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Classification of Kidney Transplant Recipients Using a Combination of Estimated GFR and Albuminuria Reflects Risk
BACKGROUND: The 2012 Kidney Dialysis Initiative Global Outcomes chronic kidney disease (CKD) classification scheme subdivides stage 3 CKD and incorporates the urinary albumin-to-creatinine ratio (ACR). The aim of this study was to evaluate whether the novel scheme provides graded risk in kidney tran...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082996/ https://www.ncbi.nlm.nih.gov/pubmed/27819037 http://dx.doi.org/10.1097/TXD.0000000000000606 |
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author | White, Christine A. Akbari, Ayub Talreja, Hari Lalani, Neha Knoll, Greg A. |
author_facet | White, Christine A. Akbari, Ayub Talreja, Hari Lalani, Neha Knoll, Greg A. |
author_sort | White, Christine A. |
collection | PubMed |
description | BACKGROUND: The 2012 Kidney Dialysis Initiative Global Outcomes chronic kidney disease (CKD) classification scheme subdivides stage 3 CKD and incorporates the urinary albumin-to-creatinine ratio (ACR). The aim of this study was to evaluate whether the novel scheme provides graded risk in kidney transplant recipients (KTRs). METHODS: Prevalent KTRs with available laboratory data were included. The primary outcome was a composite of doubling of serum creatinine, graft failure, or death. Patients were stratified using the CKD-Epidemiolgic Collaboration equation, and ACR and the event rate per 1000 patient-years in each CKD category were calculated. RESULTS: There were 269 KTRs with a mean follow-up of 4.5 ± 2.0 years. There was a graded increase in outcomes with increasing ACR and decreasing estimated glomerular filtration rate (eGFR). For the primary outcome, the event rate was 15.3 (95% confidence interval, 4.2-39.2) per 1000 patient-years for those with an eGFR greater than 60 mL/min per 1.73 m(2) and an ACR less than 30 mg/g, whereas it was 375 (95% confidence interval, 193.8-655.1) for those with an eGFR less than 30 mL/min per 1.73 m(2) and an ACR greater than 300 mg/g. CONCLUSIONS: The novel Kidney Dialysis Initiative Global Outcomes classification scheme provides graded risk for important clinical events in KTRs. This information can be used to identify high-risk patients and to tailor follow-up and management strategies aimed at improving outcomes. |
format | Online Article Text |
id | pubmed-5082996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-50829962017-03-27 Classification of Kidney Transplant Recipients Using a Combination of Estimated GFR and Albuminuria Reflects Risk White, Christine A. Akbari, Ayub Talreja, Hari Lalani, Neha Knoll, Greg A. Transplant Direct Kidney Transplantation BACKGROUND: The 2012 Kidney Dialysis Initiative Global Outcomes chronic kidney disease (CKD) classification scheme subdivides stage 3 CKD and incorporates the urinary albumin-to-creatinine ratio (ACR). The aim of this study was to evaluate whether the novel scheme provides graded risk in kidney transplant recipients (KTRs). METHODS: Prevalent KTRs with available laboratory data were included. The primary outcome was a composite of doubling of serum creatinine, graft failure, or death. Patients were stratified using the CKD-Epidemiolgic Collaboration equation, and ACR and the event rate per 1000 patient-years in each CKD category were calculated. RESULTS: There were 269 KTRs with a mean follow-up of 4.5 ± 2.0 years. There was a graded increase in outcomes with increasing ACR and decreasing estimated glomerular filtration rate (eGFR). For the primary outcome, the event rate was 15.3 (95% confidence interval, 4.2-39.2) per 1000 patient-years for those with an eGFR greater than 60 mL/min per 1.73 m(2) and an ACR less than 30 mg/g, whereas it was 375 (95% confidence interval, 193.8-655.1) for those with an eGFR less than 30 mL/min per 1.73 m(2) and an ACR greater than 300 mg/g. CONCLUSIONS: The novel Kidney Dialysis Initiative Global Outcomes classification scheme provides graded risk for important clinical events in KTRs. This information can be used to identify high-risk patients and to tailor follow-up and management strategies aimed at improving outcomes. Lippincott Williams & Wilkins 2016-07-25 /pmc/articles/PMC5082996/ /pubmed/27819037 http://dx.doi.org/10.1097/TXD.0000000000000606 Text en Copyright © 2016 The Authors. Transplantation Direct. Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. |
spellingShingle | Kidney Transplantation White, Christine A. Akbari, Ayub Talreja, Hari Lalani, Neha Knoll, Greg A. Classification of Kidney Transplant Recipients Using a Combination of Estimated GFR and Albuminuria Reflects Risk |
title | Classification of Kidney Transplant Recipients Using a Combination of Estimated GFR and Albuminuria Reflects Risk |
title_full | Classification of Kidney Transplant Recipients Using a Combination of Estimated GFR and Albuminuria Reflects Risk |
title_fullStr | Classification of Kidney Transplant Recipients Using a Combination of Estimated GFR and Albuminuria Reflects Risk |
title_full_unstemmed | Classification of Kidney Transplant Recipients Using a Combination of Estimated GFR and Albuminuria Reflects Risk |
title_short | Classification of Kidney Transplant Recipients Using a Combination of Estimated GFR and Albuminuria Reflects Risk |
title_sort | classification of kidney transplant recipients using a combination of estimated gfr and albuminuria reflects risk |
topic | Kidney Transplantation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082996/ https://www.ncbi.nlm.nih.gov/pubmed/27819037 http://dx.doi.org/10.1097/TXD.0000000000000606 |
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