Mostrar el registro sencillo

dc.contributor.authorElHafeez, Samar Abd
dc.contributor.authorKramer, Anneke
dc.contributor.authorArici, Mustafa
dc.contributor.authorArnol, Miha
dc.contributor.authorAsberg, Anders
dc.contributor.authorBell, Samira
dc.contributor.authorBelliere, Julie
dc.contributor.authorDíaz Corte, Carmen
dc.contributor.authorFernández Fresnedo, Gema 
dc.contributor.authorHemmelder, Marc
dc.contributor.authorHeylen, Line
dc.contributor.authorHommel, Kristine
dc.contributor.authorKerschbaum, Julia
dc.contributor.authorNaumovic, Radomir
dc.contributor.authorNitsch, Dorothea
dc.contributor.authorSantamaria, Rafael
dc.contributor.authorFinne, Patrick
dc.contributor.authorPalsson, Runolfur
dc.contributor.authorPippias, Maria
dc.contributor.authorResic, Halima
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2024-12-11T19:23:47Z
dc.date.available2024-12-11T19:23:47Z
dc.date.issued2024
dc.identifier.issn0931-0509
dc.identifier.issn1460-2385
dc.identifier.urihttps://hdl.handle.net/10902/34600
dc.description.abstractBackground: Primary glomerular disease (PGD) is a major cause of end-stage kidney disease (ESKD) leading to kidney replacement therapy (KRT). We aimed to describe incidence (trends) in individuals starting KRT for ESKD due to PGD and to examine their survival and causes of death. Methods: We used data from the European Renal Association (ERA) Registry on 69 854 patients who started KRT for ESKD due to PGD between 2000 and 2019. ERA primary renal disease codes were used to define six PGD subgroups. We examined age and sex standardized incidence, trend of the incidence and survival. Results: The standardized incidence of KRT for ESKD due to PGD was 16.6 per million population (pmp), ranging from 8.6 pmp in Serbia to 20.0 pmp in France. Immunoglobulin A nephropathy (IgAN) and focal segmental glomerulosclerosis (FSGS) had the highest incidences, of 4.6 pmp and 2.6 pmp, respectively. Histologically non-examined PGDs represented over 50% of cases in Serbia, Bosnia and Herzegovina, and Romania and were also common in Greece, Estonia, Belgium and Sweden. The incidence declined from 18.6 pmp in 2000 to 14.5 pmp in 2013, after which it stabilized. All PGD subgroups had 5-year survival probabilities above 50%, with crescentic glomerulonephritis having the highest risk of death [adjusted hazard ratio 1.8 (95% confidence interval 1.6-1.9)] compared with IgAN. Cardiovascular disease was the most common cause of death (33.9%). Conclusion: The incidence of KRT for ESKD due to PGD showed large differences between countries and was highest and increasing for IgAN and FSGS. Lack of kidney biopsy facilities in some countries may have affected accurate assignment of the cause of ESKD. The recognition of the incidence and outcomes of KRT among different PGD subgroups may contribute to a more individualized patient care approach.es_ES
dc.description.sponsorshipFUNDING: K.J. and V.S. report grants from the European Renal Association. A.O.’s research is supported by Comunidad de Madrid en Biomedicina P2022/BMD-7223, CIFRA_COR-CM. Instituto de Salud Carlos III (ISCIII) RICORS program to RICORS2040 (RD21/0005/0001, RD21/0005/0016) funded by European Union—NextGenerationEU, Mecanismo para la Recuperación y la Resiliencia (MRR) and SPACKDc PMP21/00 109, FEDER funds, COST Action PERMEDIK CA21165, supported by COST (European Cooperation in Science and Technology) and PREVENTCKD Consortium Project ID: 101 101 220 Programme: EU4H DG/Agency: HADEA. ACKNOWLEDGEMENTS: We would like to thank the patients and the staff of the dialysis and transplant units for contributing the data via their national and regional renal registries. Furthermore, we gratefully acknowledge the following registries and persons for their contribution of the data: Austrian