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脉冲甲基泼尼松龙输注联合环孢素为基础的免疫抑制治疗方案,在小儿肾移植后复发性局灶节段性肾小球硬化症的治疗中是安全且有效的。

Combination of pulse methylprednisolone infusions with cyclosporine-based immunosuppression is safe and effective to treat recurrent focal segmental glomerulosclerosis after pediatric kidney transplantation.

机构信息

Department of Pediatric Nephrology, School of Medicine, Toho University, Tokyo, Japan.

出版信息

Clin Transplant. 2013 Mar-Apr;27(2):E143-50. doi: 10.1111/ctr.12079. Epub 2013 Feb 6.

Abstract

BACKGROUND

Recurrence of focal segmental glomerulosclerosis (FSGS) in pediatric kidney allografts is associated with poor graft survival. Several therapeutic regimens have been proposed, with conflicting results.

METHODS

Ten pediatric patients with recurrent FSGS after kidney transplantation were treated with a protocol of methylprednisolone (MP) infusions in combination with cyclosporine (CsA)-based immunosuppression. The patients received a drug regimen with infusions of 20 mg/kg MP on three consecutive days at week 1, week 3, and week 5, and then monthly until six months after transplantation. If a complete or partial remission (PR) was obtained, MP pulse continued every three months until 24 months after transplantation. The CsA dose was adjusted according to AUC0-4.

RESULTS

Seven of 10 patients (70%) achieved complete remission (CR) with stable renal function within 18 months of beginning of treatment. One of two patients with PR entered CR 3.5 yr after transplantation. One patient lost her graft due to recurrence four months after transplantation. After observation for 26-119 months, seven patients maintained remission with normal glomerular filtration rate. Few major side effects were observed in association with the high-dose MP infusion therapy.

CONCLUSIONS

MP infusion therapy in combination with CsA-based immunosuppression could be safe and effective in treating recurrent FSGS after kidney transplantation.

摘要

背景

儿童肾移植后局灶节段性肾小球硬化症(FSGS)的复发与移植物存活率差有关。已经提出了几种治疗方案,但结果存在冲突。

方法

10 例儿童肾移植后复发性 FSGS 患者采用甲基泼尼松龙(MP)输注联合环孢素(CsA)为基础的免疫抑制方案治疗。患者接受药物治疗方案,在第 1、3 和 5 周的连续 3 天内给予 20mg/kg MP 输注,然后每月输注一次,直至移植后 6 个月。如果获得完全或部分缓解(PR),则在移植后 24 个月内每 3 个月继续使用 MP 脉冲治疗。根据 AUC0-4 调整 CsA 剂量。

结果

10 例患者中有 7 例(70%)在开始治疗后 18 个月内获得完全缓解(CR),肾功能稳定。2 例 PR 患者中有 1 例在移植后 3.5 年进入 CR。1 例患者因移植后 4 个月复发而失去移植物。观察 26-119 个月后,7 例患者肾小球滤过率正常,缓解持续。与高剂量 MP 输注治疗相关,仅观察到少数严重副作用。

结论

MP 输注联合 CsA 为基础的免疫抑制治疗可能是治疗儿童肾移植后复发性 FSGS 的安全有效的方法。

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