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Abstracts tagged "Pharmacoepidemiology"

  • Abstract Number: 2087 • ACR Convergence 2025

    Does Carbamazepine Impact Risk of Developing Osteoarthritis? Results of a Real-World Data Analysis

    Erfan Afshar1 and Andrew Long2, 1VCUSOM, Richmond, VA, 2Virginia Commonwealth University Health System, Midlothian, VA

    Background/Purpose: Carbamazepine has shown chondroprotective effects in OA animal models by modulating Nav1.7 channels. This study aimed to examine the association between Carbamazepine use and…
  • Abstract Number: 0478 • ACR Convergence 2025

    Racial and Ethnic Disparities in DMARD Use and in Medicare Part B-Covered Options Among Medicare Beneficiaries with Late-Onset Rheumatoid Arthritis

    ashkan ara1, John FitzGerald2 and Susan Ettner2, 1UCLA Health, Los Angeles, CA, 2UCLA, Los Angeles, CA

    Background/Purpose: Biologic and targeted synthetic DMARDs can substantially improve the quality of life for Medicare beneficiaries with rheumatoid arthritis (RA). However, racial and ethnic disparities…
  • Abstract Number: 2008 • ACR Convergence 2025

    Exposure to Anaerobic Antibiotics and Risk of Gout Flares: Target Trial Emulation for the Potential Role of the Gut Microbiome in Gout and Chronic Kidney Disease (CKD)

    Natalie McCormick1, Sharan Rai2, Chio Yokose3, leo lu4, Robert Terkeltaub5, Lama Nazzal6, Huilin Li6, Dylan Dodd7 and Hyon K. Choi8, 1Massachusetts General Hospital, Boston, MA, 2Massachusetts General Hospital/Harvard Medical School, Boston, MA, 3Massachusetts General Hospital, Waltham, MA, 4Arthritis Research Canada, Vancouver, BC, Canada, 5Retired, San Diego, CA, 6NYU Langone, New York, NY, 7Stanford University, Palo Alto, CA, 8MASSACHUSETTS GENERAL HOSPITAL, Lexington, MA

    Background/Purpose: As reported in Cell Press journals,1,2 intestinal commensal purine-degrading bacteria anaerobically degrade urate to anti-inflammatory short chain fatty acids, including butyrate, and thus may…
  • Abstract Number: 0267 • ACR Convergence 2025

    Pharmacosurvellience study of FDA Adverse Event Reporting System (FAERS) events of Secukinumab and Guselkumab

    NUR BARLAS1, Sait Barlas1 and Emre Adalier2, 1Florida State University College of Medicine, Cape Coral, 2University of Pavia School of Medicine & Surgery, Pavia, Italy

    Background/Purpose: Interleukin-17 (IL-17) and interleukin-23 (IL-23) inhibitors have revolutionized treatment for psoriatic arthritis, axial spondyloarthritis, and moderate-to-severe plaque psoriasis. IL-17 inhibitors block the pro-inflammatory cytokine…
  • Abstract Number: 2003 • ACR Convergence 2025

    Evaluating Patient Outcomes Pre and Post Pegloticase Initiation among Uncontrolled Gout Patients: Findings from MORE2 Registry and Medicare Fee-For-Service Claims Data

    Julia Buchfuhrer1, Niranjan Kathe2, Elizabeth Ibiloye3, Seth Kuranz4, Virginia Noxon-Wood4, Alexis Woods5 and Laurence Gozalo4, 1JB Arthritis and Rheumatology Center, Downey, CA, 2Amgen Inc, San Diego, CA, 3Amgen Inc, Thousand Oaks, CA, 4Inovalon, Bowie, MD, 5Amgen, Detroit, MI

    Background/Purpose: Among patients (pts) with chronic refractory gout (CRG), traditional urate lowering therapies are often inadequate, necessitating advanced therapies. Pegloticase, a recombinant uricase enzyme, rapidly…
  • Abstract Number: 0247 • ACR Convergence 2025

