Evidence map›Paper›PMID 36840825›Full record

ArticleAnnals of intensive care2023

Impact of renal replacement therapy strategy on beta-lactam plasma concentrations: the BETAKIKI study-an ancillary study of a randomized controlled trial.

Damien Roux, Nicolas Benichou, David Hajage, Laurent Martin-Lefèvre, Nicolas de Prost, Nicolas Lerolle, Dimitri Titeca-Beauport, Eric Boulet, Julien Mayaux, Bruno Mégarbane and 8 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Annals of intensive care, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01932190 (Artificial Kidney Initiation in Kidney Injury, a Multicenter Randomised Trial), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 43% 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.

NCT01932190 nacompletednot on this map

Artificial Kidney Initiation in Kidney Injury, a Multicenter Randomised Trial

TypeinterventionalSponsorAssistance Publique - Hôpitaux de ParisRan2013 to 2016Enrolled620ConditionsRenal Replacement Therapy for Acute Kidney Injury in Intensive Care UnitArmsEarly RRT strategy, Delayed RRT strategy
3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

18 authors at 11 institutions in 1 country.

Damien RouxDMU ESPRIT, Service de Médecine Intensive Réanimation, AP-HP, Université Paris Cité, Hôpital Louis Mourier, 92700, Colombes, France. damien.roux@aphp.fr.ORCID http://orcid.org/0000-0002-6103-6416
Nicolas BenichouDMU ESPRIT, Service de Médecine Intensive Réanimation, AP-HP, Université Paris Cité, Hôpital Louis Mourier, 92700, Colombes, France.
David HajageDépartement de Santé Publique, Centre de Pharmacoépidémiologie (Céphépi), Unité de Recherche Clinique PSL-CFX, Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, AP-HP, Hôpital Pitié Salpêtrière, CIC-1901, Paris, France.
Laurent Martin-LefèvreRéanimation Polyvalente, Centre Hospitalier Départemental - Site de La Roche-Sur-Yon, La Roche-sur-Yon, France.
Nicolas de ProstRéanimation Médicale, AP-HP, Hôpital Henri Mondor, Créteil, France.
Nicolas LerolleDépartement de Réanimation Médicale et Médecine Hyperbare, CHU Angers, Université d'Angers, Angers, France.
Dimitri Titeca-BeauportBoRealStudy Group, Medical Intensive Care Unit and EA7517, Amiens University Hospital, 80054, Amiens, France.
Eric BouletVal d'Oise, Hôpital René Dubos, Pontoise, France.
Julien MayauxMédecine Intensive Réanimation, AP-HP, Hôpital Pitié-Salpétrière, 75013, Paris, France.
Bruno MégarbaneDepartment of Medical and Toxicological Critical Care, Lariboisière Hospital, Université Paris Cité, Paris, France.
Khaoula MahjoubService de Réanimation, Hôpital Delafontaine, 93200, Saint-Denis, France.
Dorothée CarpentierMédecine Intensive Réanimation, Centre Hospitalier Universitaire Rouen, Rouen, France.
Saad NseirCentre Médecine Intensive-Réanimation, CHU de Lille and INSERM U1285, Université de Lille, CNRS, UMR 8576-UGSF, 59000, Lille, France.
Florence TubachDépartement de Santé Publique, Centre de Pharmacoépidémiologie (Céphépi), Unité de Recherche Clinique PSL-CFX, Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, AP-HP, Hôpital Pitié Salpêtrière, CIC-1901, Paris, France.
Jean-Damien RicardDMU ESPRIT, Service de Médecine Intensive Réanimation, AP-HP, Université Paris Cité, Hôpital Louis Mourier, 92700, Colombes, France.
Didier DreyfussDMU ESPRIT, Service de Médecine Intensive Réanimation, AP-HP, Université Paris Cité, Hôpital Louis Mourier, 92700, Colombes, France.
Stéphane GaudrySorbonne Université, INSERM Unit S_1155 CORAKID, 75010, Paris, France.
AKIKI Study group
Inserm · FRCentre National de la Recherche Scientifique · FRDélégation Paris 5 · FRCentre Hospitalier René-Dubos · FRCentre Hospitalier Saint-Denis · FRCentre Hospitalier Universitaire Amiens-Picardie · FRCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Rouen · FRSorbonne Université · FRUniversité Paris-Est Créteil · FR

Funding

Programme Hospitalier de Recherche Clinique National AOM12456
6 · The paper itself

Abstract

backgroundSepsis prognosis correlates with antibiotic adequacy at the early phase. This adequacy is dependent on antibacterial spectrum, bacterial resistance profile and antibiotic dosage. Optimal efficacy of beta-lactams mandates concentrations above the minimal inhibitory concentration (MIC) of the targeted bacteria for the longest time possible over the day. Septic acute kidney injury (AKI) is the most common AKI syndrome in ICU and often mandates renal replacement therapy (RRT) initiation. Both severe AKI and RRT may increase outside target antibiotic concentrations and ultimately alter patient's prognosis. PATIENTS AND

methodsThis is a secondary analysis of a randomized controlled trial that compared an early RRT initiation strategy with a delayed one in 620 critically ill patients undergoing severe AKI (defined by KDIGO 3). We compared beta-lactam trough concentrations between the two RRT initiation strategies. The primary outcome was the proportion of patients with sufficient trough plasma concentration of beta-lactams defined by trough concentration above 4 times the MIC. We hypothesized that early initiation of RRT could be associated with an insufficient antibiotic plasma trough concentration compared to patients allocated to the delayed strategy.

resultsOne hundred and twelve patients were included: 53 in the early group and 59 in the delayed group. Eighty-three patients (74%) had septic shock on inclusion. Trough beta-lactam plasma concentration was above 4 times the MIC breakpoint in 80.4% (n = 90) of patients of the whole population, without differences between the early and the delayed groups (79.2% vs. 81.4%, respectively, p = 0.78). On multivariate analysis, the presence of septic shock and a higher mean arterial pressure were significantly associated with a greater probability of adequate antibiotic trough concentration [OR 3.95 (1.14;13.64), p = 0.029 and OR 1.05 (1.01;1.10), p = 0.013, respectively). Evolution of procalcitonin level and catecholamine-free days as well as mortality did not differ whether beta-lactam trough concentration was above 4 times the MIC or not.

conclusionsIn this secondary analysis of a randomized controlled trial, renal replacement therapy initiation strategy did not significantly influence plasma trough concentrations of beta-lactams in ICU patients with severe AKI. Presence of septic shock on inclusion was the main variable associated with a sufficient beta-lactam concentration.

trial registrationThe AKIKI trial was registered on ClinicalTrials.gov (Identifier: NCT01932190) before the inclusion of the first patient.

Indexed as

Acute kidney injuryAntibioticBeta-lactamConcentrationHemofiltrationIntermittent hemodialysisRenal replacement therapySeptic shock

Identifiers

PMID36840825
PMCPMC9968363
OpenAlexW4321850233

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.