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Ester Garne

Datos Biográficos

ID7603458
NOMBREEster Garne
NOMBRESEster
APELLIDOGarne
FIRMAGARNE E
AFILIACIONESLillebaelt Hospital
ORCID0000-0003-0430-2594
VERIFICADOSí
TOTAL DE OBRAS3
TOTAL DE CITAS0
TOTAL COMO AUTOR3
TOTAL COMO EDITOR0
PRIMER AÑO DE PUBLICACIÓN2018
AÑO MÁS RECIENTE DE PUBLICACIÓN2024
ÍNDICE H0
  • The Association of Prenatal Diagnoses with Mortality and Long-Term Morbidity in Children with Specific Isolated Congenital Anomalies

    Open Access•Anna Heino, Joan K Morris et al.•ARTICLE•Maternal and Child Health Journal•2024

    Our findings do not show improved outcomes for prenatally diagnosed infants. For conditions where prenatal diagnoses were associated with greater mortality and morbidity, the findings might be attributed to increased detection of more severe anomalies. The increased mortality and morbidity in those diagnosed prenatally may be related to the lower mean gestational age (GA) at birth, leading to insufficient surfactant for respiratory effort. This i…

  • Hospital Length of Stay and Surgery among European Children with Rare Structural Congenital Anomalies—A Population-Based Data Linkage Study

    Open Access•Ester Garne, Joachim Tan et al.•ARTICLE•International Journal of…•2023

    Little is known about morbidity for children with rare structural congenital anomalies. This European, population-based data-linkage cohort study analysed data on hospitalisations and surgical procedures for 5948 children born 1995-2014 with 18 rare structural congenital anomalies from nine EUROCAT registries in five countries. In the first year of life, the median length of stay (LOS) ranged from 3.5 days (anotia) to 53.8 days (atresia of bile d…

  • Eurocat

    Open Access•F D Tucker, Joan K Morris et al.•ARTICLE•Journal of Community Genetics•2018

Sin obras prominentes en esta página.

  • Eurocat

    Open Access•F D Tucker, Joan K Morris et al.•ARTICLE•Journal of Community Genetics•2018

  • Hospital Length of Stay and Surgery among European Children with Rare Structural Congenital Anomalies—A Population-Based Data Linkage Study

    Open Access•Ester Garne, Joachim Tan et al.•ARTICLE•International Journal of…•2023

    Little is known about morbidity for children with rare structural congenital anomalies. This European, population-based data-linkage cohort study analysed data on hospitalisations and surgical procedures for 5948 children born 1995-2014 with 18 rare structural congenital anomalies from nine EUROCAT registries in five countries. In the first year of life, the median length of stay (LOS) ranged from 3.5 days (anotia) to 53.8 days (atresia of bile d…

  • The Association of Prenatal Diagnoses with Mortality and Long-Term Morbidity in Children with Specific Isolated Congenital Anomalies

    Open Access•Anna Heino, Joan K Morris et al.•ARTICLE•Maternal and Child Health Journal•2024

    Our findings do not show improved outcomes for prenatally diagnosed infants. For conditions where prenatal diagnoses were associated with greater mortality and morbidity, the findings might be attributed to increased detection of more severe anomalies. The increased mortality and morbidity in those diagnosed prenatally may be related to the lower mean gestational age (GA) at birth, leading to insufficient surfactant for respiratory effort. This i…

Congenital Anomalies and Fetal Surgery (3 obras) · Medicine (3 obras) · Pathology (2 obras) · Pediatrics (2 obras) · Public health (2 obras) · Biology (1 obra) · Cohort (1 obra) · Cohort study (1 obra) · Congenital Diaphragmatic Hernia Studies (1 obra) · Congenital Heart Disease Studies (1 obra)

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