FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2074478904> ?p ?o ?g. }

• W2074478904 endingPage "158" @default.
• W2074478904 startingPage "152" @default.
• W2074478904 abstract "BackgroundWe sought to describe current outcomes and risk factors for mortality for fetuses diagnosed with absent pulmonary valve syndrome (APV). Fetuses with APV were divided into two cohorts, those with underlying tetralogy of Fallot (TOF/APV) and those without underlying TOF and either an intact ventricular septum or small ventricular septal defect (APV/IVS).MethodsThe fetal echocardiographic database was reviewed from January 1, 2001, until June 1, 2010, and all subjects with a diagnosis of APV were included. Multiple clinical and fetal echocardiographic measurements were recorded. Statistical analysis was performed by χ2 analysis and t tests. Survival analysis was performed by Kaplan-Meier analysis. Significant relationships between variables were explored by regression analysis. Significance was set at p = 0.05.ResultsThe cohort consisted of 15 fetuses with TOF/APV and 6 fetuses with APV/IVS. There were no fetal demises in either cohort. Survival to birth was 71% in the TOF/APV cohort and 83% in the APV/IVS cohort (p = 0.62). Of subjects born alive, survival was 80% for both cohorts (p = 0.95). However, in the APV/IVS cohort, transplantation-free survival was only 20%. Underlying single-ventricle physiology strongly predicted those who underwent heart transplantation (p = 0.003, R2 = 0.50). For the entire APV cohort, left ventricular dysfunction (p = 0.005, R2 = 0.41) and a higher pulmonary artery valve–to–aortic valve ratio (p = 0.02, R2 = 0.34) predicted mortality.ConclusionsPostnatal outcomes continue to improve for fetuses with APV syndrome. Left ventricular dysfunction and higher pulmonary artery valve–to–aortic valve ratio accurately predict postnatal mortality for fetuses with APV. We sought to describe current outcomes and risk factors for mortality for fetuses diagnosed with absent pulmonary valve syndrome (APV). Fetuses with APV were divided into two cohorts, those with underlying tetralogy of Fallot (TOF/APV) and those without underlying TOF and either an intact ventricular septum or small ventricular septal defect (APV/IVS). The fetal echocardiographic database was reviewed from January 1, 2001, until June 1, 2010, and all subjects with a diagnosis of APV were included. Multiple clinical and fetal echocardiographic measurements were recorded. Statistical analysis was performed by χ2 analysis and t tests. Survival analysis was performed by Kaplan-Meier analysis. Significant relationships between variables were explored by regression analysis. Significance was set at p = 0.05. The cohort consisted of 15 fetuses with TOF/APV and 6 fetuses with APV/IVS. There were no fetal demises in either cohort. Survival to birth was 71% in the TOF/APV cohort and 83% in the APV/IVS cohort (p = 0.62). Of subjects born alive, survival was 80% for both cohorts (p = 0.95). However, in the APV/IVS cohort, transplantation-free survival was only 20%. Underlying single-ventricle physiology strongly predicted those who underwent heart transplantation (p = 0.003, R2 = 0.50). For the entire APV cohort, left ventricular dysfunction (p = 0.005, R2 = 0.41) and a higher pulmonary artery valve–to–aortic valve ratio (p = 0.02, R2 = 0.34) predicted mortality. Postnatal outcomes continue to improve for fetuses with APV syndrome. Left ventricular dysfunction and higher pulmonary artery valve–to–aortic valve ratio accurately predict postnatal mortality for fetuses with APV." @default.
• W2074478904 created "2016-06-24" @default.
• W2074478904 creator A5016817705 @default.
• W2074478904 creator A5030095581 @default.
• W2074478904 creator A5050468322 @default.
• W2074478904 creator A5061270027 @default.
• W2074478904 creator A5067306790 @default.
• W2074478904 creator A5069111250 @default.
• W2074478904 creator A5085499902 @default.
• W2074478904 date "2014-07-01" @default.
• W2074478904 modified "2023-10-10" @default.
• W2074478904 title "Anatomic Variability and Outcome in Prenatally Diagnosed Absent Pulmonary Valve Syndrome" @default.
• W2074478904 cites W1504663184 @default.
• W2074478904 cites W1602804910 @default.
• W2074478904 cites W1862834441 @default.
• W2074478904 cites W1882642303 @default.
• W2074478904 cites W1949881782 @default.
• W2074478904 cites W1972822383 @default.
• W2074478904 cites W1980219915 @default.
• W2074478904 cites W1990115816 @default.
• W2074478904 cites W1990216300 @default.
