What constitutes high-quality paediatric palliative care? : a qualitative exploration of the perspectives of children, young people, and parents

Article indépendant

BRAYBROOK, Debbie | COOMBES, Lucy | SCOTT, Hannah M. | HARÐARDOTTIR, Daney | ROACH, Anna | BARIUAN, Jemimah | ELLIS-SMITH, Clare | DOWNING, Julia | MURTAGH, Fliss E. M. | BLUEBOND-LANGNER, Myra | FRASER, Lorna K. | HARDING, Richard | BRISTOWE, Katherine

BACKGROUND: Globally, over 21 million children need palliative care each year. Although guidelines exist to support paediatric palliative care delivery, they are not informed by the experiences of children themselves. OBJECTIVE: We aimed to determine what constitutes good quality palliative care from the perspectives of children with life-limiting or life-threatening conditions and their parents. METHODS: We analysed semi-structured qualitative interviews using reflexive thematic analysis informed by the European Association for Palliative Care charter of palliative care for children and young people, and Bronfenbrenner's bioecological model. Participants included 26 children aged 5-17 years, and 40 parents of children aged 0-17 years, with a range of cancer and non-cancer diagnoses in nine UK paediatric palliative care services (hospitals and hospices). RESULTS: Quality paediatric palliative care can be both enacted or interrupted across the five domains of the bioecological model. Honest timely communication with the child and family (microsystem), and collaborative relationships between care teams and others in the child's life (mesosystem), are vital. Care experiences are negatively affected by inequities in care provision (exosystems), and society's reluctance to discuss mortality in childhood (macrosystem). Children need to enjoy what matters to them, and maintain social connections, and plan for the future, even if facing a shortened life (chronosystem). CONCLUSIONS: Children and parents are experts in their condition and should be actively involved in care discussions, through communication tailored to the child's pace and preferences, and support advocating for and coordinating care services. Fostering strong and collaborative relationships builds trust and helps children and families to feel safe, included and supported.

http://dx.doi.org/10.1007/s40271-025-00744-8

Voir la revue «The patient»

Autres numéros de la revue «The patient»

Consulter en ligne

Suggestions

Du même auteur

Achieving child-centred care for children and...

Article | COOMBES, Lucy | European journal of pediatrics

This study aims to identify the symptoms, concerns, and care priorities of children with life-limiting conditions and their families. A semi-structured qualitative interview study was conducted, seeking perspectives from multiple ...

Achieving child-centred care for children and...

Article indépendant | COOMBES, Lucy | European journal of pediatrics

This study aims to identify the symptoms, concerns, and care priorities of children with life-limiting conditions and their families. A semi-structured qualitative interview study was conducted, seeking perspectives from multiple ...

Achieving child-centred care for children and...

Article indépendant | COOMBES, Lucy | European journal of pediatrics

This study aims to identify the symptoms, concerns, and care priorities of children with life-limiting conditions and their families. A semi-structured qualitative interview study was conducted, seeking perspectives from multiple ...

De la même série

Valuing end-of-life care for older people wit...

Article indépendant | KENNY, Patricia | The patient

BACKGROUND: Most health care systems are facing the challenge of providing health services to support the increasing numbers of older people with chronic life-limiting conditions at the end of life. Many policies focus primarily o...

What aspects of quality of life are important...

Article indépendant | MCCAFFREY, Nikki | The patient

BACKGROUND AND OBJECTIVE: Preference-based outcome measures are commonly applied in economic analyses to inform healthcare resource allocation decisions. Few preference-based outcome measures have been specifically developed for p...

Community preferences for the care of older p...

Article indépendant | KENNY, Patricia | The patient

BACKGROUND: Population preferences for care at the end of life can inform palliative care policy and direction. Research investigating preferences for care at the end of life has focused predominantly on the context of advanced ca...

What constitutes high-quality paediatric pall...

Article indépendant | BRAYBROOK, Debbie | The patient

BACKGROUND: Globally, over 21 million children need palliative care each year. Although guidelines exist to support paediatric palliative care delivery, they are not informed by the experiences of children themselves. OBJECTIVE: W...

Chargement des enrichissements...