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Medical Science Review (MSR) has developed as an independent title in 2014 as a continuation of highly successful Review Section of the Medical Science Monitor (since 1995). The aim of the Journal is to gather review articles across all medical disciplines, thereby integrating international medical knowledge. Medical Science Review has adopted the Open Access publishing model which enables free access... read more

Published: 2016-04-26

Evaluation of Treatment with a Combination of Everolimus and Low-Dose Cyclosporine A in De Novo Pediatric Kidney Transplantation Patients: A Systematic Review

Jun Wang, Nannan Gu, Mingming Yu, Jingtong Sha, Hang Wu, Yulong Gong, Haobo Zhu, Zheng Ge, Rugang Lu, Gemg Ma, Yunfei Guo

(Department of Urology, Nanjing Medical University Affiliated Nanjing Children’s Hospital, Nanjing, Jiangsu, China (mainland))

Med Sci Rev 2016; 3:49-54

DOI: 10.12659/MSRev.897492

ABSTRACT: The aim of our systematic review was to determine the clinical efficacy, safety, and tolerability of everolimus and low-dose cyclosporine A (CsA) combination treatment in de novo pediatric kidney transplantation.
Our electronic literature searches of Medline, Cochrane Central Register of Controlled Trials (CENTRAL) and Embase (updated on May 1st 2015) checked all articles on everolimus and low-dose CSA treatment published in English language. Two authors independently made study selections, data extraction, and analysis.
A total of 3 case series and 3 clinical trials were included in our systematic review. The overall incidence rate of borderline changes, biopsy-proven acute rejection, interstitial fibrosis, and tubular atrophy, graft loss and death were 8.21%, 9.00%, 13.43%, 0.75%, and 0%, respectively. The incidence rate of urinary tract infection was 30.83%, but can be well-tolerated by giving proper medical treatment. Other reported severe adverse events, such as lymphocele, wound healing dysfunction, pyrexia, pneumonia, viral infections, were less than 10%.
Everolimus and low-dose CsA combination treatment is effective, safe, and well-tolerated in de novo pediatric kidney transplantation. However, an open-label randomized controlled clinical trial will provide an incentive to refine our clinical use of everolimus in children.

Keywords: Cyclosporine, Hospitals, Pediatric, Kidney Transplantation

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