Special paperThe impact of cancer on key relatives: A comparison of relative and patient concerns
References (25)
- et al.
Distress associated with cancer as measured by the Illness Distress Scale
Psychosomatics
(1990) The experience of cancer during early and advanced stages: the views of patients and their mates
Soc Sci Med
(1984)- et al.
Comparative studies of psychological function in patients with advanced cancer. 1. Self reported depressive symptoms
Psychosom Med
(1977) - et al.
A psychological analysis of cancer patients and their next of kin
Cancer
(1985) - et al.
Psychosocial aspects of mastectomy. II. The man's perspective
Am J Psychiatry
(1978) The repercussions of mastectomy on the family
Int J Family Psychiatry
(1981)Planning nursing interventions for family members of adult cancer patients
Cancer Nursing
(1981, October)Family responses to cancer hospitalisation
- et al.
Adjustment to cancer: who is the patient—the husband or the wife?
Israeli J Med Sci
(1988) - et al.
Emotional responses to the diagnosis of cancer: age related comparisons
Adjustment of patients and husbands to the initial impact of breast cancer
Nursing Res
Psychological problems and their recognition in women with cancer of the cervix
Report to Cancer Research Campaign
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The information needs of patients with head and neck cancer and their caregivers: A short report of instrument development and testing
2013, Applied Nursing ResearchCitation Excerpt :Carers also seemed to have more information needs (as indicated by percentages rating needs as ‘very important’) than patients, broadly consistent with previous work showing that carers tend to seek information more proactively than patients (James et al., 2007). The findings of greater informational need as well as previous findings of carer unmet needs exceeding patient unmet needs (Soothill et al., 2003) and levels of concern (Harrison, Haddad, & Maguire, 1995) underscore the importance of addressing carer informational needs (Morris & Thomas, 2002). The HaNiQ needs to be tested in a larger sample of HNC patients and carers, with assessments of validity such as criterion and construct validity undertaken.
Consumer perspectives of the Australian Home Medicines Review Program: Benefits and barriers
2012, Research in Social and Administrative PharmacyCitation Excerpt :Although the carers in the study by Smith et al16 reported problems of not being informed about their care recipients’ medication changes, they were at the same time aware of the prescribers’ dilemma in juggling information disclosure to carers with the care recipients’ right to privacy. Other studies found that managing medication contributed to the stress of caring,17 carers generally expressed stronger information needs and required different types of information than patients,18 and the provision of specific information to carers was vital in the process of developing competency as a carer.19,20 The undermet information need of carers has shown to cause widespread dissatisfaction of the carers 21-23 and added to the carers’ difficulty in defining their caring position in relation to the care recipient and their health care professionals.21
Telling bad news to the elderly cancer patients: The role of family caregivers in the choice of non-disclosure - The Gruppo Italiano di Oncologia Geriatrica (GIOGer) Study
2010, Journal of Geriatric OncologyCitation Excerpt :Our study also showed the NI patients’ caregivers considered more destabilising information inherent to the diagnosis. This may be due to the phase immediately following diagnosis, which is the most stressful for the caregiver.49 PI caregivers considered the prognosis to be more stressful.
A separate structured conversation with relatives of patients enrolled for advanced palliative home care: A care development project
2014, Palliative and Supportive CareAssessment of the Need for Psychological Help for Cancer Patients and Their Close Relatives
2022, Journal of Siberian Federal University - Humanities and Social Sciences