罗哌卡因与布比卡因在先兆子痫患者脊髓诱发低血压中的比较:随机对照试验

Q2 Medicine
Morteza Hashemian, Mohsen Barouni, Zahra Honarvar, K. Alidousti, Seyed Amirabbas Mohajerani, Leila Rezaeizadeh
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引用次数: 0

摘要

背景:脊髓麻醉被认为是子痫前期患者剖宫产手术中最安全的麻醉方法。先兆子痫患者在脊髓麻醉后出现严重低血压的风险会增加,这可能会对胎儿和母亲产生更深远和有害的影响。然而,布比卡因作为最常用的药物,即使剂量较低也会诱发严重低血压。本研究的目的是尽量减少母亲和胎儿在椎管内麻醉后出现低血压。研究目的确定并比较罗哌卡因组和布比卡因组对子痫前期患者脊髓麻醉后低血压的缓解程度。方法在一项随机临床试验中,共招募了 90 名接受脊髓麻醉的子痫前期孕妇,并将其随机分为两组:一组接受罗哌卡因,另一组接受布比卡因。脊髓罗哌卡因剂量为15毫克0.5%溶液,布比卡因剂量也为15毫克0.5%溶液。脊髓麻醉后记录了血液动力学参数,包括收缩压、舒张压和心率。此外,还记录了疼痛评分和运动恢复时间。结果统计分析采用 t 检验、卡方检验和方差分析对各组进行比较。两组产妇的年龄、孕龄、胎次和胎龄等人口统计学变量无显著差异。在研究的所有测量时间点,布比卡因组的平均收缩压(SBP)都明显低于罗哌卡因组(P < 0.05)。与布比卡因组相比,罗哌卡因组在脊髓麻醉后 2 分钟和 4 分钟的麻黄碱用量明显不同(P = 0.012,P = 0.025)。术后 1 小时恢复期的疼痛评分在罗哌卡因组和布比卡因组之间无明显差异(P = 0.015)。罗哌卡因组与布比卡因组相比,膝关节活动时间也明显缩短(P < 0.001)。结论与布比卡因相比,罗哌卡因可降低子痫前期患者剖宫产脊髓麻醉中低血压的发生率。这归因于脊麻引起的低血压发生率较低、血流动力学控制得到改善、麻黄碱用量减少以及患者下床活动更快。今后的研究可重点研究两种药物的不同剂量,并增加参与人数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of Ropivacaine versus Bupivacaine in Spinal-Induced Hypotension in Preeclampsia Patients: A Randomized Control Trial
Background: Spinal anesthesia is considered to be the safest method of anesthesia for cesarean sections in patients with preeclampsia. Patients with preeclampsia are at an increased risk of experiencing severe hypotension following spinal anesthesia, which could have more profound and deleterious effects on both the fetus and the mother. However, bupivacaine, the most commonly used drug, can induce severe hypotension even at low doses. The purpose of this study is to minimize post-spinal hypotension in both the mother and the fetus. Objectives: To determine and compare the reduction in hypotension following spinal anesthesia in patients with preeclampsia between the ropivacaine and bupivacaine groups. Methods: In a randomized clinical trial, a total of 90 parturients with preeclampsia undergoing spinal anesthesia were enrolled and randomly divided into 2 groups: One receiving ropivacaine and the other receiving bupivacaine. The dose of spinal ropivacaine was 15 mg of a 0.5% solution, and the dose of bupivacaine was also 15 mg of a 0.5 % solution. Hemodynamic parameters, including systolic and diastolic blood pressure and heart rate, were recorded following the administration of spinal anesthesia. Pain scores and the time until the return of motor movement were also documented. Results: For statistical analysis, the t-test, Chi-square, and ANOVA tests were utilized to compare the groups. Demographic variables, including maternal age, gestational age, parity, and gravidity, were not significantly different between the 2 groups. The trend of mean systolic blood pressure (SBP) was significantly lower in the bupivacaine group compared to the ropivacaine group at all measured time points in the study (P < 0.05). The amount of ephedrine used after spinal anesthesia was significantly different at 2 and 4 minutes in the ropivacaine group compared to the bupivacaine group (P = 0.012, P = 0.025). Post-operative pain scores at 1 hour in recovery were not significantly different between the ropivacaine and bupivacaine groups (P = 0.015). The time to knee movement was also significantly shorter in the ropivacaine group compared to the bupivacaine group (P < 0.001). Conclusions: Ropivacaine reduces the incidence of hypotension in spinal anesthesia compared to bupivacaine for cesarean section in patients with preeclampsia. This is attributed to a lower occurrence of spinal-induced hypotension, improved hemodynamic control, reduced ephedrine usage, and faster patient ambulation. A future study could focus on investigating different dosages of both drugs with a larger number of participants.
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Anesthesiology and Pain Medicine
Anesthesiology and Pain Medicine Medicine-Anesthesiology and Pain Medicine
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4.60
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