The Perspective of Cancer Patients in Palliative Care on Unmet Needs: A Qualitative Synthesis Using Meta-Ethnography.

cancer care needs end of life palliative care terminally ill unmet needs

Journal

The American journal of hospice & palliative care
ISSN: 1938-2715
Titre abrégé: Am J Hosp Palliat Care
Pays: United States
ID NLM: 9008229

Informations de publication

Date de publication:
05 Jan 2024
Historique:
medline: 5 1 2024
pubmed: 5 1 2024
entrez: 5 1 2024
Statut: aheadofprint

Résumé

As cancer patients approach the end of life, their needs become more complex, increasing the demand for palliative care. Advanced-stage cancer patients encounter increasing unmet psychological, physical, autonomy, and communication needs, reflecting the difference between patients' perceived requirements and the support from health care professionals. The objective of this study was to synthesize qualitative evidence on unmet needs in palliative cancer care among inpatient and outpatient adults. We conducted a meta-ethnographic review according to Noblit and Hare's framework and the operationalized guidelines developed by Sattar. The eMERGe Reporting Guidance was followed. A literature search was conducted in Cinahl, Embase, Medline, Scopus, Web of Science, PsycINFO and Google Scholar for gray literature. For all the studies, direct quotes from the participants and authors' results were identified, coded and analyzed in NVivo 1.7.1 and extracted as I and II order constructs from which higher third-order themes originated. Eight studies were included. Four new themes emerged, representing areas where palliative cancer care patients expressed a need for help: Palliative care patients require a secure, suffering-free end-of-life journey with informed decision-making and team support. Ensuring continuity of care, validating their suffering, and allocating sufficient time are crucial aspects of care. This involves maintaining a consistent care plan, respecting patients' emotions and experiences, and providing services tailored to individual needs.

Sections du résumé

BACKGROUND BACKGROUND
As cancer patients approach the end of life, their needs become more complex, increasing the demand for palliative care. Advanced-stage cancer patients encounter increasing unmet psychological, physical, autonomy, and communication needs, reflecting the difference between patients' perceived requirements and the support from health care professionals. The objective of this study was to synthesize qualitative evidence on unmet needs in palliative cancer care among inpatient and outpatient adults.
METHODS METHODS
We conducted a meta-ethnographic review according to Noblit and Hare's framework and the operationalized guidelines developed by Sattar. The eMERGe Reporting Guidance was followed. A literature search was conducted in Cinahl, Embase, Medline, Scopus, Web of Science, PsycINFO and Google Scholar for gray literature. For all the studies, direct quotes from the participants and authors' results were identified, coded and analyzed in NVivo 1.7.1 and extracted as I and II order constructs from which higher third-order themes originated.
RESULTS RESULTS
Eight studies were included. Four new themes emerged, representing areas where palliative cancer care patients expressed a need for help:
CONCLUSIONS CONCLUSIONS
Palliative care patients require a secure, suffering-free end-of-life journey with informed decision-making and team support. Ensuring continuity of care, validating their suffering, and allocating sufficient time are crucial aspects of care. This involves maintaining a consistent care plan, respecting patients' emotions and experiences, and providing services tailored to individual needs.

Identifiants

pubmed: 38180378
doi: 10.1177/10499091231226429
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

10499091231226429

Déclaration de conflit d'intérêts

Declaration of conflicting interestsThe author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Auteurs

Ilaria Basile (I)

Department of Biomedicine and Prevention, University of Rome "Tor Vergata", Rome, Italy.
High-Complexity Unit of Palliative Care, Pain Therapy and Rehabilitation, Foundation IRCCS, National Cancer Institute, Milan, Italy.

Letteria Consolo (L)

Department of Biomedicine and Prevention, University of Rome "Tor Vergata", Rome, Italy.
Bachelor School of Nursing, Foundation IRCCS, National Cancer Institute, Milan, Italy.

Daniele Rusconi (D)

Urology Unit, Foundation, IRCCS, National Cancer Institute, Milan, Italy.

Laura Arba (L)

Head and Neck Cancer and Rare Tumor Medical Oncology Unit, Foundation, IRCCS, National Cancer Institute, Milan, Italy.

Flavia Rampichini (F)

Library of the Central School of Medicine, University of Milan, Milan, Italy.

Augusto Caraceni (A)

High-Complexity Unit of Palliative Care, Pain Therapy and Rehabilitation, Foundation IRCCS, National Cancer Institute, Milan, Italy.
University of Milan, Milan, Italy.

Maura Lusignani (M)

Department of Biomedical Sciences for Health, Milan, Italy.

Classifications MeSH