国际麻醉学与复苏杂志   2025, Issue (6): 0-0
    
米库氯铵导致的长时间神经肌肉阻滞2例病例分析
李正钢, 薛玉红, 吴秀英1()
1.中国医科大学附属盛京医院
Analysis of two cases of prolonged neuromuscular blockade induced by mivacurium chloride
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摘要:

自1992年米库氯铵被批准上市以来,关于米库氯铵导致血浆胆碱酯酶缺乏患者长时间神经肌肉阻滞的病例就陆续的报道出来。早在1991年就有研究证实了有假性胆碱酯酶缺陷的患者使用米库氯铵会使神经肌肉阻滞时间延长,但最早的非预期的长时间神经肌肉阻滞的病例可以追溯到1993年。根据高加索人中假性胆碱酯酶基因的非典型型基因突变(A突变)纯合子的发病率(1/3000-1/2500)推测真实发生的病例要远多于报道出来的病例,而东方人中极少发生胆碱酯酶基因纯合子突变,目前中国国内的相关研究和报道也很少,所以更多的病例报道和研究是必要的,这有助于提升麻醉医生对胆碱酯酶缺乏患者的认识和重视,避免发生严重的后果。

关键词: 米库氯铵;血浆胆碱酯酶;假性胆碱酯酶(PChE);丁酰胆碱酯酶(BChE);血浆胆碱酯酶缺乏;神经肌肉阻滞
Abstract:

Since the approval of micuronium chloride in 1992 , cases of prolonged neuromuscular block caused by micuronium chloride in patients with plasma cholinesterase deficiency have been reported. As early as 1991, studies have confirmed that the use of micuronium chloride in patients with pseudocholinesterase deficiency can prolong the duration of neuromuscular block , but the earliest cases of unexpected long-term neuromuscular block can be traced back to 1993 . According to the incidence of homozygote of atypical mutation (A mutation) of pseudocholinesterase gene in Caucasians (1/3000-1/2500) , it is estimated that the actual occurrence of cases is far more than that of reported cases, while homozygote mutation of cholinesterase gene is rare in Oriental people . At present, there are few relevant studies and reports in China, so more case reports and studies are necessary, which will help to enhance anesthesiologists' understanding and attention to patients with cholinesterase deficiency and avoid serious consequences.

Key words: Micuronium chloride; Plasma cholinesterase; Pseudocholinesterase (PChE); Butyrylcholinesterase (BChE); Plasma cholinesterase deficiency; Neuromuscular block