Literature DB >> 23742065

A loss of social eating: the experience of individuals living with gastroparesis.

Jose Bennell1, Claire Taylor.   

Abstract

AIMS AND
OBJECTIVES: To report the experience of patients living with gastroparesis.
BACKGROUND: The complex illness of gastroparesis is a condition of delayed gastric emptying associated with a range of different symptoms, including nausea, vomiting and depression, resulting in altered eating patterns. Patients are often over-investigated, treatments are not always successful, and quality of life is often impaired.
DESIGN: A descriptive phenomenology study was undertaken to examine the experience of living with gastroparesis. Nine gastroparesis patients gave in-depth interviews. The interviews were transcribed, and framework analysis methods applied.
METHODS: A descriptive phenomenology study was undertaken. Nine gastroparesis patients gave in-depth interviews. The interviews were transcribed, and framework analysis methods applied.
RESULTS: Four main themes emerged: the first described their experiences and opinions of medical professionals, the second their understanding of mental health and mental illness, the third how they managed social settings and the fourth their identity and security. Their behaviour around food and mealtimes was often associated with feelings of loss, isolation and rejection, which influenced their reported quality of life. These factors resulted in their personal struggle to understand how this chronic, stigmatising illness affects their identity and their need for security.
CONCLUSIONS: The complex illness of gastroparesis affects every aspect of patients' lives. As treatments for gastroparesis continue to evolve, therapies to help these patients address the psychological impact and the feelings of loss they report must not be overlooked. RELEVANCE TO CLINICAL PRACTICE: A better understanding of these patients' sense of loss of normal eating behaviour and the associated psychological distress needs to inform gastroparesis service provision with a view to developing a more holistic service for this patient group.
© 2013 John Wiley & Sons Ltd.

Entities:  

Keywords:  chronic illness; eating; gastroparesis; psychological distress; symptom experience

Mesh:

Year:  2013        PMID: 23742065     DOI: 10.1111/jocn.12196

Source DB:  PubMed          Journal:  J Clin Nurs        ISSN: 0962-1067            Impact factor:   3.036


  3 in total

1.  Exploring Symptom Severity, Illness Perceptions, Coping Styles, and Well-Being in Gastroparesis Patients Using the Common Sense Model.

Authors:  Sally Woodhouse; Geoff Hebbard; Simon R Knowles
Journal:  Dig Dis Sci       Date:  2018-02-22       Impact factor: 3.199

2.  From ischochymia to gastroparesis: proposed mechanisms and preferred management of dyspepsia over the centuries.

Authors:  Klaus Bielefeldt
Journal:  Dig Dis Sci       Date:  2014-04-09       Impact factor: 3.199

Review 3.  A qualitative systematic review of the social eating and drinking experiences of patients following treatment for head and neck cancer.

Authors:  Mark Dornan; Cherith Semple; Anne Moorhead; Eilís McCaughan
Journal:  Support Care Cancer       Date:  2021-03-01       Impact factor: 3.603

  3 in total

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