Search results for "OUTCOME"

showing 10 items of 5148 documents

A Decision-Tree Approach to Assist in Forecasting the Outcomes of the Neonatal Brain Injury

2021

Neonatal brain injury or neonatal encephalopathy (NE) is a significant morbidity and mortality factor in preterm and full-term newborns. NE has an incidence in the range of 2.5 to 3.5 per 1000 live births carrying a considerable burden for neurological outcomes such as epilepsy, cerebral palsy, cognitive impairments, and hydrocephaly. Many scoring systems based on different risk factor combinations in regression models have been proposed to predict abnormal outcomes. Birthweight, gestational age, Apgar scores, pH, ultrasound and MRI biomarkers, seizures onset, EEG pattern, and seizure duration were the most referred predictors in the literature. Our study proposes a decision-tree approach b…

Pediatricsmedicine.medical_specialtyHealth Toxicology and MutagenesisEncephalopathyArticleCerebral palsy03 medical and health sciencesEpilepsy0302 clinical medicinePregnancySeizuresMedicinerisk factorsHumans030212 general & internal medicineRisk factorRetrospective StudiesEpilepsyneonatal brain injuryneurodevelopmentbusiness.industryNeonatal encephalopathyRPublic Health Environmental and Occupational Healthabnormal outcomesInfant NewbornGestational ageInfantElectroencephalographyOdds ratiomedicine.diseasedecision-tree algorithmsBrain InjuriesApgar ScoreMedicineApgar scoreFemalebusiness030217 neurology & neurosurgeryInternational Journal of Environmental Research and Public Health
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Electroclinical features and outcome of ANKRD11-related KBG syndrome: A novel report and literature review.

2021

KBG syndrome (OMIM #148050) is a rare autosomal dominant disorder, typically characterized by macrodontia of the upper central incisors, distinct craniofacial findings, short stature, and skeletal anomalies associated with neurological involvement including intellectual disability, behaviour difficulties, and epilepsy. KBG syndrome is associated with mutations in ANKRD11 gene that plays a chromatin regulator role of histone acetylation and gene expression during neurogenesis in the embryonic brain.

Pediatricsmedicine.medical_specialtyKBGAdolescentseizureOutcome (game theory)ANKRD11EpilepsySeizuresIntellectual DisabilityMedicineHumansAbnormalities MultipleBone Diseases Developmentalbusiness.industryTooth AbnormalitiesFaciesHigh-Throughput Nucleotide SequencingGeneral MedicineKBG SYNDROMESyndromemedicine.diseaseKBG syndromeRepressor ProteinsPhenotypeNeurologySlowing EEG activityANKRD11; KBG; Seizures; Slowing EEG activity; SyndromeFemaleNeurology (clinical)businessSeizure
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Subjective Assessment of Head and Facial Appearance in Children with Craniosynostoses after Surgical Treatment

2018

Background: Craniosynostoses are congenital defects in the construction of the skull involving premature fusion of one or more cranial sutures. Premature fusion of sutures causes characteristic skull deformation(s). This affect the structure and thus the appearance of the entire head and face. The aim of this study was to analyze parents&rsquo

Pediatricsmedicine.medical_specialtyLeadership and ManagementHead (linguistics)craniosinostosis; results of surgery; craniofacial disfigurement; clinical survey; subjective assessment; surgical outcomeslcsh:MedicineHealth Informaticscraniofacial disfigurementCraniosynostosessurgical outcomesAffect (psychology)ArticleCraniosynostosis03 medical and health sciencesInterpersonal relationship0302 clinical medicineHealth Information ManagementmedicinecraniosinostosisSurgical treatmentclinical surveybusiness.industryHealth Policylcsh:Rsubjective assessmentmedicine.diseaseFacial appearanceSkullmedicine.anatomical_structure030220 oncology & carcinogenesisresults of surgerybusiness030217 neurology & neurosurgeryHealthcare
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Efficacy of levetiracetam in the treatment of drug-resistant Rett Syndrome.

