Reconsidering early parental grief following the death of a child from cancer: a new framework for future research and bereavement support.


Journal

Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
ISSN: 1433-7339
Titre abrégé: Support Care Cancer
Pays: Germany
ID NLM: 9302957

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 11 09 2019
accepted: 12 12 2019
pubmed: 25 12 2019
medline: 10 9 2020
entrez: 25 12 2019
Statut: ppublish

Résumé

Parents of children that die from cancer are at increased risk of significant long-term psychosocial and physical morbidities. Less, however, is known about the experience of parents early in the grief process. Currently used frameworks and instruments used to understand and assess outcomes in parents early in the grief experience are inadequate and may serve to pathologize the normal grief response. Through review of the literature, previously conducted qualitative work, and extensive clinical experience working with bereaved parents, we developed a new framework for understanding, assessing, and studying parental grief during the first 2 years following the death of a child from cancer. Our novel longitudinal framework hypothesizes that short- and long-term psychosocial sequalae in parents following the death of a child from cancer depend not only on pre-death factors but on the support present through the disease experience and the oscillation between protective factors and risk factors in the post-death period. We further hypothesize that protective factors and risk factors may be modifiable, making them key potential targets for supportive interventions aimed at augmenting protective factors and diminishing the effect of risk factors. This is a new framework for understanding and assessing the grief experience of parents within the first 2 years of a child's death. Many questions about how best to support parents following the death of a child from cancer remain providing ample opportunities for future research and development of interventions to improve both short- and long-term outcomes in bereaved parents.

Identifiants

pubmed: 31872296
doi: 10.1007/s00520-019-05249-3
pii: 10.1007/s00520-019-05249-3
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4131-4139

Auteurs

Jennifer Snaman (J)

Department of Psychosocial Oncology and Palliative Care, Dana-Farber Cancer Institute, 450 Brookline Ave., Boston, MA, 02215, USA. Jennifer_snaman@dfci.harvard.edu.
Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA, USA. Jennifer_snaman@dfci.harvard.edu.
Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA. Jennifer_snaman@dfci.harvard.edu.

Sue E Morris (SE)

Department of Psychosocial Oncology and Palliative Care, Dana-Farber Cancer Institute, 450 Brookline Ave., Boston, MA, 02215, USA.
Department of Psychiatry, Boston Children's Hospital, Boston, MA, USA.
Department of Psychiatry, Brigham & Women's Hospital, Boston, MA, USA.

Abby R Rosenberg (AR)

Center for Clinical and Translational Research, Seattle Children's Research Institute, Seattle, WA, USA.
Department of Pediatrics, University of Washington School of Medicine, Seattle, WA, USA.

Rachel Holder (R)

Department of Psychosocial Oncology and Palliative Care, Dana-Farber Cancer Institute, 450 Brookline Ave., Boston, MA, 02215, USA.

Justin Baker (J)

Division of Quality of Life and Palliative Care, St. Jude Children's Research Hospital, Memphis, TN, USA.

Joanne Wolfe (J)

Department of Psychosocial Oncology and Palliative Care, Dana-Farber Cancer Institute, 450 Brookline Ave., Boston, MA, 02215, USA.
Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA.

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