A Comparative Clinical Study to Evaluate the Antinociceptive Efficacy of Intravenous versus Intraperitoneal Dexmedetomidine with Ropivacaine in Patients Undergoing Laparoscopic Cholecystectomy

A. Khare, Beena Thada, Jyoti Meena, Kuldeep Jonwal, Veena Mathur
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Abstract

Intraperitoneal (IP) local anesthetic administration has become a routine in laparoscopic surgeries. An additive to local anesthetic like alpha-2 agonist such as dexmedetomidine may enhance the efficacy of local anesthetic. Our primary objective was to compare the duration of analgesia and our secondary objectives were to compare the total amount of rescue analgesics in 24 h, hemodynamic changes, and adverse effects after the use of dexmedetomidine intraperitoneally versus intravenously in addition to 0.25% ropivacaine instillation intraperitoneally. Eighty patients aged 18–60 years of American Society of Anesthesiologists physical status I and II, undergoing laparoscopic cholecystectomy, were randomly allocated into two groups – Group V (n = 40) received 100 ml normal saline (NS) with 0.7 µg/kg dexmedetomidine over 15 min followed by 30 ml 0.25% ropivacaine intraperitoneally and Group P (n = 40) received 100 ml NS over 15 min followed by 30 ml 0.25% ropivacaine with 0.7 µg/kg dexmedetomidine intraperitoneally soon after removal of gallbladder at the end of surgery. The duration of analgesia was significantly longer in Group V (246.45 ± 27.00 min) as compared to Group P (112.83 ± 11.61 min) (P < 0.0001). The total amount of rescue analgesic consumption in 24 h was significantly reduced in Group V (185.00 ± 73.55 mg) as compared to Group P (225.00 ± 77.63 mg) (P < 0.05). As compared to Group P, patients in Group V had a statistically significant Ramsay Sedation Score. The hemodynamic parameters and side effect profile were comparable in both the groups. IV dexmedetomidine 0.7μg/kg is more efficacious as compared to IP dexmedetomidine along with IP ropivacaine 0.25% in laparoscopic cholecystectomy in terms of prolonged duration of analgesia and decreased requirement of rescue analgesia in 24 h.
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在接受腹腔镜胆囊切除术的患者中评估静脉注射右美托咪定和腹腔注射罗哌卡因的抗痛觉效果的比较临床研究
腹腔内局部麻醉已成为腹腔镜手术的常规用药。α-2激动剂(如右美托咪定)作为局麻药的添加剂可提高局麻药的疗效。我们的首要目标是比较镇痛持续时间,次要目标是比较在腹腔注射 0.25% 罗哌卡因的同时腹腔注射右美托咪定和静脉注射右美托咪定后 24 小时内的镇痛药总量、血流动力学变化和不良反应。 80 名年龄在 18-60 岁之间、美国麻醉医师协会体能状态 I 级和 II 级、接受腹腔镜胆囊切除术的患者被随机分为两组--第五组(n = 40)接受 100 毫升生理盐水(NS)和 0.7微克/千克右美托咪定,持续15分钟,然后腹腔注射30毫升0.25%罗哌卡因;P组(n = 40)在手术结束切除胆囊后不久,腹腔注射100毫升NS,持续15分钟,然后腹腔注射30毫升0.25%罗哌卡因和0.7微克/千克右美托咪定。 与 P 组(112.83 ± 11.61 分钟)相比,V 组的镇痛持续时间明显更长(246.45 ± 27.00 分钟)(P < 0.0001)。与 P 组(225.00 ± 77.63 毫克)相比,V 组 24 小时内的镇痛药总用量(185.00 ± 73.55 毫克)明显减少(P < 0.05)。与 P 组相比,V 组患者的拉姆塞镇静评分具有统计学意义。两组患者的血液动力学参数和副作用情况相当。 在腹腔镜胆囊切除术中,静脉注射右美托咪定 0.7μg/kg 与静脉注射右美托咪定和静脉注射 0.25% 罗哌卡因相比,在延长镇痛持续时间和减少 24 小时内镇痛抢救需求方面更有效。
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