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对阿曲库铵、维库溴铵和筒箭毒碱的类组胺反应。

Histaminoid responses to atracurium, vecuronium and tubocurarine.

作者信息

Lavery G G, Clarke R S, Watkins J

出版信息

Ann Fr Anesth Reanim. 1985;4(2):180-3. doi: 10.1016/S0750-7658(85)80196-9.

Abstract

Sixty patients scheduled for elective surgery underwent intradermal testing with 0.1 ml of the following solutions diluted in 0.9% saline: vecuronium and tubocurarine (1 in 1,000), atracurium (1 in 1,000 and 1 in 10,000), thiopentone (1 in 100) and also a 0.9% saline control. Thirty minutes later, an area of erythema of greater than 1.5 cm, or a wheal exceeding 1.0 cm in diameter, was recorded as a positive reaction. The patients then randomly received equipotent doses of atracurium, vecuronium or tubocurarine during a standardized anaesthetic induction. Any cutaneous reaction and the percentage fall in systolic pressure three minutes after administration of the relaxant were recorded. In 51 patients plasma IgE levels were measured. The incidence of positive cutaneous reactions to intradermal and intravenous relaxants was significantly different with each agent (p less than 0.01). The percentage fall in systolic pressure after tubocurarine was significantly different relative to the other two agents (p less than 0.01). This was regarded as reflecting potency in releasing histamine and placed the relaxants in the same order: tubocurarine, atracurium and vecuronium. The response to intradermal administration was no guide to the subsequent response after intravenous administration of the three relaxants. IgE levels below 15 IU X ml-1 occurred significantly more often in females and were associated with a significantly higher incidence of cutaneous reactions after intradermal atracurium (1 in 1,000 and 1 in 10,000) (p less than 0.05 and 0.001 respectively) and tubocurarine (1 in 1,000). With these two agents, generalized flushing after intravenous administration was also more common in this group, relative to the normal/high IgE group.

摘要

60例计划接受择期手术的患者用0.1ml以下用0.9%生理盐水稀释的溶液进行皮内试验:维库溴铵和筒箭毒碱(1:1000)、阿曲库铵(1:1000和1:10000)、硫喷妥钠(1:100),还有0.9%生理盐水作为对照。30分钟后,红斑面积大于1.5cm或风团直径超过1.0cm被记录为阳性反应。然后患者在标准化麻醉诱导期间随机接受等效剂量的阿曲库铵、维库溴铵或筒箭毒碱。记录给予松弛剂后3分钟的任何皮肤反应和收缩压下降百分比。测定了51例患者的血浆IgE水平。皮内和静脉注射松弛剂后阳性皮肤反应的发生率在每种药物之间有显著差异(p<0.01)。筒箭毒碱给药后收缩压下降百分比相对于其他两种药物有显著差异(p<0.01)。这被认为反映了释放组胺的效力,并将这些松弛剂按相同顺序排列:筒箭毒碱、阿曲库铵和维库溴铵。皮内给药后的反应并不能指导这三种松弛剂静脉给药后的后续反应。IgE水平低于15IU/ml-1在女性中明显更常见,并且与皮内注射阿曲库铵(1:1000和1:10000)(分别为p<0.05和0.001)和筒箭毒碱(1:1000)后皮肤反应的发生率显著更高相关。在这一组中,相对于正常/高IgE组,静脉注射这两种药物后全身性潮红也更常见。

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