Evidence map›Paper›PMID 38099629›Full record

ArticleThe journal of extra-corporeal technology2023

Meropenem extraction by ex vivo extracorporeal life support circuits.

Christopher Cole Honeycutt, Charles Griffin McDaniel, Autumn McKnite, J Porter Hunt, Aviva Whelan, Danielle J Green, Kevin M Watt

Open access · diamondAbstract read
In one paragraph

Article in The journal of extra-corporeal technology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Observational
  3. Article
  4. Article
  5. Article
  6. Article
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  9. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Christopher Cole HoneycuttDuke University, Durham, North Carolina, USA.ORCID 0000-0003-1813-3576
Charles Griffin McDanielDuke University, Durham, North Carolina, USA.ORCID 0000-0002-0573-0956
Autumn McKniteDepartment of Pharmacology and Toxicology, University of Utah College of Pharmacy, Salt Lake City, Utah, USA - Division of Clinical Pharmacology, Department of Pediatrics, University of Utah Medical Center, Salt Lake City, Utah, USA.
J Porter HuntDivision of Clinical Pharmacology, Department of Pediatrics, University of Utah Medical Center, Salt Lake City, Utah, USA.ORCID 0000-0003-3503-8124
Aviva WhelanDivision of Clinical Pharmacology, Department of Pediatrics, University of Utah Medical Center, Salt Lake City, Utah, USA - Division of Critical Care, Department of Pediatrics, University of Utah Medical Center, Salt Lake City, Utah, USA.
Danielle J GreenDivision of Clinical Pharmacology, Department of Pediatrics, University of Utah Medical Center, Salt Lake City, Utah, USA - Division of Critical Care, Department of Pediatrics, University of Utah Medical Center, Salt Lake City, Utah, USA.
Kevin M WattDivision of Clinical Pharmacology, Department of Pediatrics, University of Utah Medical Center, Salt Lake City, Utah, USA - Division of Critical Care, Department of Pediatrics, University of Utah Medical Center, Salt Lake City, Utah, USA.
University of Utah · USDuke University · US

Funding

The Indiana University-Ohio State University Maternal and Pediatric Precision in Therapeutics Data, Model, Knowledge, and Research Coordination Center (IU-OSU MPRINT DMKRCC)P30HD106451 · NICHD · INDIANA UNIVERSITY INDIANAPOLIS · PI Sara K Quinney · 2021 to 2026
$24.1M
Multidisciplinary Pulmonary and Critical Care Training ProgramT32HL105321 · NHLBI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Ramsey Hachem, Robert Paine · 2010 to 2026
$4.5M
Physiologically-Based Pharmacokinetic Approach to Determine Dosing on Extracorporeal Life SupportR01HD097775 · NICHD · UNIVERSITY OF UTAH · PI WATT, KEVIN M · 2019 to 2023
$2.7M
Investigation of Drug-Drug and Drug-Circuit Interactions in Children on Continuous Renal Replacement TherapyF31DK130542 · NIDDK · UNIVERSITY OF UTAH · PI MCKNITE, AUTUMN · 2022 to 2023
$74k
NHLBI NIH HHS T32 HL105321NICHD NIH HHS P30 HD106451NICHD NIH HHS R01 HD097775NIDDK NIH HHS F31 DK130542
6 · The paper itself

Abstract

backgroundMeropenem is a broad-spectrum carbapenem-type antibiotic commonly used to treat critically ill patients infected with extended-spectrum β-lactamase (ESBL)-producing Enterobacteriaceae. As many of these patients require extracorporeal membrane oxygenation (ECMO) and/or continuous renal replacement therapy (CRRT), it is important to understand how these extracorporeal life support circuits impact meropenem pharmacokinetics. Based on the physicochemical properties of meropenem, it is expected that ECMO circuits will minimally extract meropenem, while CRRT circuits will rapidly clear meropenem. The present study seeks to determine the extraction of meropenem from ex vivo ECMO and CRRT circuits and elucidate the contribution of different ECMO circuit components to extraction.

methodsStandard doses of meropenem were administered to three different configurations (n = 3 per configuration) of blood-primed ex vivo ECMO circuits and serial sampling was conducted over 24 h. Similarly, standard doses of meropenem were administered to CRRT circuits (n = 4) and serial sampling was conducted over 4 h. Meropenem was administered to separate tubes primed with circuit blood to serve as controls to account for drug degradation. Meropenem concentrations were quantified, and percent recovery was calculated for each sample.

resultsMeropenem was cleared at a similar rate in ECMO circuits of different configurations (n = 3) and controls (n = 6), with mean (standard deviation) recovery at 24 h of 15.6% (12.9) in Complete circuits, 37.9% (8.3) in Oxygenator circuits, 47.1% (8.2) in Pump circuits, and 20.6% (20.6) in controls. In CRRT circuits (n = 4) meropenem was cleared rapidly compared with controls (n = 6) with a mean recovery at 2 h of 2.36% (1.44) in circuits and 93.0% (7.1) in controls.

conclusionMeropenem is rapidly cleared by hemodiafiltration during CRRT. There is minimal adsorption of meropenem to ECMO circuit components; however, meropenem undergoes significant degradation and/or plasma metabolism at physiological conditions. These ex vivo findings will advise pharmacists and physicians on the appropriate dosing of meropenem.

Indexed as

Extracorporeal Membrane OxygenationAnti-Bacterial AgentsCarbapenemsHumansMeropenemAnti-Bacterial AgentsCarbapenemsMeropenemContinuous renal replacement therapyDrug extractionExtracorporeal membrane oxygenationMeropenemPharmacokinetics

Identifiers

PMID38099629
PMCPMC10723574
OpenAlexW4386764956

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.