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Prenatal diagnosis of persistent right umbilical vein – Incidence and clinical impact. A prospective study

BACKGROUND: Persistent right umbilical vein (PRUV) is usually an isolated finding but it may be accompanied by other fetal malformations. AIMS: We aimed to determine the incidence of prenatally diagnosed PRUV in a referral population, assess the neonatal outcome and discuss the findings together wit...

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Autores principales: Krzyżanowski, Arkadiusz, Swatowski, Dariusz, Gęca, Tomasz, Kwiatek, Maciej, Stupak, Aleksandra, Woźniak, Sławomir, Kwaśniewska, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585642/
https://www.ncbi.nlm.nih.gov/pubmed/29498037
http://dx.doi.org/10.1111/ajo.12791
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author Krzyżanowski, Arkadiusz
Swatowski, Dariusz
Gęca, Tomasz
Kwiatek, Maciej
Stupak, Aleksandra
Woźniak, Sławomir
Kwaśniewska, Anna
author_facet Krzyżanowski, Arkadiusz
Swatowski, Dariusz
Gęca, Tomasz
Kwiatek, Maciej
Stupak, Aleksandra
Woźniak, Sławomir
Kwaśniewska, Anna
author_sort Krzyżanowski, Arkadiusz
collection PubMed
description BACKGROUND: Persistent right umbilical vein (PRUV) is usually an isolated finding but it may be accompanied by other fetal malformations. AIMS: We aimed to determine the incidence of prenatally diagnosed PRUV in a referral population, assess the neonatal outcome and discuss the findings together with those from previous publications. MATERIALS AND METHODS: A total of 2360 women with low‐risk singleton pregnancies were examined in the second and third trimesters. A transabdominal convex volume transducer was used. B‐mode was applied in each patient. Scanning of the venous system included imaging of the target vessels with two‐dimensional colour Doppler mapping. The diagnosis of PRUV was made in a transverse section of the fetal abdomen. Three‐dimensional ultrasounds were performed as necessary, when anomalous cases were encountered. RESULTS: The incidence of PRUV in our population was 12/2360 = 0.5%, and it was higher than in other retrospective studies. In 75% (n = 9), PRUV was an isolated finding where delivery was uneventful and the postnatal outcome was favourable. In two cases PRUV was accompanied by omphalocele, and in one case by tetralogy of Fallot and single umbilical artery. CONCLUSIONS: PRUV is an uncommon prenatal finding. Screening for this anomaly can be easily performed in all pregnant patients. A diagnosis of PRUV should be followed by a thorough fetal morphology scan in order to exclude any other malformations, especially those of the cardiovascular system.
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spelling pubmed-65856422019-06-27 Prenatal diagnosis of persistent right umbilical vein – Incidence and clinical impact. A prospective study Krzyżanowski, Arkadiusz Swatowski, Dariusz Gęca, Tomasz Kwiatek, Maciej Stupak, Aleksandra Woźniak, Sławomir Kwaśniewska, Anna Aust N Z J Obstet Gynaecol Original Articles Obstetrics BACKGROUND: Persistent right umbilical vein (PRUV) is usually an isolated finding but it may be accompanied by other fetal malformations. AIMS: We aimed to determine the incidence of prenatally diagnosed PRUV in a referral population, assess the neonatal outcome and discuss the findings together with those from previous publications. MATERIALS AND METHODS: A total of 2360 women with low‐risk singleton pregnancies were examined in the second and third trimesters. A transabdominal convex volume transducer was used. B‐mode was applied in each patient. Scanning of the venous system included imaging of the target vessels with two‐dimensional colour Doppler mapping. The diagnosis of PRUV was made in a transverse section of the fetal abdomen. Three‐dimensional ultrasounds were performed as necessary, when anomalous cases were encountered. RESULTS: The incidence of PRUV in our population was 12/2360 = 0.5%, and it was higher than in other retrospective studies. In 75% (n = 9), PRUV was an isolated finding where delivery was uneventful and the postnatal outcome was favourable. In two cases PRUV was accompanied by omphalocele, and in one case by tetralogy of Fallot and single umbilical artery. CONCLUSIONS: PRUV is an uncommon prenatal finding. Screening for this anomaly can be easily performed in all pregnant patients. A diagnosis of PRUV should be followed by a thorough fetal morphology scan in order to exclude any other malformations, especially those of the cardiovascular system. John Wiley and Sons Inc. 2018-03-02 2019-02 /pmc/articles/PMC6585642/ /pubmed/29498037 http://dx.doi.org/10.1111/ajo.12791 Text en © 2018 The Authors. Australian and New Zealand Journal of Obstetrics and Gynaecology published by John Wiley & Sons Australia, Ltd on behalf of Royal Australian and New Zealand College of Obstetricians and Gynaecologists This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles Obstetrics
Krzyżanowski, Arkadiusz
Swatowski, Dariusz
Gęca, Tomasz
Kwiatek, Maciej
Stupak, Aleksandra
Woźniak, Sławomir
Kwaśniewska, Anna
Prenatal diagnosis of persistent right umbilical vein – Incidence and clinical impact. A prospective study
title Prenatal diagnosis of persistent right umbilical vein – Incidence and clinical impact. A prospective study
title_full Prenatal diagnosis of persistent right umbilical vein – Incidence and clinical impact. A prospective study
title_fullStr Prenatal diagnosis of persistent right umbilical vein – Incidence and clinical impact. A prospective study
title_full_unstemmed Prenatal diagnosis of persistent right umbilical vein – Incidence and clinical impact. A prospective study
title_short Prenatal diagnosis of persistent right umbilical vein – Incidence and clinical impact. A prospective study
title_sort prenatal diagnosis of persistent right umbilical vein – incidence and clinical impact. a prospective study
topic Original Articles Obstetrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585642/
https://www.ncbi.nlm.nih.gov/pubmed/29498037
http://dx.doi.org/10.1111/ajo.12791
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