期刊
AMERICAN JOURNAL OF PERINATOLOGY
卷 39, 期 10, 页码 1074-1082出版社
THIEME MEDICAL PUBL INC
DOI: 10.1055/s-0040-1721496
关键词
trisomy 13; trisomy 18; communication; interdisciplinary; palliative care
This qualitative study explores the perspectives of nurses, advanced practice practitioners, and neonatologists on the care for babies with trisomy 13 or 18 in the intensive care unit. The study reveals that the majority of NICU staff perceive care for these babies to be different from care for babies with other critical chronic illnesses. The study identifies themes of internal conflict, variable presentation and prognosis, grappling with uncertainty, family experiences, and provision of meaningful care. Nurses emphasize the provision of meaningful care, while neonatologists highlight the variability of presentation and prognosis.
Objective Care offerings vary across medical settings and between families for babies with trisomy 13 or 18. The purpose of this qualitative descriptive study was to explore nurse, advanced practice practitioner, and neonatologist perspectives on care for babies with trisomy 13 or 18 in the intensive care unit. Study Design Voice-recorded qualitative interviews occurred with 64 participants (41 bedside nurses, 14 advance practice practitioners, and 9 neonatologists) from two neonatal intensive care units (NICU) in the midwestern United States. Consolidated Criteria for Reporting Qualitative Research guidelines were followed. Content analyses occurred utilizing MAXQDA (VERBI Software, 2020). Results Over half of NICU staff perceived care for babies with trisomy 13 or 18 as different from care for other babies with critical chronic illness. Qualitative themes included internal conflict, variable presentation and prognosis, grappling with uncertainty, family experiences, and provision of meaningful care. Neonatologists emphasized the variability of presentation and prognosis, while nurses emphasized provision of meaningful care. Phrases hard/difficult were spoken 31 times; primarily describing the comorbidities, complexities, and prognostic uncertainty. Conclusion Care for babies with these genetic diagnoses reveals need for a shared dialogue not only with families but also across staff disciplines. While perspectives differ, participants depicted striving to offer compassionate, family-centered care while also balancing biomedical uncertainty about interventions for children with trisomy 13 and 18.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据