eGFR and creatinine clearance in relation to metabolic changes in an unselected patient population
Abstract Background It is widely assumed that moderate to severe renal failure (creatinine clearance < 60 ml/min; or an MDRD-4 (Modification of Diet in Renal Disease equation) < 60 ml/min/1.73 m2 ) is associated with metabolic changes, often needing further assessment and treatment. We investi...
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description | Abstract Background It is widely assumed that moderate to severe renal failure (creatinine clearance < 60 ml/min; or an MDRD-4 (Modification of Diet in Renal Disease equation) < 60 ml/min/1.73 m2 ) is associated with metabolic changes, often needing further assessment and treatment. We investigated whether such abnormalities are already present at earlier stages of kidney disease, as assessed by 24-hour urine sampling and MDRD-4 calculation. Methods A select, retrospective cohort study was conducted. Creatinine clearance was measured by collecting 24-hour urines. The individual eGFRs were calculated with the MDRD-4 formula and patients were then divided by renal function category (< 15, 15–30, 30–45, 45–60, 60–90, > 90 ml/min(/1.73 m2 )). Per clearance category the number of people with anaemia, hypokalaemia, uraemia and hyperphosphataemia was evaluated. Results The median creatinine clearance rate was 67.3 ml/min (quartiles: 42.9–95.8) versus a median MDRD-4-eGFR of 51.6 ml/min/1.73 m2 (35.8–67.7). Anaemia, hyperkalaemia, hypocalcaemia, and uraemia were found to be present at higher levels of creatinine clearance rate and eGFR than previously reported ( p < 0.0005). This increased prevalence was more pronounced in elderly subjects, particularly with respect to anaemia (OR 2.71 and 2.02 for MDRD-4 and creatinine clearance respectively, p < 0.0005). The same holds for the proportion with uraemia (OR 1.85, p < 0.0005) and hypocalcaemia (OR 1.97, p = 0.011) for MDRD-4. Conclusion Metabolic changes in an in- and outpatient hospital population are present at earlier stages than was stated in recent guidelines, especially when creatinine clearance levels are used as indicators. This might have implications for testing and treatment of patients with suspected kidney disease and/or loss of renal function. |
doi_str_mv | 10.1016/j.ejim.2009.07.002 |
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We investigated whether such abnormalities are already present at earlier stages of kidney disease, as assessed by 24-hour urine sampling and MDRD-4 calculation. Methods A select, retrospective cohort study was conducted. Creatinine clearance was measured by collecting 24-hour urines. The individual eGFRs were calculated with the MDRD-4 formula and patients were then divided by renal function category (< 15, 15–30, 30–45, 45–60, 60–90, > 90 ml/min(/1.73 m2 )). Per clearance category the number of people with anaemia, hypokalaemia, uraemia and hyperphosphataemia was evaluated. Results The median creatinine clearance rate was 67.3 ml/min (quartiles: 42.9–95.8) versus a median MDRD-4-eGFR of 51.6 ml/min/1.73 m2 (35.8–67.7). Anaemia, hyperkalaemia, hypocalcaemia, and uraemia were found to be present at higher levels of creatinine clearance rate and eGFR than previously reported ( p < 0.0005). This increased prevalence was more pronounced in elderly subjects, particularly with respect to anaemia (OR 2.71 and 2.02 for MDRD-4 and creatinine clearance respectively, p < 0.0005). The same holds for the proportion with uraemia (OR 1.85, p < 0.0005) and hypocalcaemia (OR 1.97, p = 0.011) for MDRD-4. Conclusion Metabolic changes in an in- and outpatient hospital population are present at earlier stages than was stated in recent guidelines, especially when creatinine clearance levels are used as indicators. This might have implications for testing and treatment of patients with suspected kidney disease and/or loss of renal function.]]