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Impact of renal replacement therapy strategy on beta-lactam plasma concentrations: the BETAKIKI study—an ancillary study of a randomized controlled trial

BACKGROUND: Sepsis prognosis correlates with antibiotic adequacy at the early phase. This adequacy is dependent on antibacterial spectrum, bacterial resistance profile and antibiotic dosage. Optimal efficacy of beta-lactams mandates concentrations above the minimal inhibitory concentration (MIC) of...

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Autores principales: Roux, Damien, Benichou, Nicolas, Hajage, David, Martin-Lefèvre, Laurent, de Prost, Nicolas, Lerolle, Nicolas, Titeca-Beauport, Dimitri, Boulet, Eric, Mayaux, Julien, Mégarbane, Bruno, Mahjoub, Khaoula, Carpentier, Dorothée, Nseir, Saad, Tubach, Florence, Ricard, Jean-Damien, Dreyfuss, Didier, Gaudry, Stéphane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9968363/
https://www.ncbi.nlm.nih.gov/pubmed/36840825
http://dx.doi.org/10.1186/s13613-023-01105-0
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author Roux, Damien
Benichou, Nicolas
Hajage, David
Martin-Lefèvre, Laurent
de Prost, Nicolas
Lerolle, Nicolas
Titeca-Beauport, Dimitri
Boulet, Eric
Mayaux, Julien
Mégarbane, Bruno
Mahjoub, Khaoula
Carpentier, Dorothée
Nseir, Saad
Tubach, Florence
Ricard, Jean-Damien
Dreyfuss, Didier
Gaudry, Stéphane
author_facet Roux, Damien
Benichou, Nicolas
Hajage, David
Martin-Lefèvre, Laurent
de Prost, Nicolas
Lerolle, Nicolas
Titeca-Beauport, Dimitri
Boulet, Eric
Mayaux, Julien
Mégarbane, Bruno
Mahjoub, Khaoula
Carpentier, Dorothée
Nseir, Saad
Tubach, Florence
Ricard, Jean-Damien
Dreyfuss, Didier
Gaudry, Stéphane
author_sort Roux, Damien
collection PubMed
description BACKGROUND: Sepsis prognosis correlates with antibiotic adequacy at the early phase. This adequacy is dependent on antibacterial spectrum, bacterial resistance profile and antibiotic dosage. Optimal efficacy of beta-lactams mandates concentrations above the minimal inhibitory concentration (MIC) of the targeted bacteria for the longest time possible over the day. Septic acute kidney injury (AKI) is the most common AKI syndrome in ICU and often mandates renal replacement therapy (RRT) initiation. Both severe AKI and RRT may increase outside target antibiotic concentrations and ultimately alter patient’s prognosis. PATIENTS AND METHODS: This is a secondary analysis of a randomized controlled trial that compared an early RRT initiation strategy with a delayed one in 620 critically ill patients undergoing severe AKI (defined by KDIGO 3). We compared beta-lactam trough concentrations between the two RRT initiation strategies. The primary outcome was the proportion of patients with sufficient trough plasma concentration of beta-lactams defined by trough concentration above 4 times the MIC. We hypothesized that early initiation of RRT could be associated with an insufficient antibiotic plasma trough concentration compared to patients allocated to the delayed strategy. RESULTS: One hundred and twelve patients were included: 53 in the early group and 59 in the delayed group. Eighty-three patients (74%) had septic shock on inclusion. Trough beta-lactam plasma concentration was above 4 times the MIC breakpoint in 80.4% (n = 90) of patients of the whole population, without differences between the early and the delayed groups (79.2% vs. 81.4%, respectively, p = 0.78). On multivariate analysis, the presence of septic shock and a higher mean arterial pressure were significantly associated with a greater probability of adequate antibiotic trough concentration [OR 3.95 (1.14;13.64), p = 0.029 and OR 1.05 (1.01;1.10), p = 0.013, respectively). Evolution of procalcitonin level and catecholamine-free days as well as mortality did not differ whether beta-lactam trough concentration was above 4 times the MIC or not. CONCLUSIONS: In this secondary analysis of a randomized controlled trial, renal replacement therapy initiation strategy did not significantly influence plasma trough concentrations of beta-lactams in ICU patients with severe AKI. Presence of septic shock on inclusion was the main variable associated with a sufficient beta-lactam concentration. Trial registration: The AKIKI trial was registered on ClinicalTrials.gov (Identifier: NCT01932190) before the inclusion of the first patient. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13613-023-01105-0.
