Sangeorzan Irina, Antonacci Grazia, Martin Anne, Grodzinski Ben, Zipser Carl M, Murphy Rory K J, Andriopoulou Panoraia, Cook Chad E, Anderson David B, Guest James, Furlan Julio C, Kotter Mark R N, Boerger Timothy F, Sadler Iwan, Roberts Elizabeth A, Wood Helen, Fraser Christine, Fehlings Michael G, Kumar Vishal, Jung Josephine, Milligan James, Nouri Aria, Martin Allan R, Blizzard Tammy, Vialle Luiz Roberto, Tetreault Lindsay, Kalsi-Ryan Sukhvinder, MacDowall Anna, Martin-Moore Esther, Burwood Martin, Wood Lianne, Lalkhen Abdul, Ito Manabu, Wilson Nicky, Treanor Caroline, Dugan Sheila, Davies Benjamin M
Myelopathy.org, Cambridge, United Kingdom.
Department of Primary Care and Public Health, National Institute of Health Research (NIHR) Applied Research Collaboration (ARC) Northwest London, Imperial College London, London, United Kingdom.
JMIR Res Protoc. 2023 Oct 9;12:e46809. doi: 10.2196/46809.
Health care decisions are a critical determinant in the evolution of chronic illness. In shared decision-making (SDM), patients and clinicians work collaboratively to reach evidence-based health decisions that align with individual circumstances, values, and preferences. This personalized approach to clinical care likely has substantial benefits in the oversight of degenerative cervical myelopathy (DCM), a type of nontraumatic spinal cord injury. Its chronicity, heterogeneous clinical presentation, complex management, and variable disease course engenders an imperative for a patient-centric approach that accounts for each patient's unique needs and priorities. Inadequate patient knowledge about the condition and an incomplete understanding of the critical decision points that arise during the course of care currently hinder the fruitful participation of health care providers and patients in SDM. This study protocol presents the rationale for deploying SDM for DCM and delineates the groundwork required to achieve this.
The study's primary outcome is the development of a comprehensive checklist to be implemented upon diagnosis that provides patients with essential information necessary to support their informed decision-making. This is known as a core information set (CIS). The secondary outcome is the creation of a detailed process map that provides a diagrammatic representation of the global care workflows and cognitive processes involved in DCM care. Characterizing the critical decision points along a patient's journey will allow for an effective exploration of SDM tools for routine clinical practice to enhance patient-centered care and improve clinical outcomes.
Both CISs and process maps are coproduced iteratively through a collaborative process involving the input and consensus of key stakeholders. This will be facilitated by Myelopathy.org, a global DCM charity, through its Research Objectives and Common Data Elements for Degenerative Cervical Myelopathy community. To develop the CIS, a 3-round, web-based Delphi process will be used, starting with a baseline list of information items derived from a recent scoping review of educational materials in DCM, patient interviews, and a qualitative survey of professionals. A priori criteria for achieving consensus are specified. The process map will be developed iteratively using semistructured interviews with patients and professionals and validated by key stakeholders.
Recruitment for the Delphi consensus study began in April 2023. The pilot-testing of process map interview participants started simultaneously, with the formulation of an initial baseline map underway.
This protocol marks the first attempt to provide a starting point for investigating SDM in DCM. The primary work centers on developing an educational tool for use in diagnosis to enable enhanced onward decision-making. The wider objective is to aid stakeholders in developing SDM tools by identifying critical decision junctures in DCM care. Through these approaches, we aim to provide an exhaustive launchpad for formulating SDM tools in the wider DCM community.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/46809.
医疗保健决策是慢性病发展的关键决定因素。在共同决策(SDM)中,患者和临床医生共同协作,以达成基于证据的健康决策,这些决策要符合个人情况、价值观和偏好。这种个性化的临床护理方法可能在退行性颈椎病(DCM,一种非创伤性脊髓损伤)的管理中带来巨大益处。其慢性病程、异质性临床表现、复杂的管理方式以及多变的疾病进程使得采取以患者为中心的方法成为当务之急,这种方法要考虑到每个患者的独特需求和优先事项。目前,患者对病情的了解不足以及对护理过程中出现的关键决策点缺乏全面理解,阻碍了医疗保健提供者和患者在共同决策中富有成效地参与。本研究方案阐述了对DCM应用共同决策的基本原理,并勾勒了实现这一目标所需的基础工作。
该研究的主要成果是制定一份综合检查表,在诊断时实施,为患者提供支持其知情决策所需的基本信息。这被称为核心信息集(CIS)。次要成果是创建一份详细的流程图,以图表形式展示DCM护理中涉及的全球护理工作流程和认知过程。确定患者就医过程中的关键决策点将有助于有效探索用于常规临床实践的共同决策工具,以加强以患者为中心的护理并改善临床结果。
核心信息集和流程图均通过一个协作过程迭代生成,该过程涉及关键利益相关者的投入和共识。这将由全球DCM慈善机构Myelopathy.org通过其“退行性颈椎病研究目标和通用数据元素”社区提供便利。为了制定核心信息集,将使用三轮基于网络的德尔菲法,首先从最近对DCM教育材料的范围审查、患者访谈以及专业人员的定性调查中得出的信息项目基线列表开始。明确了达成共识的先验标准。流程图将通过与患者和专业人员的半结构化访谈迭代制定,并由关键利益相关者进行验证。
德尔菲共识研究的招募工作于2023年4月开始。流程图访谈参与者的试点测试同时启动,初步基线图的制定正在进行中。
本方案标志着首次尝试为研究DCM中的共同决策提供一个起点。主要工作集中在开发一种用于诊断的教育工具,以促进更好的后续决策。更广泛的目标是通过识别DCM护理中的关键决策节点,帮助利益相关者开发共同决策工具。通过这些方法,我们旨在为在更广泛的DCM社区中制定共同决策工具提供一个详尽的起点。
国际注册报告标识符(IRRID):DERR1-10.2196/46809