Search results for "Pediatric"

showing 10 items of 4528 documents

High-Speed Video Microscopy for Primary Ciliary Dyskinesia Diagnosis: A Study of Ciliary Motility Variations with Time and Temperature

2021

Este artículo se encuentra disponible en la siguiente URL: https://www.mdpi.com/2075-4418/11/7/1301 Este artículo de investigación pertenece al número especial "Progress in Diagnosing and Managing Primary Ciliary Dyskinesia". Primary ciliary dyskinesia (PCD) is a rare disease resulting from a defect in ciliary function that generates, among other issues, chronic upper and lower respiratory tract infections. European guidelines recommend studying ciliary function (pattern (CBP) and frequency (CBF)), together with characteristic clinical symptoms, as one of the definitive tests. However, there is no “gold standard”. The present study aims to use high-speed video microscopy to describe how CBF…

medicine.medical_specialtyMedicine (General)Kartagener's syndrome - Diagnosis.Respiratory organs - Diseases in children.Clinical BiochemistryAparato respiratorio - Enfermedades en los niños.Video microscopyArticlehigh-speed video microscopy (HSVM)03 medical and health sciences0302 clinical medicineR5-920ciliary beat frequency (CBF)Microscopia.OphthalmologyMicroscopy.MicroscopymedicinePediatric otolaryngology.030212 general & internal medicinePrimary ciliary dyskinesiaDisquinesia ciliar Síndrome de - Diagnóstico.primary ciliary dyskinesia (PCD)business.industryPrimary ciliary dyskinesia - Diagnosis.Enfermedades crónicas en los niños.Otorrinolaringología pediátrica.Gold standard (test)Ciliary motilitymedicine.diseaseNasal epitheliumChronic diseases in children.ciliary beat pattern (CBP)High speed video030228 respiratory systemKartagener Síndrome de - Diagnóstico.Sample collectionbusiness
researchProduct

Expression of Human Ubiquitous Aquaporins in Chorial Villus Samples

2011

Background/objectives: Aquaporins (AQPs) are a family of proteins (AQP0-12) ubiquitously expressed acting as cell membrane water channels. AQP 1/3/8/9 expression has been found in human placenta and fetal membranes; however, AQP4 is the only identified in first trimester fetal tissue samples. We aimed to determine AQP mRNA expression in first trimester of pregnancy and compare it to the expression in placenta at delivery. Material and Methods: 26 Chorionic villus (CV) samples and 5 placental samples were collected and analyzed by real time-PCR using Taqman assay (Applied Biosystems®) for human AQP1, 2, 3, 4, 5, 6, 7, 8, 9, 11 and 18S. Results: CV expressed high mRNA levels of AQP1, 3, 9 and…

medicine.medical_specialtyMessenger RNAPregnancyFetusAquaporinBiologymedicine.diseasemedicine.anatomical_structureEndocrinologyAquaporin 2Internal medicinePlacentaPediatrics Perinatology and Child HealthmedicineTaqManChorionic villiPediatric Research
researchProduct

Which is the best ultrasound parameter for the prediction of adverse perinatal outcome within 1 day of delivery?

2021

To compare the accuracies of several sonographic parameters for the prediction of adverse perinatal outcome (APO) prior to delivery.This was a prospective study of fetuses attending the day hospital unit of a tertiary referral hospital that were scanned at 34-41 weeks and gave birth within 24 h of examination. APO was defined as a composite of abnormal intrapartum fetal heart rate or intrapartum fetal scalp pH7.20 requiring urgent cesarean section, neonatal umbilical cord pH7.10, 5' Apgar score7 and postpartum admission to neonatal or pediatric intensive care units. The accuracies of the middle cerebral, vertebral and umbilical arteries pulsatility index multiples of the median (MoM), the c…

medicine.medical_specialtyMiddle Cerebral ArteryPerinatal outcomemacromolecular substancesUltrasonography PrenatalUmbilical ArteriesPregnancyPredictive Value of Testsmedicine.arterymedicineHumansProspective StudiesProspective cohort studyChildFetusbusiness.industryObstetricsCesarean SectionUltrasoundInfant NewbornPregnancy OutcomeObstetrics and GynecologyFetal dopplerUltrasonography DopplerPulsatile FlowPediatrics Perinatology and Child HealthMiddle cerebral arteryFemalebusinessThe journal of maternal-fetalneonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians
researchProduct

Birth-weight differences at term are explained by placental dysfunction and not by maternal ethnicity. Study in newborns of first generation immigran…

