Search results for "neonatal"

showing 10 items of 581 documents

Parents' experiences of neonatal transfer. A meta-study of qualitative research 2000-2017.

2018

Transfers of critically ill neonates are frequent phenomena. Even though parents’ participation is regarded as crucial in neonatal care, a transfer often means that parents and neonates are separated. A systematic review of the parents’ experiences of neonatal transfer is lacking. This paper describes a meta-study addressing qualitative research about parents’ experiences of neonatal transfer. Through deconstruction and reflections of theories, methods and empirical data, the aim was to achieve a deeper understanding of theoretical, empirical, contextual, historical and methodological issues of qualitative studies concerning parents’ experiences of neonatal transfer over the course of this …

Value (ethics)MaleParentsPatient TransferInterviewCritical IllnessContext (language use)Developmental psychologyFamily centered caremeta-study03 medical and health sciences0302 clinical medicineexperienceIntensive Care Units NeonatalHumans030212 general & internal medicineneonatal careGeneral NursingQualitative ResearchData collection030504 nursingCritically illInfant Newbornparentstransitionfamily-centered careneonatal transferFemaleDeconstruction0305 other medical sciencePsychologyExperience family-centered care meta-study neonatal care neonatal transfer parents qualitative research transitionqualitative researchQualitative researchNursing inquiry
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Bērnu un jauniešu mirstības tendences saistībā ar makroekonomiskajiem faktoriem Baltijas valstīs (2008 – 2018)

2020

Ievads: Bērnu mirstība Latvijā un Lietuvā vēsturiski ir bijusi ļoti augsta, ņemot vērā Eiropas Savienības standartu. Iepriekšējie pētījumi liecina par to, ka iespējams tas ir saistīts ar ekonomiskiem faktoriem. Šī pētījuma galvenais mērķis ir izpētīt sakarību starp bērnu mirstību dažadās vecumu grupās; perinatālā, jaundzimušā, zīdaiņu, jaunāki par pieciem gadiem un jauniešu (5-14), un starp Baltijas valstīm; Latviju, Igauniju un Lietuvu, sakarā ar makroekonomiskajiem faktoriem. Ņemot vērā neseno ekonomijas vēsturi, tika analizēti laika posmi no 2008 – 2018 gadam. Tas ļāva apskatīt to, vai globālajai finanšu krīzei bija efekts uz bērnu mirstību šajā reģionā. Metodes: Statistiskie dati par bē…

YouthNeonatalInfantMortalityChildMedicīna
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Pentamidine rescues contractility and rhythmicity in a Drosophila model of myotonic dystrophy heart dysfunction

2015

Up to 80% of individuals with myotonic dystrophy type 1 (DM1) will develop cardiac abnormalities at some point during the progression of their disease, the most common of which is heart blockage of varying degrees. Such blockage is characterized by conduction defects and supraventricular and ventricular tachycardia, and carries a high risk of sudden cardiac death. Despite its importance, very few animal model studies have focused on the heart dysfunction in DM1. Here, we describe the characterization of the heart phenotype in a Drosophila model expressing pure expanded CUG repeats under the control of the cardiomyocyte-specific driver GMH5-Gal4. Morphologically, expression of 250 CUG repeat…

[SDV]Life Sciences [q-bio]Myotonic dystrophyMedicine (miscellaneous)lcsh:MedicineVentricular tachycardiaImmunology and Microbiology (miscellaneous)DiastoleHeart RateDrosophila ProteinsMyocytes CardiacGeneticsbiologyRNuclear ProteinsHeartPhenotype3. Good healthCell biology[SDV] Life Sciences [q-bio]Drosophila melanogasterPhenotypeDrosophilaDrosophila melanogasterDrosophila ProteinResearch Articlelcsh:RB1-214congenital hereditary and neonatal diseases and abnormalitiesSystoleLongevityNeuroscience (miscellaneous)In situ hybridizationMyotonic dystrophyGeneral Biochemistry Genetics and Molecular BiologyMuscleblindContractilitymedicinelcsh:PathologyAnimalsPentamidineHeart dysfunctionfungilcsh:RArrhythmias Cardiacbiology.organism_classificationmedicine.diseaseMyocardial ContractionSurvival AnalysisDisease Models AnimalTrinucleotide repeat expansionTrinucleotide Repeat Expansion
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Detección precoz de la hipoacusia, influencia en el diagnóstico y en el tratamiento temprano

