Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/105313
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dc.contributor.authorCormier-Daire, Valerie-
dc.contributor.authorAlSayed, Moeenaldeen-
dc.contributor.authorBen-Omran, Tawfeg-
dc.contributor.authorSousa, Sérgio Bernardo de-
dc.contributor.authorBoero, Silvio-
dc.contributor.authorFredwall, Svein O.-
dc.contributor.authorGuillen-Navarro, Encarna-
dc.contributor.authorIrving, Melita-
dc.contributor.authorLampe, Christian-
dc.contributor.authorMaghnie, Mohamad-
dc.contributor.authorMortier, Geert-
dc.contributor.authorPeijin, Zagorka-
dc.contributor.authorMohnike, Klaus-
dc.date.accessioned2023-02-16T11:15:19Z-
dc.date.available2023-02-16T11:15:19Z-
dc.date.issued2021-07-31-
dc.identifier.issn1750-1172pt
dc.identifier.urihttps://hdl.handle.net/10316/105313-
dc.description.abstractAchondroplasia 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.pt
dc.language.isoengpt
dc.publisherSpringer Naturept
dc.relationOpen Access funding enabled and organized by Projekt DEALpt
dc.relationThe initial meeting of the European Achondroplasia Forum and editorial support was funded by BioMarinpt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectAchondroplasiapt
dc.subjectGuiding principlespt
dc.subjectEuropean Achondroplasia Forumpt
dc.subject.meshAdolescentpt
dc.subject.meshAdultpt
dc.subject.meshConsensuspt
dc.subject.meshEuropept
dc.subject.meshHumanspt
dc.subject.meshLongitudinal Studiespt
dc.subject.meshReceptor, Fibroblast Growth Factor, Type 3pt
dc.subject.meshAchondroplasiapt
dc.subject.meshQuality of Lifept
dc.titleThe first European consensus on principles of management for achondroplasiapt
dc.typearticle-
degois.publication.firstPage333pt
degois.publication.issue1pt
degois.publication.titleOrphanet Journal of Rare Diseasespt
dc.peerreviewedyespt
dc.identifier.doi10.1186/s13023-021-01971-6pt
degois.publication.volume16pt
dc.date.embargo2021-07-31*
uc.date.periodoEmbargo0pt
item.openairetypearticle-
item.fulltextCom Texto completo-
item.languageiso639-1en-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
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