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儿童肾病综合征的管理

Management of nephrotic syndrome in childhood.

作者信息

Melvin T, Bennett W

机构信息

Department of Pediatrics, Oregon Health Sciences University, Portland.

出版信息

Drugs. 1991 Jul;42(1):30-51. doi: 10.2165/00003495-199142010-00003.

Abstract

Nephrotic syndrome is defined as proteinuria sufficiently severe to result in hypoalbuminaemia, oedema and hyperlipidaemia. The early modern history of this illness was characterised by the serendipitous development of renal biopsy technique at approximately the same time as the use of corticosteroids for nephrotic syndrome. The coincidence of these events set the stage for evaluating therapeutic response to corticosteroids and cytotoxic agents in relation to renal histology and ultimate clinical outcome. The International Study of Kidney Disease in Children (ISKDC) was initiated in the 1960s as a multicentre study examining these relationships in children. Over the next decade this study, as well as contributions from other investigators, helped define optimum therapy for these children. It was determined that a child with nephrotic syndrome under the age of 6 years, who did not present with hypertension, azotaemia, hypocomplementaemia or signs of systemic illness, had an approximately 85% chance of responding to corticosteroid therapy. If only those children who had minimal change histology on biopsy were considered, 94% responded. The original regimen which is still used today, was 60 mg/m2 bsa/day prednisone administered on a 3 times per day dosage schedule for 4 weeks, followed by an additional 4 weeks of therapy at a dose of 40 mg/m2 bsa given as a single oral dose every other day. Of those who respond roughly one-third will have no relapses, while almost half will have frequent relapses (greater than or equal to 2 in 6 months) and the rest will have infrequent relapses. Patients in relapse are treated as at presentation but are usually converted to the 40 mg/m2 bsa dose when the urine has been free of protein for 3 days, and are then tapered off or maintained on this dose for several weeks, depending on the individual's history of relapses and incidence of side effects from corticosteroids. For those children who are suffering frequent relapses and severe corticosteroid side effects (e.g. growth failure, morbid obesity, aseptic necrosis of bone), cytotoxic agents were identified as providing long term remission. After inducing remission with conventional corticosteroid dosages, cyclophosphamide is administered at a dose of 2 mg/kg/day given as a single dose for 8 weeks. This regimen was shown to lead to approximately 70% of patients being in remission 2 years after completion of this course of therapy. Chlorambucil given at a dose of 0.2 mg/kg/day as a single oral dose has been equally efficacious.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

肾病综合征的定义为蛋白尿严重到足以导致低白蛋白血症、水肿和高脂血症。这种疾病的早期现代史的特点是,肾活检技术与用于肾病综合征的皮质类固醇的使用大约在同一时间意外发展。这些事件的巧合为评估皮质类固醇和细胞毒性药物相对于肾组织学和最终临床结果的治疗反应奠定了基础。国际儿童肾病研究(ISKDC)于20世纪60年代发起,作为一项多中心研究,研究儿童中的这些关系。在接下来的十年里,这项研究以及其他研究人员的贡献,帮助确定了这些儿童的最佳治疗方法。已确定,6岁以下、无高血压、氮质血症、低补体血症或全身疾病体征的肾病综合征儿童,对皮质类固醇治疗有反应的几率约为85%。如果只考虑那些活检组织学为微小病变的儿童,94%有反应。至今仍在使用的原始方案是,按每日每平方米体表面积60毫克的剂量给予泼尼松,每天3次,共4周,随后再以每平方米体表面积40毫克的剂量进行4周治疗,每隔一天口服一次。在有反应的患者中,大约三分之一不会复发,而几乎一半会频繁复发(6个月内大于或等于2次),其余的会偶尔复发。复发的患者按初诊时的方法治疗,但当尿液无蛋白3天后,通常改为每平方米体表面积40毫克的剂量,然后根据个体的复发史和皮质类固醇的副作用发生率,逐渐减量或维持该剂量数周。对于那些频繁复发且有严重皮质类固醇副作用(如生长发育迟缓、病态肥胖、无菌性骨坏死)的儿童,细胞毒性药物被确定可提供长期缓解。在用常规皮质类固醇剂量诱导缓解后,给予环磷酰胺,剂量为每日每公斤体重2毫克,单次给药,共8周。该方案显示,在完成该疗程治疗2年后,约70%的患者处于缓解状态。以每日每公斤体重0.2毫克的剂量口服苯丁酸氮芥同样有效。(摘要截选至400字)

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