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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nephrology, dialysis, transplantation dialysis, transplantation, 2004-05, Vol.19 (5), p.1149-1153
Hauptverfasser: Braden, Gregory L., O'shea, Michael H., Mulhern, Jeffrey G., Germain, Michael J.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1153
container_issue 5
container_start_page 1149
container_title Nephrology, dialysis, transplantation
container_volume 19
creator Braden, Gregory L.
O'shea, Michael H.
Mulhern, Jeffrey G.
Germain, Michael J.
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
format Article
fullrecord <record><control><sourceid>istex_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1093_ndt_gfg622</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_HXZ_QCK04G28_1</sourcerecordid><originalsourceid>FETCH-LOGICAL-c351t-b2d8f6d9731bc2e1e4321477709b8a565f01d0c4740bcf7664c02c72ea7aebd13</originalsourceid><addsrcrecordid>eNpF0M9LwzAUwPEgipvTi3-A9OJFqMuvJs1xDN3EgQwUxEt4TdMtrmtH0uH631vpcKd3eJ_3Dl-Ebgl-JFixcZU341WxEpSeoSHhAseUpck5GnZLEuMEqwG6CuEbY6yolJdoQLhSjCsxRMuJ2Tc28raCMirAlXtvI6jyaN3urN9ACXbrIIIQauOgsXn045p1ZFpT1vWhXXV3wcY0ctXaZa6pfbhGFwWUwd4c5wh9PD-9T-fx4m32Mp0sYsMS0sQZzdNC5EoykhlqieWMEi6lxCpLIRFJgUmODZccZ6aQQnCDqZHUggSb5YSN0EP_1_g6BG8LvfNuC77VBOu_LrrrovsuHb7r8W6fbW1-oscQHbg_AggGysJDZVw4uURylVDVubh3LjT28L8Hv9FCMpno-eeXXk5fMZ_RVBP2C0uWe-Y</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Acute renal failure and hyperkalaemia associated with cyclooxygenase-2 inhibitors</title><source>MEDLINE</source><source>Oxford University Press Journals All Titles (1996-Current)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Braden, Gregory L. ; O'shea, Michael H. ; Mulhern, Jeffrey G. ; Germain, Michael J.</creator><creatorcontrib>Braden, Gregory L. ; O'shea, Michael H. ; Mulhern, Jeffrey G. ; Germain, Michael J.</creatorcontrib><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><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&amp;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>
fulltext fulltext
identifier ISSN: 0931-0509
ispartof Nephrology, dialysis, transplantation, 2004-05, Vol.19 (5), p.1149-1153
issn 0931-0509
1460-2385
language eng
recordid cdi_crossref_primary_10_1093_ndt_gfg622
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T18%3A08%3A53IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Acute%20renal%20failure%20and%20hyperkalaemia%20associated%20with%20cyclooxygenase-2%20inhibitors&rft.jtitle=Nephrology,%20dialysis,%20transplantation&rft.au=Braden,%20Gregory%20L.&rft.date=2004-05-01&rft.volume=19&rft.issue=5&rft.spage=1149&rft.epage=1153&rft.pages=1149-1153&rft.issn=0931-0509&rft.eissn=1460-2385&rft.coden=NDTREA&rft_id=info:doi/10.1093/ndt/gfg622&rft_dat=%3Cistex_cross%3Eark_67375_HXZ_QCK04G28_1%3C/istex_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/14993496&rfr_iscdi=true