Assessment of the Spiritual Needs of People With Amyotrophic Lateral Sclerosis and Their Caregivers

IF 3.5 2区 医学 Q2 CLINICAL NEUROLOGY Journal of pain and symptom management Pub Date : 2025-02-17 DOI:10.1016/j.jpainsymman.2025.02.012
Cornelia Brandstötter PhD, MA , Arndt Büssing MD , Magdalena Eham , Benno Littger PhD , Stefan Lorenzl MD , Manuel Memmel , Piret Paal PhD , Sarah Kristina Bublitz MD
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Abstract

Context

Amyotrophic Lateral Sclerosis (ALS) is a progressive and fatal neurodegenerative disorder which poses multidimensional burden to patients and caregivers.

Objectives

This study aimed to investigate spiritual needs in people with Amyotrophic Lateral Sclerosis (pALS) and their closest caregivers, and to identify factors which may contribute to these needs.

Methods

Spiritual needs were assessed based on the Spiritual Needs Questionnaire (SpNQ) as part of a longitudinal cohort study in pALS and their closest caregivers who were included in a multiprofessional pilot project for ALS in Southern Germany with a focus on neuropalliative care.

Results

About 61 pALS and 52 caregivers were assessed for their spiritual needs. We show that both pALS and their caregivers maintain stable and distinct spiritual needs over time, irrespective of age, gender, care setting, or perceived level of loneliness. While pALS emphasize generativity and inner peace needs, caregivers primarily focus on finding inner peace, which they value even more than pALS.

Conclusions

Both pALS and their caregivers have strong unmet spiritual, and particularly nonreligious needs, which should be regularly assessed by the interprofessional team. Documenting these needs is the initial step in the spiritual care process, which requires a collaborative response from the interprofessional team. All healthcare professionals involved in ALS care should be attuned to the potential for unmet spiritual needs in patients and their caregivers. Early identification of these needs can facilitate the initiation of appropriate support processes.
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肌萎缩侧索硬化症患者及其照顾者的精神需求评估。
背景:肌萎缩性侧索硬化症(ALS)是一种进行性和致命的神经退行性疾病,给患者和护理人员带来多方面的负担。目的:本研究旨在调查肌萎缩性侧索硬化症(pALS)患者及其最亲密的照顾者的精神需求,并确定可能导致这些需求的因素。方法:精神需求评估基于精神需求问卷(SpNQ)作为纵向队列研究的一部分,pal及其最亲密的护理人员被纳入德国南部ALS多专业试点项目,重点是神经姑息治疗。结果:对61名pal和52名照护者的精神需求进行了评估。研究表明,无论年龄、性别、护理环境或感知到的孤独程度如何,pal及其照顾者都能长期保持稳定而独特的精神需求。当朋友们强调创造性和内心平静的需求时,照顾者主要关注的是寻找内心的平静,他们甚至比朋友们更重视这一点。结论:pal及其照顾者都有强烈的未满足的精神需求,特别是非宗教需求,应由跨专业团队定期评估。记录这些需求是精神护理过程的第一步,这需要跨专业团队的协作响应。所有参与渐冻症护理的医疗保健专业人员都应该了解患者及其护理人员未满足的精神需求的潜力。及早查明这些需要有助于开展适当的支助进程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.90
自引率
6.40%
发文量
821
审稿时长
26 days
期刊介绍: The Journal of Pain and Symptom Management is an internationally respected, peer-reviewed journal and serves an interdisciplinary audience of professionals by providing a forum for the publication of the latest clinical research and best practices related to the relief of illness burden among patients afflicted with serious or life-threatening illness.
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