Akhtaruzzaman A K, Banik D, Akhtar M F, Roy J, Haque M F, Hye M A
Department of Anaesthesia, Intensive Care and Pain Medicine, Bangabandhu Sheikh Mujib Medical Univesity (BSMMU), Shahbagh, Dhaka, Bangladesh.
Mymensingh Med J. 2010 Oct;19(4):569-75.
Antinociceptive effect and safety of sub-arachnoid (SAB) midazolam is well established in animals and human beings. In this randomized, prospective placebo control clinical study, we investigated the addition of 2.5mg midazolam to bupivacaine on the quality of surgical anaesthesia and duration of first analgesic in the post operative period after lower uterine caesarean section (LUCS). Sixty ASA I or II pregnant women scheduled for elective lower uterine caesarean section were selected for the study. The patients were randomly allocated to receive 2ml of 0.5% hyperbaric bupivacaine with either 0.5ml of 5% dextrose in aqua or 2.5 mg (0.5ml) midazolam. The duration of first analgesic demand, quality of anaesthesia, haemodynamic changes and neonatal condition were assessed. The duration of analgesia (the time interval in minutes between the sub-arachnoid injection and the first analgesic demand by the patient) was significantly longer in the Group II than Group I (197min vs. 112min; p<0.001). The quality of surgical anaesthesia was excellent or good throughout the surgical procedure in 90% (n = 27) of the patients in Group II (p = 0.01). Systolic Blood pressure was significantly lower in the group I at 10 min and 20 min after administration of SAB than group II (p = 0.005 and p = 0.007) but comparable at other times. Sedation level, Apgar score was comparable in both groups. No neurological deficit or other significant adverse effects were recorded. The addition of midazolam with hyperbaric low dose bupivacaine in SAB significantly improves the quality of surgical anaesthesia and prolongs the duration of analgesia without any adverse effects.
蛛网膜下腔(SAB)注射咪达唑仑的镇痛效果及安全性在动物和人类中均已得到充分证实。在这项随机、前瞻性、安慰剂对照临床研究中,我们探讨了在布比卡因中添加2.5mg咪达唑仑对子宫下段剖宫产术(LUCS)后手术麻醉质量及术后首次镇痛持续时间的影响。选取60例计划行择期子宫下段剖宫产术的ASA I或II级孕妇作为研究对象。将患者随机分为两组,分别接受2ml 0.5%的重比重布比卡因加0.5ml 5%葡萄糖水溶液或2.5mg(0.5ml)咪达唑仑。评估首次镇痛需求的持续时间、麻醉质量、血流动力学变化及新生儿状况。II组的镇痛持续时间(蛛网膜下腔注射至患者首次镇痛需求的时间间隔,以分钟计)显著长于I组(197分钟 vs. 112分钟;p<0.001)。II组90%(n = 27)的患者在整个手术过程中手术麻醉质量为优或良(p = 0.01)。蛛网膜下腔给药后10分钟和20分钟时,I组的收缩压显著低于II组(p = 0.005和p = 0.007),但其他时间两组相当。两组的镇静水平、阿氏评分相当。未记录到神经功能缺损或其他明显不良反应。在蛛网膜下腔注射中,将咪达唑仑与低剂量重比重布比卡因联合使用可显著提高手术麻醉质量并延长镇痛持续时间,且无任何不良反应。