Wang Michael, Negrier Claude, Driessler Frank, Goodman Clifford, Skinner Mark W
University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
National Reference Center for Haemophilia, Louis Pradel Cardiology Hospital, University of Lyon, Lyon, France.
Patient Prefer Adherence. 2022 Jun 9;16:1439-1447. doi: 10.2147/PPA.S355627. eCollection 2022.
The anticipated emergence of hemophilia gene therapy will present people with hemophilia (PWH) and treating clinicians with increasingly complex treatment options. It will be critical that PWH and their families be empowered to participate fully in decision-making through transparent communication and the development of targeted educational resources.
The Council of Hemophilia Community (CHC) convened across a series of roundtable meetings to define the patient journey for hemophilia gene therapy, and to develop a question-and-answer style resource to guide discussion between healthcare professionals (HCPs) and their patients. Patient groups were also consulted during the development of this tool.
The CHC defined 5 key stages in the hemophilia gene therapy patient journey: pre-gene therapy (information-seeking and decision-making), treatment initiation, short- and long-term post-gene therapy follow-up. PWH will have different questions and concerns at each stage of their journey, which should be discussed with their HCP to aid decision-making. The resulting patient journey infographic and Q&A resource (see Supplementary Materials) has been developed for HCPs and PWH to provide a novel and practical roadmap of key issues and considerations throughout all stages.
These resources support a collaborative, patient-centric, shared decision-making approach to inform treatment decision discussions between HCPs and PWH. The value of such discussions will be influenced by the language adopted; health literacy is a particularly important consideration, and these discussions should be accessible and tailored to PWH. HCPs and PWH can benefit from awareness of the common questions and uncertainties as they progress together along the patient journey. While the contents of this article are specific to hemophilia gene therapy, the concepts developed here could be adapted to aid patients in other disease states.
血友病基因疗法的预期出现将为血友病患者(PWH)和治疗临床医生带来日益复杂的治疗选择。至关重要的是,要通过透明沟通和开发针对性的教育资源,使PWH及其家人有能力充分参与决策。
血友病社区理事会(CHC)召开了一系列圆桌会议,以确定血友病基因疗法的患者就医流程,并开发一种问答式资源,以指导医疗保健专业人员(HCP)与其患者之间的讨论。在开发此工具的过程中,还咨询了患者群体。
CHC确定了血友病基因疗法患者就医流程的5个关键阶段:基因治疗前(信息寻求和决策)、治疗开始、基因治疗后的短期和长期随访。PWH在其就医流程的每个阶段会有不同的问题和担忧,应与他们的HCP进行讨论以辅助决策。由此产生的患者就医流程信息图和问答资源(见补充材料)已为HCP和PWH开发,以提供贯穿所有阶段的关键问题和考虑因素的新颖实用路线图。
这些资源支持一种以患者为中心的协作式共同决策方法,为HCP和PWH之间的治疗决策讨论提供信息。此类讨论的价值将受所采用语言的影响;健康素养是一个特别重要的考虑因素,这些讨论应便于PWH理解并进行针对性调整。HCP和PWH在患者就医过程中共同前进时,了解常见问题和不确定性会有所裨益。虽然本文内容特定于血友病基因疗法,但此处提出的概念可加以调整,以帮助其他疾病状态的患者。