Understanding Needs for Chronic Musculoskeletal Pain Management in a Northern Dene and Métis Community: A Community Based Needs Assessment.

IF 2 Q3 CLINICAL NEUROLOGY
Tayah Zhang, Brenna Bath, Veronica McKinney, Jaris Swidrovich, Rachel Johnson, Heather Foulds, Nadia Makar, Melanie Montgrand, Stacey Lovo
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Abstract

Background: Chronic musculoskeletal (MSK) pain disproportionately affects Indigenous Peoples, and rural/remote communities face significant barriers in accessing care. La Loche, a Dene/Métis community in northern Saskatchewan, has limited access to specialized chronic pain management services and specialized health providers.

Aims: The aim of this needs assessment was to gain insight into the community's priorities, strengths, and concerns regarding chronic MSK pain management. Community engagement and relationship building were essential to ensure that cultural protocols were respected and community worldviews were accurately represented.

Methods: A community-directed needs assessment was conducted in collaboration with local health care providers and community members. To ensure appropriate representation of community-led priorities, reflexive thematic analysis was utilized and rooted within interpretive description and informed by community-based participatory research and Two-Eyed Seeing. Open discussions were conducted in person, over the phone, or via Zoom in a semistructured format. Thirteen individuals were interviewed (eight community members, five health care professionals).

Results: Interviews conducted with community members and health care providers were analyzed separately. Both yielded the same four major overarching themes: (1) impact of pain on daily living, (2) barriers limiting access to care and the understanding of pain between health care provider and patient, (3) systemic oppression and negative experiences with health care, and (4) strength-based solutions.

Conclusions: Five recommendations were developed to promote culturally safe and patient-centered environments for chronic MSK pain communication and future care delivery: (1) person-centered and community-directed care, (2) clinic model and staffing requirements, (3) practitioner education and awareness, (4) community education and awareness, and (5) community resources.

背景:慢性肌肉骨骼(MSK)疼痛对原住民的影响尤为严重,而农村/偏远社区在获得医疗服务方面面临着巨大障碍。拉洛克是萨斯喀彻温省北部的一个德尼/梅蒂斯社区,该社区获得专门的慢性疼痛管理服务和专业医疗服务提供者的机会有限。社区参与和建立关系对于确保尊重文化习俗和准确反映社区世界观至关重要:方法:与当地医疗服务提供者和社区成员合作,开展了以社区为导向的需求评估。为确保适当体现社区主导的优先事项,采用了反思性专题分析,并将其植根于解释性描述中,同时借鉴了社区参与式研究和 "双眼观察"。以半结构化的形式,通过面谈、电话或 Zoom 进行了公开讨论。共访谈了 13 人(8 名社区成员和 5 名医疗保健专业人员):对社区成员和医疗服务提供者的访谈分别进行了分析。结果:对社区成员和医疗服务提供者进行的访谈分别进行了分析,得出了相同的四大主题:(1)疼痛对日常生活的影响;(2)限制获得医疗服务的障碍以及医疗服务提供者和患者之间对疼痛的理解;(3)系统性压迫和医疗服务的负面体验;以及(4)基于力量的解决方案:为促进文化安全和以患者为中心的慢性 MSK 疼痛交流环境以及未来的医疗服务,我们提出了五项建议:(1)以人为本和社区导向的医疗服务;(2)诊所模式和人员配备要求;(3)从业人员教育和意识;(4)社区教育和意识;以及(5)社区资源。
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来源期刊
CiteScore
3.70
自引率
12.50%
发文量
36
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