Affiliation:
1. University of British Columbia, Vancouver, BC, Canada
2. University Health Network, Toronto, ON, Canada
Abstract
Survivorship concerns are common after prostate cancer with many survivors experiencing long-term and late effects of treatment. Patient navigation has been promoted to improve continuity of care. While many studies have examined the potential benefits of patient navigation by health-care professionals for the screening and diagnostic phase, few are focused on peer navigation for prostate cancer patients in the treatment and posttreatment survivorship phase. The purpose of this qualitative descriptive study was to explore the perceptions of men with prostate cancer and the partners of such men regarding their support needs and experiences. In depth, semistructured interviews were conducted with 20 men who were prostate cancer survivors and 4 partners. Qualitative thematic analysis was used to identify themes and patterns across the interviews. According to the results, participants had experienced uncertainty regarding their test results and treatment options. Many participants had dealt with these challenges by researching information and seeking support from health-care professionals, family members, and fellow prostate cancer patients. Four themes are highlighted: (a) dealing with the unknown, (b) everyone is different, (c) keep looking forward, and (d) getting on with it. Overall participants held favorable views of peer support. Sharing one’s experiences with an empathic peer who has completed treatment can reassure the patient that he is not alone. Knowing what to expect empowers men and their partners to manage the illness and effects of treatment. This research provides insights into the scope of patients’ and partners’ informational and psychosocial needs and preferred coping strategies.
Subject
Sociology and Political Science,Health(social science)
Cited by
7 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献