Vis enkel innførsel

dc.contributor.authorDerner, Ondrej
dc.contributor.authorKramer, Anneke
dc.contributor.authorHruskova, Zdenka
dc.contributor.authorArici, Mustafa
dc.contributor.authorCollart, Frederic
dc.contributor.authorFinne, Patrik
dc.contributor.authorFuentes Sánchez, Laura
dc.contributor.authorHarambat, Jérôme
dc.contributor.authorHemmelder, Marc H.
dc.contributor.authorHommel, Kristine
dc.contributor.authorKerschbaum, Julia
dc.contributor.authorDe Meester, Johan
dc.contributor.authorPalsson, Runolfur
dc.contributor.authorSegelmark, Mårten
dc.contributor.authorSkrunes, Rannveig
dc.contributor.authorTraynor, Jamie P.
dc.contributor.authorZurriaga, Oscar
dc.contributor.authorMassy, Ziad A.
dc.contributor.authorJager, Kitty J.
dc.contributor.authorStel, Vianda S.
dc.contributor.authorTesar, Vladimir
dc.date.accessioned2022-09-06T13:18:47Z
dc.date.available2022-09-06T13:18:47Z
dc.date.created2022-05-20T08:05:31Z
dc.date.issued2022
dc.identifier.issn0272-6386
dc.identifier.urihttps://hdl.handle.net/11250/3016050
dc.description.abstractRationale & Objective There is a dearth of data characterizing patients receiving kidney replacement therapy (KRT) for kidney failure due to systemic lupus erythematosus (SLE) and their clinical outcomes. The aim of this study was to describe trends in incidence and prevalence of KRT among these patients as well as to compare their outcomes versus those of patients treated with KRT for diseases other than SLE. Study Design Retrospective cohort study based on kidney registry data. Setting & Participants Patients recorded in 14 registries of patients receiving KRT that provided data to the European Renal Association Registry between 1992 and 2016. Predictor SLE as cause of kidney failure. Outcomes Incidence and prevalence of KRT, patient survival while receiving KRT, patient and graft survival after kidney transplant, and specific causes of death. Analytical Approach Kaplan-Meier methods and Cox regression models were fit to compare patient survival between the SLE and non-SLE groups, overall KRT, dialysis, and patient and graft survival after kidney transplant. Results In total, 1,826 patients commenced KRT for kidney failure due to SLE, representing an incidence of 0.80 per million population (pmp) per year. The incidence remained stable during the study period (annual percent change, 0.1% [95% CI, −0.6% to 0.8%]). Patient survival among patients with SLE receiving KRT was similar to survival in the comparator group (hazard ratio [HR], 1.11 [95% CI, 0.99-1.23]). After kidney transplant, the risk of death was greater among patients with SLE than among patients in the comparator group (HR, 1.25 [95% CI, 1.02-1.53]), whereas the risk of all-cause graft failure was similar (HR, 1.09 [95% CI, 0.95-1.27]). Ten-year patient overall survival during KRT and patient and graft survival after kidney transplant improved over the study period (HRs of 0.71 [95% CI, 0.56-0.91], 0.43 [95% CI, 0.27-0.69], and 0.60 [95% CI, 0.43-0.84], respectively). Patients with SLE receiving KRT were significantly more likely to die of infections (24.8%) than patients in the comparator group (16.9%; P < 0.001). Limitations No data were available on extrarenal manifestations of SLE, drug treatments, comorbidities, kidney transplant characteristics, or relapses of SLE. Conclusions The prognosis of patients with SLE receiving KRT has improved over time. Survival of patients with SLE who required KRT was similar compared with patients who required KRT for other causes of kidney failure. Survival following kidney transplants was worse among patients with SLE.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleIncidence of Kidney Replacement Therapy and Subsequent Outcomes Among Patients With Systemic Lupus Erythematosus: Findings From the ERA Registryen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2021 The Author(s)en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1053/j.ajkd.2021.09.016
dc.identifier.cristin2025804
dc.source.journalAmerican Journal of Kidney Diseasesen_US
dc.source.pagenumber635-645en_US
dc.identifier.citationAmerican Journal of Kidney Diseases. 2022, 79 (5), 635-645.en_US
dc.source.volume79en_US
dc.source.issue5en_US


Tilhørende fil(er)

Thumbnail

Denne innførselen finnes i følgende samling(er)

Vis enkel innførsel

Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
Med mindre annet er angitt, så er denne innførselen lisensiert som Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal