Literature DB >> 30149059

Patient, Caregiver, and Taxpayer Knowledge of Palliative Care and Views on a Model of Community-Based Palliative Care.

Nathan A Boucher1, Janet H Bull2, Sarah H Cross3, Christine Kirby4, J Kelly Davis4, Donald H Taylor5.   

Abstract

CONTEXT: Palliative care (PC) model delivered by two large hospices and PC providers.
OBJECTIVES: To understand study participants' knowledge of PC and acceptability of a new community-based PC model.
METHODS: Semistructured interview with patients and caregivers; focus groups with taxpayers. Descriptive content analysis with an inductive approach.
RESULTS: Across 10 interviews and four focus groups (n = 4-10 per group), there was varying knowledge of PC. Gaps in interview and focus group participants' knowledge related to knowing the services available in PC, how PC is paid for, how to initiate PC, and how PC affects the patient's relationship with existing providers. Regarding the model, negative feedback from interview participants included not having PC explained adequately and PC providers seen as consultants and not as full-time providers. Focus group participants indicated that the model sounded promising but noted the likely difficulty in enacting it in our current health care system. Positive feedback from interview participants included the perception that clinicians spent more time and provided more support for patients and families and the developing ability of PC services to provide care more broadly than at the very end of life. Focus group participants had similar observations related to perceived attention to care and broader application of PC. Perceptions of time-constrained care delivery and suboptimal provider-patient communication persist for some patients getting PC services.
CONCLUSION: Education for patients, caregivers, and community members about the roles and benefits of PC will be needed to successfully expand community-based PC. Published by Elsevier Inc.

Entities:  

Keywords:  Community-based palliative care; caregivers; hospice; patient knowledge

Mesh:

Year:  2018        PMID: 30149059     DOI: 10.1016/j.jpainsymman.2018.08.007

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  6 in total

1.  Policy Implications for Pain in Advanced Alzheimer's Disease.

Authors:  Alison R Anderson; Karen Hyden; Michelle D Failla; Michael A Carter
Journal:  Pain Manag Nurs       Date:  2020-07-16       Impact factor: 1.929

Review 2.  Last Aid Course. An Education For All Citizens and an Ingredient of Compassionate Communities.

Authors:  Georg Bollig; Frans Brandt; Marius Ciurlionis; Boris Knopf
Journal:  Healthcare (Basel)       Date:  2019-01-28

3.  Examining public knowledge, attitudes and perceptions towards palliative care: a mixed method sequential study.

Authors:  Sonja McIlfatrick; Paul Slater; Esther Beck; Olufikayo Bamidele; Sharon McCloskey; Karen Carr; Deborah Muldrew; Lisa Hanna-Trainor; Felicity Hasson
Journal:  BMC Palliat Care       Date:  2021-03-17       Impact factor: 3.234

4.  "That Little Bit of Time": Transition-to-Hospice Perspectives From Hospice Staff and Bereaved Family.

Authors:  Sarah H Cross; Janel R Ramkalawan; Jackie F Ring; Nathan A Boucher
Journal:  Innov Aging       Date:  2022-01-18

5.  The level of knowledge about palliative care in Iranian patients with cancer.

Authors:  Dadgari Atena; Bagheri Imane; Rassouli Maryam; Salmani Naiire; Tahani Fatemeh
Journal:  BMC Palliat Care       Date:  2022-03-10       Impact factor: 3.234

6.  Examining the International Palliative Care Systems in Rural Areas: Protocol for a Comparative Case Study.

Authors:  Meritxell Mondejar-Pont; Kristen Abbott-Anderson; Anna Ramon-Aribau; Renee Kumpula; Tammy Neiman; Hans-Peter De Ruiter
Journal:  JMIR Res Protoc       Date:  2022-07-01
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.