Does eGFR improve the diagnostic capability of S-Creatinine concentration results? A retrospective population based study

<p>The use of MDRD-eGFR to diagnose Chronic Kidney Disease (CKD) is based on the assumption that the algorithm will minimize the influence of age, gender and ethnicity that is observed in S-Creatinine concentration and thus allow a single cut-off at which further diagnostic and therapeutic act...

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Main Author: Anders Kallner, Peter A Ayling, Zahra Khatami
Format: Article
Language:English
Published: Ivyspring International Publisher 2008-01-01
Series:International Journal of Medical Sciences
Online Access:http://www.medsci.org/v05p0009.htm
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spelling doaj-69da8046c30b4d79841dad31da2476392020-11-24T21:06:08ZengIvyspring International PublisherInternational Journal of Medical Sciences1449-19072008-01-0151917Does eGFR improve the diagnostic capability of S-Creatinine concentration results? A retrospective population based studyAnders Kallner, Peter A Ayling, Zahra Khatami<p>The use of MDRD-eGFR to diagnose Chronic Kidney Disease (CKD) is based on the assumption that the algorithm will minimize the influence of age, gender and ethnicity that is observed in S-Creatinine concentration and thus allow a single cut-off at which further diagnostic and therapeutic actions should be considered. This hypothesis is tested in a retrospective analysis of outpatients (N=93,404) and hospitalised (N=35,572) patients in UK and Sweden, respectively. An algorithm based on the same model as the MDRD-eGFR algorithm was derived from simultaneously measured S-Creatinine concentrations and Iohexol GFR in a subset of 565 patients. The combined uncertainty of using this algorithm was estimated to about 15 % which is about three times that of the S-Creatinine concentration results. The diagnostic performance of S-Creatinine concentration was evaluated using the Iohexol clearance as the reference procedure. It was shown that the diagnostic capacity of MDRD-eGFR, as it stands, has no added value compared to S-Creatinine. The gender and age differences of the S-Creatinine concentrations in the dataset persist after applying the MDRD-eGFR algorithm. Thus, a general use of the MDRD-eGFR does not seem justified. Furthermore the claim that the eGFR is adjusted for body area is misleading; the algorithm does not include any body size marker. It is thus a dangerous marker for guiding drug administration.</p>http://www.medsci.org/v05p0009.htm
collection DOAJ
language English
format Article
sources DOAJ
author Anders Kallner, Peter A Ayling, Zahra Khatami
spellingShingle Anders Kallner, Peter A Ayling, Zahra Khatami
Does eGFR improve the diagnostic capability of S-Creatinine concentration results? A retrospective population based study
International Journal of Medical Sciences
author_facet Anders Kallner, Peter A Ayling, Zahra Khatami
author_sort Anders Kallner, Peter A Ayling, Zahra Khatami
title Does eGFR improve the diagnostic capability of S-Creatinine concentration results? A retrospective population based study
title_short Does eGFR improve the diagnostic capability of S-Creatinine concentration results? A retrospective population based study
title_full Does eGFR improve the diagnostic capability of S-Creatinine concentration results? A retrospective population based study
title_fullStr Does eGFR improve the diagnostic capability of S-Creatinine concentration results? A retrospective population based study
title_full_unstemmed Does eGFR improve the diagnostic capability of S-Creatinine concentration results? A retrospective population based study
title_sort does egfr improve the diagnostic capability of s-creatinine concentration results? a retrospective population based study
publisher Ivyspring International Publisher
series International Journal of Medical Sciences
issn 1449-1907
publishDate 2008-01-01
description <p>The use of MDRD-eGFR to diagnose Chronic Kidney Disease (CKD) is based on the assumption that the algorithm will minimize the influence of age, gender and ethnicity that is observed in S-Creatinine concentration and thus allow a single cut-off at which further diagnostic and therapeutic actions should be considered. This hypothesis is tested in a retrospective analysis of outpatients (N=93,404) and hospitalised (N=35,572) patients in UK and Sweden, respectively. An algorithm based on the same model as the MDRD-eGFR algorithm was derived from simultaneously measured S-Creatinine concentrations and Iohexol GFR in a subset of 565 patients. The combined uncertainty of using this algorithm was estimated to about 15 % which is about three times that of the S-Creatinine concentration results. The diagnostic performance of S-Creatinine concentration was evaluated using the Iohexol clearance as the reference procedure. It was shown that the diagnostic capacity of MDRD-eGFR, as it stands, has no added value compared to S-Creatinine. The gender and age differences of the S-Creatinine concentrations in the dataset persist after applying the MDRD-eGFR algorithm. Thus, a general use of the MDRD-eGFR does not seem justified. Furthermore the claim that the eGFR is adjusted for body area is misleading; the algorithm does not include any body size marker. It is thus a dangerous marker for guiding drug administration.</p>
url http://www.medsci.org/v05p0009.htm
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