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Dive into the research topics where Guy Putet is active.

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Featured researches published by Guy Putet.


Acta Paediatrica | 1997

Procalcitonin and C-reactive protein levels in neonatal infections

G Monneret; Jm Labaune; C Isaac; F Bienvenu; Guy Putet; J Bienvenu

In order to assess the potential of procalcitonin measurement in the management of neonatal sepsis, daily variations in serum procalcitonin (measured by an immunoluminometric assay) were evaluated in 94 control and infected newborn infants in comparison to C‐reactive protein (measured by an immunonephelometric method). High levels of procalcitonin correlated with bacterial invasion and showed no discrepancies with C‐reactive protein. Procalcitonin increased (up to 400 μg 1‐1) and returned to the normal range (< 0.1 m̈g1‐1) more quickly than C‐reactive protein, suggesting that procalcitonin may be an early marker of favourable outcome. Another finding is a significant procalcitonin peak on the first day of life in the control group, independent of any infectious stimulus. In conclusion, procalcitonin seems to be an interesting marker of neonatal sepsis but additional investigations are needed to understand better its mechanism of synthesis in order to determine its clinical usefulness.


Journal of Pediatric Gastroenterology and Nutrition | 2005

Oral vitamin A, E and D supplementation of pre-term newborns either breast-fed or formula-fed: a 3-month longitudinal study.

Edgard Delvin; Bernard L Salle; Olivier Claris; Guy Putet; Jean-Michel Hascoet; Laure Desnoulez; Sam Messai; Emile Levy

Background: In contrast to the studies of vitamin A and E status in children, adolescents and adults, information on preterm infants is scarce. In the present investigation we examined the vitamin A, D and E status of pre-term infants at birth, and verified whether, at 1 and 3 months, breast or formula feeding affected the plasma concentration of those vitamins while being supplemented with Uvesterol ADEC. Patients and Methods: In this prospective study, 2 groups of consecutively recruited preterm newborns fed either breast milk or formula received 3000 IU of vitamin A, 5 IU of vitamin E and 1000 IU of vitamin D daily. Vitamin A and E were measured by high performance liquid chromatography and spectrophotometry. 25-hydroxyvitamin D, a surrogate marker for vitamin D status, was measured by radioimmunoassay, and retinol binding-protein concentration was measured by immunonephelometry. Results: At birth, formula-fed and breast-milk fed infants had similar plasma concentrations of vitamin A (0.75 ± 0.20 and 0.64 ± 0.21 m mol/L, ns), 25-hydroxyvitamin D (34.4 ± 25.6 and 47.5 ± 26.7 nmol/L, ns) and vitamin E (9.5 ± 3.2 and 8.4 ± 3.3 μmol/L, ns). Vitamins A and E, and retinol binding-protein concentrations steadily increased with time in both groups of infants without attaining, at 3 months, values considered normal in term infants and in young children. At 3 months of age, concentrations of 25-hydroxyvitamin D reached values comparable to those observed in term infants. Conclusion: Plasma concentrations of vitamins A and E and of retinol binding-protein steadily increased during the the study without reaching full repletion values. At the conclusion of the study, the type of nutrition did not affect plasma vitamin concentrations.


Clinical Nutrition | 2003

Continuous insulin infusion in hyperglycaemic very-low-birth-weight infants receiving parenteral nutrition

F Thabet; J Bourgeois; B Guy; Guy Putet

Continuous infusion of insulin was used to improve glucose tolerance in 30 premature (26.4+/-1.4 weeks) very-low-birth-weight (750+/-211.3 g) hyperglycaemic infants receiving parenteral nutrition. Infusion of insulin was started at 159.1+/-67 h of life; while glycaemia was 12.1+/-3.3 mmol/l. Normoglycaemia was restored within 31.4h (range 2-134 h). A maximum insulin dose of 0.4 (range 0.07-4.2)IU/kg/h was required to control the blood glucose, the mean cumulative doses of insulin required was 3.27 IU/kg (range 0.09-18.1). The mean glucose infusion rate during insulin treatment was 20.3+/-1.7 g/kg/day; lipid was 4.6+/-1.1 g/kg/day and non-protein caloric intake 121.7+/-16.5 kcal/kg/day. Infants reach 85 kcal/kg/day of non-protein energy intake at 179.5+/-71.2 h after birth. During continuous insulin infusion, enteral feeding was started in all infants at 124.9+/-75.8 h of life. Insulin was continued for 317.7+/-196.6 h. Only two infants lost weight during the first week of treatment, the remaining infant gained weight steadily. In conclusion, continuous insulin infusion can rapidly and safely improve intravenous glucose tolerance, allowing higher caloric intake and growth in very-low-birth-weight infants who develop hyperglycaemia during total parenteral nutrition.


Acta Paediatrica | 1994

Plasma amino acid and protein concentrations in infants fed human milk or a whey protein hydrolysate formula during the first month of life.

J Rigo; Bernard L Salle; E Cavero; P Richard; Guy Putet; Jacques Senterre

The aim of the study was to compare growth parameters, biochemical indices of protein metabolism and plasma amino acid concentrations in infants fed either human milk (n= 12) or a whey protein hydrolysate formula (n= 13) during the first month of life. Growth and gain in skin fold thickness were similar in both groups whereas serum protein concentration was significantly decreased (57.4 ± 3.9 versus 61.2 ± 2.9 g/l) in the infants fed the whey hydrolysate formula. The discrepancies between the plasma amino acid pattern of the whey hydrolysate formula group and that of the human milk group lessened during the first month. Nevertheless, at a mean age of 33 days the plasma threonine concentration remained twice as high and the plasma tyrosine, phenylalanine and proline concentrations were Significantly lower in the whey hydrolysate formula group than in the human milk group. Thus, compared with breast‐fed infants, growth and most of the biological indices of protein metabolism were satisfactory in infants fed during the first month of life on a whey protein hydrolysate formula. Nevertheless, the decrease in total plasma protein concentration needs to be confirmed in a larger cohort of infants. In addition, further research is necessary to investigate the possible ways of reducing the hyperthreoninemia and preventing other plasma amino acid disturbances since it would be desirable to obtain plasma amino acid levels similar to those of breast‐fed infants.


