Evidence map›Paper›PMID 40735341›Full record

ArticlePalliative care and social practice2025

Experiences and perspectives by family caregivers on a palliative care journey: A case report from India.

Soumya Liz Jacob, Malathi G Nayak, Linu Sara George, Leah Macaden, Prathibha Lydia Braggs

Abstract readCase Reports
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
  2. Article
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

5 authors.

Soumya Liz JacobDepartment of Community Health Nursing, Manipal College of Nursing, Manipal Academy of Higher Education (MAHE), Karnataka, India.ORCID https://orcid.org/0000-0002-1619-0545
Malathi G NayakDepartment of Community Health Nursing, Manipal College of Nursing, Manipal Academy of Higher Education (MAHE), Karnataka, India.ORCID https://orcid.org/0000-0002-3487-0771
Linu Sara GeorgeDepartment of Fundamentals of Nursing, Manipal College of Nursing, Manipal Academy of Higher Education (MAHE), Karnataka, India.ORCID https://orcid.org/0000-0003-0022-4373
Leah MacadenNursing Studies, School of Health in Social Science, The University of Edinburgh, UK.ORCID https://orcid.org/0000-0002-2680-6462
Prathibha Lydia BraggsDepartment of Mental Health Nursing, Manipal College of Nursing, Manipal Academy of Higher Education (MAHE), Karnataka, India.ORCID https://orcid.org/0009-0004-8543-316X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Palliative care plays a vital role in supporting individuals with terminal illnesses, yet its integration and acceptance in Indian society confront significant challenges. This is despite the fact that 5.4 million people in India require palliative care annually, and <2% receive the same. Understanding the palliative care journey from the caregivers' perspective is particularly important in the Indian context, as caregivers play a central role from diagnosis to end-of-life care and beyond. This study explores the impact of caregiving on family members of terminally ill patients in India, examining the physical, emotional, psychological, and social challenges they encounter. It unfolds the coping mechanisms and the resilience they develop throughout their caregiving journey while providing insight into their experiences, perceptions, and the complexities of their decision to choose palliative care. The study utilizes a focused ethnographic approach, collecting data from the caregivers of an older gentleman who was diagnosed with terminal alveolar cancer and metastasis along with multimorbidity through three unstructured interviews at different periods of the illness trajectory, coupled with participant observation and field notes. While highlighting caregivers' various stressors, the findings indicate that access to palliative care led to benefits such as alleviating physical burden, professional support, social inclusion, and preparation for loss. However, societal reluctance and stigma toward palliative care were evident, with family caregivers feeling inadequate or a sense of failing their duties by placing their loved one in a palliative care center. Destigmatizing palliative care can foster a more supportive and understanding environment for patients and caregivers. These findings offer insights into the complexities of the caregiving process and can potentially inform future broader investigations in the region.

Indexed as

case reportfamily caregiversfocused ethnographyIndiapalliative careperspectives

Identifiers

PMID40735341
PMCPMC12304659

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Registered trials

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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.