Comparison of ciprofol-alfentanil and propofol-alfentanil sedation during bidirectional endoscopy: A prospective, double-blind, randomise d, controlle d trial

被引:7
作者
Zhang, Jiqiang [1 ]
Liu, Ruijuan [2 ,3 ]
Bi, Ruirui [2 ]
Li, Xia [2 ]
Xu, Mengjun [2 ]
Li, Lijuan [2 ,4 ]
Su, Yuxi [2 ]
Yan, Wenjun [2 ]
机构
[1] Zhengzhou Univ, Dept Anaesthesiol, Affiliated Hosp 3, Zhengzhou, Peoples R China
[2] Gansu Prov Hosp, Dept Anaesthesiol, 204 Dong Gang West Rd, Lanzhou 730030, Gansu, Peoples R China
[3] Ningxia Med Univ, Sch Clin Med, Yinchuan, Peoples R China
[4] Lanzhou Univ, Sch Clin Med 1, Lanzhou, Peoples R China
关键词
Alfentanil; Endoscopy; Propofol; INJECTION; MULTICENTER; LIDOCAINE; EMULSION; NEURONS; PAIN;
D O I
10.1016/j.dld.2023.09.016
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Although propofol is widely used for gastrointestinal endoscopic sedation, cardiopulmonary adverse events remain common. Ciprofol is a new intravenous anaesthetic agent demonstrating respiratory and hemodynamic stability. Aims: This study aimed to clarify the benefits of ciprofol combined with alfentanil in bidirectional endoscopy (esophagogastroduodenoscopy followed by colonoscopy) to reduce adverse events and improve post-endoscopic recovery. Methods: A total of 185 patients scheduled to undergo bidirectional endoscopy were randomly divided into two groups: ciprofol combined with alfentanil or propofol combined with alfentanil. All patients received 7 mu g/kg alfentanil intravenously before the study drugs were administered. The propofol group received a bolus of 1.2 mg/kg (0.12 ml/kg) propofol intravenously, whereas the ciprofol group received a bolus of 0.3 mg/kg (0.12 ml/kg) ciprofol intravenously. The primary outcome was the proportion of patients with cardiopulmonary adverse events (i.e., any one of the airway obstruction, apnoea, hypotension, hypertension, bradycardia, tachycardia or arrhythmias). Results: Compared with propofol, ciprofol reduced cardiopulmonary adverse events by 43.51 % (34.4% vs. 60.9 %, P < 0.001), mitigated respiratory adverse events by 54.74 % (17.2% vs. 38.0 %, P = 0.002) overall and by 59.05 % (12.9% vs. 31.5 %, P = 0.002) during the induction period. Conclusions: Ciprofol can significantly decrease respiratory depression events and provides a better sedative efficacy than propofol with higher recovery quality and satisfaction. (c) 2023 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:663 / 671
页数:9
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