Neonatal Jaundice
Mostrando 1-12 de 36 artigos, teses e dissertações.
-
1. Maternal-fetal alloimmunization: perinatal outcomes in a reference hospital in Northeastern Brazil
SUMMARY OBJECTIVE: To assess the prevalence of maternal alloantibodies in pregnant women at a maternity hospital in northeastern Brazil and describe their perinatal outcomes. METHODS: A retrospective cohort study reviewed maternal and newborn medical records between January 2017 and October 2018 to assess for the presence of maternal alloantibodies. RESUL
Revista da Associação Médica Brasileira. Publicado em: 2022
-
2. Cord blood bilirubin and prediction of neonatal hyperbilirubinemia and perinatal infection in newborns at risk of hemolysis
Abstract Objective To assess the accuracy of umbilical cord bilirubin values to predict jaundice in the first 48 h of life and neonatal infection. Method Newborn infants treated at a regional well-baby nursery born at ≥36 weeks of gestation were included in this retrospective cohort study. All infants born in a 3-year period from mothers with O blood typ
J. Pediatr. (Rio J.). Publicado em: 2021-08
-
3. Reply to Letter to the Editor - Association between sleep behavior and motor development in preterm infants
Abstract Objective To assess the accuracy of umbilical cord bilirubin values to predict jaundice in the first 48 h of life and neonatal infection. Method Newborn infants treated at a regional well-baby nursery born at ≥36 weeks of gestation were included in this retrospective cohort study. All infants born in a 3-year period from mothers with O blood typ
J. Pediatr. (Rio J.). Publicado em: 2021-08
-
4. AUTISM SPECTRUM DISORDER AND POSTNATAL FACTORS: A CASE-CONTROL STUDY IN BRAZIL
RESUMO Objetivo: Estimar, em uma população brasileira, a magnitude da associação entre o transtorno do espectro do autismo (TEA) e os fatores pós-natais. Métodos: Estudo de caso controle realizado com 253 indivíduos com diagnóstico do TEA e 886 sem sinais do transtorno. Foi aplicado um questionário semiestruturado e adotou-se o modelo de regress
Rev. paul. pediatr.. Publicado em: 18/07/2019
-
5. Polimorfismos nos genes das proteínas transportadoras de ânions orgânicos na hiperbilirrubinemia neonatal : um estudo de casos e controles
Jaundice usually is a physiological phenomenon among newborns; however, severe hyperbilirubinemia occurs in 5% to 6% of this population. It has been suggested that genetic variation in the genes of bilirubin transporters could enhance the risk of hyperbilirubinemia when co-expressed with other icterogenic conditions. The present study included newborns with
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 2012
-
6. Prevalência da deficiência da glicose-6-fosfato desidrogenase em doadores de sangue de Mossoró, Rio Grande do Norte
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzymopathy. It affects as many as 330 million individuals worldwide. This deficiency may determine neonatal jaundice, chronic nonspherocytic hemolytic anemia and acute hemolytic anemia induced by drugs, infections and broad bean ingestion. The efficacy of blood transfusion is decre
Revista Brasileira de Hematologia e Hemoterapia. Publicado em: 2010
-
7. Molecular characterization of glucose-6-phosphate dehidrogenase deficiency in patients from the southern brazilian city of Porto Alegre, RS
Glucose-6-phosphate dehydrogenase (G6PDH; EC 1.1.1.49) deficiency is one of the most common human enzymopathies throughout the world. Although most affected individuals are asymptomatic, there is a risk of neonatal jaundice and acute hemolytic anemia which can be triggered by infection, some pharmaceuticals and, in older individuals, eating fava beans. We ch
Publicado em: 2010
-
8. Polimorfismos genéticos em neonatos hiperbilirrubinêmicos com mais de 35 semanas de idade gestacional
A icterícia neonatal é geralmente benigna, mas desfechos desfavoráveis podem ocorrer e a identificação dos casos de maior risco seria muito útil. Alguns fatores de risco já conhecidos são prematuridade, desidratação, aleitamento materno, deficiência de G6PD e incompatibilidade sanguínea. As alterações na conjugação hepática de bilirrubina de
Publicado em: 2009
-
9. PROGRAMA DE TRIAGEM AUDITIVA NEONATAL: RESULTADOS DE SUA APLICAÇÃO EM UM HOSPITAL UNIVERSITÁRIO / NEWBORN HEARING SCREENING PROGRAM: RESULTS FROM HIS APPLICATION IN A UNIVERSITY HOSPITAL
Data collected during the implementation of the Neonatal Hearing Screening (NHS) need to be recorded, evaluated and disseminated in the scientific environment in order to ensure its quality and to encourage the creation and improvement of other services. Risk indicators (RI) for the hearing loss can influence in the occurrence of transients evoked otoacousti
Publicado em: 2009
-
10. Late-preterm birth with and without fetal growth restriction: neonatal outcomes / Prematuridade tardia com e sem restrição do crescimento fetal: resultados neonatais
The objective of this study was to compare neonatal morbidity and mortality between late-preterm infants (gestational age at birth: 34 to 36 weeks and 6 days) with and without fetal growth restriction (FGR). A longitudinal study was conducted between October 2004 and October 2006 involving 50 pregnant women with pre-term delivery associated with FGR (group I
Publicado em: 2008
-
11. Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in patients from the southern Brazilian city of Porto Alegre, RS
Glucose-6-phosphate dehydrogenase (G6PDH; EC 1.1.1.49) deficiency is one of the most common human enzymopathies throughout the world. Although most affected individuals are asymptomatic, there is a risk of neonatal jaundice and acute hemolytic anemia which can be triggered by infection, some pharmaceuticals and, in older individuals, eating fava beans. We ch
Genetics and Molecular Biology. Publicado em: 2007
-
12. Aspectos clinicos e laboratoriais da deficiencia de desidrogenase de 6 fosfato de glicose (G-6-PD) em recem-nascidos brasileiros
The etiological association of neonatal jaundice G-6-PD deficiency due to the African variant or A- variant has not been defined in previous works and Brazilian studies done in São Paulo and Bahia with different methodologies showed discordant results. The purpose of this work was to estabilish this association in a prospective study of 697 newborn infants
Publicado em: 1987