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spelling pubmed-99683632023-02-27 Impact of renal replacement therapy strategy on beta-lactam plasma concentrations: the BETAKIKI study—an ancillary study of a randomized controlled trial Roux, Damien Benichou, Nicolas Hajage, David Martin-Lefèvre, Laurent de Prost, Nicolas Lerolle, Nicolas Titeca-Beauport, Dimitri Boulet, Eric Mayaux, Julien Mégarbane, Bruno Mahjoub, Khaoula Carpentier, Dorothée Nseir, Saad Tubach, Florence Ricard, Jean-Damien Dreyfuss, Didier Gaudry, Stéphane Ann Intensive Care Research BACKGROUND: Sepsis prognosis correlates with antibiotic adequacy at the early phase. This adequacy is dependent on antibacterial spectrum, bacterial resistance profile and antibiotic dosage. Optimal efficacy of beta-lactams mandates concentrations above the minimal inhibitory concentration (MIC) of the targeted bacteria for the longest time possible over the day. Septic acute kidney injury (AKI) is the most common AKI syndrome in ICU and often mandates renal replacement therapy (RRT) initiation. Both severe AKI and RRT may increase outside target antibiotic concentrations and ultimately alter patient’s prognosis. PATIENTS AND METHODS: This is a secondary analysis of a randomized controlled trial that compared an early RRT initiation strategy with a delayed one in 620 critically ill patients undergoing severe AKI (defined by KDIGO 3). We compared beta-lactam trough concentrations between the two RRT initiation strategies. The primary outcome was the proportion of patients with sufficient trough plasma concentration of beta-lactams defined by trough concentration above 4 times the MIC. We hypothesized that early initiation of RRT could be associated with an insufficient antibiotic plasma trough concentration compared to patients allocated to the delayed strategy. RESULTS: One hundred and twelve patients were included: 53 in the early group and 59 in the delayed group. Eighty-three patients (74%) had septic shock on inclusion. Trough beta-lactam plasma concentration was above 4 times the MIC breakpoint in 80.4% (n = 90) of patients of the whole population, without differences between the early and the delayed groups (79.2% vs. 81.4%, respectively, p = 0.78). On multivariate analysis, the presence of septic shock and a higher mean arterial pressure were significantly associated with a greater probability of adequate antibiotic trough concentration [OR 3.95 (1.14;13.64), p = 0.029 and OR 1.05 (1.01;1.10), p = 0.013, respectively). Evolution of procalcitonin level and catecholamine-free days as well as mortality did not differ whether beta-lactam trough concentration was above 4 times the MIC or not. CONCLUSIONS: In this secondary analysis of a randomized controlled trial, renal replacement therapy initiation strategy did not significantly influence plasma trough concentrations of beta-lactams in ICU patients with severe AKI. Presence of septic shock on inclusion was the main variable associated with a sufficient beta-lactam concentration. Trial registration: The AKIKI trial was registered on ClinicalTrials.gov (Identifier: NCT01932190) before the inclusion of the first patient. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13613-023-01105-0. Springer International Publishing 2023-02-25 /pmc/articles/PMC9968363/ /pubmed/36840825 http://dx.doi.org/10.1186/s13613-023-01105-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Roux, Damien
Benichou, Nicolas
Hajage, David
Martin-Lefèvre, Laurent
de Prost, Nicolas
Lerolle, Nicolas
Titeca-Beauport, Dimitri
Boulet, Eric
Mayaux, Julien
Mégarbane, Bruno
Mahjoub, Khaoula
Carpentier, Dorothée
Nseir, Saad
Tubach, Florence
Ricard, Jean-Damien
Dreyfuss, Didier
Gaudry, Stéphane
Impact of renal replacement therapy strategy on beta-lactam plasma concentrations: the BETAKIKI study—an ancillary study of a randomized controlled trial
title Impact of renal replacement therapy strategy on beta-lactam plasma concentrations: the BETAKIKI study—an ancillary study of a randomized controlled trial
title_full Impact of renal replacement therapy strategy on beta-lactam plasma concentrations: the BETAKIKI study—an ancillary study of a randomized controlled trial
title_fullStr Impact of renal replacement therapy strategy on beta-lactam plasma concentrations: the BETAKIKI study—an ancillary study of a randomized controlled trial
title_full_unstemmed Impact of renal replacement therapy strategy on beta-lactam plasma concentrations: the BETAKIKI study—an ancillary study of a randomized controlled trial
title_short Impact of renal replacement therapy strategy on beta-lactam plasma concentrations: the BETAKIKI study—an ancillary study of a randomized controlled trial
title_sort impact of renal replacement therapy strategy on beta-lactam plasma concentrations: the betakiki study—an ancillary study of a randomized controlled trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9968363/
https://www.ncbi.nlm.nih.gov/pubmed/36840825
http://dx.doi.org/10.1186/s13613-023-01105-0
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