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右美托咪定联合舒芬太尼用于剖宫产术后静脉镇痛的效果:一项随机、安慰剂对照研究。

Effect of dexmedetomidine combined with sufentanil for post-caesarean section intravenous analgesia: a randomised, placebo-controlled study.

作者信息

Nie Yuyan, Liu Yuqi, Luo Qingyan, Huang Shaoqiang

机构信息

From the Department of Anesthesiology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.

出版信息

Eur J Anaesthesiol. 2014 Apr;31(4):197-203. doi: 10.1097/EJA.0000000000000011.

Abstract

BACKGROUND

Few studies have investigated the use of dexmedetomidine in obstetric anaesthesia.

OBJECTIVE

To evaluate the effect of dexmedetomidine combined with sufentanil for patient-controlled analgesia (PCA) after caesarean section under spinal anaesthesia.

DESIGN

An interventional, randomised, double-blinded, placebo-controlled clinical study.

SETTING

Department of Anaesthesiology, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China.

PATIENTS

One hundred and twenty parturients (American Society of Anesthesiologists class 1 or 2) scheduled for elective caesarean delivery under spinal anaesthesia randomly allocated into three groups (n = 40 each).

INTERVENTIONS

Group 1: physiological saline bolus after delivery and sufentanil PCA, Group 2: dexmedetomidine bolus (0.5 μg kg) after delivery and sufentanil PCA, Group 3: dexmedetomidine bolus (0.5 μg kg) after delivery and sufentanil with dexmedetomidine PCA (background infusion of 0.045 μg kg h with a bolus of 0.07 μg kg).

MAIN OUTCOME MEASURES

The total consumption of sufentanil. Pain scores at rest evaluated with a visual analogue scale (VAS) and Ramsay sedation score (RSS) were recorded at the 4, 8 and 24 h after surgery. The patients' pain threshold (PTh) and pain tolerance threshold (PTTh) were measured before surgery and 1 h after initial study drug administration. Satisfaction scores were collected 24 h after surgery.

RESULTS

Sufentanil consumption in group 3 was 43.9 ± 19.2 μg, significantly lower than in group 1 (54.5 ± 23.9 μg) and group 2 (56.3 ± 20.6 μg) (P < 0.05). Compared with group 3, VAS was increased at 4, 8 and 24 h after surgery in groups 1 and 2 (P < 0.05); there was no difference between groups 1 and 2. PTh and PTTh were significantly increased 1 h after drug administration in groups 2 (1.59 ± 0.45, 2.57 ± 0.46 mA) and 3 (1.74 ± 0.37, 2.56 ± 0.48 mA) compared with group 1 (1.49 ± 0.49, 2.42 ± 0.62 mA) (P < 0.05).

CONCLUSION

The combination of sufentanil and dexmedetomidine for PCA after caesarean section can reduce sufentanil consumption and improve parturients' satisfaction compared with sufentanil PCA alone.

TRIAL REGISTRATION

ChiCTR-TRC-11001442.

摘要

背景

很少有研究调查右美托咪定在产科麻醉中的应用。

目的

评估右美托咪定联合舒芬太尼用于腰麻下行剖宫产术后患者自控镇痛(PCA)的效果。

设计

一项干预性、随机、双盲、安慰剂对照的临床研究。

地点

中国上海复旦大学附属妇产科医院麻醉科。

患者

120例计划在腰麻下行择期剖宫产的产妇(美国麻醉医师协会分级为1或2级),随机分为三组(每组n = 40)。

干预措施

第1组:产后静脉推注生理盐水及舒芬太尼PCA;第2组:产后静脉推注右美托咪定(0.5μg/kg)及舒芬太尼PCA;第3组:产后静脉推注右美托咪定(0.5μg/kg)及舒芬太尼联合右美托咪定PCA(背景输注速率为0.045μg·kg⁻¹·h,单次推注剂量为0.07μg/kg)。

主要观察指标

舒芬太尼的总用量。术后4、8和24小时采用视觉模拟评分法(VAS)评估静息时疼痛评分及Ramsay镇静评分(RSS)。术前及首次研究用药后1小时测量患者的痛阈(PTh)和耐痛阈(PTTh)。术后24小时收集满意度评分。

结果

第3组舒芬太尼用量为43.9±19.2μg,显著低于第1组(54.5±23.9μg)和第2组(56.3±20.6μg)(P<0.05)。与第3组相比,第1组和第2组术后4、8和24小时的VAS升高(P<0.05);第1组和第

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