Recommendations for the management of MPS IVA : systematic evidence- and consensus-based guidance

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dc.contributor.author Akyol, Mehmet Umut
dc.contributor.author Alden, Tord D.
dc.contributor.author Amartino, Hernan
dc.contributor.author Ashworth, Jane
dc.contributor.author Belani, Kumar
dc.contributor.author Berger, Kenneth I.
dc.contributor.author Borgo, Andrea
dc.contributor.author Braunlin, Elizabeth
dc.contributor.author Eto, Yoshikatsu
dc.contributor.author Gold, Jeffrey I.
dc.contributor.author Jester, Andrea
dc.contributor.author Jones, Simon A.
dc.contributor.author Karsli, Cengiz
dc.contributor.author Mackenzie, William
dc.contributor.author Marinho, Diane Ruschel
dc.contributor.author McFadyen, Andrew
dc.contributor.author McGill, Jim
dc.contributor.author Mitchell, John J.
dc.contributor.author Muenzer, Joseph
dc.contributor.author Okuyama, Torayuki
dc.contributor.author Orchard, Paul J.
dc.contributor.author Stevens, Bob
dc.contributor.author Thomas, Sophie
dc.contributor.author Walker, Robert
dc.contributor.author Wynn, Robert
dc.contributor.author Giugliani, Roberto
dc.contributor.author Harmatz, Paul
dc.contributor.author Hendriksz, Christian J.
dc.contributor.author Scarpa, Maurizio
dc.date.accessioned 2020-08-18T06:09:41Z
dc.date.available 2020-08-18T06:09:41Z
dc.date.issued 2019-06
dc.description Additional file 1: Methodology: Further information regarding methodology, including: defining clinical questions using the P.I.C.O methodology, the search strategy recording form, results of the systematic literature review according to PRISMA, the Oxford Centre for Evidence-based Medicine criteria and the AGREE II evaluation.
dc.description Additional file 2: Oxford CEBM grading for MPS IVA: Tables detailing the evidence levels given to each reference supporting the MPS IVA guidance statements and the Evidence Grades applied to each guidance statement. Evidence levels were assessed using the Oxford Centre for Evidence-based Medicine and were based on the quality of evidence of each reference. For each guidance statement, an overall Evidence Grade was applied, based on the evidence levels of the supporting references.
dc.description Additional file 3: Oxford CEBM grading for MPS VI: Tables detailing the evidence levels given to each reference supporting the MPS VI guidance statements and the Evidence Grades applied to each guidance statement. Evidence levels were assessed using the Oxford Centre for Evidence-based Medicine and were based on the quality of evidence of each reference. For each guidance statement, an overall Evidence Grade was applied, based on the evidence levels of the supporting references.
dc.description Additional file 4: Modified-Delphi voting Round 1: Full results of the first round of the modified-Delphi voting, which was used to demonstrate consensus of the guidance statements.
dc.description Additional file 5: Modified-Delphi voting Round 2: Full results of the second round of the modified-Delphi voting, which was used to demonstrate consensus of the guidance statements.
dc.description.abstract INTRODUCTION: Mucopolysaccharidosis (MPS) IVA or Morquio A syndrome is an autosomal recessive lysosomal storage disorder (LSD) caused by deficiency of the N-acetylgalactosamine-6-sulfatase (GALNS) enzyme, which impairs lysosomal degradation of keratan sulphate and chondroitin-6-sulphate. The multiple clinical manifestations of MPS IVA present numerous challenges for management and necessitate the need for individualised treatment. Although treatment guidelines are available, the methodology used to develop this guidance has come under increased scrutiny. This programme was conducted to provide evidence-based, expert-agreed recommendations to optimise management of MPS IVA. METHODS: Twenty six international healthcare professionals across multiple disciplines, with expertise in managing MPS IVA, and three patient advocates formed the Steering Committee (SC) and contributed to the development of this guidance. Representatives from six Patient Advocacy Groups (PAGs) were interviewed to gain insights on patient perspectives. A modified-Delphi methodology was used to demonstrate consensus among a wider group of healthcare professionals with experience managing patients with MPS IVA and the manuscript was evaluated against the validated Appraisal of Guidelines for Research and Evaluation (AGREE II) instrument by three independent reviewers. RESULTS: A total of 87 guidance statements were developed covering five domains: (1) general management principles; (2) recommended routine monitoring and assessments; (3) disease-modifying interventions (enzyme replacement therapy [ERT] and haematopoietic stem cell transplantation [HSCT]); (4) interventions to support respiratory and sleep disorders; (5) anaesthetics and surgical interventions (including spinal, limb, ophthalmic, cardio-thoracic and ear-nosethroat [ENT] surgeries). Consensus was reached on all statements after two rounds of voting. The overall guideline AGREE II assessment score obtained for the development of the guidance was 5.3/7 (where 1 represents the lowest quality and 7 represents the highest quality of guidance). CONCLUSION: This manuscript provides evidence- and consensus-based recommendations for the management of patients with MPS IVA and is for use by healthcare professionals that manage the holistic care of patients with the intention to improve clinical- and patient-reported outcomes and enhance patient quality of life. It is recognised that the guidance provided represents a point in time and further research is required to address current knowledge and evidence gaps. en_ZA
dc.description.department Paediatrics and Child Health en_ZA
dc.description.librarian pm2020 en_ZA
dc.description.sponsorship BioMarin en_ZA
dc.description.uri https://ojrd.biomedcentral.com en_ZA
dc.identifier.citation Akyol, M.U., Alden, T.D., Amartino, H. et al. Recommendations for the management of MPS IVA: systematic evidence- and consensus-based guidance. Orphanet Journal of Rare Diseases 14, 137 (2019). https://doi.org/10.1186/s13023-019-1074-9. en_ZA
dc.identifier.issn 1750-1172 (online)
dc.identifier.other 10.1186/s13023-019-1074-9
dc.identifier.uri http://hdl.handle.net/2263/75777
dc.language.iso en en_ZA
dc.publisher BioMed Central (BMC) en_ZA
dc.rights © The Author(s)2019. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License. en_ZA
dc.subject Morquio a syndrome en_ZA
dc.subject Management guidelines en_ZA
dc.subject Elosulfase alfa en_ZA
dc.subject Enzyme replacement therapy en_ZA
dc.subject Haematopoietic stem cell transplantation en_ZA
dc.subject Surgery en_ZA
dc.subject Anaesthetics en_ZA
dc.subject Mucopolysaccharidosis (MPS) en_ZA
dc.subject Lysosomal storage disorder (LSD) en_ZA
dc.subject N-acetylgalactosamine-6-sulfatase (GALNS) en_ZA
dc.subject Haematopoietic stem cell transplantation (HSCT) en_ZA
dc.subject Enzyme replacement therapy (ERT) en_ZA
dc.subject Morquio A syndrome (MPS IVA) en_ZA
dc.title Recommendations for the management of MPS IVA : systematic evidence- and consensus-based guidance en_ZA
dc.type Article en_ZA


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