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The psychosocial impact of living with mesothelioma: Experiences and needs of patients and their carers regarding supportive care.
Prusak, Agata; van der Zwan, Jan Maarten; Aarts, Mieke J; Arber, Anne; Cornelissen, Robin; Burgers, Sjaak; Duijts, Saskia F A.
Afiliação
  • Prusak A; Department of Research & Development, Netherlands Comprehensive Cancer Organization (Integraal Kankercentrum Nederland, IKNL), Utrecht, The Netherlands.
  • van der Zwan JM; Department of Research & Development, Netherlands Comprehensive Cancer Organization (Integraal Kankercentrum Nederland, IKNL), Utrecht, The Netherlands.
  • Aarts MJ; Department of Research & Development, Netherlands Comprehensive Cancer Organization (Integraal Kankercentrum Nederland, IKNL), Utrecht, The Netherlands.
  • Arber A; School of Health and Social Care, University of Surrey, Guildford, UK.
  • Cornelissen R; Department of Pulmonary Medicine, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • Burgers S; Department of Thoracic Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Duijts SFA; Department of Research & Development, Netherlands Comprehensive Cancer Organization (Integraal Kankercentrum Nederland, IKNL), Utrecht, The Netherlands.
Eur J Cancer Care (Engl) ; 30(6): e13498, 2021 Nov.
Article em En | MEDLINE | ID: mdl-34339095
ABSTRACT

OBJECTIVE:

Mesothelioma is a rare cancer with a poor prognosis caused by exposure to asbestos. Psychosocial support and care for mesothelioma patients and their carers is limited and not tailored to their specific needs. The aim of this study was to explore patients' and carers' needs and experiences regarding psychosocial support and their coping mechanisms dealing with psychosocial problems.

METHODS:

A qualitative study was performed using semi-structured interviews with both mesothelioma patients and their carers. Participants were recruited through two specialised hospitals and two patient organisations. All interviews were transcribed verbatim and thematically analysed.

RESULTS:

Ten patients (70% male, mean age 67.7) and five carers (20% male, mean age 65) participated in the study. The main themes identified for patients were active coping, limited needs and limited knowledge and awareness about psychosocial support. The main themes for carers were passive coping and 'it's all about the patient'.

CONCLUSION:

Mesothelioma patients do not seem to have high needs for psychosocial support, whereas carers do. However, knowledge about and awareness of psychosocial support is low among mesothelioma patients. The findings from this study should be used to adjust guidelines for psychosocial support in mesothelioma patients and their carers.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mesotelioma Maligno / Mesotelioma Tipo de estudo: Prognostic_studies / Qualitative_research Limite: Aged / Female / Humans / Male Idioma: En Revista: Eur J Cancer Care (Engl) Assunto da revista: ENFERMAGEM / NEOPLASIAS Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mesotelioma Maligno / Mesotelioma Tipo de estudo: Prognostic_studies / Qualitative_research Limite: Aged / Female / Humans / Male Idioma: En Revista: Eur J Cancer Care (Engl) Assunto da revista: ENFERMAGEM / NEOPLASIAS Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Holanda