The facilitators and challenges of dying at home with dementia : a narrative synthesis

Article indépendant

MOGAN, Caroline | LLOYD-WILLIAMS, Mari | HARRISON DENING, Karen | DOWRICK, Christopher

Background: It is reported that, given the right support, most people would prefer to die at home, yet a very small minority of people with dementia do so. At present, knowledge gaps remain on how best to support end-of-life care at home for people with dementia. Aim: To identify and understand the challenges and facilitators of providing end-of-life care at home for people with dementia. Design: Narrative synthesis of qualitative and quantitative data. Data sources: The review adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. A systematic literature search was conducted across six electronic databases (AMED, BNI, CINAHL, EMBASE, MEDLINE and PsycINFO) and reference lists of key journals were searched up to July 2017. Results: Searches returned 1949 unique titles, of which seven studies met all the eligibility criteria (four quantitative and three qualitative). Six key themes were identified – four facilitators and two challenges. Facilitators included ‘support from health care professionals’, ‘informal caregiver resilience and extended social networks’, ‘medications and symptom management’ and ‘appropriate equipment and home adaptations’. Challenges included ‘issues with professional services’ and ‘worsening of physical or mental health’. Conclusion: People with dementia may not always require specialist palliative care at the end of life. Further research is required to overcome the methodological shortcomings of previous studies and establish how community development approaches to palliative care, such as compassionate communities, can support families to allow a greater number of people with dementia to die at home.

http://dx.doi.org/10.1177/0269216318760442

Voir la revue «PALLIATIVE MEDICINE, 32»

Autres numéros de la revue «PALLIATIVE MEDICINE»

Consulter en ligne

Suggestions

Du même auteur

The facilitators and challenges of dying at h...

Article | MOGAN, Caroline | PALLIATIVE MEDICINE | n°6 | vol.32

Background: It is reported that, given the right support, most people would prefer to die at home, yet a very small minority of people with dementia do so. At present, knowledge gaps remain on how best to support end-of-life care ...

Health and social care services for people wi...

Article indépendant | MOGAN, Caroline | PALLIATIVE MEDICINE | n°6 | vol.36

BACKGROUND: More people are dying at home with dementia and Alzheimer's disease. While informal caregivers are the main providers of care for people with dementia dying at home, they require support from health and social care ser...

Innovative and best models of palliative and ...

Article indépendant | MOGAN, Caroline | Current opinion in supportive and palliative care

PURPOSE OF REVIEW: The review aims to synthesize the most recent innovative models of palliative care being delivered in rural and remote locations. RECENT FINDINGS: Worldwide, as the ageing population grows, more people will requ...

De la même série

Posttraumatic growth in palliative care setti...

Article indépendant | AUSTIN, Philip D. | PALLIATIVE MEDICINE | n°2 | vol.38

BACKGROUND: Posttraumatic growth refers to positive psychological change following trauma. However, there is a need to better understand the experience of posttraumatic growth in the palliative care setting as well as the availabi...

Long-term bereavement outcomes in family memb...

Article indépendant | LAPENSKIE, Julie | PALLIATIVE MEDICINE | n°2 | vol.38

Background: Severe grief is highly distressing and prevalent up to 1 year post-death among people bereaved during the first wave of COVID-19, but no study has assessed changes in grief severity beyond this timeframe. Aim: Understa...

Understanding the extent to which PROMs and P...

Article indépendant | HOWARD, Faith D. | PALLIATIVE MEDICINE | n°2 | vol.38

BACKGROUND: Older people with severe frailty are nearing the end of life but their needs are often unknown and unmet. Systematic ways to capture and measure the needs of this group are required. Patient reported Outcome Measures (...

The perspectives of people with dementia and ...

Article indépendant | MONNET, Fanny | PALLIATIVE MEDICINE | n°2 | vol.38

BACKGROUND: Advance care planning has been defined in an international consensus paper, supported by the European Association for Palliative Care. There are concerns that this definition may not apply to dementia. Moreover, it is ...

Revised European Association for Palliative C...

Article indépendant | SURGES, Séverine M. | PALLIATIVE MEDICINE | n°2 | vol.38

BACKGROUND: The European Association for Palliative Care (EAPC) acknowledges palliative sedation as an important, broadly accepted intervention for patients with life-limiting disease experiencing refractory symptoms. The EAPC the...

Chargement des enrichissements...