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  • Abstract Number: 200 • 2016 ACR/ARHP Annual Meeting

    The Safety and Efficacy of Benzbromarone in Gout in Aotearoa New Zealand

    Lisa K. Stamp1, Janine Haslett1, Christopher Frampton1, Doug White2, David Gardner3, Simon Stebbings4, Guy Taylor5, Rebecca Grainger6, Rajesh Kumar7, Sunil Kumar8, Tracey Kain9, David Porter10, Michael Corkill11, Angela Cathro12, Scott Metcalfe12, John Wyeth12 and Nicola Dalbeth13, 1University of Otago, Christchurch, New Zealand, 2Waikato Hospital, Hamilton, New Zealand, 3Hawkes Bay DHB, Napier, New Zealand, 4Department of Medicine, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand, 5Whanganui Hospital, Whanganui, New Zealand, 6Wellington Regional Rheumatology Unit, Hutt Valley District Health Board, Lower Hutt, New Zealand, 7Taranaki Hospital, New Plymouth, New Zealand, 8Middlemore Hospital, Auckland, New Zealand, 9Tauranga Hospital, Tauranga Hospital, Tauranga, New Zealand, 10Porter Rheumatology Ltd, The Collingwood Centre, Nelson, New Zealand, 11North Shore Hospital, Auckland, New Zealand, 12Pharmaceutical Management Agency, Wellington, New Zealand, 13Department of Medicine, University of Auckland, Auckland, New Zealand

    Background/Purpose: Benzbromarone is a potent uricosuric, but is not widely available due to concerns about hepatotoxicity. In Aotearoa New Zealand benzbromarone has been available since…
  • Abstract Number: 201 • 2016 ACR/ARHP Annual Meeting

    Allopurinol Reduces the Risk of Myocardial Infarction (MI) in the Elderly: A Study of Medicare Claims

    Jasvinder A. Singh1 and Shaohua Yu2, 1Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 2University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose: To assess whether allopurinol use reduces the risk of myocardial infarction (MI) in the elderly. Methods: We used the 2006-2012 5% random sample of…
  • Abstract Number: 202 • 2016 ACR/ARHP Annual Meeting

    Allopurinol Use and the Risk of Ventricular Tachycardia in the US Elderly: A Study of Medicare Claims Data

    Jasvinder A. Singh1 and John Cleveland2, 1Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 2Rheumatology, University of Alabama at Birmingham (UAB), Birmingham, AL

    Background/Purpose: To assess whether allopurinol use reduces the risk of ventricular tachycardia in the elderly. Methods: We used the 2006-2012 5% random sample of Medicare…
  • Abstract Number: 203 • 2016 ACR/ARHP Annual Meeting

    Allopurinol Dose Escalation and Mortality Among Patients with Gout: A National Propensity-Matched Cohort Study

    Brian W Coburn1,2, Kaleb Michaud3, Debra A Bergman2 and Ted R Mikuls4,5, 1Research Service, Veterans Affairs Nebraska-Western Iowa Health Care System, Omaha, NE, 2Division of Rheumatology, University of Nebraska Medical Center, Omaha, NE, 3Internal Medicine, University of Nebraska Medical Center, Omaha, NE, 4Veteran Affairs Nebraska-Western Iowa Health Care System and University of Nebraska Medical Center, Omaha, NE, 5Internal Medicine, Division of Rheumatology, University of Nebraska Medical Center, Omaha, NE

    Allopurinol Dose Escalation and Mortality among Patients with Gout: A National Propensity-Matched Cohort Study  Background/Purpose: Numerous epidemiologic studies show that hyperuricemia and gout are associated…
  • Abstract Number: 204 • 2016 ACR/ARHP Annual Meeting

    The Safety and Efficacy of Allopurinol Dose Escalation in People with Gout, a Randomised Controlled Trial

    Lisa K. Stamp1, Peter T. Chapman2, Murray Barclay3, Anne Horne4, Christopher Frampton1, Paul Tan5, Jill Drake6 and Nicola Dalbeth5, 1University of Otago, Christchurch, New Zealand, 2Christchurch Hospital, Christchurch, New Zealand, 3Medicine, University of Otago, Christchurch, New Zealand, 4Department of Medicine, University of Auckland, Auckland, New Zealand, 5University of Auckland, Auckland, New Zealand, 6Rheumatology, Immunology and Allergy, Christchurch Hospital, Christchurch, New Zealand

