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Therapeutic variability in adult minimal change disease and focal segmental glomerulosclerosis.

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dc.contributor.author Fernandez-Juarez, Gema
dc.contributor.author Villacorta, Javier
dc.contributor.author Ruiz-Roso, Gloria
dc.contributor.author Panizo, Nayara
dc.contributor.author Martinez-Marín, Isabel
dc.contributor.author Marco, Helena
dc.contributor.author Arrizabalaga, Pilar
dc.contributor.author Díaz, Montserrat
dc.contributor.author Perez-Gómez, Vanessa
dc.contributor.author Vaca, Marco
dc.contributor.author Rodríguez García, Eva
dc.contributor.author Cobelo, Carmen
dc.contributor.author Fernandez, Loreto
dc.contributor.author Avila, Ana
dc.contributor.author Praga, Manuel
dc.contributor.author Quereda, Carlos
dc.contributor.author Ortiz, Alberto
dc.date.accessioned 2016-07-11T08:02:45Z
dc.date.available 2016-07-11T08:02:45Z
dc.date.issued 2016
dc.identifier.citation Fernandez-Juarez G, Villacorta J, Ruiz-Roso G, Panizo N, Martinez-Marín I, Marco H. et al. Therapeutic variability in adult minimal change disease and focal segmental glomerulosclerosis. Clin Kidney J. 2016 Jun;9(3):381-6. doi: 10.1093/ckj/sfw028
dc.identifier.issn 2048-8505
dc.identifier.uri http://hdl.handle.net/10230/27020
dc.description.abstract BACKGROUND: Variability in the management of glomerulonephritis may negatively impact efficacy and safety. However, there are little/no data on actual variability in the treatment of minimal change disease (MCD)/focal segmental glomerulosclerosis (FSGS) in adults. We assessed Spanish practice patterns for the management of adult nephrotic syndrome due to MCD or FSGS. The absence of reasonably good evidence on treatment for a disease often increases the variability substantially. Identification of evidence-practice gaps is the first necessary step in the knowledge-to-action cyclical process. We aim to analyse the real clinical practice in adults in hospitals in Spain and compare this with the recently released Kidney Disease: Improving Global Outcomes clinical practice guideline for glomerulonephritis. METHODS: Participating centres were required to include all adult patients (age >18 years) with a biopsy-proven diagnosis of MCD or FSGS from 2007 to 2011. Exclusion criteria included the diagnosis of secondary nephropathy. RESULTS: We studied 119 Caucasian patients with biopsy-proven MCD (n = 71) or FSGS (n = 48) from 13 Spanish hospitals. Of these patients, 102 received immunosuppressive treatment and 17 conservative treatment. The initial treatment was steroids, except in one patient in which mycophenolate mofetil was used. In all patients, the steroids were given as a single daily dose. The mean duration of steroid treatment at initial high doses was 8.7 ± 13.2 weeks and the mean global duration was 38 ± 32 weeks. The duration of initial high-dose steroids was <4 weeks in 41% of patients and >16 weeks in 10.5% of patients. We did find a weak and negative correlation between the duration of whole steroid treatment in the first episode and the number of the later relapses (r = -0.24, P = 0.023). There were 98 relapses and they were more frequent in MCD than in FSGs patients (2.10 ± 1.6 versus 1.56 ± 1.2; P = 0.09). The chosen treatment was mainly steroids (95%). Only seven relapses were treated with another drug as a first-line treatment: two relapses were treated with mycophenolate and five relapses were treated with anticalcineurinics. A second-line treatment was needed in 29 patients (24.4%), and the most frequent drugs were the calcineurin inhibitors (55%), followed by mycophenolate mofetil (31%). Although cyclophosphamide is the recommended treatment, it was used in only 14% of the patients. CONCLUSIONS: We found variation from the guidelines in the duration of initial and tapered steroid therapy, in the medical criteria for classifying a steroid-resistant condition and in the chosen treatment for the second-line treatment. All nephrologists started with a daily dose of steroids as the first-line treatment. The most frequently used steroid-sparing drug was calcineurin inhibitors. Cyclophosphamide use was much lower than expected.
dc.description.sponsorship A.O. received ISCII and FEDER funds (FIS PI13/00047ISCIII-RETIC REDinREN RD12/0021), Programa Intensificación Actividad Investigadora (ISCIII/Agencia Laín-Entralgo/CM).
dc.format.mimetype application/pdf
dc.language.iso eng
dc.publisher Oxford University Press
dc.relation.ispartof Clinical Kidney Journal. 2016 Jun;9(3):381-6
dc.rights © The Author 2016. Published by Oxford University Press on behalf of ERA-EDTA.This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://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.
dc.rights.uri https://creativecommons.org/licenses/by-nc/4.0/
dc.subject.other Glomerulonefritis -- Tractament
dc.subject.other Immunosupressió
dc.title Therapeutic variability in adult minimal change disease and focal segmental glomerulosclerosis.
dc.type info:eu-repo/semantics/article
dc.identifier.doi http://dx.doi.org/10.1093/ckj/sfw028
dc.rights.accessRights info:eu-repo/semantics/openAccess
dc.type.version info:eu-repo/semantics/publishedVersion

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