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The first European consensus on principles of management for achondroplasia

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dc.contributor.author Cormier-Daire, Valerie
dc.contributor.author AlSayed, Moeenaldeen
dc.contributor.author Ben-Omran, Tawfeg
dc.contributor.author de-Sousa, Sergio-Bernardo
dc.contributor.author Boero, Silvio
dc.contributor.author Fredwall, Svein-O
dc.contributor.author Guillén-Navarro, Encarna
dc.contributor.author Irving, Melita
dc.contributor.author Lampe, Christian
dc.contributor.author Maghnie, Mohamad
dc.contributor.author Mortier, Geert
dc.contributor.author Peijin, Zagorka
dc.contributor.author Mohnike, Klaus
dc.date.accessioned 2025-11-20T12:45:27Z
dc.date.available 2025-11-20T12:45:27Z
dc.date.issued 2021-07
dc.identifier.citation Cormier-Daire V, AlSayed M, Ben-Omran T, De Sousa SB, Boero S, Fredwall SO, et al. The first European consensus on principles of management for achondroplasia. Orphanet J Rare Dis. diciembre de 2021;16(1):333.
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/21645
dc.description.abstract Achondroplasia is the most common type of skeletal dysplasia, caused by a recurrent pathogenic variant in the fibroblast growth factor receptor 3 (FGFR3). The management of achondroplasia is multifaceted, requiring the involvement of multiple specialties across the life course. There are significant unmet needs associated with achondroplasia and substantial differences in different countries with regard to delivery of care. To address these challenges the European Achondroplasia Forum (EAF), a network of senior clinicians and orthopaedic surgeons from Europe and the Middle East representative of the achondroplasia clinical community, came together with the overall aim of improving patient outcomes. The EAF developed a consensus on guiding principles of management of achondroplasia to provide a basis for developing optimal care in Europe. All members of the EAF were invited to submit suggestions for guiding principles of management, which were consolidated and then discussed during a meeting in December 2020. The group voted anonymously on the inclusion of each principle, with the requirement of a 75% majority at the first vote to pass the principle. A vote on the level of agreement was then held. A total of six guiding principles were developed, which cover management over the lifetime of a person with achondroplasia. The principles centre on the lifelong management of achondroplasia by an experienced multidisciplinary team to anticipate and manage complications, support independence, and improve quality of life. There is focus on timely referral to a physician experienced in the management of achondroplasia on suspicion of the condition, shared decision making, the goals of management, access to adaptive measures to enable those with achondroplasia to access their environment, and the importance of ongoing monitoring throughout adolescence and adulthood. All principles achieved the 75% majority required for acceptance at the first vote (range 91-100%) and a high level of agreement (range 8.5-9.6). The guiding principles of management for achondroplasia provide all healthcare professionals, patient advocacy groups and policy makers involved in the management of achondroplasia with overarching considerations when developing health systems to support the management of achondroplasia.
dc.language.iso eng
dc.publisher BMC
dc.rights Atribución-NoComercial-SinDerivadas 3.0 España
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/3.0/es/ *
dc.subject.mesh Achondroplasia/therapy
dc.subject.mesh Adolescent
dc.subject.mesh Adult
dc.subject.mesh Consensus
dc.subject.mesh Europe
dc.subject.mesh Humans
dc.subject.mesh Longitudinal Studies
dc.subject.mesh Quality of Life
dc.subject.mesh Receptor, Fibroblast Growth Factor, Type 3/genetics
dc.title The first European consensus on principles of management for achondroplasia
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 34332609
dc.relation.publisherversion https://ojrd.biomedcentral.com/articles/10.1186/s13023-021-01971-6
dc.identifier.doi 10.1186/s13023-021-01971-6
dc.journal.title Orphanet Journal of Rare Diseases
dc.identifier.essn 1750-1172


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