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Current Transition Practice for Primary Immunodeficiencies and Autoinflammatory Diseases in Europe: a RITA-ERN Survey.
Israni, Muskan; Nicholson, Bethany; Mahlaoui, Nizar; Obici, Laura; Rossi-Semerano, Linda; Lachmann, Helen; Hayward, Georgia; Avramovic, Mojca Zajc; Guffroy, Aurelien; Dalm, Virgil; Rimmer, Rachel; Solis, Leire; Villar, Carlotta; Gennery, Andrew R; Skeffington, Stephanie; Nordin, Julia; Warnatz, Klaus; Korganow, Anne-Sophie; Antón, Jordi; Cattalini, Marco; Amin, Tania; Berg, Stephan; Soler-Palacin, Pere; Burns, Siobhan O; Campbell, Mari.
Afiliação
  • Israni M; Department of Immunology, Royal Free London NHS Foundation Trust, London, UK.
  • Nicholson B; Department of Immunology, Royal Free London NHS Foundation Trust, London, UK.
  • Mahlaoui N; Pediatric Immuno-Haematology and Rheumatology Unit, Necker Enfants Malades University Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Obici L; French National Reference Center for Primary Immune Deficiencies (CEREDIH), Necker Enfants Malades University Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Rossi-Semerano L; Fondazione IRCCS Policlinico San Matteo, Centro Per Lo Studio E La Cura Delle Amiloidosi Sistemiche, Pavia, Italy.
  • Lachmann H; Department of Pediatric Rheumatology, National Reference Centre for Auto-Inflammatory Diseases and Amyloidosis of Inflammatory Origin (CEREMAIA), Bicêtre hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Le Kremlin Bicêtre, France.
  • Hayward G; Division of Medicine, National Amyloidosis Centre, University College London, London, UK.
  • Avramovic MZ; Paediatric and Adult Rheumatology, Leeds General Infirmary and Chapel Allerton Hospital, Leeds, UK.
  • Guffroy A; Department for Allergology, Rheumatology and Clinical Immunology, University Children's Hospital Ljubljana, Ljubljana, Slovenia.
  • Dalm V; Department of Clinical Immunology and Internal Medicine, Tertiary Center for Primary Immunodeficiency, National Reference Center for Systemic Autoimmune Diseases (CNR RESO), Hôpitaux Universitaires de Strasbourg, 67000, Strasbourg, France.
  • Rimmer R; Université de Strasbourg, INSERM UMR - S1109, 67000, Strasbourg, France.
  • Solis L; Department of Internal Medicine, Division of Clinical Immunology, Erasmus University Medical Center, Rotterdam, the Netherlands.
  • Villar C; Department of Immunology, Erasmus University Medical Center, Rotterdam, the Netherlands.
  • Gennery AR; Rare Autoinflammatory Conditions Community - UK (RACC - UK), Oxford, UK.
  • Skeffington S; .
  • Nordin J; International Patient Organisation for Primary Immunodeficiencies (IPOPI), Brussels, Belgium.
  • Warnatz K; Barcelona PID Foundation, Barcelona, Spain.
  • Korganow AS; Paediatric Haematopoietic Stem Cell Transplant Unit, Great North Children's Hospital (GNCH), Royal Victoria Infirmary, Queen Victoria Road, Newcastle upon Tyne, NE1 4LP, UK.
  • Antón J; Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.
  • Cattalini M; Irish Vasculitis Organisation, Dublin, Ireland.
  • Amin T; International Patient Organisation for Primary Immunodeficiencies (IPOPI), Brussels, Belgium.
  • Berg S; Center for Chronic Immunodeficiency, Medical Center, Faculty of Medicine, University of Freiburg, University of Freiburg, Freiburg, Germany.
  • Soler-Palacin P; Department of Rheumatology and Clinical Immunology, Division of Immunodeficiency, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Burns SO; Department of Clinical Immunology and Internal Medicine, Tertiary Center for Primary Immunodeficiency, National Reference Center for Systemic Autoimmune Diseases (CNR RESO), Hôpitaux Universitaires de Strasbourg, 67000, Strasbourg, France.
  • Campbell M; Université de Strasbourg, INSERM UMR - S1109, 67000, Strasbourg, France.
J Clin Immunol ; 43(1): 206-216, 2023 01.
Article em En | MEDLINE | ID: mdl-36222999
BACKGROUND: Due to the absence of curative treatments for inborn errors of immunity (IEI), children born with IEI require long-term follow-up for disease manifestations and related complications that occur over the lifespan. Effective transition from pediatric to adult services is known to significantly improve adherence to treatment and long-term outcomes. It is currently not known what transition services are available for young people with IEI in Europe. OBJECTIVE: To understand the prevalence and practice of transition services in Europe for young people with IEI, encompassing both primary immunodeficiencies (PID) and systemic autoinflammatory disorders (AID). METHODS: A survey was generated by the European Reference Network on immunodeficiency, autoinflammatory, and autoimmune diseases Transition Working Group and electronically circulated, through professional networks, to pediatric centers across Europe looking after children with IEI. RESULTS: Seventy-six responses were received from 52 centers, in 45 cities across 17 different countries. All services transitioned patients to adult services, mainly to specialist PID or AID centers, typically transferring up to ten patients to adult care each year. The transition process started at a median age of 16-18 years with transfer to the adult center occurring at a median age of 18-20 years. 75% of PID and 68% of AID centers held at least one joint appointment with pediatric and adult services prior to the transfer of care. Approximately 75% of PID and AID services reported having a defined transition process, but few centers reported national disease-specific transition guidelines to refer to. CONCLUSIONS: Transition services for children with IEI in Europe are available in many countries but lack standardized guidelines to promote best practice.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Autoimunes / Doenças Hereditárias Autoinflamatórias / Síndromes de Imunodeficiência Tipo de estudo: Guideline / Qualitative_research / Risk_factors_studies Limite: Adolescent / Adult / Child / Humans País/Região como assunto: Europa Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Autoimunes / Doenças Hereditárias Autoinflamatórias / Síndromes de Imunodeficiência Tipo de estudo: Guideline / Qualitative_research / Risk_factors_studies Limite: Adolescent / Adult / Child / Humans País/Região como assunto: Europa Idioma: En Ano de publicação: 2023 Tipo de documento: Article