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Perinatal outcomes of intrauterine fetal arrhythmias: A 10-year retrospective cohort study

Sustained fetal arrhythmia can produce life-threatening fetal distress, fetal hemodynamic compromise, hydrops fetalis, or even fetal death. Survivors may subsequently possess severe neurologic deficits. We conducted a retrospective observational study of pregnant women hospitalized with fetal arrhyt...

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Autores principales: Hu, Qing, Liao, Hua, Xu, Tingting, Liu, Hongyan, Wang, Xiaodong, Yu, Haiyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9997811/
https://www.ncbi.nlm.nih.gov/pubmed/36897689
http://dx.doi.org/10.1097/MD.0000000000033244
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author Hu, Qing
Liao, Hua
Xu, Tingting
Liu, Hongyan
Wang, Xiaodong
Yu, Haiyan
author_facet Hu, Qing
Liao, Hua
Xu, Tingting
Liu, Hongyan
Wang, Xiaodong
Yu, Haiyan
author_sort Hu, Qing
collection PubMed
description Sustained fetal arrhythmia can produce life-threatening fetal distress, fetal hemodynamic compromise, hydrops fetalis, or even fetal death. Survivors may subsequently possess severe neurologic deficits. We conducted a retrospective observational study of pregnant women hospitalized with fetal arrhythmias from January 2011 to May 2020 at West China Second University Hospital, and fetal arrhythmias were diagnosed by specialists in cardiac ultrasonography. Of 90 cases of fetal arrhythmias, 14 (15.6%) were complicated by fetal congenital heart disease (CHD), 21 (23.33%) by fetal-hydrops, 15 (16.67%) cases by intrauterine therapy, and 6 (6.67%) by maternal auto-immune disease. In the fetal-hydrops group, the intrauterine therapy rate was significantly higher (47.62% vs 7.24%, P < .001) and the survival rate significantly lower (47.62% vs 92.75%, P < .001) than in the nonfetal hydrops group. A fetus whose arrhythmia was complicated by fetal-hydrops and CHD was delivered earlier and exhibited a lower cardiovascular profile score at diagnosis and birth, lower birth weight, and a higher rate of pregnancy termination than cases without hydrops and CHD (P < .05). Among the cases with maternal auto-immune disease, 71.43% (5/7) manifested fetal atrioventricular block. Multiple linear regression analysis revealed that 3 variables – fetal-hydrops (P < .001), body mass index (P = .014), and gestational age at diagnosis of fetal arrhythmia (P = .047) – were correlated with the gestational delivery age of arrhythmic fetuses. Parents should be counseled by the multidisciplinary team regarding the individualized management and prognosis of the arrhythmic fetus, and individualized fetal intrauterine therapy should be performed if necessary.
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spelling pubmed-99978112023-03-10 Perinatal outcomes of intrauterine fetal arrhythmias: A 10-year retrospective cohort study Hu, Qing Liao, Hua Xu, Tingting Liu, Hongyan Wang, Xiaodong Yu, Haiyan Medicine (Baltimore) 5600 Sustained fetal arrhythmia can produce life-threatening fetal distress, fetal hemodynamic compromise, hydrops fetalis, or even fetal death. Survivors may subsequently possess severe neurologic deficits. We conducted a retrospective observational study of pregnant women hospitalized with fetal arrhythmias from January 2011 to May 2020 at West China Second University Hospital, and fetal arrhythmias were diagnosed by specialists in cardiac ultrasonography. Of 90 cases of fetal arrhythmias, 14 (15.6%) were complicated by fetal congenital heart disease (CHD), 21 (23.33%) by fetal-hydrops, 15 (16.67%) cases by intrauterine therapy, and 6 (6.67%) by maternal auto-immune disease. In the fetal-hydrops group, the intrauterine therapy rate was significantly higher (47.62% vs 7.24%, P < .001) and the survival rate significantly lower (47.62% vs 92.75%, P < .001) than in the nonfetal hydrops group. A fetus whose arrhythmia was complicated by fetal-hydrops and CHD was delivered earlier and exhibited a lower cardiovascular profile score at diagnosis and birth, lower birth weight, and a higher rate of pregnancy termination than cases without hydrops and CHD (P < .05). Among the cases with maternal auto-immune disease, 71.43% (5/7) manifested fetal atrioventricular block. Multiple linear regression analysis revealed that 3 variables – fetal-hydrops (P < .001), body mass index (P = .014), and gestational age at diagnosis of fetal arrhythmia (P = .047) – were correlated with the gestational delivery age of arrhythmic fetuses. Parents should be counseled by the multidisciplinary team regarding the individualized management and prognosis of the arrhythmic fetus, and individualized fetal intrauterine therapy should be performed if necessary. Lippincott Williams & Wilkins 2023-03-10 /pmc/articles/PMC9997811/ /pubmed/36897689 http://dx.doi.org/10.1097/MD.0000000000033244 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle 5600
Hu, Qing
Liao, Hua
Xu, Tingting
Liu, Hongyan
Wang, Xiaodong
Yu, Haiyan
Perinatal outcomes of intrauterine fetal arrhythmias: A 10-year retrospective cohort study
title Perinatal outcomes of intrauterine fetal arrhythmias: A 10-year retrospective cohort study
title_full Perinatal outcomes of intrauterine fetal arrhythmias: A 10-year retrospective cohort study
title_fullStr Perinatal outcomes of intrauterine fetal arrhythmias: A 10-year retrospective cohort study
title_full_unstemmed Perinatal outcomes of intrauterine fetal arrhythmias: A 10-year retrospective cohort study
title_short Perinatal outcomes of intrauterine fetal arrhythmias: A 10-year retrospective cohort study
title_sort perinatal outcomes of intrauterine fetal arrhythmias: a 10-year retrospective cohort study
topic 5600
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9997811/
https://www.ncbi.nlm.nih.gov/pubmed/36897689
http://dx.doi.org/10.1097/MD.0000000000033244
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