Gilles Cambonie

Gilles Cambonie

orcid

Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 March 2015 in JAMA Pediatrics
Verified
Journal Article
Open access
PDF file
PAPierre-Yves Ancel
Pierre-Yves Ancel
FGFrançois Goffinet
François Goffinet
PKPierre Kuhn
Pierre Kuhn
BLBruno Langer
Bruno Langer
JMJacqueline Matis
Jacqueline Matis
MKMonique Kaminski
Monique Kaminski
Previous cohort studies1-7 suggest that survival of infants born before 27 weeks’ gestation has improved during the past 2 decades. However, disability rates remain high at these gestational ages.8-10 Moreover, countries differ substantially in their organization of care, available resources, national laws, and cultural preferences regarding provision of proactive care. Therefore, to provide the best available information for parents and medical staff to use in making treatment decisions, mortality and morbidity must be monitored, and studies should be conducted in countries with different attitudes toward active care at early gestational ages.

28 April 2021 in BMJ
Verified
Journal Article
Open access
PDF file
VPVéronique Pierrat
Véronique Pierrat
LMLaetitia Marchand-Martin
Laetitia Marchand-Martin
SMStéphane Marret
Stéphane Marret
CACatherine Arnaud
Catherine Arnaud
VBValérie Benhammou
Valérie Benhammou
PAPierre-Yves Ancel
Pierre-Yves Ancel
Objectives To describe neurodevelopment at age 5 among children born preterm. Design Population based cohort study, EPIPAGE-2. Setting France, 2011. Participants 4441 children aged 5½ born at 24-26, 27-31, and 32-34 weeks Main outcome measures Severe/moderate neurodevelopmental disabilities, defined as severe/moderate cerebral palsy (Gross Motor Function Classification System (GMFCS) ≥2), or unilateral or bilateral blindness or deafness, or full scale intelligence quotient less than minus two standard deviations (Wechsler Preschool and Primary Scale of Intelligence, 4th edition). Mild neurodevelopmental disabilities, defined as mild cerebral palsy (GMFCS-1), or visual disability ≥3.2/10 and <5/10, or hearing loss <40 dB, or full scale intelligence quotient (minus two to minus one standard deviation) or developmental coordination disorders (Movement Assessment Battery for Children, 2nd edition, total score less than or equal to the fifth centile), or behavioural difficulties (strengths and difficulties questionnaire, total score greater than or equal to the 90th centile), school assistance (mainstream class with support or special school), complex developmental interventions, and parents’ concerns about development. The distributions of the scores in contemporary term born children were used as reference. Results are given after multiple imputation as percentages of outcome measures with exact binomial 95% confidence intervals. Results Among 4441 participants, 3083 (69.4%) children were assessed. Rates of severe/moderate neurodevelopmental disabilities were 28% (95% confidence interval 23.4% to 32.2%), 19% (16.8% to 20.7%), and 12% (9.2% to 14.0%) and of mild disabilities were 38.5% (33.7% to 43.4%), 36% (33.4% to 38.1%), and 34% (30.2% to 37.4%) at 24-26, 27-31, and 32-34 weeks, respectively. Assistance at school was used by 27% (22.9% to 31.7%), 14% (12.1% to 15.9%), and 7% (4.4% to 9.0%) of children at 24-26, 27-31, and 32-34 weeks, respectively. About half of the children born at 24-26 weeks (52% (46.4% to 57.3%)) received at least one developmental intervention which decreased to 26% (21.8% to 29.4%) for those born at 32-34 weeks. Behaviour was the concern most commonly reported by parents. Rates of neurodevelopment disabilities increased as gestational age decreased and were higher in families with low socioeconomic status. Conclusions In this large cohort of children born preterm, rates of severe/moderate neurodevelopmental disabilities remained high in each gestational age group. Proportions of children receiving school assistance or complex developmental interventions might have a significant impact on educational and health organisations. Parental concerns about behaviour warrant attention.

