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抗中性粒细胞胞浆抗体(ANCA)相关血管炎的临床负担与成本:西班牙一家大学医院REDCap注册研究的主要发现

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

作者信息

Draibe Juliana, Martinez Valenzuela Laura, Gomez-Preciado Francisco, Anton-Pampols Paula, Rau Ana Melissa, Díaz-Cuervo Helena, Crespo Carlos, Cuervo Jesús, Ramirez de Arellano Antonio

机构信息

Nephrology Department, Hospital Universitari de Bellvitge, Barcelona, Spain.

Axentiva Solutions, Barcelona, Spain.

出版信息

Clinicoecon Outcomes Res. 2025 Aug 1;17:537-546. doi: 10.2147/CEOR.S529853. eCollection 2025.

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/1.73m. 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.

摘要

目的

抗中性粒细胞胞浆抗体相关性血管炎(AAV)是罕见的慢性自身免疫性疾病,有潜在致命性,且频繁复发。它们与重要器官损害相关,尤其是肾脏,常导致终末期肾病。虽然目前使用免疫抑制剂的标准治疗改善了肾功能和生存率,但长期接受免疫抑制治疗的患者面临的主要风险是感染和其他伴随疾病。本研究使用来自特定疾病登记处的患者层面数据评估了AAV的负担。

患者与方法

对西班牙一家大学医院REDCap登记处的初发AAV患者队列(2013 - 2022年)进行了研究。纳入了患有肉芽肿性多血管炎(GPA)、显微镜下多血管炎(MPA)和嗜酸性肉芽肿性多血管炎(EGPA)且至少随访一年(或在此期间死亡)的患者。分析了诊断后第一年的临床结局,包括伯明翰血管炎活动评分(BVAS)和医疗资源消耗情况。使用医院会计部门的单位成本计算了平均年度费用。

结果

共纳入75例患者(12%为EGPA,32%为GPA,56%为MPA)。52%为女性。诊断时的平均年龄为65.20±14.70岁。基线时,平均BVAS为17.35±5.70,93.33%的患者有肾脏受累,平均估计肾小球滤过率为33.32±29.93mL/min/1.73m²。作为诱导治疗,62.67%的患者接受了甲泼尼龙,37.33%接受了利妥昔单抗,25.33%接受了环磷酰胺,14.67%接受了利妥昔单抗加环磷酰胺,34.67%接受了血浆置换。在诊断后的第一年,17.33%的患者复发,78.67%的患者至少住院1次;97.33%的患者接受了类固醇治疗;13.33%的患者在某个时间点接受了透析;1例患者接受了肾移植;46.67%的患者出现感染,28%的患者出现与皮质类固醇相关的并发症;4例患者死亡,其中50%的死亡与治疗相关。观察到的第一年每位患者最高平均住院费用为11,647.95欧元。

结论

本研究揭示了AAV相当大的负担,住院率、复发率高以及需要强化医疗干预均证明了这一点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d07/12323866/a00ecf324a2b/CEOR-17-537-g0001.jpg

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