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Pharmacokinetics of meropenem in critically ill patients in Saudi Arabia
BACKGROUND: Meropenem is commonly used in the ICU to treat gram-negative infections. Due to various pathophysiological changes, critically ill patients are at higher risk of having subtherapeutic concentrations and hence have a higher risk of treatment failure—especially in regions where gram-negati...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596159/ https://www.ncbi.nlm.nih.gov/pubmed/34819789 http://dx.doi.org/10.1016/j.jsps.2021.09.017 |
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author | Alsultan, Abdullah Dasuqi, Shereen A. Aljamaan, Fadi Omran, Rasha A. Syed, Saeed Ali AlJaloud, Turki AlAhmadi, Abdullah Alqahtani, Saeed Hamad, Mohammed A. |
author_facet | Alsultan, Abdullah Dasuqi, Shereen A. Aljamaan, Fadi Omran, Rasha A. Syed, Saeed Ali AlJaloud, Turki AlAhmadi, Abdullah Alqahtani, Saeed Hamad, Mohammed A. |
author_sort | Alsultan, Abdullah |
collection | PubMed |
description | BACKGROUND: Meropenem is commonly used in the ICU to treat gram-negative infections. Due to various pathophysiological changes, critically ill patients are at higher risk of having subtherapeutic concentrations and hence have a higher risk of treatment failure—especially in regions where gram-negative drug resistance is increasing, such as Saudi Arabia. No studies have evaluated the pharmacokinetics of meropenem in critically ill patients in Saudi Arabia. Our primary objective is to assess the percentage of patients achieving the therapeutic target for meropenem. METHODS: This prospective observational study was conducted in the ICUs of King Khalid University Hospital. Patient were included if >18 years-of-age and received meropenem for a clinically suspected or proven bacterial infection. The primary outcome was to assess the percentage of patients who achieved the pharmacokinetic/pharmacodynamic (PKPD) therapeutic target of a free trough concentration four times the MIC. The secondary outcome was to estimate the pharmacokinetics of meropenem. Pharmacokinetic analysis was performed using Monolix Suite 2020R1 (Lixoft, France). RESULTS: Trough concentrations were highly variable and ranged from <0.5 µg/mL to 39 µg/mL, with a mean ± SD trough concentration of 8.5 ± 8 µg/mL. Only 46% of patients achieved the therapeutic target. The only significant predictor of failing to achieve the PKPD target was augmented renal clearance. CONCLUSION: In conclusion, more than half of our patients did not achieve the PKPD target. Thus, there is a need for better dosing strategies of meropenem in critically ill patients in Saudi Arabia such as extended and continuous infusion. |
format | Online Article Text |
id | pubmed-8596159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-85961592021-11-23 Pharmacokinetics of meropenem in critically ill patients in Saudi Arabia Alsultan, Abdullah Dasuqi, Shereen A. Aljamaan, Fadi Omran, Rasha A. Syed, Saeed Ali AlJaloud, Turki AlAhmadi, Abdullah Alqahtani, Saeed Hamad, Mohammed A. Saudi Pharm J Original Article BACKGROUND: Meropenem is commonly used in the ICU to treat gram-negative infections. Due to various pathophysiological changes, critically ill patients are at higher risk of having subtherapeutic concentrations and hence have a higher risk of treatment failure—especially in regions where gram-negative drug resistance is increasing, such as Saudi Arabia. No studies have evaluated the pharmacokinetics of meropenem in critically ill patients in Saudi Arabia. Our primary objective is to assess the percentage of patients achieving the therapeutic target for meropenem. METHODS: This prospective observational study was conducted in the ICUs of King Khalid University Hospital. Patient were included if >18 years-of-age and received meropenem for a clinically suspected or proven bacterial infection. The primary outcome was to assess the percentage of patients who achieved the pharmacokinetic/pharmacodynamic (PKPD) therapeutic target of a free trough concentration four times the MIC. The secondary outcome was to estimate the pharmacokinetics of meropenem. Pharmacokinetic analysis was performed using Monolix Suite 2020R1 (Lixoft, France). RESULTS: Trough concentrations were highly variable and ranged from <0.5 µg/mL to 39 µg/mL, with a mean ± SD trough concentration of 8.5 ± 8 µg/mL. Only 46% of patients achieved the therapeutic target. The only significant predictor of failing to achieve the PKPD target was augmented renal clearance. CONCLUSION: In conclusion, more than half of our patients did not achieve the PKPD target. Thus, there is a need for better dosing strategies of meropenem in critically ill patients in Saudi Arabia such as extended and continuous infusion. Elsevier 2021-11 2021-10-08 /pmc/articles/PMC8596159/ /pubmed/34819789 http://dx.doi.org/10.1016/j.jsps.2021.09.017 Text en © 2021 Published by Elsevier B.V. on behalf of King Saud University. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Alsultan, Abdullah Dasuqi, Shereen A. Aljamaan, Fadi Omran, Rasha A. Syed, Saeed Ali AlJaloud, Turki AlAhmadi, Abdullah Alqahtani, Saeed Hamad, Mohammed A. Pharmacokinetics of meropenem in critically ill patients in Saudi Arabia |
title | Pharmacokinetics of meropenem in critically ill patients in Saudi Arabia |
title_full | Pharmacokinetics of meropenem in critically ill patients in Saudi Arabia |
title_fullStr | Pharmacokinetics of meropenem in critically ill patients in Saudi Arabia |
title_full_unstemmed | Pharmacokinetics of meropenem in critically ill patients in Saudi Arabia |
title_short | Pharmacokinetics of meropenem in critically ill patients in Saudi Arabia |
title_sort | pharmacokinetics of meropenem in critically ill patients in saudi arabia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596159/ https://www.ncbi.nlm.nih.gov/pubmed/34819789 http://dx.doi.org/10.1016/j.jsps.2021.09.017 |
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