Evaluation of haemodialysis as a protective technique for preventing high daily dose amikacin nephrotoxicity: an experimental study in an ovine model
•Haemodialysis is an optimized technique of antibiotic dosing and delivery after administration of high dose of amikacin.•Haemodialysis reduced Cmin and time of exposure to a concentration exceeding 2.5 µg/mL after administration of high dose of amikacin.•Higher amikacin dose associated with haemodi...
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Veröffentlicht in: | International journal of antimicrobial agents 2017-08, Vol.50 (2), p.148-154 |
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creator | Pouzot-Nevoret, Céline Magnin, Mathieu Ayoub, Jean-Yves Bourguignon, Laurent Maire, Pascal Wertz, Damien Goy-Thollot, Isabelle Barthélemy, Anthony Boselli, Emmanuel Allaouchiche, Bernard Bonnet-Garin, Jeanne Marie |
description | •Haemodialysis is an optimized technique of antibiotic dosing and delivery after administration of high dose of amikacin.•Haemodialysis reduced Cmin and time of exposure to a concentration exceeding 2.5 µg/mL after administration of high dose of amikacin.•Higher amikacin dose associated with haemodialysis should be considered for intermediate resistance strains in ICU patient.
Changes in pharmacokinetic parameters of critically ill patients make the treatment of infections challenging, particularly when multidrug-resistant bacteria are involved. The aim of this study was to evaluate the ability of haemodialysis to reduce the exposure to high dose amikacin and prevent nephrotoxicity. Amikacin 50 mg/kg was administered intravenously to six adult sheep once-daily for four days. The sheep were divided into two groups according to the implementation (group 1) or not (group 2) of haemodialysis. In group 1, haemodialysis was performed for 4 h, initiated 2 h after starting amikacin infusion. Amikacin area under the curve (AUC) and trough concentrations (Cmin) were used as markers of amikacin-induced nephrotoxicity. The median haemodialysis amikacin clearance was 2.14 L/h (35.6 mL/min), 14% of the mean total body clearance for 24 h. Haemodialysis reduced Cmin (group 1: 0.3 µg/mL [0.3–1.1]; group 2: 1.4 µg/mL [1.1–3.9]; P = 0.0003). A trend towards reduced AUC with haemodialysis was observed (group 1: 1450 µg/mL⋅h [1311–1716]; group 2: 3126 µg/mL⋅h [2581–3171]; P = 0.10). In conclusion, haemodialysis seems interesting in reducing AUC and Cmin after the injection of high-dose of amikacin, parameters known to be involved in its induced nephrotoxicity, in an experimental ovine model. |
doi_str_mv | 10.1016/j.ijantimicag.2017.03.029 |
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Changes in pharmacokinetic parameters of critically ill patients make the treatment of infections challenging, particularly when multidrug-resistant bacteria are involved. The aim of this study was to evaluate the ability of haemodialysis to reduce the exposure to high dose amikacin and prevent nephrotoxicity. Amikacin 50 mg/kg was administered intravenously to six adult sheep once-daily for four days. The sheep were divided into two groups according to the implementation (group 1) or not (group 2) of haemodialysis. In group 1, haemodialysis was performed for 4 h, initiated 2 h after starting amikacin infusion. Amikacin area under the curve (AUC) and trough concentrations (Cmin) were used as markers of amikacin-induced nephrotoxicity. The median haemodialysis amikacin clearance was 2.14 L/h (35.6 mL/min), 14% of the mean total body clearance for 24 h. Haemodialysis reduced Cmin (group 1: 0.3 µg/mL [0.3–1.1]; group 2: 1.4 µg/mL [1.1–3.9]; P = 0.0003). A trend towards reduced AUC with haemodialysis was observed (group 1: 1450 µg/mL⋅h [1311–1716]; group 2: 3126 µg/mL⋅h [2581–3171]; P = 0.10). In conclusion, haemodialysis seems interesting in reducing AUC and Cmin after the injection of high-dose of amikacin, parameters known to be involved in its induced nephrotoxicity, in an experimental ovine model.