德国现实环境中系统性红斑狼疮患者器官损伤的临床和经济负担。

IF 2.1 Q3 RHEUMATOLOGY BMC Rheumatology Pub Date : 2024-05-17 DOI:10.1186/s41927-024-00387-6
Michael Schultze, Elena Garal-Pantaler, Marc Pignot, Roger A Levy, Heike Carnarius, Matthias Schneider, Kerry Gairy
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引用次数: 0

摘要

背景:系统性红斑狼疮(SLE系统性红斑狼疮(SLE)是一种慢性多系统自身免疫性疾病,极易造成器官损伤,给医疗系统带来沉重负担。系统性红斑狼疮的疾病调整旨在减少疾病活动,同时将治疗毒性降至最低,防止或尽量减少器官损伤的发生。这项真实世界的研究利用医疗行政报销数据,评估了德国系统性红斑狼疮患者器官损伤的发展、相关费用和医疗资源利用率(HCRU):从 Betriebskrankenkassen 德国疾病基金数据库中获取了 2007 年 1 月 1 日至 2017 年 12 月 31 日的理赔数据。2009年1月1日至2014年12月31日(纳入期)期间确诊为系统性红斑狼疮的成年人(大于18岁)被纳入其中。指数日期根据在此期间首次记录的系统性红斑狼疮诊断结果计算。根据年龄、性别和合并症(Charlson 合并症指数),将患者与无系统性红斑狼疮的参照队列进行倾向评分匹配(1:3)。根据系统性红斑狼疮国际合作诊所/美国风湿病学会损害指数(SDI)中描述的情况,使用ICD-10-GM诊断代码、医疗程序和/或治疗方法,采用一种算法确定器官损害。在所有系统性红斑狼疮患者中,器官损伤发生率从基线时的60.5%上升到随访6年期间的83.0%,而17.0%的系统性红斑狼疮患者没有发生器官损伤。新确诊的系统性红斑狼疮患者在基线时没有器官损伤,但在 5 年内出现器官损伤的几率几乎是对照组的两倍(52.0% 对 27.0%)。有器官损害的系统性红斑狼疮患者每名患者每年的总费用是无器官损害的系统性红斑狼疮患者的两倍多;住院人数和住院时间都更长:应用最近开发的算法,我们可以利用索赔数据,在德国一个具有代表性的大样本中阐明系统性红斑狼疮的器官损伤及其相关的高临床和经济负担。据我们所知,这是欧洲首次对在常规护理环境中接受治疗的大量系统性红斑狼疮患者进行此类分析。
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Clinical and economic burden of organ damage among patients with systemic lupus erythematosus in a real-world setting in Germany.

Background: Systemic lupus erythematosus (SLE), a chronic multisystem autoimmune disease, carries high risk of organ damage and burden to healthcare systems. SLE disease modification aims to reduce disease activity with minimal treatment toxicity and preventing or minimizing organ damage development. This real-world study utilizing healthcare administrative claims data assessed organ damage development, associated costs and healthcare resource utilization (HCRU) in patients with SLE in Germany.

Methods: Claims data from January 1, 2007, to December 31, 2017, were obtained from the Betriebskrankenkassen German Sickness Fund Database. Adults (> 18 years) with a confirmed SLE diagnosis between January 1, 2009, and December 31, 2014, (inclusion period) were included. The index date was calculated based on the first recorded SLE diagnosis during this period. Patients were propensity score-matched (1:3) to a comparator cohort without SLE by age, sex, and comorbidities (Charlson comorbidity index). Organ damage was identified using an algorithm developed based on conditions described in the Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index (SDI), using ICD-10-GM diagnostic codes, healthcare procedures, and/or treatments.

Results: 2121 patients with SLE and 6308 comparator patients were included (mean follow-up time: 6.4 years). Organ damage prevalence increased from 60.5% at baseline to 83.0% during 6 years of follow-up in all patients with SLE, while 17.0% of patients with SLE did not develop organ damage. Patients with newly confirmed SLE diagnosis without organ damage at baseline were nearly twice as likely to develop organ damage within 5 years versus the comparator cohort (52.0% vs. 27.0%). Total annual costs per patient-year for patients with SLE with organ damage were more than double those of patients with SLE without organ damage; both the number of inpatient admissions and length of stay were higher.

Conclusions: The application of a recently developed algorithm allowed us to use claims data to elucidate SLE organ damage, and its associated high clinical and economic burden, in a large, representative sample in Germany. To our knowledge, this is the first European analysis of its kind involving a broad cohort of patients with SLE treated in the routine care setting.

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来源期刊
BMC Rheumatology
BMC Rheumatology Medicine-Rheumatology
CiteScore
3.80
自引率
0.00%
发文量
73
审稿时长
15 weeks
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