Chapel Hill, Chapel Hill, NC, 5Global Healthy Living Foundation, Upper Nyack, NY, 6Division of Rheumatology & Immunology/Medical University of South Carolina, Charleston, SC, 7University of Pennsylvania, Division of Rheumatology, Philadelphia, PA, 8University California, San Diego, San Diego, 9University of Alabama at Birmingham, Birmingham, 10University of Alabama Birmingham, Birmingham, AL

    Background/Purpose: New user designs are typically preferred in pharmacoepidemiology to avoid bias. The optimal implementation of a new user design in electronic medical record (EMR)…
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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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