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Development and testing of an informative guide about palliative care for family caregivers of people with advanced dementia

机译:关于患有先进痴呆症的家庭照顾者姑息治疗的信息指南的开发与测试

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Since people with advanced dementia are usually not able to make complex decisions, it is usually the family caregivers, as proxies, who have to decide on treatments and their termination. However, these decisions are difficult for the caregivers to make, as they are often inadequately informed and cannot properly assess the consequences; moreover, they are concerned about harming the sick person. We aimed to first develop an informative booklet about palliative care issues for caregivers of people with advanced dementia. Secondly, we aimed to investigate a change in family caregivers’ knowledge regarding palliative care issues and caregivers’ involvement in medical and care decisions before and after studying this booklet. A first version of the booklet was drafted by an experienced psychiatrist and palliative care specialist based on existing booklets and guidelines; necessary cultural adaptions were taken into consideration. A nominal group process was conducted to develop the informative guide. In order to investigate the acceptance of the booklet and the possibility to implement it, 38 patient-caregiver dyads were recruited, and caregivers were interviewed both before receiving the booklet and after 3?months of receiving the booklet. Experts from various disciplines collaborated on a German booklet for family caregivers of people with advanced dementia as an information aid regarding issues of palliative care. The subsequent test showed that all caregivers had experienced a personal benefit from the booklet. Caregivers had a significant gain of knowledge after provision of the booklet. A large proportion of caregivers who had not previously considered and/or discussed medical topics reported that they had done so within 3?months after obtaining the booklet, or planned to do so in the near future. The caregivers valued the comprehensible, concise and well-structured information guide on palliative care issues in advanced dementia. They agreed it increases knowledge and prompts decision making and therefore should be developed in many languages and disseminated among family caregivers of people with dementia. clinicaltrial.gov, NCT03548142. Retrospectively registered 7 June 2018.
机译:由于患有先进性痴呆症的人通常无法做出复杂的决策,因此通常是家庭护理人员,如代理人,他们必须决定治疗和终止。然而,这些决定难以使护理人员制作,因为它们通常不充分通知,无法正确评估后果;此外,他们担心伤害病人。我们的目标是首先制定一个有关患有先进痴呆症的人们的看护人的姑息治疗问题的信息小册子。其次,我们旨在调查家庭护理人员对姑息治疗问题和护理人员在学习本手册之前和之后的医疗和护理决策的变化。一本书的第一版由经验丰富的精神科医生和基于现有的小册子和指导方针起草的专家起草;考虑了必要的文化适应。进行了一个标称小组进程,以制定信息指南。为了调查本小册子的接受和实施它的可能性,招募了38名患者 - 照顾性二元,护理人员在收到小册子之前和3个月收到小册子后进行了面试。来自各种学科的专家,在德国小册子上为具有先进痴呆症的家庭照顾者,作为关于姑息治疗问题的信息援助。随后的测试表明,所有护理人员都经历了小册子的个人福利。在提供小册子后,护理人员在提供了大量知识之后。一大部分没有考虑和/或讨论医疗主题的护理人员报告说他们在获得了一本小册子后3个月内完成了,或者计划在不久的将来这样做。护理人员对高级痴呆症的姑息治疗问题进行了理解,简洁和结构良好的信息指南。他们同意它提高了知识,并提示决策,因此应该以多种语言制定并在痴呆症的家庭照顾者中传播。 ClinicalTrial.gov,NCT03548142。回顾性地注册2018年6月7日。

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