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Therapeutic variability in adult minimal change disease and focal segmental glomerulosclerosis
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 patter...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4886920/ https://www.ncbi.nlm.nih.gov/pubmed/27274821 http://dx.doi.org/10.1093/ckj/sfw028 |
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author | Fernandez-Juarez, Gema Villacorta, Javier Ruiz-Roso, Gloria Panizo, Nayara Martinez-Marín, Isabel Marco, Helena Arrizabalaga, Pilar Díaz, Montserrat Perez-Gómez, Vanessa Vaca, Marco Rodríguez, Eva Cobelo, Carmen Fernandez, Loreto Avila, Ana Praga, Manuel Quereda, Carlos Ortiz, Alberto |
author_facet | Fernandez-Juarez, Gema Villacorta, Javier Ruiz-Roso, Gloria Panizo, Nayara Martinez-Marín, Isabel Marco, Helena Arrizabalaga, Pilar Díaz, Montserrat Perez-Gómez, Vanessa Vaca, Marco Rodríguez, Eva Cobelo, Carmen Fernandez, Loreto Avila, Ana Praga, Manuel Quereda, Carlos Ortiz, Alberto |
author_sort | Fernandez-Juarez, Gema |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-4886920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48869202016-06-03 Therapeutic variability in adult minimal change disease and focal segmental glomerulosclerosis Fernandez-Juarez, Gema Villacorta, Javier Ruiz-Roso, Gloria Panizo, Nayara Martinez-Marín, Isabel Marco, Helena Arrizabalaga, Pilar Díaz, Montserrat Perez-Gómez, Vanessa Vaca, Marco Rodríguez, Eva Cobelo, Carmen Fernandez, Loreto Avila, Ana Praga, Manuel Quereda, Carlos Ortiz, Alberto Clin Kidney J Glomerulonephritis 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. Oxford University Press 2016-06 2016-05-24 /pmc/articles/PMC4886920/ /pubmed/27274821 http://dx.doi.org/10.1093/ckj/sfw028 Text en © The Author 2016. Published by Oxford University Press on behalf of ERA-EDTA. http://creativecommons.org/licenses/by-nc/4.0/ 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. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Glomerulonephritis Fernandez-Juarez, Gema Villacorta, Javier Ruiz-Roso, Gloria Panizo, Nayara Martinez-Marín, Isabel Marco, Helena Arrizabalaga, Pilar Díaz, Montserrat Perez-Gómez, Vanessa Vaca, Marco Rodríguez, Eva Cobelo, Carmen Fernandez, Loreto Avila, Ana Praga, Manuel Quereda, Carlos Ortiz, Alberto Therapeutic variability in adult minimal change disease and focal segmental glomerulosclerosis |
title | Therapeutic variability in adult minimal change disease and focal segmental glomerulosclerosis |
title_full | Therapeutic variability in adult minimal change disease and focal segmental glomerulosclerosis |
title_fullStr | Therapeutic variability in adult minimal change disease and focal segmental glomerulosclerosis |
title_full_unstemmed | Therapeutic variability in adult minimal change disease and focal segmental glomerulosclerosis |
title_short | Therapeutic variability in adult minimal change disease and focal segmental glomerulosclerosis |
title_sort | therapeutic variability in adult minimal change disease and focal segmental glomerulosclerosis |
topic | Glomerulonephritis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4886920/ https://www.ncbi.nlm.nih.gov/pubmed/27274821 http://dx.doi.org/10.1093/ckj/sfw028 |
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