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Dive into the research topics where Jean-Charles Picaud is active.

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Featured researches published by Jean-Charles Picaud.


The Journal of Pediatrics | 2011

Dynamics and Clinical Evolution of Bacterial Gut Microflora in Extremely Premature Patients

Aurélien Jacquot; Dorine Neveu; Fabien Aujoulat; Gregoire Mercier; Hélène Marchandin; Estelle Jumas-Bilak; Jean-Charles Picaud

OBJECTIVEnTo determine baseline clinical characteristics that influence bacterial gut flora dynamics in very preterm infants and the relationship between gut flora dynamics and clinical evolution.nnnSTUDY DESIGNnProspective, monocentric study enrolling 29 consecutive very preterm infants. We collected data about growth, digestive tolerance, nutrition, and antibiotic use. Microflora in stool samples, collected between 3 and 56 days of life, was identified with direct molecular fingerprinting.nnnRESULTSnMedian (interquartile range) body weight and gestational age at birth were 950 g (760-1060 g) and 27 weeks (27-29 weeks), respectively. The diversity score (number of operational taxonomic units) increased 0.45 units/week (P < .0001), with staphylococci as the major group. Bifidobacterium was poorly represented. Gestational age (≥ 28 weeks) and caesarean delivery independently correlated with better diversity scores during follow-up (P < .05). The 6-week diversity score inversely correlated with the duration of antibiotherapy (P = .0184) and parenteral feeding (P = .013). The microflora dynamics was associated with the digestive tolerance profile. Weight gain increased with increasing diversity score (P = .0428).nnnCONCLUSIONnMicroflora diversity settled progressively in very preterm infants. Staphylococci were the major group, and few infants were colonized with Bifidobacterium spp. Measures that may improve microflora could have beneficial effects on digestive tolerance and growth.


Acta Paediatrica | 2013

Extremely low birthweight infants: how neonatal intensive care unit teams can reduce postnatal malnutrition and prevent growth retardation

Claire-Marie Loys; Delphine Maucort-Boulch; Brigitte Guy; Guy Putet; Jean-Charles Picaud; Stéphane Haÿs

To evaluate the impact of an improved nutritional policy for extremely low birthweight (ELBW) infants on nutritional deficits and postnatal growth.


Acta Paediatrica | 2010

Incidence of infectious diseases in infants fed follow-on formula containing synbiotics: an observational study.

Jean-Charles Picaud; Véronique Chapalain; Damien Paineau; Othar Zourabichvili; Francis Bornet; Jean-François Duhamel

Aim:u2002 Infectious diseases in infants are a major public health issue. Synbiotic‐enriched formulas (EF) are intended to mimic the beneficial effects of human milk on infectious diseases. We performed an observational study in infants switching to follow‐on formula to determine the effects of synbiotic‐enriched formula compared to standard formula (SF).


Neonatology | 1996

Incidence of Ischemic-Hemorrhagic Cerebral Lesions in Premature Infants of Gestational Age ≤ 28 Weeks: A Prospective Ultrasound Study

Olivier Claris; S. Besnier; Alexandre Lapillonne; Jean-Charles Picaud; Bl Salle

While it is well accepted that the incidence of intraventricular hemorrhage (IVH) increases with decreasing gestational age (GA), the majority of studies report their findings on the basis of birthweight (BW) rather than GA. Over a 5-year period, 199 infants born at or below 28 weeks of gestation were entered into a prospective cranial ultrasound study stratified according to GA. One hundred and five (53%) had normal ultrasound findings. The overall incidence of IVH, as expected, rose with decreasing GA but we were unable to show any clear influence of BW or growth retardation on its occurrence. Incidence of grades I, IIa, IIb and III IVH were 8, 10, 16 and 11%, respectively. Leukomalacia, bleeding in the posterior fossa and in the cerebellum occurred in 4, 7 and 2% of the population, respectively.


Clinical Nutrition | 2016

Probiotics and growth in preterm infants: A randomized controlled trial, PREMAPRO study

Stéphane Haÿs; Aurélien Jacquot; Hélène Gauthier; Christian Kempf; Anne Beissel; Odile Pidoux; Estelle Jumas-Bilak; Evelyne Decullier; E. Lachambre; L. Beck; Gilles Cambonie; Guy Putet; Olivier Claris; Jean-Charles Picaud