></description><identifier>ISSN: 0953-6205</identifier><identifier>EISSN: 1879-0828</identifier><identifier>DOI: 10.1016/j.ejim.2009.07.002</identifier><identifier>PMID: 19818295</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>(estimated) glomerular filtration rate ; 24-hour urine sampling ; Aged ; Anemia - epidemiology ; Anemia - metabolism ; Anemia - physiopathology ; Biochemical disturbances ; Chronic kidney disease ; Creatinine - urine ; Disease Progression ; Female ; Glomerular Filtration Rate ; Humans ; Hyperkalemia - epidemiology ; Hyperkalemia - metabolism ; Hyperkalemia - physiopathology ; Hyperphosphatemia - epidemiology ; Hyperphosphatemia - metabolism ; Hyperphosphatemia - physiopathology ; Internal Medicine ; Kidney Failure, Chronic - epidemiology ; Kidney Failure, Chronic - metabolism ; Kidney Failure, Chronic - physiopathology ; Male ; MDRD-4 ; Middle Aged ; Prevalence ; Retrospective Studies ; Uremia - epidemiology ; Uremia - metabolism ; Uremia - physiopathology</subject><ispartof>European journal of internal medicine, 2009-11, Vol.20 (7), p.722-727</ispartof><rights>European Federation of Internal Medicine.</rights><rights>2009 European Federation of Internal Medicine.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c410t-143d2ea7ee5a08600c2bc7b14ca2eef6f21808ecfe5c7392c72f39fec4ffe1693</citedby><cites>FETCH-LOGICAL-c410t-143d2ea7ee5a08600c2bc7b14ca2eef6f21808ecfe5c7392c72f39fec4ffe1693</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ejim.2009.07.002$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3541,27915,27916,45986</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19818295$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Drion, I</creatorcontrib><creatorcontrib>Joosten, H</creatorcontrib><creatorcontrib>Dikkeschei, L.D</creatorcontrib><creatorcontrib>Groenier, K.H</creatorcontrib><creatorcontrib>Bilo, H.J.G</creatorcontrib><title>eGFR and creatinine clearance in relation to metabolic changes in an unselected patient population</title><title>European journal of internal medicine</title><addtitle>Eur J Intern Med</addtitle><description><![CDATA[Abstract Background It is widely assumed that moderate to severe renal failure (creatinine clearance < 60 ml/min; or an MDRD-4 (Modification of Diet in Renal Disease equation) < 60 ml/min/1.73 m2 ) is associated with metabolic changes, often needing further assessment and treatment. We investigated whether such abnormalities are already present at earlier stages of kidney disease, as assessed by 24-hour urine sampling and MDRD-4 calculation. Methods A select, retrospective cohort study was conducted. Creatinine clearance was measured by collecting 24-hour urines. The individual eGFRs were calculated with the MDRD-4 formula and patients were then divided by renal function category (< 15, 15–30, 30–45, 45–60, 60–90, > 90 ml/min(/1.73 m2 )). Per clearance category the number of people with anaemia, hypokalaemia, uraemia and hyperphosphataemia was evaluated. Results The median creatinine clearance rate was 67.3 ml/min (quartiles: 42.9–95.8) versus a median MDRD-4-eGFR of 51.6 ml/min/1.73 m2 (35.8–67.7). Anaemia, hyperkalaemia, hypocalcaemia, and uraemia were found to be present at higher levels of creatinine clearance rate and eGFR than previously reported ( p < 0.0005). This increased prevalence was more pronounced in elderly subjects, particularly with respect to anaemia (OR 2.71 and 2.02 for MDRD-4 and creatinine clearance respectively, p < 0.0005). The same holds for the proportion with uraemia (OR 1.85, p < 0.0005) and hypocalcaemia (OR 1.97, p = 0.011) for MDRD-4. Conclusion Metabolic changes in an in- and outpatient hospital population are present at earlier stages than was stated in recent guidelines, especially when creatinine clearance levels are used as indicators. This might have implications for testing and treatment of patients with suspected kidney disease and/or loss of renal function.]]