Search results for "perinatology"

showing 10 items of 1762 documents

Epidemiology of pneumococcal disease in children in Germany

2001

UNLABELLED Recently published and as yet unpublished data allow a reasonable estimate of the annual burden of pneumococcal disease in Germany. At least 277,000 episodes of otitis media and at least 2,000 episodes of sinusitis occur in children under the age of 5 y. Pneumococcal meningitis was found in 200 children under the age of 16 y; the estimate for all age groups ranges from 450 to 1100 cases. Of approximately 150,000 cases of ambulatory pneumococcal pneumonia, at least 63,000-105,000 patients are hospitalized each year. CONCLUSION Further studies of pneumococcal epidemiology in Germany are needed, and continued surveillance will be necessary for a better understanding of the overall b…

medicine.medical_specialtyPediatricsAdolescentPrevalencemedicine.disease_causePneumococcal InfectionsGermanyEpidemiologyStreptococcus pneumoniaemedicineHumansSerotypingSinusitisChildMeningitis Pneumococcalbusiness.industryData CollectionIncidenceIncidence (epidemiology)Bacterial pneumoniaGeneral Medicinemedicine.diseaseHospitalizationOtitis MediaStreptococcus pneumoniaeOtitisPopulation SurveillancePediatrics Perinatology and Child HealthPneumococcal pneumoniaImmunologymedicine.symptombusinessMeningitisActa Paediatrica
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Does Oxygen Content Play a Role in Spontaneous Closure of Perimembranous Ventricular Septal Defects?

2021

(1) Background: the impact of a series of laboratory parameters (haemoglobin, haematocrit, foetal haemoglobin, peripheral oxygen saturation, iron, transferrin, ferritin, and albumin) on perimembranous ventricular septal defects spontaneous healing was tested. (2) Methods: one hundred and seven patients were enrolled in the study (57% males; mean age 2.1 ± 0.4 years) and were subsequently subdivided into two groups: self-healing (n = 36) and in need of intervention (n = 71). Self-healing subjects were defined on the basis of an absence of residual shunts at colorDoppler across the previous defect. (3) Results: no statistically significant differences were reported in the size of perimembrano…

medicine.medical_specialtyPediatricsArticleRJ1-570ironInternal medicinemedicineOxygen contentchemistry.chemical_classificationanaemiabiologyMultivariable linear regressionPeripheral oxygen saturationbusiness.industrySpontaneous closureAlbuminMean agecongenital heart diseasehaemoglobinventricular septal defectFerritinventricular septal defect; congenital heart disease; haemoglobin; anaemia; ironchemistryTransferrinPediatrics Perinatology and Child Healthbiology.proteinCardiologybusinessChildren
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Goitrous congenital hypothyroidism in a twin pregnancy causing respiratory obstruction at birth: Implications for management

2006

We report a twin pregnancy complicated by fetal goitrous hypothyroidism secondary to dyshormonogenesis caused by thyroglobulin deficiency. Antenatal treatment with intra-amniotic thyroxine was considered but not performed, given the late gestational age at diagnosis and the multiple nature of the pregnancy. Both twins developed airway obstruction at delivery, requiring intubation and ventilation. We review the literature and describe the practical issues relating to the antenatal assessment and perinatal management of fetal goitre.

medicine.medical_specialtyPediatricsGoiterThyroglobulinPregnancyPrenatal DiagnosisCongenital HypothyroidismDiseases in TwinsmedicineHumansTwin PregnancyPregnancyFetusThyroglobulin DeficiencyGoiterbusiness.industryInfant NewbornGestational ageGeneral MedicineAirway obstructionDelivery Obstetricmedicine.diseaseMagnetic Resonance ImagingSurgeryCongenital hypothyroidismAirway ObstructionPediatrics Perinatology and Child HealthFemalebusinessActa Paediatrica
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Nonketotic hyperglycinemia and epilepsy

2015

Nonketotic hyperglycinemia (NKH) is an autosomal recessive inborn error in the glycine degradation pathway resulting in severe neurological impairment with intractable seizures and brain damage in the majority of the affected patients. Depending on the age of onset and on the outcome of the disease, severe and attenuated forms of NKH may be discriminated. During neonatal period, patients may present with early myoclonic encephalopathy; in the course of the disease, the picture of seizures changes, and multiple forms of seizures may occur. In patients with severe NKH, seizures remain persistent and resistant to anticonvulsant treatment. Variant NKH, caused by mutations resulting in a deficie…

medicine.medical_specialtyPediatricsHyperglycinemiabusiness.industrymedicine.medical_treatmentBrain damagemedicine.diseaseGlycine encephalopathyEpilepsyEndocrinologyAnticonvulsantNeurotransmitter receptorInternal medicinePediatrics Perinatology and Child HealthmedicineNeurology (clinical)medicine.symptomAge of onsetbusinessEarly myoclonic encephalopathyJournal of Pediatric Epilepsy
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987 Emipediology and Morbidity of Late Preterm Neonates in Correlation with Maternal Risk Factors in Hessen, Germany

