Acute renal failure and hyperkalaemia associated with cyclooxygenase-2 inhibitors
Background. The renal effects of cyclooxygenase-2 (COX-2) inhibitors have been incompletely elucidated, and acute renal failure (ARF) due to COX-2 inhibitors has been reported. Methods. In order to determine the causes of ARF and hyperkalaemia in five patients during COX-2 inhibitor therapy, we care...
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Veröffentlicht in: | Nephrology, dialysis, transplantation dialysis, transplantation, 2004-05, Vol.19 (5), p.1149-1153 |
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description | Background. The renal effects of cyclooxygenase-2 (COX-2) inhibitors have been incompletely elucidated, and acute renal failure (ARF) due to COX-2 inhibitors has been reported. Methods. In order to determine the causes of ARF and hyperkalaemia in five patients during COX-2 inhibitor therapy, we carefully analysed case studies of consecutive in-patients or out-patients referred to our Renal Division over a 6-month period for ARF and hyperkalaemia who had recently received COX-2 inhibitors. Results. ARF developed 2–3 weeks after COX-2 inhibitor therapy in five patients. The ARF was consistent with pre-renal azotaemia from renal hypoperfusion. Four patients were receiving the loop diuretic, furosemide. Four patients developed hyperkalaemia and decreased serum bicarbonate despite diuretic therapy, and one patient had changes in plasma renin activity and aldosterone levels consistent with reversible hyporeninaemic hypoaldosteronism. Renal failure was reversible after discontinuation of diuretics and COX-2 inhibitors. Conclusions. COX-2 inhibitors may cause reversible ARF and hyperkalaemia in patients with oedematous conditions treated with low sodium diets and loop diuretics. |
doi_str_mv | 10.1093/ndt/gfg622 |
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The renal effects of cyclooxygenase-2 (COX-2) inhibitors have been incompletely elucidated, and acute renal failure (ARF) due to COX-2 inhibitors has been reported. Methods. In order to determine the causes of ARF and hyperkalaemia in five patients during COX-2 inhibitor therapy, we carefully analysed case studies of consecutive in-patients or out-patients referred to our Renal Division over a 6-month period for ARF and hyperkalaemia who had recently received COX-2 inhibitors. Results. ARF developed 2–3 weeks after COX-2 inhibitor therapy in five patients. The ARF was consistent with pre-renal azotaemia from renal hypoperfusion. Four patients were receiving the loop diuretic, furosemide. Four patients developed hyperkalaemia and decreased serum bicarbonate despite diuretic therapy, and one patient had changes in plasma renin activity and aldosterone levels consistent with reversible hyporeninaemic hypoaldosteronism. Renal failure was reversible after discontinuation of diuretics and COX-2 inhibitors. Conclusions. COX-2 inhibitors may cause reversible ARF and hyperkalaemia in patients with oedematous conditions treated with low sodium diets and loop diuretics.</description><identifier>ISSN: 0931-0509</identifier><identifier>EISSN: 1460-2385</identifier><identifier>DOI: 10.1093/ndt/gfg622</identifier><identifier>PMID: 14993496</identifier><identifier>CODEN: NDTREA</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Acute Kidney Injury - chemically induced ; acute renal failure ; Aged ; Aged, 80 and over ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Cyclooxygenase 2 ; Cyclooxygenase 2 Inhibitors ; Cyclooxygenase Inhibitors - adverse effects ; Diuretics - therapeutic use ; Emergency and intensive care: renal failure. Dialysis management ; Female ; Humans ; hyperkalaemia ; Hyperkalemia - chemically induced ; Intensive care medicine ; Isoenzymes - metabolism ; Male ; Medical sciences ; Membrane Proteins ; Middle Aged ; Nephrology. Urinary tract diseases ; Nephropathies. Renovascular diseases. Renal failure ; Prostaglandin-Endoperoxide Synthases - metabolism ; Renal failure ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the urinary system</subject><ispartof>Nephrology, dialysis, transplantation, 2004-05, Vol.19 (5), p.1149-1153</ispartof><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c351t-b2d8f6d9731bc2e1e4321477709b8a565f01d0c4740bcf7664c02c72ea7aebd13</citedby><cites>FETCH-LOGICAL-c351t-b2d8f6d9731bc2e1e4321477709b8a565f01d0c4740bcf7664c02c72ea7aebd13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15749529$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14993496$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Braden, Gregory L.