Exploring the Information Needs of People With Elbow Osteoarthritis Seeking Healthcare: A Qualitative Interview Study.

IF 1.6 Q3 RHEUMATOLOGY
Katy Boland, Maria Moffatt, Chris Littlewood
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引用次数: 0

Abstract

Objective: To explore the information needs of people with elbow osteoarthritis.

Design: Qualitative interview study using reflexive thematic analysis.

Setting: A single National Health Service Teaching Hospital Trust and associated primary care services, providing musculoskeletal care across the clinical pathway. Interviews were conducted in person, by phone or video call according to participant preference.

Participants: Twelve adults with clinically diagnosed elbow osteoarthritis, under the care of a general practitioner or consultant elbow surgeon, were included.

Results: Four themes were developed: (1) self-management in action, (2) experience of treatment options and navigating surgical decision making, (3) negotiating uncertainty and (4) active information seeking. Participants experiences were wide ranging and their varied information needs were at times unmet, particularly when related to treatment options, prognosis and surgical decision making. Across the clinical pathway, information was reported by some to be unclear or contradictory. Participants discussed a range of preferences for information sources. Accessing information was challenging for some participants and various barriers were discussed.

Conclusions: This is the first study to report the lived experience of people with elbow osteoarthritis and their information needs. For some, accessing information can be challenging, and the unmet information needs can affect the ability to self-manage ongoing symptoms and participate in treatment decisions. These findings provide a platform for the development of accessible, meaningful and culturally sensitive information sources capable of contributing to optimal treatment pathways.

探究肘关节骨关节炎患者寻求医疗保健的信息需求:一项定性访谈研究。
目的:了解肘关节骨关节炎患者的信息需求。设计:采用反身性主题分析的定性访谈研究。环境:一个单一的国家卫生服务教学医院信托和相关的初级保健服务,提供肌肉骨骼护理跨越临床途径。根据参与者的喜好,访谈采用面对面、电话或视频通话的方式进行。参与者:12名临床诊断为肘关节骨关节炎的成年人,在全科医生或咨询肘关节外科医生的护理下,被包括在内。结果:发展了四个主题:(1)行动中的自我管理,(2)治疗选择和导航手术决策的经验,(3)协商不确定性,(4)积极寻求信息。参与者的经历很广泛,他们不同的信息需求有时得不到满足,特别是在治疗方案、预后和手术决策方面。在整个临床过程中,一些人报告的信息不清楚或相互矛盾。与会者讨论了对信息来源的一系列偏好。对一些与会者来说,获取信息是一项挑战,讨论了各种障碍。结论:这是首次报道肘关节骨关节炎患者的生活经历及其信息需求的研究。对一些人来说,获取信息可能具有挑战性,未满足的信息需求可能影响自我管理持续症状和参与治疗决策的能力。这些发现为开发可访问的、有意义的和文化敏感的信息源提供了一个平台,这些信息源能够为最佳治疗途径做出贡献。
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来源期刊
Musculoskeletal Care
Musculoskeletal Care RHEUMATOLOGY-
CiteScore
2.30
自引率
7.70%
发文量
88
期刊介绍: Musculoskeletal Care is a peer-reviewed journal for all health professionals committed to the clinical delivery of high quality care for people with musculoskeletal conditions and providing knowledge to support decision making by professionals, patients and policy makers. This journal publishes papers on original research, applied research, review articles and clinical guidelines. Regular topics include patient education, psychological and social impact, patient experiences of health care, clinical up dates and the effectiveness of therapy.
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