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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: 1593 • ACR Convergence 2025

    Comparison of rituximab induction and maintenance regimens in ANCA-associated vasculitis: PK/PD modelling approach in real-world patients

    Blaise Pasquiers1, Benoit Blanchet2, Xavier Puéchal3, Xavier Declèves1, Pascal Cohen4, Claire Goulvestre1, Marion Casadevall1, Ines Benhabiles1, Michel Vidal1, David Ternant1, Benjamin Terrier5 and Alicja Puszkiel6, 1Hopital Cochin, Paris, France, 2National Referral Centre for Rare Autoimmune and Systemic Diseases, Hôpital Cochin, Paris, France, 3Department of Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, Hospital Cochin, and Université Paris Cité, Paris ( 75014 ), Ile-de-France, France, 4Department of Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, Hospital Cochin, Paris, France, 5Cochin Hospital, Paris, France, 6Cochin Hospital, Paris

    Background/Purpose: For the treatment of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), rituximab (RTX) may be given as a 4-dose regimen (375 mg/m2 weekly for 4…
  • Abstract Number: 1336 • ACR Convergence 2025

    Effectiveness of new initiators of tofacitinib and other biologic/targeted synthetic DMARDs in patients with rheumatoid arthritis

    Katherine Liao1, Chandrasekar Gopalakrishnan2, Jinoos Yazdany3, Griffith Bell4, Suraj Mothi5, Genevieve Gauthier6, Arne Yndestad7 and Milena Gianfrancesco8, 1Division of Rheumatology, Inflammation, and Immunity, Brigham and Women’s Hospital, Boston, MA, USA, Boston, MA, 2OM1 Inc, Boston, MA, USA, Boston, 3UCSF, San Francisco, CA, 4Pfizer Inc, New York, NY, USA, Boston, MA, 5OM1 Inc, Boston, MA, USA, Boston, MA, 6Pfizer Canada ULC, Kirkland, QC, Canada, Montreal, Canada, 7Pfizer Inc, Oslo, Norway, Oslo, Norway, 8Pfizer Inc, New York, NY, USA, New York, NY

    Background/Purpose: Though the efficacy and safety profile of tofacitinib in RA has been established in prior trials, the effectiveness of tofacitinib in routine care settings…
  • Abstract Number: 1098 • ACR Convergence 2025

    Tolerability of Apremilast: Gastrointestinal Side Effects Dominate While Cardiac Safety Remains Reassuring

    Francisco Arias1, Omar Hamdan2, Asim Khanfar3, Kristel Barturen4 and Roa’a Alshajrawi5, 1University of Texas Rio Grande Valley, McAllen, TX, 2University of Jordan, Az-Zarqa, Jordan, 3Rochester General Hospital, Rochester, NY, 4Universidad San Martin de Porres, McAllen, TX, 5University of Jordan, Amman, 'Amman, Jordan

    Background/Purpose: Apremilast, a PDE-4 inhibitor, is commonly indicated for patients with psoriasis as well as Behçet’s disease. Although this medication is generally well tolerated, numerous…
  • Abstract Number: 2627 • ACR Convergence 2025

    Risk of Adverse Pregnancy Outcomes in Individuals with Rheumatic Diseases Using Prenatal Antirheumatic Drugs: a Population-Based Cohort Study

    Shenthuraan Tharmarajah1, Dharini Mahendira2, Swaleh Hussain1, Howard Berger3, Sara Guilcher4, Lisa McCarthy4 and Mina Tadrous1, 1University of Toronto, Toronto, ON, Canada, 2St Michael's Hospital, Toronto, Canada, 3St. Michael's Hospital, Toronto, Canada, 4University of Toronto, Toronto, Canada

    Background/Purpose: Disease-modifying antirheumatic drugs (DMARDs) are the primary class of drug therapies generally used to treat rheumatic diseases, such as rheumatoid arthritis (RA), systemic lupus…
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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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