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Exploring the lived experiences of parents caring for infants with gastroschisis in Rwanda: The untold story

Pediatric surgery is a crucial pillar of health equity but is often not prioritized in the global health agenda, especially in low-and middle-income countries. Gastroschisis (GS) is a type of structural congenital anomaly that can be treated through surgical interventions. In Rwanda, neonatal surgic...

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Autores principales: Kidane, Samuel, Shamebo, Semay Desta, Ntaganda, Edmond, Petroze, Robin T., McNatt, Zahirah, Wong, Rex, Rabideau, Melany
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10021215/
https://www.ncbi.nlm.nih.gov/pubmed/36962402
http://dx.doi.org/10.1371/journal.pgph.0000439
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author Kidane, Samuel
Shamebo, Semay Desta
Ntaganda, Edmond
Petroze, Robin T.
McNatt, Zahirah
Wong, Rex
Rabideau, Melany
author_facet Kidane, Samuel
Shamebo, Semay Desta
Ntaganda, Edmond
Petroze, Robin T.
McNatt, Zahirah
Wong, Rex
Rabideau, Melany
author_sort Kidane, Samuel
collection PubMed
description Pediatric surgery is a crucial pillar of health equity but is often not prioritized in the global health agenda, especially in low-and middle-income countries. Gastroschisis (GS) is a type of structural congenital anomaly that can be treated through surgical interventions. In Rwanda, neonatal surgical care is only available in one hospital. The experience of parents of children born with gastroschisis has not been previously studied in Rwanda. The objective of this study was to explore the lived experiences of parents of children diagnosed with GS in Rwanda. A qualitative study using a semi-structured interview guide was conducted. Parents who had children with gastroschisis and were discharged alive from the hospital in Rwanda were interviewed by trained data collectors, from May to July 2021. Data were transcribed, translated, and then coded using a structured code-book. Thematic analysis was conducted with the use of Dedoose software. Sixteen parents participated in the study. Five themes emerged from the data. They were: “GS diagnosis had a significant emotional impact on the parents”, “Parents were content with the life-saving medical care provided for their children despite some dissatisfaction due to the delayed initiation of care and shortage of medications”, “GS care was accompanied by financial challenges”, “support systems were important coping mechanisms” and “the impact of GS care extended into the post-discharge period”. Having a newborn with GS was an emotional journey. The lack of pre-knowledge about the condition created a shock to the parents. Parents found support from their faith and other parents with similar experiences. The experiences with the care received were mostly positive. The overall financial burden incurred from the medical treatment and indirect costs was high and extended beyond the hospital stay. Strengthening prenatal and hospital services, providing peer, spiritual and financial support could enhance the parents’ experience.
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spelling pubmed-100212152023-03-17 Exploring the lived experiences of parents caring for infants with gastroschisis in Rwanda: The untold story Kidane, Samuel Shamebo, Semay Desta Ntaganda, Edmond Petroze, Robin T. McNatt, Zahirah Wong, Rex Rabideau, Melany PLOS Glob Public Health Research Article Pediatric surgery is a crucial pillar of health equity but is often not prioritized in the global health agenda, especially in low-and middle-income countries. Gastroschisis (GS) is a type of structural congenital anomaly that can be treated through surgical interventions. In Rwanda, neonatal surgical care is only available in one hospital. The experience of parents of children born with gastroschisis has not been previously studied in Rwanda. The objective of this study was to explore the lived experiences of parents of children diagnosed with GS in Rwanda. A qualitative study using a semi-structured interview guide was conducted. Parents who had children with gastroschisis and were discharged alive from the hospital in Rwanda were interviewed by trained data collectors, from May to July 2021. Data were transcribed, translated, and then coded using a structured code-book. Thematic analysis was conducted with the use of Dedoose software. Sixteen parents participated in the study. Five themes emerged from the data. They were: “GS diagnosis had a significant emotional impact on the parents”, “Parents were content with the life-saving medical care provided for their children despite some dissatisfaction due to the delayed initiation of care and shortage of medications”, “GS care was accompanied by financial challenges”, “support systems were important coping mechanisms” and “the impact of GS care extended into the post-discharge period”. Having a newborn with GS was an emotional journey. The lack of pre-knowledge about the condition created a shock to the parents. Parents found support from their faith and other parents with similar experiences. The experiences with the care received were mostly positive. The overall financial burden incurred from the medical treatment and indirect costs was high and extended beyond the hospital stay. Strengthening prenatal and hospital services, providing peer, spiritual and financial support could enhance the parents’ experience. Public Library of Science 2022-06-15 /pmc/articles/PMC10021215/ /pubmed/36962402 http://dx.doi.org/10.1371/journal.pgph.0000439 Text en © 2022 Kidane 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
Kidane, Samuel
Shamebo, Semay Desta
Ntaganda, Edmond
Petroze, Robin T.
McNatt, Zahirah
Wong, Rex
Rabideau, Melany
Exploring the lived experiences of parents caring for infants with gastroschisis in Rwanda: The untold story
title Exploring the lived experiences of parents caring for infants with gastroschisis in Rwanda: The untold story
title_full Exploring the lived experiences of parents caring for infants with gastroschisis in Rwanda: The untold story
title_fullStr Exploring the lived experiences of parents caring for infants with gastroschisis in Rwanda: The untold story
title_full_unstemmed Exploring the lived experiences of parents caring for infants with gastroschisis in Rwanda: The untold story
title_short Exploring the lived experiences of parents caring for infants with gastroschisis in Rwanda: The untold story
title_sort exploring the lived experiences of parents caring for infants with gastroschisis in rwanda: the untold story
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10021215/
https://www.ncbi.nlm.nih.gov/pubmed/36962402
http://dx.doi.org/10.1371/journal.pgph.0000439
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