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1000 Titel
  • Prenatal diagnosis, associated findings and postnatal outcome in fetuses with congenitally corrected transposition of the great arteries
1000 Autor/in
  1. Krummholz, Andrea |
  2. Gottschalk, I. |
  3. Geipel, A. |
  4. Herberg, U. |
  5. Berg, C. |
  6. Gembruch, U. |
  7. Hellmund, A. |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-11-20
1000 Erschienen in
1000 Quellenangabe
  • 303(6):1469-1481
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00404-020-05886-8 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8087597/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Purpose!#!To analyze anatomic features and associated malformations in 37 prenatally detected cases of congenitally corrected transposition of the great arteries (ccTGA) and to evaluate the prenatal course, neonatal outcome and mid-term follow-up.!##!Methods!#!Retrospective analysis of prenatal ultrasound of 37 patients with ccTGA in two tertiary centers between 1999 and 2019. All fetuses received fetal echocardiography and a detailed anomaly scan. Postnatal outcome and follow-up data were retrieved from pediatric reports.!##!Results!#!Isolated ccTGA without associated cardiac anomalies was found in 13.5% (5/37), in all other fetuses additional defects such as VSD (73.0%), pulmonary obstruction (35.1%), tricuspid valve anomalies (18.9%), aortic arch anomalies (13.5%), ventricular hypoplasia (5.4%) or atrioventricular block (5.4%) were present. The rate of extracardiac malformations or chromosomal aberrations was low. There were 91.9% (34/37) live births and postnatal survival rates reached 91.2% in a mean follow-up time of 4.98 years. The prenatal diagnosis of ccTGA was confirmed postnatally in all but one documented live birth and the prenatal counselling regarding the expected treatment after birth (uni- versus biventricular repair) was reassured in the majority of cases. The postnatal intervention rate was high, 64.7% (22/34) received surgery, the intervention-free survival was 36.7%, 35.0% and 25.0% at 1 month, 1 year and 10 years, respectively.!##!Conclusions!#!ccTGA is a rare heart defect often associated with additional heterogeneous cardiac anomalies that can be diagnosed prenatally. The presented study demonstrates a favorable outcome in most cases but the majority of patients require surgical treatment early in life.
1000 Sacherschließung
lokal Fetus/diagnostic imaging [MeSH]
lokal Infant, Newborn [MeSH]
lokal Female [MeSH]
lokal Fetus
lokal Prenatal Diagnosis [MeSH]
lokal Transposition of Great Vessels/surgery [MeSH]
lokal Humans [MeSH]
lokal Postnatal Care [MeSH]
lokal Ultrasonography, Prenatal [MeSH]
lokal Atrioventricular discordance
lokal Retrospective Studies [MeSH]
lokal Pregnancy Outcome [MeSH]
lokal Corrected transposition
lokal Prenatal diagnosis
lokal Male [MeSH]
lokal Transposition of Great Vessels/diagnostic imaging [MeSH]
lokal Congenital heart disease
lokal Congenitally Corrected Transposition of the Great Arteries/diagnostic imaging [MeSH]
lokal Maternal-Fetal Medicine
lokal Echocardiography/methods [MeSH]
lokal Child [MeSH]
lokal Pregnancy [MeSH]
lokal Fetal echocardiography
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-9307-2710|https://frl.publisso.de/adhoc/uri/R290dHNjaGFsaywgSS4=|https://frl.publisso.de/adhoc/uri/R2VpcGVsLCBBLg==|https://frl.publisso.de/adhoc/uri/SGVyYmVyZywgVS4=|https://frl.publisso.de/adhoc/uri/QmVyZywgQy4=|https://frl.publisso.de/adhoc/uri/R2VtYnJ1Y2gsIFUu|https://frl.publisso.de/adhoc/uri/SGVsbG11bmQsIEEu
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1000 Erstellt am 2023-11-16T20:51:53.066+0100
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1000 Zuletzt bearbeitet 2023-12-01T03:50:33.912+0100
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