BACKGROUND & AIMSnRecent studies have suggested that the gut microflora has metabolic effects. We aimed to evaluate postnatal growth in preterm infants who received different probiotic supplements, and to assess the safety of probiotic administration.nnnMETHODSnThis prospective, randomized, double-blind, controlled trial was performed at three tertiary care neonatal units. Preterm infants were randomly assigned to receive daily supplementation over 4-6 weeks with placebo (group C) or probiotics (group P). Group P comprised three subgroups: P1 received Bifidobacterium lactis, P2 received Bifidobacterium longum, and P3 received B.xa0lactis and B.xa0longum. We assessed postnatal growth during the supplementation period and up to a corrected gestational age (GA) of 41 weeks when body composition was assessed using whole-body dual-energy X-ray absorptiometry. Aerobic and anaerobic blood cultures were performed on suspicion of late-onset sepsis.nnnRESULTSnThe study comprised 199 preterm infants with a mean GA of 29.1xa0±xa01.4 weeks and a mean birth weight of 1173xa0±xa0210xa0g, who received a placebo (group C, nxa0=xa052) or probiotics (group P, nxa0=xa0147) from the first week of life. At the end of the supplementation period, no statistically significant differences were seen between the groups in relation to the mean body weight (group Cxa0=xa01906xa0±xa023xa0g, group Pxa0=xa01875xa0±xa014xa0g, pxa0=xa00.25), length, or head circumference. The incidence rates of necrotizing enterocolitis and late-onset sepsis were similar in the two groups. At the corrected GA of 41 weeks, there were no differences between the groups with respect to anthropometric measurements or body composition analysis.nnnCONCLUSIONSnPreterm infants receiving Bifidobacterium supplements did not exhibit better postnatal growth compared with those who received placebo treatment. No adverse effects were associated with probiotic administration. Registered under ClinicalTrials.gov Identifier no. NCT01379417.


Neonatology | 2013

Elective High-Frequency Oscillatory Ventilation versus Conventional Ventilation for Acute Pulmonary Dysfunction in Preterm Infants

Sung-Il Cho; Yoon Hwan Chang; Beyong Il Kim; Jung-Hwan Choi; Heui Seung Jo; Ruben Bromiker; Netanela Ernest; Maskit Bar Meir; Michael Kaplan; Cathy Hammerman; Michael S. Schimmel; Morten Breindahl; Mats Blennow; Jean-Claude Fauchère; Marta Thio Lluch; Daniele De Luca; Neil Marlow; Jean-Charles Picaud; Charles Christoph Roehr; Mireille Vanpée; Eduardo Vilamor; Gabriela Zaharie; Gorm Greisen; Lasse Dührsen; Sinno Simons; Mark Dzietko; Kerstin Genz; Ivo Bendix; Vinzenz Boos; Marco Sifringer

BACKGROUNDnRespiratory failure due to lung immaturity is a major cause of mortality in preterm infants. Although the use of intermittent positive pressure ventilation in neonates with respiratory failure saves lives, its use is associated with lung injury and chronic lung disease (CLD). A newer form of ventilation called high-frequency oscillatory ventilation (HFOV) has been shown to result in less lung injury in experimental studies.nnnOBJECTIVESnThe objective of this review is to determine the effect of the elective use of HFOV as compared to conventional ventilation (CV) on the incidence of CLD, mortality and other complications associated with prematurity and assisted ventilation in preterm infants who are mechanically ventilated for respiratory distress syndrome (RDS).nnnSEARCH METHODSnSearches were made of the Oxford Database of Perinatal Trials, MEDLINE, EMBASE, previous reviews including cross-references, abstracts, conferences and symposia proceedings, expert informants, journal hand searching by the Cochrane Collaboration, mainly in the English language. The search was updated in January 2009.nnnSELECTION CRITERIAnRandomized controlled trials comparing HFOV and CV in preterm or low birth weight infants with pulmonary dysfunction, mainly due to RDS, who required assisted ventilation. Randomization and commencement of treatment needed to be as soon as possible after the start of CV and usually in the first 12 h of life.nnnDATA COLLECTION AND ANALYSISnThe methodological quality of each trial was independently reviewed by the various authors. The standard effect measures are relative risk (RR) and risk difference (RD). From 1/RD the number needed to treat to produce one outcome were calculated. For all measures of effect, 95% confidence intervals were used. In subgroup analyses the 99% CIs are also given for summary RRs in the text. Meta-analysis was performed using a fixed effect model. Where heterogeneity was over 50%, the random effects RR is also given.nnnMAIN RESULTSnSeventeen eligible studies of 3,652 infants were included. Meta-analysis comparing HFOV with CV revealed no evidence of effect on mortality at 28-30 days of age or at approximately term equivalent age. These results were consistent across studies and in subgroup analyses. The effect of HFOV on CLD in survivors at term equivalent gestational age was inconsistent across studies and the reduction was of borderline significance overall. The effect was similar in trials with a high lung volume strategy for HFOV targeting at very low FiO(2) and trials with a high lung volume strategy with somewhat higher or unspecified target FiO(2). Subgroups of trials showed a significant reduction in CLD with HFOV when no surfactant was used, when piston oscillators were used for HFOV, when lung protective strategies for CV were not used, when randomization occurred at two to six hours of age, and when inspiratory:expiratory ratio of 1:2 was used for HFOV. In the meta-analysis of all trials, pulmonary air leaks occurred more frequently in the HFOV group. In some studies, short-term neurological morbidity with HFOV was found, but this effect was not statistically significant overall. The subgroup of two trials not using a high-volume strategy with HFOV found increased rates of grade 3 or 4 intraventricular hemorrhage and of periventricular leukomalacia. An adverse effect of HFOV on long-term neurodevelopment was found in one large trial but not in the five other trials that reported this outcome. The rate of retinopathy of prematurity is reduced overall in the HFOV group.


