美国威尔逊病患者的特征:保险索赔数据库研究

IF 2.5 Q2 GASTROENTEROLOGY & HEPATOLOGY
T. Daniel-Robin, Pradeep Kumar, Bernard Benichou, J. Combal
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引用次数: 0

摘要

背景 威尔逊病(WD)是一种影响肝脏和中枢神经系统的渐进性、潜在致命的变性疾病。由于该病发病率较低,收集大量 WD 患者的数据具有挑战性。综合保险理赔数据库为收集大量罕见病患者的回顾性数据提供了强有力的工具。目的 利用大型保险理赔数据库,描述美国 WD 患者及其治疗和临床结果。方法 该回顾性纵向研究在 Clarivate 真实世界数据产品数据库中进行。研究纳入了 2016 年至 2021 年期间所有索赔次数≥ 2 次且与 WD 国际疾病分类 10 (ICD-10) 诊断代码(E83.01)相关的患者,并对其进行随访直至死亡或研究结束。根据患者是否接受过针对 WD 的特定治疗将其分为两组。临床表现、住院治疗、肝移植和死亡情况均有记录。结果 共发现 5376 名患者的 ICD-10 诊断代码为 WD。纳入患者的平均年龄为 41.2 岁,52.0% 为男性。有 885 名患者(15.1%)接受了特定的 WD 治疗,但服用锌盐的患者人数可能因非处方药购买而被低估。纳入研究时,有治疗记录的患者平均年龄为(36.6 ± 17.8)岁,而无治疗记录的患者平均年龄为(42.2 ± 19.6)岁。在随访期间,有 273 名患者(5.1%)死亡。与美国普通人群相比,标准化死亡率为 2.19。在随访期间死亡的接受过 WD 治疗的患者比例为 4.0%,平均死亡年龄为 52.7 岁。结论 与美国人口相比,在美国接受 WD 治疗的患者早期死亡率过高。这些研究结果表明,美国对有效治疗 WD 的需求尚未得到满足。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characteristics of patients with Wilson disease in the United States: An insurance claims database study
BACKGROUND Wilson disease (WD) is a progressive, potentially fatal degenerative disease affecting the liver and central nervous system. Given its low prevalence, collecting data on large cohorts of patients with WD is challenging. Comprehensive insurance claims databases provide powerful tools to collect retrospective data on large numbers of patients with rare diseases. AIM To describe patients with WD in the United States, their treatment and clinical outcome, using a large insurance claims database. METHODS This retrospective, longitudinal study was performed in the Clarivate Real-World Data Product database. All patients with ≥ 2 claims associated with an International Classification of Diseases 10 (ICD-10) diagnostic code for WD (E83.01) between 2016 and 2021 were included and followed until death or study end. Patients were divided into two groups by whether or not they were documented to have received a specific treatment for WD. Clinical manifestations, hospitalisations, liver transplantation and death were documented. RESULTS Overall, 5376 patients with an ICD-10 diagnostic code for WD were identified. The mean age at inclusion was 41.2 years and 52.0% were men. A specific WD treatment was documented for 885 patients (15.1%), although the number of patients taking zinc salts may be underestimated due to over the counter purchase. At inclusion, the mean age of patients with a documented treatment was 36.6 ± 17.8 years vs 42.2 ± 19.6 years in those without a documented treatment. During follow-up, 273 patients (5.1%) died. Compared with the American general population, the standardised mortality ratio was 2.19. The proportion of patients with a documented WD-specific treatment who died during follow-up was 4.0% and the mean age at death 52.7 years. CONCLUSION Patients treated for WD in the United States had an excess early mortality compared with the American population. These findings indicate that there is a significant unmet need for effective treatment for WD in the United States.
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来源期刊
World Journal of Hepatology
World Journal of Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
4.10
自引率
4.20%
发文量
172
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