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依酚氯铵用于拮抗犬的神经肌肉阻滞。

Edrophonium for the antagonism of neuromuscular blockade in dogs.

作者信息

Clutton R E

机构信息

Department of Veterinary Clinical Sciences, Royal (Dick) School of Veterinary Studies, Easter Bush, Roslin, Midlothian.

出版信息

Vet Rec. 1994 Jun 25;134(26):674-8. doi: 10.1136/vr.134.26.674.

Abstract

Neuromuscular, electrocardiographic and autonomic nervous changes were studied when edrophonium and four combinations of edrophonium and atropine were used to antagonise vecuronium-induced neuromuscular blockade in 87 dogs anaesthetised with halothane. Edrophonium (500 micrograms/kg body-weight) was given alone, or with atropine (40 micrograms/kg) or one minute after a dose of 600 micrograms of atropine, and a lower dose of edrophonium (250 micrograms/kg) was used with high (40 micrograms/kg) and low (20 micrograms/kg) doses of atropine. The neuromuscular blockade was antagonised when some recovery was present. The reversal was rapid and complete in 75 cases, but the remaining 12 dogs which received the low dose of edrophonium required a second injection. Trials with the high dose of edrophonium alone were discontinued because cardiac arrest occurred in one dog and bronchosecretion with profuse salivation in another. The heart rate increased with the low dose of edrophonium and the high dose of atropine, and increased and then decreased when edrophonium was followed by 600 micrograms of atropine. The heart rate was stable when the high and low doses of atropine and edrophonium were matched. All the treatments caused atrioventricular blockade. Non-cardiac autonomic changes (salivation and bronchosecretion) occurred in only two of the 87 dogs.

摘要

在87只接受氟烷麻醉的犬中,研究了依酚氯铵以及依酚氯铵与阿托品的四种组合用于拮抗维库溴铵诱导的神经肌肉阻滞时的神经肌肉、心电图和自主神经变化。单独给予依酚氯铵(500微克/千克体重),或与阿托品(40微克/千克)一起给予,或在给予600微克阿托品一剂后一分钟给予,较低剂量的依酚氯铵(250微克/千克)与高剂量(40微克/千克)和低剂量(20微克/千克)的阿托品一起使用。当出现一定程度的恢复时,拮抗神经肌肉阻滞。75例中逆转迅速且完全,但其余12只接受低剂量依酚氯铵的犬需要第二次注射。单独使用高剂量依酚氯铵的试验停止,因为有1只犬发生心脏骤停,另1只犬出现支气管分泌和大量流涎。低剂量依酚氯铵和高剂量阿托品时心率增加,依酚氯铵后给予600微克阿托品时心率先增加后降低。高剂量和低剂量的阿托品与依酚氯铵匹配时心率稳定。所有治疗均导致房室传导阻滞。87只犬中只有2只出现非心脏自主神经变化(流涎和支气管分泌)。

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