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Development and validation of a predictive mortality risk score from a European hemodialysis cohort

Although mortality risk scores for chronic hemodialysis (HD) patients should have an important role in clinical decision-making, those currently available have limited applicability, robustness, and generalizability. Here we applied a modified Framingham Heart Study approach to derive 1- and 2-year...

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Autores principales: Floege, Jürgen, Gillespie, Iain A, Kronenberg, Florian, Anker, Stefan D, Gioni, Ioanna, Richards, Sharon, Pisoni, Ronald L, Robinson, Bruce M, Marcelli, Daniele, Froissart, Marc, Eckardt, Kai-Uwe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424813/
https://www.ncbi.nlm.nih.gov/pubmed/25651366
http://dx.doi.org/10.1038/ki.2014.419
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author Floege, Jürgen
Gillespie, Iain A
Kronenberg, Florian
Anker, Stefan D
Gioni, Ioanna
Richards, Sharon
Pisoni, Ronald L
Robinson, Bruce M
Marcelli, Daniele
Froissart, Marc
Eckardt, Kai-Uwe
author_facet Floege, Jürgen
Gillespie, Iain A
Kronenberg, Florian
Anker, Stefan D
Gioni, Ioanna
Richards, Sharon
Pisoni, Ronald L
Robinson, Bruce M
Marcelli, Daniele
Froissart, Marc
Eckardt, Kai-Uwe
author_sort Floege, Jürgen
collection PubMed
description Although mortality risk scores for chronic hemodialysis (HD) patients should have an important role in clinical decision-making, those currently available have limited applicability, robustness, and generalizability. Here we applied a modified Framingham Heart Study approach to derive 1- and 2-year all-cause mortality risk scores using a 11,508 European incident HD patient database (AROii) recruited between 2007 and 2009. This scoring model was validated externally using similar-sized Dialysis Outcomes and Practice Patterns Survey (DOPPS) data. For AROii, the observed 1- and 2-year mortality rates were 13.0 (95% confidence interval (CI; 12.3–13.8)) and 11.2 (10.4–12.1)/100 patient years, respectively. Increasing age, low body mass index, history of cardiovascular disease or cancer, and use of a vascular access catheter during baseline were consistent predictors of mortality. Among baseline laboratory markers, hemoglobin, ferritin, C-reactive protein, serum albumin, and creatinine predicted death within 1 and 2 years. When applied to the DOPPS population, the predictive risk score models were highly discriminatory, and generalizability remained high when restricted by incidence/prevalence and geographic location (C-statistics 0.68–0.79). This new model offers improved predictive power over age/comorbidity-based models and also predicted early mortality (C-statistic 0.71). Our new model delivers a robust and reproducible mortality risk score, based on readily available clinical and laboratory data.
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spelling pubmed-44248132015-05-21 Development and validation of a predictive mortality risk score from a European hemodialysis cohort Floege, Jürgen Gillespie, Iain A Kronenberg, Florian Anker, Stefan D Gioni, Ioanna Richards, Sharon Pisoni, Ronald L Robinson, Bruce M Marcelli, Daniele Froissart, Marc Eckardt, Kai-Uwe Kidney Int Clinical Investigation Although mortality risk scores for chronic hemodialysis (HD) patients should have an important role in clinical decision-making, those currently available have limited applicability, robustness, and generalizability. Here we applied a modified Framingham Heart Study approach to derive 1- and 2-year all-cause mortality risk scores using a 11,508 European incident HD patient database (AROii) recruited between 2007 and 2009. This scoring model was validated externally using similar-sized Dialysis Outcomes and Practice Patterns Survey (DOPPS) data. For AROii, the observed 1- and 2-year mortality rates were 13.0 (95% confidence interval (CI; 12.3–13.8)) and 11.2 (10.4–12.1)/100 patient years, respectively. Increasing age, low body mass index, history of cardiovascular disease or cancer, and use of a vascular access catheter during baseline were consistent predictors of mortality. Among baseline laboratory markers, hemoglobin, ferritin, C-reactive protein, serum albumin, and creatinine predicted death within 1 and 2 years. When applied to the DOPPS population, the predictive risk score models were highly discriminatory, and generalizability remained high when restricted by incidence/prevalence and geographic location (C-statistics 0.68–0.79). This new model offers improved predictive power over age/comorbidity-based models and also predicted early mortality (C-statistic 0.71). Our new model delivers a robust and reproducible mortality risk score, based on readily available clinical and laboratory data. Nature Publishing Group 2015-05 2015-02-04 /pmc/articles/PMC4424813/ /pubmed/25651366 http://dx.doi.org/10.1038/ki.2014.419 Text en Copyright © 2015 International Society of Nephrology http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Clinical Investigation
Floege, Jürgen
Gillespie, Iain A
Kronenberg, Florian
Anker, Stefan D
Gioni, Ioanna
Richards, Sharon
Pisoni, Ronald L
Robinson, Bruce M
Marcelli, Daniele
Froissart, Marc
Eckardt, Kai-Uwe
Development and validation of a predictive mortality risk score from a European hemodialysis cohort
title Development and validation of a predictive mortality risk score from a European hemodialysis cohort
title_full Development and validation of a predictive mortality risk score from a European hemodialysis cohort
title_fullStr Development and validation of a predictive mortality risk score from a European hemodialysis cohort
title_full_unstemmed Development and validation of a predictive mortality risk score from a European hemodialysis cohort
title_short Development and validation of a predictive mortality risk score from a European hemodialysis cohort
title_sort development and validation of a predictive mortality risk score from a european hemodialysis cohort
topic Clinical Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424813/
https://www.ncbi.nlm.nih.gov/pubmed/25651366
http://dx.doi.org/10.1038/ki.2014.419
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