Govil Nishith, Kumar Parag
Department of Anesthesiology, SGRRIM and HS, Dehradun, Uttarakhand, India.
Anesth Essays Res. 2017 Jan-Mar;11(1):125-128. doi: 10.4103/0259-1162.194561.
Irrigation of local anesthetic intraperitoneally in combination with opioids and non-opioids agents has been used to provide pain relief with varying success in laparoscopic surgeries. This randomized double blind placebo controlled study is designed to study the effect of intraperitoneal instillation of levo-bupivacaine along with clonidine for pain relief after laparascopic cholecystectomy.
75 patients were randomized to receive 20 ml of 0.9% normal saline as placebo (group I), 20 ml of 0.5% levo bupivacaine (group II) and 20 ml of 0.5% levo bupivacaine with 1mcg/kg clonidine (group III) intraperitoneally. The degree of postoperative pain was assessed using the VAS and VRS on the immediate arrival in the recovery room after surgery and thereafter at 2, 4, 8, 12 and 24 hours, postoperatively. Statistical analysis was performed with ANOVA, the Kruskal-Wallis test followed by the Wilcoxon matched pairs rank test was used and < 0.05 were considered significant.
VAS was maximum in placebo (group I) than in levobupivacaine alone (group II) and was minimum in levobupivacaine with clonidine (group III) at all time intervals. The difference between group I and II is statistically significant at immediate and at 2 hours postoperatively but no difference were found between group I and II after 2 hour. However, there is statistically significant difference ( < 0.05) between group I and III and group II and III at all time intervals.
Intraperitoneal instillation of levobupivacaine along with clonidine in a dose of 1mcg/kg is superior to levobupivacaine alone without having any significant adverse effects.
在腹腔镜手术中,腹腔内注射局部麻醉药并联合使用阿片类和非阿片类药物来缓解疼痛,取得了不同程度的成功。本随机双盲安慰剂对照研究旨在探讨左旋布比卡因联合可乐定腹腔内注入对腹腔镜胆囊切除术后疼痛缓解的效果。
75例患者被随机分为三组,分别腹腔内注射20 ml 0.9%生理盐水作为安慰剂(I组)、20 ml 0.5%左旋布比卡因(II组)和20 ml 0.5%左旋布比卡因加1 mcg/kg可乐定(III组)。术后立即在恢复室以及术后2、4、8、12和24小时,使用视觉模拟评分法(VAS)和视觉疼痛评分法(VRS)评估术后疼痛程度。采用方差分析进行统计分析,后续使用Kruskal-Wallis检验及Wilcoxon配对秩和检验,P<0.05被认为具有统计学意义。
在所有时间点,安慰剂组(I组)的VAS评分最高,单纯左旋布比卡因组(II组)次之,左旋布比卡因联合可乐定组(III组)最低。I组和II组在术后即刻及术后2小时差异有统计学意义,但2小时后两组无差异。然而,I组和III组以及II组和III组在所有时间点差异均有统计学意义(P<0.05)。
腹腔内注入1 mcg/kg剂量的左旋布比卡因联合可乐定优于单纯使用左旋布比卡因,且无明显不良反应。