芬太尼对老年女性患者雷马唑仑镇静有效剂量的影响:一项上下顺序分配试验。

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2024-08-22 eCollection Date: 2024-01-01 DOI:10.2147/DDDT.S473662
Xiao-Dong Huang, Jia-Bao Chen, Xiao-Yun Dong, Wei-Long Wang, Jin Zhou, Zhen-Feng Zhou
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引用次数: 0

摘要

目的:本研究旨在探讨芬太尼对接受全身麻醉的老年女性患者中瑞马唑仑诱导镇静有效剂量的影响:将接受选择性全身麻醉的 60 名 65-80 岁女性患者随机分为两组:R+F 组接受初始剂量的雷马唑仑(7.5 毫克)和芬太尼(1 微克/千克),而 R 组仅接受雷马唑仑。剂量调整(±2.5 毫克)是根据前一位患者的反应采用上下分配技术进行的。ED50 和 ED95 是通过顺序公式和概率回归计算得出的。Probit 回归法还用于评估各组之间雷马唑仑的相对效力。镇静水平采用改良观察者警觉性/镇静评估(MOAA/S)量表进行评估:结果:与 R 组相比,R+F 组瑞马唑仑的 ED50 明显较低(p= 0.007)。根据 Probit 回归估算,R+F 组的 ED50 和 ED95 值分别为 4.878 毫克(95% CI,3.845-5.859)和 8.184 毫克(95% CI,6.636-13.546)。相比之下,R 组的 ED50 和 ED95 值分别为 6.733 毫克(95% CI,5.533-8.068)和 11.298 毫克(95% CI,9.101-19.617):本研究提供了令人信服的证据,证明在老年患者的诱导过程中,使用 1 μg/kg 芬太尼可将所需的瑞马唑仑镇静剂量显著减少约 30%。重要的是,同时使用 1 μg/kg 芬太尼不会增加低血压、呼吸抑制等不良反应的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Impact of Fentanyl on the Effective Dose of Remimazolam-Induced Sedation in Elderly Female Patients: An Up-and-Down Sequential Allocation Trial.

Purpose: This study aimed to investigate the influence of fentanyl on the effective dose of remimazolam-induced sedation in elderly female patients undergoing general anesthesia.

Patients and methods: Sixty female patients aged 65-80 years undergoing selective general anesthesia were randomized into two groups: Group R+F received an initial dose of remimazolam (7.5 mg) with fentanyl (1 μg/kg), while Group R received remimazolam alone. Dosing adjustments (±2.5 mg) were made based on the response of the preceding patient using the up-and-down allocation technique. The ED50 and ED95 were calculated using a sequential formula and probit regression. Probit regression was also used to assess the relative potency of remimazolam between groups. Sedation levels were evaluated using the Modified Observer's Assessment of Alertness/Sedation (MOAA/S) scale.

Results: The ED50 for remimazolam was significantly lower in Group R+F compared to Group R (p= 0.007). Probit regression estimated the ED50 and ED95 values for Group R+F at 4.878 mg (95% CI, 3.845-5.859) and 8.184 mg (95% CI, 6.636-13.546), respectively. In contrast, Group R demonstrated ED50 and ED95 values of 6.733 mg (95% CI, 5.533-8.068) and 11.298 mg (95% CI, 9.101-19.617), respectively.

Conclusion: This study provides compelling evidence that the administration of 1 μg/kg of fentanyl significantly reduces the required sedative dose of remimazolam by approximately 30% during induction in elderly patients. Importantly, the concomitant use of 1 μg/kg of fentanyl does not increase the risk of adverse effects such as hypotension, respiratory depression.

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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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