Comparison of outcomes with low-dose anti-thymocyte globulin, basiliximab or no induction therapy in pediatric kidney transplant recipients: A retrospective study

被引:17
|
作者
Baron, Pedro W. [1 ]
Ojogho, Okechukwu N. [1 ]
Yorgin, Peter [2 ]
Sahney, Shobha [2 ]
Cutler, Drew [2 ]
Ben-Youssef, Ramzi [1 ]
Baqai, Waheed [3 ]
Weissman, Jill
Franco, Edson [1 ,4 ]
Zuppan, Craig [5 ]
Concepcion, Waldo [6 ]
机构
[1] Loma Linda Univ, Med Ctr, Inst Transplantat, Loma Linda, CA 92354 USA
[2] Loma Linda Univ, Med Ctr, Dept Pediat, Loma Linda, CA 92354 USA
[3] Loma Linda Univ, Med Ctr, Dept Hlth Res Consulting, Loma Linda, CA 92354 USA
[4] Loma Linda Univ, Med Ctr, Dept Pharm, Loma Linda, CA 92354 USA
[5] Loma Linda Univ, Med Ctr, Dept Pathol, Loma Linda, CA 92354 USA
[6] Stanford Univ, Div Transplantat, Palo Alto, CA 94304 USA
关键词
pediatric kidney transplant; induction therapy; basiliximab; anti-thymocyte globulin; acute rejection;
D O I
10.1111/j.1399-3046.2007.00764.x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
It is unclear which induction therapy yields the best outcomes in pediatric kidney transplantation. Retrospective data of 88 children receiving a renal allograft between November 1996 and October 2003 were analyzed. Patients received ATGI (n = 12), BI (n = 29), or NAI (n = 47). The mean ATG dose was 5.1 +/- 2.1 mg/kg. At 12 months, graft survival rates were 91.7%, 100%, and 97.9% for ATGI, BI, and NAI groups, respectively. Acute rejection rates at 12 months were 0 (ATGI), 20.6% (BI), and 10.7% (NAI). The mean GFR for ATGI (42.4 +/- 25.9 mL/min) was lower than for BI (78.3 +/- 27.2 mL/min), and NAI (66 +/- 28.3 mL/min) at 12 months (p < 0.05). One ATGI patient developed CMV pneumonia but none developed post-transplant lymphoproliferative disorder. Although there was no renal allograft survival benefit with either ATGI or BI, relative to NAI, the absence of acute rejection and equivalent rates of viral infections in the higher-risk ATGI recipient group suggests that the treatment strategy is promising. A large prospective study is needed to better define the role of ATGI in pediatric kidney transplantation.
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页码:32 / 39
页数:8
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