Reduced ATG‐F dosage for induction in pediatric renal transplantation: A single‐center experience. (20th January 2014)

• Record Type: Journal Article
• Authors: Shang, Wenjun; Feng, Guiwen; Gao, Shilin; Wang, Zhigang; Pang, Xinlu; Li, Jinfeng; Liu, Lei; Feng, Yonghua; Xie, Hongchang; Zhang, Shuijun; Qiao, Baoping
• Is Part Of: Pediatric transplantation. Volume 18:Number 3(2014:May)
• Page Start: 240
• Page End: 245
• Publication Date: 2014-01-20
• Subjects: Transplantation of organs, tissues, etc. in children -- Periodicals; 617.95408305
• DOI: 10.1111/petr.12224
• Languages: English
• ISSNs: 1397-3142

Abstract

<abstract abstract-type="main" id="petr12224-abs-0001"> <title>Abstract</title> <p>Rabbit antithymocyte globulin (ATG‐F) is an extensively used induction agent. To our knowledge, no study to date has assessed reduced ATG‐F dosage in children undergoing renal transplantation. This was a retrospective analysis of pediatric renal recipients in the Department of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, from May 2007 to February 2013. Thirty‐nine children underwent renal transplantation including 25 living related and 14 cardiac deceased donor transplantation. Each recipient received ATG‐F 1.5 mg/kg/d once daily for 4 days. Of the 39 recipients, five (12.8%) showed delayed graft function, including one of 25 recipients (4%) of living donor and four of 14 recipients (28.6%) of deceased donor transplantation (p &lt; 0.05). Six of the 39 recipients (15.4%) showed acute rejection on renal biopsy. Follow‐up in these children ranged from 6 to 87 months. The one‐, three‐, and five‐yr recipients and grafts survival rates postoperation were each 94.9% and 97.3%, 97.3%, and 94.6%, respectively. The incidence of postoperative infection was 35.9% (14/39), and did not differ significantly in the living related and deceased donor groups (p &gt; 0.05). Low‐dose ATG‐F can be safely used as an immune induction agent in pediatric renal transplantation.</p> </abstract>