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Abstracts tagged "classification criteria"

  • Abstract Number: 0390 • ACR Convergence 2025

    Radiographic Assessment in Juvenile Spondyloarthritis: Evaluating the axJSpA Criteria Using Radiographs Alone Versus MRI

    David M. Biko1, Nancy A. Chauvin2, Michael Francavilla3, Nele Herregods4, Walter P. Maksymowych5, Robert G. W. Lambert6, Timothy Brandon1, Ozgur Kasapcopur7, Mehmet YILDIZ8, Hemalatha Srinivasalu9 and Pamela Weiss10, 1Children's Hospital of Philadelphia, Philadelphia, PA, 2The Cleveland Clinic, Hummelstown, PA, 3Department of Pediatric Radiology, Children’s Hospital Philadelphia, Philadelphia, PA, 4Ghent University Hospital, Ghent, Belgium, 5Department of Medicine, University of Alberta, 568 Heritage Building, Edmonton, AB, Canada, 6University of Alberta, Department of Radiology & Diagnostic Imaging, Edmonton, AB, Canada, 7Istanbul University-Cerrahpasa, Cerrahpasa Medical School, istanbul, Turkey, 8Istanbul University-Cerrahpasa Department of Pediatric Rheumatology, Istanbul, Turkey, 9Children's National Hospital, Washington, DC, 10Childrens Hospital of Philadelphia, Philadelphia, PA

    Background/Purpose: Radiographs are neither sensitive nor reliable for assessing axial disease in juvenile spondyloarthritis (JSpA), though they are still used in some settings due to…
  • Abstract Number: 0389 • ACR Convergence 2025

    An International Delphi Survey for the Definition of New Classification Criteria for Juvenile Idiopathic Arthritis

    Alessandra Alongi1, Hermine Brunner2, Angelo Ravelli3, Tadej Avcin4, Michael Beresford5, RUBEN BURGOS-VARGAS6, Ruben Cuttica7, Raju Khubchandani8, Ronald laxer9, Seza Özen10, Ross Petty11, Carol Wallace12, Nico Wulffraat13, Silvia Magni-Manzoni14, Marija Jelusic15, Alessandro Consolaro16, Jordi anton17, Gerd Horneff18, Mia Glerup19, Giovanni Filocamo20, Gabriele Simonini21, ADELE CIVINO22, Agustin Remesal23, Silvia Scala24, Angela Pistorio25, Daniel Lovell2, Alberto Martini26 and Nicolino Ruperto27, 1Università Milano Bicocca, Milan, Italy, Milano, Italy, 2Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 3IRCCS Istituto Giannina Gaslini, Genoa, Italy, Genoa, Genoa, Italy, 4University Children's Hospital, University Medical Center Ljubljana, Ljubljana, Slovenia, 5Alder Hey Children's NHS Foundation Trust Hospital, Department of Women's & Children's Health, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, United Kingdom, 6Department of Rheumatology, Hospital General de Mexico, Faculty of Medicine, Universidad Nacional Autonoma de Mexico, Ciudad de México, Mexico, 7Hospital Pedro de Elizalde, Buenos Aires, Argentina, 8Jaslok Hospital and Research Center, Mumbai, India, 9The Hospital for Sick Children, Toronto, ON, Canada, 10Hacettepe University Medical Faculty, Ankara, Turkey, 11British Columbia Children’s Hospital, University of British Columbia, Vancouver, ON, Canada, 12Seattle Children's Hospital, University of Washington, Seattle, WA, 13Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, Netherlands, 14Bambino Gesù IRCCS Children's Hospital, Rome, Italy, 15University Hospital Centre Zagreb, Zagreb, Croatia, 16IRCCS Istituto Giannina Gaslini, Genoa, Italy, 17Hospital Sant Joan de Düu. Universitat de Barcelona, Barcelona, Spain, 18Asklepios Klinik, Hamburg, Germany, 19Department of Paediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark, 20Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy, 21Rheumatology Unit, ERN-ReCONNET center, Meyer Children's Hospital IRCCS, Firenze, Firenze, Italy, 22Department of Pediatric Immunology and Rheumatology, LECCE, Italy, 23Hospital Universitario La Paz, Madrid, Spain, 24Clinica Pediatrica e Reumatologia, IRCCS Istituto Giannina Gaslini, Genoa, Italy, 25Servizio di Epidemiologia e Biostatistica, IRCCS Istituto Giannina Gaslini, Genoa, Italy, 26Università degli Studi di Genova, IRCCS Istituto Giannina Gaslini, Genoa, Italy, 27Université Milano Bicocca and Fondazione IRCSS S. Gerardo dei Tintori, Monza, Monza and Brianza, Italy

