Literature DB >> 32596966

What are the psychological effects of mesothelioma on patients and their carers? A scoping review.

Virginia Sherborne1, Jane Seymour1, Bethany Taylor1, Angela Tod1.   

Abstract

OBJECTIVE: Despite recent advances in research, malignant mesothelioma remains an incurable and devastating disease, typically bringing shock and emotional distress to patients and carers. Little research has addressed the psychological impact on either group. This scoping review examines the current state of evidence on the psychological effects of mesothelioma on patients and carers, and identifies areas for further research.
METHODS: We searched PubMed, PsychINFO, CINAHL, the Cochrane Library and Web of Science for English-language peer-reviewed research articles published 1981 to 2019 reporting studies focussing on the psychological effects of mesothelioma on patients and carers. Following data extraction and quality appraisal, reflexive thematic analysis was used to identify themes.
RESULTS: Seventeen articles met the inclusion criteria. Carers' experiences were generally amalgamated with patients'. Three themes were developed. The Passing of Time included the importance of timing of interventions; delays in the medical journey; awareness of different time-phases in mesothelioma; and uncertainty/certainty. Dealing with Difficult Feelings reflected ubiquitous negative emotions, feelings about identity and states of being and associated coping strategies. Craving Good Communication covered issues related to sharing of information and to positive/negative aspects of communication.
CONCLUSIONS: Though limited, the evidence indicates that mesothelioma, with its high symptom-burden, incurability, rarity and asbestos-related causation, leads to complex and inter-relating psychological effects on patients and carers. These effects are both negative and positive. The sparse literature gives a partial picture and demonstrates an urgent need for more nuanced research. Studies exploring the experiences of specific groups are recommended, with particular attention required to carers.
© 2020 The Authors. Psycho-Oncology published by John Wiley & Sons Ltd.

Entities:  

Keywords:  cancer; caregivers; communication; diagnosis; mesothelioma; oncology; palliative care; psycho-oncology; psychological distress; review

Year:  2020        PMID: 32596966     DOI: 10.1002/pon.5454

Source DB:  PubMed          Journal:  Psychooncology        ISSN: 1057-9249            Impact factor:   3.894


  3 in total

1.  Living beyond expectations: a qualitative study into the experience of long-term survivors with pleural mesothelioma and their carers.

Authors:  Matthew Johnson; Peter Allmark; Angela Tod
Journal:  BMJ Open Respir Res       Date:  2022-05

2.  Understanding clinical decision-making in mesothelioma care: a mixed methods study.

Authors:  Catherine Henshall; Paul Dawson; Najib Rahman; Hannah Ball; Anand Sundralingam; Mitra Shahidi; Edward McKeown; John Park; Helen Walthall; Zoe Davey
Journal:  BMJ Open Respir Res       Date:  2022-07

3.  Dying of mesothelioma: A qualitative exploration of caregiver experiences.

Authors:  Jessica T Lee; Dipti L Mittal; Anne Warby; Steven Kao; Haryana M Dhillon; Janette L Vardy
Journal:  Eur J Cancer Care (Engl)       Date:  2022-06-20       Impact factor: 2.328

  3 in total

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