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A Retrospective Analysis of Intravenous Push versus Extended Infusion Meropenem in Critically Ill Patients
Emory G Johnson1,2, Kayla Maki Ortiz1, David T Adams3
1Texas Health Presbyterian Hospital Dallas, Dallas, TX 75231, USA.
Abstract:
Meropenem is a broad-spectrum antibiotic used for the treatment of multi-drug-resistant infections. Due to its pharmacokinetic profile, meropenem's activity is optimized by maintaining a specific time the serum concentration remains above the minimum inhibitory concentration (MIC) via extended infusion (EI), continuous infusion, or intermittent infusion dosing strategies. The available literature varies regarding the superiority of these dosing strategies. This study's primary objective was to determine the difference in time to clinical stabilization between intravenous push (IVP) and EI administration. We performed a retrospective pilot cohort study of 100 critically ill patients who received meropenem by IVP (n = 50) or EI (n = 50) during their intensive care unit (ICU) admission. There was no statistically significant difference in the overall achievement of clinical stabilization between IVP and EI (48% vs. 44%, p = 0.17). However, the median time to clinical stability was shorter for the EI group (20.4 vs. 66.2 h, p = 0.01). EI administration was associated with shorter hospital (13 vs. 17 days; p = 0.05) and ICU (6 vs. 9 days; p = 0.02) lengths of stay. Although we did not find a statistically significant difference in the overall time to clinical stabilization, the results of this pilot study suggest that EI administration may produce quicker clinical resolutions than IVP.
Insights
Extended infusion (EI) meropenem dosing may lead to quicker clinical recovery in critically ill patients compared to intravenous push (IVP). While overall stabilization rates were similar, EI showed faster median time to stability and shorter hospital stays.
Area of Science:
- Pharmacology and Critical Care Medicine
- Antimicrobial Stewardship
Background:
- Meropenem is a critical antibiotic for multi-drug-resistant infections.
- Optimizing meropenem efficacy requires maintaining serum concentrations above the minimum inhibitory concentration (MIC).
- Dosing strategies like extended infusion (EI), continuous infusion, and intermittent infusion are used, with varying literature on superiority.
Purpose of the Study:
- To compare the time to clinical stabilization between intravenous push (IVP) and extended infusion (EI) meropenem administration.
- To evaluate the impact of different meropenem dosing strategies on patient outcomes in the intensive care unit (ICU).
Main Methods:
- Retrospective pilot cohort study involving 100 critically ill patients.
- Patients were divided into two groups: IVP meropenem (n=50) and EI meropenem (n=50).
- Data collected included time to clinical stabilization, hospital length of stay, and ICU length of stay.
Main Results:
- No statistically significant difference in overall clinical stabilization achievement between IVP and EI groups (48% vs. 44%, p=0.17).
- Median time to clinical stability was significantly shorter in the EI group (20.4 hours) compared to the IVP group (66.2 hours, p=0.01).
- EI administration was associated with shorter hospital (13 vs. 17 days, p=0.05) and ICU (6 vs. 9 days, p=0.02) lengths of stay.
Conclusions:
- While overall stabilization rates did not differ significantly, extended infusion meropenem demonstrated a trend towards quicker clinical resolution.
- Extended infusion meropenem administration may be a more effective strategy for achieving clinical stability faster in critically ill patients.
- Further prospective studies are warranted to confirm these findings and optimize meropenem dosing for improved patient outcomes.
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