    Background/Purpose: To improve the current classification criteria for juvenile idiopathic arthritis (JIA), a multi-step initiative coordinated by PRINTO was launched in 2015, starting with a…
  • Abstract Number: 2651 • ACR Convergence 2025

    Development and Validation of the Scleroderma Clinical Trials Consortium Classification Criteria for Systemic Sclerosis Heart Involvement

    Laura Ross1, Andrew Burns2, Andre La Gerche3, Dylan Hansen4, Gerry Coghlan5, Wendy Stevens6, David Prior7, Alan Pham8, Penelope McKelvie4, Chiara Bellocchi9, Yolanda Braun Moscovici10, Cosimo Bruni11, Patricia E. Carreira12, Tracy Frech13, Sabrina Hoa14, Marie Hudson15, Vivien Hsu16, Marco Matucci-Cerinic17, Benjamin Medina Fonseca18, Andrea Low19, Sue-Ann Ng19, Tatiana Rodriguez-Reyna20, Joanne Sahhar21, Mohamed Talaat22, Susanna Proudman23, Alessandra Vacca24, Murray Baron25 and Mandana Nikpour26, 1The University of Melbourne, Melbourne, Victoria, Australia, 2St Vincent's Hospital Melbourne, Fitzroy, Australia, 3St Vincent's Institute of Medical Research, Melbourne, Victoria, Australia, 4St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia, 5Royal Free Hospital, London, United Kingdom, 6St Vincent's Hospital Melbourne & University of Melbourne, Fitzroy, Australia, 7University of Melbourne, Parkville, Australia, 8Alfred Hospital, Melbourne, Australia, 9University of Milan, Milan, Italy, 10Rambam Heath Care Campus, Haifa, Israel, 11Department of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland, 12Hospital Universitario 12 de Octubre, Madrid, Spain, 13Vanderbilt University Medical Center, Nashville, TN, 14University of Montreal, Brossard, QC, Canada, 15McGill University, Montréal, QC, Canada, 16Rutgers- RWJ Medical School, South Plainfield, NJ, 17University San Raffaele Milano, Milano, Milan, Italy, 18Universidad Nacional Autonoma de Mexico, Monterry, Mexico, 19Singapore General Hospital, Singapore, Singapore, 20Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico, 21Monash Health, Melbourne, Victoria, Australia, 22Augusta Health, Charlottesville, VA, 23Royal Adelaide Hospital and University of Adelaide, Medindie, South Australia, Australia, 24University and AOU of Cagliari, Monserrato, Italy, 25McGill University, Montreal, Canada, 26University of Sydney, School of Public Health, Faculty of Medicine and Health, Sydney, New South Wales, Australia; St Vincent’s Hospital Melbourne, Department of Rheumatology, Fitzroy, Victoria, Australia, Melbourne, Victoria, Australia

    Background/Purpose: Systemic sclerosis (SSc) heart involvement (SHI) is a serious disease manifestation associated with high mortality. This study presents newly developed classification criteria to enable…
  • Abstract Number: 0272 • ACR Convergence 2025

    Ocular Involvement in Behçet’s Disease: Comparative Study of Two Classification Criteria in Clinical Practice

