A short guideline on chronic kidney disease for medical laboratory practice / Kronik böbrek hastalığında tıbbi laboratuvar uygulamaları için kısa kılavuz
Chronic kidney disease (CKD) is asymptomatic in the early stage. Kidney function might be lost 90% when the symptoms are overt. However, in case of early detection, progression of the disease can be prevented or delayed. If not detected it results in end stage renal disease. Therefore, the level of...
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Veröffentlicht in: | Turkish Journal of Biochemistry 2016-08, Vol.41 (4), p.292-301 |
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creator | Abuşoğlu, Sedat Aydın, İlknur Bakar, Funda Bekdemir, Tan Gülbahar, Özlem İşlekel, Hüray Özarda, Yeşim Pektaş, Macit Pir, Kamil Portakal, Oytun Serdar, Muhittin Turhan, Turan Yüce, Doğan Zengi, Oğuzhan |
description | Chronic kidney disease (CKD) is asymptomatic in the early stage. Kidney function might be lost 90% when the symptoms are overt. However, in case of early detection, progression of the disease can be prevented or delayed. If not detected it results in end stage renal disease. Therefore, the level of awareness about CKD should be increased. The role of medical laboratory is utmost important for the diagnosis and staging of CKD. In this paper, the main tasks of the laboratory specialists are described and the outlines are as follows.
• Creatinine assays should be traceable to internationally recognised reference materials and methods, specifically isotope dilution mass spectrometry.
• When reporting the creatinine result, eGFR should also be reported in adult (>18 years) population. A warning expression should be included in the report form if eGFR result is 90 mL/min/1.73 m
• eGFR equations of the adult population should not be used for pediatric population. Different equations utilizing also patient height should be used. The enzymatic creatinine assay should be preferred. eGFR based on cystatin C can be used for confirmation in the pediatric population.
• Cystatin C measurements, at least when eGFR based on creatinine is not reliable and for confirmation should be encouraged.
• Proteinuria or albuminuria values should be measured in spot samples and reported in proportion to creatinine. |
doi_str_mv | 10.1515/tjb-2016-0043 |
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• Creatinine assays should be traceable to internationally recognised reference materials and methods, specifically isotope dilution mass spectrometry.
• When reporting the creatinine result, eGFR should also be reported in adult (>18 years) population. A warning expression should be included in the report form if eGFR result is <60 mL/min/1.73 m
• eGFR values should be expressed quantitatively up to 90 mL/min/1.73 m
by CKD-EPI equation. Above 90 mL/ min/1.73 m
, eGFR values can be expressed quantitatively or >90 mL/min/1.73 m
• eGFR equations of the adult population should not be used for pediatric population. Different equations utilizing also patient height should be used. The enzymatic creatinine assay should be preferred. eGFR based on cystatin C can be used for confirmation in the pediatric population.
• Cystatin C measurements, at least when eGFR based on creatinine is not reliable and for confirmation should be encouraged.
• Proteinuria or albuminuria values should be measured in spot samples and reported in proportion to creatinine.</description><identifier>ISSN: 0250-4685</identifier><identifier>EISSN: 1303-829X</identifier><identifier>DOI: 10.1515/tjb-2016-0043</identifier><language>eng</language><publisher>De Gruyter</publisher><subject>Albumin ; Albümin ; Chronic kidney disease ; Creatinine ; Cystatin C ; Glomerular filtration rate ; Glomerüler filtrasyon hızı ; İdrar ; Kreatinin ; Kronik böbrek hastalığı ; Sistatin C ; Urine</subject><ispartof>Turkish Journal of Biochemistry, 2016-08, Vol.41 (4), p.292-301</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1732-34c40c6f3f6bdff6e03ddb4ec56e6ed05f53a547f5d378b6391237f9c67638443</citedby><cites>FETCH-LOGICAL-c1732-34c40c6f3f6bdff6e03ddb4ec56e6ed05f53a547f5d378b6391237f9c67638443</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.degruyter.com/document/doi/10.1515/tjb-2016-0043/pdf$$EPDF$$P50$$Gwalterdegruyter$$H</linktopdf><linktohtml>$$Uhttps://www.degruyter.com/document/doi/10.1515/tjb-2016-0043/html$$EHTML$$P50$$Gwalterdegruyter$$H</linktohtml><link.rule.ids>314,776,780,860,27903,27904,66500,66904,68284,68688</link.rule.ids></links><search><creatorcontrib>Abuşoğlu, Sedat</creatorcontrib><creatorcontrib>Aydın, İlknur</creatorcontrib><creatorcontrib>Bakar, Funda</creatorcontrib><creatorcontrib>Bekdemir, Tan</creatorcontrib><creatorcontrib>Gülbahar, Özlem</creatorcontrib><creatorcontrib>İşlekel, Hüray</creatorcontrib><creatorcontrib>Özarda, Yeşim</creatorcontrib><creatorcontrib>Pektaş, Macit</creatorcontrib><creatorcontrib>Pir, Kamil</creatorcontrib><creatorcontrib>Portakal, Oytun</creatorcontrib><creatorcontrib>Serdar, Muhittin</creatorcontrib><creatorcontrib>Turhan, Turan</creatorcontrib><creatorcontrib>Yüce, Doğan</creatorcontrib><creatorcontrib>Zengi, Oğuzhan</creatorcontrib><title>A short guideline on chronic kidney disease for medical laboratory practice / Kronik böbrek hastalığında tıbbi laboratuvar uygulamaları için kısa kılavuz</title><title>Turkish Journal of Biochemistry</title><description>Chronic kidney disease (CKD) is asymptomatic in the early stage. Kidney function might be lost 90% when the symptoms are overt. However, in case of early detection, progression of the disease can be prevented or delayed. If not detected it results in end stage renal disease. Therefore, the level of awareness about CKD should be increased. The role of medical laboratory is utmost important for the diagnosis and staging of CKD. In this paper, the main tasks of the laboratory specialists are described and the outlines are as follows.
