Skip to main content
Top
Published in: Orphanet Journal of Rare Diseases 1/2021

Open Access 01-12-2021 | Achondroplasia | Position statement

The first European consensus on principles of management for achondroplasia

Authors: 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, Geert Mortier, Zagorka Peijin, Klaus Mohnike

Published in: Orphanet Journal of Rare Diseases | Issue 1/2021

Login to get access

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.
Literature
1.
go back to reference Coi A, Santoro M, Garne E, Pierini A, Addor M-C, Alessandri J-L, et al. Epidemiology of achondroplasia: a population-based study in Europe. Am J Med Genet Part A. 2019;179:1–8.CrossRef Coi A, Santoro M, Garne E, Pierini A, Addor M-C, Alessandri J-L, et al. Epidemiology of achondroplasia: a population-based study in Europe. Am J Med Genet Part A. 2019;179:1–8.CrossRef
2.
go back to reference Foreman PK, van Kessel F, van Hoorn R, van den Bosch J, Shediac R, Landis S. Birth prevalence of achondroplasia: a systematic literature review and meta-analysis. Am J Med Genet. 2020;182A:2297–316.CrossRef Foreman PK, van Kessel F, van Hoorn R, van den Bosch J, Shediac R, Landis S. Birth prevalence of achondroplasia: a systematic literature review and meta-analysis. Am J Med Genet. 2020;182A:2297–316.CrossRef
3.
go back to reference Marzin P, Cormier-Daire V. New perspectives on the treatment of skeletal dysplasia. Ther Adv Endocrinol Metab. 2020;11:1–16.CrossRef Marzin P, Cormier-Daire V. New perspectives on the treatment of skeletal dysplasia. Ther Adv Endocrinol Metab. 2020;11:1–16.CrossRef
4.
go back to reference Ornitz DM, Legeai-Mallet L. Achondroplasia: development, pathogenesis, and therapy. Dev Dyn. 2017;246:291–309.CrossRef Ornitz DM, Legeai-Mallet L. Achondroplasia: development, pathogenesis, and therapy. Dev Dyn. 2017;246:291–309.CrossRef
5.
go back to reference Pauli RM. Achondroplasia: a comprehensive clinical review. Orphanet J Rare Dis. 2019;14:1–19.CrossRef Pauli RM. Achondroplasia: a comprehensive clinical review. Orphanet J Rare Dis. 2019;14:1–19.CrossRef
6.
go back to reference Wright MJ, Irving MD. Clinical management of achondroplasia. Arch Dis Child. 2012;97:129–34.CrossRef Wright MJ, Irving MD. Clinical management of achondroplasia. Arch Dis Child. 2012;97:129–34.CrossRef
7.
go back to reference Ireland PJ, Pacey V, Zankl A, Edwards P, Johnston LM, Savarirayan R. Optimal management of complications associated with achondroplasia. Appl Clin Genet. 2014;7:117–25.CrossRef Ireland PJ, Pacey V, Zankl A, Edwards P, Johnston LM, Savarirayan R. Optimal management of complications associated with achondroplasia. Appl Clin Genet. 2014;7:117–25.CrossRef
8.
go back to reference Savarirayan R, Rossiter JP, Hoover-Fong JE, Irving M, Bompadre V, Goldberg MJ, et al. Best practice guidelines regarding prenatal evaluation and delivery of patients with skeletal dysplasia. Am J Obstet Gynecol. 2018;219:545–62.CrossRef Savarirayan R, Rossiter JP, Hoover-Fong JE, Irving M, Bompadre V, Goldberg MJ, et al. Best practice guidelines regarding prenatal evaluation and delivery of patients with skeletal dysplasia. Am J Obstet Gynecol. 2018;219:545–62.CrossRef
9.