    Rafael Gálvez Sánchez1, José Luis Martín-Varillas2, Lara Sánchez Bilbao3, Ivan Ferraz Amaro4, Elena Aurrecoechea5 and Ricardo Blanco3, 1Division of Rheumatology, Hospital Universitario Marqués de Valdecilla, IDIVAL, Immunopathology Group, Santander , Spain, Santander, Spain, 2Rheumatology Division, Hospital de Laredo. IDIVAL, Immunopathology Group. Santander, Spain., Laredo, Spain, 3Rheumatology Division, Hospital Universitario Marqués de Valdecilla, IDIVAL, Immunopathology Group, Santander, Spain, Santander, Cantabria, Spain, 4Hospital Universitario de Canarias, Santa Cruz de Tenerife, Spain, 5Hospital Sierrallana, CANTABRIA, Spain

    Background/Purpose: Ocular involvement is a potential severe complication of Behçet’s Disease (BD). The traditional classification, by the International Study Group (ISG, 1990) requires the mandatory…
  • Abstract Number: 2538 • ACR Convergence 2025

    Comparative Study of Two Classification Criteria Sets in Real Clinical Practice in Behçet’s Disease

    Rafael Gálvez Sánchez1, José Luis Martín-Varillas2, Lara Sánchez Bilbao3, Ivan Ferraz Amaro4, Carmen Lasa Teja5, Elena Aurrecoechea6, Diana Prieto-Peña7 and Ricardo Blanco3, 1Division of Rheumatology, Hospital Universitario Marqués de Valdecilla, IDIVAL, Immunopathology Group, Santander , Spain, Santander, Spain, 2Rheumatology Division, Hospital de Laredo. IDIVAL, Immunopathology Group. Santander, Spain., Laredo, Spain, 3Rheumatology Division, Hospital Universitario Marqués de Valdecilla, IDIVAL, Immunopathology Group, Santander, Spain, Santander, Cantabria, Spain, 4Hospital Universitario de Canarias, Santa Cruz de Tenerife, Spain, 5Division of Rheumatology, Hospital Universitario Marqués de Valdecilla, IDIVAL, Immunopathology Group, Santander, Spain., Riotuerto, Cantabria, Spain, 6Hospital Sierrallana, CANTABRIA, Spain, 7Division of Rheumatology, Hospital Universitario Marqués de Valdecilla, IDIVAL, Immunopathology Group, Santander, Spain., Santander, Spain

    Background/Purpose: Behçet´s Disease (BD) was traditionally classified according to the International Study Group (ISG) in which oral ulcers were mandatory. International Team for the Revision…
  • Abstract Number: 0270 • ACR Convergence 2025

    Diagnostic Challenge of IgG4-related Disease: Comparison Between ACR/EULAR, Umehara, and Okazaki Criteria

