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The impact of chronic breathlessness on psychological concerns and quality of life in an older, frail population in primary care

Elliott-Button, Helene Louise

Authors

Helene Louise Elliott-Button



Contributors

Miriam (Miriam J.) Johnson
Supervisor

Abstract

Background Chronic breathlessness is a debilitating symptom with major detrimental impact on individuals, carers, across health care settings. Little is known about prevalence, impact, or experience of breathlessness in the older, frail population.
Aims For older adults at risk of frailty: to explore the impact of chronic breathlessness on patients’ and carers’ psychological wellbeing and quality of life (QoL), and to explore how chronic breathlessness is identified and assessed in primary care, considering patient, carer, and health care practitioner (HCP) experiences.
Methods A multiple-methods thesis incorporating a systematic review and mixed-methods study. My quantitative narrative systematic review of published literature aimed to determine how clinicians identified and assessed breathlessness across health care settings. My mixed-methods study included: a quantitative cross-sectional survey to determine prevalence and psychological impact of chronic breathlessness, and clinical factors associated with breathlessness, in the primary care setting; qualitative in-depth interviews further explored psychological impact and experiences of management in primary care for patients, carers, and HCPs. Mixed-methods findings were synthesised using modified critical interpretative synthesis, then integrated with the systematic review results.
Findings Chronic breathlessness is prevalent (40%) in older, frail adults and associated with worse psychological outcomes and poorer QoL. People with chronic breathlessness give up activities because of their breathlessness which is conflated with the underlying disease and not recognised as therapeutic target by patient or HCPs. Chronic breathlessness is often ‘one of many’ symptoms and in the primary care context of ‘one appointment, one problem’, remains invisible and unmanaged. HCPs can feel helpless and do not routinely ask about impact of breathlessness on QoL.
Conclusions Lack of routine assessment in primary care means older, frail adults with chronic breathlessness may not access evidence-based symptom-targeted interventions. Systematic identification, assessment, and management in primary care may help improve psychological health, QoL, and overall wellbeing.

Citation

Elliott-Button, H. L. The impact of chronic breathlessness on psychological concerns and quality of life in an older, frail population in primary care. (Thesis). Hull York Medical School, the University of Hull and the University of York. https://hull-repository.worktribe.com/output/4224612

Thesis Type Thesis
Deposit Date Jan 10, 2023
Publicly Available Date Feb 24, 2023
Keywords Medical sciences
Public URL https://hull-repository.worktribe.com/output/4224612
Additional Information Hull York Medical School, The University of Hull and the University of York
Award Date Sep 1, 2022

Files

Thesis (3.9 Mb)
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Copyright Statement
© 2022 Elliott-Button, Helene Louise. All rights reserved. No part of this publication may be reproduced without the written permission of the copyright holder.




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