2020

The aim of the study was to investigate the influence of ethnicity and cerebroplacental ratio (CPR) on the birth weight (BW) of first generation Indo-Pakistan immigrants' newborns.This was a retrospective study in a mixed population of 620 term Caucasian and Indo-Pakistan pregnancies, evaluated in two reference hospitals of Spain and Italy. All fetuses underwent a scan and Doppler examination within two weeks of delivery. The influence of fetal gender, ethnicity, GA at delivery, CPR, maternal age, height, weight and parity on BW was evaluated by multivariable regression analysis.Newborns of first generation Indo-Pakistan immigrants were smaller than local Caucasian newborns (mean BW mean= 3…

medicine.medical_specialtyMiddle Cerebral Arterymedia_common.quotation_subjectBirth weightPlacentaImmigrationEthnic groupEmigrants and ImmigrantsGestational AgeUltrasonography PrenatalUmbilical ArteriesPlacental dysfunctionPregnancymedicineEthnicityBirth WeightHumanshealth care economics and organizationsmedia_commonRetrospective StudiesObstetricsbusiness.industryInfant NewbornParturitionObstetrics and GynecologyFetal dopplerFirst generationTerm (time)Pediatrics Perinatology and Child Healthpopulation characteristicsFemaleFetal nutritionbusinessgeographic locationsThe journal of maternal-fetalneonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians
researchProduct

Information and Communication Technologies to Support Early Screening of Autism Spectrum Disorder: A Systematic Review

2021

 The aim of this systematic review is to identify recent digital technologies used to detect early signs of autism spectrum disorder (ASD) in preschool children (i.e., up to six years of age). A systematic literature search was performed for English language articles and conference papers indexed in Pubmed, PsycInfo, ERIC, CINAHL, WoS, IEEE, and ACM digital libraries up until January 2020. A follow-up search was conducted to cover the literature published until December 2020 for the usefulness and interest in this area of research during the Covid-19 emergency. In total, 2427 articles were initially retrieved from databases search. Additional 481 articles were retrieved from follow-up searc…

medicine.medical_specialtyModalitiesbusiness.industryNatural user interfacescreeninglcsh:RJ1-570Information technologyautism spectrum disorderlcsh:PediatricsReviewPsycINFOCINAHLmedicine.diseaseDigital libraryprimary careinformation technologyAutism spectrum disorderInformation and Communications TechnologyPediatrics Perinatology and Child HealthmedicineMedical physicsbusinessPsychologyChildren
researchProduct

A Multivariate Age-Structured Stochastic Model with Immunization Strategies to Describe Bronchiolitis Dynamics

2021

Bronchiolitis has a high morbidity in children under 2 years old. Respiratory syncytial virus (RSV) is the most common pathogen causing the disease. At present, there is only a costly humanized monoclonal RSV-specific antibody to prevent RSV. However, different immunization strategies are being developed. Hence, evaluation and comparison of their impact is important for policymakers. The analysis of the disease with a Bayesian stochastic compartmental model provided an improved and more natural description of its dynamics. However, the consideration of different age groups is still needed, since disease transmission greatly varies with age. In this work, we propose a multivariate age-struct…

medicine.medical_specialtyMultivariate statisticsStochastic modellingstochastic Bayesian modelHealth Toxicology and Mutagenesisrespiratory syncytial virusBayesian probabilityDiseaseRespiratory Syncytial Virus InfectionsPoisson distributioninfectious diseasesArticle03 medical and health sciencessymbols.namesakemultivariate age-structured model0302 clinical medicine030225 pediatricsMedicineHumans030212 general & internal medicineIntensive care medicineChildAge structuredimmunization programsbusiness.industryPublic Health Environmental and Occupational HealthInfant NewbornRInfantBayes TheoremImmunization (finance)medicine.diseaseRespiratory Syncytial VirusesBronchiolitisChild PreschoolsymbolsMedicineImmunizationbronchiolitisbusinessInternational Journal of Environmental Research and Public Health
researchProduct

