Abstract

Objective This study sought to explore the experience of people with a diagnosis of cancer while attending for imaging procedures. The diversity and complexity of the issues described within individual interviews made it impossible to include all cancer groups in one paper. This paper focuses on the cohort of men with prostate cancer. Method An opportunistic sample of men (n = 8) were recruited from Cancer Support Groups throughout the North-east of Scotland. A qualitative, exploratory and retrospective study design was employed using semi-structured interviews. All interviews were audio taped and full transcripts produced. These were analysed following the recommendations of Miles and Huberman (1994). Main findings Men were keen to take part in the study, and described experiences from pre-diagnosis to the date of interview. Participants reported different routes to diagnosis, then having a range of diagnostic procedures indicating a very personal journey with no standardised approach. Imaging was not seen as a separate event but part of the whole story. The provision of radiology patient information material was haphazard. Participants could explain why they were having these procedures, and saw them as a ‘necessary evil’. The provision of results of their tests was complex and chaotic, and was described as an anxious time. Conclusion This study provides a unique insight into the experiences of men with prostate cancer relating to their attendance for imaging. Health professionals need to listen to their patients and learn, in order to provide a high quality, patient-centred imaging service.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call