ANCA相关性血管炎患者的复发:哥伦比亚风湿病中心的一项队列研究

Ana María Romero-Millán , Andrés Arango-Vieira , Jaime Andrés Ibarra-Burgos , Maria Antonia Mesa-Maya , María José Orrego-Garay , Santiago Gómez-Maya , Tomás Giraldo-Hinestroza , Fabio Torres-Saavedra , Diego Fernando Rojas-Gualdrón , Juan Camilo Díaz-Coronado
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引用次数: 0

摘要

导言ANCA相关性血管炎(AAV)患者复发很常见,这导致了严重的发病率、死亡率、对生活质量的影响、残疾和费用负担。本研究旨在估算哥伦比亚一家风湿病专科中心的AAV患者第一年的无复发生存率,并描述其临床和血清学变量。材料与方法本研究对18岁以上经风湿病医生确诊为AAV并获得缓解的患者的病历进行了回顾性随访。研究人员提取了AAV复发信息以及临床、免疫血清学和治疗相关特征。结果 共纳入56名患者,其中69.9%为女性,中位年龄为60岁(IQR=48-63)。根据临床表型,64.3%被归类为肉芽肿伴多血管炎(GPA),23.2%被归类为显微镜下多血管炎(MPA),12.5%被归类为嗜酸性肉芽肿伴多血管炎(EGPA)。根据欧洲血管炎研究小组(EUVAS)的分类,39.3%的患者在初次发病时患有全身性AAV,23.2%患有局部性AAV,21.4%患有严重的肾脏AAV,16.1%患有全身性AAV。五因素评分(FFS)的中位数为 1(IQR = 0-2)。结论该队列中观察到的无复发生存率与其他临床研究和AAV登记处的报告相似。
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Relapse in patients with ANCA-associated vasculitis: A cohort study from a centre for rheumatic diseases in Colombia

Introduction

Relapses are common in patients with ANCA-associated vasculitis (AAV), which results in a significant burden of morbidity, mortality, impact on quality of life, disability, and cost. However, evidence in the Colombian population is scarce.

Objective

The objective of this study was to estimate the relapse-free survival during the first year and describe clinical and serological variables of patients with AAV in a specialized centre for rheumatic diseases in Colombia.

Materials and methods

A retrospective follow-up study was conducted on a cohort based on medical records of patients over 18 years old with confirmed diagnosis of AAV by the treating rheumatologist and who had achieved remission. Information on AAV relapse and clinical, immunoserological, and treatment-related characteristics was extracted. The relapse-free survival function during the first year was estimated.

Results

A total of 56 patients were included, 69.9% of whom were women, with a median age of 60 (IQR = 48−63). According to the clinical phenotype, 64.3% were classified as granulomatosis with polyangiitis (GPA), 23.2% as microscopic polyangiitis (MPA), and 12.5% as eosinophilic granulomatosis with polyangiitis (EGPA). According to the European Vasculitis Study Group (EUVAS) classification, 39.3% had generalized AAV at debut, 23.2% had localized AAV, 21.4% had severe renal AAV, and 16.1% had systemic AAV. The median Five Factor Score (FFS) was 1 (IQR = 0−2). The cumulative relapse-free survival at one year was 82.2%.

Conclusions

The relapse-free survival observed in this cohort was similar to other reports in clinical studies and AAV registries.

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