    Rafael Gálvez Sánchez1, Ivan Ferraz Amaro2, Fernando Lopez Gutierrez3, Javier Loricera4, Pablo Martínez Calabuig5, Jorge Juan Fragío Gil6, Roxana González Mazarí7, Cristina Hormigos Martín8, DALIFER FREITES9, Maria Rodríguez Laguna8, Patricia Moya Alvarado10, Marta López I Gómez11, Hector Corominas Macia10, Maite Silva Díaz12, Guillermo González Arribas12, Angel García Aparicio13, Judit Font-Urgelles14, Ivette Casafont Solé15, Elisabet Castaneda16, Carolina Merino Argumánez17, Raquel Zas Vaamonde18, Juan Molina Collada19, Sergio Rodríguez Montero20, Rafael Melero Gonzalez21, Eva Galíndez Agirregoikoa22, Andrea Hernández23, Lucia Pantoja Zarza24, Ignacio Braña Abascal25, Vega Jovaní26, Elia Valls Pascual27, Natalia Mena Vázquez28, ADELA MARIA GALLEGO FLORES29, Noelia Cabaleiro Raña30, Raúl Veroz González31, Mariano Andrés32, Santos Castañeda Sainz33 and Ricardo Blanco34, 1Division of Rheumatology, Hospital Universitario Marqués de Valdecilla, IDIVAL, Immunopathology Group, Santander , Spain, Santander, Spain, 2Hospital Universitario de Canarias, Santa Cruz de Tenerife, Spain, 3Hospital Universitario Marqués de Valdecilla, Immunopathology Group -IDIVAL, Reumatología, Santander, Santander, Spain, 4Hospital Universitario Marqués de Valdecilla, IDIVAL, Immunopathology Group, Santander , Spain, Santander, Spain, 5Hospital General Universitario de Valencia, Spain/ Uversidad Catolica de Valencia San Vicente Martir, Valencia, Spain, Ontinyent, Spain, 6Hospital General Universitario, Valencia, Spain, 7Hospital General Universitario de Valencia, Reumatología, Valencia, Valencia, Spain, 8Hospital Clínico San Carlos, Reumatología, Madrid, Madrid, Spain, 9Rheumatology Service, San Carlos Clinical Hospital, Madrid, Madrid, Spain, 10Hospital de Sant Pau, Reumatología, Barcelona, Barcelona, Spain, 11Hospital Universitario de Araba, Reumatología, Vitoria,, Vitoria, Spain, 12Complejo Hospitalario Universitario de A Coruña, Reumatología, A Coruña, Spain, 13Hospital Universitario de Toledo, Reumatología, Toledo, Toledo, Spain, 14Hospital Universitari Germans Trias i Pujol, Badalona, Spain, 15Hospital German Trias i Pujol, Reumatología, Badalona, Badalona, Spain, 16Hospital Universitario Infanta Sofía, Reumatología, Madrid, Madrid, Spain, 17Hospital Universitario Puerta del Hierro, Reumatología, Madrid, Madrid, Spain, 18Hospital Universitario 12 de Octubre, Reumatología, Madrid, Madrid, Spain, 19Hospital General Universitario Gregorio Marañón, Reumatología, Madrid, Madrid, Spain, 20Hospital Universitario de Valme, Reumatología, Sevilla, Sevilla, Spain, 21Hospital Alvaro Cunqueiro, Reumatología, Vigo, Vigo, Spain, 22BASURTO UNIVERSITY HOSPITAL, BILBAO, Spain, 23Hospital Universitario de Gran Canaria Dr Negrin, Reumatología, Palmas de Gran Canaria, Gran Canaria, Spain, 24Hospital General de Segovia, Reumatología, Segovia, Segovia, Spain, 25Hospital Universitario Central de Asturias, Reumatología, Oviedo, Oviedo, Spain, 26Hospital General Universitario de Alicante, Reumatología, Alicante, Alicante, Comunidad Valenciana, Spain, 27Hospital General de Valencia, Reumatología, Valencia, Valencia, Spain, 28Hospital Regional Universitario de Málaga, Reumatología, Málaga, Malaga, Spain, 29Complejo Hospitalario don Benito Villanueva, Reumatología, Badajoz, Badajoz, Extremadura, Spain, 30Hospital Universitario Montecelo, Reumatología, Pontevedra, Pontevedra, Spain, 31Hospital de Mérida, Reumatología, Mérida, Mérida, Spain, 32Hospital General Universitario de Alicante, Reumatología, Alicante, Alicante, Spain, 33Hospital Universitario La Princesa, Reumatología, Madrid Grupo de cooperación nacional de enfermedad relacionada con IgG4: Blanca García Magallón (Hospital Universitario Puerta del Hierro), Maite Odriozola Gil (Hospital Universitario de Valme), Cristina Arciniega (Hospital de Mérida), Maria Lourdes Mateo Soria (Hospital German Trias i Pujol), Santiago Muñoz (Hospital Universitario Infanta Sofía), Iñigo Jesús Rua Figueroa, (Hospital Universitario de Gran Canaria Dr Negrin), Sabela Fernández Aguado, (Hospital de Montecelo)., Madrid, Spain, 34Rheumatology Division, Hospital Universitario Marqués de Valdecilla, IDIVAL, Immunopathology Group, Santander, Spain, Santander, Cantabria, Spain

    Background/Purpose: IgG4-related disease (IgG4-RD) is a rare immune-mediated condition characterized by fibro-sclerosing inflammation, elevated serum and tissue IgG4 levels, and heterogeneous clinical manifestations. Several classification…
  • Abstract Number: 2489 • ACR Convergence 2025

