ACR Meeting Abstracts

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Abstracts tagged "scleroderma and systemic sclerosis"

  • Abstract Number: 2910 • 2016 ACR/ARHP Annual Meeting

    Work Productivity in Systemic Sclerosis and Association with Health Related Quality of Life

    Kathleen Morrisroe1, Molla Huq2, Wendy Stevens3, Joanne Sahhar4, Susanna Proudman5,6, Mandana Nikpour7 and Australian Scleroderma Interest Group, 1Rheumatology, St Vincent's Hospital, Melbourne, Melbourne, Australia, 2Department of Medicine (Rheumatology), Melbourne University, Melbourne, Australia, 3Department of Rheumatology, St. Vincent’s Hospital Melbourne, Melbourne, Australia, 4Department of Rheumatology, Monash Medical Centre, Melbourne, Australia, 5Rheumatology Unit, Royal Adelaide Hospital, Adelaide, Australia, 6Discipline of Medicine, University of Adelaide, Adelaide, Australia, 7Melbourne University, Melbourne, Australia

    Background/Purpose: We sought to assess work productivity, factors associated with reduced productivity, and the relationship between work productivity and health-related quality of life (HRQoL) in…
  • Abstract Number: 826 • 2016 ACR/ARHP Annual Meeting

    Exercise Echocardiography Predicts Future Development of Pulmonary Hypertension in a High-Risk Cohort of Scleroderma Patients

    Kaitlin A. Quinn1, Tunay Kuru2, Stephanie Wappel3 and Virginia D. Steen1, 1Rheumatology, Georgetown University Medical Center, Washington, DC, 2Pulmonary, Georgetown University Medical Center, Washington, DC, 3Georgetown University Medical Center, Washington, DC

    Background/Purpose: Pulmonary hypertension (PH) is the leading cause of scleroderma related deaths and is often detected late in the disease course. Early identification of patients…
  • Abstract Number: 828 • 2016 ACR/ARHP Annual Meeting

    Survival and Health-Related Quality of Life in Incident Systemic Sclerosis Related Pulmonary Arterial Hypertension: A Multicentre Australian Cohort Study

    Kathleen Morrisroe1, Molla Huq2, Wendy Stevens3, Candice Rabusa4, Joanne Sahhar5, Gene Ngian6, Susanna Proudman7,8, Mandana Nikpour9 and Australian Scleroderma Interest Group, 1Rheumatology, St Vincent's Hospital, Melbourne, Melbourne, Australia, 2Department of Medicine (Rheumatology), Melbourne University, Melbourne, Australia, 3Department of Rheumatology, St. Vincent’s Hospital Melbourne, Melbourne, Australia, 4Rheumatology, St. Vincent’s Hospital, Melbourne, Australia, 5Department of Rheumatology, Monash Medical Centre, Melbourne, Australia, 6Department of Medicine (RMH/WH), The University of Melbourne, Melbourne, Australia, 7Rheumatology Unit, Royal Adelaide Hospital, Adelaide, Australia, 8Discipline of Medicine, University of Adelaide, Adelaide, Australia, 9Melbourne University, Melbourne, Australia

    Background/Purpose: Pulmonary arterial hypertension (PAH) is the leading cause of systemic sclerosis (SSc) related mortality. We sought to determine survival, predictors of mortality, and health…
  • Abstract Number: 833 • 2016 ACR/ARHP Annual Meeting

    A Small Proportion of Patients with Systemic Sclerosis with Suspected Pulmonary Hypertension Meet the Published Inclusion/Exclusion Criteria for Two Systemic Sclerosis Associated Pulmonary Arterial Hypertension Screening Algorithms– Results from a Single Center Cohort

    Amber Young1, Victor Moles2, Vivek Nagaraja3, Scott H. Visovatti4, Vallerie McLaughlin4 and Dinesh Khanna5, 1Department of Internal Medicine, Division of Rheumatology, University of Michigan, Ann Arbor, MI, 2Department of Internal Medicine, Division of Cardiology, University of Michigan, Ann Arbor, MI, 3Department of Medicine [Division of Rheumatology], University of Toledo, Toledo, OH, 4Internal Medicine, Division of Cardiology, University of Michigan, Ann Arbor, MI, 5University of Michigan, Ann Arbor, MI