</description><identifier>ISSN: 0924-8579</identifier><identifier>EISSN: 1872-7913</identifier><identifier>DOI: 10.1016/j.ijantimicag.2017.03.029</identifier><identifier>PMID: 28689868</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Amikacin - administration & dosage ; Amikacin - adverse effects ; Amikacin - pharmacokinetics ; Amikacin-induced nephrotoxicity ; Animals ; Anti-Bacterial Agents - administration & dosage ; Anti-Bacterial Agents - adverse effects ; Anti-Bacterial Agents - pharmacokinetics ; Disease Models, Animal ; Female ; Haemodialysis ; Human health and pathology ; Kidney Diseases - chemically induced ; Kidney Diseases - prevention & control ; Life Sciences ; Multidrug-resistant bacteria ; Pharmaceutical sciences ; Pharmacokinetics ; Plasma - chemistry ; Renal Dialysis - methods ; Sheep ; Urology and Nephrology</subject><ispartof>International journal of antimicrobial agents, 2017-08, Vol.50 (2), p.148-154</ispartof><rights>2017 Elsevier B.V. and International Society of Chemotherapy</rights><rights>Copyright © 2017 Elsevier B.V. and International Society of Chemotherapy. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-af258e53460bbe3df6d23cb22966c89dedc85c61eee84a73d7ac7a3e052d623d3</citedby><cites>FETCH-LOGICAL-c462t-af258e53460bbe3df6d23cb22966c89dedc85c61eee84a73d7ac7a3e052d623d3</cites><orcidid>0000-0002-4949-3518 ; 0000-0001-7269-8450 ; 0000-0003-0898-5425 ; 0000-0002-0226-0346 ; 0000-0003-0988-1716 ; 0000-0001-5350-338X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijantimicag.2017.03.029$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28689868$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://vetagro-sup.hal.science/hal-02458478$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Pouzot-Nevoret, Céline</creatorcontrib><creatorcontrib>Magnin, Mathieu</creatorcontrib><creatorcontrib>Ayoub, Jean-Yves</creatorcontrib><creatorcontrib>Bourguignon, Laurent</creatorcontrib><creatorcontrib>Maire, Pascal</creatorcontrib><creatorcontrib>Wertz, Damien</creatorcontrib><creatorcontrib>Goy-Thollot, Isabelle</creatorcontrib><creatorcontrib>Barthélemy, Anthony</creatorcontrib><creatorcontrib>Boselli, Emmanuel</creatorcontrib><creatorcontrib>Allaouchiche, Bernard</creatorcontrib><creatorcontrib>Bonnet-Garin, Jeanne Marie</creatorcontrib><title>Evaluation of haemodialysis as a protective technique for preventing high daily dose amikacin nephrotoxicity: an experimental study in an ovine model</title><title>International journal of antimicrobial agents</title><addtitle>Int J Antimicrob Agents</addtitle><description>•Haemodialysis is an optimized technique of antibiotic dosing and delivery after administration of high dose of amikacin.•Haemodialysis reduced Cmin and time of exposure to a concentration exceeding 2.5 µg/mL after administration of high dose of amikacin.•Higher amikacin dose associated with haemodialysis should be considered for intermediate resistance strains in ICU patient.
Changes in pharmacokinetic parameters of critically ill patients make the treatment of infections challenging, particularly when multidrug-resistant bacteria are involved. The aim of this study was to evaluate the ability of haemodialysis to reduce the exposure to high dose amikacin and prevent nephrotoxicity. Amikacin 50 mg/kg was administered intravenously to six adult sheep once-daily for four days. The sheep were divided into two groups according to the implementation (group 1) or not (group 2) of haemodialysis. In group 1, haemodialysis was performed for 4 h, initiated 2 h after starting amikacin infusion. Amikacin area under the curve (AUC) and trough concentrations (Cmin) were used as markers of amikacin-induced nephrotoxicity. The median haemodialysis amikacin clearance was 2.14 L/h (35.6 mL/min), 14% of the mean total body clearance for 24 h. Haemodialysis reduced Cmin (group 1: 0.3 µg/mL [0.3–1.1]; group 2: 1.4 µg/mL [1.1–3.9]; P = 0.0003). A trend towards reduced AUC with haemodialysis was observed (group 1: 1450 µg/mL⋅h [1311–1716]; group 2: 3126 µg/mL⋅h [2581–3171]; P = 0.10). In conclusion, haemodialysis seems interesting in reducing AUC and Cmin after the injection of high-dose of amikacin, parameters known to be involved in its induced nephrotoxicity, in an experimental ovine model.