Omote K, Satoh O, Sonoda H, Kumeta Y, Yamaya K, Namiki A
Department of Anesthesiology, Sapporo Medical University School of Medicine.
Masui. 1995 Jun;44(6):816-23.
This study was conducted to evaluate the effects of oral clonidine and tizanidine, alpha 2 adrenergic agonists, as premedication for tetracaine spinal anesthesia in 63 gynecological patients. The patients were randomly allocated to one of six groups. Group 1 (n = 7), group 2 (n = 8) and group 3 (n = 7) received 13 mg of tetracaine intrathecally in 10 % glucose solution 2.6 ml. Group 4 (n = 13), group 5 (n = 14) and group 6 (n = 13) received 13 mg of tetracaine intrathecally in a volume of 2.6 ml of 10 % glucose solution which contained 0.65 mg of phenylephrine. As premedication, group 1 and 4 received 0.25 mg of oral triazolam; group 2 and 5 received 3 mg of oral tizanidine; group 3 and 6 received 0.15 mg of oral clonidine. Group 2 and 3, or group 5 and 6 (clonidine or tizanidine group, respectively) needed significant longer time for regression of Th10 sensory blockade than group 1 or 4 (triazolam). The time for appearance of postoperative pain and the time to require postoperative analgesics were longer in the groups which had received either clonidine or tizanidine than in the groups which had received triazolam. Heart rate and systolic blood pressure in group 6 (clonidine-tetracaine-phenylephrine group) showed significant decreases (P < 0.05) after the spinal anesthesia. We concluded that oral premedication of clonidine and tizanidine prolonged tetracaine spinal anesthesia. From the view point of the prolongation of spinal anesthesia and the hemodynamic stability, oral premedication with tizanidine seems to be useful.
本研究旨在评估α2肾上腺素能激动剂口服可乐定和替扎尼定作为63例妇科患者丁卡因脊髓麻醉术前用药的效果。患者被随机分为六组。第1组(n = 7)、第2组(n = 8)和第3组(n = 7)在2.6 ml 10%葡萄糖溶液中鞘内注射13 mg丁卡因。第4组(n = 13)、第5组(n = 14)和第6组(n = 13)在2.6 ml含0.65 mg去氧肾上腺素的10%葡萄糖溶液中鞘内注射13 mg丁卡因。作为术前用药,第1组和第4组口服0.25 mg三唑仑;第2组和第5组口服3 mg替扎尼定;第3组和第6组口服0.15 mg可乐定。第2组和第3组,或第5组和第6组(分别为可乐定或替扎尼定组)Th10感觉阻滞消退所需时间显著长于第1组或第4组(三唑仑组)。接受可乐定或替扎尼定的组术后疼痛出现时间和需要术后镇痛的时间比接受三唑仑的组长。第6组(可乐定-丁卡因-去氧肾上腺素组)脊髓麻醉后心率和收缩压显著降低(P < 0.05)。我们得出结论,口服可乐定和替扎尼定作为术前用药会延长丁卡因脊髓麻醉时间。从延长脊髓麻醉时间和血流动力学稳定性的角度来看,口服替扎尼定作为术前用药似乎是有用的。