    Background/Purpose: Pulmonary arterial hypertension (PAH) is one of the leading causes of mortality in patients with systemic sclerosis (SSc). Active screening detects SSc-PAH earlier and…
  • Abstract Number: 836 • 2016 ACR/ARHP Annual Meeting

    Comprehensive Characterization of Calcinosis in a Multicenter International Cohort of Patients with Systemic Sclerosis

    Antonia Valenzuela1,2, Jessica K. Gordon3, Tatiana Sofia Rodriguez-Reyna4, Susanna Proudman5,6, Murray Baron7, Monique Hinchcliff8, Dinesh Khanna9, Amber Young10, Flavia V. Castelino11, Sara R. Schoenfeld12, Virginia D. Steen13, David Fiorentino14 and Lorinda Chung15, 1Division of Immunology and Rheumatology, Stanford University School of Medicine, Palo Alto, CA, 2Stanford University School of Medicine, Stanford, CA, 3Rheumatology, Hospital for Special Surgery, New York, NY, 4Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico, 5Rheumatology Unit, Royal Adelaide Hospital, Adelaide, Australia, 6Discipline of Medicine, University of Adelaide, Adelaide, Australia, 7Rheumatology, McGill University, Jewish General Hospital, Montreal, QC, Canada, 8Northwestern University, Feinberg School of Medicine Scleroderma Program, Chicago, IL, 9University of Michigan, Ann Arbor, MI, 10Department of Internal Medicine, Division of Rheumatology, University of Michigan, Ann Arbor, MI, 11Rheumatology, Allergy, Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, 12Rheumatology Unit, Massachusetts General Hospital, Harvard Medical School, Boston, MA, 13Rheumatology, Georgetown University Medical Center, Washington, DC, 14Department of Dermatology, Stanford University School of Medicine, Palo Alto, CA, 15Rheumatology, Stanford University Medical Center, Palo Alto, CA

    Background/Purpose: Calcinosis cutis is a debilitating complication of systemic sclerosis (SSc) affecting one quarter of patients. Repetitive trauma may be involved in the pathogenesis of…
  • Abstract Number: 971 • 2016 ACR/ARHP Annual Meeting

    Reliability and Minimal Clinically Important Differences (MCID) of Forced Vital Capacity: Post-Hoc Analyses from the Scleroderma Lung Studies (SLS-I and II)

    Suzanne Kafaja1, Philip J. Clements2, Holly Wilhalme3, Daniel E. Furst4, Chi-hong Tseng2, Kim Hyun5, Jonathan Goldin3, Elizabeth R. Volkmann3, Michael Roth2, Donald P. Tashkin6 and Dinesh Khanna7, 1Medicine/Rheumatology, University of California Los Angeles, David Geffen School of Medicine, Los Angeles, CA, 2Medicine, University of California, Los Angeles, David Geffen School of Medicine, Los Angeles, CA, 3University of California, Los Angeles, David Geffen School of Medicine, Los Angeles, CA, 4David Geffen School of Medicine at UCLA, Los Angeles, CA, 5Radiology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 6David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 7University of Michigan, Ann Arbor, MI

    Background/Purpose: Forced vital capacity (FVC) is used as a primary outcome measure in clinical trials of systemic sclerosis-related interstitial lung disease (SSc-ILD). Minimally Clinically Important…
  • Abstract Number: 973 • 2016 ACR/ARHP Annual Meeting

    Clinical Characterization of Patients with World Health Organization Group 2 Pulmonary Hypertension in the Pulmonary Hypertension Assessment and Recognition of Outcomes in Scleroderma Cohort

    Jessica K. Gordon1, Jackie Szymonifka2, Matthew R. Lammi3, Virginia D. Steen4 and PHAROS Investigators, 1Rheumatology, Hospital for Special Surgery, New York, NY, 2Epidemiology and Biostatistics, Hospital for Special Surgery, New York, NY, 3Louisiana State University Health Sciences Center, Pulmonary and Critical Medicine, New Orleans, LA, 4Rheumatology, Georgetown University Medical Center, Washington, DC

    Background/Purpose:  Pulmonary hypertension (PH) is a leading cause of death in patients (pts) with Systemic Sclerosis (SSc). The World Health Organization (WHO) classifies PH into…
  • Abstract Number: 974 • 2016 ACR/ARHP Annual Meeting

