TY - JOUR
T1 - Comparison of outcomes with low-dose anti-thymocyte globulin, basiliximab or no induction therapy in pediatric kidney transplant recipients
T2 - A retrospective study
AU - Baron, Pedro W.
AU - Ojogho, Okechukwu N.
AU - Yorgin, Peter
AU - Sahney, Shobha
AU - Cutler, Drew
AU - Ben-Youssef, Ramzi
AU - Baqai, Waheed
AU - Weissman, Jill
AU - Franco, Edson
AU - Zuppan, Craig
AU - Concepcion, Waldo
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PY - 2008/2
Y1 - 2008/2
N2 - 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. © 2007 Blackwell Munksgaard.
AB - 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. © 2007 Blackwell Munksgaard.
KW - Acute rejection
KW - Anti-thymocyte globulin
KW - Basiliximab
KW - Induction therapy
KW - Pediatric kidney transplant
KW - Graft Rejection/prevention & control
KW - Glomerular Filtration Rate
KW - T-Lymphocytes/immunology
KW - Humans
KW - Antibodies, Monoclonal/therapeutic use
KW - Immunosuppressive Agents/administration & dosage
KW - Male
KW - Kidney Transplantation/immunology
KW - Recombinant Fusion Proteins/therapeutic use
KW - Adolescent
KW - Female
KW - Retrospective Studies
KW - Child
KW - Antilymphocyte Serum/administration & dosage
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UR - http://www.scopus.com/inward/citedby.url?scp=37848999059&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/6ecd8f05-d3de-3883-80e2-3ba76b2152d6/
U2 - 10.1111/j.1399-3046.2007.00764.x
DO - 10.1111/j.1399-3046.2007.00764.x
M3 - Article
C2 - 18186886
SN - 1397-3142
VL - 12
SP - 32
EP - 39
JO - Pediatric Transplantation
JF - Pediatric Transplantation
IS - 1
ER -