2010

Rett syndrome (RTT) is a progressive neurological disorder characterized by a wide spectrum of phenotypes. Epilepsy is reported to occur in 50–90% of patients with RTT; some develop medically refractory epilepsy. The aim of this study is to investigate the efficacy of levetiracetam (LEV) in drug-resistant patients with RTT. This prospective, pragmatic, open-label study consisted of an 8-week baseline period and a 6-month evaluation period. Efficacy variable was the mean frequency of monthly seizures before, and after 3 and 6 months of treatment with LEV. Eight female patients, aged 7.5–19 years (M12.8 ± 5) entered the study. Mean age at epilepsy onset was 25.8 ± 14.1 months. All patients sh…

Pediatricsmedicine.medical_specialtyLevetiracetamAdolescentMethyl-CpG-Binding Protein 2medicine.medical_treatmentRett syndromeNeurological disorderDrug Administration ScheduleCentral nervous system diseasedrug therapy/geneticsYoung AdultEpilepsyanalogs /&/ derivatives/therapeutic useSeizuresConvulsionmedicineRett SyndromeHumansgeneticsEEGProspective StudiesMyoclonic seizuresChildProspective cohort studyPsychiatryDrug-resistanceAnalysis of Variancebusiness.industryPatient SelectionFocal seizureElectroencephalographymedicine.diseaseAdolescent Analysis of Variance Anticonvulsants; therapeutic use Child Drug Administration Schedule Electroencephalography Female Humans Methyl-CpG-Binding Protein 2; genetics Patient Selection Piracetam; analogs /&/ derivatives/therapeutic use Prospective Studies Quality of Life Rett Syndrome; drug therapy/genetics Seizures; drug therapy/genetics Treatment Outcome Young AdultPiracetamSettore MED/39 - Neuropsichiatria InfantileTreatment OutcomeAnticonvulsantNeurologytherapeutic useQuality of LifeAnticonvulsantsFemaleNeurology (clinical)Levetiracetammedicine.symptombusinessmedicine.drug
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Health Outcomes of Infants with Vitamin B12 Deficiency Identified by Newborn Screening and Early Treated

2021

Objective To evaluate the clinical outcomes at age 1.5 ± 0.5 years of infants with vitamin B12 deficiency identified by newborn screening (NBS). Study design Prospective multicenter observational study on health outcomes of 31 infants with vitamin B12 deficiency identified by NBS. Neurodevelopment was assessed by the Denver Developmental Screening Test. Results In 285 862 newborns screened between 2016 and 2019, the estimated birth prevalence of vitamin B12 deficiency was 26 in 100 000 newborns, with high seasonal variations (lowest in summer: 8 in 100 000). Infants participating in the outcome study (N = 31) were supplemented with vitamin B12 for a median (range) of 5.9 (1.1-16.2) months. …

Pediatricsmedicine.medical_specialtyNewborn screeningbusiness.industryDenver Developmental Screening TestPrenatal careHealth outcomes03 medical and health sciences0302 clinical medicine030225 pediatricsPediatrics Perinatology and Child HealthmedicineObservational study030212 general & internal medicineVitamin B12businessThe Journal of Pediatrics
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Aortopexy in esophageal atresia: Long-term experience of a parent support group

2001

Abstract Purpose: The aim of this study was to obtain the parents' view of aortopexy after esophageal atresia. Methods: A questionnaire was completed by the parents of 24 former patients, now aged from 1 to 15 years (average, 8.9; median, 9.0 years). The respondents were all members of a support group. Results: The median age of the patients receiving aortopexy was 4 months. The 24 procedures were performed in 16 different hospitals. The subjects had experienced a median of 3 apneic attacks. Technical complications occurred in 4 of the 24 children. In 71%, aortopexy was an immediate success. Conclusion: Despite its low success rate compared with centers with large cumulative experience, 90%…

Pediatricsmedicine.medical_specialtyParent supportmedicine.medical_treatmentSupport groupmedicineHumansEsophagusChildEsophageal AtresiaAortabusiness.industryEsophageal diseaseInfantAortopexyGeneral Medicinemedicine.diseaseTreatment Outcomemedicine.anatomical_structureEl NiñoPatient SatisfactionChild PreschoolAtresiaPediatrics Perinatology and Child HealthApneic attacksSurgerybusinessJournal of Pediatric Surgery
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Prematurity and twinning

