Pseudomonas aeruginosa bloodstream infections in children: a 9-year retrospective study.


Journal

European journal of pediatrics
ISSN: 1432-1076
Titre abrégé: Eur J Pediatr
Pays: Germany
ID NLM: 7603873

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 04 06 2019
accepted: 27 01 2020
revised: 24 01 2020
pubmed: 23 2 2020
medline: 31 3 2021
entrez: 22 2 2020
Statut: ppublish

Résumé

P. aeruginosa bloodstream infection (BSI) is associated with high hospital mortality. Empirical combination therapy is commonly used, but its benefit remains debated. The purpose of this study was to describe in a paediatric population, demographical characteristics and outcome of children treated for P. aeruginosa BSI receiving either a combined or single antibacterial therapy. We performed a retrospective, single-centre, cohort study of hospitalized children with P. aeruginosa BSI from 2007 to 2015. A total of 118 bloodstream infections (BSI) were analysed (102 (86.4%) hospital-acquired, including 52 (44.1%) hospitalized in intensive care unit). In immunocompromised children, 52% of BSI episodes were recorded. Recent medical history revealed that 68% were hospitalized, 31% underwent surgery and 67% had a prior antibiotic therapy within the last 3 months. In-hospital mortality was similar for patients receiving single or combined anti-Pseudomonas therapy (p = 0.78). In multivariate analysis, independent risk factors for in-hospital mortality were neutropenia (OR = 6.23 [1.94-20.01], hospitalization in ICU (OR = 5.24 [2.04-13.49]) and urinary tract infection (OR = 4.40 [1.02-19.25]).Conclusion: P. aeruginosa BSI mainly occurred in immunocompromised children. Most infections were hospital-acquired and associated with high mortality. Combination therapy did not improve survival. What is Known: • P. aeruginosa bloodstream infection (BSI) is associated with high hospital mortality. Empirical combination therapy is commonly used but its benefit remains debated. What is New: • This is the largest cohort of Pseudomonas aeruginosa bacteraemia in children ever published. P. aeruginosa Bloodstream mainly occurred in immunocompromised children. Most infections were hospital-acquired and associated with high mortality. Combination therapy did not improve survival.

Identifiants

pubmed: 32080759
doi: 10.1007/s00431-020-03598-4
pii: 10.1007/s00431-020-03598-4
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1247-1254

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Auteurs

Benoît Pilmis (B)

Université Paris Descartes, Service de Maladies Infectieuses et Tropicales, Centre d'infectiologie Necker-Pasteur, IHU Imagine, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France. benoit.pilmis@aphp.fr.
Université Paris Descartes, Equipe mobile d'infectiologie, IHU Imagine, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France. benoit.pilmis@aphp.fr.
Equipe mobile d'infectiologie- Université Paris Descartes, CHU Necker-Enfants malades, 149 rue de Sèvres, 75015 Paris, Paris, France. benoit.pilmis@aphp.fr.

Fanny Alby-Laurent (F)

Université Paris Descartes, Service de Pédiatrie Générale et maladies infectieuses Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.

Maria Letizia Fasola (ML)

Université Paris Descartes, Equipe mobile d'infectiologie, IHU Imagine, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.
Université Paris Descartes, Service de Pédiatrie Générale et maladies infectieuses Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.

Valérie Seegers (V)

SFR du pôle santé : Interactions cellulaires et Applications thérapeutiques, Université d'Angers, DRCI Data management, Angers, France.

Romain Guery (R)

Université Paris Descartes, Service de Maladies Infectieuses et Tropicales, Centre d'infectiologie Necker-Pasteur, IHU Imagine, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.

Hélène Guet-Revillet (H)

Université Paris Descartes, Service de Microbiologie, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.

Martine Postaire (M)

Service de Pharmacie, Hôpital Necker Enfants Malades, Paris, France.

Julie Toubiana (J)

Université Paris Descartes, Equipe mobile d'infectiologie, IHU Imagine, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.
Université Paris Descartes, Service de Pédiatrie Générale et maladies infectieuses Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.

Emmanuelle Bille (E)

Université Paris Descartes, Service de Microbiologie, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.

Olivier Lortholary (O)

Université Paris Descartes, Service de Maladies Infectieuses et Tropicales, Centre d'infectiologie Necker-Pasteur, IHU Imagine, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.
Université Paris Descartes, Equipe mobile d'infectiologie, IHU Imagine, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.

Jean-Ralph Zahar (JR)

Université Paris Descartes, Equipe mobile d'infectiologie, IHU Imagine, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.
Université Paris Descartes, Equipe opérationnelle d'hygiène, Hôpital Necker-Enfants Maladies, Assistance Publique-Hôpitaux de Paris, Paris, France.

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Classifications MeSH