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dc.contributor.advisorMurray, Scotten
dc.contributor.advisorKendall, Marilynen
dc.contributor.advisorBoyd, Kirstyen
dc.contributor.authorKimbell, Barbaraen
dc.date.accessioned2016-06-16T14:52:33Z
dc.date.available2016-06-16T14:52:33Z
dc.date.issued2015-07-04
dc.identifier.urihttp://hdl.handle.net/1842/15882
dc.description.abstractBackground: The number of patients dying with advanced liver disease is rising dramatically. However, little is known about the experiences of these patients and their families in respect of their care and everyday life with the disease. Palliative care services are traditionally focused on cancer and more recently on other types of organ failure, but liver disease is relatively neglected. Aim and objectives: This study aimed to broaden our understanding of the experience of living and dying with advanced liver disease. Specifically, it sought to explore the dynamic physical, psychosocial, existential and information needs of patients and their lay and professional carers, and to review their use of health, social and voluntary services. Additionally, this study examined the utility of a qualitative longitudinal, multi-perspective methodology in end-of-life research. Methods: This study employed qualitative, multi-perspective serial in-depth interviews. Patients with different aetiologies of liver disease were recruited in hospital. They and their lay carers were interviewed up to three times over one year. Single interviews were undertaken with case-linked professionals. Interviews were recorded, transcribed and analysed using grounded theory techniques and NVivo 9. Results: 15 patients, 11 lay carers and 11 professional carers were recruited, and 53 interviews conducted. Uncertainty was the key experience at all stages of the illness, across all domains, and for all participants: patients, lay carers and professionals. This uncertainty related to the nature of the illness, the unpredictability of disease pathway and prognosis, poor communication and information-sharing, and complexities of care. Coping strategies demonstrated a continuous quest to manage uncertainty. Current care arrangements were a poor fit with the high levels of physical and psychosocial need identified. The ubiquitous uncertainty meant that a care planning approach was difficult to introduce. Employing a qualitative longitudinal, multi-perspective approach emerged as a useful and effective way in which to conduct research with this patient group and contributed new learning with regard to its application in end-of-life research. Conclusion: This study identified uncertainty as the central pervasive factor in the experiences of patients, lay and professional carers. The needs of this patient group are currently poorly met from diagnosis to bereavement. Uncertainty makes advance care planning important, but difficult to know when to start. More needs to be done to ensure that people living and dying with advanced liver disease and their families benefit from appropriate and timely supportive and palliative care.en
dc.contributor.sponsorEconomic and Social Research Council (ESRC)en
dc.language.isoen
dc.publisherThe University of Edinburghen
dc.relation.hasversionBOYD, K., KIMBELL, B., MURRAY, S. & IREDALE, J. 2012. Living and dying well with end-stage liver disease: time for palliative care? Hepatology, 55, 1650-1651.en
dc.relation.hasversionKIMBELL, B. & MURRAY, S. A. 2013. What is the patient experience in advanced liver disease? A scoping review of the literature. BMJ Supportive &en
dc.subjectadvanced liver diseaseen
dc.subjectuncertaintyen
dc.subjectpalliative careen
dc.titleLiving, dying and caring in advanced liver disease: the challenge of uncertaintyen
dc.typeThesis or Dissertationen
dc.type.qualificationlevelDoctoralen
dc.type.qualificationnamePhD Doctor of Philosophyen


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