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挪威轴性脊柱关节炎患者对远程监测和患者自主护理的看法与体验:定性研究

Perspectives on and Experiences With Remote Monitoring and Patient-Initiated Care Among Norwegian Patients With Axial Spondyloarthritis: Qualitative Study.

作者信息

Hestevik Christine Hillestad, Varsi Cecilie, Østerås Nina, Tveter Anne Therese, Skandsen Jon, Eik Hedda

机构信息

Health Services Research and Innovation Unit, Diakonhjemmet Hospital, Oslo, Norway.

Centre for Treatment of Rheumatic and Musculoskeletal Diseases (REMEDY), Diakonhjemmet Hospital, Oslo, Norway.

出版信息

J Med Internet Res. 2025 Mar 28;27:e63569. doi: 10.2196/63569.

Abstract

BACKGROUND

Axial spondyloarthritis (axSpA) is a chronic inflammatory joint disease affecting the spine and sacroiliac joints, requiring frequent, lifelong monitoring and treatment. This involves regular symptom monitoring, assessing medication tolerance and side effects, and prompt therapy adjustments. Typically, patients with axSpA attend prescheduled hospital visits, but once stable disease has been attained, these seldom align with periods of high disease activity. Remote monitoring and patient-initiated care offer flexible, need-based, follow-up options. However, knowledge about how patients with axSpA perceive and experience these approaches is limited. To effectively implement these strategies in clinical practice, understanding patient perspectives is crucial.

OBJECTIVE

This study aims to explore how patients with axSpA perceive and experience remote monitoring and patient-initiated care.

METHODS

Our qualitative study was embedded in a randomized controlled trial. Participants were allocated to either usual care, remote monitoring, or patient-initiated care. The 2 intervention groups had no prescheduled visits and used a remote monitoring app, but only the remote monitoring group received monitoring by health care professionals. Semistructured interviews were conducted with 18 participants from the intervention groups to explore their experiences. The interviews were audio recorded, transcribed, anonymized, and analyzed using thematic analysis. Participants provided informed consent.

RESULTS

Eighteen patients (11 men and 7 women, aged 26-65 years) participated, 10 from the remote monitoring group and 8 from the patient-initiated care group. Transcripts were analyzed into four key themes: (1) "I don't need to go to the hospital just to report I'm doing well." When patients felt well, they perceived in-person consultations as less important. They acknowledged health care resource challenges and were willing to adapt but expressed concerns about rapid technological advancement, fearing it could exclude vulnerable groups. They emphasized the need for shared decision-making in determining follow-up strategies; (2) "It feels safer to meet healthcare personnel in person" highlighted participants' preference for in-person interactions as a safety net for detecting changes or signs of disease. They felt more secure when communicating face-to-face with health care professionals; (3) Remote monitoring can promote a sense of freedom and self-efficacy. The app provided autonomy, enabling patients to monitor their health without disrupting daily routines and promoting their health competency; and (4) Practical challenges and limitations of technology affect sense of security. Concerns about app deactivation, digital privacy, and lack of personalized settings negatively affected confidence in technology and sense of security.

CONCLUSIONS

Remote monitoring and patient-initiated care can adequately meet the needs of patients with axSpA with low disease activity, reducing unnecessary visits and enhancing self-efficacy. However, these approaches should not be one-size-fits-all. Care must adapt to evolving disease activity, circumstances, and preferences. Human interaction and support remain crucial, and future technological developments must address practical challenges to ensure user-friendly and reliable interfaces.

摘要

背景

轴性脊柱关节炎(axSpA)是一种影响脊柱和骶髂关节的慢性炎症性关节疾病,需要进行频繁的终身监测和治疗。这包括定期症状监测、评估药物耐受性和副作用,以及及时调整治疗方案。通常情况下,axSpA患者需按预定时间到医院就诊,但一旦病情稳定,这些就诊时间很少与疾病高活动期相吻合。远程监测和患者自主发起的护理提供了灵活的、基于需求的随访选择。然而,关于axSpA患者如何看待和体验这些方法的了解有限。为了在临床实践中有效实施这些策略,了解患者的观点至关重要。

目的

本研究旨在探讨axSpA患者如何看待和体验远程监测和患者自主发起的护理。

方法

我们的定性研究嵌入在一项随机对照试验中。参与者被分配到常规护理、远程监测或患者自主发起的护理组。两个干预组没有预定的就诊时间,并使用远程监测应用程序,但只有远程监测组接受医疗保健专业人员的监测。对来自干预组的18名参与者进行了半结构化访谈,以探讨他们的经历。访谈进行了录音、转录、匿名处理,并使用主题分析法进行分析。参与者提供了知情同意书。

结果

18名患者(11名男性和7名女性,年龄在26 - 65岁之间)参与了研究,其中10名来自远程监测组,8名来自患者自主发起的护理组。转录本被分析为四个关键主题:(1)“我不必仅仅为了报告自己情况良好就去医院”。当患者感觉良好时,他们认为面对面咨询不那么重要。他们认识到医疗保健资源的挑战,并愿意适应,但对技术的快速发展表示担忧,担心这可能会将弱势群体排除在外。他们强调在确定随访策略时需要共同决策;(2)“亲自见到医护人员感觉更安全”突出了参与者对面对面互动的偏好,认为这是检测疾病变化或迹象的安全保障。当与医疗保健专业人员面对面交流时,他们感觉更安心;(3)远程监测可以促进自由感和自我效能感。该应用程序提供了自主性,使患者能够在不打乱日常生活的情况下监测自己的健康状况,并提高了他们的健康能力;(4)技术的实际挑战和局限性会影响安全感。对应用程序停用、数字隐私以及缺乏个性化设置的担忧对技术信心和安全感产生了负面影响。

结论

远程监测和患者自主发起的护理能够充分满足疾病活动度低的axSpA患者的需求,减少不必要的就诊并增强自我效能感。然而,这些方法不应一刀切。护理必须适应不断变化的疾病活动度、情况和偏好。人际互动和支持仍然至关重要,未来的技术发展必须解决实际挑战,以确保界面友好且可靠。

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