Febrile urinary-tract infection due to ...
Type de document :
Article dans une revue scientifique: Article original
PMID :
URL permanente :
Titre :
Febrile urinary-tract infection due to extended-spectrum beta-lactamase-producing enterobacteriaceae in children: a french prospective multicenter study
Auteur(s) :
Madhi, Fouad [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Jung, Camille [Auteur]
Centre Hospitalier Intercommunal de Créteil [CHIC]
Timsit, Sandra [Auteur]
Hôpital Necker - Enfants Malades [AP-HP]
Levy, Corinne [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Biscardi, Sandra [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Lorrot, Mathie [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Grimprel, Emmanuel [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Hees, Laure [Auteur]
Centre Hospitalier Lyon Sud [CHU - HCL] [CHLS]
Craiu, Irina [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Galerne, Aurelien [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Dubos, Francois [Auteur]
METRICS : Evaluation des technologies de santé et des pratiques médicales - ULR 2694
Evaluation des technologies de santé et des pratiques médicales - ULR 2694 [METRICS]
Cixous, Emmanuel [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Hentgen, Veronique [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Bechet, Stéphane [Auteur]
Hôpital Necker - Enfants Malades [AP-HP]
Bonacorsi, Stéphane [Auteur]
AP-HP Hôpital universitaire Robert-Debré [Paris]
Cohen, Robert [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Jung, Camille [Auteur]
Centre Hospitalier Intercommunal de Créteil [CHIC]
Timsit, Sandra [Auteur]
Hôpital Necker - Enfants Malades [AP-HP]
Levy, Corinne [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Biscardi, Sandra [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Lorrot, Mathie [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Grimprel, Emmanuel [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Hees, Laure [Auteur]
Centre Hospitalier Lyon Sud [CHU - HCL] [CHLS]
Craiu, Irina [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Galerne, Aurelien [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Dubos, Francois [Auteur]
METRICS : Evaluation des technologies de santé et des pratiques médicales - ULR 2694
Evaluation des technologies de santé et des pratiques médicales - ULR 2694 [METRICS]
Cixous, Emmanuel [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Hentgen, Veronique [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Bechet, Stéphane [Auteur]
Hôpital Necker - Enfants Malades [AP-HP]
Bonacorsi, Stéphane [Auteur]
AP-HP Hôpital universitaire Robert-Debré [Paris]
Cohen, Robert [Auteur]
Groupe de Pathologie Infectieuse Pédiatrique [Paris] [GPIP]
Titre de la revue :
PLoS One
Nom court de la revue :
PLoS ONE
Numéro :
13
Pagination :
e0190910
Date de publication :
2018-01-01
ISSN :
1932-6203
Mot(s)-clé(s) en anglais :
Mesh:Urinary Tract Infections/drug therapy
Mesh:Child
Mesh:Preschool
Mesh:Child
Mesh:Carbapenems/adverse effects
Mesh:Anti-Bacterial Agents/therapeutic use
Mesh:Anti-Bacterial Agents/adverse effects
Mesh:Amikacin/therapeutic use
Mesh:Enterobacteriaceae/drug effects
Mesh:Enterobacteriaceae/enzymology*
Mesh:Enterobacteriaceae Infections/drug therapy
Mesh:Enterobacteriaceae Infections/epidemiology
Mesh:Enterobacteriaceae Infections/microbiology*
Mesh:Female
Mesh:Fever/drug therapy
Mesh:Fever/microbiology
Mesh:France/epidemiology
Mesh:Humans
Mesh:Adolescent
Mesh:Infant
Mesh:Infant
Mesh:Newborn
Mesh:Male
Mesh:Microbial Sensitivity Tests
Mesh:Prospective Studies
Mesh:Risk Factors
Mesh:Urinary Tract Infections/epidemiology
Mesh:Urinary Tract Infections/microbiology*
Mesh:beta-Lactamases/biosynthesis*
Mesh:Child
Mesh:Preschool
Mesh:Child
Mesh:Carbapenems/adverse effects
Mesh:Anti-Bacterial Agents/therapeutic use
Mesh:Anti-Bacterial Agents/adverse effects
Mesh:Amikacin/therapeutic use
Mesh:Enterobacteriaceae/drug effects
Mesh:Enterobacteriaceae/enzymology*
Mesh:Enterobacteriaceae Infections/drug therapy
Mesh:Enterobacteriaceae Infections/epidemiology
Mesh:Enterobacteriaceae Infections/microbiology*
Mesh:Female
Mesh:Fever/drug therapy
Mesh:Fever/microbiology
Mesh:France/epidemiology
Mesh:Humans
Mesh:Adolescent
Mesh:Infant
Mesh:Infant
Mesh:Newborn
Mesh:Male
Mesh:Microbial Sensitivity Tests
Mesh:Prospective Studies
Mesh:Risk Factors
Mesh:Urinary Tract Infections/epidemiology
Mesh:Urinary Tract Infections/microbiology*
Mesh:beta-Lactamases/biosynthesis*
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
To assess the management of febrile urinary-tract infection (FUTIs) due to extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-E) in children, the Pediatric Infectious Diseases Group of the French Pediatric ...
