去甲肾上腺素或苯肾上腺素预防剖宫产术中脊柱麻醉引起的低血压:一项胎儿脑灌注的双盲、随机、对照研究。

IF 5.1 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2025-09-02 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S535671
Jinping Liu, Zhimin Sheng, Feihe Guo, Xiao Lin, Li Xu, Lihong Sun, Xiaowei Qian
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引用次数: 0

摘要

目的:脊髓麻醉诱导的低血压对母亲和胎儿都有不利影响,这是产科麻醉中一个值得关注的问题。血管加压药的使用被认为是最可靠和有效的方法。先前的研究表明,去甲肾上腺素在维持产妇心率和心输出量方面似乎优于苯肾上腺素。因此,我们假设去甲肾上腺素比苯肾上腺素更有效地维持新生儿脑灌注,以防止脊髓麻醉引起的低血压。患者和方法:本研究是一项前瞻性、双盲、随机试验。我们招募了216名计划择期剖宫产的单胎产妇。患者预防性静脉输注去甲肾上腺素(0.08 μg/kg/min)或苯肾上腺素(0.5 μg/kg/min)。在研究期间,未对母体心输出量进行常规监测。行胎儿超声检查,测定大脑中动脉和脐动脉血流速度,计算脑胎盘比。结果:每组最终分析90例受试者。两组脊髓麻醉后3、6分钟大脑中动脉、脐动脉血流速度变化及计算的脑胎盘比差异无统计学意义。两组的ΔCPR在3分钟时的估计差异为-0.01 (95% CI, -0.05-0.02, P = 0.491),在6分钟时的估计差异为0.02 (95% CI, -0.01-0.07, P = 0.204)。结论:预防性输注同等剂量的去甲肾上腺素或苯肾上腺素对胎儿脑灌注的影响相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Norepinephrine or Phenylephrine to Prevent Spinal Anesthesia-Induced Hypotension During Cesarean Section: A Double-Blinded, Randomized, Controlled Study of Fetal Cerebral Perfusion.

Norepinephrine or Phenylephrine to Prevent Spinal Anesthesia-Induced Hypotension During Cesarean Section: A Double-Blinded, Randomized, Controlled Study of Fetal Cerebral Perfusion.

Norepinephrine or Phenylephrine to Prevent Spinal Anesthesia-Induced Hypotension During Cesarean Section: A Double-Blinded, Randomized, Controlled Study of Fetal Cerebral Perfusion.

Purpose: Spinal anesthesia-induced hypotension can cause detrimental effects on both the mother and the fetus, and it remains a significant concern in obstetric anesthesia. The use of vasopressors is considered the most reliable and effective approach. Previous studies have shown that norepinephrine appears to be superior to phenylephrine in maintaining maternal heart rate and cardiac output. Therefore, we hypothesize that norepinephrine is more effective than phenylephrine in maintaining neonatal cerebral perfusion when used to prevent spinal anesthesia-induced hypotension.

Patients and methods: This study is a prospective, double-blinded, randomized trial. We enrolled 216 singleton parturients who were scheduled for elective cesarean delivery. The patients received a prophylactic intravenous infusion of either norepinephrine (0.08 μg/kg/min) or phenylephrine (0.5 μg/kg/min). Maternal cardiac output was not routinely monitored during the study period. Fetal ultrasound examinations were performed, with blood velocity measured in the middle cerebral artery and umbilical artery, and the cerebroplacental ratio calculated.

Results: Ninety subjects were ultimately analyzed in each group. The changes in blood velocity in the middle cerebral artery and umbilical artery, as well as the calculated cerebroplacental ratio at 3 and 6 minutes after spinal anesthesia, did not differ significantly between the two groups. The estimated difference of ΔCPR in two groups was - 0.01 (95% CI, -0.05-0.02, P = 0.491) at 3 minutes and was 0.02 (95% CI, -0.01-0.07, P = 0.204) at 6 minutes.

Conclusion: Prophylactic infusion of norepinephrine or phenylephrine at comparable doses has similar effects on fetal cerebral perfusion.

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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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