What caring for a child who died was like for me: My experience of pediatric patient death as a new graduate nurse

Document
Abstract

I utilized analytical autoethnography to analyze and interpret my own experience of what caring for a child that died was like for me within the academic and institutional culture that I was educated and trained in (Chang, 2008). Themes of lack of preparedness, relationships, loss and emotion, death denial, and lasting impacts and growth were identified. Pediatric death and dying education and training for nurses should encompass nursing responsibilities, communication strategies, holistic assessments, symptom management, cultural awareness, and grief literacy (Bensoussan, 2024; Chew, Ang, & Storey, 2021; Kent, Anderson, & Ownes, 2012; RNAO, 2012). A system to accommodate, acknowledge, and value emotion. A platform to share, learn, and grow from the experience with death and dying. This autoethnographic account provides insights into the personal and professional impacts of pediatric patient death on nurses and the importance of associated education, training, and support to improve care for patients, families, and self.

Author Keywords: autoethnography, lasting impacts, metabolizing grief, nurse, pediatric patient death, self-transformation

    Item Description
    Type
    Contributors
    Creator (cre): McLean, Meghan
    Thesis advisor (ths): McIntosh, Michele
    Degree committee member (dgc): Poole, Jennifer
    Degree granting institution (dgg): Trent University
    Date Issued
    2025
    Date (Unspecified)
    2025
    Place Published
    Peterborough, ON
    Language
    Extent
    97 pages
    Rights
    Copyright is held by the author, with all rights reserved, unless otherwise noted.
    Subject (Topical)
    Local Identifier
    TC-OPET-32244060
    Publisher
    Trent University
    Degree
    Master of Science (M.Sc.): Nursing