Clinical Burden and Costs of Anti-Neutrophil Cytoplasmic Antibody-ANCA-Associated Vasculitis: Main Findings from REDCap Registry of a University Hospital in Spain.

IF 2.2 Q3 HEALTH CARE SCIENCES & SERVICES
ClinicoEconomics and Outcomes Research Pub Date : 2025-08-01 eCollection Date: 2025-01-01 DOI:10.2147/CEOR.S529853
Juliana Draibe, Laura Martinez Valenzuela, Francisco Gomez-Preciado, Paula Anton-Pampols, Ana Melissa Rau, Helena Díaz-Cuervo, Carlos Crespo, Jesús Cuervo, Antonio Ramirez de Arellano
{"title":"Clinical Burden and Costs of Anti-Neutrophil Cytoplasmic Antibody-ANCA-Associated Vasculitis: Main Findings from REDCap Registry of a University Hospital in Spain.","authors":"Juliana Draibe, Laura Martinez Valenzuela, Francisco Gomez-Preciado, Paula Anton-Pampols, Ana Melissa Rau, Helena Díaz-Cuervo, Carlos Crespo, Jesús Cuervo, Antonio Ramirez de Arellano","doi":"10.2147/CEOR.S529853","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Anti-neutrophil cytoplasmic antibody-associated vasculitis (AAV) are rare chronic autoimmune diseases, potentially fatal, with frequent relapses. They are associated with vital organ damage, especially renal, often resulting in end-stage renal disease. While current standard of care with immunosuppressants has improved renal function and survival, the main risks for patients under life-long immunosuppression are infections and other concomitant diseases. This study evaluated the burden of AAV using patient-level data from a disease-specific registry.</p><p><strong>Patients and methods: </strong>The cohort of incident AVV patients (2013-2022) in the REDCap registry in a university hospital in Spain was studied. Patients with Granulomatosis with Polyangiitis (GPA), Microscopic Polyangiitis (MPA) and Eosinophilic Granulomatosis with Polyangiitis (EGPA) with at least one year of follow-up (or deceased during the period) were included. Clinical outcomes, including Birmingham Vasculitis Activity Score (BVAS) and healthcare resource consumption were analysed for the first year after diagnosis. Mean annual costs were calculated using unitary costs from the hospital accounting department.</p><p><strong>Results: </strong>Seventy-five patients (12% EGPA, 32% GPA, and 56% MPA) were included. Fifty-two percent were women. Mean age at diagnosis was 65.20±14.70 years. At baseline, mean BVAS was 17.35±5.70, 93.33% of patients showed renal affectation, mean estimated glomerular filtration rate was 33.32±29.93mL/min/1.73m<sup>2</sup>. As induction treatment, 62.67% received methylprednisolone, 37.33% rituximab, 25.33% cyclophosphamide, 14.67% rituximab plus cyclophosphamide, 34.67% plasmapheresis. During the first year after diagnosis, 17.33% relapsed and 78.67% had at least 1 hospitalisation; 97.33% received steroids; 13.33% were on dialysis at some point; one patient received a kidney transplant; 46.67% presented infections and 28% suffered corticosteroid-associated complications; 4 patients died, being 50% of deaths treatment-related. The highest observed mean cost per patient for the first year was €11,647.95 for hospital care.</p><p><strong>Conclusion: </strong>This study revealed a considerable burden of AAV, as evidenced by high rates of hospitalisation, relapses, and the need for intensive medical interventions.</p>","PeriodicalId":47313,"journal":{"name":"ClinicoEconomics and Outcomes Research","volume":"17 ","pages":"537-546"},"PeriodicalIF":2.2000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12323866/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ClinicoEconomics and Outcomes Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2147/CEOR.S529853","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"HEALTH CARE SCIENCES & SERVICES","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: Anti-neutrophil cytoplasmic antibody-associated vasculitis (AAV) are rare chronic autoimmune diseases, potentially fatal, with frequent relapses. They are associated with vital organ damage, especially renal, often resulting in end-stage renal disease. While current standard of care with immunosuppressants has improved renal function and survival, the main risks for patients under life-long immunosuppression are infections and other concomitant diseases. This study evaluated the burden of AAV using patient-level data from a disease-specific registry.

