The role of relatives in decisions concerning life-prolonging treatment in patients with end-stage malignant disorders: informants, advocates or surrogate decision-makers?

被引:34
作者
Hauke, D. [1 ]
Reiter-Theil, S. [2 ]
Hoster, E. [3 ]
Hiddemann, W. [1 ]
Winkler, E. C. [1 ]
机构
[1] Univ Munich, Univ Hosp Grosshadern, Dept Internal Med Haematol & Oncol 3, D-81377 Munich, Germany
[2] Univ Basel Hosp, Fac Med, Dept Med & Hlth Eth, CH-4031 Basel, Switzerland
[3] Univ Munich, Dept Internal Med 3, Inst Med Informat Biometry & Epidemiol, D-81377 Munich, Germany
关键词
end-of-life decisions; ethics; family; relatives; treatment limitation; INTENSIVE-CARE-UNIT; TREATMENT PREFERENCES; SUSTAINING TREATMENT; WITHDRAWAL; SUPPORT; LIMIT; ILL; PHYSICIANS; ACCURACY; FAMILIES;
D O I
10.1093/annonc/mdr019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: This study examines the extent to which relatives of severely ill cancer patients are involved in the decision to limit treatment (DLT), their role in communicating patient wishes and the incidence of and reasons for disagreement with relatives. Patients and methods: This cohort study followed 70 patients with terminal cancer, for whom a limitation of life-prolonging treatment was being considered. 'Embedded researchers' recorded patients' wishes and the relatives' roles and disagreements with DLT. Results: Although 63 out of 70 patients had relatives present during their care, only 32% of relatives were involved in DLT. Physicians were more likely to know the end-of-life (EOL) preferences for those patients who had visiting relatives than those without them (78% versus 29%, P = 0.014). Most relatives supported patients in voicing their preferences (68%), but one-third acted against the known or presumed wishes of patients (32%). Disagreements with patients' relatives occurred in 21% of cases, and predominantly when relatives held views that contradicted known patient preferences (71% versus 7%, P = 0.001). Conclusion: If relatives are to play an important part in EOL decision making, we must devise strategies to recognise their potential as patients' advocates as well as their own needs.
引用
收藏
页码:2667 / 2674
页数:8
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