Suppr超能文献

患有先天性代谢缺陷的新生儿的肾脏替代治疗。

Renal replacement therapy in neonates with an inborn error of metabolism.

作者信息

Cho Heeyeon

机构信息

Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

出版信息

Korean J Pediatr. 2019 Feb;62(2):43-47. doi: 10.3345/kjp.2018.07143. Epub 2018 Nov 7.

Abstract

Hyperammonemia can be caused by several genetic inborn errors of metabolism including urea cycle defects, organic acidemias, fatty acid oxidation defects, and certain disorders of amino acid metabolism. High levels of ammonia are extremely neurotoxic, leading to astrocyte swelling, brain edema, coma, severe disability, and even death. Thus, emergency treatment for hyperammonemia must be initiated before a precise diagnosis is established. In neonates with hyperammonemia caused by an inborn error of metabolism, a few studies have suggested that peritoneal dialysis, intermittent hemodialysis, and continuous renal replacement therapy (RRT) are effective modalities for decreasing the plasma level of ammonia. In this review, we discuss the current literature related to the use of RRT for treating neonates with hyperammonemia caused by an inborn error of metabolism, including optimal prescriptions, prognosis, and outcomes. We also review the literature on new technologies and instrumentation for RRT in neonates.

摘要

高氨血症可由多种遗传性先天性代谢缺陷引起,包括尿素循环缺陷、有机酸血症、脂肪酸氧化缺陷以及某些氨基酸代谢紊乱。高水平的氨具有极强的神经毒性,可导致星形胶质细胞肿胀、脑水肿、昏迷、严重残疾甚至死亡。因此,必须在明确诊断之前就开始对高氨血症进行紧急治疗。对于由先天性代谢缺陷引起高氨血症的新生儿,一些研究表明,腹膜透析、间歇性血液透析和连续性肾脏替代治疗(RRT)是降低血浆氨水平的有效方式。在本综述中,我们讨论了目前有关使用RRT治疗由先天性代谢缺陷引起高氨血症新生儿的文献,包括最佳处方、预后和结局。我们还回顾了有关新生儿RRT新技术和仪器的文献。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验