    Background/Purpose: Allopurinol is the most widely used urate lowering therapy. Many patients on allopurinol fail to achieve target serum urate (SU), in part due to…
  • Abstract Number: 205 • 2016 ACR/ARHP Annual Meeting

    Serum Uric Acid Lowering Treatment Appears Unnecessary during Hemodialysis

    Raquel Soriano1, Mariano Andrés1, Eloy Oliveira2, Celia Trigo2, Eliseo Pascual3 and María Dolores Arenas4, 1Departamento de Medicina Clínica, Universidad Miguel Hernández, Alicante, Spain, 2Servicio de Análisis Clínicos, Hospital General Universitario de Alicante, Alicante, Spain, 3Departamento de Medicina Clínica, Emeritus Professor, Universidad Miguel Hernández, Alicante, Spain, 4Unidad de Nefrología, Hospital Vithas Perpetuo Socorro, Alicante, Spain

    Background/Purpose: Gout patients often suffer from renal disease, some ultimately developing end-stage renal disease (ESRD) and requiring hemodialysis (HD) replacement therapy. Though some reports suggested…
  • Abstract Number: 206 • 2016 ACR/ARHP Annual Meeting

    Renal Safety of Lesinurad: A Pooled Analysis of Phase III and Extension Studies

    Robert Terkeltaub1, Raymond Malamet2, Kathleen Bos2, Jingyi Li2, David Goldfarb3, Michael Pillinger4, Diana Jalal5, Jia Hu6 and Kenneth Saag7, 1Rheumatology, VA Medical Center, San Diego, CA, 2AstraZeneca Pharmaceuticals, Wilmington, DE, 3New York University School of Medicine, New York, NY, USA, New York, NY, 4Medicine/Rheumatology, NYU School of Medicine/NYU Hospital for Joint Diseases, New York, NY, 5University of Colorado Anschutz Medical Center, Aurora, CO, USA, Aurora, CO, 6Ardea Biosciences, Inc., San Diego, CA, 7University of Alabama at Birmingham, Birmingham, AL, USA, Birmingham, AL

    Background/Purpose: Lesinurad is a selective uric acid reabsorption inhibitor approved in the United States and European Union at 200 mg daily dose in combination with…
  • Abstract Number: 207 • 2016 ACR/ARHP Annual Meeting

    Integrated Safety of Lesinurad, a Novel Uric Acid Reabsorption Inhibitor for the Treatment of Gout

    Michael A. Becker1, Robert T. Keenan2, Puja Khanna3, Raymond Malamet4, Kathleen Bos4, Jingyi Li4, Jia Hu5 and William White6, 1University of Chicago, Chicago, IL, 2Rheumatology, Duke University, Durham, NC, 3Rheumatology, University of Michigan, Ann Arbor, MI, 4AstraZeneca Pharmaceuticals, Wilmington, DE, 5Ardea Biosciences, Inc., San Diego, CA, 6University of Connecticut School of Medicine, Farmington, CT

    Background/Purpose: Lesinurad is a selective uric acid reabsorption inhibitor recently approved at 200 mg daily in combination with a xanthine oxidase inhibitor (XOI) for treatment…
  • Abstract Number: 208 • 2016 ACR/ARHP Annual Meeting

    Examination of Serum Uric Acid (sUA) Lowering and Safety with Extended Lesinurad + Allopurinol Treatment in Subjects with Gout

    Kenneth Saag1, Michael A. Becker2, Chris Storgard3, Maple Fung3, Jia Hu3 and Thomas Bardin4, 1University of Alabama at Birmingham, Birmingham, AL, 2University of Chicago, Chicago, IL, 3Ardea Biosciences, Inc., San Diego, CA, 4Hôpital Lariboisière, Paris, France

    Background/Purpose: Two replicate, randomized, core Phase III trials (CLEAR 1 & 2) reported significantly more subjects treated with lesinurad 200 mg (LESU200) or 400 mg…
  • Abstract Number: 209 • 2016 ACR/ARHP Annual Meeting

    Clinical Response of Tophus and Flares to Extended Use of Lesinurad in Combination with a Xanthine Oxidase Inhibitor in Patients with Gout

