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大剂量静脉注射环孢素与血浆置换联合治疗对移植后复发性局灶节段性肾小球硬化有效:病例系列结果

Combination of High-Dose Intravenous Cyclosporine and Plasma Exchange Treatment Is Effective in Post-Transplant Recurrent Focal Segmental Glomerulosclerosis: Results of Case Series.

作者信息

Demir Mehmet Emin, Uyar Murathan, Merhametsiz Ozgur

机构信息

Yeni Yuzyil University, Private Gaziosmanpasa Hospital, Department of Nephrology and Organ Transplantation, Istanbul, Turkey.

Yeni Yuzyil University, Private Gaziosmanpasa Hospital, Department of Nephrology and Organ Transplantation, Istanbul, Turkey.

出版信息

Transplant Proc. 2020 Apr;52(3):843-849. doi: 10.1016/j.transproceed.2020.01.024. Epub 2020 Mar 19.

Abstract

BACKGROUND

Idiopathic focal segmental glomerulosclerosis (FSGS) commonly recurs in the early post-transplant period. The treatment protocols and results are conflictive in recurrent FSGS. We aimed to present the results of our treatment protocol and basic approach to the disease recurrences.

METHODS

This prospective, single-center study was conducted between the years 2015 and 2018. Twelve patients who fit completely the diagnosis of idiopathic FSGS by clinical, laboratory, and biopsy findings were included. A specific treatment protocol which consists of plasma exchange and high dose intravenous cyclosporine was delivered to the patients independently of induction protocols. Twenty-four months of outcomes of graft functions were evaluated.

RESULTS

Nine patients completed the treatment protocol and were documented for evaluation. All patients achieved a complete or partial remission in an average 24 months of follow-up period.

CONCLUSION

Idiopathic FSGS is more commonly recurrent than thought to be. The early detection of proteinuria is crucial because the administration of a plasma exchange-based treatment protocol can reverse proteinuria. We think our treatment protocol is a well-established, efficient, and safe choice for post-transplant recurrent FSGS in adults.

摘要

背景

特发性局灶节段性肾小球硬化(FSGS)常在移植后早期复发。复发性FSGS的治疗方案和结果存在矛盾。我们旨在介绍我们的治疗方案结果以及针对该疾病复发的基本方法。

方法

这项前瞻性单中心研究于2015年至2018年期间进行。纳入了12例通过临床、实验室和活检结果完全符合特发性FSGS诊断的患者。无论诱导方案如何,均为患者提供了一种由血浆置换和大剂量静脉注射环孢素组成的特定治疗方案。评估了移植肾功能24个月的结果。

结果

9例患者完成了治疗方案并记录在案以供评估。所有患者在平均24个月的随访期内均实现了完全或部分缓解。

结论

特发性FSGS的复发比想象中更常见。蛋白尿的早期检测至关重要,因为基于血浆置换的治疗方案可以逆转蛋白尿。我们认为我们的治疗方案是成人移植后复发性FSGS的一种成熟、有效且安全的选择。

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