Best practices in the evaluation and treatment of foramen magnum stenosis in achondroplasia during infancy

Achondroplasia is the most common inherited disorder of bone growth (skeletal dysplasia). Despite this fact, consistent and evidence‐based management approaches to recognized, life‐threatening complications, such as foramen magnum stenosis, are lacking. This study aims to outline best practice, base...

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Published inAmerican journal of medical genetics. Part A Vol. 170A; no. 1; pp. 42 - 51
Main Authors White, Klane K., Bompadre, Viviana, Goldberg, Michael J., Bober, Michael B., Campbell, Jeffrey W., Cho, Tae-Joon, Hoover-Fong, Julie, Mackenzie, William, Parnell, Shawn E., Raggio, Cathleen, Rapoport, David M., Spencer, Samantha A., Savarirayan, Ravi
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.01.2016
Wiley Subscription Services, Inc
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Summary:Achondroplasia is the most common inherited disorder of bone growth (skeletal dysplasia). Despite this fact, consistent and evidence‐based management approaches to recognized, life‐threatening complications, such as foramen magnum stenosis, are lacking. This study aims to outline best practice, based on evidence and expert consensus, regarding the diagnosis, assessment, and management of foramen magnum stenosis in achondroplasia during infancy. A panel of 11 multidisciplinary international experts on skeletal dysplasia was invited to participate in a Delphi process. They were: 1) presented with a list of 26 indications and a thorough literature review, 2) given the opportunity to anonymously rate the indications and discuss in face to face discussion; 3) edit the list and rate it in a second round. Those indications with more than 80% agreement were considered as consensual. After two rounds of rating and a face‐to‐face meeting, consensus was reached to support 22 recommendations for the evaluation and treatment of foramen magnum stenosis in infants with achondroplasia. These recommendations include indications for surgical decompression, ventriculomegaly, and hydrocephalus, sleep‐disordered breathing, physical exams and the use of polysomnography and imaging in this condition. We present a consensus‐based best practice guidelines consisting of 22 recommendations. It is hoped that these guidelines will lead to more uniform and structured evaluation, standardizing care pathways, and improving mortality and morbidity outcomes for this cohort. © 2015 Wiley Periodicals, Inc.
Bibliography:UpToDate.com - Royalties
Alexion - Grant support
Biomarin Pharmaceuticals
ark:/67375/WNG-TPJX3FK5-M
Michael J. Goldberg Skeletal Dysplasia fund
Genzyme - Speaker's honoraria and travel reimbursement
istex:11BB6624332E02013923545387D03461812DC104
ArticleID:AJMGA37394
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1552-4825
1552-4833
DOI:10.1002/ajmg.a.37394