β-Lactam antimicrobial  pharmacokinetics and target attainment in critically ill patients aged 1 day to 90 years: the ABDose study

Abstract Background The pharmacokinetics of β-lactam antibiotics in critical illness remain poorly characterized, particularly in neonates, children and the elderly. We undertook a pharmacokinetic study of commonly used β-lactam antibiotics in critically ill patients of all ages. The aims were to pr...

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Veröffentlicht in:Journal of antimicrobial chemotherapy 2020-12, Vol.75 (12), p.3625-3634
Hauptverfasser: Lonsdale, Dagan O, Kipper, Karin, Baker, Emma H, Barker, Charlotte I S, Oldfield, Isobel, Philips, Barbara J, Johnston, Atholl, Rhodes, Andrew, Sharland, Mike, Standing, Joseph F
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container_end_page 3634
container_issue 12
container_start_page 3625
container_title Journal of antimicrobial chemotherapy
container_volume 75
creator Lonsdale, Dagan O
Kipper, Karin
Baker, Emma H
Barker, Charlotte I S
Oldfield, Isobel
Philips, Barbara J
Johnston, Atholl
Rhodes, Andrew
Sharland, Mike
Standing, Joseph F
description Abstract Background The pharmacokinetics of β-lactam antibiotics in critical illness remain poorly characterized, particularly in neonates, children and the elderly. We undertook a pharmacokinetic study of commonly used β-lactam antibiotics in critically ill patients of all ages. The aims were to produce a whole-life β-lactam pharmacokinetic model and describe the extent to which standard doses achieve pharmacokinetic/pharmacodynamic targets associated with clinical cure. Patients and methods A total of 212 critically ill participants with an age range from 1 day (gestational age 24 weeks) to 90 years were recruited from a UK hospital, providing 1339 pharmacokinetic samples. Population pharmacokinetic analysis was undertaken using non-linear mixed-effects modelling (NONMEM) for each drug. Pooled data were used to estimate maturation and decline of β-lactam pharmacokinetics throughout life. Results Pharmacokinetic models for eight drugs were described, including what is thought to be the first benzylpenicillin model in critically ill adults. We estimate that 50% of adult β-lactam clearance is achieved by 43 weeks post-menstrual age (chronological plus gestational age). Fifty percent of decline from peak adult clearance occurs by 71 years. Paediatric participants were significantly less likely than adults to achieve pharmacokinetic/pharmacodynamic targets with standard antibiotic doses (P 
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We undertook a pharmacokinetic study of commonly used β-lactam antibiotics in critically ill patients of all ages. The aims were to produce a whole-life β-lactam pharmacokinetic model and describe the extent to which standard doses achieve pharmacokinetic/pharmacodynamic targets associated with clinical cure. Patients and methods A total of 212 critically ill participants with an age range from 1 day (gestational age 24 weeks) to 90 years were recruited from a UK hospital, providing 1339 pharmacokinetic samples. Population pharmacokinetic analysis was undertaken using non-linear mixed-effects modelling (NONMEM) for each drug. Pooled data were used to estimate maturation and decline of β-lactam pharmacokinetics throughout life. Results Pharmacokinetic models for eight drugs were described, including what is thought to be the first benzylpenicillin model in critically ill adults. We estimate that 50% of adult β-lactam clearance is achieved by 43 weeks post-menstrual age (chronological plus gestational age). Fifty percent of decline from peak adult clearance occurs by 71 years. Paediatric participants were significantly less likely than adults to achieve pharmacokinetic/pharmacodynamic targets with standard antibiotic doses (P &lt; 0.01). Conclusions We believe this to be the first prospective whole-life antibiotic pharmacokinetic study in the critically ill. The study provides further evidence that standard antibiotic doses fail to achieve pharmacokinetic/pharmacodynamic targets associated with clinical success in adults, children and neonates. Maturation and decline parameters estimated from this study could be adopted as a standard for future prospective studies.