Elimination of Piperacillin and Tazobactam by Renal Replacement Therapies with AN69 and Polysulfone Hemofilters: Evaluation of the Sieving Coefficient

Background/Aim: Piperacillin-tazobactam is commonly used to treat infections in ICU patients. Controversial data have been published about the sieving/saturation coefficient (Sc/Sa) of piperacillin during continuous renal replacement therapies (CRRT). The objective was to evaluate the Sc/Sa of piper...

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Veröffentlicht in:Blood purification 2006-01, Vol.24 (4), p.347-354
Hauptverfasser: Arzuaga, A., Isla, A., Gascón, A.R., Maynar, J., Corral, E., Pedraz, J.L.
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container_end_page 354
container_issue 4
container_start_page 347
container_title Blood purification
container_volume 24
creator Arzuaga, A.
Isla, A.
Gascón, A.R.
Maynar, J.
Corral, E.
Pedraz, J.L.
description Background/Aim: Piperacillin-tazobactam is commonly used to treat infections in ICU patients. Controversial data have been published about the sieving/saturation coefficient (Sc/Sa) of piperacillin during continuous renal replacement therapies (CRRT). The objective was to evaluate the Sc/Sa of piperacillin-tazobactam during continuous venovenous hemofiltration (CVVH) and continuous venovenous hemodialysis (CVVHD) using AN69 and polysulfone. Methods: Ringer lactate, BSA-containing Ringer lactate and plasma were circulated at 150 ml/min. The ultrafiltrate/dialysis flow was kept at 1,500 ml/min. A bolus was injected and samples were taken. Drugs were measured using HPLC. Sc/Sa was calculated according to standard formula. Results: Free passage of drugs through the membranes was reported with protein free solutions. In the presence of proteins the Sc/Sa lowered and correlated to protein free fraction. Polysulfone had a significantly higher permeability than AN69 during CVVH. Conclusion: Drug binding to albumin contributes to the decrease of the Sc/Sa of piperacillin but it does not completely justify the in vivo value obtained by some authors.
doi_str_mv 10.1159/000092921
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Controversial data have been published about the sieving/saturation coefficient (Sc/Sa) of piperacillin during continuous renal replacement therapies (CRRT). The objective was to evaluate the Sc/Sa of piperacillin-tazobactam during continuous venovenous hemofiltration (CVVH) and continuous venovenous hemodialysis (CVVHD) using AN69 and polysulfone. Methods: Ringer lactate, BSA-containing Ringer lactate and plasma were circulated at 150 ml/min. The ultrafiltrate/dialysis flow was kept at 1,500 ml/min. A bolus was injected and samples were taken. Drugs were measured using HPLC. Sc/Sa was calculated according to standard formula. Results: Free passage of drugs through the membranes was reported with protein free solutions. In the presence of proteins the Sc/Sa lowered and correlated to protein free fraction. Polysulfone had a significantly higher permeability than AN69 during CVVH. Conclusion: Drug binding to albumin contributes to the decrease of the Sc/Sa of piperacillin but it does not completely justify the in vivo value obtained by some authors.</description><identifier>ISSN: 0253-5068</identifier><identifier>EISSN: 1421-9735</identifier><identifier>DOI: 10.1159/000092921</identifier><identifier>PMID: 16645266</identifier><identifier>CODEN: BLPUDO</identifier><language>eng</language><publisher>Basel, Switzerland: Karger</publisher><subject>Acrylic Resins - adverse effects ; Acrylonitrile - adverse effects ; Acrylonitrile - analogs &amp; derivatives ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Anti-Bacterial Agents - pharmacokinetics ; Biocompatible Materials - adverse effects ; Biological and medical sciences ; Critical Care ; Drug Therapy, Combination ; Emergency and intensive care: renal failure. Dialysis management ; Hemofiltration - adverse effects ; Hemofiltration - instrumentation ; Humans ; In Vitro Techniques ; Intensive care medicine ; Medical sciences ; Membranes, Artificial ; Nephrology. Urinary tract diseases ; Nephropathies. Renovascular diseases. Renal failure ; Original Paper ; Penicillanic Acid - analogs &amp; derivatives ; Penicillanic Acid - pharmacokinetics ; Piperacillin - pharmacokinetics ; Polymers - adverse effects ; Renal failure ; Statistics, Nonparametric ; Sulfones - adverse effects</subject><ispartof>Blood purification, 2006-01, Vol.24 (4), p.347-354</ispartof><rights>2006 S. Karger AG, Basel</rights><rights>2006 INIST-CNRS</rights><rights>Copyright 2006 S. 