Search results for "newborn."

showing 10 items of 1433 documents

Congenital pelvic skeletal anomalies: Clinical and radiographic evaluation of newborns with gastrointestinal malformation

2020

Abstract Background Congenital pelvic skeletal anomalies (CPSA) may appear as isolated defects or in association with other anomalies like congenital malformations of the digestive system (CMDS). Minor CPSA in non-syndromic patients are often overlooked. We aimed to assess the frequency of CPSA in newborns with CMDS to review the diagnostic approaches. Study design A retrospective review of medical records of 201 newborns who underwent X-rays for different neonatal indications was conducted. In 122 patients CMDS were diagnosed and classified according to the ICD-10 classification; 79 non-CMDS patients acted as controls. Pelvic skeletal segments were examined by X-rays. Results Patients with…

AdultMalePediatricsmedicine.medical_specialtySkeletal anomaliesRadiographyPelvic bones Musculoskeletal system Congenital abnormalities VACTERL association Radiography International classification of diseasesInfant Newborn DiseasesPelvismedicineHumansbusiness.industryIncidenceMedical recordInfant NewbornObstetrics and GynecologyOdds ratiomedicine.diseaseVACTERL associationHypoplasiaMusculoskeletal AbnormalitiesRadiographyAgenesisPediatrics Perinatology and Child HealthFemaleHigh incidencebusinessDigestive System Abnormalities
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Incidence and risk factors in sudden unexpected death in epilepsy: a prospective cohort study.

2001

Objective: To determine incidence of and risk factors for sudden unexpected death in epilepsy (SUDEP). Methods: Three epilepsy centers enrolled 4,578 patients and prospectively followed these patients for 16,463 patient-years. The cohort was screened for death annually. Deaths were investigated to determine whether SUDEP occurred. Potential risk factors were compared in SUDEP cases and in controls enrolled contemporaneously at the same center. Results: Incidence of SUDEP was 1.21/1,000 patient-years and was higher among women (1.45/1,000) than men (0.98/1,000). SUDEP accounted for 18% of all deaths. Occurrence of tonic-clonic seizures, treatment with more than two anticonvulsant medications…

AdultMalePediatricsmedicine.medical_specialtyTime FactorsAdolescentSudden deathCohort StudiesEpilepsyDeath SuddenRisk FactorsCause of DeathEpidemiologymedicineHumansProspective StudiesRisk factorProspective cohort studyChildCause of deathAgedAged 80 and overEpilepsybusiness.industryIncidenceInfant NewbornInfantepilepsy death sudepMiddle Agedmedicine.diseaseSurgeryChild PreschoolCohortSettore MED/26 - NeurologiaFemaleNeurology (clinical)businessEpidemiologic MethodsCohort studyNeurology
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A retrospective follow up study on maternal age and infant mortality in two Sicilian districts

2011

Abstract Background Infant mortality rate (IMR) is a key public health indicator. Maternal age is a well-known determinant of pregnancy and delivery complications and of infant morbidity and mortality. In Italy the Infant Mortality Rate was 3.7/1000 during 2005, lower than the average IMR for the European Union (4.94/1000). Sicily is the Italian region with the highest IMR, 5/1000, and neonatal mortality rate (NMR), 3.8/1000, with substantial variation among its nine districts. The present study compared a high IMR/NMR district (Messina) with a low IMR/NMR district (Palermo) during the period 2004-2006 to evaluate potential determinants of the IMRs' differences between the two districts and…

AdultMalePediatricsmedicine.medical_specialtyretrospective studySettore MED/42 - Igiene Generale E Applicatasymbols.namesakeEpidemiologyInfant Mortalitymedicinemedia_common.cataloged_instanceHumansAdvanced maternal agePoisson regressioninfant mortality rateRegistriesEuropean unionSicilymedia_commonRetrospective StudiesPregnancybusiness.industrylcsh:Public aspects of medicinePublic healthPublic Health Environmental and Occupational HealthInfant NewbornInfantlcsh:RA1-1270medicine.diseaseInfant mortalitysymbolsFemaleLive birthbusinessDemographyResearch ArticleFollow-Up StudiesMaternal AgeBMC Public Health
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The value of the short-term fetal heart rate variation for timing the delivery of growth-retarded fetuses.

