Anxiety, depression, and quality of life in caregivers of patients with cancer in late palliative phase
Top Cited Papers
Open Access
- 22 April 2005
- journal article
- research article
- Published by Elsevier BV in Annals of Oncology
- Vol. 16 (7), 1185-1191
- https://doi.org/10.1093/annonc/mdi210
Abstract
Background:: Limited research has been done on mental health and health-related quality of life (QOL) of primary caregivers (PCs) to patients staying at home with advanced cancer. This study examines anxiety, depression, and QOL in PCs of patients with cancer in the late palliative phase. Patients and methods:: The sample consisted of 49 PCs of women with breast cancer and 47 PCs of men with prostate cancer. QOL was rated with the Medical Outcome Study Short Form (SF-36), and mental health with the Hospital Anxiety and Depression Scale (HADS). The findings were compared with age-adjusted norm data (norm). Results:: Physical QOL was significantly higher than norm in both genders, while mental QOL was significantly lower in male PCs. The level of anxiety was significantly higher than norm in both genders. No significant difference for level of depression was found in either gender, while caseness of HADS-defined depression was significantly more prevalent in female PCs compared with norm. Conclusion:: PCs of both genders had significantly more anxiety than norm samples. Health care personnel in contact with PCs should consider screening them for mental symptoms and QOL and, if necessary, recommend further evaluation by their doctors.This publication has 37 references indexed in Scilit:
- Measuring the mental health status of the Norwegian population: A comparison of the instruments SCL-25, SCL-10, SCL-5 and MHI-5 (SF-36)Nordic Journal of Psychiatry, 2003
- Lifestyle interference and emotional distress in family caregivers of advanced cancer patientsCancer, 2002
- Effect of Caregiver Perception of Preparedness on Burden in an Oncology PopulationOncology Nursing Forum, 2002
- A Norwegian Psychiatric Epidemiological StudyAmerican Journal of Psychiatry, 2001
- Family Caregiver Quality of Life: Differences Between Curative and Palliative Cancer Treatment SettingsJournal of Pain and Symptom Management, 1999
- Identifying the concerns of informal carers in palliative carePalliative Medicine, 1999
- Identifying the concerns of informal carers in palliative carePalliative Medicine, 1999
- Family Care Giving at Home as a Solitary JourneyImage: the Journal of Nursing Scholarship, 1996
- A problem solving intervention for caregivers of cancer patientsSocial Science & Medicine (1982), 1995
- Measurement and the Analysis of BurdenResearch on Aging, 1985