Variability in protein binding of teicoplanin and achievement of therapeutic drug monitoring targets in critically ill patients: lessons from the DALI Study.
Identifieur interne : 001863 ( Ncbi/Checkpoint ); précédent : 001862; suivant : 001864Variability in protein binding of teicoplanin and achievement of therapeutic drug monitoring targets in critically ill patients: lessons from the DALI Study.
Auteurs : J A Roberts [Australie] ; V. Stove [Belgique] ; J J De Waele [Belgique] ; B. Sipinkoski [Australie] ; B. Mcwhinney [Australie] ; J P J. Ungerer [Australie] ; M. Akova [Turquie] ; M. Bassetti [Italie] ; G. Dimopoulos [Grèce] ; K-M Kaukonen [Australie] ; D. Koulenti [Grèce] ; C. Martin [France] ; P. Montravers [France] ; J. Rello [Espagne] ; A. Rhodes [Royaume-Uni] ; T. Starr [Australie] ; S C Wallis [Australie] ; J. Lipman [Australie]Source :
- International journal of antimicrobial agents [ 1872-7913 ] ; 2014.
Descripteurs français
- KwdFr :
- Adulte, Adulte d'âge moyen, Antibactériens (administration et posologie), Antibactériens (métabolisme), Antibactériens (pharmacocinétique), Chromatographie, Coopération internationale, Femelle, Humains, Jeune adulte, Liaison aux protéines, Maladie grave, Mâle, Plasma sanguin (), Sujet âgé, Surveillance pharmacologique, Téicoplanine (administration et posologie), Téicoplanine (métabolisme), Téicoplanine (pharmacocinétique).
- MESH :
- administration et posologie : Antibactériens, Téicoplanine.
- métabolisme : Antibactériens, Téicoplanine.
- pharmacocinétique : Antibactériens, Téicoplanine.
- Adulte, Adulte d'âge moyen, Chromatographie, Coopération internationale, Femelle, Humains, Jeune adulte, Liaison aux protéines, Maladie grave, Mâle, Plasma sanguin, Sujet âgé, Surveillance pharmacologique.
English descriptors
- KwdEn :
- Adult, Aged, Anti-Bacterial Agents (administration & dosage), Anti-Bacterial Agents (metabolism), Anti-Bacterial Agents (pharmacokinetics), Chromatography, Critical Illness, Drug Monitoring, Female, Humans, International Cooperation, Male, Middle Aged, Plasma (chemistry), Protein Binding, Teicoplanin (administration & dosage), Teicoplanin (metabolism), Teicoplanin (pharmacokinetics), Young Adult.
- MESH :
- chemical , administration & dosage : Anti-Bacterial Agents, Teicoplanin.
- chemical , metabolism : Anti-Bacterial Agents, Teicoplanin.
- chemical , pharmacokinetics : Anti-Bacterial Agents, Teicoplanin.
- chemistry : Plasma.
- Adult, Aged, Chromatography, Critical Illness, Drug Monitoring, Female, Humans, International Cooperation, Male, Middle Aged, Protein Binding, Young Adult.
Abstract
The aims of this study were to describe the variability in protein binding of teicoplanin in critically ill patients as well as the number of patients achieving therapeutic target concentrations. This report is part of the multinational pharmacokinetic DALI Study. Patients were sampled on a single day, with blood samples taken both at the midpoint and the end of the dosing interval. Total and unbound teicoplanin concentrations were assayed using validated chromatographic methods. The lower therapeutic range of teicoplanin was defined as total trough concentrations from 10 to 20 mg/L and the higher range as 10-30 mg/L. Thirteen critically ill patients were available for analysis. The following are the median (interquartile range) total and free concentrations (mg/L): midpoint, total 13.6 (11.2-26.0) and free 1.5 (0.7-2.5); trough, total 11.9 (10.2-22.7) and free 1.8 (0.6-2.6). The percentage free teicoplanin for the mid-dose and trough time points was 6.9% (4.5-15.6%) and 8.2% (5.5-16.4%), respectively. The correlation between total and free antibiotic concentrations was moderate for both the midpoint (ρ = 0.79, P = 0.0021) and trough (ρ = 0.63, P = 0.027). Only 42% and 58% of patients were in the lower and higher therapeutic ranges, respectively. In conclusion, use of standard dosing for teicoplanin leads to inappropriate concentrations in a high proportion of critically ill patients. Variability in teicoplanin protein binding is very high, placing significant doubt on the validity of total concentrations for therapeutic drug monitoring in critically ill patients.
