Psychosocial Impact of Cancer Patients on Their Family Members
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Purpose A population-based study was conducted in order to examine the characteristics of family members of cancer patients in comparison with the general population and also to evaluate the psychosocial impact of cancer patients on their family members. Materials and Methods From the Fourth Korea National Health and Nutrition Examination Surveys (KNHANES IV) (2007-2009) dataset, we identified 460 cancer patients and then selected family members of these patients who were aged 20 years or older (n=565). The control group was sampled from members of families without a cancer patient with matching for sex and age (n=2,260). Serial conditional logistic regression models were used for comparison of characteristics between family members of cancer patients and subjects in the control group. Results Family members of cancer patients were less employed (57.9% vs. 63.0%, p < 0.001),more functionally limited (20.2% vs. 16.5%, p=0.032), and had lower self-rated health (p=0.023) compared with sex and age-matched control subjects. They also had a significantly higher level of stress (79.7% vs. 76.1%, p=0.008), history of depression (12.9% vs. 10.2%, p=0.035), and current depressive symptoms (5.5% vs. 3.5%,p=0.038). However, higher physical activity was reported in family members of cancer patients (13.6% vs. 9.6%, p=0.003) than in control subjects. The presence of a cancer patient in the family showed an association with current depressive symptoms (odds ratio, 1.62; 95% confidence interval, 1.05 to 2.48; p=0.028), however, the association was no longer significant after adjustment for household income, education level,and employment status (p=0.304). Conclusion Family members of cancer patients are more susceptible to depression, probably due to adverse change in socioeconomic status. Use of multidisciplinary approaches for promotion of psychological health and well-being is essential.
Abstract
Purpose A population-based study was conducted in order to examine the characteristics of family members of cancer patients in comparison with the general population and also to evaluate the psychosocial impact of cancer patients on their family members. Materials and Methods From the Fourth Korea National Health and Nutrition Examination Surveys (KNHANES IV) (2007-2009) dataset, we identified 460 cancer patients and then selected family members of these patients who were aged 20 years or older (n=565). The control group was sampled from members of families without a cancer patient with matching for sex and age (n=2,260). Serial conditional logistic regression models were used for comparison of characteristics between family members of cancer patients and subjects in the control group. Results Family members of cancer patients were less employed (57.9% vs. 63.0%, p < 0.001),more functionally limited (20.2% vs. 16.5%, p=0.032), and had lower self-rated health (p=0.023) compared with sex and age-matched control subjects. They also had a significantly higher level of stress (79.7% vs. 76.1%, p=0.008), history of depression (12.9% vs. 10.2%, p=0.035), and current depressive symptoms (5.5% vs. 3.5%,p=0.038). However, higher physical activity was reported in family members of cancer patients (13.6% vs. 9.6%, p=0.003) than in control subjects. The presence of a cancer patient in the family showed an association with current depressive symptoms (odds ratio, 1.62; 95% confidence interval, 1.05 to 2.48; p=0.028), however, the association was no longer significant after adjustment for household income, education level,and employment status (p=0.304). Conclusion Family members of cancer patients are more susceptible to depression, probably due to adverse change in socioeconomic status. Use of multidisciplinary approaches for promotion of psychological health and well-being is essential.
참고문헌 (25)
- Luckett T, "Psychological morbidity and quality of life of ethnic minority patients with cancer: a systematic review and meta-analysis", Lancet Oncol, 12, pp.1240~1248 (2011)
- Shi Q, "Symptom burden in cancer survivors 1 year after diagnosis: a report from the American Cancer Society’s Studies of Cancer Survivors", Cancer, 117, pp.2779~2790 (2011)
- Collins LG, "Caregiver care", Am Fam Physician, 83, pp.1309~1317 (2011)
- Bevans M, "Caregiving burden, stress, and health effects among family caregivers of adult cancer patients", JAMA, 307, pp.398~403 (2012)
- Kim Y, "Family caregivers’ strains: comparative analysis of cancer caregiving with dementia, diabetes, and frail elderly caregiving", J Aging Health, 20, pp.483~503 (2008)
- Hagedoorn M, "Couples dealing with cancer: role and gender differences regarding psychological distress and quality of life", Psychooncology, 9, pp.232~242 (2000)
- Hodges LJ, "A meta-analytic investigation of the relationship between the psychological distress of cancer patients and their carers", Soc Sci Med, 60, pp.1~12 (2005)
- Palos GR, "Caregiver symptom burden: the risk of caring for an underserved patient with advanced cancer", Cancer, 117, pp.1070~1079 (2011)
- Weaver KE, "Forgoing medical care because of cost: assessing disparities in healthcare access among cancer survivors living in the United States", Cancer, 116, pp.3493~3504 (2010)
- Choi YJ, "Prevalence and management of diabetes in Korean adults: Korea National Health and Nutrition Examination Surveys 1998- 2005", Diabetes Care, 32, pp.2016~2020 (2009)
- World Health Organization, "International guide for monitoring alcohol consumption and related harm", ~ (2000)
- "EuroQol: a new facility for the measurement of health-related quality of life. The EuroQol Group", Health Policy, 16, pp.199~208 (1990)
- Brooks R, "EuroQol: the current state of play", Health Policy, 37, pp.53~72 (1996)
- Chen X, "The family and harmonious medical decision making: cherishing an appropriate Confucian moral balance", J Med Philos, 35, pp.573~586 (2010)
- Given BA, "Family and caregiver needs over the course of the cancer trajectory", J Support Oncol, 10, pp.57~64 (2012)
- Northouse LL, "Living with prostate cancer: patients’ and spouses’ psychosocial status and quality of life", J Clin Oncol, 25, pp.4171~4177 (2007)
- Edwards B, "The psychological impact of a cancer diagnosis on families: the influence of family functioning and patients’ illness characteristics on depression and anxiety", Psychooncology, 13, pp.562~576 (2004)
- Meropol NJ, "American Society of Clinical Oncology guidance statement: the cost of cancer care", J Clin Oncol, 27, pp.3868~3874 (2009)
- Byers TE, "The impact of socioeconomic status on survival after cancer in the United States: findings from the National Program of Cancer Registries Patterns of Care Study", Cancer, 113, pp.582~591 (2008)
- Boyd C, "Associations between community income and cancer survival in Ontario, Canada, and the United States", J Clin Oncol, 17, pp.2244~2255 (1999)
- Burke L, "Smoking behaviors among cancer survivors: an observational clinical study", J Oncol Pract, 5, pp.6~9 (2009)
- McBride CM, "Teachable moments for promoting smoking cessation: the context of cancer care and survivorship", Cancer Control, 10, pp.325~333 (2003)
- Mackillop WJ, "Associations between community income and cancer incidence in Canada and the United States", Cancer, 89, pp.901~912 (2000)
- Northouse LL, "Interventions with family caregivers of cancer patients: metaanalysis of randomized trials", CA Cancer J Clin, 60, pp.317~339 (2010)
- Northouse L, "Psychosocial care for family caregivers of patients with cancer", J Clin Oncol, 30, pp.1227~1234 (2012)
