Evidence map›Paper›PMID 35698202›Full record

ArticleOrphanet journal of rare diseases2022

Literature review and expert opinion on the impact of achondroplasia on medical complications and health-related quality of life and expectations for long-term impact of vosoritide: a modified Delphi study.

Ravi Savarirayan, Wagner Baratela, Thomas Butt, Valérie Cormier-Daire, Melita Irving, Bradley S Miller, Klaus Mohnike, Keiichi Ozono, Ron Rosenfeld, Angelo Selicorni and 4 more

Open access · goldAbstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Guideline
  2. Review
  3. Review
  4. Experiences and treatment perspectives of adolescents and young adults with achondroplasia and caregivers: a qualitative interview study.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Observational
  10. Article
  11. Article
  12. The Treatment of Growth Disorders in Childhood and Adolescence.Deutsches Arzteblatt international · 2024
    Review
  13. Article
  14. Article
  15. Review
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

14 authors at 14 institutions in 9 countries.

Ravi SavarirayanMurdoch Children's Research Institute, and University of Melbourne, Parkville, Melbourne, VIC, 3052, Australia. ravi.savarirayan@vcgs.org.au.ORCID 0000-0002-5105-8427
Wagner BaratelaHospital Sirio-Libanes, São Paolo, Brazil.
Thomas ButtBioMarin International Ltd, London, UK.
Valérie Cormier-DaireUniversité de Paris, Reference Center for Skeletal Dysplasia, Hôpital Necker-Enfants Malades, Paris, France.
Melita IrvingGuy's and St. Thomas' NHS Foundation Trust, London, UK.
Bradley S MillerUniversity of Minnesota Medical School, Minneapolis, MN, USA.
Klaus MohnikeUniversitätskinderklinik, Otto-Von-Guericke Universität, Magdeburg, Germany.
Keiichi OzonoOsaka University Graduate School of Medicine, Osaka, Japan.
Ron RosenfeldOregon Health and Science University, Portland, OR, USA.
Angelo SelicorniASST Lariana, Como, Italy.
Dominic ThompsonGreat Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.ORCID 0000-0002-1114-9869
Klane K WhiteUniversity of Washington, Seattle Children's Hospital, Seattle, WA, USA.
Michael WrightNorthern Genetics Service, Institute of Human Genetics, Newcastle-Upon-Tyne Hospitals, NHS Foundation Trust, Newcastle-upon-Tyne, UK.
Svein O FredwallTRS National Resource Centre for Rare Disorders, Sunnaas Rehabilitation Hospital, Nesodden, Norway.
Azienda Socio Sanitaria Territoriale Lariana · ITBioMarin (United Kingdom) · GBGreat Ormond Street Hospital for Children NHS Foundation Trust · GBGuy's and St Thomas' NHS Foundation Trust · GBHôpital Necker-Enfants Malades · FRHospital Sírio-Libanês · BRNewcastle upon Tyne Hospitals NHS Foundation Trust · GBOregon Health & Science University · USSeattle Children's Hospital · USSunnaas sykehus · NOThe University of Melbourne · AUThe University of Osaka · JPUniversitätskinderklinik · DEUniversity of Minnesota Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAchondroplasia is associated with disproportionate short stature and significant and potentially severe medical complications. Vosoritide is the first medicine to treat the underlying cause of achondroplasia and data from phase 3 and phase 2 extension studies showed effects on growth and body proportions. However, there are currently no long-term data available on the direct impact on endpoints such as medical complications and health-related quality of life (HRQoL). This study explored the perceived impact of achondroplasia on medical complications, HRQoL, healthcare resource use and mortality, and potential modifying effects of vosoritide, based on published evidence and expert opinion. Structured expert opinion was obtained by an international modified Delphi study among 14 experts in managing achondroplasia performed on a virtual platform and consisting of an explorative phase followed by an anonymous individual rating round.

resultsOverall, the panelists expect that in individuals starting long-term treatment between 2 years of age and puberty, growth velocity increases observed in the clinical trials will be maintained until final height is reached (92% agreement) and will likely result in clinically meaningful improvements in upper-to-lower body segment ratio (85%). Earlier treatment initiation will likely result in a greater final height (100%) and more likely improve proportionality (92%) than later treatment. Although current data are limited, ≥ 75% of panelists find it conceivable that the earlier long-term treatment is started, the greater the probability of a positive effect on the lifetime incidence of symptomatic spinal stenosis, kyphosis, obstructive sleep apnea, and foramen magnum stenosis. These are among the most clinically important complications of achondroplasia because of their high impact on comorbidity, mortality, and/or HRQoL. A positive effect of vosoritide on the incidence of surgeries through lifetime was considered more likely with earlier long-term treatment (90%).

conclusionsThis explorative study, based on international expert opinion, provides further insight into the medical and functional impacts of achondroplasia and how these might be modified through long-term use of vosoritide. The results can be used to guide the direction and design of future research to validate the assumptions and to discuss potential treatment outcomes with disease modifying therapies with families and clinicians.

Indexed as

AchondroplasiaQuality of LifeDelphi TechniqueHumansMotivationNatriuretic Peptide, C-TypeNatriuretic Peptide, C-TypevosoritideAchondroplasiaActivities of daily livingComplicationsDelphi techniqueExpert opinionGrowthHealth-related quality of lifeVosoritide

Identifiers

PMID35698202
PMCPMC9195406
OpenAlexW4282830236

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.