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.


Archives of Disease in Childhood-fetal and Neonatal Edition | 2009

Rapid quantitative procalcitonin measurement to diagnose nosocomial infections in newborn infants

Aurélien Jacquot; Jean-Marc Labaune; Thierry-Pascal Baum; Guy Putet; Jean-Charles Picaud

Background and objective: Serum procalcitonin (PCT) monitoring may help clinicians to manage nosocomial infections in neonates. This study investigated the diagnostic value of a new, rapid method to measure PCT and sought to determine the best cut-off value. Methods: This monocentric, prospective study included all newborn infants with clinical suspicion of infection in a neonatal intensive care unit. Rapid, automated PCT measurements were performed on blood samples obtained for C-reactive protein (CRP) measurement. Negative and positive predictive values, sensitivity and specificity were calculated. Logistic regression analysis determined the best cut-off value to obtain a negative predictive value of PCT that was at least 15% above that of CRP. Results: Between June 2005 and May 2006, 73 newborn infants with a median (Q25–Q75) gestational age of 28 (26–30) weeks and a birth weight of 995 (720–1350) g were included. Thirty (41%) were infected. The best PCT cut-off value was 0.6 ng/ml, which provided a negative predictive value of 100%. The sensitivity, specificity and positive predictive value were 100%, 65%, and 67%, respectively, for PCT at the 0.6 ng/ml cut-off value. Conclusion: Rapid measurement of PCT could help to rule out nosocomial infection in newborn infants hospitalised in intensive care units.


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.


British Journal of Nutrition | 2016

Effect of dietary protein on plasma insulin-like growth factor-1, growth, and body composition in healthy term infants: a randomised, double-blind, controlled trial (Early Protein and Obesity in Childhood (EPOCH) study).

Guy Putet; Jean-Marc Labaune; Katherine Macé; Philippe Steenhout; Dominik Grathwohl; Véronique Raverot; Yves Morel; Jean-Charles Picaud

The effect of protein intake on growth velocity in infancy may be mediated by insulin-like growth factor-1 (IGF-1). This study aimed to determine the effects of formulae containing 1·8 (F1·8) or 2·7 g (F2·7) protein/418·4 kJ (100 kcal) on IGF-1 concentrations and growth. Healthy term infants were randomly assigned to receive F1·8 (n 74) or F2·7 (n 80) exclusively for the first 4 months of life. A group of breast-fed infants (n 84) was followed-up simultaneously (reference). Growth and body composition were measured at 0·5, 4, 6, 12, 36, 48 and 60 months of life. The IGF-1 concentrations at 4 months (primary outcome) were similar in the F1·8 (67·1 (sd 20·8) ng/l; n 70) and F2·7 (71·2 (sd 27·5) ng/l; n 73) groups (P=0·52). Both formula groups had higher IGF-1 concentrations than the breast-fed group at 4 and 9 months of age (P≤0·0001). During the first 60 months of life, anthropometric parameters in the F1·8 group were lower compared with the F2·7 group, and the differences were significant for head circumference from 2 to 60 months, body weight at 4 and 6 months and length at 9, 12 and 36 months of age. There were no significant differences in body composition between these two groups at any age. We conclude that, in formula-fed infants, although increased protein intake did not affect the IGF-1 concentration during the first 12 months of life, it did affect length and head circumference growth, suggesting that factors other than IGF-1 could play roles in determining growth velocity.


Medecine Et Maladies Infectieuses | 1999

Influence des manipulations des tubulures de perfusion reliées à un cathéter central sur les infections à staphylocoques coagulase négative chez les prématurés

H. Constant; G. Crassard; Massimo Girelli; Guy Putet; G. Aulagner

Resume Objectifs — Le but de ce travail etait de determiner les types de manipulations de tubulures et de catheters susceptibles d’entrainer des infections a staphylocoques coagulase negative chez les prematures porteurs de catheters centraux. Materiels et methodes — Les parametres environnementaux ont ete etudies chez 22 enfants (sept infectes et 15 non infectes tires au sort parmi 37) de facon retrospective grâce a une fiche remplie par les infirmieres. Resultats — Les facteurs influencant le risque infectieux de facon significative sont: le nombre de piqures lors de la mise en place du catheter, la duree du catheterisme, les deconnections proches du point d’insertion du catheter. L’âge gestationnel et a la pose, le poids et ses variations, le nombre de catheters utilises a la pose et le temps de pose, les deconnections des flacons en bout de ligne ne sont pas des facteurs de risque.


Pediatric Research | 1998

Auditory Screening in High Risk Preterm and Fullterm Neonates Using Evoked Otoacoustic Emissions and Brainstem Auditory Evoked Potentials 1300

Thierry T Morlet; Chantal Ferber-Viart; Guy Putet; François Sevin; Monique M Fau; Roland Duclaux

Auditory Screening in High Risk Preterm and Fullterm Neonates Using Evoked Otoacoustic Emissions and Brainstem Auditory Evoked Potentials 1300

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Chantal Ferber-Viart

Centre national de la recherche scientifique

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Delphine Maucort-Boulch

Centre national de la recherche scientifique

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