德国杜氏肌萎缩症的流行病学、疾病负担和费用:一项观察性、回顾性健康声明数据分析。

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY
Joanna Diesing, Janbernd Kirschner, Astrid Pechmann, Jörg König, Leonie Kunk, Tarcyane Barata Garcia, Carolina Schwedhelm, Carsta Militzer-Horstmann, Ivonne Hänsel, Agnes Kisser
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引用次数: 0

摘要

背景:杜氏肌营养不良症(DMD)是一种罕见的遗传性疾病,主要影响男性。从儿童期开始,患者会出现无法走动、心力衰竭和需要通气的情况。疾病管理已经有所改善,然而,DMD仍然使人衰弱,并且无法治愈。这种疾病的罕见性给研究带来了困难,而且缺乏德国的流行数据。成本和资源利用估计是基于小样本量或自我报告的数据,限制了普遍性,并增加了回忆偏差的可能性。通过对医疗索赔数据库的回顾性研究,我们采用算法来识别DMD患者,并根据疾病进展的1-4期(早期门诊、晚期门诊、早期非门诊、晚期非门诊)对患者进行分类。按观察时间(患者年)分析年度患病率、疾病负担、医疗资源利用和直接医疗费用。结果:从2016年到2021年,我们确定了134例可以确定疾病分期的患者,并确定了德国40岁以下男性DMD的外推患病率在14.85 (95%CI 12.17, 17.95)和18.91 (95%CI 15.70, 22.61) / 100,000之间。我们确定的大多数患者符合DMD 4期组标准(47.01%),其次是3期(37.31%),2期(33.58%),1期只有4.48%。随着疾病的进展,患者的平均年龄从第一阶段的4.27岁增加到第二、第三和第四阶段的11.43岁、18.86岁和23.21岁。在2期组中,记录了反映活动支持和骨科手术干预的诊断代码(占组的15.56%)。在3期组中,记录了卧位预防,在4期组中增加到大约一半的患者。每位患者每年的直接平均医疗费用总额随着疾病严重程度的增加而大幅增加,从第一阶段的2,180.73欧元(标准差16,258.90);第二阶段€13,599.83(瑞典克朗33,756.07);第三阶段为14,472.08欧元(标准差27,245.78),第四阶段为41,888.70欧元(标准差117,718.13)。特别是在第3和第4阶段,医疗辅助费用约占总费用的一半。结论:我们提出了一种算法,该算法可以作为进一步研究的基础,并提供了德国DMD流行病学,疾病负担和医疗保健利用以及直接成本的当前图景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epidemiology, disease burden and costs of Duchenne muscular dystrophy in Germany: an observational, retrospective health claims data analysis.

Background: Duchenne muscular dystrophy (DMD) is a rare genetic disorder that primarily affects males. Beginning in childhood, patients experience ambulatory loss, heart failure and need ventilation. Disease management has improved, however, DMD remains debilitating, and has no cure. The rarity of the disease makes research difficult, and German prevalence data are lacking. Cost and resource utilization estimations are based on small sample sizes or self-reported data, limiting generalizability and adds the potential for recall bias. With a retrospective study on a healthcare claims database, we adapted algorithms to identify DMD patients and categorized them by disease stages 1-4 (early ambulatory, late ambulatory, early non-ambulatory, late non-ambulatory) with increasing disease progression. We analyzed annual prevalence, burden of disease, healthcare resource utilization and direct medical care costs, by time under observation (patient year).

Results: From 2016 to 2021, we identified 134 patients for which we could determine a disease stage and determined an extrapolated prevalence of DMD in Germany between 14.85 (95%CI 12.17, 17.95) and 18.91 (95%CI 15.70, 22.61) per 100,000 males under 40 years of age. Most patients we identified met DMD stage 4 group criteria (47.01%), followed by stage 3 (37.31%), stage 2 (33.58%) and only 4.48% in stage 1. The average age increased with progressing disease, from 4.27 years in stage 1, to 11.43, 18.86 and 23.21 in stage groups 2, 3 and 4, respectively. In the stage 2 group, diagnosis codes reflecting mobility support and orthopedic surgical interventions (15.56% of the group) were documented. In the stage 3 group, decubitus prevention was documented, increasing to around half of patients in the stage 4 group. Total direct mean healthcare costs per patient year increased substantially with disease severity group, from €2,180.73 (SD 16,258.90) in stage 1; €13,599.83 (SD 33,756.07) in stage 2; €14,472.08 (SD 27,245.78) in stage 3 and finally €41,888.70 (SD 117,718.13) in stage 4. Especially in stage groups 3 and 4, medical aids accounted for about half of total costs.

Conclusions: We present an algorithm on which further research can be based, and provide a current picture of epidemiology, burden of disease and healthcare utilization and direct costs of DMD in Germany.

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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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