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

dc.contributor.authorAkyol, Mehmet Umut
dc.contributor.authorAlden, Tord D.
dc.contributor.authorAmartino, Hernan
dc.contributor.authorAshworth, Jane
dc.contributor.authorBelani, Kumar
dc.contributor.authorBerger, Kenneth I.
dc.contributor.authorBorgo, Andrea
dc.contributor.authorBraunlin, Elizabeth
dc.contributor.authorEto, Yoshikatsu
dc.contributor.authorGold, Jeffrey I.
dc.contributor.authorJester, Andrea
dc.contributor.authorJones, Simon A.
dc.contributor.authorKarsli, Cengiz
dc.contributor.authorMackenzie, William
dc.contributor.authorMarinho, Diane Ruschel
dc.contributor.authorMcFadyen, Andrew
dc.contributor.authorMcGill, Jim
dc.contributor.authorMitchell, John J.
dc.contributor.authorMuenzer, Joseph
dc.contributor.authorOkuyama, Torayuki
dc.contributor.authorOrchard, Paul J.
dc.contributor.authorStevens, Bob
dc.contributor.authorThomas, Sophie
dc.contributor.authorWalker, Robert
dc.contributor.authorWynn, Robert
dc.contributor.authorGiugliani, Roberto
dc.contributor.authorHarmatz, Paul
dc.contributor.authorHendriksz, Christian J.
dc.contributor.authorScarpa, Maurizio
dc.date.accessioned2020-08-18T06:09:41Z
dc.date.available2020-08-18T06:09:41Z
dc.date.issued2019-06
dc.descriptionAdditional 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.descriptionAdditional 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.descriptionAdditional 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.descriptionAdditional 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.descriptionAdditional 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.abstractINTRODUCTION: 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.departmentPaediatrics and Child Healthen_ZA
dc.description.librarianpm2020en_ZA
dc.description.sponsorshipBioMarinen_ZA
dc.description.urihttps://ojrd.biomedcentral.comen_ZA
dc.identifier.citationAkyol, 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.issn1750-1172 (online)
dc.identifier.other10.1186/s13023-019-1074-9
dc.identifier.urihttp://hdl.handle.net/2263/75777
dc.language.isoenen_ZA
dc.publisherBioMed 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.subjectMorquio a syndromeen_ZA
dc.subjectManagement guidelinesen_ZA
dc.subjectElosulfase alfaen_ZA
dc.subjectEnzyme replacement therapyen_ZA
dc.subjectHaematopoietic stem cell transplantationen_ZA
dc.subjectSurgeryen_ZA
dc.subjectAnaestheticsen_ZA
dc.subjectMucopolysaccharidosis (MPS)en_ZA
dc.subjectLysosomal storage disorder (LSD)en_ZA
dc.subjectN-acetylgalactosamine-6-sulfatase (GALNS)en_ZA
dc.subjectHaematopoietic stem cell transplantation (HSCT)en_ZA
dc.subjectEnzyme replacement therapy (ERT)en_ZA
dc.subjectMorquio A syndrome (MPS IVA)en_ZA
dc.titleRecommendations for the management of MPS IVA : systematic evidence- and consensus-based guidanceen_ZA
dc.typeArticleen_ZA

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