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班布特罗对血浆胆碱酯酶活性异常的杂合子受试者血浆胆碱酯酶活性及琥珀胆碱诱导的神经肌肉阻滞的影响

The effect of bambuterol on plasma cholinesterase activity and suxamethonium-induced neuromuscular blockade in subjects heterozygous for abnormal plasma cholinesterase.

作者信息

Bang U, Viby-Mogensen J, Wirén J E

机构信息

Department of Anaesthesia, University of Copenhagen, Herlev Hospital, Denmark.

出版信息

Acta Anaesthesiol Scand. 1990 Oct;34(7):600-4. doi: 10.1111/j.1399-6576.1990.tb03153.x.

Abstract

Bambuterol is a new bronchodilator which is also a reversible inhibitor of plasma cholinesterase. In patients with normal plasma cholinesterase genotype, bambuterol prolongs suxamethonium-induced neuromuscular blockade. In the present study, we investigated the interaction of bambuterol and suxamethonium in nine patients heterozygous for abnormal plasma cholinesterase during anaesthesia with fentanyl, thiopentone, halothane and nitrous oxide in oxygen. The patients (seven E1uE1a and two E1uE1s) were given 20 mg of bambuterol orally 2 h before anaesthesia. Suxamethonium 1 mg.kg-1 was given for tracheal intubation. The neuromuscular function was monitored using train-of-four (TOF) stimulation of the ulnar nerve and a force displacement transducer. Plasma cholinesterase activity decreased in all patients following bambuterol (P less than 0.001). In patients with genotype E1uE1a, median time to 90% recovery of twitch height and TOF ratio greater than or equal to 0.7 (37.5 min) was prolonged compared to 28 E1uE1a patients not treated with bambuterol (14.0 min) (P less than 0.001). Four of these patients developed a phase II block apparently not correlated to plasma cholinesterase activity. In the E1uE1s; patients, full recovery was seen after 22.0 and 31.4 min, respectively. It is concluded that in patients heterozygous for abnormal plasma cholinesterase, bambuterol 20 mg taken 2 h before anaesthesia causes a 2-3 times prolongation of the neuromuscular blockade following suxamethonium 1 mg.kg-1 and in some patients a phase II block.

摘要

班布特罗是一种新型支气管扩张剂,也是血浆胆碱酯酶的可逆抑制剂。在血浆胆碱酯酶基因型正常的患者中,班布特罗可延长琥珀胆碱引起的神经肌肉阻滞。在本研究中,我们调查了9例血浆胆碱酯酶异常的杂合子患者在芬太尼、硫喷妥钠、氟烷和一氧化二氮-氧气麻醉期间班布特罗与琥珀胆碱的相互作用。这些患者(7例E1uE1a和2例E1uE1s)在麻醉前2小时口服20毫克班布特罗。给予1毫克/千克的琥珀胆碱用于气管插管。使用尺神经的四个成串刺激(TOF)和力位移换能器监测神经肌肉功能。所有患者服用班布特罗后血浆胆碱酯酶活性均下降(P<0.001)。与28例未用班布特罗治疗的E1uE1a患者(14.0分钟)相比,E1uE1a基因型患者抽搐高度恢复90%和TOF比值大于或等于0.7的中位时间(37.5分钟)延长(P<0.001)。其中4例患者出现II期阻滞,显然与血浆胆碱酯酶活性无关。在E1uE1s患者中,分别在22.0分钟和31.4分钟后观察到完全恢复。结论是,在血浆胆碱酯酶异常的杂合子患者中,麻醉前2小时服用20毫克班布特罗可使1毫克/千克琥珀胆碱后的神经肌肉阻滞延长2至3倍,并且在一些患者中会出现II期阻滞。

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