"I can't get it into my head that I have cancer…"-A qualitative interview study on needs of patients with lung cancer.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 24 11 2017
accepted: 29 04 2019
entrez: 16 5 2019
pubmed: 16 5 2019
medline: 23 1 2020
Statut: epublish

Résumé

Caring for patients with advanced lung cancer is of high relevance in different clinical settings. Lung cancer is among the most common causes of death from malignant neoplasms worldwide; with increasing prevalence and mortality. To get a better understanding of individual patients' needs, exploring the experiences and meaning of living with advanced lung cancer at the end of life, and to develop strategies for improving patient-centred care in Germany. Qualitative explorative interview study with patients, using grounded theory. A sample of 17 adults living with advanced lung cancer in Lower Saxony/Germany was recruited in two university hospitals. Patients were asked to tell of their experiences of living with advanced lung cancer. The emphasis of this study was the period of palliative tumour therapy. The main phenomenon of living with advanced lung cancer is the feeling of having to redefine one's own existence, such as social roles within and outside the family. The diagnosis trigger powerlessness, which can lead to information passivity, followed by acceptance of aggressive tumour treatment. Patients perceive a high degree of psychological and social stress, without being able to express this. There is a lack of regular appropriate psychosocial care accompanying chemotherapy. Patients ascribe their physical suffering to the side effects of tumour treatment, which may trigger a desire to die. Finally, patients tend to hide their individual needs, even when asked. Regarding the patients' needs, greater emphasis must be placed on psychosocial care as part of the biopsychosocial model to adequately consider the patients' concerns. Assessments can be helpful to enhance communication at an early stage across all professions into the multi-professional therapy.

Sections du résumé

BACKGROUND
Caring for patients with advanced lung cancer is of high relevance in different clinical settings. Lung cancer is among the most common causes of death from malignant neoplasms worldwide; with increasing prevalence and mortality.
AIM
To get a better understanding of individual patients' needs, exploring the experiences and meaning of living with advanced lung cancer at the end of life, and to develop strategies for improving patient-centred care in Germany.
DESIGN
Qualitative explorative interview study with patients, using grounded theory.
SETTING/PARTICIPANTS
A sample of 17 adults living with advanced lung cancer in Lower Saxony/Germany was recruited in two university hospitals. Patients were asked to tell of their experiences of living with advanced lung cancer. The emphasis of this study was the period of palliative tumour therapy.
RESULTS
The main phenomenon of living with advanced lung cancer is the feeling of having to redefine one's own existence, such as social roles within and outside the family. The diagnosis trigger powerlessness, which can lead to information passivity, followed by acceptance of aggressive tumour treatment. Patients perceive a high degree of psychological and social stress, without being able to express this. There is a lack of regular appropriate psychosocial care accompanying chemotherapy. Patients ascribe their physical suffering to the side effects of tumour treatment, which may trigger a desire to die. Finally, patients tend to hide their individual needs, even when asked.
CONCLUSIONS
Regarding the patients' needs, greater emphasis must be placed on psychosocial care as part of the biopsychosocial model to adequately consider the patients' concerns. Assessments can be helpful to enhance communication at an early stage across all professions into the multi-professional therapy.

Identifiants

pubmed: 31086395
doi: 10.1371/journal.pone.0216778
pii: PONE-D-17-41100
pmc: PMC6516640
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0216778

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Henrikje Stanze (H)

Department of Palliative Medicine, University Medical Center Göttingen, Göttingen, Germany.
Institute for General Practice, Hannover Medical School, Hannover, Germany.

Nils Schneider (N)

Institute for General Practice, Hannover Medical School, Hannover, Germany.

Friedemann Nauck (F)

Department of Palliative Medicine, University Medical Center Göttingen, Göttingen, Germany.

Gabriella Marx (G)

Department of Palliative Medicine, University Medical Center Göttingen, Göttingen, Germany.
Department of General Practice / Primary Care, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

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Classifications MeSH