Search results for "newborn."

showing 10 items of 1433 documents

Cardiac pacing in premature infants and neonates: steroid eluting leads and automatic output adaptation

1999

Abstract Background . Appropriate generator and lead selection as well as techniques of implantation are most important aspects of cardiac pacing in the extremely young patient. Here we report the clinical results using a new technique with automatic output adaptation based on evoked response in combination with steroid-eluting epicardial leads in small children. Methods . One neonate and 2 premature infants underwent permanent pacemaker implantation because of congenital high-degree atrioventricular block or postoperative complete heart block, respectively. Steroid-eluting epicardial leads and a multiprogrammable pacemaker with automatic output adaptation were used. Results . Intermuscular…

Heart Defects CongenitalPulmonary and Respiratory MedicinePacemaker ArtificialCardiac pacingInfant Premature DiseasesPostoperative complete heart blockmedicineHumansLead (electronics)Bipolar leadbusiness.industryCardiac Pacing ArtificialInfant NewbornSmall childrenInfantmedicine.diseasePatient populationAnesthesiaFemaleSurgeryPermanent pacemakerCardiology and Cardiovascular MedicinebusinessAtrioventricular blockAlgorithmsInfant PrematureThe Annals of Thoracic Surgery
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Transcatheter radiofrequency perforation and stent implantation for palliation of pulmonary atresia in a 3060-g infant

1995

In a 3060-g infant with fibromuscular pulmonary atresia an open right ventricular outflow tract was created by means of interventional cardiological methods. Following two inadvertent perforations without sequelae or clinical symptoms, radiofrequency perforation and subsequent balloon dilatation were successfully performed. The implantation of a Palmaz iliac stent led to a predictable communication between the right ventricle and pulmonary artery.

Heart Septal Defects VentricularCardiac Catheterizationmedicine.medical_specialtymedicine.medical_treatmentPerforation (oil well)Coronary Angiographymedicine.arterymedicineHumansVentricular outflow tractmedicine.diagnostic_testbusiness.industryInfant NewbornStentmedicine.diseaseSurgerymedicine.anatomical_structureEchocardiographyPulmonary AtresiaVentricleAtresiaAngiographyPulmonary arteryCatheter AblationFemaleStentsRadiologyCardiology and Cardiovascular MedicinePulmonary atresiabusinessCatheterization and Cardiovascular Diagnosis
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Congenital anomalies among live births in a high environmental risk area—A case-control study in Brindisi (southern Italy)

2013

Maternal exposure to ambient pollution has been increasingly linked to the risk of congenital anomalies (CAs) in the fetus and newborns. Recently, a descriptive study in the high environmental risk city of Brindisi (Italy) revealed an increased prevalence of total CAs, especially congenital heart disease (CHD) and ventricular septal defects (VSDs), both at the local level and in comparison with the pool of EUROCAT registries. This paper concerns a population-based case control study to investigate the association between maternal exposure to air pollutants - sulfur dioxide (SO2) and total suspended particulate (TSP) matter - and the risk of CA. Cases were newborns up to 28 days of age, born…

Heart Septal Defects VentricularCongenital anomaliesPediatricsmedicine.medical_specialtyPercentilePopulationAir pollutionAir pollutionmedicine.disease_causeBiochemistryIndustrial exposureEnvironmental riskPregnancyEnvironmental healthBrindisimedicineHumansCitieseducationGeneral Environmental Scienceeducation.field_of_studyPregnancybusiness.industryInfant NewbornCase-control studyOdds ratiomedicine.diseaseIncreased riskItalySulfur dioxideMaternal ExposureCase-Control StudiesFemaleParticulate MatterbusinessEnvironmental Research
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VATER/VACTERL association: clinical variability and expanding phenotype including laryngeal stenosis.

1992

Vertebral abnormalities and anorectal and tracheoesophageal defects are the main manifestations in the VATER/VACTERL association. Radial defects vary from radial aplasia to thumb duplication. Heart and renal defects are reported with lower frequency. Additional malformations, such as the laryngeal stenosis described in the present patient, may expand the phenotype of the association. The wide spectrum of congenital abnormalities confirms the high clinical variability of VATER/VACTERL association which seems to be due to a disruption of blastogenesis. © 1992 Wiley-Liss, Inc.

