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1.
BMC Pediatr ; 15: 204, 2015 Dec 09.
Article de Anglais | MEDLINE | ID: mdl-26645894

RÉSUMÉ

BACKGROUND: The acquisition and development of infant gut microbiota can be influenced by numerous factors, of which early antibiotic treatment is an important one. However, studies on the effects of antibiotic treatment in early life on clinical outcomes and establishment and development of the gut microbiota of term infants are limited. Disturbed microbiota composition is hypothesized to be an underlying mechanism of an aberrant development of the immune system. This study aims to investigate the potential clinical and microbial consequences of empiric antibiotic use in early life. METHODS/DESIGN: 450 term born infants, of whom 150 are exposed to antibiotic treatment in early life and 300 are not (control group), are included in this observational cohort study with a one-year follow-up. Clinical outcomes, including coughing, wheezing, fever >38 °C, runny nose, glue ear, rash, diarrhea and >3 crying hours a day, are recorded daily by parents and examined by previously defined doctor's diagnosis. A blood sample is taken at closure to investigate the infant's vaccination response and sensitization for food and inhalant allergens. Fecal samples are obtained at eight time points during the first year of life. Potential differences in microbial profiles of infants treated with antibiotics versus healthy controls will be determined by use of 16S-23S rRNA gene analysis (IS-pro). Microbiota composition will be described by means of abundance, diversity and (dis)similarity. Diversity is calculated using the Shannon index. Dissimilarities between samples are calculated as the cosine distance between each pair of samples and analyzed with principal coordinate analysis. Clinical variables and possible associations are assessed by appropriate statistics. DISCUSSION: Both clinical quantitative and qualitative microbial effects of antibiotic treatment in early life may be demonstrated. These findings can be important, since there is evidence that manipulation of the infant microbiota by using pre- or probiotics can restore the ecological balance of the microbiota and may mitigate potential negative effects on the developing immune system, when use of antibiotics cannot be avoided. TRIAL REGISTRATION: ClinicalTrials.gov NCT02536560. Registered 28 August 2015.


Sujet(s)
Antibactériens/usage thérapeutique , Microbiome gastro-intestinal/effets des médicaments et des substances chimiques , Infections/traitement médicamenteux , Muqueuse intestinale/microbiologie , Femelle , Études de suivi , Humains , Nouveau-né , Infections/immunologie , Muqueuse intestinale/effets des médicaments et des substances chimiques , Muqueuse intestinale/immunologie , Mâle , Facteurs temps
4.
J Inherit Metab Dis ; 27(1): 111-2, 2004.
Article de Anglais | MEDLINE | ID: mdl-15065575

RÉSUMÉ

Resting energy expenditure (REE) was investigated in 8 children with propionic and methylmalonic acidaemias because a lowered REE has been reported in the literature. We observed a marginally elevated REE and think that adequate caloric intake and the use of a synthetic amino acid mixture are responsible for this.


Sujet(s)
Aminoacidopathies congénitales/métabolisme , Métabolisme énergétique , Acide méthyl-malonique/métabolisme , Propionates/métabolisme , Aminoacidopathies congénitales/traitement médicamenteux , Acides aminés/usage thérapeutique , Enfant , Enfant d'âge préscolaire , Association médicamenteuse , Ration calorique , Femelle , Humains , Nourrisson , Mâle
5.
Eur J Obstet Gynecol Reprod Biol ; 73(2): 145-8, 1997 Jun.
Article de Anglais | MEDLINE | ID: mdl-9228495

RÉSUMÉ

myotonic dystrophy, also called the Curschmann-Steinert syndrome, is an autosomal dominant inherited neuromuscular disorder characterized by progressive muscular dystrophy, muscle weakness and myotonia, which can affect both mother and child. Complications may arise during pregnancy, delivery, including anaesthetic problems, and in the neonatal period. During pregnancy hydramnion can be a first sign of the disease leading to premature labor and also muscle weakness and myotonia can aggravate complicating the course of delivery. The affected neonate may display severe hypotonia, facial diplegia and respiratory distress. The clinical diagnosis can be confirmed by direct DNA analysis in serum and in chorionvillus biopsy material. In this case report two sisters with myotonic dystrophy are described, their pregnancies, deliveries and the outcome of their affected babies.


Sujet(s)
Dystrophie myotonique/génétique , Complications de la grossesse/étiologie , Adulte , Femelle , Humains , Dystrophie myotonique/congénital , Pedigree , Grossesse
6.
Eur J Pediatr ; 155(4): 338-40, 1996 Apr.
Article de Anglais | MEDLINE | ID: mdl-8777931

RÉSUMÉ

Two cases of caecal duplication are presented, one in a neonate and one in an infant. The diagnosis was made at laparotomy, which had been undertaken for the presumptive diagnosis of intestinal atresia and torsion of an ovarian cyst respectively. Also the literature on alimentary tract duplications is reviewed, referring to the incidence, presenting symptoms, and location of the duplication, in particular that of the caecum.


Sujet(s)
Caecum/malformations , Occlusion intestinale/congénital , Caecum/chirurgie , Diagnostic différentiel , Femelle , Humains , Nourrisson , Nouveau-né , Occlusion intestinale/diagnostic , Occlusion intestinale/chirurgie
7.
Ned Tijdschr Geneeskd ; 138(40): 2001-4, 1994 Oct 01.
Article de Néerlandais | MEDLINE | ID: mdl-7935957

RÉSUMÉ

OBJECTIVE: Evaluation of patients with toxic shock syndrome (TSS) in a paediatric hospital. DESIGN: Retrospective analysis. SETTING: Paediatric Intensive Care Unit, University Hospital, Rotterdam, the Netherlands. METHOD: Analysis of the medical records on 155 patients admitted between January 1982 and January 1992 suffering from shock, 8 of whom had TSS. RESULTS: Five out of 8 TSS patients were under 5 years of age. All the patients needed mechanical ventilation. All patients survived. In 7 patients a probably causative focus of infection was found. The cultures of 6 patients showed growth of Staphylococcus aureus, those of 2 patients showed Lancefield group A beta-haemolytic streptococci (bacterial culture in one, increased antibody titer in the other). Systematic phage typing was not performed. CONCLUSION: Although TSS is a relatively rare disease in young children, it is a potentially lethal one, early recognition of which is very important.


Sujet(s)
Choc septique/diagnostic , Infections à staphylocoques/diagnostic , Facteurs âges , Enfant , Enfant d'âge préscolaire , Femelle , Humains , Nourrisson , Mâle , Études rétrospectives , Choc septique/microbiologie , Infections à staphylocoques/microbiologie , Staphylococcus aureus/isolement et purification , Infections à streptocoques/diagnostic , Infections à streptocoques/microbiologie , Streptococcus pyogenes/isolement et purification
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