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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Martínez Casanova, Javier</mods:namePart>
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                  <mods:namePart>Esteve Pitarch, Erika</mods:namePart>
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                  <mods:namePart>Colom Codina, Helena</mods:namePart>
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                  <mods:namePart>Gumucio Sanguino, Víctor Daniel</mods:namePart>
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                  <mods:namePart>Cobo Sacristán, Sara</mods:namePart>
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                  <mods:namePart>Shaw, Evelyn</mods:namePart>
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                  <mods:namePart>Maisterra Santos, Kristel</mods:namePart>
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                  <mods:namePart>Sabater Riera, Joan</mods:namePart>
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                  <mods:namePart>Pérez Fernández, Xosé Luis</mods:namePart>
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                  <mods:namePart>Rigo Bonnin, Raúl</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Tubau Quintano, Fe</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Carratalà, Jordi</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Padullés Zamora, Ariadna</mods:namePart>
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               <mods:originInfo>
                  <mods:dateIssued encoding="iso8601">2023-05-23T11:37:04Z2023-05-23T11:37:04Z2023-03-072023-04-21T12:19:37Z</mods:dateIssued>
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               <mods:abstract>Critically ill patients undergo significant pathophysiological changes that affect antibiotic pharmacokinetics. Piperacillin/tazobactam administered by continuous infusion (CI) improves pharmacokinetic/pharmacodynamic (PK/PD) target attainment. This study aimed to characterize piperacillin PK after CI administration of piperacillin/tazobactam in critically ill adult patients with preserved renal function and to determine the empirical optimal dosing regimen. A total of 218 piperacillin concentrations from 106 patients were simultaneously analyzed through the population PK approach. A two-compartment linear model best described the data. Creatinine clearance (CLCR) estimated by CKD-EPI was the covariate, the most predictive factor of piperacillin clearance (CL) interindividual variability. The mean (relative standard error) parameter estimates for the final model were: CL: 12.0 L/h (6.03%); central and peripheral compartment distribution volumes: 20.7 L (8.94%) and 62.4 L (50.80%), respectively; intercompartmental clearance: 4.8 L/h (26.4%). For the PK/PD target of 100% fT(>1xMIC), 12 g of piperacillin provide a probability of target attainment > 90% for MIC &lt; 16 mg/L, regardless of CLCR, but higher doses are needed for MIC = 16 mg/L when CLCR > 100 mL/min. For 100% fT(>4xMIC), the highest dose (24 g/24 h) was not sufficient to ensure adequate exposure, except for MICs of 1 and 4 mg/L. Our model can be used as a support tool for initial dose guidance and during therapeutic drug monitoring.</mods:abstract>
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               <mods:accessCondition type="useAndReproduction">cc by (c) Martínez Casanova, Javier et al., 2023 http://creativecommons.org/licenses/by/3.0/es/ info:eu-repo/semantics/openAccess</mods:accessCondition>
               <mods:subject>
                  <mods:topic>Antibiòtics betalactàmics</mods:topic>
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               <mods:subject>
                  <mods:topic>Farmacocinètica</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Farmacovigilància</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Beta lactam antibiotics</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Pharmacokinetics</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Drug monitoring</mods:topic>
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               <mods:titleInfo>
                  <mods:title>Predictive Factors of Piperacillin Exposure and the Impact on Target Attainment after Continuous Infusion Administration to Critically Ill Patients</mods:title>
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