依托咪酯联合舒芬太尼、芬太尼或地佐辛对无痛胃镜患者意识指数和不良反应的影响:一项随机对照单盲试点研究

Ji Liu, Ming Sun, Weiwu Fang, Changqing Zhong, Xuewu Xu, Yan Lv, Lin Zhao, Qiang Li, Ying Zhang, Ming Zou, Yong Wang, Xiaochen Wang
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IoC was measured before anesthesia (T1), opioids (T2), etomidate (T3), the start of endoscopy (T4), drug withdrawal (T5), OAA/S ​&gt; ​2 (T6), and OAA/S ​&gt; ​4) (T7). The primary outcome was the observation of IoC at T6 and T7. The adverse reaction and recovery time were secondary outcomes.</p></div><div><h3>Results</h3><p>With 20 patients in each group, there were no differences in the operation and awakening times among the four groups (P ​&gt; ​0.05). Compared with group C, the IoC values of groups S and F at T5, T6, and T7 were increased after drug administration (P ​&lt; ​0.05), with intragroup differences (P ​&lt; ​0.001). Compared with group C, the IoC values of groups S, F, and D were higher at T6 and T7 (P<sub>S-T6</sub> ​= ​0.003, P<sub>F-T6</sub> ​= ​0.013, P<sub>D-T6</sub> ​= ​0.015; P<sub>S-T7</sub> ​= ​0.015, P<sub>F-T7</sub> ​= ​0.040, P<sub>D-T7</sub> ​= ​0.028). 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引用次数: 0

摘要

目的使用依托咪酯与不同的阿片类药物(舒芬太尼、芬太尼和德佐辛),从患者意识指数(IoC)方面比较几种麻醉方案,2020年12月至2022年5月。患者被随机分为对照组(依托咪酯)、S组(舒芬太尼​+​依托咪酯)、F(芬太尼​+​依托咪酯)和D(脱佐辛​+​乙酰胺)。在麻醉(T1)、阿片类药物(T2)、依托咪酯(T3)、内窥镜检查开始(T4)、停药(T5)、OAA/S前测量IoC​>;​2(T6)和OAA/S​>;​4) (T7)。主要结果是在T6和T7时观察到IoC。不良反应和恢复时间是次要结果。结果每组20例,四组患者的手术时间和苏醒时间差异无统计学意义(P​>;​与C组相比,S组和F组在给药后T5、T6和T7的IoC值均升高(P​<;​0.05),组内差异有统计学意义(P​<;​0.001)。与C组相比,S、F和D组的IoC值在T6和T7时更高(PS-T6​=​0.003,PF-T6​=​0.013,PD-T6​=​0.015;PS-T7​=​0.015,PF-T7​=​0.040,PD-T7​=​0.028)。D组和C组之间的恶心和呕吐有差异(PD-C​=​0.044)和肌阵挛(PS–CPF-C<0.001和PD-C<0.001);观察到90%(S组2例,F组1例)。结论IoC值与OAA/S评分具有良好的相关性,可以准确监测依托咪酯联合阿片类药物对无痛胃镜麻醉患者麻醉深度的影响。试验注册ChiCTR,ChiCTR200040927。注册日期:2020年12月16日-预期注册,http://www.chictr.org.cn/ChiCTR2000040927.
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Comparison of the effects of etomidate combined with sufentanil, fentanyl, or dezocine on the consciousness index and adverse reactions for painless gastroscopy: A randomized controlled single-blinded pilot study

Objective

To use etomidate in combination with different opioids (sufentanil, fentanyl, and dezocine) to compare several anesthesia options from the aspects of the patient's index of consciousness (IoC).

Methods

This was a prospective pilot study of consecutive patients who were scheduled for elective painless gastroscopy at PLA Strategic Force Characteristic Medical Center, Beijing, China, between December 2020 and May 2022. The patients were randomized to control (etomidate), S (sufentanil ​+ ​etomidate), F (fentanyl ​+ ​etomidate), and D (dezocine ​+ ​etimidate). IoC was measured before anesthesia (T1), opioids (T2), etomidate (T3), the start of endoscopy (T4), drug withdrawal (T5), OAA/S ​> ​2 (T6), and OAA/S ​> ​4) (T7). The primary outcome was the observation of IoC at T6 and T7. The adverse reaction and recovery time were secondary outcomes.

Results

With 20 patients in each group, there were no differences in the operation and awakening times among the four groups (P ​> ​0.05). Compared with group C, the IoC values of groups S and F at T5, T6, and T7 were increased after drug administration (P ​< ​0.05), with intragroup differences (P ​< ​0.001). Compared with group C, the IoC values of groups S, F, and D were higher at T6 and T7 (PS-T6 ​= ​0.003, PF-T6 ​= ​0.013, PD-T6 ​= ​0.015; PS-T7 ​= ​0.015, PF-T7 ​= ​0.040, PD-T7 ​= ​0.028). There were differences in nausea and vomiting between groups D and C (PD-C ​= ​0.044) and myoclonus (PSCPF-C<0.001, and PD-C<0.001). SpO2 <90% (two cases in group S and one in group F) were observed.

Conclusion

IoC value has a good correlation with OAA/S score, which can accurately monitor the effect of etomidate combined with opioids on the depth of anesthesia of patients undergoing painless gastroscopic anesthesia.

Trial registration

ChiCTR, ChiCTR2000040927. Registered December 16, 2020 –Prospective registration, http://www.chictr.org.cn/ChiCTR2000040927.

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