首页> 美国卫生研究院文献>Gerontology and Geriatric Medicine >Now I Don’t Have to Guess: Using Pamphlets to Encourage Residents and Families/Friends to Engage in Advance Care Planning in Long-Term Care
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Now I Don’t Have to Guess: Using Pamphlets to Encourage Residents and Families/Friends to Engage in Advance Care Planning in Long-Term Care

机译:现在我不必猜测:使用小册子鼓励居民和家人/朋友参与长期护理的预先护理规划

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摘要

>Objective: This article explores whether access to illness trajectory pamphlets for five conditions with high prevalence in long-term care (LTC) can encourage residents and families/friends to openly engage in advance care planning (ACP) discussions with one another and with health providers. >Method: In all, 57 residents and families/friends in LTC completed surveys and 56 participated in seven focus groups that explored whether the pamphlets supported ACP engagement. >Results: Survey results suggested that access to pamphlets encouraged residents and families/friends to reflect on future care (48/57, 84%), clarified what questions to ask (40/57, 70%), and increased comfort in talking about end of life (EOL) care (36/57, 63%). Discussions between relatives and friends/families (32/57, 56%) or with health providers (21/57, 37%) were less common. Focus group deliberations illuminated that while reading illness-specific information was validating, a tendency to protect one another from an emotional topic, prevented residents and families/friends from conversing with one another about EOL issues. >Discussion: Having access to pamphlets with information about EOL care provides important and welcome opportunities for reflection for both residents in LTC and their families/friends. Moving residents and families/friends from reflecting on issues to discussing them together could require staff support through planned care conferences or staff initiated conversations at the bedside.
机译:>目标:本文探讨了在长期护理(LTC)中患病率高的五个条件下获得疾病轨迹手册的方法是否可以鼓励居民和家人/朋友公开参与预先护理计划(ACP)的讨论彼此之间以及与健康提供者。 >方法:LTC共有57位居民和家人/朋友完成了调查,有56位参与者参加了七个焦点小组,探讨了这些小册子是否支持ACP参与。 >结果:调查结果表明,使用小册子会鼓励居民和家人/朋友反思未来的护理(48 / 57,84%),阐明了要问的问题(40 / 57,70%),在谈论寿命终止(EOL)护理时增加了舒适感(36/57,63%)。亲朋好友/家人(32 / 57,56%)或与医疗人员(21 / 57,37%)之间的讨论较少见。焦点小组的讨论表明,在阅读特定于疾病的信息时,这是一种相互保护的趋势,可以防止居民和家人/朋友就EOL问题进行交流。 >讨论:获得有关EOL护理信息的小册子为LTC的居民及其家人/朋友提供了重要且值得欢迎的反思机会。让居民和家人/朋友从思考问题转移到一起讨论问题,可能需要通过计划的护理会议或员工在床边发起的对话来要求员工的支持。

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