Minimum Local Anesthetic Dose of Ropivacaine in Cesarean Section for Real-Time Ultrasound-Guided Spinal Anesthesia Using 24-Gauge versus 26-Gauge Needles Based on Fluid Simulation Technology: A Randomized Controlled Trial.

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL Drug Design, Development and Therapy Pub Date : 2024-10-01 eCollection Date: 2024-01-01 DOI:10.2147/DDDT.S476710
Chunying Zheng, Hanliang Fan, Peng Ye, Xing Zhang, Xiaochun Zheng, Ting Zheng
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Abstract

Purpose: Previous research has demonstrated that real-time ultrasound-guided (UG) spinal anesthesia requires a higher minimum local anesthetic dose (MLAD) compared to traditional methods. However, the precise MLAD of ropivacaine for UG cesarean sections remains undetermined. In this study, we ascertained the MLAD of ropivacaine for cesarean section. We also investigated the mechanism underlying the diffusion of ropivacaine within the spinal canal using fluid simulation technology.

Patients and methods: We randomly placed 60 healthy parturients undergoing elective cesarean section with real-time UG spinal anesthesia into Groups I (26-gauge spinal needle) and II (24-gauge spinal needle). For the first parturient in both groups, 15 mg of ropivacaine was administered intrathecally. Based on the effective or ineffective response of the previous parturient, the dose for the subsequent parturient was increased or decreased by 1 mg. Spinal anesthesia characteristics and side effects were recorded. A computer-generated spinal canal model was developed. Leveraging fluid dynamics simulation technology, we documented the diffusion of ropivacaine in the spinal canal using 26-and 24-gauge spinal needles.

Results: The MLADs in Groups I and II were 12.728 mg (12.339-13.130 mg) and 9.795 mg (9.491-10.110 mg), respectively. No significant difference was observed in the onset times and durations of sensory or motor blocks, incidence of complications, or neonatal Apgar scores between both groups. Fluid simulation modeling indicated that the 26-gauge spinal needle achieved a higher distribution level more quickly; however, its peak drug concentration was lower compared to the 24-gauge spinal needle.

Conclusion: For cesarean section anesthetization, the required MLAD of ropivacaine when using a real-time UG 26-gauge spinal needle is significantly greater than that with a 24-gauge needle. The spinal needle diameter influences ropivacaine's MLAD by markedly affecting its diffusion rate within the spinal canal.

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基于流体模拟技术的剖宫产手术中使用 24 号针头与 26 号针头进行实时超声引导脊柱麻醉的罗哌卡因最小局麻药剂量:随机对照试验。
目的:先前的研究表明,与传统方法相比,实时超声引导(UG)脊髓麻醉需要更高的最小局麻药剂量(MLAD)。然而,用于 UG 剖宫产术的罗哌卡因的精确 MLAD 仍未确定。在本研究中,我们确定了罗哌卡因在剖宫产术中的最小局麻药剂量。我们还利用流体模拟技术研究了罗哌卡因在椎管内扩散的机制:我们将 60 名接受择期剖宫产手术的健康产妇随机分为 I 组(26 号椎管针)和 II 组(24 号椎管针)。两组的第一名产妇均鞘内注射了 15 毫克罗哌卡因。根据前一位产妇的有效或无效反应,后一位产妇的剂量增加或减少 1 毫克。记录脊髓麻醉的特点和副作用。开发了计算机生成的椎管模型。利用流体动力学模拟技术,我们用26号和24号椎管针记录了罗哌卡因在椎管内的扩散情况:结果:第一组和第二组的 MLAD 分别为 12.728 毫克(12.339-13.130 毫克)和 9.795 毫克(9.491-10.110 毫克)。两组在感觉或运动阻滞的发生时间和持续时间、并发症发生率或新生儿阿普加评分方面均无明显差异。流体模拟模型显示,26 号脊柱针能更快地达到较高的分布水平,但与 24 号脊柱针相比,其峰值药物浓度较低:结论:在剖腹产麻醉中,使用实时 UG 26 号脊柱针所需的罗哌卡因 MLAD 明显高于使用 24 号针时的 MLAD。椎管针直径会明显影响罗哌卡因在椎管内的扩散速度,从而影响其 MLAD。
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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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