</description><subject>Amikacin - administration & dosage</subject><subject>Amikacin - adverse effects</subject><subject>Amikacin - pharmacokinetics</subject><subject>Amikacin-induced nephrotoxicity</subject><subject>Animals</subject><subject>Anti-Bacterial Agents - administration & dosage</subject><subject>Anti-Bacterial Agents - adverse effects</subject><subject>Anti-Bacterial Agents - pharmacokinetics</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Haemodialysis</subject><subject>Human health and pathology</subject><subject>Kidney Diseases - chemically induced</subject><subject>Kidney Diseases - prevention & control</subject><subject>Life Sciences</subject><subject>Multidrug-resistant bacteria</subject><subject>Pharmaceutical sciences</subject><subject>Pharmacokinetics</subject><subject>Plasma - chemistry</subject><subject>Renal Dialysis - methods</subject><subject>Sheep</subject><subject>Urology and Nephrology</subject><issn>0924-8579</issn><issn>1872-7913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkduO0zAQhi0EYsvCKyBzyUWCDzk43K2qhUWqxA1cW1N70kxJ4hKn0eZBeF9cFVZcItkayfN_c_DP2Dspcilk9eGY0xHGmQZycMiVkHUudC5U84xtpKlVVjdSP2cb0agiM2Xd3LBXMR6FkKUuypfsRpnKNOlu2K_7BfozzBRGHlreAQ7BE_RrpMghHX6awoxupgV5it1IP8_I2zClBC6YphgPvKNDxz1Qv3IfInIY6Ac4GvmIpy7x4ZEczetHDiPHxxNONCQSeh7ns195EqZEWGhEntpj_5q9aKGP-OZPvGXfP91_2z5ku6-fv2zvdpkrKjVn0KrSYNqpEvs9at9WXmm3V6qpKmcaj96Z0lUSEU0BtfY1uBo0ilL5Smmvb9n7a90OentKU8G02gBkH-529vImVFGaojaLTNrmqnVTiHHC9gmQwl5ssUf7jy32YosVOpVoEvv2yp7O-wH9E_nXhyTYXgWYtl0IJxsd4ejQ05Q-3_pA_9HmNxMXqPI</recordid><startdate>201708</startdate><enddate>201708</enddate><creator>Pouzot-Nevoret, Céline</creator><creator>Magnin, Mathieu</creator><creator>Ayoub, Jean-Yves</creator><creator>Bourguignon, Laurent</creator><creator>Maire, Pascal</creator><creator>Wertz, Damien</creator><creator>Goy-Thollot, Isabelle</creator><creator>Barthélemy, Anthony</creator><creator>Boselli, Emmanuel</creator><creator>Allaouchiche, Bernard</creator><creator>Bonnet-Garin, Jeanne Marie</creator><general>Elsevier B.V</general><general>Elsevier</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>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-4949-3518</orcidid><orcidid>https://orcid.org/0000-0001-7269-8450</orcidid><orcidid>https://orcid.org/0000-0003-0898-5425</orcidid><orcidid>https://orcid.org/0000-0002-0226-0346</orcidid><orcidid>https://orcid.org/0000-0003-0988-1716</orcidid><orcidid>https://orcid.org/0000-0001-5350-338X</orcidid></search><sort><creationdate>201708</creationdate><title>Evaluation of haemodialysis as a protective technique for preventing high daily dose amikacin nephrotoxicity: an experimental study in an ovine model</title><author>Pouzot-Nevoret, Céline ; Magnin, Mathieu ; Ayoub, Jean-Yves ; Bourguignon, Laurent ; Maire, Pascal ; Wertz, Damien ; Goy-Thollot, Isabelle ; Barthélemy, Anthony ; Boselli, Emmanuel ; Allaouchiche, Bernard ; Bonnet-Garin, Jeanne Marie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-af258e53460bbe3df6d23cb22966c89dedc85c61eee84a73d7ac7a3e052d623d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Amikacin - administration & dosage</topic><topic>Amikacin - adverse effects</topic><topic>Amikacin - pharmacokinetics</topic><topic>Amikacin-induced nephrotoxicity</topic><topic>Animals</topic><topic>Anti-Bacterial Agents - administration & dosage</topic><topic>Anti-Bacterial Agents - adverse effects</topic><topic>Anti-Bacterial Agents - pharmacokinetics</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Haemodialysis</topic><topic>Human health and pathology</topic><topic>Kidney Diseases - chemically induced</topic><topic>Kidney Diseases - prevention & control</topic><topic>Life Sciences</topic><topic>Multidrug-resistant bacteria</topic><topic>Pharmaceutical sciences</topic><topic>Pharmacokinetics</topic><topic>Plasma - chemistry</topic><topic>Renal Dialysis - methods</topic><topic>Sheep</topic><topic>Urology and Nephrology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pouzot-Nevoret, Céline</creatorcontrib><creatorcontrib>Magnin, Mathieu</creatorcontrib><creatorcontrib>Ayoub, Jean-Yves</creatorcontrib><creatorcontrib>Bourguignon, Laurent</creatorcontrib><creatorcontrib>Maire, Pascal</creatorcontrib><creatorcontrib>Wertz, Damien</creatorcontrib><creatorcontrib>Goy-Thollot, Isabelle</creatorcontrib><creatorcontrib>Barthélemy, Anthony</creatorcontrib><creatorcontrib>Boselli, Emmanuel</creatorcontrib><creatorcontrib>Allaouchiche, Bernard</creatorcontrib><creatorcontrib>Bonnet-Garin, Jeanne