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Immunosuppressive therapy in children with primary nephrotic syndrome: single center experience, Karachi, Pakistan

机译:原发性肾病综合征儿童免疫抑制治疗:单中心经验,卡拉奇,巴基斯坦

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摘要

Abstract Background Majority of children with nephrotic syndrome are steroid sensitive, but treatment of difficult to treat nephrotic (frequent relapsing, steroid dependent and steroid resistant) syndrome is challenging. Low dose steroid, levamisole, cyclophosphamide (CPM), mycophenolate mofetil (MMF) and calcineurin inhibitors (CNIs) are the common options of treatment. Objective of the study was to determine the response to steroid and alternative immunosuppressive agents (ISAs) in children with difficult nephrotic syndrome (DNS). Methods This is a retrospective cohort study of 176 children with DNS, managed over 12 years at The Kidney Center-Postgraduate Training Institute, Karachi- Pakistan from 2005 to 2017. Initial episode was treated with daily oral prednisolone (OP) for 4–8 weeks followed by alternate day OP for 12–24 weeks. Subsequently low dose OP, levamisole (Leva)and cyclophosphamide was used for frequent relapsing (FR)/ steroid dependent (SD). All with initial steroid resistance and non- responders to leva and or cyclophosphamide were biopsied and treated with CNIs and MMF. Data was analyzed using descriptive statistics. Results There were 130(73.86%) children with FR/SD and 46(26.13%) with SRNS. All children with SR (46) and 86 with FR/SD were biopsied. Minimal change disease (60.60%) and focal segmental glomerulosclerosis (FSGS 23%) were the two common lesions. Majority (73.86%) received single OP whereas divided doses were administered in 26.13% cases. Daily OP was used for 4, 6 and 8 weeks in 61.36,28.4 and10.22% respectively. Steroids were tapered over 3 (31.81%),4 (52.27%) and 6 months (15.90%). Levamisole, CPM, cyclosporin (CS) and MMF were used sequentially in 45, 54.23, 50 and 20% respectively. Combination of MMF and CS was used in 11.29% of cases. Levamisole was effective in 80%, CPM induced complete remission (CR, 57.77%) or partial remission (PR, 22.22%), CS induced CR 46.59% and PR 39.77%. MMF showed PR and CR 69 and 12.82% respectively. At last follow up, 46% were maintaining remission while off treatment, whereas 35% are maintaining remission on therapy,10.23% lost- to-follow, 5.68% progressed to chronic kidney disease. Mortality was 2.84% and it was due to infection and uremia. Conclusion Majority had steroid sensitive MCD. Levamisole and cyclophosphamide were effective in maintaining remission in FR/ SD. FSGS was responsible for resistance to steroid and alternative ISAs. Cyclosporin was effective in inducing remission in SRNS. Mortality was less than 3%.
机译:摘要背景大多数肾病综合征的儿童是类固醇敏感性,但治疗难以治疗肾病(频繁复发,类固醇依赖性和类固醇)综合征挑战。低剂量类固醇,左旋咪唑,环磷酰胺(CPM),霉酚酸酯MOFETIL(MMF)和钙调解素抑制剂(CNIS)是治疗的常见选择。该研究的目的是确定患有困难肾病综合征(DNS)的儿童的类固醇和替代免疫抑制剂(ISAS)的反应。方法是,这是一项回顾性队列队列,可在2005年至2017年的Karachi-Pakistan在肾脏中心研究生培训研究所管理12年,在12年内进行了一系列的DNS。初步发作是用日常口服泼尼松(OP)治疗4-8周其次是12-24周的交替日期。随后的低剂量OP,左旋氨酸(Leva)和环膦酰胺用于频繁复发(FR)/类固醇依赖(SD)。所有具有初始类固醇抗性和左旋磷酰胺的非响应者都是活检并用CNI和MMF处理。使用描述性统计分析数据。结果130名(73.86%)儿童FR / SD和46(26.13%),SRNS。所有带有FR / SD的SR(46)和86的儿童都是活检的。最小的变化疾病(60.60%)和局灶性节段性肾小球粥样硬化(FSGS 23%)是两种常见病变。大多数(73.86%)接受单一OP,而分裂剂量在26.13%的情况下施用。每日OP分别用于61.36,28.4和10.22%的4,6和8周。类固醇超过3(31.81%),4(52.27%)和6个月(15.90%)。左旋吲哚,CPM,环孢菌素(CS)和MMF分别在45,54.23,50%和20%中依次使用。 MMF和Cs的组合用于11.29%的病例。 Levamisole在80%中有效,CPM诱导完全缓解(Cr,57.77%)或部分缓解(Pr,22.22%),Cs诱导Cr 46.59%和Pr 39.77%。 MMF显示PR和CR 69和12.82%。最后跟进,46%的人在脱离治疗时维持缓解,而35%正在保持治疗缓解,减少10.23%,5.68%进展到慢性肾病。死亡率为2.84%,它是由于感染和尿毒症。结论大多数有类固醇敏感MCD。 Levamisole和环磷酰胺在维持FR / SD中的缓解方面是有效的。 FSGS负责抵抗类固醇和替代ISA。环孢菌素有效在SRNS中诱导缓解。死亡率小于3%。

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