Ahmed Fareed, Garg Ashish, Chawla Vipul, Khandelwal Mamta
Department of Anaesthesia and Critical Care, Sawai Man Singh Medical College and Hospital, Jaipur - 302 004, Rajasthan, India.
Indian J Anaesth. 2010 Jan;54(1):24-8. doi: 10.4103/0019-5049.60492.
This study was carried out to assess the effect of nitroglycerine (transdermal) on intrathecal neostigmine with bupivacaine on postoperative analgesia and note the incidence of adverse effects, if any. After taking informed consent, 120 patients of ASA Grade I and II were systematically randomised into four groups of 30 each. Patients were premedicated with midazolam 0.05 mg/kg intravenously and hydration with Ringer's lactate solution 10ml/kg preoperatively in the holding room. Group I patients received Intrathecal injection of 15 mg bupivacaine with 1ml of normal saline and transdermal placebo patch. Group II patients received Intrathecal injection of 15 mg bupivacaine with 5 mcg of neostigmine and transdermal placebo patch. Group III patients received Intrathecal injection of 15 mg bupivacaine with 1ml of normal saline with transdermal nitroglycerine patch (5 mg/24 hours). Group IV patients received Intrathecal injection of 15 mg bupivacaine with 5mcg of neostigmine and transdermal nitroglycerine patch (5 mg/24 hours), applied on a non anaesthetised area after 20 minutes. Groups were demographically similar and did not differ in intraoperative characteristics like sensory block, motor block, haemodynamic parameters and SpO(2). The mean duration of analgesia was 202.17 minutes, 407.20 minutes, 207.53 minutes and 581.63 minutes in control group (I), neostigmine group (II), nitroglycerine group (III) and nitroglycerine neostigmine group (IV) respectively (P<0.01). To conclude, our results show that transdermal nitroglycerine itself does not show any analgesic potential but it enhances the analgesic potential of intrathecal neostigmine.
本研究旨在评估硝酸甘油(经皮给药)对鞘内注射新斯的明联合布比卡因术后镇痛的影响,并记录不良反应的发生率(如有)。在获得知情同意后,将120例ASA I级和II级患者系统地随机分为四组,每组30例。患者在麻醉前准备室静脉注射咪达唑仑0.05mg/kg进行术前用药,并在术前用10ml/kg乳酸林格氏液进行补液。I组患者接受鞘内注射15mg布比卡因加1ml生理盐水及经皮安慰剂贴片。II组患者接受鞘内注射15mg布比卡因加5μg新斯的明及经皮安慰剂贴片。III组患者接受鞘内注射15mg布比卡因加1ml生理盐水及经皮硝酸甘油贴片(5mg/24小时)。IV组患者接受鞘内注射15mg布比卡因加5μg新斯的明及经皮硝酸甘油贴片(5mg/24小时),20分钟后贴于未麻醉区域。各组在人口统计学上相似,在感觉阻滞、运动阻滞、血流动力学参数和SpO₂等术中特征方面无差异。对照组(I组)、新斯的明组(II组)、硝酸甘油组(III组)和硝酸甘油新斯的明组(IV组)的平均镇痛时间分别为202.17分钟、407.20分钟、207.53分钟和581.63分钟(P<0.01)。总之,我们的结果表明,经皮硝酸甘油本身不具有任何镇痛潜力,但它可增强鞘内新斯的明的镇痛潜力。