首页> 美国卫生研究院文献>International Journal of Clinical and Experimental Medicine >Hyperbaric spinal anesthesia with ropivacaine coadministered with sufentanil for cesarean delivery: a dose-response study
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Hyperbaric spinal anesthesia with ropivacaine coadministered with sufentanil for cesarean delivery: a dose-response study

机译:罗哌卡因与舒芬太尼联合应用高压脊髓麻醉进行剖宫产的剂量反应研究

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摘要

Adjuvant sufentanil could achieve effective spinal anesthesia with low dose of hyperbaric ropivacaine for cesarean delivery. Two previous studies had calculated the 50% effective dose (ED50) of intrathecal ropivacaine coadministered with sufentanil for cesarean delivery. However, the 95% effective dose (ED95) of intrathecal hyperbaric ropivacaine coadministered with sufentanil for cesarean delivery remains uncertain. This study determined the ED95 of intrathecal hyperbaric ropivacaine coadministered with sufentanil for cesarean delivery. 80 ASA physical status I or II parturients undergoing elective cesarean delivery were enrolled in this prospective, randomized, double-blind investigation. A combined spinal and epidural anesthesia was performed at the L3-L4 interspace. Patients received a dose of spinal ropivacaine coadministered with sufentanil 5 μg diluted to 3.0 ml with normal saline and 0.5 ml of 10% dextrose: 7.5 mg (n = 20), 9.0 mg (n = 20), 10.5 mg (n = 20), or 12 mg (n = 20). An effective dose was defined as a dose that provided bilateral sensory block to T7 within 10 min after intrathecal drug administration and required no epidural top-up for surgery to be completed. The ED50 and ED95 values for successful anesthesia were determined using a logistic regression model. The ED50 (95% confidence interval [CI]) for successful anesthesia was 8.4 (4.0-9.8) mg and the ED95 (95% CI) was 11.4 (9.7-13.9) mg. The results show that the ED95 of intrathecal hyperbaric ropivacaine coadministered with sufentanil 5 μg for cesarean delivery was 11.4 mg. The addition of sufentanil could significantly reduce the dosage of ropivacaine.
机译:舒芬太尼佐剂可通过小剂量高压罗哌卡因用于剖宫产,实现有效的脊柱麻醉。先前的两项研究计算了鞘内罗哌卡因与舒芬太尼联合剖宫产的50%有效剂量(ED50)。然而,鞘内高压罗哌卡因与舒芬太尼联合用于剖宫产的95%有效剂量(ED95)仍不确定。这项研究确定鞘内高压罗哌卡因与舒芬太尼联合剖宫产的ED95。在这项前瞻性,随机,双盲研究中,选择了80名接受择期剖宫产的ASA身体状况I或II产妇。在L3-L4间隙进行脊髓和硬膜外联合麻醉。患者接受一定剂量的罗哌卡因与5克舒芬太尼联合稀释至3.0毫升生理盐水和0.5毫升10%右旋糖共同给药:7.5毫克(n = 20),9.0毫克(n = 20),10.5毫克(n = 20)或12毫克(n = 20)。有效剂量定义为在鞘内注射药物后10分钟内可提供双侧感觉阻滞至T7且不需要硬膜外充注即可完成手术的剂量。使用逻辑回归模型确定成功麻醉的ED50和ED95值。成功麻醉的ED50(95%置信区间[CI])为8.4(4.0-9.8)mg,ED95(95%CI)为11.4(9.7-13.9)mg。结果显示,鞘内高压罗哌卡因与舒芬太尼5μg联合剖宫产的ED95为11.4 mg。舒芬太尼的添加可以显着减少罗哌卡因的剂量。

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