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Childhood Steroid-resistant Nephrotic Syndrome: Long-term Outcomes from a Tertiary Care Center
INTRODUCTION: Steroid-resistant nephrotic syndrome (SRNS) is a rare condition that accounts for about 10% to 20% of all nephrotic syndromes in children. While calcineurin inhibitors induce remission in the majority, the data on long-term outcomes are limited. This retrospective study aimed to look a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364992/ https://www.ncbi.nlm.nih.gov/pubmed/35967537 http://dx.doi.org/10.4103/ijn.ijn_258_21 |
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author | Agrwal, Shipra Mantan, Mukta Dabas, Aashima Batra, Vineeta V. |
author_facet | Agrwal, Shipra Mantan, Mukta Dabas, Aashima Batra, Vineeta V. |
author_sort | Agrwal, Shipra |
collection | PubMed |
description | INTRODUCTION: Steroid-resistant nephrotic syndrome (SRNS) is a rare condition that accounts for about 10% to 20% of all nephrotic syndromes in children. While calcineurin inhibitors induce remission in the majority, the data on long-term outcomes are limited. This retrospective study aimed to look at the clinical profile, biopsy findings, and long-term treatment outcomes in children with SRNS. METHODS: The records of all children (1–18 years) with SRNS with biopsy findings of minimal change disease (MCD), focal segmental glomerulosclerosis (FSGS), or mesangioproliferative glomerulonephritis, who received treatment for a minimum period of 12 months and were in follow-up during the years 2007–2018 at a tertiary care teaching hospital were retrieved. The clinical, histopathological, and biochemical factors and treatment outcomes were recorded and analyzed. RESULTS: Ninety-one (72 boys) children with a median (interquartile range [IQR]) age of onset of nephrotic syndrome as 48 (24–87) months were included. MCD and FSGS were the most common histopathological types (57.1% and 36.3%, respectively) and 62 (68.1%) patients had late steroid resistance. Calcineurin inhibitors (CNIs) were used in 86.8% of the children, and response rates with cyclosporine and tacrolimus for complete remission (CR) were 80% and 73.7%, respectively, with median (IQR) time to response being 3 (2–4) months. The presence of MCD on histology and the use of CNIs were significantly associated with CR (P < 0.01). At a median (IQR) follow-up of 5 (3–7) years, 76 (83.5%) children had either CR or partial remission, four (4.4%) developed chronic kidney disease and five (5.5%) died (three due to end-stage renal disease and two of infective complications). CONCLUSION: SRNS children with MCD on biopsy, late resistance, and response to CNIs have better long-term outcomes. Most patients respond to CNIs within the first 6 months of use and need therapy for at least 24 to 36 months. |
format | Online Article Text |
id | pubmed-9364992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-93649922022-08-11 Childhood Steroid-resistant Nephrotic Syndrome: Long-term Outcomes from a Tertiary Care Center Agrwal, Shipra Mantan, Mukta Dabas, Aashima Batra, Vineeta V. Indian J Nephrol Original Article INTRODUCTION: Steroid-resistant nephrotic syndrome (SRNS) is a rare condition that accounts for about 10% to 20% of all nephrotic syndromes in children. While calcineurin inhibitors induce remission in the majority, the data on long-term outcomes are limited. This retrospective study aimed to look at the clinical profile, biopsy findings, and long-term treatment outcomes in children with SRNS. METHODS: The records of all children (1–18 years) with SRNS with biopsy findings of minimal change disease (MCD), focal segmental glomerulosclerosis (FSGS), or mesangioproliferative glomerulonephritis, who received treatment for a minimum period of 12 months and were in follow-up during the years 2007–2018 at a tertiary care teaching hospital were retrieved. The clinical, histopathological, and biochemical factors and treatment outcomes were recorded and analyzed. RESULTS: Ninety-one (72 boys) children with a median (interquartile range [IQR]) age of onset of nephrotic syndrome as 48 (24–87) months were included. MCD and FSGS were the most common histopathological types (57.1% and 36.3%, respectively) and 62 (68.1%) patients had late steroid resistance. Calcineurin inhibitors (CNIs) were used in 86.8% of the children, and response rates with cyclosporine and tacrolimus for complete remission (CR) were 80% and 73.7%, respectively, with median (IQR) time to response being 3 (2–4) months. The presence of MCD on histology and the use of CNIs were significantly associated with CR (P < 0.01). At a median (IQR) follow-up of 5 (3–7) years, 76 (83.5%) children had either CR or partial remission, four (4.4%) developed chronic kidney disease and five (5.5%) died (three due to end-stage renal disease and two of infective complications). CONCLUSION: SRNS children with MCD on biopsy, late resistance, and response to CNIs have better long-term outcomes. Most patients respond to CNIs within the first 6 months of use and need therapy for at least 24 to 36 months. Medknow Publications & Media Pvt Ltd 2022 2022-07-16 /pmc/articles/PMC9364992/ /pubmed/35967537 http://dx.doi.org/10.4103/ijn.ijn_258_21 Text en Copyright: © Indian Journal of Nephrology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Agrwal, Shipra Mantan, Mukta Dabas, Aashima Batra, Vineeta V. Childhood Steroid-resistant Nephrotic Syndrome: Long-term Outcomes from a Tertiary Care Center |
title | Childhood Steroid-resistant Nephrotic Syndrome: Long-term Outcomes from a Tertiary Care Center |
title_full | Childhood Steroid-resistant Nephrotic Syndrome: Long-term Outcomes from a Tertiary Care Center |
title_fullStr | Childhood Steroid-resistant Nephrotic Syndrome: Long-term Outcomes from a Tertiary Care Center |
title_full_unstemmed | Childhood Steroid-resistant Nephrotic Syndrome: Long-term Outcomes from a Tertiary Care Center |
title_short | Childhood Steroid-resistant Nephrotic Syndrome: Long-term Outcomes from a Tertiary Care Center |
title_sort | childhood steroid-resistant nephrotic syndrome: long-term outcomes from a tertiary care center |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364992/ https://www.ncbi.nlm.nih.gov/pubmed/35967537 http://dx.doi.org/10.4103/ijn.ijn_258_21 |
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