DOI: 10.1016/j.ijantimicag.2014.01.023
PubMed: 24630304
Affiliations:
- Australie, Belgique, Espagne, France, Grèce, Italie, Royaume-Uni, Turquie
- Angleterre, Attique (région), Catalogne, Grand Londres, Victoria (État), Île-de-France
- Athènes, Barcelone, Londres, Melbourne, Paris
- Université autonome de Barcelone, Université de Londres
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pubmed:24630304Le document en format XML
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<author><name sortKey="Roberts, J A" sort="Roberts, J A" uniqKey="Roberts J" first="J A" last="Roberts">J A Roberts</name>
<affiliation wicri:level="1"><nlm:affiliation>Burns, Trauma and Critical Care Research Centre, The University of Queensland, Brisbane, Queensland, Australia; Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia. Electronic address: j.roberts2@uq.edu.au.</nlm:affiliation>
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<author><name sortKey="Stove, V" sort="Stove, V" uniqKey="Stove V" first="V" last="Stove">V. Stove</name>
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<author><name sortKey="Sipinkoski, B" sort="Sipinkoski, B" uniqKey="Sipinkoski B" first="B" last="Sipinkoski">B. Sipinkoski</name>
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<author><name sortKey="Ungerer, J P J" sort="Ungerer, J P J" uniqKey="Ungerer J" first="J P J" last="Ungerer">J P J. Ungerer</name>
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<author><name sortKey="Akova, M" sort="Akova, M" uniqKey="Akova M" first="M" last="Akova">M. Akova</name>
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<author><name sortKey="Bassetti, M" sort="Bassetti, M" uniqKey="Bassetti M" first="M" last="Bassetti">M. Bassetti</name>
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<author><name sortKey="Dimopoulos, G" sort="Dimopoulos, G" uniqKey="Dimopoulos G" first="G" last="Dimopoulos">G. Dimopoulos</name>
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<author><name sortKey="Koulenti, D" sort="Koulenti, D" uniqKey="Koulenti D" first="D" last="Koulenti">D. Koulenti</name>
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<author><name sortKey="Rello, J" sort="Rello, J" uniqKey="Rello J" first="J" last="Rello">J. Rello</name>
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<country xml:lang="fr">Espagne</country>
<wicri:regionArea>CIBERES, Vall d'Hebron Institute of Research, Universitat Autònoma de Barcelona, Barcelona</wicri:regionArea>
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<wicri:regionArea>St George's Healthcare NHS Trust and St George's University of London, London</wicri:regionArea>
<placeName><settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
<settlement type="city">Londres</settlement>
</placeName>
<orgName type="university">Université de Londres</orgName>
</affiliation>
</author>
<author><name sortKey="Starr, T" sort="Starr, T" uniqKey="Starr T" first="T" last="Starr">T. Starr</name>
<affiliation wicri:level="1"><nlm:affiliation>Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Royal Brisbane and Women's Hospital, Brisbane, Queensland</wicri:regionArea>
<wicri:noRegion>Queensland</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Wallis, S C" sort="Wallis, S C" uniqKey="Wallis S" first="S C" last="Wallis">S C Wallis</name>
<affiliation wicri:level="1"><nlm:affiliation>Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Royal Brisbane and Women's Hospital, Brisbane, Queensland</wicri:regionArea>
<wicri:noRegion>Queensland</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Lipman, J" sort="Lipman, J" uniqKey="Lipman J" first="J" last="Lipman">J. Lipman</name>
<affiliation wicri:level="1"><nlm:affiliation>Burns, Trauma and Critical Care Research Centre, The University of Queensland, Brisbane, Queensland, Australia; Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Burns, Trauma and Critical Care Research Centre, The University of Queensland, Brisbane, Queensland, Australia; Royal Brisbane and Women's Hospital, Brisbane, Queensland</wicri:regionArea>
