Literature DB >> 28957884

Palliative and end-of-life care for adults with advanced chronic obstructive pulmonary disease: a rapid review focusing on patient and family caregiver perspectives.

Gillian Mathews1, Bridget Johnston.   

Abstract

PURPOSE OF REVIEW: The aim of the review was to explore patient and family caregiver perspectives on key issues for ensuring quality of end-of-life care for people with chronic obstructive pulmonary disease (COPD). The growing evidence on the value of specialist palliative care services demonstrates significant improvements in treatments and provisions; however, much of the literature is generic in nature or centred on people with a cancer diagnosis. In this review, we examine the literature to ascertain the views and needs of patients and carers affected by advanced COPD, a highly debilitating condition that can have a profoundly negative impact on the quality of end-of-life experience. RECENT
FINDINGS: A total of 19 papers were included in the review. The main themes in the literature were Holistic Care, Illness Trajectory and Technology.
SUMMARY: Areas of unmet need emphasized across physical, psychosocial and spiritual domains were identified, particularly in relation to appropriate and timely conversations. Positive developments in the care and treatment of advanced COPD include the use of the STIOLTO Respimat inhaler, a brief educative and psychosocial intervention based on cognitive-behavioural therapy, and high-intensity exercise training. There is some evidence regarding the use of technology in end-stage COPD.

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Year:  2017        PMID: 28957884     DOI: 10.1097/SPC.0000000000000303

Source DB:  PubMed          Journal:  Curr Opin Support Palliat Care        ISSN: 1751-4258            Impact factor:   2.302


  3 in total

1.  Support to informal caregivers of patients with severe chronic obstructive pulmonary disease: a qualitative study of caregivers' and professionals' experiences in Swedish hospitals.

Authors:  Susann Strang; Josefin Fährn; Peter Strang; Agneta Ronstad; Louise Danielsson
Journal:  BMJ Open       Date:  2019-08-10       Impact factor: 2.692

2.  Exploring social capital for family caregivers of patients with chronic organ failure: study protocol for a concept mapping study.

Authors:  Marques Shek Nam Ng; Winnie Kwok Wei So; Kai Chow Choi; Wallace Chi Ho Chan; Helen Yue Lai Chan; Carmen Wing Han Chan
Journal:  BMJ Open       Date:  2022-06-17       Impact factor: 3.006

3.  The experience of caring for patients at the end-of-life stage in non-palliative care settings: a qualitative study.

Authors:  Xiao Bin Lai; Frances Kam Yuet Wong; Shirley Siu Yin Ching
Journal:  BMC Palliat Care       Date:  2018-10-17       Impact factor: 3.234

  3 in total

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