Understanding the early presentation of mucopolysaccharidoses disorders : results of a systematic literature review and physician survey
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/194763 |
Resumo: | As therapies are developed for rare disorders, challenges of early diagnosis become particularly relevant. This article focuses on clinical recognition of mucopolysaccharidoses (MPS), a group of rare genetic diseases related to abnormalities in lysosomal function. As quality of outcomes with current therapies is impacted by timing of intervention, minimizing time to diagnosis is critical. The objective of this study was to characterize how, when, and to whom patients with MPS first present and develop tools to stimulate earlier recognition of MPS. A tripartite approach was used, including a systematic literature review yielding 194 studies, an online physician survey completed by 209 physicians who described 859 MPS cases, and a global panel of MPS experts who distilled the findings. Red flag signs/symptoms were identified for cardiology, pediatric neurology, otorhinolaryngology, rheumatology, orthopedics, pediatrics, and general medicine and converted into simple, specialty-specific tools intended to facilitate early diagnosis of MPS, enabling improved patient outcomes. |
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Clarke, Lorne A.Wijburg, FritsGiugliani, Roberto2019-05-30T02:40:16Z20182326-4594http://hdl.handle.net/10183/194763001090234As therapies are developed for rare disorders, challenges of early diagnosis become particularly relevant. This article focuses on clinical recognition of mucopolysaccharidoses (MPS), a group of rare genetic diseases related to abnormalities in lysosomal function. As quality of outcomes with current therapies is impacted by timing of intervention, minimizing time to diagnosis is critical. The objective of this study was to characterize how, when, and to whom patients with MPS first present and develop tools to stimulate earlier recognition of MPS. A tripartite approach was used, including a systematic literature review yielding 194 studies, an online physician survey completed by 209 physicians who described 859 MPS cases, and a global panel of MPS experts who distilled the findings. Red flag signs/symptoms were identified for cardiology, pediatric neurology, otorhinolaryngology, rheumatology, orthopedics, pediatrics, and general medicine and converted into simple, specialty-specific tools intended to facilitate early diagnosis of MPS, enabling improved patient outcomes.application/pdfengJournal of inborn errors of metabolism & screeing. Thousand Oaks. vol. 6 (2018), 12 p.MucopolissacaridosesDiagnósticoMucopolysaccharidosesMucopolysaccharidosis IMucopolysaccharidosis IIMucopolysaccharidosis IIIMucopolysaccharidosis IVMucopolysaccharidosis VIMucopolysaccharidosis VIIDiagnosisUnderstanding the early presentation of mucopolysaccharidoses disorders : results of a systematic literature review and physician surveyEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001090234.pdf.txt001090234.pdf.txtExtracted Texttext/plain47461http://www.lume.ufrgs.br/bitstream/10183/194763/2/001090234.pdf.txt43c54486e2da3dd02f63aa944668a510MD52ORIGINAL001090234.pdfTexto completo (inglês)application/pdf681467http://www.lume.ufrgs.br/bitstream/10183/194763/1/001090234.pdfb1d686d707b6e2f49108766dc2bd8303MD5110183/1947632019-05-31 02:45:31.607243oai:www.lume.ufrgs.br:10183/194763Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2019-05-31T05:45:31Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Understanding the early presentation of mucopolysaccharidoses disorders : results of a systematic literature review and physician survey |
title |
Understanding the early presentation of mucopolysaccharidoses disorders : results of a systematic literature review and physician survey |
spellingShingle |
Understanding the early presentation of mucopolysaccharidoses disorders : results of a systematic literature review and physician survey Clarke, Lorne A. Mucopolissacaridoses Diagnóstico Mucopolysaccharidoses Mucopolysaccharidosis I Mucopolysaccharidosis II Mucopolysaccharidosis III Mucopolysaccharidosis IV Mucopolysaccharidosis VI Mucopolysaccharidosis VII Diagnosis |
title_short |
Understanding the early presentation of mucopolysaccharidoses disorders : results of a systematic literature review and physician survey |
title_full |
Understanding the early presentation of mucopolysaccharidoses disorders : results of a systematic literature review and physician survey |
title_fullStr |
Understanding the early presentation of mucopolysaccharidoses disorders : results of a systematic literature review and physician survey |
title_full_unstemmed |
Understanding the early presentation of mucopolysaccharidoses disorders : results of a systematic literature review and physician survey |
title_sort |
Understanding the early presentation of mucopolysaccharidoses disorders : results of a systematic literature review and physician survey |
author |
Clarke, Lorne A. |
author_facet |
Clarke, Lorne A. Wijburg, Frits Giugliani, Roberto |
author_role |
author |
author2 |
Wijburg, Frits Giugliani, Roberto |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Clarke, Lorne A. Wijburg, Frits Giugliani, Roberto |
dc.subject.por.fl_str_mv |
Mucopolissacaridoses Diagnóstico |
topic |
Mucopolissacaridoses Diagnóstico Mucopolysaccharidoses Mucopolysaccharidosis I Mucopolysaccharidosis II Mucopolysaccharidosis III Mucopolysaccharidosis IV Mucopolysaccharidosis VI Mucopolysaccharidosis VII Diagnosis |
dc.subject.eng.fl_str_mv |
Mucopolysaccharidoses Mucopolysaccharidosis I Mucopolysaccharidosis II Mucopolysaccharidosis III Mucopolysaccharidosis IV Mucopolysaccharidosis VI Mucopolysaccharidosis VII Diagnosis |
description |
As therapies are developed for rare disorders, challenges of early diagnosis become particularly relevant. This article focuses on clinical recognition of mucopolysaccharidoses (MPS), a group of rare genetic diseases related to abnormalities in lysosomal function. As quality of outcomes with current therapies is impacted by timing of intervention, minimizing time to diagnosis is critical. The objective of this study was to characterize how, when, and to whom patients with MPS first present and develop tools to stimulate earlier recognition of MPS. A tripartite approach was used, including a systematic literature review yielding 194 studies, an online physician survey completed by 209 physicians who described 859 MPS cases, and a global panel of MPS experts who distilled the findings. Red flag signs/symptoms were identified for cardiology, pediatric neurology, otorhinolaryngology, rheumatology, orthopedics, pediatrics, and general medicine and converted into simple, specialty-specific tools intended to facilitate early diagnosis of MPS, enabling improved patient outcomes. |
publishDate |
2018 |
dc.date.issued.fl_str_mv |
2018 |
dc.date.accessioned.fl_str_mv |
2019-05-30T02:40:16Z |
dc.type.driver.fl_str_mv |
Estrangeiro info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
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article |
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http://hdl.handle.net/10183/194763 |
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2326-4594 |
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001090234 |
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http://hdl.handle.net/10183/194763 |
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eng |
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Journal of inborn errors of metabolism & screeing. Thousand Oaks. vol. 6 (2018), 12 p. |
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