Habibi Ali, Alipour Abbas, Baradari Afshin Gholipour, Gholinataj Abdolmajid, Habibi Mohammad Reza, Peivandi Saloumeh
Student Research Committee, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Department of Epidemiology, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Open Access Maced J Med Sci. 2019 Jun 26;7(12):1946-1950. doi: 10.3889/oamjms.2019.545. eCollection 2019 Jun 30.
Caesarean section is one of the commonest gynaecological surgeries.
Given the importance of pain relief after caesarean section surgery as well as contradictions in the studies conducted on intravenous lidocaine analgesic effects, this study aimed to evaluate the effect of adding lidocaine to patient-controlled analgesia (PCA) with morphine on pain intensity after caesarean section surgery.
In a double-blinded, randomised clinical trial, 80 women who were scheduled for caesarean section surgery with spinal anaesthesia at Sari Imam Khomeini Hospital in 2017 were randomly assigned into two intervention and control groups. After surgery, all patients were connected to a morphine PCA pump. The PCA solution (total volume = 100 ml) in intervention group contained 50 ml of 2% lidocaine and 30 mg (3 ml) of morphine in 47 ml normal saline. In the control group, the PCA pump contained 30 mg (3 ml) of morphine, and the rest (97 cc) was normal saline. Patients' pain intensity was assessed at 2, 4, 6, 12, 18 and 24 hours after surgery using a visual analogue scale (VAS). Additionally, their postoperative nausea and vomiting, duration of hospitalisation, duration of ileus relapse after surgery, and patients' satisfaction after surgery were evaluated. Data were analysed using SPSS version 22 software.
The mean and standard deviation of pain intensity in all patients at the intervals of 2, 4, 6, 12, 18 and 24 hours after surgery were 5.91 ± 1.57, 4.97 ± 1.55, 3.84 ± 1.60, 3.54 ± 1.45, 2.56 ± 1.70 and 0.94 ± 1.70, respectively. Data analysis revealed that, regardless of the groups, postoperative pain intensity significantly decreased (P < 0.0001). However, there were no significant differences between the two groups in terms of mean postoperative pain intensity at any time interval (p > 0.05). Also, there was no significant difference between the two groups in terms of frequency of receiving the diclofenac suppositories after the surgery (p > 0.05). Additionally, there was no statistically significant difference between the two groups in terms of postoperative nausea and vomiting, duration of hospitalisation, duration of postoperative ileus relapse and patients' satisfaction (p > 0.05).
Based on the results of this study, it seems that adding lidocaine to PCA with morphine, compared with morphine PCA alone, do not have a significant effect on reducing the pain intensity after cesarean section using spinal anaesthesia. Although, further studies with larger sample size are warranted.
剖宫产是最常见的妇科手术之一。
鉴于剖宫产术后疼痛缓解的重要性以及关于静脉注射利多卡因镇痛效果的研究存在矛盾,本研究旨在评估在吗啡自控镇痛(PCA)中添加利多卡因对剖宫产术后疼痛强度的影响。
在一项双盲随机临床试验中,2017年在萨里伊玛目霍梅尼医院计划接受腰麻剖宫产手术的80名女性被随机分为两个干预组和对照组。手术后,所有患者均连接到吗啡PCA泵。干预组的PCA溶液(总体积 = 100 ml)包含50 ml 2%利多卡因和30 mg(3 ml)吗啡,溶入47 ml生理盐水中。对照组的PCA泵包含30 mg(3 ml)吗啡,其余(97 cc)为生理盐水。使用视觉模拟量表(VAS)在术后2、4、6、12、18和24小时评估患者的疼痛强度。此外,评估他们术后的恶心和呕吐情况、住院时间、术后肠梗阻复发持续时间以及患者术后满意度。使用SPSS 22版软件进行数据分析。
所有患者在术后2、4、6、12、18和24小时各时间点的疼痛强度均值及标准差分别为5.91±1.57、4.97±1.55、3.84±1.60、3.54±1.45、2.56±1.70和0.94±1.70。数据分析显示,无论组别如何,术后疼痛强度均显著降低(P < 0.0001)。然而,两组在任何时间间隔的术后平均疼痛强度方面均无显著差异(p > 0.05)。此外,两组术后使用双氯芬酸栓剂的频率也无显著差异(p > 0.05)。另外,两组在术后恶心和呕吐、住院时间、术后肠梗阻复发持续时间以及患者满意度方面均无统计学显著差异(p > 0.05)。
基于本研究结果,与单纯吗啡PCA相比,在吗啡PCA中添加利多卡因似乎对腰麻剖宫产术后疼痛强度的降低没有显著影响。尽管如此,仍需要进行更大样本量的进一步研究。