</description><identifier>ISSN: 0305-7453</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/dkaa363</identifier><identifier>PMID: 32989452</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><ispartof>Journal of antimicrobial chemotherapy, 2020-12, Vol.75 (12), p.3625-3634</ispartof><rights>The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com. 2020</rights><rights>The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-1722507d7f848ba1113b15701ec5f64c639d33ae37d488668e261a8858f472263</citedby><cites>FETCH-LOGICAL-c357t-1722507d7f848ba1113b15701ec5f64c639d33ae37d488668e261a8858f472263</cites><orcidid>0000-0002-4561-7173 ; 0000-0003-0838-921X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32989452$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lonsdale, Dagan O</creatorcontrib><creatorcontrib>Kipper, Karin</creatorcontrib><creatorcontrib>Baker, Emma H</creatorcontrib><creatorcontrib>Barker, Charlotte I S</creatorcontrib><creatorcontrib>Oldfield, Isobel</creatorcontrib><creatorcontrib>Philips, Barbara J</creatorcontrib><creatorcontrib>Johnston, Atholl</creatorcontrib><creatorcontrib>Rhodes, Andrew</creatorcontrib><creatorcontrib>Sharland, Mike</creatorcontrib><creatorcontrib>Standing, Joseph F</creatorcontrib><title>β-Lactam antimicrobial  pharmacokinetics and target attainment in critically ill patients aged 1 day to 90 years: the ABDose study</title><title>Journal of antimicrobial chemotherapy</title><addtitle>J Antimicrob Chemother</addtitle><description>Abstract Background The pharmacokinetics of β-lactam antibiotics in critical illness remain poorly characterized, particularly in neonates, children and the elderly. We undertook a pharmacokinetic study of commonly used β-lactam antibiotics in critically ill patients of all ages. The aims were to produce a whole-life β-lactam pharmacokinetic model and describe the extent to which standard doses achieve pharmacokinetic/pharmacodynamic targets associated with clinical cure. Patients and methods A total of 212 critically ill participants with an age range from 1 day (gestational age 24 weeks) to 90 years were recruited from a UK hospital, providing 1339 pharmacokinetic samples. Population pharmacokinetic analysis was undertaken using non-linear mixed-effects modelling (NONMEM) for each drug. Pooled data were used to estimate maturation and decline of β-lactam pharmacokinetics throughout life. Results Pharmacokinetic models for eight drugs were described, including what is thought to be the first benzylpenicillin model in critically ill adults. We estimate that 50% of adult β-lactam clearance is achieved by 43 weeks post-menstrual age (chronological plus gestational age). Fifty percent of decline from peak adult clearance occurs by 71 years. Paediatric participants were significantly less likely than adults to achieve pharmacokinetic/pharmacodynamic targets with standard antibiotic doses (P &lt; 0.01). Conclusions We believe this to be the first prospective whole-life antibiotic pharmacokinetic study in the critically ill. The study provides further evidence that standard antibiotic doses fail to achieve pharmacokinetic/pharmacodynamic targets associated with clinical success in adults, children and neonates. Maturation and decline parameters estimated from this study could be adopted as a standard for future prospective studies.</description><issn>0305-7453</issn><issn>1460-2091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kDtOxDAQhi0EYpdHRY9c0aCAHceOQ8cbpJVooI4mtrPr3bwUe4t0lHALzsAROACH4CQY7UJJNSPN9__SfAgdUHJCScZO56BO9QKACbaBxjQRJIpJRjfRmDDCozThbIR2nJsTQgQXchuNWJzJLOHxGL18vkcTUB5qDI23tVV9W1io8MdbN4O-BtUubGO8VS4AGnvop8Zj8B5sU5vGY9tg1dsAQFUN2FYV7sDbcAmBqdGYfj2_ahiwb3FGwj4Y6N0Z9jODzy-uWmew80s97KGtEipn9tdzFz3dXD9e3kWTh9v7y_NJpBhPfUTTOOYk1WkpE1kApZQVlKeEGsVLkSjBMs0YGJbqREohpIkFBSm5LJMQFWwXHa96w6PO9abMu97W0A85JfmPzzz4zNc-A324ortlURv9x_4KDMDRCmiX3b9N3w1BgpI</recordid><startdate>20201201</startdate><enddate>20201201</enddate><creator>Lonsdale, Dagan O</creator><creator>Kipper, Karin</creator><creator>Baker, Emma H</creator><creator>Barker, Charlotte I S</creator><creator>Oldfield, Isobel</creator><creator>Philips, Barbara J</creator><creator>Johnston, Atholl</creator><creator>Rhodes, Andrew</creator><creator>Sharland, Mike</creator><creator>Standing, Joseph