Elution of gentamicin and vancomycin from polymethylmethacrylate beads and hip spacers in vivo
Background and purpose Late infections after total hip arthroplasty are still a problem. Treatment procedures include resection arthroplasty with implantation of antibiotic-loaded beads or implantation of an antibiotic-impreganted spacer. However, little is known about antibiotic elution from bone c...
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description | Background and purpose Late infections after total hip arthroplasty are still a problem. Treatment procedures include resection arthroplasty with implantation of antibiotic-loaded beads or implantation of an antibiotic-impreganted spacer. However, little is known about antibiotic elution from bone cement beyond the first 2-3 postoperative days in humans.
Methods 17 hip spacers (80g PMMA, 1g gentamicin, and 4 g vancomycin) and 11 chains (40 g PMMA, 0.5 g gentamicin, and 2 g vancomycin) in 28 patients were studied. The release of both agents was measured in the drainage fluid on a daily basis. The drains were left in situ until less than 50 mL was produced per day. The elution of both antibiotics was determined by fluorescence polarization immunoassay. Systemic antibiotics were given postoperatively according to antibiogram. If possible, no gentamicin or vancomycin was given.
Results Peak mean concentrations from beads and spacers were reached for gentamicin (1,160 (12-371) µg/mL and 21 (0.7-39) µg/mL, respectively) and for vancomycin (80 (21-198) µg/mL and 37 (3.3-72) µg/mL) on day 1. The last concentrations to be determined were 3.7 µg/mL gentamicin and 23 µg/mL vancomycin in the beads group after 13 days, and 1.9 µg/mL gentamicin and 6.6 µg/mL vancomycin in the spacer group after 7 days. Between the fifth and seventh day, an intermittent increase in elution of vancomycin from both beads and spacers and of gentamicin from spacers was noticed. No renal or hepatic dysfunction was observed.
Interpretation Beads showed higher elution characteristics in vivo than the spacers due to their larger surface area; however, a great amount of inter-subject variability was seen for both beads and spacers. The inferior elution properties of spacers emphasize the importance of additional systemic antibiotics for this treatment procedure during the postoperative period. Future studies should clarify whether the dose of antibiotics or length of antibiotic therapy may be reduced in the case of bead implantation, without jeopardizing the control of infection. |
doi_str_mv | 10.3109/17453670902884700 |
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Methods 17 hip spacers (80g PMMA, 1g gentamicin, and 4 g vancomycin) and 11 chains (40 g PMMA, 0.5 g gentamicin, and 2 g vancomycin) in 28 patients were studied. The release of both agents was measured in the drainage fluid on a daily basis. The drains were left in situ until less than 50 mL was produced per day. The elution of both antibiotics was determined by fluorescence polarization immunoassay. Systemic antibiotics were given postoperatively according to antibiogram. If possible, no gentamicin or vancomycin was given.
Results Peak mean concentrations from beads and spacers were reached for gentamicin (1,160 (12-371) µg/mL and 21 (0.7-39) µg/mL, respectively) and for vancomycin (80 (21-198) µg/mL and 37 (3.3-72) µg/mL) on day 1. The last concentrations to be determined were 3.7 µg/mL gentamicin and 23 µg/mL vancomycin in the beads group after 13 days, and 1.9 µg/mL gentamicin and 6.6 µg/mL vancomycin in the spacer group after 7 days. Between the fifth and seventh day, an intermittent increase in elution of vancomycin from both beads and spacers and of gentamicin from spacers was noticed. No renal or hepatic dysfunction was observed.