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Controversial data have been published about the sieving/saturation coefficient (Sc/Sa) of piperacillin during continuous renal replacement therapies (CRRT). The objective was to evaluate the Sc/Sa of piperacillin-tazobactam during continuous venovenous hemofiltration (CVVH) and continuous venovenous hemodialysis (CVVHD) using AN69 and polysulfone. Methods: Ringer lactate, BSA-containing Ringer lactate and plasma were circulated at 150 ml/min. The ultrafiltrate/dialysis flow was kept at 1,500 ml/min. A bolus was injected and samples were taken. Drugs were measured using HPLC. Sc/Sa was calculated according to standard formula. Results: Free passage of drugs through the membranes was reported with protein free solutions. In the presence of proteins the Sc/Sa lowered and correlated to protein free fraction. Polysulfone had a significantly higher permeability than AN69 during CVVH. Conclusion: Drug binding to albumin contributes to the decrease of the Sc/Sa of piperacillin but it does not completely justify the in vivo value obtained by some authors.</description><subject>Acrylic Resins - adverse effects</subject><subject>Acrylonitrile - adverse effects</subject><subject>Acrylonitrile - analogs &amp; derivatives</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Anti-Bacterial Agents - pharmacokinetics</subject><subject>Biocompatible Materials - adverse effects</subject><subject>Biological and medical sciences</subject><subject>Critical Care</subject><subject>Drug Therapy, Combination</subject><subject>Emergency and intensive care: renal failure. Dialysis management</subject><subject>Hemofiltration - adverse effects</subject><subject>Hemofiltration - instrumentation</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Intensive care medicine</subject><subject>Medical sciences</subject><subject>Membranes, Artificial</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Nephropathies. Renovascular diseases. Renal failure</subject><subject>Original Paper</subject><subject>Penicillanic Acid - analogs &amp; derivatives</subject><subject>Penicillanic Acid - pharmacokinetics</subject><subject>Piperacillin - pharmacokinetics</subject><subject>Polymers - adverse effects</subject><subject>Renal failure</subject><subject>Statistics, Nonparametric</subject><subject>Sulfones - adverse effects</subject><issn>0253-5068</issn><issn>1421-9735</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0E1vEzEQBmALgWgoHDgjIV964LDgj7V3za2KQotUQQXhHI2948bg9a7sTVH4IfxetiRK5zBzeWZGegl5zdl7zpX5wOYywgj-hCx4LXhlGqmekgUTSlaK6faMvCjlJ2O81so8J2dc61oJrRfk7yqGPiSYwpDo4OltGDGDCzGGRCF1dA1_Bgtugp7aPf2GCeLcxwgOe0wTXW9nPwYs9HeYtvTyizb_926HuC-76IeE9Br7wYc4YS4f6eoe4u70b9oi_R7wPqQ7uhzQ--DCfPYleeYhFnx1nOfkx6fVenld3Xy9-ry8vKmclHKqRNcIsIY5aZSQ1rZW8FYy2TTC2KZuBYdGqZozbbuuZV63YBEZc1Z3wJiW5-Td4a7LQykZ_WbMoYe833C2ech2c8p2tm8PdtzZHrtHeQxzBhdHAMVB9BmSC-XRtYw3sm5m9-bgfkG-w3wChzf_AMmgiwI</recordid><startdate>20060101</startdate><enddate>20060101</enddate><creator>Arzuaga, A.</creator><creator>Isla, A.</creator><creator>Gascón, A.R.</creator><creator>Maynar, J.</creator><creator>Corral, E.</creator><creator>Pedraz, J.L.</creator><general>Karger</general><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>20060101</creationdate><title>Elimination of Piperacillin and Tazobactam by Renal Replacement Therapies with AN69 and Polysulfone Hemofilters: Evaluation of the Sieving Coefficient</title><author>Arzuaga, A. ; Isla, A. ; Gascón, A.R. ; Maynar, J. ; Corral, E. ; Pedraz, J.L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c333t-2d72ab90c39523bb8b2183037729b74821a7554106bdd80f68abee00cb6da0063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Acrylic Resins - adverse effects</topic><topic>Acrylonitrile - adverse effects</topic><topic>Acrylonitrile - analogs &amp; derivatives</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Anti-Bacterial Agents - pharmacokinetics</topic><topic>Biocompatible Materials - adverse effects</topic><topic>Biological and medical sciences</topic><topic>Critical Care</topic><topic>Drug Therapy, Combination</topic><topic>Emergency and