Caring for a loved one with advanced cancer:: Determinants of psychological distress in family caregivers

被引:154
作者
Dumont, Serge
Turgeon, Jean
Allard, Pierre
Gagnon, Pierre
Charbonneau, Cecile
Vezina, Lucie
机构
[1] Univ Laval, Ecole Serv Social, Fac Sci Sociales, Ctr Rech Cancerol, Quebec City, PQ G1K 7P4, Canada
[2] Univ Laval, Fac Med, Quebec City, PQ G1K 7P4, Canada
[3] Univ Ottawa, Div Palliat Care, Ottawa, ON, Canada
[4] Sister Char Ottawa Hlth Serv Partnership, Ottawa, ON, Canada
[5] Univ Laval, Fac Pharm, Ctr Hosp Univ Quebec, Ctr Rech Cancerol, Quebec City, PQ G1K 7P4, Canada
[6] Univ Laval, Ctr Rech, Univ Laval Robert Giffard, Quebec City, PQ G1K 7P4, Canada
[7] Ctr Jeunesse Quebec, Quebec City, PQ, Canada
[8] Hop Laval, Unite Med Familiale, Quebec City, PQ, Canada
关键词
D O I
10.1089/jpm.2006.9.912
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: Family caregivers caring for a patient with terminal cancer may experience significant psychological distress. Objective: The purpose of this study was to determine the extent to which the family caregivers' psychological distress is influenced by the patients' performance status while taking into account individual characteristics of caregivers and their unmet needs. Methods: Two hundred twelve family caregivers were assigned to three cohorts according to the patient's performance status, as measured by the Eastern Collaborative Oncology Group Functional Scale (ECOGS). Interview information was collected on the services and care provided, as well as on the caregivers' characteristics and level of psychological distress. Results: Family caregivers' psychosocial distress is strongly associated with the patients' terminal disease progress and declined functioning. The level of psychological distress varies from 25.2 to 33.5 (p = 0.0008) between the groups. Moreover, the percentage of caregivers with a high level of psychological distress varies from 41% to 62%, while this percentage is estimated at 19.2% in general population. A high distress index was significantly associated with the caregiver's burden, the patient's young age, the patient's symptoms, the caregiver's young age and gender, a poor perception of his/her health and dissatisfaction with emotional and tangible support. Conclusions: Family caregivers of patients in the advanced stages of cancer experience a high level of psychological distress, which increases significantly as the patient loses autonomy. Health care policies and programs need to be revisited in order to take the reality of these patients and their families into account.
引用
收藏
页码:912 / 921
页数:10
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