Interpretation Beads showed higher elution characteristics in vivo than the spacers due to their larger surface area; however, a great amount of inter-subject variability was seen for both beads and spacers. The inferior elution properties of spacers emphasize the importance of additional systemic antibiotics for this treatment procedure during the postoperative period. Future studies should clarify whether the dose of antibiotics or length of antibiotic therapy may be reduced in the case of bead implantation, without jeopardizing the control of infection.</description><identifier>ISSN: 1745-3674</identifier><identifier>EISSN: 1745-3682</identifier><identifier>DOI: 10.3109/17453670902884700</identifier><identifier>PMID: 19404802</identifier><language>eng</language><publisher>Basingstoke: Informa UK Ltd</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Anti-Bacterial Agents - adverse effects ; Anti-Bacterial Agents - pharmacokinetics ; Antibacterial agents ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Arthroplasty, Replacement, Hip - adverse effects ; Biological and medical sciences ; Bone Cements ; Diseases of the osteoarticular system ; Female ; Gentamicins - administration & dosage ; Gentamicins - pharmacokinetics ; Humans ; Male ; Medical sciences ; Middle Aged ; Pharmacology. Drug treatments ; Polymethyl Methacrylate ; Prospective Studies ; Prosthesis Failure ; Prosthesis-Related Infections - drug therapy ; Prosthesis-Related Infections - microbiology ; Prosthesis-Related Infections - surgery ; Reoperation ; Time Factors ; Vancomycin - administration & dosage ; Vancomycin - pharmacokinetics</subject><ispartof>Acta orthopaedica, 2009-01, Vol.80 (2), p.193-197</ispartof><rights>2009 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2009</rights><rights>2009 INIST-CNRS</rights><rights>Copyright: © Nordic Orthopedic Federation 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c555t-fa457a08fff179dd051ed7126faef4e4441dad0d64fe7bf7074747464abd75613</citedby><cites>FETCH-LOGICAL-c555t-fa457a08fff179dd051ed7126faef4e4441dad0d64fe7bf7074747464abd75613</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2823164/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2823164/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21431410$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19404802$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Anagnostakos, Konstantinos</creatorcontrib><creatorcontrib>Wilmes, Philippe</creatorcontrib><creatorcontrib>Schmitt, Eduard</creatorcontrib><creatorcontrib>Kelm, Jens</creatorcontrib><title>Elution of gentamicin and vancomycin from polymethylmethacrylate beads and hip spacers in vivo</title><title>Acta orthopaedica</title><addtitle>Acta Orthop</addtitle><description>Background and purpose Late infections after total hip arthroplasty are still a problem. Treatment procedures include resection arthroplasty with implantation of antibiotic-loaded beads or implantation of an antibiotic-impreganted spacer. However, little is known about antibiotic elution from bone cement beyond the first 2-3 postoperative days in humans.
Methods 17 hip spacers (80g PMMA, 1g gentamicin, and 4 g vancomycin) and 11 chains (40 g PMMA, 0.5 g gentamicin, and 2 g vancomycin) in 28 patients were studied. The release of both agents was measured in the drainage fluid on a daily basis. The drains were left in situ until less than 50 mL was produced per day. The elution of both antibiotics was determined by fluorescence polarization immunoassay. Systemic antibiotics were given postoperatively according to antibiogram. If possible, no gentamicin or vancomycin was given.
Results Peak mean concentrations from beads and spacers were reached for gentamicin (1,160 (12-371) µg/mL and 21 (0.7-39) µg/mL, respectively) and for vancomycin (80 (21-198) µg/mL and 37 (3.3-72) µg/mL) on day 1. The last concentrations to be determined were 3.7 µg/mL gentamicin and 23 µg/mL vancomycin in the beads group after 13 days, and 1.9 µg/mL gentamicin and 6.6 µg/mL vancomycin in the spacer group after 7 days. Between the fifth and seventh day, an intermittent increase in elution of vancomycin from both beads and spacers and of gentamicin from spacers was noticed. No renal or hepatic dysfunction was observed.