    Use of Nintedanib in Patients with Progressive Pulmonary Fibrosis

    Elizabeth Volkmann1, Steven Nathan2, Karen Coeytaux3, Yanni Fan4, Jill Curran3, Haikun Bao3, Kamila Sroka-Saidi5, Ann Chauffe6 and Jeffrey J Swigris7, 1Division of Rheumatology, Department of Medicine, University of California, David Geffen School of Medicine, Los Angeles, CA, USA, Los Angeles, CA, 2Inova Advanced Lung Disease and Transplant Program, Falls Church, VA, USA, Falls Church, 3Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT, USA, Ridgefield, 4Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT, USA, Ridgefield, CT, 5Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany, Ingelheim am Rhein, Germany, 6Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT, USA, Newberry, FL, 7Center for Interstitial Lung Disease, Division of Pulmonary, Critical Care and Sleep Medicine, National Jewish Health, Denver, CO, USA, Denver

    Background/Purpose: Nintedanib was approved in the US for the treatment of chronic fibrosing interstitial lung diseases (ILDs) with a progressive phenotype (progressive pulmonary fibrosis [PPF])…
  • Abstract Number: 1926 • ACR Convergence 2025

    Real World  Rate of Efficacy of Adalimumab Biosimilars Following a Mandated Switch in an Academic Medical Center

    Katharine McCarthy, viktoriya avlasevich and Darren Tabechian, URMC, Rochester, NY

    Background/Purpose: The proliferation of similar biotherapeutic products (biosimilars) has helped to reduce the cost burden of biologic therapies for health care systems1. Multiple studies have…
  • Abstract Number: 0165 • ACR Convergence 2025

    Per-Protocol Analysis of the Effectiveness of GLP1 Agonists Against SGLT2 Inhibitors on Osteoarthritis Outcomes

    Nene Ukonu1, David Felson2, Michael LaValley3 and S. Reza Jafarzadeh4, 1Boston University School of Public Health, Boston, MA, 2Boston University, Boston, MA, 3Boston University School of Public Health, Arlington, MA, 4Boston University Chobanian & Avedisian School of Medicine, Boston, MA

    Background/Purpose: Anti-diabetic medications often have effects on other conditions. GLP1 agonists (GLP1a) have shown protective effects on OA outcomes in trials and short-term trial emulations,…
  • Abstract Number: 1895 • ACR Convergence 2025

    Assessing the Validity of Self-Reported Medication Data Through Metabolite Analysis: Data from the Osteoarthritis Initiative

    Kate Lapane1, Anne Hume2, Jeffrey Driban3, Shao-Hsien Liu1, Timothy McAlington4, Charles Eaton5, Shike Xu6 and Bing Lu7, 1UMass Chan Medical School, Worcester, MA, 2College of Pharmacy, University of Rhode Island, Kingston, RI, 3University of Massachusetts Chan Medical School, Marlborough, NH, 4UMass Chan School of Medicine, Arlington, MA, 5Brown University, Pawtucket, RI, 6University of Connecticut Health Center, Farmington, CT, 7UConn Health Center, Newton, MA

    Background/Purpose: Pharmacotherapy, including non-steroidal anti-inflammatory agents (NSAIDs), is commonly used to alleviate symptoms of osteoarthritis (OA); however, these medications may increase the risk of adverse…
  • Abstract Number: 1657 • ACR Convergence 2025

    Extracting TNF Inhibitor Switching Reasons and Trajectories From Real-World Data Using Large Language Models

    Brenda Miao1, Marie Binvignat2, Augusto Garcia-Agundez3, Maxim Bravo4, Christopher Williams5, Claire Miao4, Ahmed Alaa6, Vivek Rudrapatna5, gabriela Schmajuk7 and Jinoos Yazdany3, 1UCSF, Fremont, CA, 2Sorbonne University, Paris, France, 3UCSF, San Francisco, CA, 4UC Berkeley, San Francisco, 5UCSF, San Francisco, 6UC Berkeley, Berkeley, 7University of California, San Francisco, and San Francisco Veterans Affairs Medical Center, San Francisco, CA

    Background/Purpose: Tumor necrosis factor inhibitors (TNFi) are cornerstones of autoimmune‑disease therapy, yet many patients switch agents because of loss of effectiveness, adverse events, or insurance…
  • Abstract Number: 1656 • ACR Convergence 2025

    Risk of Serious Infection associated with non-TNF biologic initiation after Anti-TNF Use in Older Adults with Rheumatoid Arthritis

    Jiha Lee1, Sofia Pedro2 and Kaleb Michaud3, 1University of Michigan, Ann Arbor, 2Forward, The National Databank for Rheumatic Diseases, Wichita, KS, 3University of Nebraska Medical Center, Omaha, NE

