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Living beyond placenta accreta spectrum: parent’s experience of the postnatal journey and recommendations for an integrated care pathway

BACKGROUND: Placenta Accreta Spectrum is associated with significant clinical maternal morbidity and mortality, which has been extensively described in the literature. However, there is a dearth of research on the lived experiences of pregnant people and their support partners. The aim of this study...

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Autores principales: Bartels, Helena C., Horsch, Antje, Cooney, Naomi, Brennan, Donal J., Lalor, Joan G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092796/
https://www.ncbi.nlm.nih.gov/pubmed/35538441
http://dx.doi.org/10.1186/s12884-022-04726-8
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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 BACKGROUND: Placenta Accreta Spectrum is associated with significant clinical maternal morbidity and mortality, which has been extensively described in the literature. However, there is a dearth of research on the lived experiences of pregnant people and their support partners. The aim of this study is to describe living beyond a pregnancy and birth complicated by PAS for up to four years postpartum. Participants experiences inform the development of an integrated care pathway of family centered support interventions. METHODS: An Interpretative Phenomenological Analysis approach was applied to collect data through virtual interviews over a 3-month period from February to April 2021. Twenty-nine participants shared their stories; six people with a history of PAS and their support partners were interviewed together (n = 12 participants), six were interviewed separately (n = 12 participants), and five were interviewed without their partner. Pregnant people were eligible for inclusion if they had a diagnosis of PAS within the previous 5 years. This paper focuses on the postnatal period, with data from the antenatal and intrapartum periods described separately. RESULTS: One superordinate theme “Living beyond PAS” emerged from interviews, with 6 subordinate themes as follows; “Living with a different body”, “The impact on relationships”, “Coping strategies”, “Post-traumatic growth”, “Challenges with normal care” and recommendations for “What needs to change”. These themes informed the development of an integrated care pathway for pregnant people and their support partners to support them from diagnosis up to one year following the birth. CONCLUSION: Parents described the challenges of the postnatal period in terms of the physical and emotional impact, and how some were able to make positive life changes in the aftermath of a traumatic event. An integrated care pathway of simple supportive interventions, based on participant recommendations, delivered as part of specialist multidisciplinary team care may assist pregnant people and their support partners in alleviating some of these challenges.
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spelling pubmed-90927962022-05-12 Living beyond placenta accreta spectrum: parent’s experience of the postnatal journey and recommendations for an integrated care pathway Bartels, Helena C. Horsch, Antje Cooney, Naomi Brennan, Donal J. Lalor, Joan G. BMC Pregnancy Childbirth Research BACKGROUND: Placenta Accreta Spectrum is associated with significant clinical maternal morbidity and mortality, which has been extensively described in the literature. However, there is a dearth of research on the lived experiences of pregnant people and their support partners. The aim of this study is to describe living beyond a pregnancy and birth complicated by PAS for up to four years postpartum. Participants experiences inform the development of an integrated care pathway of family centered support interventions. METHODS: An Interpretative Phenomenological Analysis approach was applied to collect data through virtual interviews over a 3-month period from February to April 2021. Twenty-nine participants shared their stories; six people with a history of PAS and their support partners were interviewed together (n = 12 participants), six were interviewed separately (n = 12 participants), and five were interviewed without their partner. Pregnant people were eligible for inclusion if they had a diagnosis of PAS within the previous 5 years. This paper focuses on the postnatal period, with data from the antenatal and intrapartum periods described separately. RESULTS: One superordinate theme “Living beyond PAS” emerged from interviews, with 6 subordinate themes as follows; “Living with a different body”, “The impact on relationships”, “Coping strategies”, “Post-traumatic growth”, “Challenges with normal care” and recommendations for “What needs to change”. These themes informed the development of an integrated care pathway for pregnant people and their support partners to support them from diagnosis up to one year following the birth. CONCLUSION: Parents described the challenges of the postnatal period in terms of the physical and emotional impact, and how some were able to make positive life changes in the aftermath of a traumatic event. An integrated care pathway of simple supportive interventions, based on participant recommendations, delivered as part of specialist multidisciplinary team care may assist pregnant people and their support partners in alleviating some of these challenges. BioMed Central 2022-05-10 /pmc/articles/PMC9092796/ /pubmed/35538441 http://dx.doi.org/10.1186/s12884-022-04726-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Bartels, Helena C.
Horsch, Antje
Cooney, Naomi
Brennan, Donal J.
Lalor, Joan G.
Living beyond placenta accreta spectrum: parent’s experience of the postnatal journey and recommendations for an integrated care pathway
title Living beyond placenta accreta spectrum: parent’s experience of the postnatal journey and recommendations for an integrated care pathway
title_full Living beyond placenta accreta spectrum: parent’s experience of the postnatal journey and recommendations for an integrated care pathway
title_fullStr Living beyond placenta accreta spectrum: parent’s experience of the postnatal journey and recommendations for an integrated care pathway
title_full_unstemmed Living beyond placenta accreta spectrum: parent’s experience of the postnatal journey and recommendations for an integrated care pathway
title_short Living beyond placenta accreta spectrum: parent’s experience of the postnatal journey and recommendations for an integrated care pathway
title_sort living beyond placenta accreta spectrum: parent’s experience of the postnatal journey and recommendations for an integrated care pathway
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092796/
https://www.ncbi.nlm.nih.gov/pubmed/35538441
http://dx.doi.org/10.1186/s12884-022-04726-8
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