Patients and methods: The cohort of incident AVV patients (2013-2022) in the REDCap registry in a university hospital in Spain was studied. Patients with Granulomatosis with Polyangiitis (GPA), Microscopic Polyangiitis (MPA) and Eosinophilic Granulomatosis with Polyangiitis (EGPA) with at least one year of follow-up (or deceased during the period) were included. Clinical outcomes, including Birmingham Vasculitis Activity Score (BVAS) and healthcare resource consumption were analysed for the first year after diagnosis. Mean annual costs were calculated using unitary costs from the hospital accounting department.

Results: Seventy-five patients (12% EGPA, 32% GPA, and 56% MPA) were included. Fifty-two percent were women. Mean age at diagnosis was 65.20±14.70 years. At baseline, mean BVAS was 17.35±5.70, 93.33% of patients showed renal affectation, mean estimated glomerular filtration rate was 33.32±29.93mL/min/1.73m2. As induction treatment, 62.67% received methylprednisolone, 37.33% rituximab, 25.33% cyclophosphamide, 14.67% rituximab plus cyclophosphamide, 34.67% plasmapheresis. During the first year after diagnosis, 17.33% relapsed and 78.67% had at least 1 hospitalisation; 97.33% received steroids; 13.33% were on dialysis at some point; one patient received a kidney transplant; 46.67% presented infections and 28% suffered corticosteroid-associated complications; 4 patients died, being 50% of deaths treatment-related. The highest observed mean cost per patient for the first year was €11,647.95 for hospital care.

Conclusion: This study revealed a considerable burden of AAV, as evidenced by high rates of hospitalisation, relapses, and the need for intensive medical interventions.

Abstract Image

Abstract Image

Abstract Image

抗中性粒细胞细胞质抗体- anca相关血管炎的临床负担和费用:来自西班牙一所大学医院REDCap注册的主要发现
目的:抗中性粒细胞细胞质抗体相关血管炎(AAV)是一种罕见的慢性自身免疫性疾病,具有潜在的致命性,复发频繁。它们与重要器官损害有关,尤其是肾脏,常导致终末期肾脏疾病。虽然目前使用免疫抑制剂的护理标准改善了肾功能和生存率,但终身免疫抑制患者的主要风险是感染和其他伴随疾病。本研究使用来自疾病特异性登记处的患者水平数据来评估AAV的负担。患者和方法:对西班牙某大学医院REDCap登记的AVV患者队列(2013-2022)进行研究。纳入随访至少1年(或期间死亡)的肉芽肿病合并多血管炎(GPA)、显微镜下多血管炎(MPA)和嗜酸性肉芽肿病合并多血管炎(EGPA)患者。临床结果包括诊断后第一年的伯明翰血管炎活动评分(BVAS)和医疗资源消耗。平均年成本采用医院会计部门的单一成本计算。结果:纳入75例患者(EGPA 12%, GPA 32%, MPA 56%)。52%是女性。平均诊断年龄65.20±14.70岁。基线时,BVAS平均值为17.35±5.70,93.33%的患者表现为肾功能不全,肾小球滤过率平均值为33.32±29.93mL/min/1.73m2。诱导治疗中,62.67%采用甲基强龙,37.33%采用利妥昔单抗,25.33%采用环磷酰胺,14.67%采用利妥昔单抗联合环磷酰胺,34.67%采用血浆置换。在诊断后的一年内,17.33%复发,78.67%至少住院一次;97.33%接受类固醇治疗;13.33%接受过透析治疗;一名患者接受了肾脏移植;46.67%出现感染,28%出现皮质类固醇相关并发症;4例死亡,50%的死亡与治疗有关。观察到的第一年每位患者住院治疗的最高平均费用为11,647.95欧元。结论:这项研究揭示了AAV的相当大的负担,证明了高住院率、复发率和强化医疗干预的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
ClinicoEconomics and Outcomes Research
ClinicoEconomics and Outcomes Research HEALTH CARE SCIENCES & SERVICES-
CiteScore
3.70
自引率
0.00%
发文量
83
审稿时长
16 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信