Standardization of the management of rheumatoid purpura nephropathy in the West of France. What are the repercussions on the renal sequelae?

Nephrologie & therapeutique Pub Date : 2024-02-28 Epub Date: 2024-01-31 DOI:10.1684/ndt.2024.65
Margaux Salmon, Chloé Rousseau, Gwenaëlle Roussey, Nadine Jay, Sylvie Cloarec, Maud Injeyan, Amélie Ryckewaert, Sophie Taque
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Abstract

Introduction: Rheumatoid purpura is the most common vasculitis in children, and its renal involvement determines the prognosis. To date, no national protocol exists for its management. A protocol was drafted for the French Grand Ouest inter-region in 2011 in order to standardize practices.

Objectives: The main objective is to evaluate renal sequelae with a median follow-up of 2 years since the implementation of this protocol. The secondary objectives are to evaluate the different therapeutic and diagnostic management.

Method: Inclusion of all children from 2006 to 2018 with nephropathy due to rheumatoid purpura followed in the university hospitals of Rennes, Nantes, Tours, Angers and Brest.

Results: 169 patients were included, of whom 104 were treated accroding to protocol and 65 differently. Sequels at 2-year follow-up concerned 27.0% of patients with no significant difference according to whether or not the protocol was followed. A significant decrease of 26.1% in the number of renal biopsies was observed in the group that followed the protocol. The latter was performed with a median delay of less than 30 days.

Conclusion: The protocol allowed a standardization of practices without deleterious consequences at 2 years of follow-up and a decrease in renal biopsy punctures. It is in agreement with the recommendations of KDIGO (Kidney Disease Improving Global Outcomes) and European experts. On the other hand, in view of recent studies and the physiopathology, immunosuppressive drugs other than corticosteroids could be introduced earlier in severe forms.

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法国西部类风湿性紫癜肾病管理的标准化。对肾脏后遗症有何影响?
简介类风湿性紫癜是儿童中最常见的血管炎,其肾脏受累情况决定了预后。迄今为止,尚无全国性的治疗方案。2011年,法国大西部跨大区起草了一份方案,以规范诊疗行为:主要目的是评估自该方案实施以来,中位随访时间为 2 年的肾脏后遗症情况。次要目标是评估不同的治疗和诊断方法:方法:纳入2006年至2018年期间在雷恩、南特、图尔、昂热和布雷斯特大学医院就诊的所有类风湿性紫癜肾病患儿:共纳入169名患者,其中104人按照方案治疗,65人采用不同方案治疗。在两年的随访中,27.0%的患者出现了并发症,但是否按照方案治疗并无明显差异。按方案治疗组的肾活检次数明显减少了 26.1%。后者的中位延迟时间少于30天:结论:该方案实现了标准化操作,在 2 年的随访中没有造成不良后果,并减少了肾活检穿刺次数。这与 KDIGO(肾脏疾病改善全球结果)和欧洲专家的建议一致。另一方面,考虑到近期的研究和生理病理情况,对于病情严重的患者,可以更早地使用皮质类固醇以外的免疫抑制剂。
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