MT Álvarez-Román , S Bonanad , C Herrera , MR López , DA García-Diego , S García , JB Montoro , JP Quintero , JL Poveda , A Gil , I Gómez , I Cortés
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引用次数: 0
Abstract
Background
The approval of the first gene therapy for haemophilia B represents a disruptive innovation in its management. Its practical integration into the Spanish national healthcare system presents unique challenges and opportunities, requiring the development of a structured, coordinated and multidisciplinary patient journey roadmap to ensure high-quality patient care and outcomes measurement.
Methods
A multidisciplinary panel of 10 experts was established. The project involved a literature review, structured questionnaires, individual interviews, practical exercises and validation of results by focus group with nominal group methodology.
Results
No specific patient journey for haemophilia B or for gene therapy were identified in Spain. Associated changes required for current treatment of haemophilia B were identified and proposals made: 1) selection of candidates to receive gene therapy involves individualised assessment of eligibility criteria by a multidisciplinary committee including additional profiles; 2) providing adequate training on gene therapy to healthcare professionals is a must to ensure quality of care; 3) the generation of a specific informed consent document and processes involving hepatology and psychology are essential, with the patient association playing a crucial role; 4) centres without prior practical experience in gene therapy must adapt specific areas to ensure correct preparation and administration; 5) short- and long-term patient follow-up should incorporate continuous monitoring of the patient's liver health and inclusion in registries for evaluation of outcomes.
背景批准首例血友病 B 基因疗法是血友病治疗领域的一次颠覆性创新。将该疗法实际纳入西班牙国家医疗保健系统既是独特的挑战,也是机遇,需要制定一个结构化、协调和多学科的患者旅程路线图,以确保高质量的患者护理和疗效评估。该项目包括文献综述、结构化问卷调查、个人访谈、实践练习,并通过采用名义小组方法的焦点小组对结果进行验证。确定了目前治疗 B 型血友病所需的相关变化,并提出了建议:1)选择接受基因治疗的候选者需要由一个多学科委员会对资格标准进行个性化评估,包括额外的资料;2)为医护人员提供有关基因治疗的充分培训是确保治疗质量的必要条件;3)制定专门的知情同意文件以及涉及肝病学和心理学的程序是必不可少的,患者协会在其中发挥着至关重要的作用;4)没有基因治疗实践经验的中心必须对特定领域进行调整,以确保正确的准备和管理;5)对患者的短期和长期随访应包括持续监测患者的肝脏健康状况,并将其纳入登记册以评估结果。