Evidence map›Paper›PMID 38107537›Full record

ArticleCritical care explorations2023

Anakinra Removal by Continuous Renal Replacement Therapy: An Ex Vivo Analysis.

Samuel D J Dubinsky, Kevin M Watt, Carina E Imburgia, Autumn M Mcknite, J Porter Hunt, Cassandra Rice, Joseph E Rower, Andrea N Edginton

Open access · goldAbstract read
In one paragraph

Article in Critical care explorations, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Samuel D J DubinskyUniversity of Waterloo, School of Pharmacy, Faculty of Science, Waterloo, ON, Canada.
Kevin M WattDepartment of Pediatrics, University of Utah, School of Medicine, Salt Lake City, UT.
Carina E ImburgiaDepartment of Pediatrics, University of Utah, School of Medicine, Salt Lake City, UT.
Autumn M MckniteDepartment of Pharmacology and Toxicology, University of Utah, Salt Lake City, UT.
J Porter HuntDepartment of Pediatrics, University of Utah, School of Medicine, Salt Lake City, UT.
Cassandra RiceDepartment of Pharmacology and Toxicology, Center for Human Toxicology, University of Utah, Salt Lake City, UT.
Joseph E RowerDepartment of Pharmacology and Toxicology, Center for Human Toxicology, University of Utah, Salt Lake City, UT.
Andrea N EdgintonUniversity of Waterloo, School of Pharmacy, Faculty of Science, Waterloo, ON, Canada.
University of Utah · US

Funding

Physiologically-Based Pharmacokinetic Approach to Determine Dosing on Extracorporeal Life SupportR01HD097775 · NICHD · UNIVERSITY OF UTAH · PI WATT, KEVIN M · 2019 to 2023
$2.7M
NICHD NIH HHS R01 HD097775
6 · The paper itself

Abstract

objectivesPatients with sepsis are at significant risk for multiple organ dysfunction, including the lungs and kidneys. To manage the morbidity associated with kidney impairment, continuous renal replacement therapy (CRRT) may be required. The extent of anakinra pharmacokinetics in CRRT remains unknown. The objectives of this study were to investigate the anakinra-circuit interaction and quantify the rate of removal from plasma.

designThe anakinra-circuit interaction was evaluated using a closed-loop ex vivo CRRT circuit. CRRT was performed in three phases based on the method of solute removal: 1) hemofiltration, 2) hemodialysis, and 3) hemodiafiltration. Standard control samples of anakinra were included to assess drug degradation.

settingUniversity research laboratory. PATIENTS: None.

interventionsAnakinra was administered to the CRRT circuit and serial prefilter blood samples were collected along with time-matched control and hemofiltrate samples. Each circuit was run in triplicate to assess inter-run variability. Concentrations of anakinra in each reference fluid were measured by enzyme-linked immunosorbent assay. Transmembrane filter clearance was estimated by the product of the sieving coefficient/dialysate saturation constant and circuit flow rates. MEASUREMENTS AND MAIN

resultsRemoval of anakinra from plasma occurred within minutes for each CRRT modality. Average drug remaining (%) in plasma following anakinra administration was lowest with hemodiafiltration (34.9%). The average sieving coefficient was 0.34, 0.37, and 0.41 for hemodiafiltration, hemofiltration, and hemodialysis, respectively. Transmembrane clearance was fairly consistent across each modality with the highest during hemodialysis (5.53 mL/min), followed by hemodiafiltration (4.99 mL/min), and hemofiltration (3.94 mL/min). Percent drug remaining within the control samples (93.1%) remained consistent across each experiment, indicating negligible degradation within the blood.

conclusionsThe results of this analysis are the first to demonstrate that large molecule therapeutic proteins such as anakinra, are removed from plasma with modern CRRT technology. Current dosing recommendations for patients with severe renal impairment may result in subtherapeutic anakinra concentrations in those receiving CRRT.

Indexed as

anakinracontinuous renal replacement therapyex vivopharmacokinetics

Identifiers

PMID38107537
PMCPMC10723863
OpenAlexW4389727296

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.