• Creatinine assays should be traceable to internationally recognised reference materials and methods, specifically isotope dilution mass spectrometry.
• When reporting the creatinine result, eGFR should also be reported in adult (>18 years) population. A warning expression should be included in the report form if eGFR result is <60 mL/min/1.73 m
• eGFR values should be expressed quantitatively up to 90 mL/min/1.73 m
by CKD-EPI equation. Above 90 mL/ min/1.73 m
, eGFR values can be expressed quantitatively or >90 mL/min/1.73 m
• eGFR equations of the adult population should not be used for pediatric population. Different equations utilizing also patient height should be used. The enzymatic creatinine assay should be preferred. eGFR based on cystatin C can be used for confirmation in the pediatric population.
• Cystatin C measurements, at least when eGFR based on creatinine is not reliable and for confirmation should be encouraged.
• Proteinuria or albuminuria values should be measured in spot samples and reported in proportion to creatinine.</description><subject>Albumin</subject><subject>Albümin</subject><subject>Chronic kidney disease</subject><subject>Creatinine</subject><subject>Cystatin C</subject><subject>Glomerular filtration rate</subject><subject>Glomerüler filtrasyon hızı</subject><subject>İdrar</subject><subject>Kreatinin</subject><subject>Kronik böbrek hastalığı</subject><subject>Sistatin C</subject><subject>Urine</subject><issn>0250-4685</issn><issn>1303-829X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNptkLtu1EAUhkeISCwhZfrzAiZz966oooibiEQDEp115rY7u7N2NGMHmZdBoqF2wwvED5a1Ah3N-U_xf0dHHyGXjL5miqmrfm8qTpmuKJXiGVkxQUW15ptvz8mKckUrqdfqBXlZyp5SVXPJV-TXNZRdl3vYDtH5FFsPXQt2l7s2WjhE1_oRXCwei4fQZTh6Fy0mSGi6jH2XR7jLaPtoPVzBp4U7gHn4Y7I_wA5Lj2me5p_z1DqEfp6Mif_Y4R4zDON2SHjEhHmeID78ji0c5qngMhPeDz9ekbOAqfiLv3lOvr57--XmQ3X7-f3Hm-vbyrJa8EpIK6nVQQRtXAjaU-Gckd4q7bV3VAUlUMk6KCfqtdFiw7iow8bqWou1lOKcVE93be5KyT40dzkeMY8No80iuDkJbhbBzSL41H_z1P-OqffZ-W0extPS7Lsht6dP_89JJvmGi0cYR4xU</recordid><startdate>20160801</startdate><enddate>20160801</enddate><creator>Abuşoğlu, Sedat</creator><creator>Aydın, İlknur</creator><creator>Bakar, Funda</creator><creator>Bekdemir, Tan</creator><creator>Gülbahar, Özlem</creator><creator>İşlekel, Hüray</creator><creator>Özarda, Yeşim</creator><creator>Pektaş, Macit</creator><creator>Pir, Kamil</creator><creator>Portakal, Oytun</creator><creator>Serdar, Muhittin</creator><creator>Turhan, Turan</creator><creator>Yüce, Doğan</creator><creator>Zengi, Oğuzhan</creator><general>De Gruyter</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20160801</creationdate><title>A short guideline on chronic kidney disease for medical laboratory practice / Kronik böbrek hastalığında tıbbi laboratuvar uygulamaları için kısa kılavuz</title><author>Abuşoğlu, Sedat ; Aydın, İlknur ; Bakar, Funda ; Bekdemir, Tan ; Gülbahar, Özlem ; İşlekel, Hüray ; Özarda, Yeşim ; Pektaş, Macit ; Pir, Kamil ; Portakal, Oytun ; Serdar, Muhittin ; Turhan, Turan ; Yüce, Doğan ; Zengi, Oğuzhan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1732-34c40c6f3f6bdff6e03ddb4ec56e6ed05f53a547f5d378b6391237f9c67638443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Albumin</topic><topic>Albümin</topic><topic>Chronic kidney disease</topic><topic>Creatinine</topic><topic>Cystatin C</topic><topic>Glomerular filtration rate</topic><topic>Glomerüler filtrasyon hızı</topic><topic>İdrar</topic><topic>Kreatinin</topic><topic>Kronik böbrek hastalığı</topic><topic>Sistatin