2021

Detección precoz de la hipoacusia, influencia en el diagnóstico y en el tratamiento temprano. INTRODUCCIÓN: La hipoacusia es el déficit sensorial mas frecuente en los países desarrollados. La prevalencia de cualquier grado de hipoacusia es de un 2-3 % de la población infantil y el 80% de las mismas, está presente al nacimiento. Los programa de screening auditivo (SA) se justifican por la alta incidencia de la hipoacusia y sus consecuencias devastadoras para el lenguaje cuando no se detecta precozmente. OBJETIVO: Establecer el número de niños diagnosticados de hipoacusia congénita gracias al SA en el hospital Universitario La Fe. Analizamos las técnicas utilizadas en el cribado, los parámetr…

age at screenotoacoustic emissions:CIENCIAS MÉDICAS [UNESCO]neonatal hearing screeninguniversal newborn hearing screeningearly interventionautomated auditory brainstem responsehearing impairment aetiologyevoked potentials auditoryUNESCO::CIENCIAS MÉDICASrisk factorsepidemiologyreferral ratecongenital hearing lossearly diagnosis
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Long-Term Potentiation in the Neonatal Rat Barrel Cortex In Vivo

2012

Long-term potentiation (LTP) is important for the activity-dependent formation of early cortical circuits. In the neonatal rodent barrel cortex, LTP has been studied only in vitro . We combined voltage-sensitive dye imaging with extracellular multielectrode recordings to study whisker stimulation-induced LTP in the whisker-to-barrel cortex pathway of the neonatal rat barrel cortex in vivo . Single whisker stimulation at 2 Hz for 10 min induced an age-dependent expression of LTP in postnatal day (P) 0 to P14 rats, with the strongest expression of LTP at P3–P5. The magnitude of LTP was largest in the activated barrel-related column, smaller in the surrounding septal region, and no LTP could b…

animal structuresPatch-Clamp TechniquesLong-Term PotentiationBiophysicsStimulationBiologyIn Vitro TechniquesStatistics NonparametricIn vivoCortex (anatomy)Evoked Potentials SomatosensoryExtracellularmedicineAnimalsNeuronsSerotonin Plasma Membrane Transport ProteinsCortical circuitsNeonatal ratAfferent PathwaysGeneral Neurosciencemusculoskeletal neural and ocular physiologyAge FactorsLong-term potentiationSomatosensory CortexBarrel cortexElectric StimulationVoltage-Sensitive Dye ImagingRatsmedicine.anatomical_structurenervous systemAnimals NewbornVibrissaeBiophysicsBrief CommunicationsNeuroscience
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Grave ipotonia neonatale con artrogriposi: descrizione di un caso clinico e problematiche diagnostiche

2014

atrogriposi ipotonia neonatale
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Segmentation et métrologie des sinus de Valsalva à partir de ciné-IRM

2012

Automatic segmentation of Valsalva sinuses from cine-MRI

body regionscongenital hereditary and neonatal diseases and abnormalities[ INFO.INFO-IM ] Computer Science [cs]/Medical Imaging[INFO.INFO-IM] Computer Science [cs]/Medical Imagingcardiovascular system[INFO.INFO-IM]Computer Science [cs]/Medical Imagingcardiovascular diseasescirculatory and respiratory physiology
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No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Data…

