Ni Yuan, Min Li, Shan-Shan Wang, Hua-Xin Yu, Ya-Qun Wang, Fan-Yu Dong, Han-Xiang Chen, Sheng-Nan Duan, Ji Luo
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Data were collected through an online questionnaire, which included basic patient information, disease status, self-assessment of quality of life, diagnosis and treatment, as well as direct and indirect medical costs. The demographic and diagnosis and treatment profile of patients were analyzed by descriptive statistics. Furthermore, univariate and multiple linear regression were used to explore the economic burden and influencing factors of patients with MPS II.</p><p><strong>Results: </strong>The survival data of 145 patients were collected, the majority (98.62%) were male, and 78 were less than or equal to 10 years old. All patients were covered by medical insurance, mainly urban residents (135 cases). In terms of expenses, the 124 patients in the year before the survey incurred a total cost of about 14.7895 million yuan, and the direct economic burden accounted for 87.19%. 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引用次数: 0
摘要
研究背景本研究调查了中国黏多醣症II型(MPS II)患者人群,了解了患者的基本情况、患病率和诊治现状,以及患者的经济负担,并分析了影响因素:方法:2023 年在中国开展了一项以 MPS II 患者为研究对象的横断面研究。研究对象来自北京正宇粘多糖罕见病关爱中心,该中心是中国大陆唯一一家在民政部门注册的以粘多糖病为主要研究对象的非营利性机构。数据通过在线问卷收集,包括患者基本信息、疾病状况、生活质量自评、诊断和治疗情况以及直接和间接医疗费用。通过描述性统计分析了患者的人口统计学、诊断和治疗概况。此外,还采用单变量和多元线性回归法探讨了 MPS II 患者的经济负担和影响因素:收集了 145 名患者的生存数据,其中大多数(98.62%)为男性,78 名患者的年龄小于或等于 10 岁。所有患者都参加了医疗保险,主要是城镇居民(135 例)。在费用方面,124 例患者在调查前一年的总费用约为 1478.95 万元,直接经济负担占 87.19%。单变量分析显示,年龄、住院次数、住院时间、门诊/急诊次数、造血干细胞移植(HSCT)和酶替代疗法(ERT)与疾病经济负担显著相关。多元回归分析显示,住院次数、住院天数、门诊/急诊次数和造血干细胞移植治疗是主要影响因素:本研究发现,MPS II 患者难以诊断且容易误诊,他们的身体机能在很多方面都受到损害。现有的治疗方案在经济性和有效性方面存在不足,也缺乏相应的政策保障和支持,使患者及其家庭面临巨大的经济压力。
Study on the disease burden of patients with mucopolysaccharidosis type II in China.
Background: In this study, we investigated the patient population of Mucopolysaccharidosis type II (MPS II) in China, understood the basic situation, prevalence and diagnosis and treatment status of the patients, as well as the economic burden of the patients, and analyzed the influencing factors.
Methods: A cross-sectional study focusing on patients with MPS II was conducted in China in 2023. Participants in the study were drawn from the Beijing Zhengyu Mucopolysaccharide Rare Disease Care Center, which is the only non-profit organization in mainland China registered with the civil affairs department that focuses on mucopolysaccharidosis. Data were collected through an online questionnaire, which included basic patient information, disease status, self-assessment of quality of life, diagnosis and treatment, as well as direct and indirect medical costs. The demographic and diagnosis and treatment profile of patients were analyzed by descriptive statistics. Furthermore, univariate and multiple linear regression were used to explore the economic burden and influencing factors of patients with MPS II.
Results: The survival data of 145 patients were collected, the majority (98.62%) were male, and 78 were less than or equal to 10 years old. All patients were covered by medical insurance, mainly urban residents (135 cases). In terms of expenses, the 124 patients in the year before the survey incurred a total cost of about 14.7895 million yuan, and the direct economic burden accounted for 87.19%. Univariate analysis showed that age, number of hospitalizations, length of hospital stay, number of outpatient/emergency departments, hematopoietic stem cell transplantation (HSCT), and enzyme replacement therapy (ERT) were significantly associated with the economic burden of disease. Multiple regression analysis showed that the number of hospitalizations, days of hospitalization, number of outpatient/emergency departments and HSCT treatment were the main influencing factors.
Conclusions: This study found that patients with MPS II were difficult to diagnose and easily misdiagnosed, their physical functions were impaired in many aspects. The existing treatment options are not sufficient in terms of economy and effectiveness, and there is also a lack of corresponding policy guarantees and support, which makes patients and their families have to face huge financial pressure.
期刊介绍:
Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.