安定在有机磷酯农药中毒治疗中的应用。

Timothy C Marrs
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引用次数: 51

摘要

尽管地西泮和其他苯二氮卓类药物一样,其主要作用部位是γ -氨基丁酸A (GABAA)受体,但地西泮对有机磷酯农药中毒的有益作用在多大程度上是通过GABAA受体介导的,一直存在争议。虽然在大多数OP中毒系列中,抽搐相对不常见,但抽搐可能通过引起结构损伤而在中枢神经系统中产生长期后遗症。动物研究表明,地西泮可预防和治疗OPs引起的惊厥,并可预防此类惊厥引起的中枢神经系统损伤所造成的晚期影响。因此,使用地西泮是严重OP中毒治疗方案的重要组成部分,因为它可以防止或至少缩短抽搐的持续时间。此外,病例报告表明,地西泮也会改善肌束,这是OP农药中毒的主观上令人不快的特征。没有数据,无论是实验还是临床,证明单独使用地西泮对OP中毒的致死率有任何明确的影响。事实上,在一项对大型动物的研究中,单独服用地西泮会增加死亡率。在实验性OPs中毒的动物中,与单独使用阿托品相比,阿托品和地西泮联合治疗显著降低了致死率,表明明显的有益效果。有许多使用地西泮的病例报告,通常作为其他更具体的OP解毒剂的辅助剂,如阿托品和/或肟吡啶。根据这一证据和实验动物的药理学研究,当OPs中毒患者出现抽搐或明显的肌肉束动时,应给予地西泮。在严重中毒的情况下,甚至在这些并发症发生之前就应考虑给予地西泮。虽然地西泮有很大的治疗指数,但在OP中毒中似乎没有常规使用的余地。在医院接受治疗的OP中毒患者应静脉给予地西泮,尽管在医院外,如在战场上,当使用自动注射器时,肌肉注射途径用于给药。然而,应该认识到,肌内途径的吸收很差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diazepam in the treatment of organophosphorus ester pesticide poisoning.

Although the main site of action of diazepam, as with other benzodiazepines, is at the gamma-aminobutyric acid A (GABAA) receptor, the degree to which the beneficial actions of diazepam in organophosphorus (OP) ester pesticide poisoning are mediated through the GABAA receptor has been a matter of controversy. Although in most series of OP intoxications, convulsions have been relatively uncommon, it is probable that convulsions produce long-term sequelae in the central nervous system by causing structural damage. Animal studies have demonstrated that diazepam prevents and treats convulsions produced by OPs and may prevent the late effects caused by damage to the central nervous system induced by such convulsions. Consequently, the use of diazepam is an important part of the treatment regimen of severe OP poisoning as it prevents, or at least reduces the duration of, convulsions. In addition, case reports suggest that diazepam will also ameliorate muscle fasciculation, a subjectively unpleasant feature of OP pesticide poisoning. There are no data, either experimental or clinical, demonstrating any clear effect of diazepam alone on lethality in OP poisoning. In fact, in one study of large animals, diazepam, given alone, increased lethality. In animals experimentally poisoned with OPs, combined treatment with atropine and diazepam significantly lowered lethality compared with atropine treatment alone, indicating a clear beneficial effect. There are numerous case reports of the use of diazepam, generally as an adjunct to other more specific OP antidotes such as atropine and/or pyridinium oximes. Based on this evidence and pharmacodynamic studies in experimental animals, diazepam should be given to patients poisoned with OPs whenever convulsions or pronounced muscle fasciculation are present. In severe poisoning, diazepam administration should be considered even before these complications develop. Although diazepam has a large therapeutic index, there appears to be no place for its routine use in OP poisoning. Diazepam should be given intravenously to patients treated in hospital for OP poisoning, although the intramuscular route is used to administer diazepam outside hospital, such as on the battlefield, when an auto-injector is employed. It should be recognised, however, that absorption by the intramuscular route is poor.

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