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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorBonanad, Santiago
dc.contributor.authorHerrera, Concha
dc.contributor.authorRodriguez Lopez, Manuel
dc.contributor.authorGarcía-Diego, Daniel-Aníbal
dc.contributor.authorGarcía, S
dc.contributor.authorÁlvarez Román, María Teresa
dc.contributor.authorMontoro-Ronsano, J. Bruno
dc.date.accessioned2025-05-07T07:25:57Z
dc.date.available2025-05-07T07:25:57Z
dc.date.issued2025
dc.identifier.citationÁlvarez-Román MT, Bonanad S, Herrera C, López R. M, Garcia-Diego DA, García S, et al. Proposal of an Integrated Patient Journey roadmap for the introduction of the first gene therapy for haemophilia B in Spain – The BHEMOGEN project. Rare. 2025;3:100078.
dc.identifier.issn2950-0087
dc.identifier.urihttp://hdl.handle.net/11351/13045
dc.descriptionGene therapy; Haemophilia B; Patient journey roadmap
dc.description.abstractBackground 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.
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesRare;3
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectTeràpia genètica
dc.subjectSang - Coagulació - Trastorns - Tractament
dc.subjectAtenció centrada en el pacient
dc.subject.meshGenetic Therapy
dc.subject.meshHemophilia B
dc.subject.mesh/therapy
dc.subject.meshPatient-Centered Care
dc.titleProposal of an Integrated Patient Journey roadmap for the introduction of the first gene therapy for haemophilia B in Spain – The BHEMOGEN project
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.rare.2025.100078
dc.subject.decsterapia genética
dc.subject.decshemofilia B
dc.subject.decs/terapia
dc.subject.decsatención centrada en el paciente
dc.relation.publishversionhttps://doi.org/10.1016/j.rare.2025.100078
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Álvarez-Román MT, García S] La Paz University Hospital, Madrid, Spain. [Bonanad S] La Fe University and Polytechnic Hospital, Valencia, Spain. [Herrera C] Reina Sofía General University Hospital, Córdoba, Spain. [Rodríguez López M] Álvaro Cunqueiro University Hospital, Vigo, Spain. [García-Diego DA] Spanish Federation of Haemophilia (FEDHEMO), Spain. [Montoro JB] Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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