Clerc Steve, Vuilleumier Henri, Frascarolo Philippe, Spahn Donat R, Gardaz Jean-Patrice
Department of Anesthesiology, University Hospital, Lausanne, Switzerland.
Clin J Pain. 2005 Jan-Feb;21(1):101-5. doi: 10.1097/00002508-200501000-00012.
The aim of the study was to assess whether coadministration of S(+) ketamine or ketorolac would enhance or prolong local analgesic effect of bupivacaine after inguinal hernia repair.
Prospective double-blind randomized study evaluating pain intensity after surgery under general anesthesia.
Outpatient facilities of the University Hospital of Lausanne.
Thirty-six ASA I-II outpatients scheduled for elective day-case inguinal herniorraphy.
Analgesia strategy consisted of a wound infiltration and an inguinal field block either with 30 mL bupivacaine (0.5%) or with the same volume of a mixture of 27 mL bupivacaine (0.5%) + 3 mL S(+) ketamine (75 mg) or a 28 mL bupivacaine (0.5%) + 2 mL ketorolac (60 mg). Postoperative analgesic regimen was standardized.
Pain intensity was assessed with a Visual Analog Scale, a verbal rating score, and by pressure algometry 2, 4, 6, 24, and 48 hours after surgery.
The 3 groups of patients experienced the highest Visual Analog Scale pain score at 24 hours, which was different from those at 6 and 48 hours (P < 0.05). Apart from a significantly lower pain sensation (verbal rating score) in the ketorolac group at 24 and 48 hours and only at 48 hours with ketamine, there were no other differences in pain scores, pain pressure thresholds, or rescue analgesic consumption between groups throughout the 48-hour study period.
The addition of S(+)-ketamine or ketorolac only minimally improves the analgesic effect of bupivacaine. This may be related to the tension-free hernia repair technique associated with low postoperative pain.
本研究旨在评估S(+)氯胺酮或酮咯酸联合使用是否会增强或延长布比卡因在腹股沟疝修补术后的局部镇痛效果。
前瞻性双盲随机研究,评估全身麻醉下手术后的疼痛强度。
洛桑大学医院门诊设施。
36例ASA I-II级择期日间腹股沟疝修补术门诊患者。
镇痛策略包括伤口浸润和腹股沟区域阻滞,分别使用30 mL布比卡因(0.5%)或相同体积的混合液,其中一组为27 mL布比卡因(0.5%)+ 3 mL S(+)氯胺酮(75 mg),另一组为28 mL布比卡因(0.5%)+ 2 mL酮咯酸(60 mg)。术后镇痛方案标准化。
术后2、4、6、24和48小时,采用视觉模拟评分法、语言评分法和压力痛觉测定法评估疼痛强度。
3组患者在术后24小时的视觉模拟评分疼痛得分最高,与术后6小时和48小时的得分不同(P < 0.05)。除酮咯酸组在术后24小时和48小时以及氯胺酮组仅在术后48小时的疼痛感觉(语言评分)明显较低外,在整个48小时研究期间,各组之间的疼痛评分、疼痛压力阈值或补救性镇痛药消耗量没有其他差异。
添加S(+)-氯胺酮或酮咯酸仅能轻微改善布比卡因的镇痛效果。这可能与无张力疝修补技术导致术后疼痛较低有关。