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Parents' experiences of pediatric palliative care and the impact on long-term parental grief

Parents' experiences of pediatric palliative care and the impact on long-term parental grief
Parents' experiences of pediatric palliative care and the impact on long-term parental grief
Context: approximately 25% of children diagnosed with cancer eventually die. Losing a child puts parents at increased risk for developing psychological problems.

Objectives: to explore parents' perceptions of the interaction with health care professionals (communication, continuity of care, and parental involvement) and symptom management during the pediatric palliative phase, and to investigate the influence on long-term grief in parents who lost a child to cancer.

Methods: a total of 89 parents of 57 children who died of cancer between 2000 and 2004 participated in this retrospective cross-sectional study by completing a set of questionnaires measuring grief (Inventory of Traumatic Grief), parents' perceptions of the interaction with health care professionals (communication, continuity of care, and parental involvement), and symptom management during the palliative phase. Care was assessed on a five point Likert scale (1 = disagree and 5 = agree).

Results: parents highly rated communication (4.6 ± 0.6), continuity of care (4.3 ± 0.6), and parental involvement (4.6 ± 0.7) during the palliative phase. Parents' most often reported physical and psychological symptoms of their child during the palliative phase were fatigue (75%), pain (74%), anxiety to be alone (52%), and anger (48%). Higher ratings of parents on communication (? = ?9.08, P = 0.03) and continuity of care (? = ?11.74, P = 0.01) were associated with lower levels of long-term parental grief. The severity of the child's dyspnea (? = 2.96, P = 0.05), anxiety to be alone (? = 4.52, P < 0.01), anxiety about the future (? = 5.02, P < 0.01), anger (? = 4.90, P < 0.01), and uncontrolled pain (? = 6.60, P < 0.01) were associated with higher levels of long-term parental grief. Multivariate models combining the interaction with health care professionals and symptom management showed a significant influence of both aspects on long-term parental grief.

Conclusion: both interaction with health care professionals, especially communication and continuity of care, and symptom management in children dying of cancer are associated with long-term parental grief levels
0885-3924
van der Geest, Ivana M.M.
b3e44c5a-03a8-40cf-8485-fb3307c2a302
Darlington, Anne-Sophie E.
472fcfc9-160b-4344-8113-8dd8760ff962
Streng, Isabelle C.
f0ed162b-9c17-4f1e-87c5-5222f3a71385
Michiels, Erna M.C.
c738c978-2d6d-45f8-a7c4-aa3a04673a07
Pieters, Rob
958e8db6-8c78-4019-ac64-d9b46a80670f
van den Heuvel-Eibrink, Marry M.
093a9aa2-cb40-4839-b6e5-50cfbfb9df15
van der Geest, Ivana M.M.
b3e44c5a-03a8-40cf-8485-fb3307c2a302
Darlington, Anne-Sophie E.
472fcfc9-160b-4344-8113-8dd8760ff962
Streng, Isabelle C.
f0ed162b-9c17-4f1e-87c5-5222f3a71385
Michiels, Erna M.C.
c738c978-2d6d-45f8-a7c4-aa3a04673a07
Pieters, Rob
958e8db6-8c78-4019-ac64-d9b46a80670f
van den Heuvel-Eibrink, Marry M.
093a9aa2-cb40-4839-b6e5-50cfbfb9df15

van der Geest, Ivana M.M., Darlington, Anne-Sophie E., Streng, Isabelle C., Michiels, Erna M.C., Pieters, Rob and van den Heuvel-Eibrink, Marry M. (2013) Parents' experiences of pediatric palliative care and the impact on long-term parental grief. Journal of Pain and Symptom Management. (doi:10.1016/j.jpainsymman.2013.07.007). (PMID:24120185)

Record type: Article

Abstract

Context: approximately 25% of children diagnosed with cancer eventually die. Losing a child puts parents at increased risk for developing psychological problems.

Objectives: to explore parents' perceptions of the interaction with health care professionals (communication, continuity of care, and parental involvement) and symptom management during the pediatric palliative phase, and to investigate the influence on long-term grief in parents who lost a child to cancer.

Methods: a total of 89 parents of 57 children who died of cancer between 2000 and 2004 participated in this retrospective cross-sectional study by completing a set of questionnaires measuring grief (Inventory of Traumatic Grief), parents' perceptions of the interaction with health care professionals (communication, continuity of care, and parental involvement), and symptom management during the palliative phase. Care was assessed on a five point Likert scale (1 = disagree and 5 = agree).

Results: parents highly rated communication (4.6 ± 0.6), continuity of care (4.3 ± 0.6), and parental involvement (4.6 ± 0.7) during the palliative phase. Parents' most often reported physical and psychological symptoms of their child during the palliative phase were fatigue (75%), pain (74%), anxiety to be alone (52%), and anger (48%). Higher ratings of parents on communication (? = ?9.08, P = 0.03) and continuity of care (? = ?11.74, P = 0.01) were associated with lower levels of long-term parental grief. The severity of the child's dyspnea (? = 2.96, P = 0.05), anxiety to be alone (? = 4.52, P < 0.01), anxiety about the future (? = 5.02, P < 0.01), anger (? = 4.90, P < 0.01), and uncontrolled pain (? = 6.60, P < 0.01) were associated with higher levels of long-term parental grief. Multivariate models combining the interaction with health care professionals and symptom management showed a significant influence of both aspects on long-term parental grief.

Conclusion: both interaction with health care professionals, especially communication and continuity of care, and symptom management in children dying of cancer are associated with long-term parental grief levels

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Published date: 2013
Organisations: Faculty of Health Sciences

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Local EPrints ID: 362957
URI: http://eprints.soton.ac.uk/id/eprint/362957
ISSN: 0885-3924
PURE UUID: c288f22c-3193-462e-8f28-e0f093ea4f4d

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Date deposited: 17 Mar 2014 12:15
Last modified: 14 Mar 2024 16:16

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Contributors

Author: Ivana M.M. van der Geest
Author: Isabelle C. Streng
Author: Erna M.C. Michiels
Author: Rob Pieters
Author: Marry M. van den Heuvel-Eibrink

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