2008

OBJECTIVE: To assess the clinical value of the short-term fetal heart rate variation (STV) for timing the delivery of severely growth-retarded fetuses, many associated with pre-eclampsia. DESIGN: Retrospective cohort study. SETTING: John Radcliffe Maternity Hospital, Oxford, UK. POPULATION: Two hundred and fifty-seven fetuses with a birthweight less than third percentile and a last computerised cardiotocography performed within 24 h of delivery. METHODS: Analysis of the relationship between antepartum STV and the perinatal outcome. MAIN OUTCOME MEASURES: Stillbirth rate and the acid-base status at birth. RESULTS: There were no stillbirths or neonatal deaths (NNDs) within 24 h in the study p…

AdultMalePercentilemedicine.medical_specialtyTime FactorsAdolescentCardiotocographyGestational AgeAcid-Base ImbalanceHeart ratemedicineHumansCardiotocographyreproductive and urinary physiologyRetrospective StudiesFetusPregnancyFetal Growth Retardationmedicine.diagnostic_testbusiness.industryObstetricsInfant NewbornObstetrics and GynecologyRetrospective cohort studyHeart Rate Fetalmedicine.diseaseDelivery ObstetricGestationPopulation studyFemalebusinessBJOG : an international journal of obstetrics and gynaecology
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Placental metal concentrations and birth outcomes: The Environment and Childhood (INMA) project

2019

To examine the association of placental levels of arsenic (As), cadmium (Cd), mercury (Hg), lead (Pb), manganese (Mn), and chromium (Cr) with birth outcomes (birth weight, length, and head circumference, low birth weight [LBW], gestational age, preterm delivery, and small for gestational age [SGA]) in mother-child pairs from the Environment and Childhood (INMA) Project in Spain.Metal concentrations were measured in placenta tissue samples randomly selected from five INMA cohorts. Data on birth outcomes were obtained from medical records. Associations were assessed in a sub-sample of 327 mother-infant pairs by regression models adjusted for confounding factors and for all metals simultaneous…

AdultMalePlacentaBirth weightPhysiologyGestational Age010501 environmental sciences01 natural sciencesArsenicCohort StudiesFetal Development03 medical and health sciences0302 clinical medicinePregnancyMetals HeavyPlacentaBirth WeightHumansMedicine030212 general & internal medicineMaternal-Fetal ExchangePreterm delivery0105 earth and related environmental sciencesbusiness.industryConfoundingInfant NewbornPublic Health Environmental and Occupational HealthGestational agemedicine.diseaseLow birth weightmedicine.anatomical_structureMaternal ExposureSpainIn uteroSmall for gestational ageEnvironmental PollutantsFemalemedicine.symptombusinessHeadBiological MonitoringInternational Journal of Hygiene and Environmental Health
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Gastric outlet obstruction in a neonate because of Peutz-Jeghers syndrome

2012

Neonatal detection of Peutz-Jeghers syndrome is unusual with only 2 cases previously reported in the literature. We describe a neonate presenting with gastric outlet obstruction owing to 2 large Peutz-Jeghers polyps. The child's father and grandmother were known to have Peutz-Jeghers syndrome. On the ninth day of life, the infant underwent colonoscopy, abdominal exploration, and complete surgical resection of 3 polyps. The postoperative course was uneventful, and the patient was discharged home at the age of 3 weeks on full oral feeds. This is the first case report of inherited Peutz-Jeghers syndrome causing gastric outlet obstruction in a neonate.

AdultMalePolyhydramniosSurgical resectioncongenital hereditary and neonatal diseases and abnormalitiesmedicine.medical_specialtyDay of lifePeutz-Jeghers SyndromeColonoscopyPeutz–Jeghers syndromePolypsPregnancyStomach NeoplasmsAbdominal explorationmedicineHumansskin and connective tissue diseasesmedicine.diagnostic_testGastric Outlet Obstructionbusiness.industryInfant NewbornGastric outlet obstructionGeneral Medicinemedicine.diseasedigestive system diseasesSurgeryPediatrics Perinatology and Child HealthFemaleSurgerybusinessJournal of Pediatric Surgery
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Autosomal dominant and sporadic radio-ulnar synostosis.

1997

We report on seven cases of congenital radio-ulnar synostosis (RUS). Five were found in the same family and two were sporadic. In six the synostosis was bilateral and consistently involved the proximal end of the radius and ulna. In the familial cases the anomaly was inherited as an autosomal dominant trait and was associated with a Dubois sign and relative shortness of metacarpals number 4 and 5 in two patients, and of number 2 in another patient, and of all phalanges of the 5th fingers. These observations suggest involvement of an ulnar developmental field. RUS does not seem to be rare in the Sicilian population.

