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Parental terminal cancer and dependent children: a systematic review
Alexandra Wray1, Julie Seymour2, Sarah Greenley3
1Wolfson Palliative Care Research Centre, Hull York Medical School, Univeristy of Hull, Hull, UK Alexandra.wray@hyms.ac.uk.
Background:
When a parent has terminal cancer, their children are part of that experience. Parents often want to protect their children from their disease and prognosis. Knowledge of dependent children's experience will help ensure they receive appropriate support. To date, there is lack of synthesis of this evidence examining children's perspectives.
Objectives:
To systematically search and synthesise the qualitative literature exploring the experiences of dependent children when their parent has terminal cancer.
Methods:
Databases of MEDLINE, Embase, PsycINFO, CINAHL, Assia and the Cochrane library were searched systematically from inception to July 2020 to determine eligible studies. Included studies were appraised for quality and thematically synthesised using Thomas and Harden's thematic synthesis framework.
Results:
Fourteen studies were included, which interviewed children about their experiences (n=654 children aged 4-18 years at the time of parental death), from six countries. Five descriptive themes were identified, further categorised into two broad themes: (1) finding out about parental cancer and its impact on the family and (2) coping with life with parental cancer, death and beyond.
Conclusion:
Children want to be involved in their parent's cancer experience and to help support the family. Healthcare professionals are ideally placed to support and encourage parents to include their children. They should reassure parents that children can cope well and that maintaining normality will help, and explain the benefits of honest and open communication and how they can include dependent children from diagnosis and beyond.
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