Health Status of Children Alive 10 Years after Pediatric Liver Transplantation Performed in the US and Canada: Report of the Studies of Pediatric Liver Transplantation Experience

被引:181
|
作者
Ng, Vicky L. [2 ,3 ]
Alonso, Estella M. [4 ,5 ]
Bucuvalas, John C. [6 ]
Cohen, Geoff [1 ]
Limbers, Christine A. [7 ]
Varni, James W. [8 ,9 ]
Mazariegos, George [10 ,11 ]
Magee, John
McDiarmid, Susan V. [12 ,13 ,14 ]
Anand, Ravinder [1 ]
机构
[1] EMMES Corp, Rockville, MD 20850 USA
[2] Hosp Sick Children, SickKids Transplant Ctr, Toronto, ON M5G 1X8, Canada
[3] Univ Toronto, Toronto, ON, Canada
[4] Childrens Mem Hosp, Siragusa Transplant Ctr, Chicago, IL 60614 USA
[5] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
[6] Cincinnati Childrens Hosp, Med Ctr, Pediat Liver Care Ctr, Cincinnati, OH USA
[7] Baylor Univ, Dept Psychol & Neurosci, Waco, TX 76798 USA
[8] Texas A&M Univ, Dept Pediat, College Stn, TX USA
[9] Texas A&M Univ, Dept Landscape Architecture & Urban Planning, College Stn, TX USA
[10] Childrens Hosp Pittsburgh, Hillman Ctr Pediat Transplantat, Pittsburgh, PA 15213 USA
[11] Univ Pittsburgh, Med Ctr, Thomas E Starzl Transplantat Inst, Pittsburgh, PA USA
[12] Univ Michigan Hlth Syst, Div Transplantat, Ann Arbor, MI USA
[13] Dumont Univ Calif Los Angeles, Liver Transplant Ctr, UCLA Sch Med, Los Angeles, CA USA
[14] Mattel Childrens Hosp, Los Angeles, CA USA
来源
JOURNAL OF PEDIATRICS | 2012年 / 160卷 / 05期
关键词
QUALITY-OF-LIFE; GLOMERULAR-FILTRATION-RATE; GRAFT FIBROSIS; RECIPIENTS; PEDSQL(TM)-4.0; RELIABILITY; DISEASE;
D O I
10.1016/j.jpeds.2011.10.038
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
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. (J Pediatr 2012; 160: 820-6).
引用
收藏
页码:820 / U372
页数:10
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