No Negative Impact of Palliative Sedation on Relatives' Experience of the Dying Phase and Their Wellbeing after the Patient's Death: An Observational Study

被引:9
作者
Bruinsma, S. M. [1 ]
van der Heide, A. [1 ]
van der Lee, M. L. [2 ]
Vergouwe, Y. [1 ]
Rietjens, J. A. C. [1 ]
机构
[1] Erasmus MC, Dept Publ Hlth, Rotterdam, Netherlands
[2] Helen Dowling Inst, Bilthoven, Netherlands
来源
PLOS ONE | 2016年 / 11卷 / 02期
基金
英国经济与社会研究理事会;
关键词
CONTINUOUS DEEP SEDATION; OF-LIFE CARE; RANDOMIZED CONTROLLED-TRIAL; FAMILY-MEMBERS; BEREAVED RELATIVES; CANCER-PATIENTS; EUROPEAN COUNTRIES; MEDICAL-CARE; UNTIL DEATH; EUTHANASIA;
D O I
10.1371/journal.pone.0149250
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Palliative sedation is the widely-used intervention of administering sedating agents to induce a state of unconsciousness to take away a dying patient's perception of otherwise irrelievable symptoms. However, it remains questionable whether this ethically complex intervention is beneficial for patients and whether the associated lack of communication in the last phase of life has a negative impact on relatives' wellbeing. Methods An observational questionnaire study was conducted among relatives of a consecutive sample of patients who died a non-sudden death in the Erasmus MC Cancer Institute or in the hospice 'Laurens Cadenza' (both in Rotterdam) between 2010 and 2013. Results Relatives filled in questionnaires regarding 151 patients who had been sedated and 90 patients who had not been sedated. The median time since all patients had passed away was 21 (IQR 14-32) months. No significant differences were found in relatives 'assessments of the quality of end-of-life care, patients 'quality of life in the last week before death and their quality of dying, between patients who did and did not receive sedation, or in relatives' satisfaction with their own life, their general health and their mental wellbeing after the patient's death. Conclusions The use of sedation in these patients appears to have no negative effect on bereaved relatives' evaluation of the patient's dying phase, or on their own wellbeing after the patient's death.
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页数:13
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