2012

Aim of the study: Newborns from multiple pregnancies are increasing in number and demonstrate a higher perinatal morbidity and mortality compared to singletons. Prematurity is the main reason for most neonatal diseases in twins, but other variables may play a role and their prenatal evaluation may improve the overall outcome. Main findings: Prematurity is six times more frequent in twins and therefore birth weight is significantly lower compared to singletons. Thus, twins are more exposed to prematurity related diseases (respiratory, cardiovas- cular, infectious, etc.) and to long-term complications (especially neurological disabilities). Results: It is very difficult to estimate the increa…

Pediatricsmedicine.medical_specialtyPregnancybusiness.industryDiscordance growth morbidity mortality outcome prematurity twinningInfant NewbornTwinsMEDLINEObstetrics and Gynecologymedicine.diseaseNervous SystemPerinatal morbiditySettore MED/38 - Pediatria Generale E SpecialisticaPregnancyPediatrics Perinatology and Child HealthmedicineHumansPremature BirthEthics MedicalFemalePregnancy MultiplebusinessInfant PrematureThe Journal of Maternal-Fetal & Neonatal Medicine
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Symptomatic seizures in preterm newborns: A review on clinical features and prognosis

2018

Abstract Neonatal seizures are the most common neurological event in newborns, showing higher prevalence in preterm than in full-term infants. In the majority of cases they represent acute symptomatic phenomena, the main etiologies being intraventricular haemorrhage, hypoxic-ischemic encephalopathy, central nervous system infections and transient metabolic derangements. Current definition of neonatal seizures requires detection of paroxysmal EEG-changes, and in preterm newborns the incidence of electrographic-only seizures seems to be particularly high, further stressing the crucial role of electroencephalogram monitoring in this population. Imaging work-up includes an integration of serial…

Pediatricsmedicine.medical_specialtyPrognosiDevelopmental DisabilitiesPopulationEncephalopathyInfant Premature DiseasesReviewElectroencephalographyCerebral palsy03 medical and health sciencesEpilepsy0302 clinical medicineRisk FactorsSeizures030225 pediatricsmedicineNewborn; Outcome; Prognosis; Seizures; TreatmentHumanseducationNeurophysiological MonitoringUltrasonographyOutcomeeducation.field_of_studymedicine.diagnostic_testbusiness.industryInfant Newbornlcsh:RJ1-570BrainSymptomatic seizuresElectroencephalographylcsh:PediatricsGeneral MedicineOff-Label Usemedicine.diseaseNewbornPrognosisMagnetic Resonance ImagingNeurophysiological MonitoringSeizureTreatmentEtiologyAnticonvulsantsbusiness030217 neurology & neurosurgeryInfant Premature
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Multi-spectral Pattern of Clinical Presentation and the Resultant Outcome in Central Nervous System Tuberculosis: A Single Center Study on the Ubiqui…

2020

Central nervous system (CNS) tuberculosis (TB) is a great medical masquerader having a multi-spectral pattern of clinical presentation, thereby complicating early diagnosis and appropriate management. This review article describes clinical presentation of CNS TB in a group of 47 patients, who were managed in the Nobel Medical College and Teaching Hospital in Biratnagar, Nepal during the last 2 years. We evaluated demographic profile, mode of management, and clinical outcome in these patients. The findings were that intracranial TB was present in 27 (57.5%) patients and the spinal involvement was in 20 (42.5%) patients. The most frequent presentation of the former was TB meningitis with hydr…

Pediatricsmedicine.medical_specialtyTuberculosisClinical outcomebusiness.industryDifferential diagnosimedicine.diseaseSingle CenterHydrocephalusReview articleMeningiti03 medical and health sciences0302 clinical medicineCentral nervous systemPott’s spinemedicineTuberculosis030212 general & internal medicinePresentation (obstetrics)Differential diagnosisbusinessAbscessMeningitis
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Experience with the Hellp-Syndrohe

1988

A total of 13 patients with HELLP-Syndrome were treated between 1980 and 1986 at the Mainz University Gynecology Clinic. The course of disease, complications, and fetal outcome observed do not permit generalized recommendations concerning treatment of this syndrome. The treatment plan should rather be based on the Individual situation, whereby the cesarean section has proven to be the preferred mode of delivery in almost all cases.

Pediatricsmedicine.medical_specialtybusiness.industryGeneral surgerySection (typography)Obstetrics and GynecologyDisease courseMode of deliveryTreatment planInternal MedicineGynecology clinicMedicineFetal outcomebusinessClinical and Experimental Hypertension. Part B: Hypertension in Pregnancy
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