Hyperammonemia in review: pathophysiology, diagnosis, and treatment

被引:156
作者
Auron, Ari [2 ]
Brophy, Patrick D. [1 ]
机构
[1] Univ Iowa, Childrens Hosp, Dept Pediat Pediat Nephrol Dialysis & Transplanta, Iowa City, IA 52242 USA
[2] Blank Mem Hosp Children, Des Moines, IA 50309 USA
关键词
Hyperammonemia; Dialysis; Urea cycle defects; Treatment; Pathophysiology; UREA CYCLE DISORDERS; ORNITHINE TRANSCARBAMYLASE DEFICIENCY; SPARSE-FUR MICE; INBORN-ERRORS; PERITONEAL-DIALYSIS; LIVER-TRANSPLANTATION; N-CARBAMYLGLUTAMATE; NITROGEN-METABOLISM; ACUTE HEMODIALYSIS; HYPER-AMMONEMIA;
D O I
10.1007/s00467-011-1838-5
中图分类号
R72 [儿科学];
学科分类号
100202 [儿科学];
摘要
Ammonia is an important source of nitrogen and is required for amino acid synthesis. It is also necessary for normal acid-base balance. When present in high concentrations, ammonia is toxic. Endogenous ammonia intoxication can occur when there is impaired capacity of the body to excrete nitrogenous waste, as seen with congenital enzymatic deficiencies. A variety of environmental causes and medications may also lead to ammonia toxicity. Hyperammonemia refers to a clinical condition associated with elevated ammonia levels manifested by a variety of symptoms and signs, including significant central nervous system (CNS) abnormalities. Appropriate and timely management requires a solid understanding of the fundamental pathophysiology, differential diagnosis, and treatment approaches available. The following review discusses the etiology, pathogenesis, differential diagnosis, and treatment of hyperammonemia.
引用
收藏
页码:207 / 222
页数:16
相关论文
共 108 条
[1]
Efficacy of L-Ornithine L-Aspartate in Acute Liver Failure: A Double-Blind, Randomized, Placebo-Controlled Study [J].
Acharya, Subrat Kumar ;
Bhatia, Vikram ;
Sreenivas, Vishnubhatla ;
Khanal, Shankar ;
Panda, Subrat Kumar .
GASTROENTEROLOGY, 2009, 136 (07) :2159-2168
[2]
Carbamazepine-induced hyperammonemia [J].
Adams, Erin N. ;
Marks, Alla ;
Lizer, Mitsi H. .
AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY, 2009, 66 (16) :1468-1470
[3]
HYPERAMMONEMIA IN ASTERIXIS INDUCED BY CARBAMAZEPINE - 2 CASE-REPORTS [J].
AMBROSETTO, G ;
RIVA, R ;
BARUZZI, A .
ACTA NEUROLOGICA SCANDINAVICA, 1984, 69 (03) :186-189
[4]
Continuous venovenous haemodialysis (CVVHD) and continuous peritoneal dialysis (CPD) in the acute management of 21 children with inborn errors of metabolism [J].
Arbeiter, Anja K. ;
Kranz, Birgitta ;
Wingen, Anne-Margret ;
Bonzel, Klaus-Eugen ;
Dohna-Schwake, Christian ;
Hanssler, Ludwig ;
Neudorf, Ulrich ;
Hoyer, Peter F. ;
Buescher, Rainer .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2010, 25 (04) :1257-1265
[5]
Estimation of the total number of disease-causing mutations in ornithine transcarbamylase (OTC) deficiency.: Value of the OTC structure in predicting a mutation pathogenic potential [J].
Arranz, J. A. ;
Riudor, E. ;
Marco-Marin, C. ;
Rubio, V. .
JOURNAL OF INHERITED METABOLIC DISEASE, 2007, 30 (02) :217-226
[6]
INCREASE OF TRYPTOPHAN AND 5-HYDROXYINDOLE ACETIC-ACID IN THE BRAIN OF ORNITHINE CARBAMOYLTRANSFERASE DEFICIENT SPARSE-FUR MICE [J].
BACHMANN, C ;
COLOMBO, JP .
PEDIATRIC RESEARCH, 1984, 18 (04) :372-375
[7]
Batshaw M L, 1984, Curr Probl Pediatr, V14, P1
[8]
TREATMENT OF HYPERAMMONEMIC COMA CAUSED BY INBORN-ERRORS OF UREA SYNTHESIS [J].
BATSHAW, ML ;
BRUSILOW, SW .
JOURNAL OF PEDIATRICS, 1980, 97 (06) :893-900
[9]
Alternative pathway therapy for urea cycle disorders: Twenty years later [J].
Batshaw, ML ;
MacArthur, RB ;
Tuchman, M .
JOURNAL OF PEDIATRICS, 2001, 138 (01) :S46-S54
[10]
QUINOLINIC ACID IN CHILDREN WITH CONGENITAL HYPERAMMONEMIA [J].
BATSHAW, ML ;
ROBINSON, MB ;
HYLAND, K ;
DJALI, S ;
HEYES, MP .
ANNALS OF NEUROLOGY, 1993, 34 (05) :676-681