Literature DB >> 31866198

The experiences and perspectives of family surrogate decision-makers: A systematic review of qualitative studies.

Ya Su1, Michiko Yuki2, Kengo Hirayama3.   

Abstract

OBJECTIVE: Surrogate decision-makers play an increasingly important role in the lives of older adults who have lost their ability to make decisions. Currently, there is a lack of evidence to support family surrogates in making a variety of decisions. Additionally, a greater understanding of family caregivers' experiences and perspectives toward making surrogate decisions is needed.
METHODS: This study employed a qualitative systematic review and thematic synthesis of the research evidence using the methodologies of the Joanna Briggs Institute (2014) and Thomas and Harden (2008).
RESULTS: Decisions were classified per three main types: intensive care treatment, end-of-life treatment, and placement. Six themes were identified concerning surrogates' experiences: struggle and reluctance, seeking reassurance, communication with healthcare professionals, family support, older adults' wishes, and negative impact.
CONCLUSION: Family surrogates often lack adequate preparation and education regarding decision-making. Quality communication between surrogates and healthcare providers helps reduce the anxiety and guilt experienced when making surrogate decisions. Further research is required to elucidate these experiences with more cultural and racial nuances. PRACTICE IMPLICATIONS: This review informs healthcare providers' awareness of the challenges faced by surrogates and fosters improved surrogate decision-making experiences.
Copyright © 2019 The Authors. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Family caregiver; Healthcare provider; Older adults; Patients; Surrogate decision-making

Year:  2019        PMID: 31866198     DOI: 10.1016/j.pec.2019.12.011

Source DB:  PubMed          Journal:  Patient Educ Couns        ISSN: 0738-3991


  5 in total

1.  Do surrogates predict patient preferences more accurately after a physician-led discussion about advance directives? A randomized controlled trial.

Authors:  Catarina Sampaio Martins; Iva Sousa; Cláudia Barros; Alexandra Pires; Luisa Castro; Cristina da Costa Santos; Rui Nunes
Journal:  BMC Palliat Care       Date:  2022-07-12       Impact factor: 3.113

2.  (Re)Conceptualising 'good' proxy decision-making for research: the implications for proxy consent decision quality.

Authors:  Victoria Shepherd
Journal:  BMC Med Ethics       Date:  2022-07-18       Impact factor: 2.834

3.  Individual, interpersonal, and health care factors associated with informal and formal advance care planning in a nationally-representative sample of midlife and older adults.

Authors:  Daniel Siconolfi; Julia Bandini; Emily Chen
Journal:  Patient Educ Couns       Date:  2020-12-25

Review 4.  Quality indicators of palliative care for cardiovascular intensive care.

Authors:  Yoshimitsu Takaoka; Yasuhiro Hamatani; Tatsuhiro Shibata; Shogo Oishi; Akemi Utsunomiya; Fujimi Kawai; Nobuyuki Komiyama; Atsushi Mizuno
Journal:  J Intensive Care       Date:  2022-03-14

5.  Cultural adaptation of a community-based advance serious illness planning decision aid to the Quebec context involving end-users.

Authors:  Ariane Plaisance; Yoanna Skrobik; Mathieu Moreau; Felix Pageau; Diane Tapp; Daren K Heyland
Journal:  Health Expect       Date:  2022-02-02       Impact factor: 3.318

  5 in total

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