Recommendations for Assessment and Management of Health-Related Quality of Life in Patients with Mucopolysaccharidoses in Latin America

R. Giugliani, A. Fainboim, C. Kim, D. Horovitz, E. T. Sakata, A. Damiano, T. Magalhães, Martha L. Solano Villareal
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引用次数: 1

Abstract

Mucopolysaccharidoses (MPS) constitute a heterogeneous group of rare genetic disorders caused by enzymatic deficiencies that lead to the accumulation of glycosaminoglycans (GAGs). Clinical observations suggest a health-related impairment in quality of life in patients with MPS. Professionals with extensive experience in the care of patients with inborn errors of metabolism, such as MPS, held a meeting in April 2017 to discuss and propose recommendations for the evaluation and management of quality of life in MPS patients in Latin America. In the light of this scenario, the present work summarizes the content of the discussions and presents the recommendations produced at the meeting. The panel had suggested the use of the following tools for the assessment of health-related quality of life (HRQoL): Children’s Health Assessment Questionnaire (CHAQ) for children and patients unable to express their feelings, Health Assessments Questionnaire (HAQ) and EuroQol 5 Domains (EQ-5D) scales for adult patients. Based on the scores verified in these scales, the panel proposes interventions that aim reducing the impairment of the quality of life in patients with MPS disorders.
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拉丁美洲黏多糖病患者健康相关生活质量评估和管理建议
粘多糖病(MPS)是由酶缺陷引起的罕见遗传疾病,导致糖胺聚糖(GAGs)的积累。临床观察表明MPS患者的生活质量存在健康相关损害。在先天性代谢错误(如MPS)患者护理方面拥有丰富经验的专业人员于2017年4月举行了一次会议,讨论并提出了评估和管理拉丁美洲MPS患者生活质量的建议。鉴于这种情况,本工作总结了讨论的内容,并提出了会议所提出的建议。专家小组建议使用以下工具评估与健康有关的生活质量(HRQoL):儿童和无法表达自己感受的患者使用儿童健康评估问卷(CHAQ),成年患者使用健康评估问卷(HAQ)和EuroQol 5域(EQ-5D)量表。根据这些量表中验证的分数,专家组提出旨在减少MPS障碍患者生活质量损害的干预措施。
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来源期刊
CiteScore
0.60
自引率
0.00%
发文量
7
审稿时长
12 weeks
期刊介绍: The Journal of Inborn Errors of Metabolism and Screening (JIEMS) is an online peer-reviewed open access journal devoted to publishing clinical and experimental research in inherited metabolic disorders and screening, for health professionals and scientists. Original research articles published in JIEMS range from basic findings that have implications for disease pathogenesis and therapy, passing through diagnosis and screening of metabolic diseases and genetic conditions, and therapy development and outcomes as well. Original articles, reviews on specific topics, brief communications and case reports are welcome. JIEMS aims to become a key resource for geneticists, genetic counselors, biochemists, molecular biologists, reproductive medicine researchers, obstetricians/gynecologists, neonatologists, pediatricians, pathologists and other health professionals interested in inborn errors of metabolism and screening.
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