2010
DOI: 10.1097/mop.0b013e32833683fd
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Pediatric renal transplantation: an overview and update

Abstract: This review presents a comprehensive discussion of the major issues in pediatric renal transplantation, the newer immunosuppression approaches to limit toxicities of therapies in children and some critical issues that remain to be addressed, specific to the care of the transplanted child. The ultimate goal of designing optimum conditions for equating graft survival to patient survival still remains a major goal for pediatric organ transplantation.

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Cited by 59 publications
(64 citation statements)
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References 50 publications
(51 reference statements)
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“…Transplants were categorized into 4 time periods (1987-1993, 1994-2001, 2002-2004, and 2005-2012) to reflect changes in immunosuppression practices over time (in general, increased use of tacrolimus and mycophenolate mofetil, decreased use of cyclosporine and azathioprine, and introduction of interleukin-2 receptor monoclonal antibodies) 4 and implementation in 2005 of the Share-35 allocation policy, which includes preference to pediatric recipients in the allocation of organs from deceased donors under age 35. 6 Outcome Ascertainment Death-censored graft survival (DCGS) was defined as the time between date of KT and either date of graft failure (marked by retransplantation or return to dialysis) or last date of follow-up with a functioning graft, censoring for death and administrative end of study.…”
Section: Study Populationmentioning
confidence: 99%
See 1 more Smart Citation
“…Transplants were categorized into 4 time periods (1987-1993, 1994-2001, 2002-2004, and 2005-2012) to reflect changes in immunosuppression practices over time (in general, increased use of tacrolimus and mycophenolate mofetil, decreased use of cyclosporine and azathioprine, and introduction of interleukin-2 receptor monoclonal antibodies) 4 and implementation in 2005 of the Share-35 allocation policy, which includes preference to pediatric recipients in the allocation of organs from deceased donors under age 35. 6 Outcome Ascertainment Death-censored graft survival (DCGS) was defined as the time between date of KT and either date of graft failure (marked by retransplantation or return to dialysis) or last date of follow-up with a functioning graft, censoring for death and administrative end of study.…”
Section: Study Populationmentioning
confidence: 99%
“…The field of pediatric KT has evolved over the past 25 years, including changes in immunosuppression, surgical technique, organ allocation policy, and rates of living donor transplantation. 4 However, the relationship between these changes and post-KT outcomes remains unclear, both in terms of which patient phenotypes have been affected and when any changes in outcomes have occurred (ie, early versus late post-KT).The objective of this study was to examine changes in pediatric KToutcomes over the last 25 years. In particular, our work sought to assess trends in graft survival, rates of primary nonfunction (PNF) and delayed graft function (DGF), and patient survival independent of concurrent variations in recipient and donor characteristics, to compare the early and late posttransplant periods with regard to trends in graft and patient survival, and to evaluate whether any changes in graft and patient survival differ in particular recipient subgroups.…”
mentioning
confidence: 99%
“…LD reduces the additional morbidity and mortality factors associated with the waiting time for a DBD organ [17]. Parents represent 80 % of LD [18]. The minimum legal age for living donation varies by jurisdiction, ranging from no minimum age limit (in England, Wales and North Ireland) to age 19 years in some Canadian provinces, with underaged living donation even forbidden in some European countries, including France [19].…”
Section: Pediatric Organ Donors and Their Managementmentioning
confidence: 99%
“…At present times the risk of post-surgical immediate graft failure is uncommon [1], and new immunosuppressive protocols have greatly reduced the risk of immunological acute rejection; chronic rejection and subclinical rejection, as well as allograft nephropathy remain the great challenges of paediatric KT. [2] Through the use of aggressive treatment protocols for acute rejection, the susceptibility to infection and secondary neoplastic disease were greatly increased, as shown in our 2 case presentations.…”
Section: (Figure 1)mentioning
confidence: 99%