Combined Use of Remimazolam and Ciprofol Reduces Hypoxemia and Shortens Recovery Time During Sedated Gastrointestinal Endoscopy.

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2025-05-06 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S515783
Hai-Ding Zou, Cong Luo, Zhao-Lan Hu, Pei Zhou, Ru-Yi Luo
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引用次数: 0

Abstract

Background: Hypoxemia is the most common adverse event during painless gastrointestinal endoscopy (PGIE). This study aimed to evaluate whether the combined use of remimazolam besylate and ciprofol (group RC) reduces the incidence of hypoxemia compared to ciprofol alone (group C) in patients undergoing PGIE under deep sedation.

Methods: A total of 246 patients scheduled for PGIE were recruited from the Second Xiangya Hospital of Central South University and randomly assigned to group C or RC. The primary outcome measured was the incidence of intraoperative hypoxemia. Secondary outcomes included physiological parameters such as blood pressure, heart rate, and oxygen saturation (SpO2) during the procedure, along with time to loss of consciousness (LoC), time to awakening, and major adverse effects (MAEs). Additionally, correlations between minimum SpO2 and factors like body mass index (BMI), age, and preoperative SpO2 were examined.

Results: Group C exhibited a significantly higher incidence and frequency of hypoxemia compared to group RC. Correlation analysis revealed that minimum SpO2 was inversely related to age and BMI, while showing a positive correlation with preoperative SpO2. Additionally, the RC group demonstrated significantly decreased induction and shorter times to LoC and awakening than group C.

Conclusion: The combined administration of ciprofol and remimazolam besylate may enhance the safety profile of deep sedation for PGIE compared to ciprofol alone, offering reduced hypoxemia incidence and improved procedural efficiency.

Trial registration: www.chictr.org.cn (Registration number: ChiCTR2400092506, Registration date: November 18, 2024).

联合使用雷马唑仑和环丙酚减少低氧血症和缩短恢复时间镇静胃肠道内镜检查。
背景:低氧血症是无痛胃肠内镜检查(PGIE)中最常见的不良事件。本研究旨在评估在深度镇静下,与单独使用环丙酚(C组)相比,联合使用贝磺酸雷马唑仑和环丙酚(RC组)是否能降低PGIE患者低氧血症的发生率。方法:从中南大学湘雅第二医院招募246例PGIE患者,随机分为C组和RC组。测量的主要结果是术中低氧血症的发生率。次要结局包括生理参数,如手术过程中的血压、心率和血氧饱和度(SpO2),以及意识丧失时间(LoC)、苏醒时间和主要不良反应(MAEs)。此外,还检查了最低SpO2与体重指数(BMI)、年龄和术前SpO2等因素之间的相关性。结果:C组低氧血症的发生率和频率明显高于RC组。相关分析显示,最低SpO2与年龄、BMI呈负相关,与术前SpO2呈正相关。此外,RC组的诱导作用明显降低,LoC和苏醒时间比c组短。结论:与单独使用环丙酚相比,环丙酚和苯磺酸雷马唑仑联合使用可提高PGIE深度镇静的安全性,降低低氧血症发生率,提高手术效率。试验注册:www.chictr.org.cn(注册号:ChiCTR2400092506,注册日期:2024年11月18日)。
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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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