    Diffuse Scleroderma, Male Sex, and Myopathy Are Associated with Severe Gastrointestinal Dysmotility in Scleroderma

    Zsuzsanna McMahan1, Livia Casciola-Rosen2 and Fredrick M. Wigley3, 1Department of Internal Medicine, Johns Hopkins University, Baltimore, MD, 2Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 3Rheum Div/Mason F Lord, Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: Despite the fact that up to 90% of scleroderma (SSc) patients are affected by gastrointestinal (GI) dysmotility, features associated with severe GI disease are…
  • Abstract Number: 1189 • 2016 ACR/ARHP Annual Meeting

    Inpatient Trends for Adults with Scleroderma in the United States: A 20 Year Analysis

    Noopur Goel1, Ishan Lalani2 and Iram Moledina3, 1Internal Medicine, Monmouth Medical Center, monmouth beach, NJ, 2Internal Medicine, Monmouth Medical Center, Ocean, NJ, 3Gujarat Adani Institute of Medical Sciences, New Haven, CT

  • Abstract Number: 1432 • 2016 ACR/ARHP Annual Meeting

    The EULAR Systemic Sclerosis Impact of Disease Score – a New Patient-Reported Outcome Measure for Patients with Systemic Sclerosis Under Development

    Rucsandra Dobrota1, Mike Becker2, Kim Fligelstone3,4, Jaap Fransen5, Ann Kennedy6, Yannick Allanore7, Patricia Carreira8, László Czirják9, Christopher Denton10, Roger Hesselstrand11, Gunnel Sandqvist11, Otylia Kowal-Bielecka12, Marco Matucci Cerinic13, Carina Mihai14, Ana Maria Gheorghiu15, Ulf Müller-Ladner16, Marc Frerix17, Turid Heiberg18 and Oliver Distler1, 1Department of Rheumatology, University Hospital Zurich, Zurich, Switzerland, 2Division of Rheumatology, University Hospital Zurich, Zurich, Switzerland, 3Royal Free Hospital, Scleroderma Unit and Scleroderma Society, London, United Kingdom, 4Federation of European Scleroderma Associations (FESCA), London, United Kingdom, 5Rheumatology, Radboud University Medical Center, Nijmegen, Netherlands, 6Federation of European Scleroderma Associations (FESCA), Tournai, Belgium, 7Department of Rheumatology, University Paris Descartes and Cochin Hospital, Paris, France, 8Department of Rheumatology, Hospital Universitario 12 de Octubre, Madrid, Spain, 9Department of Rheumatology and Immunology, University of Pécs, Faculty of Medicine, Pécs, Hungary, 10Division of Medicine, Centre for Rheumatology and Connective Tissue Disease, University College London, London, United Kingdom, 11Department of Rheumatology, Lund University, Lund, Sweden, 12Department of Rheumatology and Internal Medicine, Medical University of Bialystok, Bialystok, Poland, 13Department of Rheumatology, University of Florence, Florence, Italy, 14Department of Internal Medicine and Rheumatology, Carol Davila University of Medicine and Pharmacy, Cantacuzino Hospital, Bucharest, Romania, 15Carol Davila University of Medicine and Pharmacy, Internal Medicine and Rheumatology Department, Cantacuzino Clinical Hospital, Bucharest, Romania, 16Department of Internal Medicine and Rheumatology, Justus-Liebig-University Giessen, Kerckhoff-Klinik, Bad Nauheim, Germany, 17Department of Rheumatology and Clinical Immunology, Justus-Liebig-University Giessen, Kerckhoff-Klinik, Bad Nauheim, Germany, 18Department of Health and Social Sciences, Oestfold University College, Oslo, Norway

    Background/Purpose: Patient reported outcome measures (PROM) are required as key outcomes in disease modifying therapeutic trials in systemic sclerosis (SSc). A PROM tool in SSc,…
  • Abstract Number: 1865 • 2016 ACR/ARHP Annual Meeting

    Urinary Cell Adhesion Molecules As Markers of Renal Involvement in Systemic Sclerosis

    Edward Stern1, Voon H. Ong2, Aine Burns3, Robert Unwin4 and Christopher Denton5, 1UCL Division of Medicine, London, United Kingdom, 2Rheumatology, UCL Division of Medicine, London, United Kingdom, 3Nephrology, Royal Free Hospital, London, United Kingdom, 4Nephrology, UCL Division of Medicine, London, United Kingdom, 5Division of Medicine, Centre for Rheumatology and Connective Tissue Disease, University College London, London, United Kingdom

