Allegri Massimo, Ornaghi Martina, Ferland Catherine E, Bugada Dario, Meghani Yash, Calcinati Serena, De Gregori Manuela, Lovisari Federica, Radhakrishnan Krishnaprabha, Cusato Maria, Scalia Catenacci Stefano, Somaini Marta, Fanelli Guido, Ingelmo Pablo
Department of Anaesthesia, ICU and Pain Therapy, University Hospital of Parma, Parma, Italy; Department of Surgical Sciences, University of Parma, Parma, Italy; SIMPAR Group (Study in Multidisciplinary Pain Research), Parma, Italy.
Department of Anaesthesia and Intensive Care, San Gerardo Hospital of Monza, Milan Bicocca University, Milan, Italy.
Pain Res Manag. 2017;2017:4260702. doi: 10.1155/2017/4260702. Epub 2017 Feb 20.
. Intraperitoneal nebulization of ropivacaine reduces postoperative pain and morphine consumption after laparoscopic surgery. The aim of this multicenter double-blind randomized controlled trial was to assess the efficacy of different doses and dose-related absorption of ropivacaine when nebulized in the peritoneal cavity during laparoscopic cholecystectomy. . Patients were randomized to receive 50, 100, or 150 mg of ropivacaine 1% by peritoneal nebulization through a nebulizer. Morphine consumption, pain intensity in the abdomen, wound and shoulder, time to unassisted ambulation, discharge time, and adverse effects were collected during the first 48 hours after surgery. The pharmacokinetics of ropivacaine was evaluated using high performance liquid chromatography. . Nebulization of 50 mg of ropivacaine had the same effect of 100 or 150 mg in terms of postoperative morphine consumption, shoulder pain, postoperative nausea and vomiting, activity resumption, and hospital discharge timing (>0.05). Plasma concentrations did not reach toxic levels in any patient, and no significant differences were observed between groups ( > 0.05). . There is no enhancement in analgesic efficacy with higher doses of nebulized ropivacaine during laparoscopic cholecystectomy. When administered with a microvibration-based aerosol humidification system, the pharmacokinetics of ropivacaine is constant and maintains an adequate safety profile for each dosage tested.
罗哌卡因腹腔雾化可减轻腹腔镜手术后的疼痛并减少吗啡用量。本多中心双盲随机对照试验的目的是评估在腹腔镜胆囊切除术期间,罗哌卡因在腹腔内雾化时不同剂量及其相关吸收的疗效。患者通过雾化器随机接受1%罗哌卡因50、100或150mg腹腔雾化。在术后48小时内收集吗啡用量、腹部、伤口和肩部的疼痛强度、自主活动时间、出院时间及不良反应。采用高效液相色谱法评估罗哌卡因的药代动力学。就术后吗啡用量、肩部疼痛、术后恶心呕吐、活动恢复及出院时间而言,50mg罗哌卡因雾化与100mg或150mg具有相同效果(>0.05)。所有患者血浆浓度均未达到中毒水平,各组间未观察到显著差异(>0.05)。在腹腔镜胆囊切除术期间,较高剂量的罗哌卡因雾化并未增强镇痛效果。当与基于微振动的气溶胶加湿系统一起给药时,罗哌卡因的药代动力学恒定,且对每个测试剂量均保持足够的安全性。