The Recovery of Ciprofol, Remimazolam and Remimazolam-Flumazenil for General Anesthesia Undergoing Fundus Surgery: A Single-Center, Prospective, Randomized, Controlled Clinical Study.

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2025-05-05 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S512431
Shuang Zhang, Yunfei Liu, Yanyu Liu, Ting Xu
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引用次数: 0

Abstract

Purpose: Ciprofol (HSK3486 injectable emulsion) is a 2.6-disubstituted phenol derivative that acts similarly to propofol with a fast onset, quick, and stable recovery. Moreover, remimazolam is a new benzodiazepine with a faster onset and recovery than midazolam, and more stable hemodynamics than propofol. We found no relevant literature that directly compared these two drugs. The primary objective of this study was to compare the recovery of HSK3486 with that of remimazolam during successful general anesthesia.

Patients and methods: This prospective, randomized, double-blind study included 93 patients who had undergone fundus surgery. The patients were divided into three groups: HSK3486 (H group), remimazolam-saline (RS group), and remimazolam-flumazenil (RF group). The primary outcome was the time from drug withdrawal to eye opening, and the secondary outcome was the time from drug withdrawal to laryngeal mask removal, the time for Aldrete modified score ≥ 9, intraoperative hemodynamic changes, post-operative adverse events (nausea, vomiting, pain, delirium, re-sedation), and the Quality of Recovery-15 score before surgery and at 1, 7, and 14 days post-operatively.

Results: The RF group showed the shortest eye-opening time: 3.8 (2.8) min vs 13.3 (5.2) min for the H group, P < 0.001; and 11.5 (5.5) min for the RS group, P < 0.001. And laryngeal mask removal time was 5.2 (3.1) min for the RF group vs 14.1 (5.2) min for the H group, P < 0.001; and 12.4 (5.5) min for the RS group, P < 0.001. There were no significant differences in other post-operative outcomes.

Conclusion: The incorporation of flumazenil with remimazolam for total intravenous anesthesia provided rapid and reliable recovery of consciousness, although there were no significant visible differences between HSK3486 and Remimazolam-saline.

环丙酚、雷马唑仑和雷马唑仑-氟马西尼用于全麻眼底手术的恢复:一项单中心、前瞻性、随机对照临床研究。
目的:环丙酚(HSK3486注射用乳剂)是一种2.6双取代苯酚衍生物,作用类似于异丙酚,起效快,恢复快,稳定。雷马唑仑是一种新型苯二氮卓类药物,比咪达唑仑起效和恢复更快,血流动力学比异丙酚更稳定。我们没有发现直接比较这两种药物的相关文献。本研究的主要目的是比较HSK3486和雷马唑仑在成功全身麻醉期间的恢复情况。患者和方法:这项前瞻性、随机、双盲研究纳入了93例接受过眼底手术的患者。患者分为HSK3486组(H组)、雷马唑仑-生理盐水组(RS组)、雷马唑仑-氟马西尼组(RF组)。主要观察指标为停药至睁眼时间,次要观察指标为停药至取喉罩时间,Aldrete修正评分≥9的时间,术中血流动力学变化,术后不良事件(恶心、呕吐、疼痛、谵妄、再镇静),术前及术后1、7、14天恢复质量-15评分。结果:RF组睁眼时间最短,分别为3.8 (2.8)min和13.3 (5.2)min, P < 0.001;RS组为11.5 (5.5)min, P < 0.001。取喉罩时间RF组为5.2 (3.1)min, H组为14.1 (5.2)min, P < 0.001;RS组为12.4 (5.5)min, P < 0.001。其他术后结果无显著差异。结论:氟马西尼联合雷马唑仑全静脉麻醉可快速可靠地恢复意识,但HSK3486与雷马唑仑生理盐水间无明显差异。
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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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