Evidence map›Paper›PMID 31109283›Full record

ArticleBMC infectious diseases2019

Acute kidney injury during daptomycin versus vancomycin treatment in cardiovascular critically ill patients: a propensity score matched analysis.

Philippe Gaudard, Marine Saour, David Morquin, Hélène David, Jacob Eliet, Maxime Villiet, Jean-Pierre Daures, Pascal Colson

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
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  3. Article
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  5. Review
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  7. 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

8 authors at 3 institutions in 3 countries.

Philippe GaudardPhyMedExp, University of Montpellier, CNRS, INSERM, Department of cardiothoracic Anaesthesiology and Critical Care Medicine, CHU Montpellier, Montpellier, France. p-gaudard@chu-montpellier.fr.ORCID http://orcid.org/0000-0003-1192-8704
Marine SaourDepartment of cardiothoracic Anaesthesiology and Critical Care Medicine, CHU Montpellier, Montpellier, France.
David MorquinInfectious and Tropical Diseases Department, CHU Montpellier, Montpellier, France.
Hélène DavidPhyMedExp, University of Montpellier, CNRS, INSERM, Department of cardiothoracic Anaesthesiology and Critical Care Medicine, CHU Montpellier, Montpellier, France.
Jacob ElietDepartment of cardiothoracic Anaesthesiology and Critical Care Medicine, CHU Montpellier, Montpellier, France.
Maxime VillietClinical Pharmacy Department, CHU Montpellier, Montpellier, France.
Jean-Pierre DauresLaboratory of Biostatistics and Epidemiology EA2415, University Institute for Clinical Research, Montpellier, France.
Pascal ColsonDepartment of cardiothoracic Anaesthesiology and Critical Care Medicine, CHU Montpellier, Montpellier, France.
Centre Hospitalier Universitaire de Montpellier · FRCentre National de la Recherche Scientifique · FRBiologie Labor · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGram-positive organisms are a leading cause of infection in cardiovascular surgery. Furthermore, these patients have a high risk of developing postoperative renal failure in intensive care unit (ICU). Some antibiotic drugs are known to impair renal function. The aim of the study was to evaluate whether patients treated for Gram-positive cardiovascular infection with daptomycin (DAP) experienced a lower incidence of acute kidney injury (AKI) when compared to patients treated with vancomycin (VAN), with comparable efficacy.

methodsICU patients who received either DAP or VAN, prior to or after cardiovascular surgery or mechanical circulatory support, from January 2010 to December 2012, were included in this observational retrospective cohort study. We excluded patients with end stage renal disease and antibiotic prophylaxis. The primary endpoint was the incidence of AKI within the first week of treatment. Secondary endpoints were the incidence of AKI within the first 14 days of treatment, the severity of AKI including renal replacement therapy (RRT), the rates of clinical failure (unsuccessful infection treatment) and of premature discontinuation and mortality. To minimize selection bias, we used a propensity score to compare the 2 groups. Univariate and multivariate analysis were performed to determine factors associated with AKI.

resultsSeventy two patients, treated for infective endocarditis, cardiovascular foreign body infection, or surgical site infection were included (DAP, n = 28 and VAN, n = 44). AKI at day 7 was observed in 28 (64%) versus 6 (21%) of the VAN and DAP patients, respectively (p = 0.001). In the multivariate analysis adjusted to the propensity score, vancomycin treatment was the only factor associated with AKI (Odds Ratio 4.42; 95% CI: 1.39-15.34; p = 0.014). RRT was required for 2 (7%) DAP patients and 13 (30%) VAN patients, p = 0.035. Premature discontinuation and clinical failure occurred more frequently in VAN group than in DAP group (25% versus 4%, p = 0.022 and 42% versus 12%, respectively, p = 0.027).

conclusionsDaptomycin appears to be safer than vancomycin in terms of AKI risk in ICU patients treated for cardiovascular procedure-related infection. Daptomycin could be considered as a first line treatment to prevent AKI in high-risk patients.

Indexed as

Acute Kidney InjuryAgedAnti-Bacterial AgentsCardiovascular DiseasesCritical IllnessDaptomycinEndocarditisFemaleHumansIncidenceIntensive Care UnitsMaleMiddle AgedOdds RatioPropensity ScoreRetrospective StudiesAnti-Bacterial AgentsDaptomycinVancomycinAcute kidney injuryCardiovascular surgeryDaptomycinForeign body associated infectionInfective endocarditisNephrotoxicityVancomycin

Identifiers

PMID31109283
PMCPMC6528203
OpenAlexW2947329786

What OpenQuestion holds

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LicenceCC BY
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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.