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Living with a diagnosis of Placenta Accreta Spectrum: Mothers’ and Fathers’ experience of the antenatal journey and the birth
OBJECTIVE: Much research into Placenta Accreta Spectrum (PAS) has focussed on the associated maternal morbidity and mortality. However, mothers’ and fathers’ lived experiences of the aftermath of a diagnosis of PAS up to the birth and beyond has received little attention. Therefore, the aim of this...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10202293/ https://www.ncbi.nlm.nih.gov/pubmed/37216388 http://dx.doi.org/10.1371/journal.pone.0286082 |
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author | Bartels, Helena C. Horsch, Antje Cooney, Naomi Brennan, Donal J. Lalor, Joan G. |
author_facet | Bartels, Helena C. Horsch, Antje Cooney, Naomi Brennan, Donal J. Lalor, Joan G. |
author_sort | Bartels, Helena C. |
collection | PubMed |
description | OBJECTIVE: Much research into Placenta Accreta Spectrum (PAS) has focussed on the associated maternal morbidity and mortality. However, mothers’ and fathers’ lived experiences of the aftermath of a diagnosis of PAS up to the birth and beyond has received little attention. Therefore, the aim of this study was to increase our understanding of the psychological consequences of PAS on women and their partners during pregnancy, up to and including the birth. METHODS: In-depth interviews were conducted with 29 participants; 6 couples were interviewed together (n = 12), 6 couples were interviewed separately (n = 12), and 5 women were interviewed without their partner. Data from the antenatal and intrapartum periods are presented. Couples were eligible for inclusion if they had a diagnosis of PAS within the previous 5 years. An Interpretative Phenomenological Analysis approach was used to gather and analyse data. Virtual interviews were conducted over a 3-month period from February to April 2021. RESULTS: Themes emerged relating to two distinct timepoints, the antenatal period and birth. The antenatal period had two main themes: the first antenatal main theme was “Living with PAS”, which had two sub-themes: “Lack of knowledge of PAS” and “Experiences of varied approaches to care”. The second antenatal main theme was “Coping with uncertainty”, which had two sub-themes of “Getting on with it”, and “Emotional toll”. Relating to birth, two main themes emerged. The first main theme was “A traumatic experience”, with three sub-themes of “Saying goodbye”, “Experiencing trauma” and the “Witnessing of trauma” (by fathers). The second main theme which emerged was “Feeling safe in the hands of experts”, with two subthemes of “Safety in expert team” and “Relief at surviving”. CONCLUSIONS: This study highlights the significant psychological consequences a diagnosis of PAS has on mothers and fathers, how they try to come to terms with the diagnosis and the experience of a traumatic birth, and how management within a specialist team can alleviate some of these fears. |
format | Online Article Text |
id | pubmed-10202293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-102022932023-05-23 Living with a diagnosis of Placenta Accreta Spectrum: Mothers’ and Fathers’ experience of the antenatal journey and the birth Bartels, Helena C. Horsch, Antje Cooney, Naomi Brennan, Donal J. Lalor, Joan G. PLoS One Research Article OBJECTIVE: Much research into Placenta Accreta Spectrum (PAS) has focussed on the associated maternal morbidity and mortality. However, mothers’ and fathers’ lived experiences of the aftermath of a diagnosis of PAS up to the birth and beyond has received little attention. Therefore, the aim of this study was to increase our understanding of the psychological consequences of PAS on women and their partners during pregnancy, up to and including the birth. METHODS: In-depth interviews were conducted with 29 participants; 6 couples were interviewed together (n = 12), 6 couples were interviewed separately (n = 12), and 5 women were interviewed without their partner. Data from the antenatal and intrapartum periods are presented. Couples were eligible for inclusion if they had a diagnosis of PAS within the previous 5 years. An Interpretative Phenomenological Analysis approach was used to gather and analyse data. Virtual interviews were conducted over a 3-month period from February to April 2021. RESULTS: Themes emerged relating to two distinct timepoints, the antenatal period and birth. The antenatal period had two main themes: the first antenatal main theme was “Living with PAS”, which had two sub-themes: “Lack of knowledge of PAS” and “Experiences of varied approaches to care”. The second antenatal main theme was “Coping with uncertainty”, which had two sub-themes of “Getting on with it”, and “Emotional toll”. Relating to birth, two main themes emerged. The first main theme was “A traumatic experience”, with three sub-themes of “Saying goodbye”, “Experiencing trauma” and the “Witnessing of trauma” (by fathers). The second main theme which emerged was “Feeling safe in the hands of experts”, with two subthemes of “Safety in expert team” and “Relief at surviving”. CONCLUSIONS: This study highlights the significant psychological consequences a diagnosis of PAS has on mothers and fathers, how they try to come to terms with the diagnosis and the experience of a traumatic birth, and how management within a specialist team can alleviate some of these fears. Public Library of Science 2023-05-22 /pmc/articles/PMC10202293/ /pubmed/37216388 http://dx.doi.org/10.1371/journal.pone.0286082 Text en © 2023 Bartels et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Bartels, Helena C. Horsch, Antje Cooney, Naomi Brennan, Donal J. Lalor, Joan G. Living with a diagnosis of Placenta Accreta Spectrum: Mothers’ and Fathers’ experience of the antenatal journey and the birth |
title | Living with a diagnosis of Placenta Accreta Spectrum: Mothers’ and Fathers’ experience of the antenatal journey and the birth |
title_full | Living with a diagnosis of Placenta Accreta Spectrum: Mothers’ and Fathers’ experience of the antenatal journey and the birth |
title_fullStr | Living with a diagnosis of Placenta Accreta Spectrum: Mothers’ and Fathers’ experience of the antenatal journey and the birth |
title_full_unstemmed | Living with a diagnosis of Placenta Accreta Spectrum: Mothers’ and Fathers’ experience of the antenatal journey and the birth |
title_short | Living with a diagnosis of Placenta Accreta Spectrum: Mothers’ and Fathers’ experience of the antenatal journey and the birth |
title_sort | living with a diagnosis of placenta accreta spectrum: mothers’ and fathers’ experience of the antenatal journey and the birth |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10202293/ https://www.ncbi.nlm.nih.gov/pubmed/37216388 http://dx.doi.org/10.1371/journal.pone.0286082 |
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