Lire la suite >To assess the management of febrile urinary-tract infection (FUTIs) due to extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-E) in children, the Pediatric Infectious Diseases Group of the French Pediatric Society set up an active surveillance network in pediatric centers across France in 2014. We prospectively analysed data from 2014 to 2016 for all children < 18 years old who received antibiotic treatment for FUTI due to ESBL-E in 24 pediatric centers. Baseline demographic, clinical features, microbiological data and antimicrobials prescribed were collected. 301 children were enrolled in this study. The median age was 1 year (IQR 0.02-17.9) and 44.5% were male. These infections occurred in children with history of UTIs (27.3%) and urinary malformations (32.6%). Recent antibiotic use was the main associated factor for FUTIs due to ESBL-E, followed by a previous hospitalization and travel history. Before drug susceptibility testing (DST), third-generation cephalosporins (3GC) PO/IV were the most-prescribed antibiotics (75.5%). Only 13% and 24% of children received amikacine alone for empirical or definitive therapy, respectively, whereas 88.7% of children had isolates susceptible to amikacin. In all, 23.2% of children received carbapenems in empirical and/or definitive therapy. Cotrimoxazole (24.5%), ciprofloxacin (15.6%) and non-orthodox clavulanate-cefixime combination (31.3%) were the most frequently prescribed oral options after obtaining the DST. The time to apyrexia and length of hospital stay did not differ with or without effective empirical therapy. We believe that amikacin should increasingly take on a key role in the choice of definitive therapy of FUTI due to ESBL-E in children by avoiding the use of carbapenems.Lire moins >
Lire la suite >To assess the management of febrile urinary-tract infection (FUTIs) due to extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-E) in children, the Pediatric Infectious Diseases Group of the French Pediatric Society set up an active surveillance network in pediatric centers across France in 2014. We prospectively analysed data from 2014 to 2016 for all children < 18 years old who received antibiotic treatment for FUTI due to ESBL-E in 24 pediatric centers. Baseline demographic, clinical features, microbiological data and antimicrobials prescribed were collected. 301 children were enrolled in this study. The median age was 1 year (IQR 0.02-17.9) and 44.5% were male. These infections occurred in children with history of UTIs (27.3%) and urinary malformations (32.6%). Recent antibiotic use was the main associated factor for FUTIs due to ESBL-E, followed by a previous hospitalization and travel history. Before drug susceptibility testing (DST), third-generation cephalosporins (3GC) PO/IV were the most-prescribed antibiotics (75.5%). Only 13% and 24% of children received amikacine alone for empirical or definitive therapy, respectively, whereas 88.7% of children had isolates susceptible to amikacin. In all, 23.2% of children received carbapenems in empirical and/or definitive therapy. Cotrimoxazole (24.5%), ciprofloxacin (15.6%) and non-orthodox clavulanate-cefixime combination (31.3%) were the most frequently prescribed oral options after obtaining the DST. The time to apyrexia and length of hospital stay did not differ with or without effective empirical therapy. We believe that amikacin should increasingly take on a key role in the choice of definitive therapy of FUTI due to ESBL-E in children by avoiding the use of carbapenems.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
CHU Lille
Université de Lille
Université de Lille
Date de dépôt :
2019-12-09T16:55:47Z
2020-05-26T08:37:40Z
2020-05-26T08:37:40Z
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