Covid-19 疫苗相关肾小球疾病 (CVAGD) 的治疗结果--印度的一个病例系列

Pub Date : 2024-07-15 DOI:10.25259/ijn_479_23
V. Rajarathinam, Jayalakshmi Seshadri, G. Senthilkumaran, V. Jibia, Vinoj Murugesan, P. Devaraju, C. M. Balasubramanian, Dinesh Kumar, T. Lamech, Natarajan Gopalakrishnan
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摘要

据报道,接种 Covid-19 疫苗(尤其是 mRNA 疫苗)后出现肾小球疾病的病例不在少数。然而,有关印度广泛使用的两种疫苗(Covaxin 和 Covishield)引起的肾小球疾病及其长期结果的数据却很少。这是一项前瞻性观察研究,在 2021 年 5 月至 2023 年 5 月期间进行。这项前瞻性观察研究在 2021 年 5 月至 2023 年 5 月期间进行。研究纳入了在接种 Covid-19 疫苗 30 天内新发或复发蛋白尿、血尿或肾衰竭的患者。研究人员收集了原有肾脏疾病、疫苗类型、症状、实验室报告、肾活检结果和治疗细节等数据。研究了 16 名 Covid-19 疫苗相关肾小球疾病(CVAGD)患者的临床病程和长期肾脏疗效。中位年龄为 28 岁(IQR 20.5-40),中位症状出现时间为接种疫苗后 14 天(IQR 10-16.5)。七名患者(43.75%)出现肾病综合征,七名患者(43.75%)出现肾炎综合征,两名患者(12.5%)出现快速进展性肾衰竭。肾活检显示,5 名患者(31.2%)患有微小病变;4 名患者(25%)患有 IgA 肾病;2 名患者(12.5%)患有 C3 肾小球病、狼疮性肾炎和局灶节段性肾小球硬化症;1 名患者(6.25%)患有贫免疫性肾小球肾炎(ANCA 相关性血管炎)。11名患者接受了免疫抑制剂治疗。中位随访时间为 20 个月(IQR 18-21)。在最后一次随访中,11 名患者的肾衰竭和蛋白尿完全恢复,4 名患者部分恢复。CVAGD的总体远期疗效良好。
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Outcomes of Covid-19 Vaccine-Associated Glomerular Diseases (CVAGD) – A Case Series from India
Several cases of glomerular diseases following Covid-19 vaccination, especially mRNA vaccines, have been reported. However, there is little data on glomerular diseases associated with the two vaccines widely available in India (Covaxin and Covishield) and their long-term outcomes. This was a prospective observational study conducted between May 2021 and May 2023. Patients with new-onset or relapse of proteinuria, hematuria, or renal failure within 30 days of Covid-19 vaccination were included. Data on pre-existing renal disease, vaccine type, symptomatology, laboratory reports, kidney biopsy findings, and treatment details were collected. The clinical course and long-term renal outcomes were studied. Sixteen patients with Covid-19 vaccine associated glomerular disease (CVAGD) were studied. The median age was 28 years (IQR 20.5–40) and median time of symptom onset was 14 days (IQR 10–16.5) after vaccination. Renal syndromes at presentation were nephrotic syndrome in seven patients (43.75%), nephritic syndrome in seven patients (43.75%), and rapidly progressive renal failure in two patients (12.5%). Kidney biopsy revealed minimal change disease in five patients (31.2%); IgA nephropathy in four patients (25%); C3 glomerulopathy, lupus nephritis, and focal segmental glomerulosclerosis in two patients each (12.5%); and pauci-immune glomerulonephritis (ANCA-associated vasculitis) in one patient (6.25%). Eleven patients were treated with immunosuppressive drugs. Median duration of follow-up was 20 months (IQR 18–21). At last follow-up, 11 patients had complete recovery of renal failure and proteinuria and 4 patients had partial recovery. The most common lesions in this series were minimal change disease and IgA nephropathy. The overall long-term outcome of CVAGD appears good.
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