</creatorcontrib><creatorcontrib>O'shea, Michael H.</creatorcontrib><creatorcontrib>Mulhern, Jeffrey G.</creatorcontrib><creatorcontrib>Germain, Michael J.</creatorcontrib><title>Acute renal failure and hyperkalaemia associated with cyclooxygenase-2 inhibitors</title><title>Nephrology, dialysis, transplantation</title><addtitle>Nephrol. Dial. Transplant</addtitle><description>Background. The renal effects of cyclooxygenase-2 (COX-2) inhibitors have been incompletely elucidated, and acute renal failure (ARF) due to COX-2 inhibitors has been reported. Methods. In order to determine the causes of ARF and hyperkalaemia in five patients during COX-2 inhibitor therapy, we carefully analysed case studies of consecutive in-patients or out-patients referred to our Renal Division over a 6-month period for ARF and hyperkalaemia who had recently received COX-2 inhibitors. Results. ARF developed 2–3 weeks after COX-2 inhibitor therapy in five patients. The ARF was consistent with pre-renal azotaemia from renal hypoperfusion. Four patients were receiving the loop diuretic, furosemide. Four patients developed hyperkalaemia and decreased serum bicarbonate despite diuretic therapy, and one patient had changes in plasma renin activity and aldosterone levels consistent with reversible hyporeninaemic hypoaldosteronism. Renal failure was reversible after discontinuation of diuretics and COX-2 inhibitors. Conclusions. COX-2 inhibitors may cause reversible ARF and hyperkalaemia in patients with oedematous conditions treated with low sodium diets and loop diuretics.</description><subject>Acute Kidney Injury - chemically induced</subject><subject>acute renal failure</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Cyclooxygenase 2</subject><subject>Cyclooxygenase 2 Inhibitors</subject><subject>Cyclooxygenase Inhibitors - adverse effects</subject><subject>Diuretics - therapeutic use</subject><subject>Emergency and intensive care: renal failure. Dialysis management</subject><subject>Female</subject><subject>Humans</subject><subject>hyperkalaemia</subject><subject>Hyperkalemia - chemically induced</subject><subject>Intensive care medicine</subject><subject>Isoenzymes - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Membrane Proteins</subject><subject>Middle Aged</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Nephropathies. Renovascular diseases. Renal failure</subject><subject>Prostaglandin-Endoperoxide Synthases - metabolism</subject><subject>Renal failure</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the urinary system</subject><issn>0931-0509</issn><issn>1460-2385</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0M9LwzAUwPEgipvTi3-A9OJFqMuvJs1xDN3EgQwUxEt4TdMtrmtH0uH631vpcKd3eJ_3Dl-Ebgl-JFixcZU341WxEpSeoSHhAseUpck5GnZLEuMEqwG6CuEbY6yolJdoQLhSjCsxRMuJ2Tc28raCMirAlXtvI6jyaN3urN9ACXbrIIIQauOgsXn045p1ZFpT1vWhXXV3wcY0ctXaZa6pfbhGFwWUwd4c5wh9PD-9T-fx4m32Mp0sYsMS0sQZzdNC5EoykhlqieWMEi6lxCpLIRFJgUmODZccZ6aQQnCDqZHUggSb5YSN0EP_1_g6BG8LvfNuC77VBOu_LrrrovsuHb7r8W6fbW1-oscQHbg_AggGysJDZVw4uURylVDVubh3LjT28L8Hv9FCMpno-eeXXk5fMZ_RVBP2C0uWe-Y</recordid><startdate>20040501</startdate><enddate>20040501</enddate><creator>Braden, Gregory L.</creator><creator>O'shea, Michael H.</creator><creator>Mulhern, Jeffrey G.</creator><creator>Germain, Michael J.