    Background/Purpose: Renal involvement in systemic sclerosis (SSc) includes scleroderma renal crisis as well as progressive organ fibrosis. Detection and management of these disease complications is…
  • Abstract Number: 1877 • 2016 ACR/ARHP Annual Meeting

    Confirmatory Factor Analysis and Assessment of Differential Item Functioning of the Satisfaction with Appearance Scale in Systemic Sclerosis: A Comparison Across Sex, Race/Ethnicity and Disease Subtype

    Lisa Jewett1, Linda Kwakkenbos2, Vanessa L. Malcarne3, Marie-Eve Carrier2 and Brett D. Thombs4, 1Department of Psychiatry, McGill University, Montreal, QC, Canada, 2McGill University, Montreal, QC, Canada, 3SDSU/UC San Diego Joint Doctoral Program in Clinical Psychology, San Diego, CA, 4Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada

    Background/Purpose: The Satisfaction with Appearance Scale (SWAP) has been used to assess dissatisfaction with appearance and social discomfort relative to disfigurement in systemic sclerosis (scleroderma,…
  • Abstract Number: 1880 • 2016 ACR/ARHP Annual Meeting

    A Large Proportion of Patients in an Early Systemic Sclerosis-Associated Interstitial Lung Disease Cohort Have Coexisting Pulmonary Hypertension

    Amber Young1, Caitlyn Fisher1, Rajaie Namas2, Holly Wilhalme3 and Dinesh Khanna4, 1Department of Internal Medicine, Division of Rheumatology, University of Michigan, Ann Arbor, MI, 2Department of Medicine [Division of Rheumatology], University of Michigan, Ann Arbor, MI, 3University of California, Los Angeles, David Geffen School of Medicine, Los Angeles, CA, 4University of Michigan, Ann Arbor, MI

    Background/Purpose: Systemic Sclerosis (SSc) is a multi-organ system disease manifested by fibrosis, vascular damage and dysregulation of the immune system. The leading causes of death…
  • Abstract Number: 2019 • 2016 ACR/ARHP Annual Meeting

    Faces in Motion: Clinical Subtyping in Scleroderma Using Changes in Forced Vital Capacity

    Colin Ligon1, Peter Schulam2, Suchi Saria3, Fredrick M. Wigley4, Robert Wise5 and Laura K. Hummers6, 1Rheumatology, University of Pennsylvania School of Medicine, Philadelphia, PA, 2Johns Hopkins University, Baltimore, MD, 3Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, 4Rheum Div/Mason F Lord, Johns Hopkins University School of Medicine, Baltimore, MD, 5Department of Pulmonology, Johns Hopkins University School of Medicine, Baltimore, MD, 6Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: Prognostication in scleroderma has historically depended on using static measures such as antibody status and extent of skin involvement to stratify risk of mortality…
  • Abstract Number: 2895 • 2016 ACR/ARHP Annual Meeting

    Adaptation of UCLA Scleroderma Clinical Trial Consortium Gastrointestinal Tract 2.0 Questionnaire into Turkish

    Murat Yasar Tas1, Gozde Dervis Hakim2, Pembe Keskinoglu3, Gokce Kenar4, Handan Yarkan5, Berrin Zengin4, Gerçek Can5, Fatos Onen4, Nurullah Akkoc4, Mesut Akarsu6 and Merih Birlik4, 1Internal Medicine, Dokuz Eylul University Faculty of Medicine, Izmir, Turkey, 2Gastroenterology, Ataturk State Hospital, Sinop, Turkey, 3Department of Biostatistics and Medical Informatics, Dokuz Eylul University Faculty of Medicine, Izmir, Turkey, 4Rheumatology, Dokuz Eylul University Faculty of Medicine, Izmir, Turkey, 5Rheumatology, Dokuz Eylul University Faculty of Medicine, İzmir, Turkey, 6Gastroenterology, Dokuz Eylul University Faculty of Medicine, Izmir, Turkey

    Background/Purpose:  Nearly 90% of patients with scleroderma (SSc) have gastrointestinal tract(GIT) involvement in variable severities and is a challenging process for clinicians.The University of California…
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