    Background/Purpose: In older adults with rheumatoid arthritis (RA), anti-TNF therapies are typically used as first-line biologic treatment. However, many patients require a switch to non-TNF…
  • Abstract Number: 0989 • ACR Convergence 2024

    Malignancy Risk Between JAK Inhibitors and Anti-TNF Therapy Across Disease Indications: A Bayesian Network Meta-analysis

    Mark Gibson1, Benjamin Zuckerman2, Maryam Adas1, Mark Russell3, Katie Bechman1 and James Galloway4, 1King's College London, London, United Kingdom, 2King's College London, London, England, United Kingdom, 3King's College London, London, United Kingdom, 4Centre for Rheumatic Diseases, King's College London, London, United Kingdom

    Background/Purpose: To estimate the relative risk of malignancy between Janus kinase inhibitors (JAKi), tumour necrosis factor-α inhibitors (TNFi) and placebo in individuals with immune-mediated inflammatory…
  • Abstract Number: 2479 • ACR Convergence 2024

    Mepolizumab Treatment Decreased Oral Corticosteroid Use and Improved Clinical Response, Control Status, and Remission in Patients with Eosinophilic Granulomatosis with Polyangiitis: Results up to 24 Months from a Large Network of US Allergy Practices

    Michael E Wechsler1, Anna Kovalszki2, Jared Silver3, Brian Stone4, Lior Seluk5, Lynn Huynh6, Wilson da Costa Junior6, Mingchen Ye6, Jeremiah Hwee7, Mei Sheng Duh6, William McCann4 and Amy G. Edgecomb8, 1Department of Medicine, National Jewish Health, Denver, CO, 2Division of Allergy and Clinical Immunology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, 3US Medical Affairs - Respiratory, GSK, Durham, 4Allergy Partners, Asheville, NC, 5Division of Pulmonary, Critical Care and Sleep Medicine, National Jewish Health, Denver, 6Analysis Group, Boston, MA, 7Value Evidence and Outcomes, GSK, Mississauga, Canada, 8US Value, Evidence, & Outcomes, Anti-Infectives and Respiratory, GSK, Philadelphia

    Background/Purpose: Eosinophilic granulomatosis with polyangiitis (EGPA) is a severe rare systemic inflammatory disease characterized by elevated blood eosinophil counts ≥1000 cells/µL and vasculitis of small-…
  • Abstract Number: 1005 • ACR Convergence 2024

    Pharmacosurvellience Study of FDA Adverse Event Reporting System (FAERS) Events of Tofacitinib and Upadacitinib

    Nur Barlas, Sait Barlas, Stefan Milutinovic and Shristi Basnyat, Florida State University College of Medicine Internal Medicine Residency Program at Lee Health, Cape Coral

    Background/Purpose: Janus Kinase (JAK) inhibitors are the agents of choice for the treatment of rheumatoid arthritis, psoriatic arthritis, and ankylosing spondylitis when other DMARDs are…
  • Abstract Number: 2566 • ACR Convergence 2024

    Detrimental Effects of Proton Pump Inhibitors on Bone Mineral Density Are Not Mediated by Changes in Serum Calcium or Parathyroid Hormone in Patients with Inflammatory Rheumatic Diseases: A Cross-sectional Study

    andriko Palmowski1, Zhivana Boydzhieva2, Paula Hoff3, Sandra Hermann3, burkhard Muche3, David Simon4, Gerhard Krönke3, Edgar Wiebe5 and FRANK HARTMUT DR. BUTTGEREIT5, 1Charité - Universittsmedizin Berlin, Berlin, Germany, 2Charité Universittsmedizin, Berlin, Germany, 3Rheumatology, Charité, Berlin, Germany, 4Department of Rheumatology and Clinical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany/ Department of Internal Medicine 3, University of Erlangen-Nuremberg and Universitätsklinikum Erlangen, Erlangen, Germany/Deutsches Zentrum für Immuntherapie (DZI), University of Erlangen-Nuremberg and Universitätsklinikum Erlangen, Erlangen, Germany, Berlin, Germany, 5Charité University Medicine Berlin, Berlin, Germany

    Background/Purpose: In a previous study, we found daily proton pump inhibitor (PPI) intake to be associated with decreased bone mineral density in patients with inflammatory…
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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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