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Clinical Course and Outcome of Non-Immune Fetal Hydrops in Singleton Pregnancies

Nonimmune fetal hydrops is a condition defined by abnormal fluid accumulation in two or more body compartments. The aim is to evaluate factors associated with adverse outcome in diagnosed fetal hydrops and to investigate the aspects for the decision making in the case of termination of pregnancy. Th...

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Autores principales: Reischer, Theresa, Muth, Bernadette, Catic, Anja, Monod, Cécile, Linder, Tina, Göbl, Christian, Yerlikaya-Schatten, Gülen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836777/
https://www.ncbi.nlm.nih.gov/pubmed/35160154
http://dx.doi.org/10.3390/jcm11030702
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author Reischer, Theresa
Muth, Bernadette
Catic, Anja
Monod, Cécile
Linder, Tina
Göbl, Christian
Yerlikaya-Schatten, Gülen
author_facet Reischer, Theresa
Muth, Bernadette
Catic, Anja
Monod, Cécile
Linder, Tina
Göbl, Christian
Yerlikaya-Schatten, Gülen
author_sort Reischer, Theresa
collection PubMed
description Nonimmune fetal hydrops is a condition defined by abnormal fluid accumulation in two or more body compartments. The aim is to evaluate factors associated with adverse outcome in diagnosed fetal hydrops and to investigate the aspects for the decision making in the case of termination of pregnancy. Therefore, a retrospective data analysis of pregnancies complicated by non-immune hydrops fetalis between 2004 and 2018 was performed in a single tertiary referral center. Of 361 pregnancies with diagnosed fetal hydrops, in 183 cases (50.7%), the parents decided to terminate the pregnancy. A strong relationship between etiology and termination of pregnancy was demonstrated, whereas the highest rates of termination of pregnancy were found if a chromosomal aberration was diagnosed. Of the remaining 178 cases, 51 cases (28.7%) had a miscarriage, 33 cases (18.5%) had an intrauterine fetal death, and 94 cases (52.8%) were live born, whereas 26 (27.7%) of these offspring died within the first week of life. The risk of an adverse outcome increased with lower gestational age at diagnosis (p < 0.001). A nuchal translucency thickness greater than 2.5 mm was associated with an adverse outcome (p < 0.01). Furthermore, pregnancies with adverse outcome had significantly more affected compartments (median: 3; IQR 2), compared with live born cases (median: 2; IQR 1; p < 0.01). In conclusion, adverse outcome in pregnancies with fetal hydrops was associated with a lower gestational age at diagnosis, nuchal translucency greater than 2.5 mm and a higher count of affected compartments. These results confirm that a precise clinical workup to identify the underlying etiology of non-immune fetal hydrops is essential for a better prognostic assessment and accurate counselling of parents.
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spelling pubmed-88367772022-02-12 Clinical Course and Outcome of Non-Immune Fetal Hydrops in Singleton Pregnancies Reischer, Theresa Muth, Bernadette Catic, Anja Monod, Cécile Linder, Tina Göbl, Christian Yerlikaya-Schatten, Gülen J Clin Med Article Nonimmune fetal hydrops is a condition defined by abnormal fluid accumulation in two or more body compartments. The aim is to evaluate factors associated with adverse outcome in diagnosed fetal hydrops and to investigate the aspects for the decision making in the case of termination of pregnancy. Therefore, a retrospective data analysis of pregnancies complicated by non-immune hydrops fetalis between 2004 and 2018 was performed in a single tertiary referral center. Of 361 pregnancies with diagnosed fetal hydrops, in 183 cases (50.7%), the parents decided to terminate the pregnancy. A strong relationship between etiology and termination of pregnancy was demonstrated, whereas the highest rates of termination of pregnancy were found if a chromosomal aberration was diagnosed. Of the remaining 178 cases, 51 cases (28.7%) had a miscarriage, 33 cases (18.5%) had an intrauterine fetal death, and 94 cases (52.8%) were live born, whereas 26 (27.7%) of these offspring died within the first week of life. The risk of an adverse outcome increased with lower gestational age at diagnosis (p < 0.001). A nuchal translucency thickness greater than 2.5 mm was associated with an adverse outcome (p < 0.01). Furthermore, pregnancies with adverse outcome had significantly more affected compartments (median: 3; IQR 2), compared with live born cases (median: 2; IQR 1; p < 0.01). In conclusion, adverse outcome in pregnancies with fetal hydrops was associated with a lower gestational age at diagnosis, nuchal translucency greater than 2.5 mm and a higher count of affected compartments. These results confirm that a precise clinical workup to identify the underlying etiology of non-immune fetal hydrops is essential for a better prognostic assessment and accurate counselling of parents. MDPI 2022-01-28 /pmc/articles/PMC8836777/ /pubmed/35160154 http://dx.doi.org/10.3390/jcm11030702 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Reischer, Theresa
Muth, Bernadette
Catic, Anja
Monod, Cécile
Linder, Tina
Göbl, Christian
Yerlikaya-Schatten, Gülen
Clinical Course and Outcome of Non-Immune Fetal Hydrops in Singleton Pregnancies
title Clinical Course and Outcome of Non-Immune Fetal Hydrops in Singleton Pregnancies
title_full Clinical Course and Outcome of Non-Immune Fetal Hydrops in Singleton Pregnancies
title_fullStr Clinical Course and Outcome of Non-Immune Fetal Hydrops in Singleton Pregnancies
title_full_unstemmed Clinical Course and Outcome of Non-Immune Fetal Hydrops in Singleton Pregnancies
title_short Clinical Course and Outcome of Non-Immune Fetal Hydrops in Singleton Pregnancies
title_sort clinical course and outcome of non-immune fetal hydrops in singleton pregnancies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836777/
https://www.ncbi.nlm.nih.gov/pubmed/35160154
http://dx.doi.org/10.3390/jcm11030702
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