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Abstracts tagged "outcomes and vasculitis"

  • Abstract Number: 2717 • 2017 ACR/ARHP Annual Meeting

    Late Onset of IgA Vasculitis Is Associated with More Severe Renal Involvement

    Alexandra Audemard-Verger1, Aurélie Baldolli2, Noemie Le Gouellec3, Loic Raffray4, Alban Deroux5, Julie Goutte6, Bertrand Lioger7, Zahir Amoura8, Patrice Cacoub9, Sébastien Sanges10, Evangeline Pillebout11, Loïc Guillevin for the French Vasculitis Study Group12 and Benjamin Terrier13, 1Internal Medicine, Caen, France, 2Internal Medicine, CHU, Caen, France, 3Internal Medicine, Lille, France, 4Internal Medicine, CHU de Bordeaux, Bordeaux, France, 5Internal Medicine, CHU de Grenoble, Grenoble, France, 6Internal Medicine, Saint Etienne, France, 7GICC UMR 7292, University François Rabelais, Tours, France, 8Department of Internal Medicine 2. Referal center for SLE/APS, Hôpital Pitié-Salpêtrière, AP-HP, UPMC Univ Paris 06 & French National Reference Center For Systemic Lupus and Antiphospholipid Syndrome, Paris, France, 9Internal Medicine Department, University Hospital “Pitié-Salpêtrière”, “Pierre et Marie Curie Paris VI” University, Paris, France, 10Université Lille Nord de France, Faculté de Médecine Henri Warembourg, Lille, Lille, France, 11Nephrology, Saint Louis, Paris, France, 12Service de Médecine Interne, Centre de Référence Maladies Auto-Immunes et Auto-Inflammatoires Systémiques Rares, Hôpital Cochin, Paris, France, 13Internal Medicine, Cochin University Hospital, Paris, France

    Background/Purpose: Immunoglobulin A vasculitis (IgAV), formerly called Henoch–Schönlein purpura, is a small-vessel vasculitis characterized by immune-complex deposits with predominant IgA. Although the disease is often…
  • Abstract Number: 126 • 2016 ACR/ARHP Annual Meeting

    Anti-Neutrophil Cytoplasmic Antibodies (ANCA) in African-American Patients: Disease Associations and Clinical Outcomes in an Urban Cohort

    Philip McCarthy1, Jenna Hudy2, Marie Melville2, Danielle Robson1, John McKinnon2, Sandeep Soman2 and Kathleen Maksimowicz-McKinnon3, 1Michigan State University College of Osteopathic Medicine, East Lansing, MI, 2Henry Ford Hospital, Detroit, MI, 3Rheumatology, Henry Ford Hospital, Detroit, MI

    Background/Purpose: Antineutrophil cytoplasmic antibody-associated vasculitis (AAV) has been most extensively described and studied in non-African-American populations. The significance of and associations with ANCA in African-Americans,…
  • Abstract Number: 127 • 2016 ACR/ARHP Annual Meeting

    Disease Characteristics and Outcomes in African-American Patients with Antineutrophil Cytoplasmic Antibody-Associated Vasculitis:  a High Risk Group for Poor Outcomes

    Philip McCarthy1, Danielle Robson1, Jenna Hudy2, Marie Melville2, John McKinnon2, Sandeep Soman2 and Kathleen Maksimowicz-McKinnon3, 1Michigan State University College of Osteopathic Medicine, East Lansing, MI, 2Henry Ford Hospital, Detroit, MI, 3Rheumatology, Henry Ford Hospital, Detroit, MI

    Background/Purpose: Antineutrophil antibody-associated vasculitis (AAV) has been most extensively described and studied in non-African American populations. Little is known about the characteristics and outcomes of…
  • Abstract Number: 1000 • 2016 ACR/ARHP Annual Meeting

    Subclinical Cytomegalovirus Viremia Is Associated with Increased Nosocomial Infections and Prolonged Hospitalization in Patients with Systemic Autoimmune Diseases

    John McKinnon1, Junying Zhou2, Jenna Hudy1, Sara Hegab1 and Kathleen Maksimowicz-McKinnon3, 1Henry Ford Hospital, Detroit, MI, 2Infectious Diseases, Henry Ford Hospital, Detroit, MI, 3Rheumatology, Henry Ford Hospital, Detroit, MI

    Background/Purpose: Both subclinical cytomegalovirus (CMV) viremia and CMV disease have been associated with adverse outcomes in select immunosuppressed populations, including an increased incidence of other…
  • Abstract Number: 1943 • 2016 ACR/ARHP Annual Meeting

    Factors Predictive of ANCA-Associated Vasculitis Relapse

    Maxime Samson1, Hervé Devilliers2, Xavier Puéchal3, Christian Pagnoux4, Pascal Cohen3, Luc Mouthon3, Benjamin Terrier5 and Loïc Guillevin3, 1Department of Internal Medicine and Clinical Immunology, Hôpital François Mitterrand, CHU de Dijon, Dijon, France, 2Department of Internal Medicine and Systemic Diseases, Hôpital François Mitterrand, CHU de Dijon, Dijon, France, 3Department of Internal Medicine, Referral Center for Rare Autoimmune and Systemic Diseases, Hôpital Cochin, AP–HP, Université Paris Descartes, Paris, France, Paris, France, 4Division of Rheumatology, Mount Sinai Hospital, University Health Network, University of Toronto, Toronto, Canada, Toronto, ON, Canada, 5National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochin, AP–HP, Université Paris Descartes, Paris, France