go back to reference Hoover-Fong J, Scott CI, Jones ME, AAP Committee on Genetics. Health supervision for people with achondroplasia. Pediatrics. 2020;145:e20201010.CrossRef Hoover-Fong J, Scott CI, Jones ME, AAP Committee on Genetics. Health supervision for people with achondroplasia. Pediatrics. 2020;145:e20201010.CrossRef
10.
go back to reference Van der Heijde D, Aletaha D, Carmona L, Edwards CJ, Kvien TK, Kouloumas M, et al. 2014 update of the EULAR standardised operating procedures for EULAR-endorsed recommendations. Ann Rheum Dis. 2015;74:8–13.CrossRef Van der Heijde D, Aletaha D, Carmona L, Edwards CJ, Kvien TK, Kouloumas M, et al. 2014 update of the EULAR standardised operating procedures for EULAR-endorsed recommendations. Ann Rheum Dis. 2015;74:8–13.CrossRef
11.
go back to reference Wynn J, King TM, Gambello MJ, Waller DK, Hecht JT. Mortality in achondroplasia study: a 42-year follow-up. Am J Med Genet. 2007;143A:2502–11.CrossRef Wynn J, King TM, Gambello MJ, Waller DK, Hecht JT. Mortality in achondroplasia study: a 42-year follow-up. Am J Med Genet. 2007;143A:2502–11.CrossRef
13.
go back to reference Schulze KJ, Alade YA, McGready J, Hoover-Fong JE. Body Mass Index (BMI): the case for condition-specific cut-offs for overweight and obesity in skeletal dysplasias. Am J Med Genet. 2013;161A:2110–2.CrossRef Schulze KJ, Alade YA, McGready J, Hoover-Fong JE. Body Mass Index (BMI): the case for condition-specific cut-offs for overweight and obesity in skeletal dysplasias. Am J Med Genet. 2013;161A:2110–2.CrossRef
14.
go back to reference Dhiman N, Albaghdadi A, Zogg CK, Sharma M, Hoover-Fong JE, Ain MC, et al. Factors associated with health-related quality of life (HRQOL) in adults with short stature skeletal dysplasias. Qual Life Res. 2017;26:1337–48.CrossRef Dhiman N, Albaghdadi A, Zogg CK, Sharma M, Hoover-Fong JE, Ain MC, et al. Factors associated with health-related quality of life (HRQOL) in adults with short stature skeletal dysplasias. Qual Life Res. 2017;26:1337–48.CrossRef
15.
go back to reference Fredwall SO, Maanum G, Johansen H, Snekkevik H, Savarirayan R, Lidal IB. Current knowledge of medical complications in adults with achondroplasia: a scoping review. Clin Genet. 2020;97:179–97.CrossRef Fredwall SO, Maanum G, Johansen H, Snekkevik H, Savarirayan R, Lidal IB. Current knowledge of medical complications in adults with achondroplasia: a scoping review. Clin Genet. 2020;97:179–97.CrossRef
18.
go back to reference Baumbusch J, Mayer S, Sloan-Yip I. Alone in a crowd? Parents of children with rare diseases’ experiences of navigating the healthcare system. J Genet Couns. 2019;28:80–90.CrossRef Baumbusch J, Mayer S, Sloan-Yip I. Alone in a crowd? Parents of children with rare diseases’ experiences of navigating the healthcare system. J Genet Couns. 2019;28:80–90.CrossRef
20.
go back to reference Baujat G, Legeai-Mallet L, Finidori G, Cormier-Daire V, Le Merrer M. Achondroplasia. Best Pract Res Clin Rheumatol. 2008;22:3–18.CrossRef Baujat G, Legeai-Mallet L, Finidori G, Cormier-Daire V, Le Merrer M. Achondroplasia. Best Pract Res Clin Rheumatol. 2008;22:3–18.CrossRef
21.
go back to reference Cheung MS, Irving M, Cocca A, Santos R, Shaunak M, Dougherty H, et al. Achondroplasia foramen magnum score: screening for infants for stenosis. Arch Dis Child. 2021;106:180–4.CrossRef Cheung MS, Irving M, Cocca A, Santos R, Shaunak M, Dougherty H, et al. Achondroplasia foramen magnum score: screening for infants for stenosis. Arch Dis Child. 2021;106:180–4.CrossRef
