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首页> 外文期刊>Australasian journal on ageing >Dissonance on perceptions of end‐of‐life needs between health‐care providers and members of the public: Quantitative cross‐sectional surveys
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Dissonance on perceptions of end‐of‐life needs between health‐care providers and members of the public: Quantitative cross‐sectional surveys

机译:对卫生保健提供者和公众成员之间的生活终止需求的看法的不和谐:量化横断面调查

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Objective To investigate views, determinants and barriers to end‐of‐life discussions for doctors, nurses and members of the public (MoP) and their acceptability of risk prediction tools. Methods Concurrent surveys of 360 doctors and nurses and 497 MoP. Results Sixty per cent of clinicians reported high confidence in initiating end‐of‐life discussions, and 55.8% regularly engaged in them. Barriers to end‐of‐life communication reported by clinicians were uncertainty on the likely time to death (44.7%) and family requests to withhold information from patients (44.2%). By contrast, most (92.8%) MoP wanted information about life expectancy; 89.9% wanted involvement in treatment decisions if the likelihood of death was high; and 23.8% already had an advance care directive. Conclusions A dissonance exists between doctor/nurses perception of older peoples’ preference for receiving prognostic information and the public desire for involvement in decision‐making at the end of life. As public attitudes change, strategies for greater involvement of patients in shared end‐of‐life planning are warranted.
机译:目的探讨对寿命讨论的意见,决定因素和障碍对医生,护士和公众成员(MOP)及其风险预测工具的可接受性。方法并发调查360名医生和护士和497拖把。结果六十百百分人的临床医生报告了启动生活终止讨论的高度信心,55.8%定期参与其中。临床医生报告的生活终止通信的障碍是对可能的死亡时间(44.7%)和家庭要求扣留患者信息的不确定性(44.2%)。相比之下,大多数(92.8%)MOP想要关于预期寿命的信息; 89.9%的人想要参与治疗决定如果死亡的可能性高; 23.8%已有提前护理指令。结论医生/护士之间存在不和谐,对老年人民的偏好接受预后信息和公众参与生命结束时的决策的公众愿望。随着公众态度的变化,有必要进行患者在共同的寿命规划中参与患者的策略。

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