Modern strategies in therapy of organophosphate poisoning

被引:118
作者
Thiermann, H
Szinicz, L
Eyer, F
Worek, F
Eyer, P
Felgenhauer, N
Zilker, T
机构
[1] Sanitatsakad Bundeswehr, Inst Pharmakol & Toxikol, D-85748 Garching, Germany
[2] Univ Munich, Walther Straub Inst Pharmakol & Toxikol, D-80336 Munich, Germany
[3] Tech Univ Munich, Klinikum Rechts Isar, Med Klin 2, Toxicol Abt, D-81664 Munich, Germany
关键词
organophosphate poisoning; obidoxime; pralidoxime; parathion; oxydemeton methyl;
D O I
10.1016/S0378-4274(99)00052-1
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Considering the various microscopic reactions as well as toxicokinetic and pharmacokinetic principles in therapy of organophosphate poisoning, the administration of obidoxime by an initial bolus dose followed by continuous infusion appears rational. Using this protocol, six patients each with parathion or oxydemeton methyl poisoning were treated. In parathion poisoning, reactivation was possible up to 7 days. At paraoxon concentrations >0.1 mu M obidoxime only partially reactivated acetylcholinesterase (AChE) of erythrocytes in vivo although reactivation could be assessed in vitro, which roughly fitted theoretical calculations. AChE-inhibitory material was detected up to 5 days. Cholinergic signs soon subsided when AChE was above 20% of normal, and atropine plasma levels could be kept below 7 ng/ml. In one patient brain damage persisted. Oxydemeton methyl poisoning responded to obidoxime therapy only when the oxime was instituted shortly after poisoning. Out of six patients one died. No intermediate syndrome and no signs of permanent hepatic dysfunction were found in the 12 patients. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:233 / 239
页数:7
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