26 January 2017 in Intensive Care Medicine
Verified
Journal Article
Closed access
PDF file
CMChristophe Milési
Christophe Milési
SESandrine Essouri
Sandrine Essouri
RPRobin Pouyau
Robin Pouyau
JLJean-Michel Liet
Jean-Michel Liet
MAMickael Afanetti
Mickael Afanetti
G(Groupe Francophone de Réanimation Et D’uRgences Pédiatriques (Gfrup)
Groupe Francophone de Réanimation Et D’uRgences Pédiatriques (Gfrup)

1 August 2013 in Pediatrics
Verified
Journal Article
Closed access
AMAyoub Mitha
Ayoub Mitha
LFLaurence Foix-L’hÉlias
Laurence Foix-L’hÉlias
CACatherine Arnaud
Catherine Arnaud
SMStéphane Marret
Stéphane Marret
RVRachel Vieux
Rachel Vieux
PAPierre-Yves Ancel
Pierre-Yves Ancel
OBJECTIVE: To determine whether neonatal infections are associated with a higher risk of adverse neurodevelopment at 5 years of age in a population-based cohort of very preterm children.METHODS: We included all live births between 22 and 32 weeks of gestation, from 9 regions in France, in 1997 (EPIPAGE study). Of the 2665 live births, 2277 were eligible for a follow-up evaluation at 5 years of age: 1769 had a medical examination and 1495 underwent cognitive assessment. Cerebral palsy and cognitive impairment were studied as a function of early-onset sepsis (EOS) and late-onset sepsis (LOS), after adjustment for potential confounding factors, in multivariate logistic regression models.RESULTS: A total of 139 (5%) of the 2665 live births included in the study presented with EOS alone (without associated LOS), 752 (28%) had LOS alone (without associated EOS), and 64 (2%) displayed both EOS and LOS. At 5 years of age, the frequency of cerebral palsy was 9% (157 of 1769) and that of cognitive impairment was 12% (177 of 1495). The frequency of cerebral palsy was higher in infants with isolated EOS (odds ratio [OR]: 1.70 [95% confidence interval (CI): 0.84−3.45]) or isolated LOS (OR: 1.71 [95% CI: 1.14−2.56]) than in uninfected infants, and this risk was even higher in cases of combined EOS and LOS (OR: 2.33 [95% CI: 1.02−5.33]). There was no association between neonatal infection and cognitive impairment.CONCLUSIONS: Neonatal infections in these very preterm infants were associated with a higher risk of cerebral palsy at the age of 5 years, particularly in infants presenting with both EOS and LOS.

1 October 2003 in The Journal of Pediatrics
Verified
Journal Article
Closed access
BLBéatrice Larroque
Béatrice Larroque
SMStéphane Marret
Stéphane Marret
PAPierre-Yves Ancel
Pierre-Yves Ancel
CACatherine Arnaud
Catherine Arnaud
LMLoic Marpeau
Loic Marpeau
GBGérard Bréart
Gérard Bréart

30 September 2014 in Annals of Intensive Care
Verified
Journal Article
Open access
PDF file
CMChristophe Milési
Christophe Milési
MBMathilde Boubal
Mathilde Boubal
AJAurélien Jacquot
Aurélien Jacquot
JBJulien Baleine
Julien Baleine
SDSabine Durand
Sabine Durand
GCGilles Cambonie
Gilles Cambonie
High-flow nasal cannula (HFNC) is a relatively new device for respiratory support. In pediatrics, HFNC use continues to increase as the system is easily set up and is well tolerated by patients. The use of nasal cannula adapted to the infant’s nares size to deliver heated and humidified gas at high flow rates has been associated with improvements in washout of nasopharyngeal dead space, lung mucociliary clearance, and oxygen delivery compared with other oxygen delivery systems. HFNC may also create positive pharyngeal pressure to reduce the work of breathing, which positions the device midway between classical oxygen delivery systems, like the high-concentration face mask and continuous positive airway pressure (CPAP) generators. Currently, most of the studies in the pediatric literature suggest the benefits of HFNC therapy only for moderately severe acute viral bronchiolitis. But, the experience with this device in neonatology and adult intensive care may broaden the pediatric indications to include weaning from invasive ventilation and acute asthma. As for any form of respiratory support, HFNC initiation in patients requires close monitoring, whether it be for pre- or inter-hospital transport or in the emergency department or the pediatric intensive care unit.