Early orthotopic liver transplantation in urea cycle defects: Follow up of a developmental outcome study

被引:40
作者
Campeau, Philippe M.
Pivalizza, Penelope J. [1 ]
Miller, Geoffrey [2 ]
McBride, Kim [3 ]
Karpen, Saul
Goss, John [4 ]
Lee, Brendan H. [1 ,5 ]
机构
[1] Texas Childrens Hosp, Baylor Coll Med, Ctr Dev Pediat, Dept Neurol, Houston, TX 77030 USA
[2] Yale Univ, Sch Med, Dept Pediat, New Haven, CT 06510 USA
[3] Nationwide Childrens Hosp, Res Inst, Columbus, OH USA
[4] Baylor Coll Med, Ctr Liver, Houston, TX 77030 USA
[5] Howard Hughes Med Inst, Houston, TX 77030 USA
关键词
Urea cycle; Liver transplantation; Ornithine transcarbamylase; Carbamoyl phosphate synthase; Griffiths Scales; ORNITHINE TRANSCARBAMYLASE DEFICIENCY; DISORDERS; DIAGNOSIS; MANAGEMENT; METABOLISM;
D O I
10.1016/j.ymgme.2010.02.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Patients with neonatal urea cycle defects (UCDs) typically have high mortality and poor neurological outcome unless they receive liver transplantation. Neurologic outcome may be better with liver transplantation before age one year. We report on a follow up on an initial prospective study performed to assess developmental outcome after early liver transplant using the Griffiths Scales. Developmental testing up to 7 years after transplantation showed average developmental quotients (DQs) of 69 for four children who underwent transplantation before one year of age (latest DQs were 47, 63, 95 and 96), and 80 for a patient who underwent transplantation at 3 years of age (latest DQ was 88). We conclude that a combination of early liver transplantation, aggressive metabolic management and early childhood intervention improve the neurologic outcome of children with UCDs. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:S84 / S87
页数:4
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