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Outcomes of sustained fetal tachyarrhythmias after transplacental treatment
BACKGROUND: Fetal tachyarrhythmia is a condition that may lead to cardiac dysfunction, hydrops, and death. Despite a transplacental treatment, failure to obtain or maintain sinus rhythm may occur. OBJECTIVE: We aimed to analyze the perinatal outcomes of sustained fetal tachyarrhythmias after in uter...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183966/ https://www.ncbi.nlm.nih.gov/pubmed/34113918 http://dx.doi.org/10.1016/j.hroo.2021.02.006 |
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author | Bartin, Raphael Maltret, Alice Nicloux, Muriel Ville, Yves Bonnet, Damien Stirnemann, Julien |
author_facet | Bartin, Raphael Maltret, Alice Nicloux, Muriel Ville, Yves Bonnet, Damien Stirnemann, Julien |
author_sort | Bartin, Raphael |
collection | PubMed |
description | BACKGROUND: Fetal tachyarrhythmia is a condition that may lead to cardiac dysfunction, hydrops, and death. Despite a transplacental treatment, failure to obtain or maintain sinus rhythm may occur. OBJECTIVE: We aimed to analyze the perinatal outcomes of sustained fetal tachyarrhythmias after in utero treatment. METHODS: We performed a retrospective evaluation of 69 cases with sustained fetal tachyarrhythmia. We compared the perinatal and long-term outcomes of prenatally converted and drug-resistant fetuses. Tachyarrhythmia subtypes were also evaluated. RESULTS: Conversion to sinus rhythm was obtained in 74% of cases; 26% of cases were drug-resistant and delivered arrhythmic. Three perinatal deaths occurred in both groups (6.7% vs 17%, P = .34). Neonates delivered arrhythmic were more frequently admitted to neonatal intensive care units (75% vs 31%, P < .01), and their hospital stay was longer (20.9 vs 6.64 days, P < .001). Multiple neonatal recurrences (81% vs 11%, P < .001), temporary hemodynamic dysfunction or heart failure (50% vs 6.7%, P < .001), and postnatal use of a combination treatment (44% vs 13%, P = .028) were also more frequent in this population. Beyond the neonatal period, rates of recurrences within the first 16 months were higher in drug-resistant fetuses (HR = 16.14, CI 95% [4.485; 193.8], P < .001). In this population, postnatal electrocardiogram revealed an overrepresentation of rare mechanisms, especially permanent junctional reciprocating tachycardia (PJRT) (31%). CONCLUSION: Prenatal conversion to stable sinus rhythm is a major determinant of perinatal and long-term outcomes in fetal tachyarrhythmias. The underlying electrophysiological mechanisms have a major role in predicting these differential outcomes with an overrepresentation of PJRT in the drug-resistant population. |
format | Online Article Text |
id | pubmed-8183966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-81839662021-06-09 Outcomes of sustained fetal tachyarrhythmias after transplacental treatment Bartin, Raphael Maltret, Alice Nicloux, Muriel Ville, Yves Bonnet, Damien Stirnemann, Julien Heart Rhythm O2 Devices BACKGROUND: Fetal tachyarrhythmia is a condition that may lead to cardiac dysfunction, hydrops, and death. Despite a transplacental treatment, failure to obtain or maintain sinus rhythm may occur. OBJECTIVE: We aimed to analyze the perinatal outcomes of sustained fetal tachyarrhythmias after in utero treatment. METHODS: We performed a retrospective evaluation of 69 cases with sustained fetal tachyarrhythmia. We compared the perinatal and long-term outcomes of prenatally converted and drug-resistant fetuses. Tachyarrhythmia subtypes were also evaluated. RESULTS: Conversion to sinus rhythm was obtained in 74% of cases; 26% of cases were drug-resistant and delivered arrhythmic. Three perinatal deaths occurred in both groups (6.7% vs 17%, P = .34). Neonates delivered arrhythmic were more frequently admitted to neonatal intensive care units (75% vs 31%, P < .01), and their hospital stay was longer (20.9 vs 6.64 days, P < .001). Multiple neonatal recurrences (81% vs 11%, P < .001), temporary hemodynamic dysfunction or heart failure (50% vs 6.7%, P < .001), and postnatal use of a combination treatment (44% vs 13%, P = .028) were also more frequent in this population. Beyond the neonatal period, rates of recurrences within the first 16 months were higher in drug-resistant fetuses (HR = 16.14, CI 95% [4.485; 193.8], P < .001). In this population, postnatal electrocardiogram revealed an overrepresentation of rare mechanisms, especially permanent junctional reciprocating tachycardia (PJRT) (31%). CONCLUSION: Prenatal conversion to stable sinus rhythm is a major determinant of perinatal and long-term outcomes in fetal tachyarrhythmias. The underlying electrophysiological mechanisms have a major role in predicting these differential outcomes with an overrepresentation of PJRT in the drug-resistant population. Elsevier 2021-03-09 /pmc/articles/PMC8183966/ /pubmed/34113918 http://dx.doi.org/10.1016/j.hroo.2021.02.006 Text en © 2021 Heart Rhythm Society. Published by Elsevier Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Devices Bartin, Raphael Maltret, Alice Nicloux, Muriel Ville, Yves Bonnet, Damien Stirnemann, Julien Outcomes of sustained fetal tachyarrhythmias after transplacental treatment |
title | Outcomes of sustained fetal tachyarrhythmias after transplacental treatment |
title_full | Outcomes of sustained fetal tachyarrhythmias after transplacental treatment |
title_fullStr | Outcomes of sustained fetal tachyarrhythmias after transplacental treatment |
title_full_unstemmed | Outcomes of sustained fetal tachyarrhythmias after transplacental treatment |
title_short | Outcomes of sustained fetal tachyarrhythmias after transplacental treatment |
title_sort | outcomes of sustained fetal tachyarrhythmias after transplacental treatment |
topic | Devices |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183966/ https://www.ncbi.nlm.nih.gov/pubmed/34113918 http://dx.doi.org/10.1016/j.hroo.2021.02.006 |
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