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铝毒理学的最新进展。

Recent developments in aluminum toxicology.

作者信息

Monteagudo F S, Cassidy M J, Folb P I

机构信息

Department of Pharmacology, Medical School, University of Cape Town, South Africa.

出版信息

Med Toxicol Adverse Drug Exp. 1989 Jan-Feb;4(1):1-16. doi: 10.1007/BF03259899.

DOI:10.1007/BF03259899
PMID:2651849
Abstract

Aluminum is now recognised as an important toxin causing considerable morbidity and mortality, particularly in patients with chronic renal failure. Diseases that have been associated with aluminium include dialysis dementia, renal osteodystrophy and Alzheimer's disease. Aluminum also has an effect on red blood cells, parathyroid glands and chromosomes. Accumulation of aluminium in the body tends to occur when the gastrointestinal barrier is circumvented. This has been identified as a problem during dialysis or intravenous fluid administration. Renal functional impairment results in decreased aluminum excretion and promotes accumulation of the element in the body. Many sources have been shown to be contaminated with aluminium. These include the water used for dialysis; medicines containing aluminium, such as aluminium-containing phosphate binding gels; total parenteral nutrition solutions; processed human serum albumin; intravenous fluids in infants; and other environmental and industrial sources. The management of aluminium toxicity involves the identification of these contaminated sources and subsequent removal of the element. This includes regular monitoring of water used in dialysis. The use of aluminium-containing phosphate binding gels in patients with compromised renal function should be reviewed and alternatives sought. The development of effective aluminium-free phosphate binders is desirable. Once a patient has aluminium toxicity, desferrioxamine (deferoxamine) has been shown to be an effective agent in its chelation and removal.

摘要

铝现在被认为是一种重要的毒素,会导致相当高的发病率和死亡率,尤其是在慢性肾衰竭患者中。与铝相关的疾病包括透析性痴呆、肾性骨营养不良和阿尔茨海默病。铝对红细胞、甲状旁腺和染色体也有影响。当胃肠道屏障被绕过,体内就容易发生铝蓄积。这已被确定为透析或静脉输液过程中的一个问题。肾功能损害会导致铝排泄减少,并促进体内该元素的蓄积。已证明许多来源都被铝污染。这些包括用于透析的水;含铝药物,如含铝的磷酸盐结合凝胶;全胃肠外营养溶液;加工过的人血清白蛋白;婴儿静脉输液;以及其他环境和工业来源。铝中毒的处理包括识别这些污染源并随后去除该元素。这包括定期监测透析用水。对于肾功能受损患者使用含铝的磷酸盐结合凝胶的情况应进行审查并寻找替代方法。开发有效的无铝磷酸盐结合剂是很有必要的。一旦患者出现铝中毒,去铁胺已被证明是一种有效的螯合和去除剂。

相似文献

1
Recent developments in aluminum toxicology.铝毒理学的最新进展。
Med Toxicol Adverse Drug Exp. 1989 Jan-Feb;4(1):1-16. doi: 10.1007/BF03259899.
2
Aluminium intoxication in renal disease.
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3
1alpha(OH)D3 One-alpha-hydroxy-cholecalciferol--an active vitamin D analog. Clinical studies on prophylaxis and treatment of secondary hyperparathyroidism in uremic patients on chronic dialysis.1α(OH)D3 一α-羟基胆钙化醇——一种活性维生素 D 类似物。关于慢性透析的尿毒症患者继发性甲状旁腺功能亢进症预防和治疗的临床研究。
Dan Med Bull. 2008 Nov;55(4):186-210.
4
Clinical experience with desferrioxamine in dialysis patients with aluminium toxicity.去铁胺治疗铝中毒透析患者的临床经验。
Q J Med. 1990 Mar;74(275):257-76.
5
The use of desferrioximine in dialysis-associated aluminium disease.
Contrib Nephrol. 1993;102:125-34. doi: 10.1159/000421919.
6
Aluminium toxicity in chronic renal insufficiency.
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[Aluminum poisoning in dialysis patients--diagnosis and therapy].[透析患者的铝中毒——诊断与治疗]
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8
Deferoxamine for aluminum toxicity in dialysis patients.去铁胺用于透析患者铝中毒的治疗
ANNA J. 1990 Jun;17(3):224-8.
9
[Renal osteodystrophy (3); its treatment in dialysis patients].[肾性骨营养不良(3);透析患者的治疗]
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10
Kinetics of aluminium removal by desferrioxamine VIA hemodialysis in a case with aluminium bone disease.
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