    Unraveling IPAF, VEDOSS and connective tissue diseases classifications through the mixed connective tissue disease spectrum

    Kevin Chevalier1, Benjamin Torreau2, Marc Michel3, Bertrand Godeau3, Christian AGARD4, Thomas Papo5, Karim Sacré6, Brigitte Bader-Meunier7, Raphaele Seror8, Xavier Mariette9, Cacoub Patrice10, Ygal Benhamou11, Hervé Levesque12, Cécile goujard13, Olivier Lambotte14, Bernard Bonnotte15, Maxime Samson16, Félix Ackermann17, Jean Schmidt18, Pierre Duhaut18, Isabelle Kone-Paut14, Jean-Emmanuel Kahn19, Thomas Hanslik19, Nathalie Costedoat-Chalumeau20, Benjamin Terrier20, Alexis REGENT21, bertrand Dunogue22, Pascal Cohen23, Véronique Le Guern20, Eric HACHULLA24, Benjamin Chaigne22 and Luc Mouthon22, 1Université Paris Cité, Montrouge, France, 2Internal Medicine and Immunology, CHU Tours, Tours, France, 3Henri Mondor hospital, Créteil, France, 4Internal medicine, Nantes University Hospital, Nantes, France, 5Bichat hospital, Paris, France, 6Department of Internal Medicine, Bichat University Hospital, Université Paris Cité, AP-HP, Paris, France, Paris, France, 7Necker hospital, Paris, France, 8Department of Rheumatology, National referral center for auto immune disease and Sjogren disease, Université Paris-Saclay, INSERM UMR1184: Centre for Immunology of Viral Infections and Autoimmune Diseases, Assistance Publique-Hôpitaux de Paris, Hôpital Bicêtre, Le Kremlin Bicêtre, Paris, France., le kremlin bicetre, France, 9Université Paris-Saclay, Le Kremlin Bicetre, France, 10Department of Internal Medicine and Clinical Immunology, Sorbonne Universités, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Centre national de références Maladies Autoimmunes et systémiques rares, Centre national de références Maladies Autoinflammatoires rares et Amylose inflammatoire (CEREMAIA), INSERM, UMR S959, Immunology-Immunopathology-Immunotherapy (I3), Paris, France, Paris, France, 11Internal Medicine, CHU Rouen, Rouen, France, 12Rouen hospital, Rouen, France, 13Université Paris Saclay, Department of Internal Medicine and Clinical Immunology, Bicêtre Hospital, APHP, UMR1184 Inserm, CEA, Le Kremlin Bicêtre, France, Kremlin Bicêtre, France, 14Bicêtre hospital, Kremlin Bicêtre, France, 15Internal medicine and clinical immunology, Université Bourgogne Europe , CHU Dijon Bourgogne, Dijon, France, 16CHU Dijon Bourgogne, Dijon, France, 17Foch hospital, Suresnes, France, 18Amiens hospital, Amiens, France, 19Ambroise Paré hospital, Boulogne, France, 20Cochin hospital, Paris, France, 21Hopital Cochin, Paris, France, 22Department of Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, Cochin University Hospital, Université Paris Cité, AP-HP, Paris, France, 23Department of Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, Hospital Cochin, Paris, France, 24CHU Lille, Département de Médecine Interne et Immunologie Clinique, Centre de Référence des Maladies Auto-Immunes et Auto-Inflammatoires Rares du Nord, Nord-Ouest, Méditerranée et Guadeloupe (CeRAINOM), Lille, France, Lille, France

    Background/Purpose: Mixed connective tissue disease (MCTD) is a rare systemic disorder that belongs to connective tissue diseases (CTD). Approximately 25% of MCTD patients will meet…
  • Abstract Number: 0126 • ACR Convergence 2025

    Performance of the 2023 and 2006 APS Classification Criteria in Pediatric Patients Diagnosed with APS: A Multisite Cohort Study

