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Counseling for personal care options at neonatal end of life: a quantitative and qualitative parent survey

BACKGROUND: The death of a newborn is a traumatic life changing event in the lives of parents. We hypothesized that bereaved parents of newborn infants want to have choices in the personal care of their infant at the end of life. METHODS: Parents who had suffered a perinatal or neonatal loss between...

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Autores principales: Shelkowitz, Emily, Vessella, Sharon L., O’Reilly, Patricia, Tucker, Richard, Lechner, Beatrice E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667527/
https://www.ncbi.nlm.nih.gov/pubmed/26626572
http://dx.doi.org/10.1186/s12904-015-0063-6
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author Shelkowitz, Emily
Vessella, Sharon L.
O’Reilly, Patricia
Tucker, Richard
Lechner, Beatrice E.
author_facet Shelkowitz, Emily
Vessella, Sharon L.
O’Reilly, Patricia
Tucker, Richard
Lechner, Beatrice E.
author_sort Shelkowitz, Emily
collection PubMed
description BACKGROUND: The death of a newborn is a traumatic life changing event in the lives of parents. We hypothesized that bereaved parents of newborn infants want to have choices in the personal care of their infant at the end of life. METHODS: Parents who had suffered a perinatal or neonatal loss between 1 and 6 years before the survey in a regional level IV neonatal intensive care unit (NICU) and associated labor and delivery room were invited to participate. Parents chose between an online survey, paper survey or telephone interview. The survey included multiple choice and open ended questions. RESULTS: Parents prefer multiple options for the personal care of their infant at the end of life. Emergent themes were need for guidance by the medical team, memory making, feeling cared for and respected by staff, and regrets related to missed opportunities. CONCLUSION: While parents differ in their preferences in utilizing specific personal care options for their infant’s end of life, they share a common preference for being presented with multiple options to choose from and in being guided and supported by healthcare providers, while being afforded the opportunity to make memories with their infant by bonding with and parenting them. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12904-015-0063-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-46675272015-12-03 Counseling for personal care options at neonatal end of life: a quantitative and qualitative parent survey Shelkowitz, Emily Vessella, Sharon L. O’Reilly, Patricia Tucker, Richard Lechner, Beatrice E. BMC Palliat Care Research Article BACKGROUND: The death of a newborn is a traumatic life changing event in the lives of parents. We hypothesized that bereaved parents of newborn infants want to have choices in the personal care of their infant at the end of life. METHODS: Parents who had suffered a perinatal or neonatal loss between 1 and 6 years before the survey in a regional level IV neonatal intensive care unit (NICU) and associated labor and delivery room were invited to participate. Parents chose between an online survey, paper survey or telephone interview. The survey included multiple choice and open ended questions. RESULTS: Parents prefer multiple options for the personal care of their infant at the end of life. Emergent themes were need for guidance by the medical team, memory making, feeling cared for and respected by staff, and regrets related to missed opportunities. CONCLUSION: While parents differ in their preferences in utilizing specific personal care options for their infant’s end of life, they share a common preference for being presented with multiple options to choose from and in being guided and supported by healthcare providers, while being afforded the opportunity to make memories with their infant by bonding with and parenting them. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12904-015-0063-6) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-02 /pmc/articles/PMC4667527/ /pubmed/26626572 http://dx.doi.org/10.1186/s12904-015-0063-6 Text en © Shelkowitz et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Shelkowitz, Emily
Vessella, Sharon L.
O’Reilly, Patricia
Tucker, Richard
Lechner, Beatrice E.
Counseling for personal care options at neonatal end of life: a quantitative and qualitative parent survey
title Counseling for personal care options at neonatal end of life: a quantitative and qualitative parent survey
title_full Counseling for personal care options at neonatal end of life: a quantitative and qualitative parent survey
title_fullStr Counseling for personal care options at neonatal end of life: a quantitative and qualitative parent survey
title_full_unstemmed Counseling for personal care options at neonatal end of life: a quantitative and qualitative parent survey
title_short Counseling for personal care options at neonatal end of life: a quantitative and qualitative parent survey
title_sort counseling for personal care options at neonatal end of life: a quantitative and qualitative parent survey
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667527/
https://www.ncbi.nlm.nih.gov/pubmed/26626572
http://dx.doi.org/10.1186/s12904-015-0063-6
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