C</topic><topic>Urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abuşoğlu, Sedat</creatorcontrib><creatorcontrib>Aydın, İlknur</creatorcontrib><creatorcontrib>Bakar, Funda</creatorcontrib><creatorcontrib>Bekdemir, Tan</creatorcontrib><creatorcontrib>Gülbahar, Özlem</creatorcontrib><creatorcontrib>İşlekel, Hüray</creatorcontrib><creatorcontrib>Özarda, Yeşim</creatorcontrib><creatorcontrib>Pektaş, Macit</creatorcontrib><creatorcontrib>Pir, Kamil</creatorcontrib><creatorcontrib>Portakal, Oytun</creatorcontrib><creatorcontrib>Serdar, Muhittin</creatorcontrib><creatorcontrib>Turhan, Turan</creatorcontrib><creatorcontrib>Yüce, Doğan</creatorcontrib><creatorcontrib>Zengi, Oğuzhan</creatorcontrib><collection>CrossRef</collection><jtitle>Turkish Journal of Biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abuşoğlu, Sedat</au><au>Aydın, İlknur</au><au>Bakar, Funda</au><au>Bekdemir, Tan</au><au>Gülbahar, Özlem</au><au>İşlekel, Hüray</au><au>Özarda, Yeşim</au><au>Pektaş, Macit</au><au>Pir, Kamil</au><au>Portakal, Oytun</au><au>Serdar, Muhittin</au><au>Turhan, Turan</au><au>Yüce, Doğan</au><au>Zengi, Oğuzhan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A short guideline on chronic kidney disease for medical laboratory practice / Kronik böbrek hastalığında tıbbi laboratuvar uygulamaları için kısa kılavuz</atitle><jtitle>Turkish Journal of Biochemistry</jtitle><date>2016-08-01</date><risdate>2016</risdate><volume>41</volume><issue>4</issue><spage>292</spage><epage>301</epage><pages>292-301</pages><issn>0250-4685</issn><eissn>1303-829X</eissn><abstract>Chronic kidney disease (CKD) is asymptomatic in the early stage. Kidney function might be lost 90% when the symptoms are overt. However, in case of early detection, progression of the disease can be prevented or delayed. If not detected it results in end stage renal disease. Therefore, the level of awareness about CKD should be increased. The role of medical laboratory is utmost important for the diagnosis and staging of CKD. In this paper, the main tasks of the laboratory specialists are described and the outlines are as follows.
• Creatinine assays should be traceable to internationally recognised reference materials and methods, specifically isotope dilution mass spectrometry.
• When reporting the creatinine result, eGFR should also be reported in adult (>18 years) population. A warning expression should be included in the report form if eGFR result is <60 mL/min/1.73 m
• eGFR values should be expressed quantitatively up to 90 mL/min/1.73 m
by CKD-EPI equation. Above 90 mL/ min/1.73 m
, eGFR values can be expressed quantitatively or >90 mL/min/1.73 m
• eGFR equations of the adult population should not be used for pediatric population. Different equations utilizing also patient height should be used. The enzymatic creatinine assay should be preferred. eGFR based on cystatin C can be used for confirmation in the pediatric population.
• Cystatin C measurements, at least when eGFR based on creatinine is not reliable and for confirmation should be encouraged.
• Proteinuria or albuminuria values should be measured in spot samples and reported in proportion to creatinine.</abstract><pub>De Gruyter</pub><doi>10.1515/tjb-2016-0043</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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source | De Gruyter Open Access Journals; DOAJ Directory of Open Access Journals; De Gruyter journals |
subjects | Albumin Albümin Chronic kidney disease Creatinine Cystatin C Glomerular filtration rate Glomerüler filtrasyon hızı İdrar Kreatinin Kronik böbrek hastalığı Sistatin C Urine |
title | A short guideline on chronic kidney disease for medical laboratory practice / Kronik böbrek hastalığında tıbbi laboratuvar uygulamaları için kısa kılavuz |
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