intensive care: renal failure. Dialysis management</topic><topic>Hemofiltration - adverse effects</topic><topic>Hemofiltration - instrumentation</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>Intensive care medicine</topic><topic>Medical sciences</topic><topic>Membranes, Artificial</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Nephropathies. Renovascular diseases. Renal failure</topic><topic>Original Paper</topic><topic>Penicillanic Acid - analogs &amp; derivatives</topic><topic>Penicillanic Acid - pharmacokinetics</topic><topic>Piperacillin - pharmacokinetics</topic><topic>Polymers - adverse effects</topic><topic>Renal failure</topic><topic>Statistics, Nonparametric</topic><topic>Sulfones - adverse effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arzuaga, A.</creatorcontrib><creatorcontrib>Isla, A.</creatorcontrib><creatorcontrib>Gascón, A.R.</creatorcontrib><creatorcontrib>Maynar, J.</creatorcontrib><creatorcontrib>Corral, E.</creatorcontrib><creatorcontrib>Pedraz, J.L.</creatorcontrib><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>Blood purification</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arzuaga, A.</au><au>Isla, A.</au><au>Gascón, A.R.</au><au>Maynar, J.</au><au>Corral, E.</au><au>Pedraz, J.L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Elimination of Piperacillin and Tazobactam by Renal Replacement Therapies with AN69 and Polysulfone Hemofilters: Evaluation of the Sieving Coefficient</atitle><jtitle>Blood purification</jtitle><addtitle>Blood Purif</addtitle><date>2006-01-01</date><risdate>2006</risdate><volume>24</volume><issue>4</issue><spage>347</spage><epage>354</epage><pages>347-354</pages><issn>0253-5068</issn><eissn>1421-9735</eissn><coden>BLPUDO</coden><abstract>Background/Aim: Piperacillin-tazobactam is commonly used to treat infections in ICU patients. Controversial data have been published about the sieving/saturation coefficient (Sc/Sa) of piperacillin during continuous renal replacement therapies (CRRT). The objective was to evaluate the Sc/Sa of piperacillin-tazobactam during continuous venovenous hemofiltration (CVVH) and continuous venovenous hemodialysis (CVVHD) using AN69 and polysulfone. Methods: Ringer lactate, BSA-containing Ringer lactate and plasma were circulated at 150 ml/min. The ultrafiltrate/dialysis flow was kept at 1,500 ml/min. A bolus was injected and samples were taken. Drugs were measured using HPLC. Sc/Sa was calculated according to standard formula. Results: Free passage of drugs through the membranes was reported with protein free solutions. In the presence of proteins the Sc/Sa lowered and correlated to protein free fraction. Polysulfone had a significantly higher permeability than AN69 during CVVH. Conclusion: Drug binding to albumin contributes to the decrease of the Sc/Sa of piperacillin but it does not completely justify the in vivo value obtained by some authors.</abstract><cop>Basel, Switzerland</cop><pub>Karger</pub><pmid>16645266</pmid><doi>10.1159/000092921</doi><tpages>8</tpages></addata></record>
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ispartof Blood purification, 2006-01, Vol.24 (4), p.347-354
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language eng
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source MEDLINE; Karger Journals
subjects Acrylic Resins - adverse effects
Acrylonitrile - adverse effects
Acrylonitrile - analogs & derivatives
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Anti-Bacterial Agents - pharmacokinetics
Biocompatible Materials - adverse effects
Biological and medical sciences
Critical Care
Drug Therapy, Combination
Emergency and intensive care: renal failure. Dialysis management
Hemofiltration - adverse effects
Hemofiltration - instrumentation
Humans
In Vitro Techniques
Intensive care medicine
Medical sciences
Membranes, Artificial
Nephrology. Urinary tract diseases
Nephropathies. Renovascular diseases. Renal failure
Original Paper
Penicillanic Acid - analogs & derivatives
Penicillanic Acid - pharmacokinetics
Piperacillin - pharmacokinetics
Polymers - adverse effects
Renal failure
Statistics, Nonparametric
Sulfones - adverse effects
title Elimination of Piperacillin and Tazobactam by Renal Replacement Therapies with AN69 and Polysulfone Hemofilters: Evaluation of the Sieving Coefficient
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