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用抗胆碱酯酶药进行预充——不同预充剂量依酚氯铵的作用。

Priming with anti-cholinesterases--the effect of different priming doses of edrophonium.

作者信息

Naguib M, Abdulatif M

机构信息

Department of Anesthesiology, King Faisal University, King Fahd Hospital, Al-Khobar, Saudi Arabia.

出版信息

Can J Anaesth. 1988 Jan;35(1):53-7. doi: 10.1007/BF03010545.

DOI:10.1007/BF03010545
PMID:3349555
Abstract

The effect of different priming doses of edrophonium were studied in 77 patients divided into seven groups (n = 11 in each). Edrophonium 1.0 mg.kg-1 was administered either in a single bolus dose (Group I; controls) or in an initial dose of 0.05, 0.1, 0.15, 0.2, 0.25 or 0.3 mg.kg-1 followed one minute later by the remainder of the 1.0 mg.kg-1 dose in Groups II to VII respectively. Reversal was attempted at ten per cent spontaneous recovery of twitch height (T1) from atracurium-induced neuromuscular blockade. Increasing the size of the priming dose from 0.05 to 0.2 mg.kg-1 resulted in a stepwise increase (p less than 0.05) in recovery of T1 and train-of-four (TOF) ratio. Higher priming doses (0.25 and 0.3 mg.kg-1) were not associated with further improvement in T1 and TOF recovery. Reversal time, that is the time taken from the first injection of edrophonium until the TOF ratio value had reached 0.75 was significantly faster (p less than 0.01) following priming with edrophonium 0.2 mg.kg-1 (Group V) when compared to Groups I, II, III, IV and VI. Reversal times were also significantly faster in Groups IV and VI when compared to the control group. It is concluded that 0.2 mg.kg-1 appears to be the optimal priming dose for administration of edrophonium in divided doses.

摘要

在77例患者中研究了不同预注剂量依酚氯铵的效果,这些患者被分为七组(每组n = 11)。依酚氯铵1.0mg.kg-1以单次推注剂量给药(I组;对照组),或分别在II至VII组中先给予初始剂量0.05、0.1、0.15、0.2、0.25或0.3mg.kg-1,1分钟后再给予剩余的1.0mg.kg-1剂量。当自阿曲库铵诱导的神经肌肉阻滞出现10%的单次颤搐高度(T1)自发恢复时尝试进行逆转。将预注剂量从0.05mg.kg-1增加至0.2mg.kg-1会导致T1和四个成串刺激(TOF)比值的恢复呈逐步增加(p < 0.05)。更高的预注剂量(0.25和0.3mg.kg-1)与T1和TOF恢复的进一步改善无关。与I、II、III、IV和VI组相比,0.2mg.kg-1依酚氯铵预注(V组)后逆转时间(即从首次注射依酚氯铵直至TOF比值达到0.75所花费的时间)明显更快(p < 0.01)。与对照组相比,IV组和VI组的逆转时间也明显更快。得出的结论是,0.2mg.kg-1似乎是分次给药依酚氯铵的最佳预注剂量。

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Priming with anti-cholinesterases--the effect of different priming doses of edrophonium.用抗胆碱酯酶药进行预充——不同预充剂量依酚氯铵的作用。
Can J Anaesth. 1988 Jan;35(1):53-7. doi: 10.1007/BF03010545.
2
Train-of-four ratio after antagonism of atracurium with edrophonium: influence of different priming doses of edrophonium.依酚氯铵拮抗阿曲库铵后的四个成串刺激比值:不同预注剂量依酚氯铵的影响。
Can J Anaesth. 1989 Jan;36(1):25-9. doi: 10.1007/BF03010882.
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Priming with anti-cholinesterases--the effect of different combinations of anti-cholinesterases and different priming intervals.抗胆碱酯酶药物预充——抗胆碱酯酶药物不同组合及不同预充间隔的影响
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Antagonism of atracurium-induced neuromuscular blockade by neostigmine or edrophonium.新斯的明或依酚氯铵对阿曲库铵所致神经肌肉阻滞的拮抗作用。
Br J Anaesth. 1986 Nov;58(11):1290-5. doi: 10.1093/bja/58.11.1290.

引用本文的文献

1
"Priming" with neostigmine: failure to accelerate reversal of single twitch and train-of-four responses.
Can J Anaesth. 1989 Jan;36(1):30-4. doi: 10.1007/BF03010883.
2
Train-of-four ratio after antagonism of atracurium with edrophonium: influence of different priming doses of edrophonium.依酚氯铵拮抗阿曲库铵后的四个成串刺激比值:不同预注剂量依酚氯铵的影响。
Can J Anaesth. 1989 Jan;36(1):25-9. doi: 10.1007/BF03010882.
3
Edrophonium priming for antagonism of atracurium neuromuscular blockade.
Can J Anaesth. 1990 Mar;37(2):197-201. doi: 10.1007/BF03005469.
4

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Neuromuscular blockade by neostigmine in anaesthetized man.新斯的明对麻醉状态下人体的神经肌肉阻滞作用。
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Pharmacokinetics of edrophonium and neostigmine when antagonizing d-tubocurarine neuromuscular blockade in man.依酚氯铵和新斯的明在人体中拮抗筒箭毒碱神经肌肉阻滞作用时的药代动力学。
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Edrophonium priming alters the course of neuromuscular recovery from a pipecuronium neuromuscular blockade.依酚氯铵预充可改变哌库溴铵神经肌肉阻滞作用后的神经肌肉恢复过程。
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Accelerated reversal of atracurium blockade with divided doses of neostigmine.新斯的明分次给药加速阿曲库铵阻滞的逆转
Can Anaesth Soc J. 1986 Nov;33(6):723-8. doi: 10.1007/BF03027121.
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