Evidence map›Paper›PMID 41181374›Full record

ArticlePalliative care and social practice2025

A qualitative study of the palliative care needs of primary care patients with COPD: Experiences of COPD patients, their families and healthcare professionals.

Liz Gwyther, Lindsay Farrant, Joy Hunter, Olona Mzimkulu, Kennedy Nkhoma, Richard Harding

Abstract read
In one paragraph

Article in Palliative care and social practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Liz GwytherFaculty of Health Sciences, University of Cape Town, South Africa.ORCID https://orcid.org/0000-0001-7602-6168
Lindsay FarrantDivision of Interdisciplinary Palliative Care and Medicine, University of Cape Town, South Africa.ORCID https://orcid.org/0000-0002-1997-429X
Joy HunterDivision of Interdisciplinary Palliative Care and Medicine, University of Cape Town, South Africa.
Olona MzimkuluDivision of Interdisciplinary Palliative Care and Medicine, University of Cape Town, South Africa.
Kennedy NkhomaFlorence Nightingale Faculty of Nursing Midwifery & Palliative Care, Cicely Saunders Institute, Kings College London, UK.ORCID https://orcid.org/0000-0002-2991-8160
Richard HardingFlorence Nightingale Faculty of Nursing Midwifery & Palliative Care, Cicely Saunders Institute, Kings College London, UK.ORCID https://orcid.org/0000-0001-9653-8689

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The majority of deaths from chronic obstructive pulmonary disease (COPD) occur in low- and middle-income countries. Primary palliative care is commonly proposed as the best model to ensure access to appropriate care. However, the existing evidence on needs, models and outcomes comes from high-income settings. The purpose of the study was to determine the experiences of adults with COPD attending primary care, their informal caregivers and healthcare professionals to identify current care provided and gaps in this care in primary care settings in South Africa. Methods: Cross-sectional qualitative interview study collected in-depth data from three stakeholder groups: adults with COPD attending one of five primary care settings, informal carers of patients and healthcare professionals. The cross-national research team developed a coding frame through inductive thematic analysis. Results: The study participants comprised 22 COPD patients, 19 family caregivers and 22 healthcare professionals. Four main themes emerged. (1) Importance of communication to quality primary palliative care, with poor health literacy regarding the diagnosis and its progression. (2) Symptoms and concerns among patients and caregivers, with multidimensional impact on social participation, poverty and family mental health. (3) The role of health systems in promoting quality primary palliative care, with unreliable drug supply, the need for rapid access pathways during exacerbations and continuity of care from the acute sector through primary care into the home. (4) Patient preferences and agency, with patients favouring holistic assessment, self-management and adequate information and consultation to participate in decision-making. Discussion: Palliative care health literacy for COPD patients, families and staff attending primary settings may ensure well-planned continuous care, symptom management and support care at home.

Indexed as

COPDpalliative careprimary careSouth Africa

Identifiers

PMID41181374
PMCPMC12579134

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.