• W2074478904 cites W1994442197 @default.
• W2074478904 cites W1995949968 @default.
• W2074478904 cites W2001910652 @default.
• W2074478904 cites W2026579017 @default.
• W2074478904 cites W2033583026 @default.
• W2074478904 cites W2041217621 @default.
• W2074478904 cites W2048260781 @default.
• W2074478904 cites W2060656764 @default.
• W2074478904 cites W2069373747 @default.
• W2074478904 cites W2077268685 @default.
• W2074478904 cites W2086370232 @default.
• W2074478904 cites W2092203519 @default.
• W2074478904 cites W2096420428 @default.
• W2074478904 cites W2113786392 @default.
• W2074478904 cites W2131960198 @default.
• W2074478904 cites W2936648692 @default.
• W2074478904 doi "https://doi.org/10.1016/j.athoracsur.2014.03.002" @default.
• W2074478904 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24793686" @default.
• W2074478904 hasPublicationYear "2014" @default.
• W2074478904 type Work @default.
• W2074478904 sameAs 2074478904 @default.
• W2074478904 citedByCount "33" @default.
• W2074478904 countsByYear W20744789042015 @default.
• W2074478904 countsByYear W20744789042016 @default.
• W2074478904 countsByYear W20744789042017 @default.
• W2074478904 countsByYear W20744789042018 @default.
• W2074478904 countsByYear W20744789042019 @default.
• W2074478904 countsByYear W20744789042020 @default.
• W2074478904 countsByYear W20744789042021 @default.
• W2074478904 countsByYear W20744789042022 @default.
• W2074478904 countsByYear W20744789042023 @default.
• W2074478904 crossrefType "journal-article" @default.
• W2074478904 hasAuthorship W2074478904A5016817705 @default.
• W2074478904 hasAuthorship W2074478904A5030095581 @default.
• W2074478904 hasAuthorship W2074478904A5050468322 @default.
• W2074478904 hasAuthorship W2074478904A5061270027 @default.
• W2074478904 hasAuthorship W2074478904A5067306790 @default.
• W2074478904 hasAuthorship W2074478904A5069111250 @default.
• W2074478904 hasAuthorship W2074478904A5085499902 @default.
• W2074478904 hasBestOaLocation W20744789041 @default.
• W2074478904 hasConcept C126322002 @default.
• W2074478904 hasConcept C141071460 @default.
• W2074478904 hasConcept C164705383 @default.
• W2074478904 hasConcept C172680121 @default.
• W2074478904 hasConcept C201903717 @default.
• W2074478904 hasConcept C2778646171 @default.
• W2074478904 hasConcept C2778921608 @default.
• W2074478904 hasConcept C2779234561 @default.
• W2074478904 hasConcept C2779895586 @default.
• W2074478904 hasConcept C2780074459 @default.
• W2074478904 hasConcept C2780940725 @default.
• W2074478904 hasConcept C54355233 @default.
• W2074478904 hasConcept C71924100 @default.
• W2074478904 hasConcept C72563966 @default.
• W2074478904 hasConcept C86803240 @default.
• W2074478904 hasConceptScore W2074478904C126322002 @default.
• W2074478904 hasConceptScore W2074478904C141071460 @default.
• W2074478904 hasConceptScore W2074478904C164705383 @default.
• W2074478904 hasConceptScore W2074478904C172680121 @default.
• W2074478904 hasConceptScore W2074478904C201903717 @default.
• W2074478904 hasConceptScore W2074478904C2778646171 @default.
• W2074478904 hasConceptScore W2074478904C2778921608 @default.
• W2074478904 hasConceptScore W2074478904C2779234561 @default.
• W2074478904 hasConceptScore W2074478904C2779895586 @default.
• W2074478904 hasConceptScore W2074478904C2780074459 @default.
• W2074478904 hasConceptScore W2074478904C2780940725 @default.
• W2074478904 hasConceptScore W2074478904C54355233 @default.
• W2074478904 hasConceptScore W2074478904C71924100 @default.
• W2074478904 hasConceptScore W2074478904C72563966 @default.
• W2074478904 hasConceptScore W2074478904C86803240 @default.
• W2074478904 hasIssue "1" @default.
• W2074478904 hasLocation W20744789041 @default.
• W2074478904 hasLocation W20744789042 @default.
• W2074478904 hasOpenAccess W2074478904 @default.
• W2074478904 hasPrimaryLocation W20744789041 @default.
• W2074478904 hasRelatedWork W2013930956 @default.
• W2074478904 hasRelatedWork W2016296403 @default.

• next