Attitudes of oncology health professionals to information from the Internet and other media.

OBJECTIVE: To investigate attitudes of Australian health professionals working in oncology to health-related information in the media and on the Internet and to patients who search for this information. DESIGN: Questionnaire-based survey. SETTING AND PARTICIPANTS: Questionnaires were mailed in January 2003 to all 333 health professionals belonging to the Victorian Cooperative Oncology Group. MAIN OUTCOME MEASURES: 27 items about attitudes to information in the media and the Internet, patient information-seeking and its effects on the doctor-patient relationship. RESULTS: 226 surveys (68%) were returned and assessable. Most respondents took notice of medical information reported on television/radio, in newspapers (80% each) and on the Internet (56%), mainly to be informed when patients ask questions (82%) and to check its accuracy (60%). Most were concerned about this accuracy (64% believed it accurate only sometimes, and 23% rarely), and 91% believed information from the Internet had the potential to cause harm to patients. Nevertheless, they generally supported patients' information-searching, believing it allowed them to be better informed (58%), and did not affect their ability to cope with their illness (49%), or their trust in, and relationship with, their doctor (69% and 67%, respectively). CONCLUSIONS: Oncology health professionals are aware of patients' use of the Internet and other media to obtain medical information. To ensure oncology patients find reliable and relevant information and to minimise the risk of harm, the health professionals treating them should provide guidance in finding information sources, and assistance in interpreting the information obtained.

'It's not the easy part': the experience of significant others of women with early stage breast cancer, at treatment completion.

Partners of women with breast cancer are intimately affected by their disease. This study describes the lived experience of the significant others of women with early stage breast cancer at the point of their partners' completion of adjuvant therapies. Significant others describe their need to adapt to the fear of losing their partner, the impact on their own mortality and their new role of caregiver for which they were unprepared. The greatest divergence between patient and partner was at the point of treatment completion. Whereas the women were continuing to experience difficulties at this time, their significant others were focused on 'getting back to normal.' There is a need to increase our understanding of the psychosocial needs of primary carers in order to better support them, as integral members of the care team.