    Background/Purpose:  To identify associations between patients’ clinical and biological characteristics at diagnosis of antineutrophil cytoplasmic antibody-associated vasculitides (AAVs), and their relapse during follow-up. Methods:  Long-term…
  • Abstract Number: 1953 • 2016 ACR/ARHP Annual Meeting

    Management and Outcomes of ANCA-Associated Vasculitis in Unselected Cases within a Large Health Region of England

    Fiona Pearce1, Catherine McGrath2, Ravinder Sandhu3, Jon Packham4, Karen Obrenovich5, Richard A. Watts6, Peter Lanyon7 and for the East Midlands, West Midlands and East of England regional audit groups, 1Epidemiology and Public Health, University of Nottingham, Nottingham, United Kingdom, 2Department of Rheumatology, The Dudley Group NHS Foundation Trust, Dudley, United Kingdom, 3The Dudley Group NHS Foundation Trust, Dudley, Great Britain, 4University of Keele, Keele, United Kingdom, 5The Dudley Group NHS Foundation Trust, Dudley, United Kingdom, 6Rheumatology Department, Ipswich Hospital, Ipswich, Great Britain, 7Department of Rheumatology, Nottingham University Hospitals NHS trust, Nottingham, United Kingdom

    Background/Purpose: Most data on management and outcomes of ANCA-associated vasculitis (AAV) come from highly selected populations in tertiary referral centres, or clinical trials. These results…
  • Abstract Number: 1954 • 2016 ACR/ARHP Annual Meeting

    Clinical Features and Long Term Outcome of 105 Patients of Granulomatosis with Polyangiitis: A Single Centre Experience from North India

    Aman Sharma1, Shankar Naidu2, Manish Rathi3, Benzeeta Pinto4, Kusum Sharma5, Varun Dhir6, Ritambhra Nada7, Ranjana Minz8 and Surjit Singh9, 1Internal Medicine, Postgraduate Institute of Medical Education and Research, Chandigarh, India, 2PGIMER, cHANDIGARH, India, 3Department of Nephrology,, Postgraduate Institute of Medical Education and Research, Chandigarh, India, 4PGIMER, CHANDIGARH, India, 5Department of Medical Microbiology,, PGIMER,, Chandigarh, India, 6Internal Medicine (Rheumatology Unit), Postgraduate Institute of Medical Education and Research, Chandigarh, India, 7Histopathology, Professor, Chandigarh, India, 8Department of Immunopathology,, PGIMER,, Chandigarh, India, 9Department of Internal Medicine,, Postgraduate Institute of Medical Education and Research, Chandigarh, India

    Background/Purpose: The published Indian data on Granulomatosis with Polyangiitis (GPA) is sparse and only in the form of few small case series. The purpose of this study…
  • Abstract Number: 2856 • 2014 ACR/ARHP Annual Meeting

    Update on Long-Term Outcomes after Reversible Cerebral Vasoconstriction Syndrome (RCVS)

    Seby John1, Aneesh Singhal2, Leonard H. Calabrese3, Ken Uchino4, Tariq Hammad3, Stewart Tepper3, Mark Stillman3 and Rula A Hajj-Ali5, 19500 Euclid Avenue S10-C, Cleveland Clinic Foundation, Cleveland, OH, 2Neurology, Massachusetts General Hospital, Boston, MA, 3Cleveland Clinic Foundation, Cleveland, OH, 4Neurology, Cleveland Clinic Foundation, Cleveland, OH, 5Rheumatology, Cleveland Clinic Foundation, Cleveland, OH

    Background/Purpose RCVS is characterized by acute onset of severe headaches, with or without neurologic deficit with evidence of reversible cerebral vasoconstriction. We have previously reported…
  • Abstract Number: 1781 • 2014 ACR/ARHP Annual Meeting

    Long-Term Outcomes Among Patients with Renal Disease Secondary to ANCA-Associated Vasculitis: Temporal Trends over 25 Years

    Rennie L. Rhee1, Susan L Hogan2, Caroline J. Poulton2, Julie Anne G. McGregor2, J. Richard Landis3, Ronald Falk4 and Peter A. Merkel5, 1Rheumatology, University of Pennsylvania, Philadelphia, PA, 2UNC Kidney Center, Chapel Hill, NC, 3Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania, Philadelphia, PA, 4Dept of Nephrology and Hypertension, UNC Kidney Center, Chapel Hill, NC, 5University of Pennsylvania, Philadelphia, PA

    Background/Purpose Significant advances have been made in the diagnosis and treatment of patients with ANCA-associated vasculitis (AAV).  However, little is known about how these advances…
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