Heart Septal Defects VentricularMalemedicine.medical_specialtyRadial aplasiaTerminology as TopicmedicineHumansEsophageal AtresiaLungGenetics (clinical)Polydactylybusiness.industryVATER/VACTERL ASSOCIATIONInfant NewbornLaryngostenosisAnatomySyndromemedicine.diseaseAnusPhenotypeVACTERL associationStenosismedicine.anatomical_structurePhenotypeRadiologyLaryngeal StenosisbusinessTracheoesophageal FistulaAmerican journal of medical genetics
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The Association of H1N1 Pandemic Influenza with Congenital Anomaly Prevalence in Europe

2015

BACKGROUND: In the context of the European Surveillance of Congenital Anomalies (EUROCAT) surveillance response to the 2009 influenza pandemic, we sought to establish whether there was a detectable increase of congenital anomaly prevalence among pregnancies exposed to influenza seasons in general, and whether any increase was greater during the 2009 pandemic than during other seasons.METHODS: We performed an ecologic time series analysis based on 26,967 pregnancies with nonchromosomal congenital anomaly conceived from January 2007 to March 2011, reported by 15 EUROCAT registries. Analysis was performed for EUROCAT-defined anomaly subgroups, divided by whether there was a prior hypothesis of…

Heart Septal Defects VentricularPediatricsmedicine.medical_specialtyEpidemiologyEPIDEMICSPrevalenceCRITICAL PERIODSContext (language use)DiseaseILLNESSmedicine.disease_causeTricuspid AtresiaDISEASECongenital AbnormalitiesInfluenza A Virus H1N1 SubtypePregnancyCystic Adenomatoid Malformation of Lung CongenitalInfluenza HumanPandemicPrevalenceInfluenza A virusHumansMedicineNeural Tube DefectsRegistriesPregnancy Complications InfectiousPandemicsTetralogy of FallotRISKPregnancyOUTCOMESbusiness.industryABNORMALITIESInfant NewbornPOLICIESmedicine.diseaseEuropeVaccinationTetralogy of FallotVACCINATIONFemaleTricuspid Valve StenosisbusinessPREGNANT-WOMENEpidemiology
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Coronary Artery Fistula in Down Syndrome: A Hidden Association

2017

Heart Septal Defects VentricularVena Cava SuperiorFistula Down Syndrome AssociationCoronary Vessel AnomaliesInfant NewbornCoronary VesselsUltrasonography PrenatalDiagnosis DifferentialEchocardiographyArteriovenous FistulaHumansFemaleDown Syndrome
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CK-BB as indicator of prenatal brain-cell injury in fetuses with absent or reverse end-diastolic flow velocities of the umbilical arteries

1994

The purpose of this study is to determine the levels of brain type isoenzyme of creatine kinase (CK-BB) as a possible indicator of a pre-existing intrauterine brain-cell damage in cord blood sera of fetuses with preceding absent or reverse end-diastolic flow velocities of the umbilical arteries (AREDFV). CK-BB isoenzyme activities were determined in umbilical cord sera of 13 newborn infants with preceding AREDFV and in 14 fetuses with low end-diastolic flow velocities (LEDFV) of the umbilical arteries. 50 newborn infants with elective cesarean section and normal umbilical artery blood flow velocity waveforms were used as controls. Two-tailed Student's t-test and Fischer's exact test were us…

HemodynamicsUmbilical cordUmbilical ArteriesAndrologyPregnancymedicine.arteryHumansMedicineCreatine KinaseBrain DiseasesFetusbiologybusiness.industryInfant NewbornObstetrics and GynecologyGestational ageUmbilical arteryBlood flowAnatomyFetal BloodIsoenzymesFetal Diseasesmedicine.anatomical_structureCord bloodPediatrics Perinatology and Child Healthbiology.proteinFemaleCreatine kinasebusinessBlood Flow Velocityjpme
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Immunohistochemical Study as a Tool in Differential Diagnosis of Pediatric Malignant Rhabdoid Tumor