</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20040501</creationdate><title>Acute renal failure and hyperkalaemia associated with cyclooxygenase-2 inhibitors</title><author>Braden, Gregory L. ; O'shea, Michael H. ; Mulhern, Jeffrey G. ; Germain, Michael J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c351t-b2d8f6d9731bc2e1e4321477709b8a565f01d0c4740bcf7664c02c72ea7aebd13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Acute Kidney Injury - chemically induced</topic><topic>acute renal failure</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Cyclooxygenase 2</topic><topic>Cyclooxygenase 2 Inhibitors</topic><topic>Cyclooxygenase Inhibitors - adverse effects</topic><topic>Diuretics - therapeutic use</topic><topic>Emergency and intensive care: renal failure. Dialysis management</topic><topic>Female</topic><topic>Humans</topic><topic>hyperkalaemia</topic><topic>Hyperkalemia - chemically induced</topic><topic>Intensive care medicine</topic><topic>Isoenzymes - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Membrane Proteins</topic><topic>Middle Aged</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Nephropathies. Renovascular diseases. Renal failure</topic><topic>Prostaglandin-Endoperoxide Synthases - metabolism</topic><topic>Renal failure</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the urinary system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Braden, Gregory L.</creatorcontrib><creatorcontrib>O'shea, Michael H.</creatorcontrib><creatorcontrib>Mulhern, Jeffrey G.</creatorcontrib><creatorcontrib>Germain, Michael J.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Nephrology, dialysis, transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Braden, Gregory L.</au><au>O'shea, Michael H.</au><au>Mulhern, Jeffrey G.</au><au>Germain, Michael J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute renal failure and hyperkalaemia associated with cyclooxygenase-2 inhibitors</atitle><jtitle>Nephrology, dialysis, transplantation</jtitle><addtitle>Nephrol. Dial. Transplant</addtitle><date>2004-05-01</date><risdate>2004</risdate><volume>19</volume><issue>5</issue><spage>1149</spage><epage>1153</epage><pages>1149-1153</pages><issn>0931-0509</issn><eissn>1460-2385</eissn><coden>NDTREA</coden><abstract>Background. The renal effects of cyclooxygenase-2 (COX-2) inhibitors have been incompletely elucidated, and acute renal failure (ARF) due to COX-2 inhibitors has been reported. Methods. In order to determine the causes of ARF and hyperkalaemia in five patients during COX-2 inhibitor therapy, we carefully analysed case studies of consecutive in-patients or out-patients referred to our Renal Division over a 6-month period for ARF and hyperkalaemia who had recently received COX-2 inhibitors. Results. ARF developed 2–3 weeks after COX-2 inhibitor therapy in five patients. The ARF was consistent with pre-renal azotaemia from renal hypoperfusion. Four patients were receiving the loop diuretic, furosemide. Four patients developed hyperkalaemia and decreased serum bicarbonate despite diuretic therapy, and one patient had changes in plasma renin activity and aldosterone levels consistent with reversible hyporeninaemic hypoaldosteronism. Renal failure was reversible after discontinuation of diuretics and COX-2 inhibitors. Conclusions. COX-2 inhibitors may cause reversible ARF and hyperkalaemia in patients with oedematous conditions treated with low sodium diets and loop diuretics.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>14993496</pmid><doi>10.1093/ndt/gfg622</doi><tpages>5</tpages></addata></record> |
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source | MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Acute Kidney Injury - chemically induced acute renal failure Aged Aged, 80 and over Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences Cyclooxygenase 2 Cyclooxygenase 2 Inhibitors Cyclooxygenase Inhibitors - adverse effects Diuretics - therapeutic use Emergency and intensive care: renal failure. Dialysis management Female Humans hyperkalaemia Hyperkalemia - chemically induced Intensive care medicine Isoenzymes - metabolism Male Medical sciences Membrane Proteins Middle Aged Nephrology. Urinary tract diseases Nephropathies. Renovascular diseases. Renal failure Prostaglandin-Endoperoxide Synthases - metabolism Renal failure Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the urinary system |
title | Acute renal failure and hyperkalaemia associated with cyclooxygenase-2 inhibitors |
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