Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.785769
Title: Patient-reported long term complications after ileal conduit surgery and the implementation of a surveillance protocol
Author: Abdelbaky, Ather Mohamed Taha
ISNI:       0000 0004 7971 2640
Awarding Body: Newcastle University
Current Institution: University of Newcastle upon Tyne
Date of Award: 2018
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Abstract:
Introduction and aim of the study: Ileal conduit(IC) is the most frequent urinary diversion following radical cystectomy. Reports highlighted high rates of long term complications but the best schedule of surveillance remains undecided. The main aim of this study to investigate IC patients' experience after surgery and to explore current practice of surveillance and investigate stakeholders' views about alternative models. Materials and Methods: This study was formed of two parts. Part A: 2000 IC patients were invited to complete a postal questionnaire. The questionnaire explored patients' experience of complications and their views of follow up. Statistical analysis was conducted using Stata®14 software to identify association between reporting complications, patients' satisfaction or views and patient characteristics. Part B: A multicentre qualitative study, using semi-structured interviews among health professionals involved in IC care was conducted. Interviews explored participants' views of current practice and best surveillance model. Following thematic analysis, the framework of the NPT was used to analyse the data. Results: Part A: 1092 completed questionnaires were analysed (response rate= 60%). 88% of respondents reported ≥1 complication, and 45% ≥1 frequent complication. UTIs, hernia and appliances problems are the most reported ones. Multivariable logistic regression showed female gender, age < 60 years, benign indication for surgery and difficult access to stoma nurse were associated with reporting complications. Of the 44% who felt GP follow up is inappropriate; lack of experience was the main cause. Part B: 17 interviews were conducted with different types of health professionals at three centres. Participants described good understanding of surveillance scope and value. They highlighted the need for change due to lack of guidelines and service workload. The stoma nurse role was seen as pivotal in making surveillance workable. There was a lack of agreement over surveillance length. Participants raised concern regarding GPs willingness to participate and about lack of resources. Conclusion: The high and cumulative incidence of IC related complications suggest the development of a standardised, evidence based long term surveillance protocol. A shared care community based nurse led scheme could be a suitable model.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.785769  DOI: Not available
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