中国儿童线粒体疾病经济成本的初步调查。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Chaolong Xu, Dan Zhao, Xin Duan, Zhimei Liu, Tongyue Li, Yunxi Zhang, Zixuan Zhang, Tianyu Song, Ying Zou, Huafang Jiang, Fang Fang
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引用次数: 0

摘要

背景:线粒体疾病的患病率正在上升,给家庭和社会带来了巨大的经济负担。然而,有关它们对中国经济影响的全国性成本数据仍然有限。本研究旨在调查中国儿童线粒体疾病的经济成本,分析相关影响因素,为制定降低儿童线粒体疾病医疗负担的策略提供依据。方法:在这项单中心横断面研究中,对2012年1月至2022年1月诊断为线粒体疾病的儿科患者随机进行在线问卷调查。调查问卷的问题包括人口统计数据、临床信息和与支出相关的费用。使用广义线性伽马共轭模型(A1)进行经济成本的多变量分析。结果:对102份问卷的回复进行了分析。诊断线粒体疾病的直接经济费用中位数为8,520.19美元,其中直接医疗费用和非医疗费用分别为6,769.06美元和2,092.98美元,间接费用为3,162.93美元。医疗保险支付27.29%的直接医疗费用。多因素分析显示,诊断线粒体疾病的经济成本与疾病发病年份显著相关(P)。结论:研究结果表明,线粒体疾病患者的诊断和治疗经济负担都很大。应更加重视初级和二级预防战略,以进一步减少线粒体病等罕见遗传疾病的总体经济负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preliminary investigation on the economic cost of mitochondrial disease in Chinese children.

Background: The prevalence of mitochondrial diseases is increasing, leading to a significant economic burden on families and society. However, nationwide cost data on their effects on China's economy remain limited. This study aimed to investigate the economic cost of mitochondrial diseases in Chinese children, analyse the relevant influencing factors, and provide a foundation for strategies to reduce the healthcare burden.

Methods: In this single-centre, cross-sectional study, an online questionnaire was randomly administered to paediatric patients diagnosed with mitochondrial diseases between January 2012 and January 2022. The questionnaire included questions regarding demographic data, clinical information, and expenditure-related costs. Multivariate analysis of economic cost was performed using a generalised linear gamma conjugate model (A1).

Results: The responses to 102 questionnaires were analysed. The median direct economic cost incurred for the diagnosis of mitochondrial disease was $8,520.19, with direct medical and non-medical costs of $6,769.06 and $2,092.98, respectively, and an indirect cost of $3,162.93. Healthcare insurance covers 27.29% of direct medical expenses. Multivariate analysis showed that the economic cost of diagnosing mitochondrial diseases was significantly correlated with the year of disease onset (P < 0.001). The median annual economic cost for treatment and symptom management after diagnosis was $12,292.79, with direct medical and non-medical costs of $10,887.53 and $1,360.44, respectively, and an indirect cost of $5,442.21. Healthcare insurance covered only 15.16% of direct medical expenses. No significant differences were observed between the subgroups after diagnosis and the annual economic costs of treatment or symptom management.

Conclusion: The study findings indicated that the economic burden of both the diagnosis and treatment of patients with mitochondrial diseases was substantial. Increased emphasis should be placed on primary and secondary prevention strategies to further reduce the overall economic burden of rare genetic diseases, such as mitochondrial diseases.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
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.
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