首页> 外文期刊>Journal of developmental and behavioral pediatrics >Long-term outcomes of adaptive functions for children with mucopolysaccharidosis I (Hurler syndrome) treated with hematopoietic stem cell transplantation.
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Long-term outcomes of adaptive functions for children with mucopolysaccharidosis I (Hurler syndrome) treated with hematopoietic stem cell transplantation.

机译:造血干细胞移植治疗的I型粘多糖贮积症(Hurler综合征)患儿的适应功能的长期结果。

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摘要

Advances in medical treatment have prolonged the lives of children with Hurler syndrome or mucopolysaccharidosis I requiring increased attention to the assessment of their long-term outcomes and functional abilities. Adaptive functions are critical for understanding functional outcomes after treatment and developing focused interventions. We investigated the development of various adaptive functions in children who have had hematopoietic stem cell transplant (HSCT) for Hurler syndrome and risk factors that are associated with the development of these functions. We examined the development of 41 children who had 3 or more Vineland Adaptive Behavior Scales records assessed before and after transplant. Communication, daily living skills, socialization, and motor functions were measured. While standard scores decline over time, development of skills continue with a slower than average rate compared with peers. A cross-sectional nontransplanted comparison group showed more deficits after age 2 years than the transplanted group. In contrast to cognitive ability, age at transplant was not significantly associated with ultimate adaptive level. Baseline cognitive level before HSCT and growth of cognition after HSCT were associated with adaptive functions especially for communication and daily living skills. Socialization was predicted by cumulative medical risk factors, likely due to restricted social exposure in children with complicated transplant courses. Overall, measurement of adaptive behaviors demonstrated that HSCT allows long-term slow improvement of functional outcomes for children with Hurler syndrome. Children with Hurler syndrome with good cognitive levels before HSCT and continued growth of cognition after HSCT show good adaptive functions. Although cognitive and orthopedic problems as well as medical complications limit adaptive ability, identifying these problems early allow beneficial targeted interventions.
机译:医学的进步已延长了Hurler综合征或粘多糖贮积症儿童的寿命,因此我需要更加重视对其长期结局和功能能力的评估。适应性功能对于理解治疗后的功能结局和制定有针对性的干预措施至关重要。我们调查了患有Hurler综合征的造血干细胞移植(HSCT)儿童的各种适应性功能的发展以及与这些功能的发展有关的危险因素。我们检查了41名儿童的发展情况,这些儿童在移植前后评估了3个或更多的Vineland适应行为量表记录。测量了沟通,日常生活技能,社交和运动功能。尽管标准分数会随着时间的推移而下降,但与同龄人相比,技能的发展速度仍低于平均水平。与移植组相比,横断面非移植比较组显示2岁后的缺陷更多。与认知能力相反,移植时的年龄与最终适应水平没有显着相关。 HSCT之前的基线认知水平和HSCT之后的认知增长与适应功能有关,尤其是在交流和日常生活技能方面。社会化是由累积的医学风险因素预测的,这可能是由于患有复杂移植过程的儿童的社会接触受限所致。总体而言,对适应行为的测量表明,HSCT可以长期缓慢改善Hurler综合征患儿的功能结局。患有Hurler综合征的儿童在HSCT之前具有良好的认知水平,在HSCT之后具有持续的认知增长,显示出良好的适应性功能。尽管认知和矫形问题以及医疗并发症限制了适应能力,但尽早发现这些问题可以进行有益的针对性干预。

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