<wicri:noRegion>Queensland</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series><title level="j">International journal of antimicrobial agents</title>
<idno type="eISSN">1872-7913</idno>
<imprint><date when="2014" type="published">2014</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>Anti-Bacterial Agents (administration & dosage)</term>
<term>Anti-Bacterial Agents (metabolism)</term>
<term>Anti-Bacterial Agents (pharmacokinetics)</term>
<term>Chromatography</term>
<term>Critical Illness</term>
<term>Drug Monitoring</term>
<term>Female</term>
<term>Humans</term>
<term>International Cooperation</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Plasma (chemistry)</term>
<term>Protein Binding</term>
<term>Teicoplanin (administration & dosage)</term>
<term>Teicoplanin (metabolism)</term>
<term>Teicoplanin (pharmacokinetics)</term>
<term>Young Adult</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Antibactériens (administration et posologie)</term>
<term>Antibactériens (métabolisme)</term>
<term>Antibactériens (pharmacocinétique)</term>
<term>Chromatographie</term>
<term>Coopération internationale</term>
<term>Femelle</term>
<term>Humains</term>
<term>Jeune adulte</term>
<term>Liaison aux protéines</term>
<term>Maladie grave</term>
<term>Mâle</term>
<term>Plasma sanguin ()</term>
<term>Sujet âgé</term>
<term>Surveillance pharmacologique</term>
<term>Téicoplanine (administration et posologie)</term>
<term>Téicoplanine (métabolisme)</term>
<term>Téicoplanine (pharmacocinétique)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="administration & dosage" xml:lang="en"><term>Anti-Bacterial Agents</term>
<term>Teicoplanin</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Anti-Bacterial Agents</term>
<term>Teicoplanin</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacokinetics" xml:lang="en"><term>Anti-Bacterial Agents</term>
<term>Teicoplanin</term>
</keywords>
<keywords scheme="MESH" qualifier="administration et posologie" xml:lang="fr"><term>Antibactériens</term>
<term>Téicoplanine</term>
</keywords>
<keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Plasma</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Antibactériens</term>
<term>Téicoplanine</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacocinétique" xml:lang="fr"><term>Antibactériens</term>
<term>Téicoplanine</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>Chromatography</term>
<term>Critical Illness</term>
<term>Drug Monitoring</term>
<term>Female</term>
<term>Humans</term>
<term>International Cooperation</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Protein Binding</term>
<term>Young Adult</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Chromatographie</term>
<term>Coopération internationale</term>
<term>Femelle</term>
<term>Humains</term>
<term>Jeune adulte</term>
<term>Liaison aux protéines</term>
<term>Maladie grave</term>
<term>Mâle</term>
<term>Plasma sanguin</term>
<term>Sujet âgé</term>
<term>Surveillance pharmacologique</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">The aims of this study were to describe the variability in protein binding of teicoplanin in critically ill patients as well as the number of patients achieving therapeutic target concentrations. This report is part of the multinational pharmacokinetic DALI Study. Patients were sampled on a single day, with blood samples taken both at the midpoint and the end of the dosing interval. Total and unbound teicoplanin concentrations were assayed using validated chromatographic methods. The lower therapeutic range of teicoplanin was defined as total trough concentrations from 10 to 20 mg/L and the higher range as 10-30 mg/L. Thirteen critically ill patients were available for analysis. The following are the median (interquartile range) total and free concentrations (mg/L): midpoint, total 13.6 (11.2-26.0) and free 1.5 (0.7-2.5); trough, total 11.9 (10.2-22.7) and free 1.8 (0.6-2.6). The percentage free teicoplanin for the mid-dose and trough time points was 6.9% (4.5-15.6%) and 8.2% (5.5-16.4%), respectively. The correlation between total and free antibiotic concentrations was moderate for both the midpoint (ρ = 0.79, P = 0.0021) and trough (ρ = 0.63, P = 0.027). Only 42% and 58% of patients were in the lower and higher therapeutic ranges, respectively. In conclusion, use of standard dosing for teicoplanin leads to inappropriate concentrations in a high proportion of critically ill patients. Variability in teicoplanin protein binding is very high, placing significant doubt on the validity of total concentrations for therapeutic drug monitoring in critically ill patients.</div>
</front>
</TEI>
<affiliations><list><country><li>Australie</li>
<li>Belgique</li>
<li>Espagne</li>
<li>France</li>
<li>Grèce</li>
<li>Italie</li>
<li>Royaume-Uni</li>
<li>Turquie</li>
</country>
<region><li>Angleterre</li>
<li>Attique (région)</li>
<li>Catalogne</li>
<li>Grand Londres</li>
<li>Victoria (État)</li>
<li>Île-de-France</li>
</region>
<settlement><li>Athènes</li>
<li>Barcelone</li>
<li>Londres</li>
<li>Melbourne</li>
<li>Paris</li>
</settlement>
<orgName><li>Université autonome de Barcelone</li>
<li>Université de Londres</li>
</orgName>
</list>
<tree><country name="Australie"><noRegion><name sortKey="Roberts, J A" sort="Roberts, J A" uniqKey="Roberts J" first="J A" last="Roberts">J A Roberts</name>
</noRegion>
<name sortKey="Kaukonen, K M" sort="Kaukonen, K M" uniqKey="Kaukonen K" first="K-M" last="Kaukonen">K-M Kaukonen</name>
<name sortKey="Lipman, J" sort="Lipman, J" uniqKey="Lipman J" first="J" last="Lipman">J. Lipman</name>
<name sortKey="Mcwhinney, B" sort="Mcwhinney, B" uniqKey="Mcwhinney B" first="B" last="Mcwhinney">B. Mcwhinney</name>
<name sortKey="Sipinkoski, B" sort="Sipinkoski, B" uniqKey="Sipinkoski B" first="B" last="Sipinkoski">B. Sipinkoski</name>
<name sortKey="Starr, T" sort="Starr, T" uniqKey="Starr T" first="T" last="Starr">T. Starr</name>
<name sortKey="Ungerer, J P J" sort="Ungerer, J P J" uniqKey="Ungerer J" first="J P J" last="Ungerer">J P J. Ungerer</name>
<name sortKey="Wallis, S C" sort="Wallis, S C" uniqKey="Wallis S" first="S C" last="Wallis">S C Wallis</name>
</country>
<country name="Belgique"><noRegion><name sortKey="Stove, V" sort="Stove, V" uniqKey="Stove V" first="V" last="Stove">V. Stove</name>
</noRegion>
<name sortKey="De Waele, J J" sort="De Waele, J J" uniqKey="De Waele J" first="J J" last="De Waele">J J De Waele</name>
</country>
<country name="Turquie"><noRegion><name sortKey="Akova, M" sort="Akova, M" uniqKey="Akova M" first="M" last="Akova">M. Akova</name>
</noRegion>
</country>
<country name="Italie"><noRegion><name sortKey="Bassetti, M" sort="Bassetti, M" uniqKey="Bassetti M" first="M" last="Bassetti">M. Bassetti</name>
</noRegion>
</country>
<country name="Grèce"><region name="Attique (région)"><name sortKey="Dimopoulos, G" sort="Dimopoulos, G" uniqKey="Dimopoulos G" first="G" last="Dimopoulos">G. Dimopoulos</name>
</region>
<name sortKey="Koulenti, D" sort="Koulenti, D" uniqKey="Koulenti D" first="D" last="Koulenti">D. Koulenti</name>
</country>
<country name="France"><noRegion><name sortKey="Martin, C" sort="Martin, C" uniqKey="Martin C" first="C" last="Martin">C. Martin</name>
</noRegion>
<name sortKey="Montravers, P" sort="Montravers, P" uniqKey="Montravers P" first="P" last="Montravers">P. Montravers</name>
</country>
<country name="Espagne"><region name="Catalogne"><name sortKey="Rello, J" sort="Rello, J" uniqKey="Rello J" first="J" last="Rello">J. Rello</name>
</region>
</country>
<country name="Royaume-Uni"><region name="Angleterre"><name sortKey="Rhodes, A" sort="Rhodes, A" uniqKey="Rhodes A" first="A" last="Rhodes">A. Rhodes</name>
</region>
</country>
</tree>
</affiliations>
</record>
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