Interpretation Beads showed higher elution characteristics in vivo than the spacers due to their larger surface area; however, a great amount of inter-subject variability was seen for both beads and spacers. The inferior elution properties of spacers emphasize the importance of additional systemic antibiotics for this treatment procedure during the postoperative period. Future studies should clarify whether the dose of antibiotics or length of antibiotic therapy may be reduced in the case of bead implantation, without jeopardizing the control of infection.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anti-Bacterial Agents - adverse effects</subject><subject>Anti-Bacterial Agents - pharmacokinetics</subject><subject>Antibacterial agents</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Arthroplasty, Replacement, Hip - adverse effects</subject><subject>Biological and medical sciences</subject><subject>Bone Cements</subject><subject>Diseases of the osteoarticular system</subject><subject>Female</subject><subject>Gentamicins - administration & dosage</subject><subject>Gentamicins - pharmacokinetics</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>Polymethyl Methacrylate</subject><subject>Prospective Studies</subject><subject>Prosthesis Failure</subject><subject>Prosthesis-Related Infections - drug therapy</subject><subject>Prosthesis-Related Infections - microbiology</subject><subject>Prosthesis-Related Infections - surgery</subject><subject>Reoperation</subject><subject>Time Factors</subject><subject>Vancomycin - administration & dosage</subject><subject>Vancomycin - pharmacokinetics</subject><issn>1745-3674</issn><issn>1745-3682</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kF1L5DAUhoMozqy7P8CbpTdezm7SnjYtK4KI-wGCN3prOJMPmyFtStIZ6b-33RnHHRYkkJwk7_Mm5yXknNFvGaPVd8YhzwpOK5qWJXBKj8h8OltkRZke72sOM_IpxhWlWQkVPSUzVgGFkqZz8nTr1r31beJN8qzbHhsrbZtgq5INttI3w7Q1wTdJ593Q6L4e3DSjDIPDXidLjSr-BWrbJbFDqUNMRmhjN_4zOTHoov6yW8_I48_bh5vfi7v7X39uru8WMs_zfmEQco60NMYwXilFc6YVZ2lhUBvQAMAUKqoKMJovDaccplEALhXPC5adkautb7deNlrJsZOATnTBNhgG4dGKw5vW1uLZb0RaphkrYDRgWwMZfIxBmz3LqJjCFv-FPTJf_330ndilOwoudgKMEp0JY6I27nUpg4wBm4wutzrbGh8afPHBKdHj4Hx4g7KP_vHjAK81ur6WGLRY-XVox-A_6OIViSCvgg</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Anagnostakos, Konstantinos</creator><creator>Wilmes, Philippe</creator><creator>Schmitt, Eduard</creator><creator>Kelm, Jens</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><general>Informa Healthcare</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><scope>5PM</scope></search><sort><creationdate>20090101</creationdate><title>Elution of gentamicin and vancomycin from polymethylmethacrylate beads and hip spacers in vivo</title><author>Anagnostakos, Konstantinos ; Wilmes, Philippe ; Schmitt, Eduard ; Kelm, Jens</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c555t-fa457a08fff179dd051ed7126faef4e4441dad0d64fe7bf7074747464abd75613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anti-Bacterial Agents - adverse effects</topic><topic>Anti-Bacterial Agents - pharmacokinetics</topic><topic>Antibacterial agents</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Arthroplasty, Replacement, Hip - adverse effects</topic><topic>Biological and medical sciences</topic><topic>Bone Cements</topic><topic>Diseases of the osteoarticular system</topic><topic>Female</topic><topic>Gentamicins - administration & dosage</topic><topic>Gentamicins - pharmacokinetics</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. Drug treatments</topic><topic>Polymethyl Methacrylate</topic><topic>Prospective Studies</topic><topic>Prosthesis Failure</topic><topic>Prosthesis-Related Infections - drug therapy</topic><topic>Prosthesis-Related Infections - microbiology</topic><topic>Prosthesis-Related Infections - surgery</topic><topic>Reoperation</topic><topic>Time Factors</topic><topic>Vancomycin - administration & dosage</topic><topic>Vancomycin - pharmacokinetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Anagnostakos, Konstantinos</creatorcontrib><creatorcontrib>Wilmes, Philippe</creatorcontrib><creatorcontrib>Schmitt, Eduard</creatorcontrib><creatorcontrib>Kelm, Jens</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Acta orthopaedica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Anagnostakos, Konstantinos</au><au>Wilmes, Philippe</au><au>Schmitt, Eduard</au><au>Kelm, Jens</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Elution of gentamicin and vancomycin from polymethylmethacrylate beads and hip spacers in vivo</atitle><jtitle>Acta orthopaedica</jtitle><addtitle>Acta Orthop</addtitle><date>2009-01-01</date><risdate>2009</risdate><volume>80</volume><issue>2</issue><spage>193</spage><epage>197</epage><pages>193-197</pages><issn>1745-3674</issn><eissn>1745-3682</eissn><abstract>Background and purpose Late infections after total hip arthroplasty are still a problem. Treatment procedures include resection arthroplasty with implantation of antibiotic-loaded beads or implantation of an antibiotic-impreganted spacer. However, little is known about antibiotic elution from bone cement beyond the first 2-3 postoperative days in humans.
Methods 17 hip spacers (80g PMMA, 1g gentamicin, and 4 g vancomycin) and 11 chains (40 g PMMA, 0.5 g gentamicin, and 2 g vancomycin) in 28 patients were studied. The release of both agents was measured in the drainage fluid on a daily basis. The drains were left in situ until less than 50 mL was produced per day. The elution of both antibiotics was determined by fluorescence polarization immunoassay. Systemic antibiotics were given postoperatively according to antibiogram. If possible, no gentamicin or vancomycin was given.
Results Peak mean concentrations from beads and spacers were reached for gentamicin (1,160 (12-371) µg/mL and 21 (0.7-39) µg/mL, respectively) and for vancomycin (80 (21-198) µg/mL and 37 (3.3-72) µg/mL) on day 1. The last concentrations to be determined were 3.7 µg/mL gentamicin and 23 µg/mL vancomycin in the beads group after 13 days, and 1.9 µg/mL gentamicin and 6.6 µg/mL vancomycin in the spacer group after 7 days. Between the fifth and seventh day, an intermittent increase in elution of vancomycin from both beads and spacers and of gentamicin from spacers was noticed. No renal or hepatic dysfunction was observed.
Interpretation Beads showed higher elution characteristics in vivo than the spacers due to their larger surface area; however, a great amount of inter-subject variability was seen for both beads and spacers. The inferior elution properties of spacers emphasize the importance of additional systemic antibiotics for this treatment procedure during the postoperative period. Future studies should clarify whether the dose of antibiotics or length of antibiotic therapy may be reduced in the case of bead implantation, without jeopardizing the control of infection.</abstract><cop>Basingstoke</cop><pub>Informa UK Ltd</pub><pmid>19404802</pmid><doi>10.3109/17453670902884700</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Aged, 80 and over Anti-Bacterial Agents - adverse effects Anti-Bacterial Agents - pharmacokinetics Antibacterial agents Antibiotics. Antiinfectious agents. Antiparasitic agents Arthroplasty, Replacement, Hip - adverse effects Biological and medical sciences Bone Cements Diseases of the osteoarticular system Female Gentamicins - administration & dosage Gentamicins - pharmacokinetics Humans Male Medical sciences Middle Aged Pharmacology. Drug treatments Polymethyl Methacrylate Prospective Studies Prosthesis Failure Prosthesis-Related Infections - drug therapy Prosthesis-Related Infections - microbiology Prosthesis-Related Infections - surgery Reoperation Time Factors Vancomycin - administration & dosage Vancomycin - pharmacokinetics |
title | Elution of gentamicin and vancomycin from polymethylmethacrylate beads and hip spacers in vivo |
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