Coming to terms with dying : advance care planning as a conduit between clinicians, patients, and conversations about death and dying : a qualitative interview study

Article

EASON, Rowena Jane | BRIGHTON, Lisa Jane | KOFFMAN, Jonathan | BRISTOWE, Katherine

BACKGROUND: Advance care planning discussions exploring future care and support needs can be beneficial to people with advanced illness. While research has focussed on barriers, outcomes, and completion, little is known about how discussions influence thoughts, feelings, and behaviours. AIM: To explore experiences of advance care planning for people with incurable life-limiting illnesses, to understand the impact of discussions on individuals, and factors influencing psychological responses. DESIGN: Semi-structured qualitative interviews were conducted. Data were analysed using framework analysis. Reflexive journalling and discussion of coding framework and themes supported rigour. SETTING/PARTICIPANTS: Twenty purposively sampled adults receiving hospice care, aged 30–93 with cancer (n = 15) and non-cancer (n = 5) diagnoses were interviewed. RESULTS: Advance care planning elicits multiple complex thoughts, emotions, and behaviours, with responses ranging from the procedural to the profound. Discussions empowered and instilled confidence, promoted openness with relatives, encouraged people to make the most of their time remaining, and sometimes contributed to coming to terms with their mortality. Factors influencing experiences of discussions reflected the complexity and diversity in participants' lives, personalities, and life experiences, with discussions exposing the realities of living with terminal illness. CONCLUSION: Individuals' unique lives and experiences shape their responses to, and the impact of advance care planning on how they think, feel and behave. Advance care planning is not simply a means to document end-of-life care preferences, but can empower and instil confidence in patients, and may form part of the process of coming to terms with mortality, allowing clinicians to shift focus from process-related outcomes.

http://dx.doi.org/10.1177/02692163251318907

Voir la revue «PALLIATIVE MEDICINE»

Autres numéros de la revue «PALLIATIVE MEDICINE»

Consulter en ligne

Suggestions

Du même auteur

Coming to terms with dying : advance care pla...

Article indépendant | EASON, Rowena Jane | PALLIATIVE MEDICINE

BACKGROUND: Advance care planning discussions exploring future care and support needs can be beneficial to people with advanced illness. While research has focussed on barriers, outcomes, and completion, little is known about how ...

"Difficult conversations" : evaluation of mul...

Article indépendant | BRIGHTON, Lisa Jane | BMJ supportive & palliative care | n°1 | vol.8

Objectives: Evidence-based communication skills training for health and social care professionals is essential to improve the care of seriously ill patients and their families. We aimed to evaluate the self-reported impact of 'Dif...

Emotional labour in palliative and end-of-lif...

Article | BRIGHTON, Lisa Jane | Patient education and counseling | n°3 | vol.102

OBJECTIVE: To explore generalist palliative care providers' experiences of emotional labour when undertaking conversations around palliative and end-of-life care with patients and families, to inform supportive strategies. METHODS...

De la même série

Improving family grief outcomes : a scoping r...

Article | HØEG, Beverley Lim | PALLIATIVE MEDICINE | n°3 | vol.38

BACKGROUND: Experiencing the illness and death of a child is a traumatic experience for the parents and the child's siblings. However, knowledge regarding effective grief interventions targeting the whole family is limited, includ...

Death education interventions for people with...

Article | WANG, Tong | PALLIATIVE MEDICINE | n°4 | vol.38

BACKGROUND: People with life-threatening diseases and their family caregivers confront psychosocial and spiritual issues caused by the persons' impending death. Reviews of death education interventions in the context of life-threa...

Research methods in palliative care

Article | DELIENS, Luc | PALLIATIVE MEDICINE | n°6 | vol.38

Research in palliative care is challenging and complex and it uses a range of research designs and research methods, derived from many different scientific disciplines: from medicine and nursing over health sciences, communication...

What are we planning, exactly? The perspectiv...

Article | BRUUN, Andrea | PALLIATIVE MEDICINE | n°6 | vol.38

BACKGROUND: Deaths of people with intellectual disabilities are often unplanned for and poorly managed. Little is known about how to involve people with intellectual disabilities in end-of-life care planning. AIM: To explore the p...

Face and content validity, acceptability, fea...

Article | NAMISANGO, Eve | PALLIATIVE MEDICINE | n°7 | vol.37

Background: The Children’s Palliative Care Outcome Scale (C-POS) is the first measure developed for children with life-limiting and -threatening illness. It is essential to determine whether the measure addresses what matter...

Chargement des enrichissements...