scholarly journals The Cyclosporine-A Treatment does not have Harmful Effect on the Linear Growth of Pediatric Patients with Steroid-dependent and Steroid-resistant Nephrotic Syndrome

2016 ◽  
Vol 20 (2) ◽  
pp. 45-49
Author(s):  
Sang Soo Lee ◽  
Ji Hoon Kim ◽  
Chung Ho Kim ◽  
Byoung-Soo Cho ◽  
Deog Yoon Kim ◽  
...  
Medicine ◽  
2021 ◽  
Vol 100 (49) ◽  
pp. e28186
Author(s):  
Juan Lv ◽  
Shizhi Luo ◽  
Yunxia Zhang ◽  
Enlai Dai

2007 ◽  
Vol 22 (4) ◽  
pp. 600-602 ◽  
Author(s):  
Jens Drube ◽  
Christoph Geerlings ◽  
Ruth Taylor ◽  
Michael Mengel ◽  
Jochen H. H. Ehrich

2020 ◽  
Vol 7 (8) ◽  
pp. 1762
Author(s):  
Sabnam Ara Begum ◽  
Santanu Kumar Tripathi ◽  
Mousumi Nandy ◽  
Sanat Kumar Ghosh ◽  
Shatavisa Mukherjee ◽  
...  

Background: In patients with frequently relapsing nephrotic syndrome (FRNS), steroid-dependent nephrotic syndrome (SDNS) and steroid resistant nephrotic syndrome (SRNS) steroids are either used for prolonged period of time or ineffective. To reduce the degree of steroid dependency and avoid steroid toxicity, several immunosuppressive steroid sparing agents (SPAs) have been proposed to treat these children. The present study tried to study the relative safety of most commonly steroid sparing agent in such children.Methods: A multi-centred, prospective observational study was conducted in paediatric nephrology OPD of two tertiary care hospitals in Kolkata over a period of 24 months. All consecutive children with diagnosed FRNS, SDNS and SRNS who were started on steroid sparing agents were enrolled and followed up for at least 6 months. Records of clinical examination, laboratory tests were collected and measured at the baseline and regular intervals. Safety parameters were noted and statistically analysed.Results: A total 110 patients were screened, examined and enrolled. Levamisole, cyclophosphamide and MMF were commonly used SPAs. Of the two tertiary care hospitals, all the patients of FRNS and SDNS were started with levamisole and SRNS with cyclophosphamide in one set-up, while in the other hospital some SDNS patients were started with cyclophosphamide and SRNS with MMF but without clinically significant outcomes. In comparison with few minor adverse events in MMF group, some serious adverse events were documented in the both cyclophosphamide and levamisole groups.Conclusions: Levamisole being a very efficacious, safe and easily affordable drug, should be used as an initial first line SPA in treating FRNS and SDNS children. The side effect profiles of levamisole and MMF are much more patient friendly.


2018 ◽  
Vol 35 (3-4) ◽  
pp. 403-412
Author(s):  
Mohamed S. El-Farsy ◽  
Magid A. A. F. Ibrahim ◽  
Fathy N. Fatouh ◽  
Ahmed T. Abd El-Fattah

2017 ◽  
Vol 129 (15-16) ◽  
pp. 579-582 ◽  
Author(s):  
Danica Batinić ◽  
Danko Milošević ◽  
Boris Filipović-Grčić ◽  
Marija Topalović-Grković ◽  
Nina Barišić ◽  
...  

2019 ◽  
Vol 59 (4) ◽  
pp. 175-82
Author(s):  
Agomoni Chaki ◽  
Farhana Rahman ◽  
Jahanara Arju ◽  
Abdullah- Al Mamun ◽  
Tahmina Jesmin ◽  
...  

Background Nephrotic syndrome (NS) is one of the most common glomerular disease in children, characterized by massive proteinuria, hypoalbuminemia, dyslipidemia and edema. Steroid-resistant nephrotic syndrome (SRNS) and steroid-dependent nephrotic syndrome (SDNS) present challenges in pharmaceutical management. Patient need several immunosuppressant for optimal control, each of which has significant side effect and difficult to get  desired results. Rituximab (RTX) is a monoclonal antibody that targets B cells and has been shown to be effective for patients with SRNS and SDNS. Objective To see efficacy of RTX in pediatric patients with SRNS. Method This retrospective study took place in Pediatric Nephrology Department of Bangabandhu Sheikh Mujib Medical University from July 2017 to June 2019. Patients diagnosed with SRNS who were treated with RTX and followed up for 6 months were enrolled in this study. Primary endpoint was achievement of remission after rituximab infusion; secondary endpoint was relapse-free survival rate in 6 months period following rituximab infusion. Results Total  7 patients were recruited in this study. Among them 4 were male. Clinical and lab parameters of all patients before and after RTX  were compared. Complete remission achieved in 4/7 patients, partial remission in 2/7 patients and no response in 1/7 patient. Mean number of relapse in 3 patients before RTX infusion was 3.67 (SD 0.57) and after 0.33 (SD 0.00) (P=0.038). Conclusion RTX is a biological agent that is effective and promising drug in children with SRNS. Rituximab is useful to induce and maintain remission.


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