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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Series: | International Journal of Medical Sciences |
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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 |
work_keys_str_mv |
AT anderskallnerpeteraaylingzahrakhatami doesegfrimprovethediagnosticcapabilityofscreatinineconcentrationresultsaretrospectivepopulationbasedstudy |
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