使用 "照顾者警示温度计 "工具识别需求并为运动神经元病患者的家庭照顾者提供支持:超越需求评估。

IF 2.7 Q2 HEALTH CARE SCIENCES & SERVICES
Palliative Care and Social Practice Pub Date : 2024-02-11 eCollection Date: 2024-01-01 DOI:10.1177/26323524241228306
Samar M Aoun, Mary R O'Brien, Katherine Knighting
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引用次数: 0

摘要

背景:运动神经元病患者(MND)的家庭照顾者因其照顾经历而对健康产生不利影响。如果能够系统、及时地识别并满足他们的支持需求,就可以缓解这种状况。这项试点研究旨在从 MND 家庭护理者的角度评估 "护理者警示温度计"(CAT)在家庭护理中的可行性和相关性。该工具提供了一个正式的结构,便于与照护者进行讨论,从而满足他们的需求:这项混合方法研究在西澳大利亚州进行(2020-2021 年)。41 名照护者和 5 名 MND 顾问参与了 CAT 干预试验,其中包括与顾问的两次会面(间隔 6-8 周),以通过行动计划确定和满足支持需求。通过电话采访获得了护理人员的反馈,并进行了主题分析:结果:30 名护理人员完成了两次 CAT 评估。护理人员确定了支持的优先事项,包括管理他们的情绪和忧虑、提供情感或精神关怀、提供有关患者病情的信息以及他们的护理需求可能会如何变化。我们对 17 名护理人员进行了访谈,他们认为这一评估过程充分满足了他们的需求,应该继续进行下去,因为这可以让他们集中精力来澄清问题并找出解决办法。根据他们提出的改进建议,包括在姑息关怀方面提供更好的信息/教育,开发了一个在线支持/信息工具包,通过获取相关信息和资源来增强关怀者和工作人员的能力:结论:计算机辅助姑息治疗工具包(CAT)在对最需要额外支持的姑息关怀者进行分流方面发挥了作用,并为他们提供了获取额外信息和自主获取支持的途径。要使任何工具成为护理的综合组成部分,服务提供者的支持是实施的关键,这需要时间资源以及适当的教育和支持结构。MND协会在与支持性社区网络建立更牢固的伙伴关系方面发挥着重要作用,通过关爱社区的护理模式,以更可持续和全面的方式满足MND家庭已确定的需求。需求评估是在正式和非正式网络之间建立这种能力的一种手段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Using the Carers' Alert Thermometer tool to identify needs and support family caregivers of people with motor neurone disease: moving beyond needs assessments.

Background: Family caregivers of people with motor neurone disease (MND) experience adverse health outcomes as a result of their caregiving experience. This may be alleviated if their support needs are identified and addressed in a systematic and timely manner. The objective of this pilot study was to assess the feasibility and relevance of the Carers' Alert Thermometer (CAT) in home-based care, from the perspective of MND family caregivers. The tool provides a formal structure to facilitate discussions with caregivers to enable needs to be addressed.

Methods: This mixed-method study was conducted in Western Australia (2020-2021). Forty-one caregivers and five MND Advisors participated in trialling the CAT intervention which consisted of two encounters with Advisors (6-8 weeks apart) to identify and address support needs through action plans. Caregivers' feedback was obtained via telephone interviews and a thematic analysis was undertaken.

Results: Thirty caregivers completed two CAT assessments. Caregivers identified support priorities of managing their feelings and worries, providing emotional or spiritual care, information about the person's condition and how their care needs might change. Seventeen caregivers were interviewed and found that this assessment process adequately addressed their needs and it should be continued, it brought the focus onto them to clarify problems and work through solutions. The improvements that were suggested by them, including better information/education in palliative care, led to the development of an online support/information toolkit, which served to empower caregivers and staff by accessing relevant information and resources.

Conclusions: The CAT demonstrated utility for triaging caregivers most in need of additional support and those whom signposting to additional information and self-directed access to support was most appropriate. For any tool to become an integrated part of care, service provider support is key for implementation, allowing for the time resource required and an appropriate education and support structure. MND Associations have an important role in building stronger partnerships with supportive community networks, through compassionate communities models of care, to address the identified needs of MND families in a more sustainable and wholistic manner. Needs assessment is a means towards building this capacity between formal and informal networks.

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来源期刊
Palliative Care and Social Practice
Palliative Care and Social Practice Nursing-Advanced and Specialized Nursing
CiteScore
2.90
自引率
0.00%
发文量
37
审稿时长
9 weeks
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