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依酚氯铵和新斯的明对深度阿曲库铵阻滞的预激逆转作用。

Priming reversal of profound atracurium blockade by edrophonium and neostigmine.

作者信息

Liu C H, Lin I S, Liu C G, Peng T H, Yeh Y J, Chuu L J, Lin S Y

机构信息

Department of Anesthesiology, Provincial Tao-Yuan General Hospital, Republic of China.

出版信息

Gaoxiong Yi Xue Ke Xue Za Zhi. 1995 May;11(5):257-64.

PMID:7602663
Abstract

Accelerated reversal of moderate neuromuscular blockade has been reported to be effective by giving anticholinesterase in divided doses (priming reversal). To evaluate its effectiveness in profound blockade, forty ASA physical status I or II patients were studied. After receiving 0.5mg/kg of atracurium during N2O-O2-halothane anesthesia, they were reversed at 5% spontaneous recovery of first twitch height (T1) measured by train-of-four (TOF) stimulation. Edrophonium 1mg/kg was administered intravenously either in a single bolus dose (Group I, n = 10) or in an initial priming dose of 0.2mg/kg followed one minute later by 0.8mg/kg (Group II, n = 10). Neostigmine 0.05mg/kg was administered in a single bolus dose (Group III, n = 10) or in divided priming dose of 0.01 mg/kg followed one minute later by 0.04mg/kg (Group IV, n = 10). The recovery time from the first injection of the reversal agents until the TOF ratio reached 75% was significantly longer (p < 0.05) in Group III (681.5 +/- 77.5 sec) compared to Groups I, II, and IV (451.3 +/- 72.3 sec, 470.6 +/- 39.8 sec, and 448.1 +/- 42.5 sec, respectively; no statistical difference among these three groups). It is concluded that priming reversal by neostigmine, but not edrophonium, produced a significantly faster recovery of profound atracurium blockade. Using the priming method, neostigmine may reach a similar recovery time as edrophonium in profound blockade under equipotent doses.

摘要

据报道,通过分次给予抗胆碱酯酶药物(预注逆转法)可有效加速中度神经肌肉阻滞的逆转。为评估其在深度阻滞中的有效性,对40例ASA身体状况I或II级的患者进行了研究。在N2O - O2 - 氟烷麻醉期间给予0.5mg/kg阿曲库铵后,当四个成串刺激(TOF)测得的第一个肌颤搐高度(T1)自发恢复至5%时进行逆转。依酚氯铵1mg/kg静脉注射,要么单次推注(I组,n = 10),要么初始预注剂量0.2mg/kg,1分钟后再给予0.8mg/kg(II组,n = 10)。新斯的明0.05mg/kg单次推注(III组,n = 10),要么分次预注剂量0.01mg/kg,1分钟后再给予0.04mg/kg(IV组,n = 10)。与I组、II组和IV组(分别为451.3 +/- 72.3秒、470.6 +/- 39.8秒和448.1 +/- 42.5秒;这三组之间无统计学差异)相比,III组从首次注射逆转药物至TOF比值达到75%的恢复时间明显更长(p < 0.05)(681.5 +/- 77.5秒)。得出的结论是,新斯的明预注逆转法而非依酚氯铵能显著加快深度阿曲库铵阻滞的恢复。采用预注法,在等效剂量下,新斯的明在深度阻滞中的恢复时间可能与依酚氯铵相似。

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