P.10.18 Common data elements for muscle biopsy reporting

2013

Physicians commonly utilize the muscle biopsy to assist in the diagnosis of neuromuscular diseases. However, there is no current standard for evaluating or reporting on findings, and the resulting variability can impede accurate diagnoses and limit the utility of the muscle biopsy as a tool for clinical care, research, and stratifying patients for clinical trials. The National Institutes of Neurological Disorders and Stroke (NINDS) recently launched a Common Data Element (CDE) in an effort to standardize neuromuscular data collected in clinical reports. For this study, the authors adapted the NINDS Muscle Biopsy CDE to generate a form for prospective muscle biopsy reporting (CDE-R). This fo…

medicine.medical_specialtyMuscle biopsymedicine.diagnostic_testbusiness.industryConcordanceDiseaseMuscle disorderChecklistClinical trialNeurologyPediatrics Perinatology and Child HealthmedicinePhysical therapyNeurology (clinical)Medical diagnosisIntensive care medicinebusinessPathologicalGenetics (clinical)Neuromuscular Disorders
researchProduct

Significance of I313V mutation of NLPR3 gene in two pediatric patients

2011

Results Both case #1 (M.T) and #2 (V.C) displayed a mild clinical phenotype (episodes of urticarial rash and arthralgia associated with elevation of acute phase reactants), compatible with FCAS and Muckle-Wells syndrome, respectively. Both patients displayed good response to NSAID and/or steroid on demand. Compared to HD controls, patients displayed enhanced and delayed IL1b secretion. This was accompanied by higher levels of lL1Ra and IL-6 without any significant differences in IL-8. Interestingly, parents carrying the mutation also displayed higher levels of secreted IL-1b compared to HD control group. Conclusion The I313V mutation is associated with a mild CAPS phenotype and with an incr…

medicine.medical_specialtyMutationlcsh:Diseases of the musculoskeletal systembusiness.industryAcute-phase proteinlcsh:RJ1-570lcsh:Pediatricsmedicine.disease_causePhenotypeRheumatologyEndocrinologyRheumatologyUrticarial rashInternal medicineOn demandPoster PresentationPediatrics Perinatology and Child HealthmedicineImmunology and AllergySecretionPediatrics Perinatology and Child Healthlcsh:RC925-935businessGenePediatric Rheumatology
researchProduct

Monitoring and use of antimycotic (micafungin) for systemic use provided by the pharmacy of Marsala Hospital, Italy

2016

Micafungin is an antimycotic drug and represents an important addition to the available therapies for the treatment of systemic fungal infections. Micafungin is used: in the treatment of invasive candidiasis, oesophageal and prophylaxis of <em>Candida</em> infections. It inhibits, in a non-competitive way, the synthesis of 1,3-β-D-glucan, a component of fungal cell wall and is rapidly distributed into the tissues. It has a high-rate respectful bond with plasma protein, which is independent from the concentration of the drug. It is metabolized through the liver, being not subject to intense metabolic transformations until the excretion. There is no evidence of systemic accumulati…

medicine.medical_specialtyNauseaAnemiaPharmacyPlant SciencePharmacyGeneral Biochemistry Genetics and Molecular BiologyHypomagnesemiaExcretion03 medical and health sciencesHospital Pharmacy0302 clinical medicine030225 pediatricsInternal medicineIntensive caremedicineAntimycotic030212 general & internal medicineSicilylcsh:QH301-705.5Antimycotic; Micafungin; Hospital Pharmacybusiness.industryBiochemistry (medical)Micafunginmedicine.diseaseHypokalemiaSurgerylcsh:Biology (General)MicafunginSettore BIO/14 - Farmacologiamedicine.symptombusinessmedicine.drug
researchProduct

Diaphragmatic Hernia following Pediatric Liver Transplantation: An Underappreciated Complication Prone to Recur.

2020

Abstract Introduction Postoperative diaphragmatic hernia (DH) is a rare but potentially life-threatening complication following pediatric liver transplantation (LT). In the current literature, a total of 49 such hernias have been reported in 17 case series. We present eight additional cases, three of which reoccurred after surgical correction, and review the current literature with a focus on recurrence. Materials and Methods The study sample included children (<18 years of age) who underwent LT between June 2013 and June 2020 at five large transplant centers and who subsequently presented with DH. During the study period, a total of 907 LT was performed. Eight DH were recognized, and ri…

medicine.medical_specialtyNauseamedicine.medical_treatment030230 surgeryLiver transplantationAsymptomatic03 medical and health sciences0302 clinical medicinePostoperative ComplicationsRecurrencemedicineHumansDiaphragmatic herniaChildRetrospective StudiesSurgical repairHernia DiaphragmaticRespiratory distressbusiness.industryInfantmedicine.diseaseSurgeryLiver TransplantationChild PreschoolPediatrics Perinatology and Child HealthVomiting030211 gastroenterology & hepatologySurgerymedicine.symptombusinessComplicationEuropean journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie
researchProduct