2012

Short and long term morbidity in late preterm neonates (LP) and their correlation to maternal risk factors are relevant as shown in multiple studies in North America and European countries. Epidemiological studies showed an increase in LP birth over time. Corresponding data for Germany have not yet been published. Our goal was to evaluate the epidemiology of LP over a 7 year period and the correlation to potential maternal risk factors in Hessen, Germany. Data was collected from the perinatal und neonatal quality assurance in Hessen form 2001 to 2007. For some calculations the two data sets were merged. Overall the data sets of 360.000 births and 44.000 neonatal hospitalizations were availa…

medicine.medical_specialtyPediatricsMaternal risk factorsbusiness.industryMaternal morbidityPlacental insufficiencymedicine.diseaseObesityGestational diabetesCorrelationPediatrics Perinatology and Child HealthEpidemiologymedicineLate pretermbusinessArchives of Disease in Childhood
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Reduction of earwax with hypoacusia in Saharawi children

2010

Summary We report case reports of earwax with hypoacusia (1.8%) in 270 Saharawi children, aged from 6 to 13 years, for a two-month period during the summer according to the “Holidays in Peace” program developed in collaboration with a local non-governmental organization (NGO). Our values are lower than those of other authors due to an initiative of systematic checks carried out by trained general doctors and nursing on children's hearing in Saharawi refugee camps in the last years.

medicine.medical_specialtyPediatricsOtorhinolaryngologybusiness.industryRefugeeFamily medicinePediatrics Perinatology and Child HealthMedicinebusinessInternational Journal of Pediatric Otorhinolaryngology Extra
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Epidemiological study of Italian patients with Fabry disease.

2007

medicine.medical_specialtyPediatricsPathologyFabry diseaseSettore MED/38 - PEDIATRIA GENERALE E SPECIALISTICAbusiness.industryPediatrics Perinatology and Child HealthEpidemiologymedicineGeneral Medicinebusinessmedicine.diseaseFabry disease
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Newborn screening of inherited metabolic disorders by tandem mass spectrometry: past, present and future

2013

Inborn errors of metabolism are inherited biochemical disorders caused by lack of a functional enzyme, transmembrane transporter, or similar protein, which then results in blockage of the corresponding metabolic pathway. Taken individually, inborn errors of metabolism are rare. However, as a group these diseases are relatively frequent and they may account for most of neonatal mortality and need of health resources. The detection of genetic metabolic disorders should occur in a pre-symptomatic phase. Recently, the introduction of the tandem mass spectrometric methods for metabolite analysis has changed our ability to detect intermediates of metabolism in smaller samples and provides the mea…

medicine.medical_specialtyPediatricsPopulationlcsh:Surgeryinborn errors of metabolismPredictive Value of TestSensitivity and SpecificityNeonatal ScreeningSettore MED/38 - Pediatria Generale E SpecialisticaPredictive Value of TestsnewbornTandem Mass SpectrometryHealth caremedicineHumansIntensive care medicineeducationPreventive healthcareeducation.field_of_studyNewborn screeningbusiness.industrylcsh:RJ1-570Infant Newbornlcsh:Pediatricslcsh:RD1-811Metabolite analysisPlace of birthMass spectrometricPediatrics Perinatology and Child HealthEthical dilemmaSurgerymetabolic screeningbusinessMetabolism Inborn ErrorMetabolism Inborn ErrorsHuman
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Endemic Treponemal Infections in International Adoptees and Immigrant Children: How Common are they?

2011

medicine.medical_specialtyPediatricsTreponemal Infectionbusiness.industrymedia_common.quotation_subjectFamily medicinePediatrics Perinatology and Child HealthImmigrationmedicineDermatologybusinessmedia_commonPediatric Dermatology
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Risk factors for refractory Kawasaki disease: clinical records of the paediatric clinic of palermo

2014

Kawasaki disease (KD) is an acute, self-limited febrile illness that mainly affecting small- to medium-sized vessels and occurs in early childhood. The etiology is currently unknown, however it likely results from an immunologic response triggered by microbial agents, with documented genetic susceptibility. Intravenous administration of immunoglobulin (IVIG) is the gold standard therapy for coronary arteritis in the acute phase of KD; some patients do not respond to IVIG and coronary aneurysms continue to develop in 5%. The most serious complications are coronary vasculitis and aneurysms. 15% of these patients do not respond to IVIG (Refractory KD:RMK) and have a higher risk of aneurysms.

medicine.medical_specialtyPediatricsbiologybusiness.industryGold standardmedicine.diseaseRheumatologySettore MED/38 - Pediatria Generale E SpecialisticaRefractoryRheumatologyhemic and lymphatic diseasesInternal medicinePoster PresentationPediatrics Perinatology and Child HealthmedicineGenetic predispositionEtiologybiology.proteinImmunology and AllergyKawasaki diseaseKawasaki disease risk factorsPediatrics Perinatology and Child HealthAntibodyVasculitisbusinessPediatric Rheumatology
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