The Joint Vasculitis Registry in German-speaking countries (GeVas) – a prospective, multicenter registry for the follow-up of long-term outcomes in vasculitis

Abstract Background Vasculitides comprise a group of rare diseases which affect less than 5 in 10.000 individuals. Most types of vasculitis can become organ- and life-threatening and are characterized by chronicity, high morbidity and relapses, altogether resulting in significant morbidity and morta...

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Main Authors: Christof Iking-Konert, Pia Wallmeier, Sabrina Arnold, Sabine Adler, Kirsten de Groot, Bernhard Hellmich, Bimba F. Hoyer, Konstanze Holl-Ulrich, Gabriele Ihorst, Margit Kaufmann, Ina Kötter, Ulf Müller-Ladner, T. Magnus, Jürgen Rech, Fabian Schubach, Hendrik Schulze-Koops, Nils Venhoff, Thorsten Wiech, Peter Villiger, Peter Lamprecht
Format: Article
Language:English
Published: BMC 2021-07-01
Series:BMC Rheumatology
Subjects:
Online Access:https://doi.org/10.1186/s41927-021-00206-2
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language English
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author Christof Iking-Konert
Pia Wallmeier
Sabrina Arnold
Sabine Adler
Kirsten de Groot
Bernhard Hellmich
Bimba F. Hoyer
Konstanze Holl-Ulrich
Gabriele Ihorst
Margit Kaufmann
Ina Kötter
Ulf Müller-Ladner
T. Magnus
Jürgen Rech
Fabian Schubach
Hendrik Schulze-Koops
Nils Venhoff
Thorsten Wiech
Peter Villiger
Peter Lamprecht
spellingShingle Christof Iking-Konert
Pia Wallmeier
Sabrina Arnold
Sabine Adler
Kirsten de Groot
Bernhard Hellmich
Bimba F. Hoyer
Konstanze Holl-Ulrich
Gabriele Ihorst
Margit Kaufmann
Ina Kötter
Ulf Müller-Ladner
T. Magnus
Jürgen Rech
Fabian Schubach
Hendrik Schulze-Koops
Nils Venhoff
Thorsten Wiech
Peter Villiger
Peter Lamprecht
The Joint Vasculitis Registry in German-speaking countries (GeVas) – a prospective, multicenter registry for the follow-up of long-term outcomes in vasculitis
BMC Rheumatology
Vasculitis
GeVas
ANCA
Prospective
Registry
Giant cell arteritis
author_facet Christof Iking-Konert
Pia Wallmeier
Sabrina Arnold
Sabine Adler
Kirsten de Groot
Bernhard Hellmich
Bimba F. Hoyer
Konstanze Holl-Ulrich
Gabriele Ihorst
Margit Kaufmann
Ina Kötter
Ulf Müller-Ladner
T. Magnus
Jürgen Rech
Fabian Schubach
Hendrik Schulze-Koops
Nils Venhoff
Thorsten Wiech
Peter Villiger
Peter Lamprecht
author_sort Christof Iking-Konert
title The Joint Vasculitis Registry in German-speaking countries (GeVas) – a prospective, multicenter registry for the follow-up of long-term outcomes in vasculitis
title_short The Joint Vasculitis Registry in German-speaking countries (GeVas) – a prospective, multicenter registry for the follow-up of long-term outcomes in vasculitis
title_full The Joint Vasculitis Registry in German-speaking countries (GeVas) – a prospective, multicenter registry for the follow-up of long-term outcomes in vasculitis
title_fullStr The Joint Vasculitis Registry in German-speaking countries (GeVas) – a prospective, multicenter registry for the follow-up of long-term outcomes in vasculitis
title_full_unstemmed The Joint Vasculitis Registry in German-speaking countries (GeVas) – a prospective, multicenter registry for the follow-up of long-term outcomes in vasculitis
title_sort joint vasculitis registry in german-speaking countries (gevas) – a prospective, multicenter registry for the follow-up of long-term outcomes in vasculitis
publisher BMC
series BMC Rheumatology
issn 2520-1026
publishDate 2021-07-01
description Abstract Background Vasculitides comprise a group of rare diseases which affect less than 5 in 10.000 individuals. Most types of vasculitis can become organ- and life-threatening and are characterized by chronicity, high morbidity and relapses, altogether resulting in significant morbidity and mortality. Previous studies have been either monocentric or mainly retrospective – studies with a prospective design mostly consisted of rather small cohorts of 100 to 200 patients. The aim of the Joint Vasculitis Registry in German-speaking countries (GeVas) is to record all patients who have been recently diagnosed with vasculitis or who have changed their treatment due to a relapse (inception cohort). In GeVas, data are collected prospectively in a multicenter design in Germany, Austria and Switzerland. By this approach, courses of vasculitis and their outcomes can be monitored over an extended period. Methods GeVas is a prospective, web-based, multicenter, clinician-driven registry for the documentation of organ manifestations, damage, long-term progress and other outcomes of various types of vasculitis. The registry started recruiting in June 2019. As of October 2020, 14 centers have been initiated and started recruiting patients in Germany. Involvement of sites in Austria and the German-speaking counties of Switzerland is scheduled in the near future. Discussion In June 2019, we successfully established a prospective multicenter vasculitis registry being the first of its kind in German-speaking countries. The participating centers are currently recruiting, and systematic analysis of long-term vasculitis outcomes is expected in the ensuing period. Trial registration German Clinical Trials Register (Deutsches Register Klinischer Studien): DRKS00011866 . Registered 10 May 2019.