    Jacqueline Madison1, Elizabeth Sloan2, Cristina Saez3, Olivia Kwan4, Kevin Lewis1, Jonathan Marilao5, Blake Baay6, Rasha Elrefai4, Marissa Dale7, Deborah McCurdy8, Jheel Bhatt9, Sasidhar Goteti10, Ekemini Ogbu11, Jason S. Knight1 and Yu (Ray) Zuo1, 1University of Michigan, Ann Arbor, MI, 2UT Southwestern, Children's Medical Center, and Scottish Rite for Children, Dallas, TX, 3Children's Hospital Colorado, Glendale, CO, 4Baylor College of Medicine, Houston, TX, 5University of Texas Southwestern, Dallas, TX, 6Scottish Rite for Children, Dallas, TX, 7Hospital for Special Surgery/NYP Cornell, New York, NY, 8UCLA Medical Center, Los Angeles, CA, 9Advent Health Orlando, Orlando, FL, 10University of Utah, Salt Lake City, UT, 11Cincinnati Children's Hospital Medical Center, Cincinnati, OH

    Background/Purpose: Antiphospholipid syndrome (APS) is a thrombo-inflammatory disorder that causes significant morbidity and mortality, even in children. The 2023 ACR/EULAR classification criteria, which use weighted…
  • Abstract Number: 2405 • ACR Convergence 2025

    Machine Learning in SLE Diagnosis: Performance of the SLE Risk Probability Index Questionnaire in a Multicenter Cohort of Patients with Systemic Lupus Erythematosus

    Joan Manuel Dapeña1, Eliana Serrano1, Juan Manuel Bande2, María Alejandra Medina2, Diana klajn2, José Caracciolo2, Cecilia Castro3, Julieta Morbiducci4, Aixa Lucia Merce5, Rossella Tralice6, Gabriela Vanesa Espasa7, Yessika Jackeline Soria7, Maria Lilia Leguizamón8, Mariana Pera7, Inés Verónica Bellomio9, María Silvia Yacuzzi10, Maximiliano Machado Escobar11, Máximo Cosentino12, Lucila Garcia13, Mercedes Garcia12, Carolina Aeschlimann14, Graciela Noemi Gomez15, Nicolas Perez16 and Silvia Beatriz Papasidero2, 1Sanatorio Dr Julio Méndez, CABA, Ciudad Autonoma de Buenos Aires, Argentina, 2Hospital General de Agudos Dr. Enrique Tornú, Buenos Aires, Argentina, 3Hospital Z.G.A Dr. Isidoro Iriarte de Quilmes, Quilmes, Buenos Aires, Argentina, 4Hospital General de Agudos Bernardino Rivadavia, Capital Federal, Ciudad Autonoma de Buenos Aires, Argentina, 5Hospital General de Agudos Bernardino Rivadavia, Buenos Aires, Ciudad Autonoma de Buenos Aires, Argentina, 6Hospital General de Agudos Bernardino Rivadavia, Buenos Aires, Argentina, 7Hospital Padilla de Tucumán, Tucumán, Argentina, 8Hospital Padilla de Tucumán, San Miguel de Tucuman, Argentina, 9Hospital Padilla, Tucumán, Argentina, San Miguel de Tucumán, Argentina, 10Hospital Eva Perón de Tucumán, Tucuman, Argentina, 11Hospital Eva Perón de Tucumán, Tucumán, Argentina, 12Hospital Interzonal General de Agudos “General San Martín” de la plata, La Plata, Argentina, 13Hospital San Martin de La Plata, La Plata, Argentina, La Plata, Argentina, 14Hospital Provincial de Rosario, Rosario, Argentina, 15Instituto de Investigaciones Médicas Dr. Alfredo Lanari, Don Torcuato, Argentina, 16Instituto de Investigaciones Médicas Dr. Alfredo Lanari, Buenos Aires, Argentina

    Background/Purpose: The SLE Risk Probability Index (SLERPI), a clinical prediction model for systemic lupus erythematosus (SLE), was developed using machine‑learning variable‑selection techniques (Random Forest, LASSO).…
  • Abstract Number: 0117 • ACR Convergence 2025

    Are Thrombotic or Obstetric Events Associated with Additional Clinical Domains in Triple Antiphospholypid Syndrome?

