低剂量右美托咪定降低异丙酚对宫腔镜手术患者身体运动抑制的剂量要求。

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2025-02-18 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S503538
Xu-Feng Zhang, Fei Xiao, Ying-Ying Lou, Ke-Wei Wu, Jing Qian, Guo-Wei Zhu
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引用次数: 0

摘要

背景:右美托咪定是一种中枢α-2肾上腺素能激动剂,具有镇静、镇痛和解交感神经的特性。我们研究了低剂量右美托咪定对手术宫腔镜患者异丙酚镇静的剂量-反应关系的影响。方法:将患者随机分为丙泊酚+芬太尼组(P组,n = 100)和丙泊酚+右美托咪定+芬太尼组(DP组,n = 100)。随后,参与者进一步随机接受1.0、1.5、2.0和2.5 mg/kg剂量的异丙酚P组,0.5、1.0、1.5和2.0 mg/kg剂量的DP组。本研究的主要结局是达到异丙酚有效剂量的患者的发生率,定义为患者在宫颈扩张期间没有身体运动且BIS值低于60的剂量。采用Probit法计算异丙酚在宫腔镜手术中对宫颈扩张体运动反应的抑制作用ED50和ED95。结果:P组异丙酚抑制宫腔镜手术中宫颈扩张体运动反应的ED50和ED95值分别为1.781 (95% CI 1.507~2.118)和4.670 (95% CI 3.555~7.506) mg/kg;DP组分别为0.983 (95% CI 0.800~1.173)和2.578 (95% CI 2.013~3.895) mg/kg。结论:低剂量右美托咪定(0.5μg/kg)可降低手术宫腔镜患者对异丙酚的体运动抑制需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low-Dose Dexmedetomidine Attenuates the Dose Requirement of Propofol for Suppression of Body Movement in Patients Undergoing Operative Hysteroscopy.

Background: Dexmedetomidine is a central α-2 adrenergic agonist characterized by its sedative, analgesic, and sympatholytic properties. We investigated the effect of low dose dexmedetomidine on the dose-response relationship of propofol for sedation in patients undergoing operative hysteroscopy.

Methods: The patients were firstly randomly assigned to receive either propofol and fentanyl (P group, n = 100) or a combination of propofol, dexmedetomidine, and fentanyl (DP group, n = 100). Subsequently, participants were further randomized to receive propofol at doses of 1.0, 1.5, 2.0, and 2.5 mg/kg in P group, and 0.5, 1.0, 1.5, and 2.0 mg/kg in DP group. The primary outcome of this study was the incidence of patients achieving effective propofol dose, defined as the dosage at which a patient exhibited no body movement during cervical dilation and had a BIS value below60. The Probit method was used to calculate the ED50 and ED95 of propofol in the inhibition of body movement reaction to cervical dilation during hysteroscopic surgery.

Results: The ED50 and ED95 values for propofol in the inhibition of body movement reaction to cervical dilation during hysteroscopic surgery were 1.781 (95% CI 1.507~2.118) and 4.670 (95% CI 3.555~7.506) mg/kg, respectively, in P group; while in the DP group, these values were found to be 0.983 (95% CI 0.800~1.173) and 2.578 (95% CI 2.013~3.895) mg/kg.

Conclusion: Low-dose dexmedetomidine (0.5μg/kg) could reduce the requirement of propofol for suppression of body movement in patients undergoing operative hysteroscopy.

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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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