topic Vasculitis
GeVas
ANCA
Prospective
Registry
Giant cell arteritis
url https://doi.org/10.1186/s41927-021-00206-2
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spelling doaj-8f59c30451b24487839dad2ba4d31aca2021-08-01T11:29:26ZengBMCBMC Rheumatology2520-10262021-07-01511710.1186/s41927-021-00206-2The Joint Vasculitis Registry in German-speaking countries (GeVas) – a prospective, multicenter registry for the follow-up of long-term outcomes in vasculitisChristof Iking-Konert0Pia Wallmeier1Sabrina Arnold2Sabine Adler3Kirsten de Groot4Bernhard Hellmich5Bimba F. Hoyer6Konstanze Holl-Ulrich7Gabriele Ihorst8Margit Kaufmann9Ina Kötter10Ulf Müller-Ladner11T. Magnus12Jürgen Rech13Fabian Schubach14Hendrik Schulze-Koops15Nils Venhoff16Thorsten Wiech17Peter Villiger18Peter Lamprecht19Sektion Rheumatologie, III Med. Klinik, Universitätsklinikum Hamburg EppendorfSektion Rheumatologie, III Med. Klinik, Universitätsklinikum Hamburg EppendorfDepartment of Rheumatology and Clinical Immunology, University of LübeckSimZentrum ErfurtMed Klinik III, Innere Medizin, Rheumatologie, Nephrologie, Sana Klinikum Offenbach/MainKlinik für Innere Medizin, Rheumatologie und Immunologie medius KLINIK KirchheimRheumatologie/klinische Immunologie und Exzellenzzentrum Entzündungsmedizin, Klinik für Innere Medizin IPathologie Hamburg, Labor Lademannbogen MVZ GmbHClinical Trials Unit, Faculty of Medicine, Medical Center – University of Freiburg, University of FreiburgClinical Trials Unit, Faculty of Medicine, Medical Center – University of Freiburg, University of FreiburgSektion Rheumatologie, III Med. Klinik, Universitätsklinikum Hamburg Eppendorf und Klinikum Bad BramstedtAbt. Rheumatologie und Klinische Immunologie, JLU GiessenNeurologische Klinik, Universitätsklinikum Hamburg EppendorfUni-Klinikum Erlangen, Department of Internal Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander University (FAU) Erlangen-Nürnberg and Universitätsklinikum ErlangenClinical Trials Unit, Faculty of Medicine, Medical Center – University of Freiburg, University of FreiburgDivision of Rheumatology and Clinical Immunology, Department of Internal Medicine IV, Ludwig-Maximilians-University MunichDepartment of Rheumatology and Clinical Immunology, Faculty of Medicine, Medical Center – University of Freiburg, University of FreiburgSektion Nephropathologie, Institut für Pathologie, Universitätsklinikum Hamburg-EppendorfUniversity Hospital and University of BernDepartment of Rheumatology and Clinical Immunology, University of LübeckAbstract Background Vasculitides comprise a group of rare diseases which affect less than 5 in 10.000 individuals. Most types of vasculitis can become organ- and life-threatening and are characterized by chronicity, high morbidity and relapses, altogether resulting in significant morbidity and mortality. Previous studies have been either monocentric or mainly retrospective – studies with a prospective design mostly consisted of rather small cohorts of 100 to 200 patients. The aim of the Joint Vasculitis Registry in German-speaking countries (GeVas) is to record all patients who have been recently diagnosed with vasculitis or who have changed their treatment due to a relapse (inception cohort). In GeVas, data are collected prospectively in a multicenter design in Germany, Austria and Switzerland. By this approach, courses of vasculitis and their outcomes can be monitored over an extended period. Methods GeVas is a prospective, web-based, multicenter, clinician-driven registry for the documentation of organ manifestations, damage, long-term progress and other outcomes of various types of vasculitis. The registry started recruiting in June 2019. As of October 2020, 14 centers have been initiated and started recruiting patients in Germany. Involvement of sites in Austria and the German-speaking counties of Switzerland is scheduled in the near future. Discussion In June 2019, we successfully established a prospective multicenter vasculitis registry being the first of its kind in German-speaking countries. The participating centers are currently recruiting, and systematic analysis of long-term vasculitis outcomes is expected in the ensuing period. Trial registration German Clinical Trials Register (Deutsches Register Klinischer Studien): DRKS00011866 . Registered 10 May 2019.https://doi.org/10.1186/s41927-021-00206-2VasculitisGeVasANCAProspectiveRegistryGiant cell arteritis