巴西II型粘多糖病的回顾性研究——来自巴西卫生系统(DATASUS)的数据

Q3 Medicine
Fernanda Tenório, Carolina Fischinger Moura de Souza
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引用次数: 0

摘要

拉丁美洲关于II型粘多糖病(MPS II)的数据很少。这项回顾性数据库研究使用巴西卫生系统信息部(DATASUS)的数据,旨在估计2008年至2020年巴西MPSII的患病率,并描述正在接受治疗的患者的人口统计学和临床资料。研究人群来源于巴西诊断的MPS II (ICD-10 E76.1)的DATASUS记录。最初发现455例患者,但只有181例接受伊杜硫酶治疗的患者被纳入本研究。在这些病例中,正如在x连锁疾病中所预期的那样,所有病例均为男性,40%的病例记录在东南地区,另外34%在东北地区。最大比例的患者(39%)在10-19岁时被诊断出来。MPSII的主要合并症包括:腹股沟疝、呼吸系统并发症和腕管综合征,但有212种临床症状与MPSII相关。呼吸系统疾病是这些患者记录的第五大常见合并症。在巴西,更多参与MPS II诊断的医疗保健专业人员是放射科医生,其次是遗传学家和心脏病专家。尽管存在一些局限性,但DATASUS是一个提供罕见病(如MPS II)信息的相关数据库。大多数病例分别报告在东南和东北地区。这些信息对于帮助设计有针对性的公共政策至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Retrospective Study of Mucopolysaccharidosis Type II in Brazil - Data from Brazilian Health System (DATASUS)
Data on Mucopolysaccharidosis type II (MPS II) in Latin America are scarce. This retrospective database study, using data from the Informatics Department of the Brazilian Health System (DATASUS), aimed to estimate the prevalence of MPSII in Brazil from 2008 to 2020 and to describe demographic and clinical profiles from patients under treatment. The study population was derived from DATASUS records of MPS II (ICD-10 E76.1) diagnosed in Brazil. Initially 455 patients were found, but only 181 patients who were receiving idursulfase treatment were included in this study. Among these cases, as expected in a X-linked disease, all were males and 40% of the cases were recorded in the Southeast region, and another 34% in the Northeast region. The biggest proportion of patients (39%) were diagnosed when they were 10-19 years old. There are 212 clinical conditions associated with MPS II, although the main comorbidities related to MPSII include: abdominal/inguinal hernia, respiratory complications, and carpal tunnel syndrome. Respiratory disorders were the fifth most frequent comorbidity recorded in these patients. The healthcare professionals in Brazil more involved in the diagnosis of MPS II were radiologists, followed by geneticists and cardiologists. Despite some limitations, DATASUS is a relevant database to provide information on rare diseases such as MPS II. Most cases were reported in southeast and northeast regions, respectively. This information is crucial to help design targeted public policies.
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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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