Evidence map›Paper›PMID 34332609›Full record

ArticleOrphanet journal of rare diseases2021

The first European consensus on principles of management for achondroplasia.

Valerie Cormier-Daire, Moeenaldeen AlSayed, Tawfeg Ben-Omran, Sérgio Bernardo de Sousa, Silvio Boero, Svein O Fredwall, Encarna Guillen-Navarro, Melita Irving, Christian Lampe, Mohamad Maghnie and 3 more

Open access · goldAbstract readConsensus Statement
In one paragraph

Article in Orphanet journal of rare diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 3 pooled it
7.3field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 3 syntheses or guidelines pooled it, 62 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 12 institutions in 10 countries.

Valerie Cormier-DaireCentre of Reference for Constitutional Bone Diseases (MOC), Department of Clinical Genetics, Paris Centre University, INSERM UMR 1163, Imagine Institute, Paris Centre University, Paris, France.
Moeenaldeen AlSayedDepartment of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia.
Tawfeg Ben-OmranDivision of Genetic and Genomic Medicine, Department of Medical Genetic, Sidra Medicine and Hamad Medical Corporation, Doha, Qatar.
Sérgio Bernardo de SousaMedical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
Silvio BoeroDepartment for Limb Lengthening and Axial Correction, Istituto Giannina Gaslini, Genoa, Italy.
Svein O FredwallTRS National Resource Centre for Rare Disorders, Sunnaas Rehabilitation Hospital, Nesodden, Norway.
Encarna Guillen-NavarroMedical Genetics Section. Department of Pediatrics, Virgen de la Arrixaca University Hospital, IMIB, University of Murcia-UMU, CIBERER-ISCIII, Murcia, Spain.
Melita IrvingDepartment of Clinical Genetics, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Christian LampeClinic of Neuropediatrics, Epileptology and Social Pediatrics, University Hospital Giessen and Marburg, Giessen, Germany.
Mohamad MaghnieDepartment of Pediatrics, School of Medicine IRCCS Istituto Giannina Gaslini, University of Genoa, Genoa, Italy.
Geert MortierDepartment of Medical Genetics, Antwerp University Hospital and University of Antwerp, Antwerp, Belgium.
Zagorka PeijinOrthopaedic Surgery and Paediatric Trauma, Hôpital Necker-Enfants Malades, Paris, France.
Klaus MohnikeCentral German Competence Network for Rare Diseases (MKSE), Dept of Pediatrics, University Hospital, Otto-von-Guericke University, Magdeburg, Germany. klaus.mohnike@med.ovgu.de.ORCID 0000-0001-5113-8657
Istituto Giannina Gaslini · ITAlfaisal University · SAGuy's and St Thomas' NHS Foundation Trust · GBHamad Medical Corporation · QAHôpital Necker-Enfants Malades · FRHospitais da Universidade de Coimbra · PTInserm · FRInstituto de Salud Carlos III · ESOtto-von-Guericke-Universität Magdeburg · DESunnaas sykehus · NOUniversitätsklinikum Gießen und Marburg · DEUniversity of Antwerp · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

AchondroplasiaQuality of LifeAdolescentAdultEuropeHumansLongitudinal StudiesReceptor, Fibroblast Growth Factor, Type 3Receptor, Fibroblast Growth Factor, Type 3AchondroplasiaEuropean Achondroplasia ForumGuiding principles

Identifiers

PMID34332609
PMCPMC8325831
OpenAlexW3192767729

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.