></description><subject>(estimated) glomerular filtration rate</subject><subject>24-hour urine sampling</subject><subject>Aged</subject><subject>Anemia - epidemiology</subject><subject>Anemia - metabolism</subject><subject>Anemia - physiopathology</subject><subject>Biochemical disturbances</subject><subject>Chronic kidney disease</subject><subject>Creatinine - urine</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Glomerular Filtration Rate</subject><subject>Humans</subject><subject>Hyperkalemia - epidemiology</subject><subject>Hyperkalemia - metabolism</subject><subject>Hyperkalemia - physiopathology</subject><subject>Hyperphosphatemia - epidemiology</subject><subject>Hyperphosphatemia - metabolism</subject><subject>Hyperphosphatemia - physiopathology</subject><subject>Internal Medicine</subject><subject>Kidney Failure, Chronic - epidemiology</subject><subject>Kidney Failure, Chronic - metabolism</subject><subject>Kidney Failure, Chronic - physiopathology</subject><subject>Male</subject><subject>MDRD-4</subject><subject>Middle Aged</subject><subject>Prevalence</subject><subject>Retrospective Studies</subject><subject>Uremia - epidemiology</subject><subject>Uremia - metabolism</subject><subject>Uremia - physiopathology</subject><issn>0953-6205</issn><issn>1879-0828</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kctq3TAURUVpaG6T_EAHRbOO7BzJD1lQCiU0aSAQ6GMs5OPjVq4tu5IdyN9X5l4odNCR4LD2Bq3N2BsBuQBRXw85DW7KJYDOQeUA8gU7iEbpDBrZvGQH0FWR1RKqc_Y6xgFAKIDiFTsXuhGN1NWBtXR3-4Vb33EMZFfnnSeOI9lgPRJ3ngca0332fJ35RKtt59Ehx5_W_6C4A9bzzUcaCVfq-JJg8itf5mU7Bi_ZWW_HSFen94J9v_307eZz9vB4d3_z8SHDUsCaibLoJFlFVFloagCULapWlGglUV_3UjTQEPZUoSq0RCX7QveEZd-TqHVxwd4de5cw_94ormZyEWkcrad5i0YVZfKi5E7KI4lhjjFQb5bgJhuejQCzqzWD2dWaXa0BZZLaFHp7qt_aibq_kZPLBLw_ApQ--eQomIhJBVLnQnJjutn9v__DP3Ec0xxox1_0THGYt-CTPiNMlAbM133cfVvQaVfZ6OIPLBagvw</recordid><startdate>20091101</startdate><enddate>20091101</enddate><creator>Drion, I</creator><creator>Joosten, H</creator><creator>Dikkeschei, L.D</creator><creator>Groenier, K.H</creator><creator>Bilo, H.J.G</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20091101</creationdate><title>eGFR and creatinine clearance in relation to metabolic changes in an unselected patient population</title><author>Drion, I ; Joosten, H ; Dikkeschei, L.D ; Groenier, K.H ; Bilo, H.J.G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-143d2ea7ee5a08600c2bc7b14ca2eef6f21808ecfe5c7392c72f39fec4ffe1693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>(estimated) glomerular filtration rate</topic><topic>24-hour urine sampling</topic><topic>Aged</topic><topic>Anemia - epidemiology</topic><topic>Anemia - metabolism</topic><topic>Anemia - physiopathology</topic><topic>Biochemical disturbances</topic><topic>Chronic kidney disease</topic><topic>Creatinine - urine</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Glomerular Filtration Rate</topic><topic>Humans</topic><topic>Hyperkalemia - epidemiology</topic><topic>Hyperkalemia - metabolism</topic><topic>Hyperkalemia - physiopathology</topic><topic>Hyperphosphatemia - epidemiology</topic><topic>Hyperphosphatemia - metabolism</topic><topic>Hyperphosphatemia - physiopathology</topic><topic>Internal Medicine</topic><topic>Kidney Failure, Chronic - epidemiology</topic><topic>Kidney Failure, Chronic - metabolism</topic><topic>Kidney Failure, Chronic - physiopathology</topic><topic>Male</topic><topic>MDRD-4</topic><topic>Middle Aged</topic><topic>Prevalence</topic><topic>Retrospective Studies</topic><topic>Uremia - epidemiology</topic><topic>Uremia - metabolism</topic><topic>Uremia - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Drion, I</creatorcontrib><creatorcontrib>Joosten, H</creatorcontrib><creatorcontrib>Dikkeschei, L.D</creatorcontrib><creatorcontrib>Groenier, K.H</creatorcontrib><creatorcontrib>Bilo, H.J.G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of internal medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Drion, I</au><au>Joosten, H</au><au>Dikkeschei, L.D</au><au>Groenier, K.H</au><au>Bilo, H.J.G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>eGFR and creatinine clearance in relation to metabolic changes in an unselected patient population</atitle><jtitle>European journal of internal medicine</jtitle><addtitle>Eur J Intern Med</addtitle><date>2009-11-01</date><risdate>2009</risdate><volume>20</volume><issue>7</issue><spage>722</spage><epage>727</epage><pages>722-727</pages><issn>0953-6205</issn><eissn>1879-0828</eissn><abstract><![CDATA[Abstract Background It is widely assumed that moderate to severe renal failure (creatinine clearance < 60 ml/min; or an MDRD-4 (Modification of Diet in Renal Disease equation) < 60 ml/min/1.73 m2 ) is associated with metabolic changes, often needing further assessment and treatment. We investigated whether such abnormalities are already present at earlier stages of kidney disease, as assessed by 24-hour urine sampling and MDRD-4 calculation. Methods A select, retrospective cohort study was conducted. Creatinine clearance was measured by collecting 24-hour urines. The individual eGFRs were calculated with the MDRD-4 formula and patients were then divided by renal function category (< 15, 15–30, 30–45, 45–60, 60–90, > 90 ml/min(/1.73 m2 )). Per clearance category the number of people with anaemia, hypokalaemia, uraemia and hyperphosphataemia was evaluated. Results The median creatinine clearance rate was 67.3 ml/min (quartiles: 42.9–95.8) versus a median MDRD-4-eGFR of 51.6 ml/min/1.73 m2 (35.8–67.7). Anaemia, hyperkalaemia, hypocalcaemia, and uraemia were found to be present at higher levels of creatinine clearance rate and eGFR than previously reported ( p < 0.0005). This increased prevalence was more pronounced in elderly subjects, particularly with respect to anaemia (OR 2.71 and 2.02 for MDRD-4 and creatinine clearance respectively, p < 0.0005). The same holds for the proportion with uraemia (OR 1.85, p < 0.0005) and hypocalcaemia (OR 1.97, p = 0.011) for MDRD-4. Conclusion Metabolic changes in an in- and outpatient hospital population are present at earlier stages than was stated in recent guidelines, especially when creatinine clearance levels are used as indicators. This might have implications for testing and treatment of patients with suspected kidney disease and/or loss of renal function.]]></abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>19818295</pmid><doi>10.1016/j.ejim.2009.07.002</doi><tpages>6</tpages></addata></record> |
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subjects | (estimated) glomerular filtration rate 24-hour urine sampling Aged Anemia - epidemiology Anemia - metabolism Anemia - physiopathology Biochemical disturbances Chronic kidney disease Creatinine - urine Disease Progression Female Glomerular Filtration Rate Humans Hyperkalemia - epidemiology Hyperkalemia - metabolism Hyperkalemia - physiopathology Hyperphosphatemia - epidemiology Hyperphosphatemia - metabolism Hyperphosphatemia - physiopathology Internal Medicine Kidney Failure, Chronic - epidemiology Kidney Failure, Chronic - metabolism Kidney Failure, Chronic - physiopathology Male MDRD-4 Middle Aged Prevalence Retrospective Studies Uremia - epidemiology Uremia - metabolism Uremia - physiopathology |
title | eGFR and creatinine clearance in relation to metabolic changes in an unselected patient population |
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