患者对基于电子健康记录的类风湿关节炎结果仪表板的看法:一项混合方法研究。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-12 DOI:10.1186/s12911-024-02696-9
Catherine Nasrallah, Cherish Wilson, Alicia Hamblin, Christine Hariz, Cammie Young, Jing Li, Jinoos Yazdany, Gabriela Schmajuk
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引用次数: 0

摘要

背景:结果测量对于支持类风湿性关节炎(RA)治疗的 "靶向治疗 "方法至关重要,但它们与临床实践的结合仍不一致。我们开发了一款集成了电子病历、面向患者的侧载应用程序,用于在临床就诊期间显示类风湿关节炎的治疗结果(疾病活动度、功能状态、疼痛评分)、用药和化验结果("RA PRO Dashboard")。该研究旨在采用混合方法评估患者对在临床就诊期间实施面向患者的新型仪表盘的看法和态度:方法:我们邀请临床医生在临床访问期间至少使用过一次该仪表板的 RA 患者完成一份关于其在护理中的实用性的调查。我们还对部分患者进行了半结构化访谈,以评估他们对仪表板的看法。我们对访谈内容进行了逐字记录,并使用演绎和归纳技术对访谈内容进行了专题分析。新出现的主题和次主题被归纳为健康生态模型的四个领域:在 173 名调查对象中,79% 的人表示有兴趣在今后就诊时再次查看仪表板,71% 的人认为仪表板增进了他们对自身疾病的了解,65% 的人认为仪表板有助于他们做出 RA 护理决策。许多患者表示,仪表板有助于他们与临床医生讨论自己的 RA 症状(76%)和药物治疗(72%)。对 29 名 RA 患者的访谈揭示了 10 个关键主题:仪表板被认为是一种有价值的可视化工具,可提高患者对 RA 结果测量的理解,增强他们对护理的参与,并增加他们对临床医生和诊所的信任。普遍报告的局限性包括一些RA患者对RA结果问卷的可靠性感到担忧,以及临床医生收集和解释这些指标的方式不一致:结论:在研究的定量和定性部分中,患者均报告称仪表板提高了他们对自身 RA 的了解,加强了患者与医生之间的沟通,支持共同决策,并提高了患者在护理中的参与度。这些发现支持在 RA 护理中使用仪表板或类似的数据可视化工具,并可用于未来的干预措施,以应对数据收集和患者教育方面的挑战。
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Patient perceptions of an electronic-health-record-based rheumatoid arthritis outcomes dashboard: a mixed-methods study.

Background: Outcome measures are crucial to support a treat-to-target approach to rheumatoid arthritis (RA) care, yet their integration into clinical practice remains inconsistent. We developed an Electronic Heath Record-integrated, patient-facing side-car application to display RA outcomes (disease activity, functional status, pain scores), medications, and lab results during clinical visits ("RA PRO Dashboard"). The study aimed to evaluate patient perceptions and attitudes towards the implementation of a novel patient-facing dashboard during clinical visits using a mixed-methods approach.

Methods: RA patients whose clinicians used the dashboard at least once during their clinical visit were invited to complete a survey regarding its usefulness in care. We also conducted semi-structured interviews with a subset of patients to assess their perceptions of the dashboard. The interviews were transcribed verbatim and analyzed thematically using deductive and inductive techniques. Emerging themes and subthemes were organized into four domains of the Ecological Model of Health.

Results: Out of 173 survey respondents, 79% were interested in seeing the dashboard again at a future visit, 71% felt it improved their understanding of their disease, and 65% believed it helped with decision-making about their RA care. Many patients reported that the dashboard helped them discuss their RA symptoms (76%) and medications (72%) with their clinician. Interviews with 29 RA patients revealed 10 key themes: the dashboard was perceived as a valuable visual tool that improved patients' understanding of RA outcome measures, enhanced their involvement in care, and increased their trust in clinicians and the clinic. Common reported limitations included concerns about reliability of RA outcome questionnaires for some RA patients and inconsistent collection and explanation of these measures by clinicians.

Conclusions: In both the quantitative and qualitative components of the study, patients reported that the dashboard improved their understanding of their RA, enhanced patient-clinician communication, supported shared decision-making, and increased patient engagement in care. These findings support the use of dashboards or similar data visualization tools in RA care and can be used in future interventions to address challenges in data collection and patient education.

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