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信息、参与、自我护理和支持 - 脑卒中患者照顾者的需求:扎根理论方法。

Information, involvement, self-care and support-The needs of caregivers of people with stroke: A grounded theory approach.

机构信息

School of Information Technology, Deakin University, Geelong, VIC, Australia.

Department of Public Health, University of Copenhagen, Copenhagen, Denmark.

出版信息

PLoS One. 2023 Jan 31;18(1):e0281198. doi: 10.1371/journal.pone.0281198. eCollection 2023.

Abstract

BACKGROUND

Globally, stroke is a leading cause of death and disability, with most care undertaken by caregivers who are generally family and friends without prior experience of care. The lack of experience or unpreparedness results in feelings of uncertainty, burnout, anxiety, burden, etc. Hence, it is necessary to identify the needs of caregivers to better support them in their caregiving journey and improve the quality of care delivered.

METHODS

The study employed a grounded theory methodology that utilizes information gathered from literature reviews and social media to represent the needs and create a storyline visually. The storyline is further refined and evaluated using an online survey of 72 participants recruited through online stroke caregiving communities.

RESULTS

The study identified four core categories of needs: (i) Information: sufficient information delivered in layman's terms based on the individual situation of the caregiver and survivor through oral and hands-on demonstrations, (ii) Involvement: inclusion in the decision-making processes at different stages of recovery through face-to-face communication at the hospital, (iii) Self-care: ability to engage in work and leisure activities, (iv) Support: receive support in the form of resources, services and finances from different other stakeholders.

CONCLUSIONS

There is a need to create a caregiver-centered approach in stroke recovery to ensure limited obstruction to care and reduced uncertainty in stroke recovery. Moreover, through the inclusion of caregivers in stroke recovery, it may be possible to reduce the burden of care to the caregiver and ensure the satisfaction of the healthcare system throughout stroke recovery.

摘要

背景

在全球范围内,中风是导致死亡和残疾的主要原因,大多数护理工作由没有护理经验的家属和朋友等照顾者承担。由于缺乏经验或准备不足,照顾者会感到不确定、精疲力竭、焦虑、负担过重等。因此,有必要确定照顾者的需求,以便更好地支持他们的护理工作,并提高护理质量。

方法

本研究采用扎根理论方法,利用文献综述和社交媒体收集的信息来代表需求,并通过在线中风护理社区招募的 72 名参与者的在线调查来进一步完善和评估。

结果

研究确定了四个核心需求类别:(i)信息:根据照顾者和幸存者的个人情况,以通俗易懂的方式提供足够的信息,并通过口头和实际演示进行传授,(ii)参与:通过在医院进行面对面的沟通,在康复的不同阶段参与决策过程,(iii)自我护理:能够从事工作和休闲活动,(iv)支持:从不同的利益相关者那里获得资源、服务和资金方面的支持。

结论

需要在中风康复中建立以照顾者为中心的方法,以确保对护理的限制最小,并减少中风康复中的不确定性。此外,通过让照顾者参与中风康复,可能会减轻照顾者的负担,并确保整个中风康复过程中医疗保健系统的满意度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d866/9888718/4cc5014c64a1/pone.0281198.g001.jpg

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