    Thomas Bardin1, Nicola Dalbeth2, Robert Terkeltaub3, Chris Storgard4, Maple Fung4, Jia Hu4 and Fernando Perez-Ruiz5, 1Hôpital Lariboisière, Paris, France, 2University of Auckland, Auckland, New Zealand, 3Medicine-Rheumatology, VA Medical Ctr/University of California San Diego, San Diego, CA, 4Ardea Biosciences, Inc., San Diego, CA, 5Hospital de Cruces and Biocruces Health Research Institute, Vizcaya, Spain

    Background/Purpose: Three randomized, double-blind, Phase III trials reported that greater proportions of patients treated with lesinurad 200 mg (LESU200) or 400 mg (LESU400), combined with…
  • Abstract Number: 210 • 2016 ACR/ARHP Annual Meeting

    Skin Events with Febuxostat in Gout Patients and Previous Skin Reactions to Allopurinol. a Retrospective Review

    Neus Quilis1, Mariano Andrés1,2, Carlos Muñoz3, Paloma Vela1,2 and Eliseo Pascual4, 1Sección de Reumatología, Hospital General Universitario de Alicante, Alicante, Spain, 2Departamento de Medicina Clínica, Universidad Miguel Hernández, Alicante, Spain, 3Sección de Inmunología, Hospital General Universitario de Alicante, Alicante, Spain, 4Departamento de Medicina Clínica, Emeritus Professor, Universidad Miguel Hernández, Alicante, Spain

    Background/Purpose: Allopurinol is the most used urate-lowering agent for patients with gout, but around 10% of patients show intolerance to this drug, often at skin,…
  • Abstract Number: 211 • 2016 ACR/ARHP Annual Meeting

    Safety and Efficacy of Febuxostat in Advanced CKD Patients with Hyperuricemia

    Yoon-Jeong Oh1, Seung Min Jung1, Sang-Won Lee2, Yong-Beom Park2 and Jason Jungsik Song2, 1Division of Rheumatology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea, The Republic of, 2Division of Rheumatology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, South Korea

    Background/Purpose:  Dosing adjustments and increased risk of serious side effects of uric acid lowering agents in patients with reduced renal function lead to undercorrection of…
  • Abstract Number: 212 • 2016 ACR/ARHP Annual Meeting

    Pegloticase Provides Clinical Benefit in Patients with Chronic Refractory Gout Who Did Not Meet the Clinical Trial Biochemical Definition of Response

    Brian F. Mandell1, Michael Weisman2, Anthony Yeo3 and Peter E. Lipsky4, 1Rheumatology, Cleveland Clinic, Cleveland, OH, 2Rheumatology, Cedars-Sinai Medical Center, West Hollywood, CA, 3Horizon Pharma, Lake Forest, IL, 4AMPEL BioSolutions, Charlottesville, VA

    Background/Purpose: Pegloticase is a recombinant uricase conjugated to polyethylene glycol approved for the treatment of chronic refractory gout refractory. The pivotal clinical trials for pegloticase…
  • Abstract Number: 213 • 2016 ACR/ARHP Annual Meeting

    Prophylaxis for Infusion Reactions to Pegloticase: An Analyis of Two Different Corticosteroid Pre-Infusion Regimens in US Community Rheumatology Practices

    Amar Majjhoo1, Kome Okposo2 and Michael Zdanis3, 1Shores Rheumatology, St. Clair Shores, MI, 2Horizon Pharma, Lake Forest, IL, 3Cetus Group, LLC, Towson, MD

    Background/Purpose: Corticosteroids are commonly utilized, along with other agents in clinical practice for pre-infusion prophylaxis prior to the administration of therapeutic biologic proteins. Two steroids,…
  • Abstract Number: 214 • 2016 ACR/ARHP Annual Meeting

    Anakinra Compared to Prednisone on the Treatment of Acute CPPD Crystal Arthritis, a Randomized, Controlled, Double-Blind Study

    Alexandre Dumusc1, Borbala Pazar Maldonado1, Charles Benaim2, Isabelle Fabreguet1, Pascal Zufferey1, Bérengère Aubry-Rozier1 and Alexander So1, 1Rheumatology Department, Lausanne University Hospital, Switzerland, Lausanne, Switzerland, 2Physical Medicine and Rehabilitation Department, Lausanne University Hospital, Switzerland, Lausanne, Switzerland

    Background/Purpose:   Calcium pyrophosphate crystal-induced arthritis (CPPD) is an acute crystal arthritis, frequently involving the wrist or the knee. Monosodium urate in gout or CPPD…
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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.).

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