F</creator><general>Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-4561-7173</orcidid><orcidid>https://orcid.org/0000-0003-0838-921X</orcidid></search><sort><creationdate>20201201</creationdate><title>β-Lactam antimicrobial  pharmacokinetics and target attainment in critically ill patients aged 1 day to 90 years: the ABDose study</title><author>Lonsdale, Dagan O ; Kipper, Karin ; Baker, Emma H ; Barker, Charlotte I S ; Oldfield, Isobel ; Philips, Barbara J ; Johnston, Atholl ; Rhodes, Andrew ; Sharland, Mike ; Standing, Joseph F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-1722507d7f848ba1113b15701ec5f64c639d33ae37d488668e261a8858f472263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lonsdale, Dagan O</creatorcontrib><creatorcontrib>Kipper, Karin</creatorcontrib><creatorcontrib>Baker, Emma H</creatorcontrib><creatorcontrib>Barker, Charlotte I S</creatorcontrib><creatorcontrib>Oldfield, Isobel</creatorcontrib><creatorcontrib>Philips, Barbara J</creatorcontrib><creatorcontrib>Johnston, Atholl</creatorcontrib><creatorcontrib>Rhodes, Andrew</creatorcontrib><creatorcontrib>Sharland, Mike</creatorcontrib><creatorcontrib>Standing, Joseph F</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of antimicrobial chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lonsdale, Dagan O</au><au>Kipper, Karin</au><au>Baker, Emma H</au><au>Barker, Charlotte I S</au><au>Oldfield, Isobel</au><au>Philips, Barbara J</au><au>Johnston, Atholl</au><au>Rhodes, Andrew</au><au>Sharland, Mike</au><au>Standing, Joseph F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>β-Lactam antimicrobial  pharmacokinetics and target attainment in critically ill patients aged 1 day to 90 years: the ABDose study</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><addtitle>J Antimicrob Chemother</addtitle><date>2020-12-01</date><risdate>2020</risdate><volume>75</volume><issue>12</issue><spage>3625</spage><epage>3634</epage><pages>3625-3634</pages><issn>0305-7453</issn><eissn>1460-2091</eissn><abstract>Abstract Background The pharmacokinetics of β-lactam antibiotics in critical illness remain poorly characterized, particularly in neonates, children and the elderly. We undertook a pharmacokinetic study of commonly used β-lactam antibiotics in critically ill patients of all ages. The aims were to produce a whole-life β-lactam pharmacokinetic model and describe the extent to which standard doses achieve pharmacokinetic/pharmacodynamic targets associated with clinical cure. Patients and methods A total of 212 critically ill participants with an age range from 1 day (gestational age 24 weeks) to 90 years were recruited from a UK hospital, providing 1339 pharmacokinetic samples. Population pharmacokinetic analysis was undertaken using non-linear mixed-effects modelling (NONMEM) for each drug. Pooled data were used to estimate maturation and decline of β-lactam pharmacokinetics throughout life. Results Pharmacokinetic models for eight drugs were described, including what is thought to be the first benzylpenicillin model in critically ill adults. We estimate that 50% of adult β-lactam clearance is achieved by 43 weeks post-menstrual age (chronological plus gestational age). Fifty percent of decline from peak adult clearance occurs by 71 years. Paediatric participants were significantly less likely than adults to achieve pharmacokinetic/pharmacodynamic targets with standard antibiotic doses (P &lt; 0.01). Conclusions We believe this to be the first prospective whole-life antibiotic pharmacokinetic study in the critically ill. The study provides further evidence that standard antibiotic doses fail to achieve pharmacokinetic/pharmacodynamic targets associated with clinical success in adults, children and neonates. Maturation and decline parameters estimated from this study could be adopted as a standard for future prospective studies.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>32989452</pmid><doi>10.1093/jac/dkaa363</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-4561-7173</orcidid><orcidid>https://orcid.org/0000-0003-0838-921X</orcidid><oa>free_for_read</oa></addata></record>
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title β-Lactam antimicrobial  pharmacokinetics and target attainment in critically ill patients aged 1 day to 90 years: the ABDose study
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