Abstract:Objective To compare the anesthetic effect and hemodynamic changes of Mivacurium Chloride and Cisatracurium Besylate in ear-nose-throat surgery. Methods From January 2017 to January 2018, 80 patients with planed operation of ear, nose and throat under general anesthesia in the Second Hospital of Baoding were divided into observation group and control group according to random number table, 40 cases in each group. Patients were given muscle relaxants for general anesthesia induction, and the control group was given the Cisatracurium Besylate, the observation group was given Mivacurium Chloride. The MAP, HR, SpO2, BIS and four TOF value at seven time points of the home invasion (T1), anesthetic induction immediately (T2), intubation (T3), end of the surgery (T4), consciousness recovery (T5), tube drawing (T6), leaving the room (T7) were recorded. The time of recover, open eyes, extubation, and the restlessness and complications of patients were recorded. Results There were no significant differences in MAP, HR, and SpO2 between the two groups from T1 to T7 (P > 0.05). Compared with T1 and T2 of the same group, the levels of SpO2 in the control group at T5, T6 and the observation group at T7 decreased, and the differences were statistically significant (P < 0.05). Compared with the control group, the BIS values at T4, T7 and the TOF values at T4 to T7 were increased in the observation group, and the differences were statistically significant (P < 0.05); the BIS and TOF values of other time points between two groups were not statistically significant (P > 0.05). Compared with T1 and T2 of the same group, TOF values of T4, T5, T6, T7 in the control group and T4, T5, T6 in the observation group decreased, and the BIS of T3, T4, T5 in the two groups decreased and the differences were statistically significant (P < 0.05). The time of recovery, open eyes, extubation in observation group were shorter than those in control group, the incidence of extubation after agitation and complications was lower than those in control group, the differences were statistically significant (P < 0.05). Conclusion The effects of Mivacurium Chloride on hemodynamics perioperative anesthesia is small, work quickly, short induction time, fast recovery of muscle contraction function, and without the effect of neuromuscular blockade accumulation, it has less postoperative muscle relaxant residual, and is suitable for the ear, nose and throat surgery, safe and effective, which is worth popularizing clinically.
[1] Kochhar A,Banday J,Ahmad Z,et al. Pregabalin in monitored anesthesia care for ear-nose-throat surgery [J]. Anesth Essays Res,2017,11(2):350-353.
[2] Vermi■li S,Cukurova ■,Baydur H,et al. Relationship between preoperative patient learning need and anxiety of patients hospitalized at Ear Nose Throat and Head Neck Surgery clinic for surgical treatment [J]. Kulak Burun Bogaz Ihtis Derg,2016,26(2):79-91.
[3] 段宏伟,吴海星,吴一鸣,等.维库溴铵的麻醉药理学研究进展[J].中国临床研究,2018,31(2):266-269.
[4] 胡振华,鲁华,代山等.同步间歇指令通气用于喉罩通气无肌松药全麻下支气管镜检查术患者气道管理的效果[J].中华麻醉学杂志,2015,35(11):1407-1408.
[5] 鲁显福,曾因明.米库氯铵的过去、现在与未来[J].国际麻醉学与复苏杂志,2010,31(5):423-426,430.
[6] 吕慧,马鹤,朱卓,等.新型非去极化肌松药-米库氯铵[J].中国实验诊断学,2013,17(7):1359-1361.
[7] 曾春红.地佐辛对小儿耳鼻喉手术全身麻醉苏醒期躁动的影响[J].中国医药导刊,2015,(10):1045-1046,1049.
[8] 柳春玲.两种不同麻醉方式在老年耳鼻喉手术中的麻醉效果比较[J].当代医学,2015,21(35):66-67.
[9] 何雨竹,沈丹敏,房永利,等.不同因素对耳鼻喉手术术后疼痛的影响[J].北京医学,2015,37(2):154-156.
[10] 赵海琴.全麻手术患者麻醉复苏期的躁动因素分析与护理[J].实用临床医药杂志,2017,21(18):88-90.
[11] 杨沁岩,陈钰铨,陈强,等.监护麻醉对局部麻醉手术应激反应的调控效果[J].中国医师进修杂志,2015,38(7):518-521.
[12] 王馥婧,李聪,魏骐,等.麻醉后监测治疗室中应用肌松监测仪必要性的临床观察[J].国际麻醉学与复苏杂志,2018,39(2):132-135.
[13] Zeng R,Liu X,Zhang J,et al. The efficacy and safety of mivacurium in pediatric patients [J]. BMC Anesthesiol,2017,17,17(1):58.
[14] Wichmann S,F?覸rk G,Bundgaard JR,et al. Patients with prolonged effect of succinylcholine or mivacurium had novel mutations in the butyrylcholinesterase gene [J]. Pharmacogenet Genomics,2016,26(7):351-356.
[15] Eskildsen KZ,G?覿tke MR. Danish Cholinesterase Research Unit diagnoses patients with prolonged paralysis after succinylcholine and mivacurium [J]. Ugeskr Laeger,2015, 177(18):866-868.
[16] Dimov D,Kanev K,Dimova I. Correlation between butyrylcholinesterase variants and sensitivity to soman toxicity [J]. Acta Biochim Pol,2012,59(2):313-316.
[17] Ozdamar D,Dayioglu H,Anik I,et al. Evaluation of the neurotoxicity of intrathecal dexmedetomidine on rat spinal cord (electromicroscopic observations)[J]. Saudi J Anaesth,2018,12(1):10-15.
[18] Jiang L,Li H,Zhao N. Thymoquinone protects against cobalt chloride-induced neurotoxicity via Nrf2/GCL-regulated glutathione homeostasis [J]. J Biol Regul Homeost Agents,2017,31(4):843-853.
[19] Al-Ajmi AM,Morad MA,Cooper PE,et al. Reversible ethyl chloride Neurotoxicity:a case report [J]. Can J Neurol Sci,2018,45(1):119-120.
[20] Abulfadl YS,El-Maraghy NN,Ahmed AAE,et al. Protective effects of thymoquinone on D-galactose and aluminum chloride induced neurotoxicity in rats:biochemical,histological and behavioral changes [J]. Neurol Res,2018,40(4):324-333.