Literature DB >> 24292156

Home-based palliative care: a systematic literature review of the self-reported unmet needs of patients and carers.

Adriana D Ventura1, Susan Burney, Joanne Brooker, Jane Fletcher, Lina Ricciardelli.   

Abstract

BACKGROUND: There have been many studies on the unmet needs of palliative care patients and carers from the perspective of bereaved caregivers. However, the unmet needs of palliative care patients and carers from the perspective of current patients and their carers have received little research attention. AIM: As home-based services have become one of the main delivery models of palliative care, the aim of this review was to describe, evaluate and summarise the literature on the unmet needs of palliative home care patients and carers.
DESIGN: The systematic review of qualitative and quantitative studies was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. DATA SOURCES: PubMed, CINAHL, Embase, MEDLINE, PsycINFO, AMED and CareSearch were searched to find empirical studies on the self-reported unmet needs of palliative home care patients and carers.
RESULTS: Nine qualitative studies, three quantitative studies and three mixed-design studies were identified. The most frequently reported unmet need was effective communication with health-care professionals, the lack of which negatively impacted on the care received by patients and carers. Physical care needs were met, which indicates that the examined palliative home care services were delivering satisfactory care in this domain, but lacking in other areas.
CONCLUSIONS: The focus therefore should be on improving other aspects of patient care, including communication by health professionals to prevent or reduce suffering in areas such as psychosocial domains. Valid and reliable quantitative measures of unmet needs in palliative care are needed to examine this area more rigorously.

Entities:  

Keywords:  Palliative care; home care services; needs assessment; systematic review

Mesh:

Year:  2013        PMID: 24292156     DOI: 10.1177/0269216313511141

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  44 in total

1.  Education, Training, and Mentorship of Caregivers of Canadians Experiencing a Life-Limiting Illness.

Authors:  Allison M Williams
Journal:  J Palliat Med       Date:  2018-01       Impact factor: 2.947

Review 2.  A Review of the Essential Components of Quality Palliative Care in the Home.

Authors:  Hsien Seow; Daryl Bainbridge
Journal:  J Palliat Med       Date:  2018-01       Impact factor: 2.947

3.  Teaching Home-Based Primary Care.

Authors:  Jennifer M Reckrey; Katherine A Ornstein; Ania Wajnberg; M Victoria Kopke; Linda V DeCherrie
Journal:  Home Healthc Now       Date:  2017 Nov/Dec

4.  Strategies to Improve Quality of Life at the End of Life: Interdisciplinary Team Perspectives.

Authors:  Rana Sagha Zadeh; Paul Eshelman; Judith Setla; Hessam Sadatsafavi
Journal:  Am J Hosp Palliat Care       Date:  2017-06-02       Impact factor: 2.500

5.  Identifying the prevalence of unmet supportive care needs among family caregivers of cancer patients: an Italian investigation on home palliative care setting.

Authors:  Veronica Zavagli; Melania Raccichini; Rita Ostan; Giacomo Ercolani; Luca Franchini; Silvia Varani; Raffaella Pannuti
Journal:  Support Care Cancer       Date:  2022-01-09       Impact factor: 3.603

6.  Factors influencing adult carer support planning for unpaid caregiving at the end of life in Scotland: Qualitative insights from triangulated interviews and focus groups.

Authors:  Susan Swan; Richard Meade; Debbie Cavers; Barbara Kimbell; Anna Lloyd; Emma Carduff
Journal:  Health Soc Care Community       Date:  2021-08-24

7.  Delivering and participating in a psycho-educational intervention for family caregivers during palliative home care: a qualitative study from the perspectives of health professionals and family caregivers.

Authors:  Maja Holm; Ida Carlander; Carl-Johan Fürst; Yvonne Wengström; Kristofer Årestedt; Joakim Öhlen; Anette Henriksson
Journal:  BMC Palliat Care       Date:  2015-04-24       Impact factor: 3.234

Review 8.  Death in the Digital Age: A Systematic Review of Information and Communication Technologies in End-of-Life Care.

Authors:  Kirsten Ostherr; Peter Killoran; Ross Shegog; Eduardo Bruera
Journal:  J Palliat Med       Date:  2015-12-29       Impact factor: 2.947

9.  Engaging family caregivers and health system partners in exploring how multi-level contexts in primary care practices affect case management functions and outcomes of patients and family caregivers at end of life: a realist synthesis.

Authors:  Grace Warner; Lisa Garland Baird; Brendan McCormack; Robin Urquhart; Beverley Lawson; Cheryl Tschupruk; Erin Christian; Lori Weeks; Kothai Kumanan; Tara Sampalli
Journal:  BMC Palliat Care       Date:  2021-07-16       Impact factor: 3.234

10.  Can comprehensive specialised end-of-life care be provided at home? Lessons from a study of an innovative consultant-led community service in the UK.

Authors:  B Noble; N King; A Woolmore; P Hughes; M Winslow; J Melvin; J Brooks; A Bravington; C Ingleton; P A Bath
Journal:  Eur J Cancer Care (Engl)       Date:  2014-04-15       Impact factor: 2.520

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