Survivorship issues following treatment completion—results from focus groups with Australian cancer survivors and health professionals

Background The number of cancer survivors is increasing dramatically. Many survivors report long-term psychosocial, physical and other consequences. To understand the issues faced by Australian cancer survivors we conducted focus groups with cancer patients and health professionals. Methods Patients...

Full description

Saved in:
Bibliographic Details
Published in:Journal of cancer survivorship 2008-03, Vol.2 (1), p.20-32
Main Authors: Jefford, Michael, Karahalios, Emily, Pollard, Annabel, Baravelli, Carl, Carey, Mariko, Franklin, Jennie, Aranda, Sanchia, Schofield, Penelope
Format: Article
Language:English
Subjects:
Adaptation, Psychological
Adult
Aged
Cancer
Emotions
Female
Focus groups
Health Informatics
Health Personnel - statistics & numerical data
Health Promotion and Disease Prevention
Humans
Male
Medicine
Medicine & Public Health
Middle Aged
Neoplasms - classification
Neoplasms - physiopathology
Neoplasms - psychology
Oncology
Primary Care Medicine
Psychotherapy
Public Health
Quality of Life
Quality of Life Research
Social Identification
Social Support
Survivor
Survivors - psychology
Survivors - statistics & numerical data
Victoria
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Background The number of cancer survivors is increasing dramatically. Many survivors report long-term psychosocial, physical and other consequences. To understand the issues faced by Australian cancer survivors we conducted focus groups with cancer patients and health professionals. Methods Patients were identified through a peer support program at a major cancer treatment center (Peter Mac). Health professionals were also recruited from Peter Mac. Focus groups followed a semi-structured format based on themes identified from the literature. Questions focused on treatment completion, and 1 year post-treatment. Participants were also asked to suggest solutions to address identified issues. Focus groups were taped, transcribed, cross-checked for accuracy, and analyzed independently. Results The most common needs (in terms of both frequency and intensity) reported at treatment completion by both survivors and professionals were dealing with fatigue, anxiety about cancer recurrence, others expecting you to be back to normal, having to create new expectations about physical ability, and anxiety about leaving the hospital system. The most common needs at 1 year were anxiety about check-ups and results, and going into early menopause. The most frequently suggested ways of meeting these perceived needs were reassuring survivors the way they feel is normal and putting them in contact with others who have been through the same experience. Discussion There was a high level of congruence in the themes identified by survivors and health professionals. Implications for cancer survivors These results provide a clear direction for the development of resources to support cancer survivors following treatment completion.
ISSN:1932-2259
1932-2267
DOI:10.1007/s11764-008-0043-4