Caregiver-Reported Roles in Treatment Decision Making in Advanced Cancer and Associated Caregiving Burden and Psychological Distress: A Longitudinal Study

被引:12
作者
Ozdemir, Semra [1 ,2 ,3 ]
Ng, Sean [1 ,2 ]
Chaudhry, Isha [1 ,2 ]
Teo, Irene [1 ,2 ,4 ]
Malhotra, Chetna [1 ,2 ]
Finkelstein, Eric Andrew [1 ,2 ,3 ,5 ]
机构
[1] Duke NUS Med Sch, Lien Ctr Palliat Care, 8 Coll Rd, Singapore 169857, Singapore
[2] Duke NUS Med Sch, Signat Programme Hlth Serv & Syst Res, Singapore, Singapore
[3] Natl Univ Singapore, Saw Swee Hock Sch Publ Hlth, Singapore, Singapore
[4] Natl Canc Ctr Singapore, Singapore, Singapore
[5] Duke Univ, Duke Global Hlth Inst, Durham, NC USA
关键词
caregiving; treatment decision making; anxiety; depression; FAMILY INVOLVEMENT; PREFERENCES; PATIENT; RELIABILITY; EXPERIENCES; ATTITUDES; CARE;
D O I
10.1177/0272989X221125408
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
Objective To longitudinally examine caregiver-reported treatment decision-making roles and to investigate the associations of these roles with caregiver burden, caregiving esteem, caregiver anxiety, and depression. Methods 281 caregivers of patients with stage IV solid cancers were recruited from outpatient clinics in Singapore. Caregivers were eligible if they were aged >= 21 y, primary informal caregiver, and involved in treatment decision making. We used 3 y of longitudinal data. The decision-making roles were grouped into 4 categories: no family involvement, patient/physician-led, joint, and family-led/alone decision making. Mixed-effects linear regressions were used to assess associations between decision-making roles and caregiver outcomes. Results On average, 72% of caregivers reported family involvement in decision making. Compared with baseline, a higher proportion of caregivers at the 36-mo follow-up reported no family involvement (from 23% to 34%, P = 0.05) and patient/physician-led decision making (from 22% to 34%, P = 0.02), while a lower proportion reported family-led/alone (from 19% to 7%, P = 0.01) decision making. Compared with family-led/alone decision making, caregivers reporting no family involvement reported lower impact on finances (-0.15 [-0.28, -0.01], P = 0.03) while caregivers who reported patient/physician-led decision making reported lower impact on schedule and health (-0.12 [-0.20, -0.03], P = 0.01), and finances (-0.15 [-0.28, -0.03], P = 0.02), and lower anxiety (-0.69 [-1.17, -0.22], P < 0.01), and depressive symptoms (-0.69 [-1.12, -0.26], P < 0.01). Caregivers who reported joint decision making reported higher caregiving esteem (0.07 [0.01, 0.14], P = 0.02). Conclusions Higher family involvement in decision making was associated with higher caregiver burden and psychological distress. Help should be given so that family caregivers can support patient decision-making in a meaningful way.
引用
收藏
页码:191 / 202
页数:12
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