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Inhaled milrinone in cardiac surgical patients: pharmacokinetic and pharmacodynamic exploration

Mean arterial pressure to mean pulmonary arterial pressure ratio (mAP/mPAP) has been identified as a strong predictor of perioperative complications in cardiac surgery. We therefore investigated the pharmacokinetic/pharmacodynamic (PK/PD) relationship of inhaled milrinone in these patients using thi...

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Autores principales: Nguyen, Anne Quynh-Nhu, Denault, André Y., Théoret, Yves, Varin, France
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981759/
https://www.ncbi.nlm.nih.gov/pubmed/36864229
http://dx.doi.org/10.1038/s41598-023-29945-7
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author Nguyen, Anne Quynh-Nhu
Denault, André Y.
Théoret, Yves
Varin, France
author_facet Nguyen, Anne Quynh-Nhu
Denault, André Y.
Théoret, Yves
Varin, France
author_sort Nguyen, Anne Quynh-Nhu
collection PubMed
description Mean arterial pressure to mean pulmonary arterial pressure ratio (mAP/mPAP) has been identified as a strong predictor of perioperative complications in cardiac surgery. We therefore investigated the pharmacokinetic/pharmacodynamic (PK/PD) relationship of inhaled milrinone in these patients using this ratio (R) as a PD marker. Following approval by the ethics and research committee and informed consent, we performed the following experiment. Before initiation of cardiopulmonary bypass in 28 pulmonary hypertensive patients scheduled for cardiac surgery, milrinone (5 mg) was nebulized, plasma concentrations measured (up to 10 h) and compartmental PK analysis carried out. Baseline (R(0)) and peak (R(max)) ratios as well as magnitude of peak response (∆(Rmax-R0)) were measured. During inhalation, individual area under effect-time (AUEC) and plasma concentration–time (AUC) curves were correlated. Potential relationships between PD markers and difficult separation from bypass (DSB) were explored. In this study, we observed that milrinone peak concentrations (41–189 ng ml(−1)) and Δ(Rmax-R0) (− 0.12–1.5) were obtained at the end of inhalation (10–30 min). Mean PK parameters agreed with intravenous milrinone published data after correction for the estimated inhaled dose. Paired comparisons yielded a statistically significant increase between R(0) and R(max) (mean difference, 0.58: 95% CI 0.43–0.73; P < 0.001). Individual AUEC correlated with AUC (r = 0.3890, r(2) = 0.1513; P = 0.045); significance increased after exclusion of non-responders (r = 4787, r(2) = 0.2292; P = 0.024). Individual AUEC correlated with ∆R(max-R0) (r = 5973, r(2) = 0.3568; P = 0.001). Both ∆R(max-R0) (P = 0.009) and CPB duration (P < 0.001) were identified as predictors of DSB. In conclusion, both magnitude of peak response of the mAP/mPAP ratio and CPB duration were associated with DSB.
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spelling pubmed-99817592023-03-04 Inhaled milrinone in cardiac surgical patients: pharmacokinetic and pharmacodynamic exploration Nguyen, Anne Quynh-Nhu Denault, André Y. Théoret, Yves Varin, France Sci Rep Article Mean arterial pressure to mean pulmonary arterial pressure ratio (mAP/mPAP) has been identified as a strong predictor of perioperative complications in cardiac surgery. We therefore investigated the pharmacokinetic/pharmacodynamic (PK/PD) relationship of inhaled milrinone in these patients using this ratio (R) as a PD marker. Following approval by the ethics and research committee and informed consent, we performed the following experiment. Before initiation of cardiopulmonary bypass in 28 pulmonary hypertensive patients scheduled for cardiac surgery, milrinone (5 mg) was nebulized, plasma concentrations measured (up to 10 h) and compartmental PK analysis carried out. Baseline (R(0)) and peak (R(max)) ratios as well as magnitude of peak response (∆(Rmax-R0)) were measured. During inhalation, individual area under effect-time (AUEC) and plasma concentration–time (AUC) curves were correlated. Potential relationships between PD markers and difficult separation from bypass (DSB) were explored. In this study, we observed that milrinone peak concentrations (41–189 ng ml(−1)) and Δ(Rmax-R0) (− 0.12–1.5) were obtained at the end of inhalation (10–30 min). Mean PK parameters agreed with intravenous milrinone published data after correction for the estimated inhaled dose. Paired comparisons yielded a statistically significant increase between R(0) and R(max) (mean difference, 0.58: 95% CI 0.43–0.73; P < 0.001). Individual AUEC correlated with AUC (r = 0.3890, r(2) = 0.1513; P = 0.045); significance increased after exclusion of non-responders (r = 4787, r(2) = 0.2292; P = 0.024). Individual AUEC correlated with ∆R(max-R0) (r = 5973, r(2) = 0.3568; P = 0.001). Both ∆R(max-R0) (P = 0.009) and CPB duration (P < 0.001) were identified as predictors of DSB. In conclusion, both magnitude of peak response of the mAP/mPAP ratio and CPB duration were associated with DSB. Nature Publishing Group UK 2023-03-02 /pmc/articles/PMC9981759/ /pubmed/36864229 http://dx.doi.org/10.1038/s41598-023-29945-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Article
Nguyen, Anne Quynh-Nhu
Denault, André Y.
Théoret, Yves
Varin, France
Inhaled milrinone in cardiac surgical patients: pharmacokinetic and pharmacodynamic exploration
title Inhaled milrinone in cardiac surgical patients: pharmacokinetic and pharmacodynamic exploration
title_full Inhaled milrinone in cardiac surgical patients: pharmacokinetic and pharmacodynamic exploration
title_fullStr Inhaled milrinone in cardiac surgical patients: pharmacokinetic and pharmacodynamic exploration
title_full_unstemmed Inhaled milrinone in cardiac surgical patients: pharmacokinetic and pharmacodynamic exploration
title_short Inhaled milrinone in cardiac surgical patients: pharmacokinetic and pharmacodynamic exploration
title_sort inhaled milrinone in cardiac surgical patients: pharmacokinetic and pharmacodynamic exploration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981759/
https://www.ncbi.nlm.nih.gov/pubmed/36864229
http://dx.doi.org/10.1038/s41598-023-29945-7
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