Sammarco J L, Conzemius M G, Perkowski S Z, Weinstein M J, Gregor T P, Smith G K
Department of Clinical Studies, Veterinary Hospital of the University of Pennsylvania, Philadelphia, USA.
Vet Surg. 1996 Jan-Feb;25(1):59-69. doi: 10.1111/j.1532-950x.1996.tb01377.x.
A prospective study was undertaken to compare the analgesic effect of intra-articular bupivacaine, morphine, or saline in the 24-hour period following cranial cruciate ligament repair in dogs. Thirty-six clinical patients with ruptured cranial cruciate ligaments were randomly assigned to one of three groups. After surgical stabilization, and before skin closure, an intra-articular injection was given; group one (n = 12) received 0.5% bupivacaine HCl at 0.5 mL/kg, group two (n = 12) received morphine at 0.1 mg/kg diluted with saline to a volume of 0.5 mL/kg, and group three (n = 12) received saline at 0.5 mL/kg. Heart rate, respiratory rate, mean arterial blood pressure, cumulative pain score, visual analog pain score, and pain threshold test on both stifles were recorded preoperatively and at 0 to 6 and 24 hours postoperatively. Surgeons and pain scoring investigators were unaware of the intra-articular medication given. Supplemental analgesia, if needed, was provided in the postoperative period according to subjective assessment of patient discomfort. Postoperative pain scores were lowest in the bupivacaine group and highest in the saline group. Pain threshold, measured by applying calibrated loads to the knee, was higher postoperatively in the bupivacaine group than in the saline group. Dogs in the morphine and bupivacaine groups required less supplemental analgesia than dogs in the saline group. The local provision of analgesia reduces the need for systemic drugs with potential side effects. Both intra-articular morphine and intra-articular bupivacaine provided better postoperative analgesia than intra-articular saline, with intra-articular bupivacaine showing the greatest effect.
进行了一项前瞻性研究,以比较关节内注射布比卡因、吗啡或生理盐水对犬颅十字韧带修复术后24小时的镇痛效果。36例颅十字韧带断裂的临床病犬被随机分为三组。手术固定后、皮肤缝合前,进行关节内注射;第一组(n = 12)接受0.5%盐酸布比卡因,剂量为0.5 mL/kg;第二组(n = 12)接受吗啡,剂量为0.1 mg/kg,用生理盐水稀释至体积为0.5 mL/kg;第三组(n = 12)接受生理盐水,剂量为0.5 mL/kg。术前以及术后0至6小时和24小时记录心率、呼吸频率、平均动脉血压、累积疼痛评分、视觉模拟疼痛评分以及双侧 stifles 的疼痛阈值测试。外科医生和疼痛评分研究者不知道所给予的关节内用药。术后根据对患者不适的主观评估,必要时提供补充镇痛。布比卡因组术后疼痛评分最低,生理盐水组最高。通过对膝关节施加校准负荷测量的疼痛阈值,布比卡因组术后高于生理盐水组。吗啡组和布比卡因组的犬比生理盐水组的犬需要更少的补充镇痛。局部提供镇痛可减少对有潜在副作用的全身药物的需求。关节内注射吗啡和关节内注射布比卡因均比关节内注射生理盐水提供更好的术后镇痛效果,其中关节内注射布比卡因效果最佳。