AdultMalePopulationUlnaFingersElbow JointmedicineHumanseducationSicilyGenetics (clinical)Agededucation.field_of_studybusiness.industryUlnaInfant NewbornAutosomal dominant traitInfantAnatomySyndromeSynostosisPhalanxmedicine.diseasePedigreeRadiographyRadiusmedicine.anatomical_structureSynostosisFemalebusinessAmerican journal of medical genetics
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Risk factors for cystic fibrosis arthropathy: Data from the German cystic fibrosis registry

2021

Epidemiology and potential risk factors for cystic fibrosis arthropathy (CFA) were studied in a relevant cystic fibrosis (CF) patient cohort.Cohort study of patients included in the German CF registry in 2016-2017. Descriptive analysis, exploratory tests and multivariable logistic regression were used to assess prevalence of CFA and associated potential risk factors for adult patients with/without chronic Pseudomonas aeruginosa infection.6069 CF patients aged from 0 to 78 years were analysed. CFA was observed in 4.9% of the patients. Prevalence was significantly higher in adult patients (8.4%) compared to patients18 years (0.7%; p0.0001). Logistic regression analyses in adult patients (n=33…

AdultMalePulmonary and Respiratory Medicinemedicine.medical_specialtyAdolescentCystic FibrosisCystic fibrosis-related diabetesmedicine.disease_causeLogistic regressionCystic fibrosisDiabetes ComplicationsSex FactorsRisk FactorsGermanyInternal medicineArthropathyEpidemiologyPrevalencemedicineHumansPseudomonas InfectionsRegistriesSinusitisChildAgedPseudomonas aeruginosabusiness.industryAge FactorsInfant NewbornInfantMiddle Agedmedicine.diseaseChild PreschoolPediatrics Perinatology and Child HealthCohortExocrine Pancreatic InsufficiencyFemaleJoint DiseasesbusinessCohort studyJournal of Cystic Fibrosis
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Prevention of ventricular catheter obstruction and slit ventricle syndrome by the prophylactic use of the Integra antisiphon device in shunt therapy …

2010

Object This 25-year follow-up study was performed on 120 children with hypertensive hydrocephalus to evaluate the influence of the early prophylactic implantation of the Integra antisiphon device (ASD, Integra Neurosciences Ltd.) on the rate of proximal shunt obstructions and the frequency of symptomatic slit ventricle syndrome (SVS). The adaptability of the ASD to growth, proper positioning of the ASD as a necessity for its successful performance, and the 3 phases of SVS development are discussed. Method Since 1978, the ASD has consistently been implanted either at the time of primary shunt insertion (66 neonates, mean follow-up 11 years) or during revisions of preexisting shunts (54 chil…

AdultMaleReoperationmedicine.medical_specialtyAdolescentIntracranial PressureHydrostatic pressureInfant Premature DiseasesSlit Ventricle SyndromeCentral nervous system diseaseYoung AdultPostoperative ComplicationsRisk FactorsHydrostatic PressuremedicineHumansYoung adultChildbusiness.industryInfant NewbornInfantEquipment DesignGeneral Medicinemedicine.diseaseSlit Ventricle SyndromeCerebrospinal Fluid ShuntsHydrocephalusSurgeryEquipment Failure AnalysisCatheterEl NiñoChild PreschoolFemaleIntracranial HypertensionbusinessShunt (electrical)Follow-Up StudiesHydrocephalusJournal of Neurosurgery: Pediatrics
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Development of a New Nordic Diet score and its association with gestational weight gain and fetal growth - A study performed in the Norwegian Mother …

2014

AbstractObjectiveTo construct a diet score for assessing degree of adherence to a healthy and environmentally friendly New Nordic Diet (NND) and to investigate its association with adequacy of gestational weight gain and fetal growth in a large prospective birth cohort.DesignMain exposure was NND adherence, categorized as low, medium or high adherence. Main outcomes were adequacy of gestational weight gain, described as inadequate, optimal or excessive according to the 2009 Institute of Medicine guidelines, and fetal growth, categorized as being small, appropriate or large for gestational age. Associations of NND adherence with gestational weight gain and fetal growth were estimated with mu…

AdultMaleRiskPediatricsmedicine.medical_specialtyAdolescentVDP::Gynekologi og obstetrikk: 756Birth weightMedicine (miscellaneous)Health PromotionWeight GainModels BiologicalNutrition PolicyCohort StudiesFetal DevelopmentNutrient densityYoung AdultPregnancymedicineHumansProspective StudiesProspective cohort studyVDP::Gynaecology and obstetrics: 756PregnancyFetal Growth RetardationNutrition and DieteticsNorwaybusiness.industryObstetricsInfant NewbornPublic Health Environmental and Occupational HealthGestational ageMaternal Nutritional Physiological PhenomenaOverweightmedicine.diseaseDietPregnancy ComplicationsPatient ComplianceSmall for gestational ageFemalemedicine.symptombusinessWeight gainFollow-Up StudiesCohort study
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