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Incidence of Initial Renal Replacement Therapy Over the Course of Kidney Disease in Children

The Chronic Kidney Disease in Children Study, a prospective cohort study with data collected from 2003 to 2018, provided the first opportunity to characterize the incidence of renal replacement therapy (RRT) initiation over the life course of pediatric kidney diseases. In the current analysis, param...

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Autores principales: Ng, Derek K, Matheson, Matthew B, Warady, Bradley A, Mendley, Susan R, Furth, Susan L, Muñoz, Alvaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036655/
https://www.ncbi.nlm.nih.gov/pubmed/31595948
http://dx.doi.org/10.1093/aje/kwz220
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author Ng, Derek K
Matheson, Matthew B
Warady, Bradley A
Mendley, Susan R
Furth, Susan L
Muñoz, Alvaro
author_facet Ng, Derek K
Matheson, Matthew B
Warady, Bradley A
Mendley, Susan R
Furth, Susan L
Muñoz, Alvaro
author_sort Ng, Derek K
collection PubMed
description The Chronic Kidney Disease in Children Study, a prospective cohort study with data collected from 2003 to 2018, provided the first opportunity to characterize the incidence of renal replacement therapy (RRT) initiation over the life course of pediatric kidney diseases. In the current analysis, parametric generalized gamma models were fitted and extrapolated for RRT overall and by specific treatment modality (dialysis or preemptive kidney transplant). Children were stratified by type of diagnosis: nonglomerular (mostly congenital; n = 650), glomerular–hemolytic uremic syndrome (HUS; n = 49), or glomerular–non-HUS (heterogeneous childhood onset; n = 216). Estimated durations of time to RRT after disease onset for 99% of the nonglomerular and glomerular–non-HUS groups were 42.5 years (95% confidence interval (CI): 31.0, 54.1) and 25.4 years (95% CI: 14.9, 36.0), respectively. Since onset for the great majority of children in the nonglomerular group was congenital, disease duration equated with age. A simulation-based estimate of age at RRT for 99% of the glomerular population was 37.9 years (95% CI: 33.6, 63.2). These models performed well in cross-validation. Children with glomerular disease received dialysis earlier and were less likely to have a preemptive kidney transplant, while the timing and proportions of dialysis and transplantation were similar for the nonglomerular group. These diagnosis-specific estimates provide insight into patient-centered prognostic information and can assist in RRT planning efforts for children with moderate-to-severe kidney disease who are receiving regular specialty care.
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spelling pubmed-70366552020-03-02 Incidence of Initial Renal Replacement Therapy Over the Course of Kidney Disease in Children Ng, Derek K Matheson, Matthew B Warady, Bradley A Mendley, Susan R Furth, Susan L Muñoz, Alvaro Am J Epidemiol Original Contribution The Chronic Kidney Disease in Children Study, a prospective cohort study with data collected from 2003 to 2018, provided the first opportunity to characterize the incidence of renal replacement therapy (RRT) initiation over the life course of pediatric kidney diseases. In the current analysis, parametric generalized gamma models were fitted and extrapolated for RRT overall and by specific treatment modality (dialysis or preemptive kidney transplant). Children were stratified by type of diagnosis: nonglomerular (mostly congenital; n = 650), glomerular–hemolytic uremic syndrome (HUS; n = 49), or glomerular–non-HUS (heterogeneous childhood onset; n = 216). Estimated durations of time to RRT after disease onset for 99% of the nonglomerular and glomerular–non-HUS groups were 42.5 years (95% confidence interval (CI): 31.0, 54.1) and 25.4 years (95% CI: 14.9, 36.0), respectively. Since onset for the great majority of children in the nonglomerular group was congenital, disease duration equated with age. A simulation-based estimate of age at RRT for 99% of the glomerular population was 37.9 years (95% CI: 33.6, 63.2). These models performed well in cross-validation. Children with glomerular disease received dialysis earlier and were less likely to have a preemptive kidney transplant, while the timing and proportions of dialysis and transplantation were similar for the nonglomerular group. These diagnosis-specific estimates provide insight into patient-centered prognostic information and can assist in RRT planning efforts for children with moderate-to-severe kidney disease who are receiving regular specialty care. Oxford University Press 2019-12 2019-10-09 /pmc/articles/PMC7036655/ /pubmed/31595948 http://dx.doi.org/10.1093/aje/kwz220 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Johns Hopkins Bloomberg School of Public Health. https://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/ (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
spellingShingle Original Contribution
Ng, Derek K
Matheson, Matthew B
Warady, Bradley A
Mendley, Susan R
Furth, Susan L
Muñoz, Alvaro
Incidence of Initial Renal Replacement Therapy Over the Course of Kidney Disease in Children
title Incidence of Initial Renal Replacement Therapy Over the Course of Kidney Disease in Children
title_full Incidence of Initial Renal Replacement Therapy Over the Course of Kidney Disease in Children
title_fullStr Incidence of Initial Renal Replacement Therapy Over the Course of Kidney Disease in Children
title_full_unstemmed Incidence of Initial Renal Replacement Therapy Over the Course of Kidney Disease in Children
title_short Incidence of Initial Renal Replacement Therapy Over the Course of Kidney Disease in Children
title_sort incidence of initial renal replacement therapy over the course of kidney disease in children
topic Original Contribution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036655/
https://www.ncbi.nlm.nih.gov/pubmed/31595948
http://dx.doi.org/10.1093/aje/kwz220
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