    Cristina Rocamora-Gisbert1, Francina salabert-Carreras2, Raquel Ugena-García3, Cristina Calomarde-Gómez3, Clara Churtichaga Domenech2, Judith Vidal-Ripoll2, Laia Gifre-Sala2, Agueda Prior-Español2, Annika Nack1, Susana Holgado4, Maria Aparicio1, Melania Martínez-Morillo2, LOURDES MATEO SORIA5, Anne Riveros frutos1, Ivette Casafont-Solé3 and Judit Font-Urgelles3, 1Hospital Germans Trias i Pujol, Barcelona, Spain, 2Hospital Germans Trias i Pujol, Barcelona, 3Hospital Universitari Germans Trias i Pujol, Badalona, Spain, 4Hospital Germans Trias i Pujol, Barcelona, Catalonia, Spain, 5HOSPITAL GERMANS TRIAS I PUJOL, BADALONA, Spain

    Background/Purpose: It is known that triple positive antiphospholipid syndrome (APS-TP) is related to an increased presence of thrombotic and obstetric manifestations. Triple positivity is referred…
  • Abstract Number: 2404 • ACR Convergence 2025

    Clinical features of Elderly-onset Systemic Lupus Erythematosus

    Jessica Dai1, Erin Carter2, Mala Masson3, Amit Saxena4, H Michael Belmont5, Peter Izmirly6 and Jill Buyon4, 1New York University Grossman School of Medicine, Tenafly, NJ, 2New York University Grossman School of Medicine, New York, NY, 3NYU Langone Medical Center- Division of Rheumatology, New York, NY, 4NYU Grossman School of Medicine, New York, NY, 5NYU School of Medicine, New York, NY, 6New York University Grossman School of Medicine, New York, NY

    Background/Purpose: Systemic lupus erythematosus (SLE) is a multisystemic chronic disease characterized by a wide range of clinical and serological manifestations. It most commonly affects young…
  • Abstract Number: 2156 • ACR Convergence 2025

    Bridging the Gap: Juvenile Spondyloarthritis (JSpA) vs. Chronic Non-Bacterial Osteomyelitis (CNO)

    Sophia Elfrink1, Timothy Brandon1, Jahan Jazayeri1 and Pamela Weiss2, 1Children's Hospital of Philadelphia, Philadelphia, PA, 2Childrens Hospital of Philadelphia, Philadelphia, PA

    Background/Purpose: The relationship between juvenile spondyloarthritis (JSpA) and chronic nonbacterial osteomyelitis (CNO) remains poorly defined. This study aimed to assess the proportion of pediatric patients…
  • Abstract Number: 2136 • ACR Convergence 2025

    Confirming The Validity Of The New EULAR/ACR Classification Criteria For Pediatric Chronic Nonbacterial Osteomyelitis

    Greta Mastrangelo1, Edan Itzkovitz2, Katherine Sawicka3, Ingrid Goh4, Ari Bitnun5, Sevan Hopyan5, Paul Nathan2, Ronald laxer1 and Brian Feldman1, 1The Hospital for Sick Children, Toronto, ON, Canada, 2The Hospital for Sick Children, Toronto, 3The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada, 4University of Toronto The Hospital for Sick Children, Toronto, ON, Canada, 5The Hospital for Sick Children, Toronto, Canada

    Background/Purpose: Chronic nonbacterial osteomyelitis (CNO) is a noninfectious autoinflammatory bone disease which remains a diagnosis of exclusion, as existing diagnostic criteria are not widely accepted.…
  • Abstract Number: 1672 • ACR Convergence 2025

    Classification criteria, disease phenotypes and long-term outcomes of childhood Sjögren’s Disease into adulthood

    Coziana Ciurtin1, Ruby Gotch2, Hannah Peckham1, Robert Wilson2, Muthana AlObaidi3 and Elizabeth C Jury1, 1University College London, London, United Kingdom, 2University College London Hospital NHS Trust, London, United Kingdom, 3Great Ormond Street Hospital, London, United Kingdom

    Background/Purpose: Childhood Sjögren Disease (cSjD) is a rare clinical phenotype lacking research on long-term outcomes and impact on the quality of life of young people…
  • Abstract Number: 1575 • ACR Convergence 2025

    Clinical presentation, course, treatment and outcome of juvenile onset versus adult onset mixed connective tissue disease patients: a multicenter retrospective cohort.

