Efficacy and safety of ciprofol versus propofol for anesthesia in patients undergoing gastrointestinal endoscope: a systematic review and meta-analysis of randomized controlled trials (RCT).

IF 2.3 3区 医学 Q2 ANESTHESIOLOGY
Zhaoxuan Wang, Siru Wang, Lu Liu, Xiaolu Zhang, Meijuan Ren, Qianqian Zhang, Chang Liu
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引用次数: 0

Abstract

Background: Ciprofol is considered an alternative to propofol and can be used to achieve anesthesia at a lower dose with a lower incidence of adverse events. The primary objective of this study was to compare the efficacy and safety of ciprofol and propofol used in patients undergoing gastrointestinal endoscopes.

Methods: The databases of PubMed, Embase, Cochrane Library, Web of Science, and China National Knowledge Infrastructure were retrieved for randomized controlled trials of ciprofol and propofol used in gastrointestinal endoscopes from inception to May 10, 2024. All statistical analyses were conducted using Stata 14.0. Primary outcomes encompassed a successful rate of sedation and other safety outcomes, including injection pain, hypotension, bradycardia, overall respiratory disorders, and hypoxemia. Secondary outcomes concluded time to onset of successful induction, waking time, and discharge time.

Results: A total of 20 studies were included, involving 3779 patients. The results of the meta-analysis showed that the successful rate of anesthesia and waking time were not significantly different between ciprofol and propofol, while ciprofol was better than propofol in injection pain (RR: 0.10, 95% CI: 0.07 to 0.16, p < 0.001, I2 = 46.4%, moderate certainty), hypotension (RR: 0.68, 95% CI: 0.59 to 0.77, p < 0.001, I2 = 49.2%, moderate certainty), bradycardia (RR: 0.67, 95% CI: 0.52 to 0.85, p = 0.001, I2 = 0.0%, moderate certainty), hypoxemia (RR: 0.45, 95% CI: 0.33 to 0.61, p < 0.001, I2 = 9.2%, moderate certainty), and overall respiratory disorders (RR: 0.45, 95% CI: 0.27 to 0.75, p < 0.001, I2 = 77.1%, moderate certainty). In addition, compared to propofol, shorter time to onset of successful induction (MD: -0.16, 95% CI: -0.24 to - 0.08, p < 0.001, I2 = 97.2%, very low certainty) and longer discharge time (MD: 0.420, 95% CI: 0.29 to 0.54, p < 0.001, I2 = 29.4%, moderate certainty) were related to ciprofol.

Conclusion: Based on the results of pooled analysis, we conclude that ciprofol takes longer for cipofol to recover after surgery, it may greatly improve the pain problem and hemodynamic stability of intravenous propofol. Therefore, we believe that ciprofol can be used as an excellent substitute for propofol.

环丙酚与异丙酚在胃肠内镜患者麻醉中的有效性和安全性:随机对照试验(RCT)的系统回顾和荟萃分析。
背景:环丙酚被认为是异丙酚的替代品,可以在较低剂量和较低不良事件发生率下实现麻醉。本研究的主要目的是比较环丙酚和异丙酚用于胃肠内窥镜患者的疗效和安全性。方法:检索PubMed、Embase、Cochrane Library、Web of Science、中国国家知识基础设施数据库,检索自成立至2024年5月10日胃肠道内窥镜中使用环丙酚和异丙酚的随机对照试验。所有统计分析均使用Stata 14.0进行。主要结局包括镇静成功率和其他安全性结局,包括注射疼痛、低血压、心动过缓、整体呼吸系统疾病和低氧血症。次要结局包括诱导成功开始时间、苏醒时间和出院时间。结果:共纳入20项研究,涉及3779例患者。荟萃分析的结果表明,麻醉和清醒时间的成功率没有显著不同ciprofol和异丙酚,而ciprofol比异丙酚注射痛(RR: 0.10, 95% CI: 0.07 ~ 0.16, p < 0.001, I2 = 46.4%,中度确定性),低血压(RR: 0.68, 95% CI: 0.59 ~ 0.77, p < 0.001, I2 = 49.2%,中度确定性),心动过缓(RR: 0.67, 95% CI: 0.52 ~ 0.85, p = 0.001, I2 = 0.0%,中度的确定性),血氧不足(RR: 0.45, 95%置信区间CI:0.33 ~ 0.61, p < 0.001, I2 = 9.2%,中等确定性)和整体呼吸系统疾病(RR: 0.45, 95% CI: 0.27 ~ 0.75, p < 0.001, I2 = 77.1%,中等确定性)。此外,与异丙酚相比,环丙酚与较短的诱导成功起始时间(MD: -0.16, 95% CI: -0.24 ~ - 0.08, p < 0.001, I2 = 97.2%,极低确定性)和较长的出院时间(MD: 0.420, 95% CI: 0.29 ~ 0.54, p < 0.001, I2 = 29.4%,中等确定性)相关。结论:综合分析结果,我们认为环丙酚可使环丙酚术后恢复时间较长,可大大改善静脉注射异丙酚的疼痛问题和血流动力学稳定性。因此,我们认为环丙酚可以作为异丙酚的优良替代品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Anesthesiology
BMC Anesthesiology ANESTHESIOLOGY-
CiteScore
3.50
自引率
4.50%
发文量
349
审稿时长
>12 weeks
期刊介绍: BMC Anesthesiology is an open access, peer-reviewed journal that considers articles on all aspects of anesthesiology, critical care, perioperative care and pain management, including clinical and experimental research into anesthetic mechanisms, administration and efficacy, technology and monitoring, and associated economic issues.
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