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A Review of Clinical Outcomes Associated with Two Meropenem Dosing Strategies
Meropenem is a carbapenem antibiotic that exhibits time-dependent bactericidal activity, traditionally dosed intravenously at 1 g every 8 h. In order to maximize its pharmacodynamic activity and reduce costs, an alternative regimen employed by many institutions is 500 mg every 6 h. The objective of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318341/ https://www.ncbi.nlm.nih.gov/pubmed/28101836 http://dx.doi.org/10.1007/s40268-017-0173-0 |
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author | Wilby, Kyle John Nasr, Ziad Ghantous Elazzazy, Shereen Lau, Tim T. Y. Hamad, Anas |
author_facet | Wilby, Kyle John Nasr, Ziad Ghantous Elazzazy, Shereen Lau, Tim T. Y. Hamad, Anas |
author_sort | Wilby, Kyle John |
collection | PubMed |
description | Meropenem is a carbapenem antibiotic that exhibits time-dependent bactericidal activity, traditionally dosed intravenously at 1 g every 8 h. In order to maximize its pharmacodynamic activity and reduce costs, an alternative regimen employed by many institutions is 500 mg every 6 h. The objective of this review was to summarize and evaluate published literature comparing clinical outcomes associated with these two meropenem dosing regimens. The literature was searched up to October 2016 using the MEDLINE, EMBASE, and Google Scholar databases. Three retrospective cohort studies were identified that compared clinical outcomes in general infectious disease patients (two studies) and patients with febrile neutropenia (one study). All studies reported no difference in clinical outcomes (clinical success, time to defervescence, sign or symptom resolution, length of stay, mortality, need for other antibiotics, and seizure rates). One study reported reduced economic costs with the alternative dosing. Interpretation of findings was primarily limited by small sample sizes and generalizability. Based on the data reviewed, the alternative dosing regimen of meropenem 500 mg intravenously every 6 h could be considered a therapeutic option. Future studies are needed to confirm the findings of this review, especially in high-risk populations such as immunocompromised patients or those with severe infections. |
format | Online Article Text |
id | pubmed-5318341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-53183412017-03-03 A Review of Clinical Outcomes Associated with Two Meropenem Dosing Strategies Wilby, Kyle John Nasr, Ziad Ghantous Elazzazy, Shereen Lau, Tim T. Y. Hamad, Anas Drugs R D Review Article Meropenem is a carbapenem antibiotic that exhibits time-dependent bactericidal activity, traditionally dosed intravenously at 1 g every 8 h. In order to maximize its pharmacodynamic activity and reduce costs, an alternative regimen employed by many institutions is 500 mg every 6 h. The objective of this review was to summarize and evaluate published literature comparing clinical outcomes associated with these two meropenem dosing regimens. The literature was searched up to October 2016 using the MEDLINE, EMBASE, and Google Scholar databases. Three retrospective cohort studies were identified that compared clinical outcomes in general infectious disease patients (two studies) and patients with febrile neutropenia (one study). All studies reported no difference in clinical outcomes (clinical success, time to defervescence, sign or symptom resolution, length of stay, mortality, need for other antibiotics, and seizure rates). One study reported reduced economic costs with the alternative dosing. Interpretation of findings was primarily limited by small sample sizes and generalizability. Based on the data reviewed, the alternative dosing regimen of meropenem 500 mg intravenously every 6 h could be considered a therapeutic option. Future studies are needed to confirm the findings of this review, especially in high-risk populations such as immunocompromised patients or those with severe infections. Springer International Publishing 2017-01-18 2017-03 /pmc/articles/PMC5318341/ /pubmed/28101836 http://dx.doi.org/10.1007/s40268-017-0173-0 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Review Article Wilby, Kyle John Nasr, Ziad Ghantous Elazzazy, Shereen Lau, Tim T. Y. Hamad, Anas A Review of Clinical Outcomes Associated with Two Meropenem Dosing Strategies |
title | A Review of Clinical Outcomes Associated with Two Meropenem Dosing Strategies |
title_full | A Review of Clinical Outcomes Associated with Two Meropenem Dosing Strategies |
title_fullStr | A Review of Clinical Outcomes Associated with Two Meropenem Dosing Strategies |
title_full_unstemmed | A Review of Clinical Outcomes Associated with Two Meropenem Dosing Strategies |
title_short | A Review of Clinical Outcomes Associated with Two Meropenem Dosing Strategies |
title_sort | review of clinical outcomes associated with two meropenem dosing strategies |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318341/ https://www.ncbi.nlm.nih.gov/pubmed/28101836 http://dx.doi.org/10.1007/s40268-017-0173-0 |
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