2021

Background. Lynch syndrome is the most common genetic predisposition for hereditary cancer. Carriers of pathogenic changes in mismatch repair (MMR) genes have an increased risk of developing colorectal (CRC), endometrial, ovarian, urinary tract, prostate, and other cancers, depending on which gene is malfunctioning. In Lynch syndrome, differences in cancer incidence (penetrance) according to the gene involved have led to the stratification of cancer surveillance. By contrast, any differences in penetrance determined by the type of pathogenic variant remain unknown. Objective. To determine cumulative incidences of cancer in carriers of truncating and missense or aberrant splicing pathogenic …

cancer incidence0302 clinical medicineMalalties hereditàriesMissense mutation8Q23.3CàncerCancerGenetics0303 health sciencesmedicine.diagnostic_testFactors de risc en les malaltiesMISMATCH REPAIR GENESRMLH1General MedicinePenetranceLynch syndrome3. Good healthsyöpägeenit030220 oncology & carcinogenesisMedicinesyöpätauditilmaantuvuusGenetic diseasescongenital hereditary and neonatal diseases and abnormalitiesmissense11Q23.1Risk factors in diseasesCANCER-RISKMLH1Articleaberrant splicing03 medical and health sciencesAGEmedicineGenetic predispositionddc:610<i>MSH2</i>Lynchin oireyhtymäpenetrance030304 developmental biologyGenetic testingMLH1; MSH2; penetrance; cancer incidence; truncating; missense; aberrant splicing; Lynch syndromeperinnölliset tauditbusiness.industryMUTATIONSHMSH2Cancernutritional and metabolic diseasesmedicine.diseasedigestive system diseasesMSH2Lynch syndromeMSH23121 General medicine internal medicine and other clinical medicine<i>MLH1</i>businesstruncating
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Effects of Gestational Diabetes Mellitus on Cholesterol Metabolism in Women with High-Risk Pregnancies: Possible Implications for Neonatal Outcome

2022

Metabolic disorders in pregnancy, particularly gestational diabetes mellitus (GDM), are associated with an increased risk for adverse pregnancy outcome and long-term cardiometabolic health of mother and child. This study analyzed changes of serum cholesterol synthesis and absorption markers during the course of high-risk pregnancies, with respect to the development of GDM. Possible associations of maternal lipid biomarkers with neonatal characteristics were also investigated. The study included 63 women with high risk for development of pregnancy complications. Size and proportions of small low-density (LDL) and high-density lipoprotein (HDL) particles were assessed across trimesters (T1&nd…

cholesterol synthesis and absorptionEndocrinology Diabetes and Metabolismhigh-risk pregnancy; gestational diabetes; cholesterol synthesis and absorption; LDL and HDL particles; neonatal outcomeLDL and HDL particles cholesterol synthesis and absorption gestational diabetes high-risk pregnancy neonatal outcomehigh-risk pregnancygestational diabetesLDL and HDL particlesMolecular BiologyBiochemistryneonatal outcome
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Severe Perinatal Hypoxic-Ischemic Brain Injury Induces Long-Term Sensorimotor Deficits, Anxiety-Like Behaviors and Cognitive Impairment in a Sex-, Ag…

2019

Perinatal brain injury (PBI) leads to neurological disabilities throughout life, from motor deficits, cognitive limitations to severe cerebral palsy. Yet, perinatal brain damage has limited therapeutic outcomes. Besides, the immature brain of premature children is at increased risk of hypoxic/ischemic (HI) injury, with males being more susceptible to it and less responsive to protective/therapeutical interventions. Here, we model in male and female C57BL/6 mice, the impact of neonatal HI and the protective effects of neonatal handling (NH), an early life tactile and proprioceptive sensory stimulation. From postnatal day 1 (PND1, modeling pre-term) to PND21 randomized litters received either…

cognitionsensory stimulationCognitive NeurosciencePhysiologyBrain damageCorpus callosumlcsh:RC321-571Cerebral palsy03 medical and health sciencesBehavioral Neuroscience0302 clinical medicineAtrophyCognitionmedicinesexAnimal modelneonatal hypoxic ischemic injurylcsh:Neurosciences. Biological psychiatry. Neuropsychiatry030304 developmental biologyOriginal Research0303 health sciencesBehaviorSensory stimulation therapyNeocortexbusiness.industrybehaviorPutamenanimal modelNeophobiagender medicineNeonatal handlingmedicine.diseaseSensory stimulationmedicine.anatomical_structureNeuropsychology and Physiological PsychologyNeonatal hypoxic ischemic injuryneonatal handlingSexGender medicinemedicine.symptombusiness030217 neurology & neurosurgeryNeuroscienceFrontiers in Behavioral Neuroscience
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