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dc.contributor.authorAkyol, Mehmet Umutpt_BR
dc.contributor.authorGiugliani, Robertopt_BR
dc.contributor.authorMarinho, Diane Ruschelpt_BR
dc.contributor.authorScarpa, Mauriziopt_BR
dc.date.accessioned2019-10-25T03:46:49Zpt_BR
dc.date.issued2019pt_BR
dc.identifier.issn1750-1172pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/200998pt_BR
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 gapsen
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofOrphanet journal of rare diseases. [London] : BioMed Central. Vol. 14 (2019), 137, 25 p.pt_BR
dc.rightsOpen Accessen
dc.subjectMucopolissacaridose IVpt_BR
dc.subjectMorquio a syndromeen
dc.subjectGuia de prática clínicapt_BR
dc.subjectMucopolysaccharidosisen
dc.subjectMPS IVAen
dc.subjectAvaliação de sintomaspt_BR
dc.subjectMonitorização fisiológicapt_BR
dc.subjectManagement guidelinesen
dc.subjectElosulfase alfaen
dc.subjectTranstornos do sono-vigíliapt_BR
dc.subjectTerapia de reposição de enzimaspt_BR
dc.subjectEnzyme replacement therapyen
dc.subjectTransplante de células-tronco hematopoéticaspt_BR
dc.subjectERTen
dc.subjectHaematopoietic stem cell transplantationen
dc.subjectProcedimentos cirúrgicos operatóriospt_BR
dc.subjectAnestésicospt_BR
dc.subjectHSCTen
dc.subjectSurgeryen
dc.subjectAnaestheticsen
dc.subjectVIMIZIMen
dc.titleRecommendations for the management of MPS IVA : systematic evidence- and consensus-based guidancept_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001104093pt_BR
dc.type.originEstrangeiropt_BR


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