22.
go back to reference Nadel JL, Wilkinson DA, Garton HJL, Muraszko KM, Maher CO. Screening and surgery for foramen magnum stenosis in children with achondroplasia: a large, national database analysis. J Neurosurg Pediatr. 2018;23:374–80.CrossRef Nadel JL, Wilkinson DA, Garton HJL, Muraszko KM, Maher CO. Screening and surgery for foramen magnum stenosis in children with achondroplasia: a large, national database analysis. J Neurosurg Pediatr. 2018;23:374–80.CrossRef
23.
go back to reference Margalit A, McKean G, Lawing C, Galey S, Ain MC. Walking out of the curve: thoracolubar kyphosis in achondroplasia. J Pedatr Orthop. 2018;38:491–7.CrossRef Margalit A, McKean G, Lawing C, Galey S, Ain MC. Walking out of the curve: thoracolubar kyphosis in achondroplasia. J Pedatr Orthop. 2018;38:491–7.CrossRef
24.
go back to reference Pauli RM, Breed A, Horton VK, Glinski LP, Reiser CA. Prevention of fixed, angular kyphosis in achondroplasia. J Pediatr Orthop. 1997;17:726–33.PubMed Pauli RM, Breed A, Horton VK, Glinski LP, Reiser CA. Prevention of fixed, angular kyphosis in achondroplasia. J Pediatr Orthop. 1997;17:726–33.PubMed
25.
go back to reference Trotter TL, Hall JG, AAP Committee on Genetics. Health supervision for children with achondroplasia. Pediatrics. 2005;116:771–83.CrossRef Trotter TL, Hall JG, AAP Committee on Genetics. Health supervision for children with achondroplasia. Pediatrics. 2005;116:771–83.CrossRef
26.
29.
go back to reference Ireland PJ, Johnson S, Donaghey S, Johnston L, Ware RS, Zankl A, et al. Medical management of children with achondroplasia: evaluation of an Australasian cohort aged 0–5 years. J Pediatr Child Health. 2012;48:443–9.CrossRef Ireland PJ, Johnson S, Donaghey S, Johnston L, Ware RS, Zankl A, et al. Medical management of children with achondroplasia: evaluation of an Australasian cohort aged 0–5 years. J Pediatr Child Health. 2012;48:443–9.CrossRef
30.
go back to reference Cohen GJ, Weitzman CC, Committee on Psychological Aspects of Child and Family Health. Helping children and families deal with divorce and separation. Pediatrics. 2016;138:e20163020.CrossRef Cohen GJ, Weitzman CC, Committee on Psychological Aspects of Child and Family Health. Helping children and families deal with divorce and separation. Pediatrics. 2016;138:e20163020.CrossRef
31.
go back to reference Saint-Laurent C, Garde-Etayo L, Gouze E. Obesity in achondroplasia patients: from evidence to medical monitoring. Orphanet J Rare Dis. 2019;14:253.CrossRef Saint-Laurent C, Garde-Etayo L, Gouze E. Obesity in achondroplasia patients: from evidence to medical monitoring. Orphanet J Rare Dis. 2019;14:253.CrossRef
32.
go back to reference Witt S, Kolb B, Mohnike K, Bullinger M, Quitmann J. Quality of life of children with achondroplasia and their parents—a German cross-sectional study. Orphanet J Rare Dis. 2019;14:194.CrossRef Witt S, Kolb B, Mohnike K, Bullinger M, Quitmann J. Quality of life of children with achondroplasia and their parents—a German cross-sectional study. Orphanet J Rare Dis. 2019;14:194.CrossRef
33.
go back to reference Cortinovis I, Luraschi E, Intini S, Sessa M, Delle FA. The daily experience of people with achondroplasia. Apply Psychol Health Well Being. 2011;3:207–27.CrossRef Cortinovis I, Luraschi E, Intini S, Sessa M, Delle FA. The daily experience of people with achondroplasia. Apply Psychol Health Well Being. 2011;3:207–27.CrossRef