Dialysis and Transplant Registry (OEDTR) (F. Engler, G. Mayer and the Austrian Society of Nephrology); Dutch-speaking Belgian Society of Nephrology (NBVN]) (M. Couttenye, F. Schroven and J. De Meester); French-speaking Belgian Society of Nephrology (GNFB) (J.M. des Grottes and F. Collart); Estonian Society of Nephrology (Ü. Pechter and K. Lilienthal); Finnish Registry for Kidney Diseases (J. Helve and H. Niemelä); France: The Epidemiology and Information Network in Nephrology (REIN) (M. Lassalle and C. Couchoud); Hellenic Renal Registry (G. Moustakas); Norwegian Renal Registry (A.V. Reisæter); Romanian Renal Registry (RRR) (G. Mircescu, L. Garneata, and E. Podgoreanu); Renal Registry in Serbia (M. Lausevic, all of the Serbian renal units, and the Serbian Society of Nephrology); Spain Renal Registry (B. Mahillo Durán and M.O. Valentín Muñoz); Swedish Renal Registry (SRR) (K.G. Prütz, M. Stendahl, M. Evans, S. Schön, T. Lundgren and H. Rydell); Swiss Dialysis Registry (P. Ambühl and R. Guidotti); Dutch Renal Registry (RENINE) (L. Heuveling, S. Vogelaar and M. ten Dam); UK Renal Registry (all the staff of the UK Renal Registry and of the renal units submitting data); Scottish Renal Registry (SRR) (all of the Scottish renal units); and the regional registries of Andalusia (SICATA) [P. Castro de la Nuez (on behalf of all users of SICATA)], Aragon (F. Arribas Monzón), Asturias (P. Beltrán, M. Rodríguez, J.R. Quirós and RERCA Working Group), Basque country (UNIPAR) (Á. Magaz, J. Aranzabal, M. Rodrigo and I. Moina), Cantabria (J.C. Ruiz San Millán), Castile and León (M.A. Palencia García and P. Ucio Mingo), Castile-La Mancha (G. Gutiérrez Ávila and I. Moreno Alía), Catalonia (RMRC) (J. Comas and J. Tort), Community of Madrid (M.I. Aparicio de Madre and F. Tornero Molina), Extremadura [all the renal units (Nephrology and Dialysis)], Galicia (E. Bouzas-Caamaño), Murcia (I. Marín Sánchez and C. Santiuste de Pablos), Navarre (M.F. Slon Roblero, J. Manrique Escola and J. Arteaga Coloma) and Valencian region (O.L. Rodríguez-Arévalo and O. Zurriaga); and the other ERA Registry committee members not mentioned above for their advice in the analysis and the drafting of this paper: C. Wanner, P. Ambühl, P.M. Ferraro, J. Harambat, J. Helve, J.E. Sánchez-Alvarez, R. Boenink and B.A. Boerstra, and M.E. Astley in the AMC Registry office for data collection and management. The ERA Registry is funded by the European Renal Association (ERA).es_ES
dc.format.extent12 p.es_ES
dc.language.isoenges_ES
dc.publisherOxford University Presses_ES
dc.rights© The Author(s) 2024. Published by Oxford University Press on behalf of the ERA. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.comes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.sourceNephrology, Dialysis, Transplantation, 2024, 39, 1449-1460es_ES
dc.subject.otherDialysises_ES
dc.subject.otherEpidemiologyes_ES
dc.subject.otherKidney replacement therapyes_ES
dc.subject.otherOutcomees_ES
dc.subject.otherPrimary glomerular diseasees_ES
dc.titleIncidence and outcomes of kidney replacement therapy for end-stage kidney disease due to primary glomerular disease in Europe: findings from the ERA Registryes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1093/ndt/gfae034es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1093/ndt/gfae034
dc.type.versionpublishedVersiones_ES


Ficheros en el ítem

Thumbnail

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo

© The Author(s) 2024. Published by Oxford University Press on behalf of the ERA. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.comExcepto si se señala otra cosa, la licencia del ítem se describe como © The Author(s) 2024. Published by Oxford University Press on behalf of the ERA. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com