Severe bacterial infections (SBI) are responsible for significant morbidity and mortality in the paediatric population. There is considerable individual variability in children's susceptibility to developing SBIs. This variability is multifactorial, and the mechanisms at work are not yet fully understood. The investigators of this study therefore propose to study a population of children who had particularly severe bacterial infections requiring hospitalization in a pediatric intensive care unit in France between 2015 and 2018. This study is part of a global approach to understanding the mechanisms favoring the occurrence of IBS in pediatrics. The study will initially focus on analyzing the clinical phenotype of these children in terms of the type of infection presented, as well as immunologically with an immune workup of all these patients. The investigators also plan to contact each family individually to identify other episodes of personal or family IBS or other elements suggestive of immune deficiency (opportunistic infections, autoimmune manifestations, severe atopy). The investigators will also assess the persistent sequelae since their infectious episode, and their quality of life following this IBS. In parallel, the genetic analysis of these patients and their parents will be carried out using whole-exome sequencing. The investigators will compare the results with those obtained in 2 IBS-free control populations (N=70 and N=116). The goal is to identify genetic variants that favor the occurrence of IBS in general, and some that are specific to certain bacteria or clinical presentations.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
1,401
Extended phenotyping (analysis performed at Nantes University Hospital, MANDATORY DELIVERY WITHIN 24 HOURS) = 1 EDTA 3 mL tube for patients included in Nantes.
Blood sample for WES : 1 x 3 mL EDTA tube (if not included in DIABACT IV biocollection)
Blood sample for PBMC freezing integrated into the biocollection: 1 EDTA tube = 3 mL
Assessment of POPC score (Pediatric Overall Performance Category)
Questionnaires completed by parents or children: * SDQ * PedSQL4.0
Nantes University Hospital
Nantes, Loire Atlantique, France
CHU de Brest
Brest, France
Hospices Civils de Lyon
Lyon, France
Hôpital Armand Trousseau
Paris, France
Hôpital Necker enfants malades
Paris, France
CHU de Saint-Étienne
Saint-Etienne, France
Identification of innate errors of immunity involved in the development of IBS in pediatrics.
List of rare genetic variants significantly more frequently found in cases than in controls and/or absent in healthy parents.
Time frame: At the enrollment
Identification of inborn errors of immunity involved in the development of IBS and their association with abnormalities of the immune balance,
Time frame: At the enrollment
Identification of rare genetic variants favoring certain clinical types of infection, or certain biological and immunological abnormalities.
Time frame: At the enrollment
Identification of immune deficiencies in patients who have developed a severe bacterial infection
Time frame: At the enrollment
Assessment of sequelae with the POPC sequelae score (Pediatric Overall Performance Category) at a distance from the IBS episode.
The POPC sequelae score is a scale from 1 to 6, with 6 being the worst possible outcome.
Time frame: At the enrollment
Assessment of sequelae at a distance from the IBS episode with the Strengths and Weaknesses Questionnaire (SDQ-Fra).
The SDQ-Fra score is a scale from 0 to 2, with 2 being the worst possible outcome.
Time frame: At the enrollment
Assessment of quality of life at a distance from the IBS episode.
Quality of life will be assessed in this patient population using the Pediatric Quality of Life InventoryTM (scale from 0 to 4, with 4 corresponding to the worst outcome).
Time frame: At the enrollment
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