34.
go back to reference Witt S, Rohenkohl A, Bullinger M, Sommer R, Kahrs C, Klingebiel KH, et al. Understanding, assessing and improving health-related quality of life on young people with achondroplaisa—a collaboration between a patient organisation and academic medicine. Pediatr Endocrinol Rev. 2017;15:109–18.PubMed Witt S, Rohenkohl A, Bullinger M, Sommer R, Kahrs C, Klingebiel KH, et al. Understanding, assessing and improving health-related quality of life on young people with achondroplaisa—a collaboration between a patient organisation and academic medicine. Pediatr Endocrinol Rev. 2017;15:109–18.PubMed
35.
go back to reference Pfeiffer KM, Brod M, Smith A, Gianettoni J, Viuff D, Ota S, et al. Assessing physical symptoms, daily functioning, and well-being in children with achondroplasia. Am J Med Genet. 2021;185A:33–45.CrossRef Pfeiffer KM, Brod M, Smith A, Gianettoni J, Viuff D, Ota S, et al. Assessing physical symptoms, daily functioning, and well-being in children with achondroplasia. Am J Med Genet. 2021;185A:33–45.CrossRef
36.
go back to reference Fredwall SO, Steen U, de Vries O, Rustad CF, Eggesbø HB, Weedon-Fekjaer H, et al. High prevalence of symptomatic spinal stenosis in Norwegian adults with achondroplasia: a population-based study. Orphanet J Rare Dis. 2020;15:123.CrossRef Fredwall SO, Steen U, de Vries O, Rustad CF, Eggesbø HB, Weedon-Fekjaer H, et al. High prevalence of symptomatic spinal stenosis in Norwegian adults with achondroplasia: a population-based study. Orphanet J Rare Dis. 2020;15:123.CrossRef
37.
go back to reference Blomemeke J, Sommer R, Witt S, Dabs M, Badia FJ, Bullinger M, et al. Piloting and psychometric properties of a patient-reported outcome instrument for young people with achondroplasia based on the International Classification of Functioning Disability and Health: the Achondroplasia Personal Life Experience Scale (APLES). Disabil Rehabil. 2019;41:1815–25.CrossRef Blomemeke J, Sommer R, Witt S, Dabs M, Badia FJ, Bullinger M, et al. Piloting and psychometric properties of a patient-reported outcome instrument for young people with achondroplasia based on the International Classification of Functioning Disability and Health: the Achondroplasia Personal Life Experience Scale (APLES). Disabil Rehabil. 2019;41:1815–25.CrossRef
38.
go back to reference Alade Y, Tunkel D, Schulze K, McGready J, Jallo G, Ain M, et al. Cross-sectional assessment of pain and physical function in skeletal dysplasia patients. Clin Genet. 2013;84:237–43.CrossRef Alade Y, Tunkel D, Schulze K, McGready J, Jallo G, Ain M, et al. Cross-sectional assessment of pain and physical function in skeletal dysplasia patients. Clin Genet. 2013;84:237–43.CrossRef
Metadata
Title
The first European consensus on principles of management for achondroplasia
Authors
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
Geert Mortier
Zagorka Peijin
Klaus Mohnike
Publication date
01-12-2021
Publisher
BioMed Central
Keyword
Achondroplasia
Published in
Orphanet Journal of Rare Diseases / Issue 1/2021
Electronic ISSN: 1750-1172
DOI
https://doi.org/10.1186/s13023-021-01971-6

Other articles of this Issue 1/2021

Orphanet Journal of Rare Diseases 1/2021 Go to the issue