Literature DB >> 33206952

The experience of uncertainty for patients, families and healthcare providers in post-stroke palliative and end-of-life care: a qualitative meta-synthesis.

Teresa Connolly1, Heather Coats1, Kristen DeSanto2, Jacqueline Jones1.   

Abstract

PURPOSE: recent data show that there is limited evidence and guidance regarding the best practices for the integration of palliative care (PC) and end-of-life (EOL) post-stroke. The purpose of this meta-synthesis is to understand the PC/EOL experiences after a stroke.
METHODS: a meta-synthesis was conducted to answer the following research question-What are post-stroke PC/EOL experiences from the perspectives of patients, families and healthcare professionals (HCPs)? This approach was completed through two main phases-a systematic search and appraisal of the literature and reciprocal translation with interpretive triangulation of the extracted data. Databases searched were MEDLINE, EMBASE, PsycINFO, Joanna Briggs Institute and CINAHL databases (from their inception to April 2020). After data were extracted, a qualitative exploratory design was used to evaluate the PC/EOL in post-stroke experiences.
RESULTS: the search identified 696 studies. A total of 14 studies were included in this meta-synthesis as they satisfied our eligibility criteria. Uncertainty post-stroke was the overarching main theme that emerged across post-stroke PC/EOL experiences. Within this theme of uncertainty, opportunities to decrease uncertainty emerged from two interdependent themes-presence of cohesive communication and shared dynamic decision process for both families and HCPs.
CONCLUSIONS: to mitigate the degree of uncertainty post-stroke, HCPs should be present, provide clear direct communication and incorporate the value-based goals of care within their medical treatment plan. These findings suggest that future research is needed to focus on how PC approaches can be integrated into stroke care programmes.
© The Author(s) 2020. Published by Oxford University Press on behalf of the British Geriatrics Society. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  communication; older people; palliative care; qualitative research; shared decision-making; stroke; value-based care

Mesh:

Year:  2021        PMID: 33206952     DOI: 10.1093/ageing/afaa229

Source DB:  PubMed          Journal:  Age Ageing        ISSN: 0002-0729            Impact factor:   10.668


  3 in total

1.  International consensus-based policy recommendations to advance universal palliative care access from the American Academy of Nursing Expert Panels.

Authors:  William E Rosa; Harleah G Buck; Allison P Squires; Sharon L Kozachik; Huda Abu-Saad Huijer; Marie Bakitas; Juli McGowan Boit; Patricia K Bradley; Pamela Z Cacchione; Garrett K Chan; Nigel Crisp; Constance Dahlin; Pat Daoust; Patricia M Davidson; Sheila Davis; Myrna A A Doumit; Regina M Fink; Keela A Herr; Pamela S Hinds; Tonda L Hughes; Viola Karanja; Deborah J Kenny; Cynthia R King; Hester C Klopper; Ann R Knebel; Ann E Kurth; Elizabeth A Madigan; Pamela Malloy; Marianne Matzo; Polly Mazanec; Salimah H Meghani; Todd B Monroe; Patricia J Moreland; Judith A Paice; J Craig Phillips; Cynda H Rushton; Judith Shamian; Mona Shattell; Julia A Snethen; Connie M Ulrich; Dorothy Wholihan; Lucia D Wocial; Betty R Ferrell
Journal:  Nurs Outlook       Date:  2021-10-06       Impact factor: 3.250

2.  When Should Neuroendovascular Care for Patients With Acute Stroke Be Palliative?

Authors:  Michael J Young; Robert W Regenhardt; Leonard L Sokol; Thabele M Leslie-Mazwi
Journal:  AMA J Ethics       Date:  2021-10-01

3.  Top Ten Tips Palliative Clinicians Should Know About Evidence-Based Advocacy.

Authors:  William E Rosa; Katherine I Pettus; Liliana De Lima; Allison Silvers; Stacie Sinclair; Lukas Radbruch
Journal:  J Palliat Med       Date:  2021-04-30       Impact factor: 2.947

  3 in total

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