    Kevin Chevalier1, Brigitte Bader-Meunier2, Isabelle Kone-Paut3, Benjamin Torreau4, Marc Michel5, Bertrand Godeau5, Christian AGARD6, Thomas Papo7, Karim Sacré8, Raphaele Seror9, Xavier Mariette10, Cacoub Patrice11, Ygal Benhamou12, Mathilde Leclercq13, Cécile goujard14, Olivier Lambotte3, Bernard Bonnotte15, Maxime Samson16, Félix Ackermann17, Jean Schmidt18, Pierre Duhaut18, Jean-Emmanuel Kahn19, Thomas Hanslik19, Nathalie Costedoat-Chalumeau20, Benjamin Terrier20, Alexis REGENT21, bertrand Dunogue22, Pascal Cohen23, Véronique Le Guern20, Eric HACHULLA24, Luc Mouthon22 and Benjamin Chaigne22, 1Université Paris Cité, Montrouge, France, 2Necker hospital, Paris, France, 3Bicêtre hospital, Kremlin Bicêtre, France, 4Internal Medicine and Immunology, CHU Tours, Tours, France, 5Henri Mondor hospital, Créteil, France, 6Internal medicine, Nantes University Hospital, Nantes, France, 7Bichat hospital, Paris, France, 8Department of Internal Medicine, Bichat University Hospital, Université Paris Cité, AP-HP, Paris, France, Paris, France, 9Department of Rheumatology, National referral center for auto immune disease and Sjogren disease, Université Paris-Saclay, INSERM UMR1184: Centre for Immunology of Viral Infections and Autoimmune Diseases, Assistance Publique-Hôpitaux de Paris, Hôpital Bicêtre, Le Kremlin Bicêtre, Paris, France., le kremlin bicetre, France, 10Université Paris-Saclay, Le Kremlin Bicetre, France, 11Department of Internal Medicine and Clinical Immunology, Sorbonne Universités, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Centre national de références Maladies Autoimmunes et systémiques rares, Centre national de références Maladies Autoinflammatoires rares et Amylose inflammatoire (CEREMAIA), INSERM, UMR S959, Immunology-Immunopathology-Immunotherapy (I3), Paris, France, Paris, France, 12Internal Medicine, CHU Rouen, Rouen, France, 13Rouen hospital, Rouen, France, 14Université Paris Saclay, Department of Internal Medicine and Clinical Immunology, Bicêtre Hospital, APHP, UMR1184 Inserm, CEA, Le Kremlin Bicêtre, France, Kremlin Bicêtre, France, 15Internal medicine and clinical immunology, Université Bourgogne Europe , CHU Dijon Bourgogne, Dijon, France, 16CHU Dijon Bourgogne, Dijon, France, 17Foch hospital, Suresnes, France, 18Amiens hospital, Amiens, France, 19Ambroise Paré hospital, Boulogne, France, 20Cochin hospital, Paris, France, 21Hopital Cochin, Paris, France, 22Department of Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, Cochin University Hospital, Université Paris Cité, AP-HP, Paris, France, 23Department of Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, Hospital Cochin, Paris, France, 24CHU Lille, Département de Médecine Interne et Immunologie Clinique, Centre de Référence des Maladies Auto-Immunes et Auto-Inflammatoires Rares du Nord, Nord-Ouest, Méditerranée et Guadeloupe (CeRAINOM), Lille, France, Lille, France

    Background/Purpose: Mixed connective tissue disease (MCTD) is an entity defined by clinical features of differentiated connective tissue diseases (dCTD), such as systemic lupus erythematosus (SLE),…
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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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