Evidence map›Paper›PMID 34529722›Full record

ArticlePloS one2021

Relay oral therapy in febrile urinary tract infections caused by extended spectrum beta-lactamase-producing Enterobacteriaceae in children: A French multicenter study.

Gabriel Lignieres, André Birgy, Camille Jung, Stéphane Bonacorsi, Corinne Levy, François Angoulvant, Emmanuel Grimprel, Marie Aliette Dommergues, Yves Gillet, Irina Craiu and 13 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

1 citing paper in PubMed, 29 citations in OpenAlex.

  1. Observational
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

23 authors at 10 institutions in 1 country.

Gabriel LignieresService de Pédiatrie Générale, Centre Hospitalier Intercommunal de Créteil, Créteil, France.
André BirgyService de Microbiologie, CHU Robert Debré, Centre National de Référence (CNR) associé Escherichia coli, Paris, France.
Camille JungCentre de Recherche Clinique (CRC), Centre Hospitalier Intercommunal de Créteil, Créteil, France.
Stéphane BonacorsiService de Microbiologie, CHU Robert Debré, Centre National de Référence (CNR) associé Escherichia coli, Paris, France.
Corinne LevyCentre de Recherche Clinique (CRC), Centre Hospitalier Intercommunal de Créteil, Créteil, France.ORCID 0000-0002-1927-6360
François AngoulvantGPIP (Groupe de Pathologie Infectieuse Pédiatrique) de la SFP (Société Française de Pédiatrie), Paris, France.
Emmanuel GrimprelGPIP (Groupe de Pathologie Infectieuse Pédiatrique) de la SFP (Société Française de Pédiatrie), Paris, France.
Marie Aliette DommerguesGPIP (Groupe de Pathologie Infectieuse Pédiatrique) de la SFP (Société Française de Pédiatrie), Paris, France.ORCID 0000-0003-1632-9241
Yves GilletGPIP (Groupe de Pathologie Infectieuse Pédiatrique) de la SFP (Société Française de Pédiatrie), Paris, France.
Irina CraiuGPIP (Groupe de Pathologie Infectieuse Pédiatrique) de la SFP (Société Française de Pédiatrie), Paris, France.
Alexis RybakGPIP (Groupe de Pathologie Infectieuse Pédiatrique) de la SFP (Société Française de Pédiatrie), Paris, France.
Loic De PontualGPIP (Groupe de Pathologie Infectieuse Pédiatrique) de la SFP (Société Française de Pédiatrie), Paris, France.
François DubosGPIP (Groupe de Pathologie Infectieuse Pédiatrique) de la SFP (Société Française de Pédiatrie), Paris, France.
Emmanuel CixousGPIP (Groupe de Pathologie Infectieuse Pédiatrique) de la SFP (Société Française de Pédiatrie), Paris, France.
Vincent GajdosGPIP (Groupe de Pathologie Infectieuse Pédiatrique) de la SFP (Société Française de Pédiatrie), Paris, France.
Didier PinquierGPIP (Groupe de Pathologie Infectieuse Pédiatrique) de la SFP (Société Française de Pédiatrie), Paris, France.
Isabelle AndriantahinaService de Pédiatrie Générale, Centre Hospitalier de Saint-Camille, Bry sur Marne, France.
Valérie Soussan-BaniniService des Urgences Pédiatriques, CHU Ambroise Paré, Boulogne Billancourt, France.
Emilie GeorgetService de Pédiatrie Générale, Centre Hospitalier de Villeneuve-Saint-Georges, Villeneuve-Saint-Georges, France.
Elise LaunayGPIP (Groupe de Pathologie Infectieuse Pédiatrique) de la SFP (Société Française de Pédiatrie), Paris, France.
Olivier VignaudGPIP (Groupe de Pathologie Infectieuse Pédiatrique) de la SFP (Société Française de Pédiatrie), Paris, France.
Robert CohenGPIP (Groupe de Pathologie Infectieuse Pédiatrique) de la SFP (Société Française de Pédiatrie), Paris, France.
Fouad MadhiService de Pédiatrie Générale, Centre Hospitalier Intercommunal de Créteil, Créteil, France.ORCID 0000-0001-6816-5272
Société Française de Cardiologie · FRHôpital Intercommunal de Créteil · FRCentre Hospitalier de Roubaix · FRCentre Hospitalier Intercommunal de Villeneuve-Saint-Georges · FRCentre Hospitalier Universitaire de Lille · FRCentre Hospitalier Universitaire de Nantes · FRHôpital Ambroise-Paré · FRHôpital Necker-Enfants Malades · FRHôpital Robert-Debré · FRHôpital Saint- Camille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWe need studies assessing therapeutic options for oral relay in febrile urinary tract infection (FUTI) due to ESBL-producing Enterobacteriaceae (ESBL-E) in children. Amoxicillin-clavulanate/cefixime (AC-cefixime) combination seems to be a suitable option. We sought to describe the risk of recurrence at 1 month after the end of treatment for FUTI due to ESBL-E according to the oral relay therapy used. MATERIALS AND

methodsWe retrospectively identified children <18 years who were included in a previous prospective observational multicentric study on managing FUTI due to ESBL-E between 2014 and 2017 in France. We collected whether children who received cotrimoxazole, ciprofloxacin or the AC-cefixime combination as the oral relay therapy reported a recurrence within the first month after the end of treatment. Then, we analyzed the susceptibility drug-testing of the strains involved.

resultsWe included 199 children who received an oral relay therapy with cotrimoxazole (n = 72, 36.2%), ciprofloxacin (n = 38, 19.1%) or the AC-cefixime combination (n = 89, 44.7%). Nine (4.5%) patients had a recurrence within the first month after the end of treatment, with no difference between the 3 groups of oral relay (p = 0.8): 4 (5.6%) cotrimoxazole, 2 (5.3%) ciprofloxacin and 3 (3.4%) AC-cefixime combination. Phenotype characterization of 249 strains responsible for FUTI due to ESBL-E showed that 97.6% were susceptible to the AC-cefixime combination.

conclusionsThe AC-cefixime combination represents an interesting therapeutic option for oral relay treatment of FUTI due to ESBL-E as the recurrence rate at 1 month after the end of treatment was the same when compared to cotrimoxazole and ciprofloxacin.

Indexed as

Administration, OralAdolescentAmoxicillin-Potassium Clavulanate Combinationbeta-LactamasesCefiximeChildChild, PreschoolCiprofloxacinEnterobacteriaceaeFemaleFeverFranceHumansInfantInfant, NewbornMaleAmoxicillin-Potassium Clavulanate Combinationbeta-LactamasesCefiximeCiprofloxacinTrimethoprim, Sulfamethoxazole Drug Combination

Identifiers

PMID34529722
PMCPMC8445429
OpenAlexW3199599890

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.