Petkar Shubham, Bele Amol, Priya Vishnu, Bawiskar Dushyant
Anaesthesiology, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.
Sports Medicine, Abhinav Bindra Targeting Performance, Bangalore, IND.
Cureus. 2024 Aug 28;16(8):e68034. doi: 10.7759/cureus.68034. eCollection 2024 Aug.
Ciprofol (HSK3486) is a novel intravenous anaesthetic developed as an alternative to propofol, offering a safer and more effective option in anaesthesia. It works primarily by modulating the gamma-aminobutyric acid (GABA) receptors in the central nervous system, leading to sedation and hypnosis. Ciprofol's unique pharmacological properties include a rapid onset of action, shorter duration, and reduced cardiovascular and respiratory depression compared to propofol, making it particularly suitable for outpatient and day surgery procedures. Molecular changes in ciprofol appear to be superior to those of other cibenzolines; it is more potent and has a stable hemodynamic effect. It has been used in primary surgery, inpatients and outpatients, and even for sedation of intensive care patients. The reported clinical data indicate that ciprofol is a powerful sedative that is characterised by a high-enough speed of emergence from the state of anaesthesia, which is necessary for outpatient conditions and intensive operating modes. It can be considered a new and important perspective in the technology of intravenous anaesthetics with its improved pharmacological characteristics and clinical effects. With the further accumulation of clinical data, ciprofol will undeniably become an essential agent in today's anaesthetic practice and contribute to an enhancement of healthcare efficiency by providing a more secure approach to numerous kinds of surgical interventions. The purpose of the current study is to provide a review of the pharmacology and clinical use of ciprofol, a new intravenous anaesthetic agent. Various studies demonstrate the functionality and safety profile of ciprofol, which solidifies it as a potential contender for propofol. Regarding respiratory depression, hypoxemia, and injection pain during hysteroscopy, ciprofol was shown to be a relatively safer option than propofol. Ciprofol can, therefore, be recommended for intravenous anaesthesia because of its effectiveness and safety, which has been clearly demonstrated. Randomised trials uniformly report the ability to achieve quicker onset of sedation and lower risk with the agent compared to propofol. These findings imply that ciprofol has many benefits concerning a variety of applications in patients due to a lower rate of adverse reactions and increased patient comfort.
环泊酚(HSK3486)是一种新型静脉麻醉药,作为丙泊酚的替代品开发,在麻醉中提供了更安全、更有效的选择。它主要通过调节中枢神经系统中的γ-氨基丁酸(GABA)受体起作用,从而导致镇静和催眠。与丙泊酚相比,环泊酚独特的药理特性包括起效迅速、作用时间短以及心血管和呼吸抑制作用减轻,这使其特别适用于门诊手术和日间手术。环泊酚的分子变化似乎优于其他西苯唑啉类药物;它更强效且具有稳定的血流动力学效应。它已用于初次手术、住院患者和门诊患者,甚至用于重症监护患者的镇静。报道的临床数据表明,环泊酚是一种强效镇静剂,其特点是从麻醉状态苏醒的速度足够快,这对于门诊手术条件和高强度手术模式是必要的。由于其改善的药理特性和临床效果,它可被视为静脉麻醉技术中的一个新的重要视角。随着临床数据的进一步积累,环泊酚无疑将成为当今麻醉实践中的一种重要药物,并通过为多种手术干预提供更安全的方法来提高医疗效率。本研究的目的是对新型静脉麻醉药环泊酚的药理学和临床应用进行综述。各种研究证明了环泊酚的功能和安全性,这使其成为丙泊酚的潜在竞争者。在宫腔镜检查期间的呼吸抑制、低氧血症和注射疼痛方面,环泊酚被证明是比丙泊酚相对更安全的选择。因此,由于环泊酚的有效性和安全性已得到明确证明,可推荐用于静脉麻醉。随机试验一致报告,与丙泊酚相比,该药物能更快起效镇静且风险更低。这些发现意味着,由于不良反应发生率较低且患者舒适度提高,环泊酚在患者的各种应用中具有许多益处。