2010

Malignant rhabdoid tumors (MRTs) are aggressive childhood neoplasms, occurring mainly in the kidney and brain. We describe 2 unusual cases of extrarenal and noncranial location (liver and soft tissue with dissemination) mimicking hepatoblastoma, neuroblastoma or Ewing sarcoma. Both cases revealed a polyphenotypic profile, combined with cytokeratin, vimentin, and CD99 expression. INI1/BAF-47 showed negative protein nuclear expression in both cases, suggesting a diagnosis of MRT. An extensive immunohistochemical panel was performed to exclude pediatric tumors reminiscent of MRT. The genetic studies failed to detected MYCN amplification, 11q23 deletion, and EWS break-apart positivity. No alter…

HepatoblastomaPathologymedicine.medical_specialtySkin NeoplasmsHistologyDesmoplastic small-round-cell tumorChromosomal Proteins Non-HistoneCD9912E7 AntigenN-Myc Proto-Oncogene ProteinPathology and Forensic MedicineDiagnosis DifferentialNeoplasms Multiple PrimaryFatal OutcomeAntigens CDNeuroblastomaAntineoplastic Combined Chemotherapy ProtocolsmedicineHumansVimentinRhabdoid TumorChromosome AberrationsOncogene ProteinsN-Myc Proto-Oncogene Proteinbusiness.industryLiver NeoplasmsInfant NewbornInfantNuclear ProteinsWilms' tumorSMARCB1 Proteinmedicine.diseaseImmunohistochemistryDNA-Binding ProteinsMedical Laboratory TechnologyDrug Resistance NeoplasmKeratinsFemaleSarcomaRNA-Binding Protein EWSDifferential diagnosisbusinessCell Adhesion MoleculesTranscription FactorsApplied Immunohistochemistry & Molecular Morphology
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Spatial shaping of cochlear innervation by temporally regulated neurotrophin expression.

2001

Previous work suggested qualitatively different effects of neurotrophin 3 (NT-3) in cochlear innervation patterning in different null mutants. We now show that all NT-3 null mutants have a similar phenotype and lose all neurons in the basal turn of the cochlea. To understand these longitudinal deficits in neurotrophin mutants, we have compared the development of the deficit in the NT-3 mutant to the spatial–temporal expression patterns of brain-derived neurotrophic factor (BDNF) and NT-3, using lacZ reporters in each gene and with expression of the specific neurotrophin receptors, trkB and trkC. In the NT-3 mutant, almost normal numbers of spiral ganglion neurons form, but fiber outgrowth t…

HeterozygoteCell SurvivalCell CountNeurotrophin-3Tropomyosin receptor kinase BTropomyosin receptor kinase CArticleMiceNeurotrophin 3Neurotrophic factorsGenes ReportermedicineAnimalsReceptor trkBReceptor trkCNeurons AfferentCochleaSpiral ganglionBrain-derived neurotrophic factorAfferent PathwaysbiologyGeneral NeuroscienceBrain-Derived Neurotrophic FactorHomozygoteGene Expression Regulation DevelopmentalImmunohistochemistryMice Mutant StrainsCochleamedicine.anatomical_structurePhenotypenervous systemAnimals NewbornLac OperonMutationbiology.proteinSpiral GanglionNeuroscienceNeurotrophin
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Amino acid profile of milk-based infant formulas

2000

The protein content and amino acid profile of three milk-based infant formulas, two of which were powdered (adapted and follow-on) and the third liquid, were determined to check their compliance with the EU directive and to evaluate whether or not they fulfil an infant's nutritional needs. To obtain the amino acid profile proteins were subjected to acid hydrolysis, prior to which the sulfur-containing amino acids were oxidized with performic acid. The amino acids were derivatized with phenylisothiocyanate (PITC) and then determined by ion-pair reverse phase high performance liquid chromatography (HPLC) In the case of tryptophan a basic hydrolysis was applied and there was no need of derivat…

High-performance liquid chromatographychemistry.chemical_compoundHydrolysisAnimalsHumansmedia_common.cataloged_instanceEuropean UnionAmino AcidsEuropean unionInfant Nutritional Physiological PhenomenaChromatography High Pressure Liquidmedia_commonchemistry.chemical_classificationAnalysis of VariancePerformic acidChromatographyMilk HumanInfant NewbornNutritional RequirementsTryptophanTryptophanInfantLegislation FoodAmino acidMilkchemistryInfant formulaInfant FoodAcid hydrolysisDietary ProteinsFood ScienceInternational Journal of Food Sciences and Nutrition
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