Acta Paediatrica | 2012

Neonatal mortality and morbidity in preterm infants born from assisted reproductive technologies

Jean-Charles Picaud; S Chalies; C Combes; G Mercier; H Dechaud; Gilles Cambonie

Aim:u2002 Premature birth is frequent in infants conceived with assisted reproductive technologies (ART). We sought to determine whether neonatal outcome in ART preterm infants differs from that of spontaneously conceived (SC) preterm infants.


Acta Paediatrica | 2011

Lipid peroxidation in all-in-one admixtures for preterm neonates: impact of amount of lipid, type of lipid emulsion and delivery condition.

Anne Jalabert; Anaïs Grand; Jean-Paul Steghens; Eric Barbotte; Christelle Pigue; Jean-Charles Picaud

Aim:u2002 To evaluate the effect of lipid emulsion composition and delivery condition on lipid peroxidation in typical all‐in‐one parenteral admixtures for preterm neonates.


Neonatology | 2007

Myocardial Adaptation to Anemia and Red Blood Cell Transfusion in Premature Infants Requiring Ventilation Support in the 1st Postnatal Week

Gilles Cambonie; Stephan Matecki; Christophe Milési; Michel Voisin; Sophie Guillaumont; Jean-Charles Picaud

Background: Although transfusion practice in very premature infants is becoming more restrictive, little is known about myocardial adaptation to anemia during the 1st postnatal week. Objectives: To determine the central hemodynamic effects of anemia and red blood cell transfusion in very preterm infants undergoing intensive care. Methods: Twenty-nine neonates of less than 30 weeks gestational age were treated for respiratory distress syndrome, following a strict protocol. Echocardiographies were performed at the 4th and 6th postnatal days, which corresponded to, respectively, just before and 48 h after an erythrocyte transfusion of 15 ml/kg in the 12 anemic infants. Results: Anemic infants had increased stroke volume [2.1 (1.8–2.3) vs. 1.5 (1.3–1.6) ml/kg] and left ventricular (LV) output [312 (271–345) vs. 206 (177–240) ml/min/kg]. The relationship of the heart rate-corrected velocity of circumferential fiber shortening to LV end-systolic meridional wall stress indicated a higher contractile state in the anemic infants, with a higher y-intercept (p = 0.03) and a steeper slope (p = 0.05) of the regression line than in the nonanemic patients. Posttransfusion, the stroke volume, LV output, shortening fraction, and contractile state decreased to the values observed in the nonanemic infants. Conclusions: Myocardial contractility was a major component of the circulatory adjustments in the anemic premature infants requiring ventilation support in the early neonatal period. Changes in LV performance associated with anemia were reversed by transfusion with no detrimental effect on right ventricular function, LV preload or the respiratory status of these patients.


Oxidative Medicine and Cellular Longevity | 2013

Malondialdehyde Adduct to Hemoglobin: A New Marker of Oxidative Stress Suitable for Full-Term and Preterm Neonates

Cécile Cipierre; Stéphane Haÿs; Delphine Maucort-Boulch; Jean-Paul Steghens; Jean-Charles Picaud

Oxidative stress may play a central role in the onset of many diseases during the neonatal period. Malondialdehyde (MDA) is a marker of lipid peroxidation. The aim of this study was to evaluate a new marker, the malondialdehyde adduct to hemoglobin (MDA-Hb), which is measured in red blood cells (RBCs) and thus does not require that an additional blood sample be drawn. In this prospective study, we first adapted the measurement method previously described to Hb solutions obtained from washed RBCs and then evaluated the suitability of the method for use in neonates. MDA-Hb concentrations were measured by liquid chromatography-mass spectrometry. We compared the concentrations of MDA-Hb between preterm and term neonates. Erythrocyte samples were collected at birth from 60 healthy neonates (29 full-term and 31 preterm), as well as from 50 preterm neonates with uncomplicated postnatal evolution during the first months of life. We found a significantly higher MDA-Hb concentration at birth in preterm neonates (P = 0.002). During the first months of life, MDA-Hb concentrations were 9.4u2009nanomol/g Hb in hospitalized preterm neonates. MDA-Hb could be used to assess oxidative stress in preterm neonates. Together with clinical variables, it could be a useful marker for oxidative stress exposition in these higher risk patients.

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Delphine Maucort-Boulch

Centre national de la recherche scientifique

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Gilles Cambonie

Centre national de la recherche scientifique

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Gilles Cambonie

Centre national de la recherche scientifique

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