Marie</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>International journal of antimicrobial agents</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pouzot-Nevoret, Céline</au><au>Magnin, Mathieu</au><au>Ayoub, Jean-Yves</au><au>Bourguignon, Laurent</au><au>Maire, Pascal</au><au>Wertz, Damien</au><au>Goy-Thollot, Isabelle</au><au>Barthélemy, Anthony</au><au>Boselli, Emmanuel</au><au>Allaouchiche, Bernard</au><au>Bonnet-Garin, Jeanne Marie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of haemodialysis as a protective technique for preventing high daily dose amikacin nephrotoxicity: an experimental study in an ovine model</atitle><jtitle>International journal of antimicrobial agents</jtitle><addtitle>Int J Antimicrob Agents</addtitle><date>2017-08</date><risdate>2017</risdate><volume>50</volume><issue>2</issue><spage>148</spage><epage>154</epage><pages>148-154</pages><issn>0924-8579</issn><eissn>1872-7913</eissn><abstract>•Haemodialysis is an optimized technique of antibiotic dosing and delivery after administration of high dose of amikacin.•Haemodialysis reduced Cmin and time of exposure to a concentration exceeding 2.5 µg/mL after administration of high dose of amikacin.•Higher amikacin dose associated with haemodialysis should be considered for intermediate resistance strains in ICU patient.
Changes in pharmacokinetic parameters of critically ill patients make the treatment of infections challenging, particularly when multidrug-resistant bacteria are involved. The aim of this study was to evaluate the ability of haemodialysis to reduce the exposure to high dose amikacin and prevent nephrotoxicity. Amikacin 50 mg/kg was administered intravenously to six adult sheep once-daily for four days. The sheep were divided into two groups according to the implementation (group 1) or not (group 2) of haemodialysis. In group 1, haemodialysis was performed for 4 h, initiated 2 h after starting amikacin infusion. Amikacin area under the curve (AUC) and trough concentrations (Cmin) were used as markers of amikacin-induced nephrotoxicity. The median haemodialysis amikacin clearance was 2.14 L/h (35.6 mL/min), 14% of the mean total body clearance for 24 h. Haemodialysis reduced Cmin (group 1: 0.3 µg/mL [0.3–1.1]; group 2: 1.4 µg/mL [1.1–3.9]; P = 0.0003). A trend towards reduced AUC with haemodialysis was observed (group 1: 1450 µg/mL⋅h [1311–1716]; group 2: 3126 µg/mL⋅h [2581–3171]; P = 0.10). In conclusion, haemodialysis seems interesting in reducing AUC and Cmin after the injection of high-dose of amikacin, parameters known to be involved in its induced nephrotoxicity, in an experimental ovine model.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>28689868</pmid><doi>10.1016/j.ijantimicag.2017.03.029</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-4949-3518</orcidid><orcidid>https://orcid.org/0000-0001-7269-8450</orcidid><orcidid>https://orcid.org/0000-0003-0898-5425</orcidid><orcidid>https://orcid.org/0000-0002-0226-0346</orcidid><orcidid>https://orcid.org/0000-0003-0988-1716</orcidid><orcidid>https://orcid.org/0000-0001-5350-338X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amikacin - administration & dosage Amikacin - adverse effects Amikacin - pharmacokinetics Amikacin-induced nephrotoxicity Animals Anti-Bacterial Agents - administration & dosage Anti-Bacterial Agents - adverse effects Anti-Bacterial Agents - pharmacokinetics Disease Models, Animal Female Haemodialysis Human health and pathology Kidney Diseases - chemically induced Kidney Diseases - prevention & control Life Sciences Multidrug-resistant bacteria Pharmaceutical sciences Pharmacokinetics Plasma - chemistry Renal Dialysis - methods Sheep Urology and Nephrology |
title | Evaluation of haemodialysis as a protective technique for preventing high daily dose amikacin nephrotoxicity: an experimental study in an ovine model |
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