TY - JOUR
T1 - Health status of children alive 10 years after pediatric liver transplantation performed in the US and Canada
T2 - Report of the studies of pediatric liver transplantation experience
AU - Ng, Vicky L.
AU - Alonso, Estella M.
AU - Bucuvalas, John C.
AU - Cohen, Geoff
AU - Limbers, Christine A.
AU - Varni, James W.
AU - Mazariegos, George
AU - Magee, John
AU - McDiarmid, Susan V.
AU - Anand, Ravinder
N1 - Funding Information:
The SPLIT Research Group is supported by National Institute of Diabetes and Digestive and Kidney Diseases (grant U01-DK061693-01A1 ), unrestricted grants from Astellas Pharma US, Inc, and Roche Laboratories . An American Recovery and Reinvestment Act (ARRA) 2009 grant awarded to the SPLIT Research Group supported the current study design, data analysis, and interpretation, with writing and completion of the manuscript being entirely investigator-initiated. J.V. holds the copyright and the trademark for PedsQL and receives financial compensation from the Mapi Research Trust, a nonprofit research institute that charges distribution fees to for-profit companies that use the PedsQL. The authors declare no conflicts of interest.
Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 2012/5
Y1 - 2012/5
N2 - Objectives: To determine clinical and health-related quality of life outcomes, and to derive an "ideal" composite profile of children alive 10 years after pediatric liver transplantation (LT) performed in the US and Canada. Study design: This was a multicenter cross-sectional analysis characterizing patients enrolled in the Studies of Pediatric Liver Transplantation database registry who have survived >10 years from LT. Results: A total of 167 10-year survivors were identified, all of whom received daily immunosuppression therapy. Comorbidities associated with the post-LT course included post-transplantation lymphoproliferative disease (in 5% of patients), renal dysfunction (9%), and impaired linear growth (23%). Health-related quality of life, as assessed by the PedsQL 4.0 Generic Core Scales, revealed lower patient self-reported total scale scores for 10-year survivors compared with matched healthy children (77.2 ± 12.9 vs 84.9 ± 11.7; P <.001). At 10 years post-LT, only 32% of patients achieved an ideal profile of a first allograft stable on immunosuppression monotherapy, normal growth, and absence of common immunosuppression-induced sequelae. Conclusion: Success after pediatric LT has moved beyond patient survival. Availability of an ideal composite profile at follow-up provides opportunities for patients, families, and healthcare providers to identify broader sets of outcomes at earlier stages, ultimately contributing to improved outcomes after pediatric LT.
AB - Objectives: To determine clinical and health-related quality of life outcomes, and to derive an "ideal" composite profile of children alive 10 years after pediatric liver transplantation (LT) performed in the US and Canada. Study design: This was a multicenter cross-sectional analysis characterizing patients enrolled in the Studies of Pediatric Liver Transplantation database registry who have survived >10 years from LT. Results: A total of 167 10-year survivors were identified, all of whom received daily immunosuppression therapy. Comorbidities associated with the post-LT course included post-transplantation lymphoproliferative disease (in 5% of patients), renal dysfunction (9%), and impaired linear growth (23%). Health-related quality of life, as assessed by the PedsQL 4.0 Generic Core Scales, revealed lower patient self-reported total scale scores for 10-year survivors compared with matched healthy children (77.2 ± 12.9 vs 84.9 ± 11.7; P <.001). At 10 years post-LT, only 32% of patients achieved an ideal profile of a first allograft stable on immunosuppression monotherapy, normal growth, and absence of common immunosuppression-induced sequelae. Conclusion: Success after pediatric LT has moved beyond patient survival. Availability of an ideal composite profile at follow-up provides opportunities for patients, families, and healthcare providers to identify broader sets of outcomes at earlier stages, ultimately contributing to improved outcomes after pediatric LT.
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U2 - 10.1016/j.jpeds.2011.10.038
DO - 10.1016/j.jpeds.2011.10.038
M3 - Article
C2 - 22192813
AN - SCOPUS:84859906325
SN - 0022-3476
VL - 160
SP - 820-826.e3
JO - Journal of Pediatrics
JF - Journal of Pediatrics
IS - 5
ER -