Atef Hossam, El-Kasaby Alaa El-Din, Omera Magdy, Badr Mohamed
Department of Anesthesia and Intensive Care, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
Middle East J Anaesthesiol. 2012 Feb;21(4):591-8.
To determine the dose of hyperbaric bupivacaine 0.5% required for unilateral spinal anesthesia during diagnostic knee arthroscopy.
This prospective, randomized, clinical study was performed in 80 patients who were assigned to four groups to receive different doses of intrathecal hyperbaric bupivacaine (5 mg, 7.5 mg, 10 mg and 12.5 mg in Groups 1, 2, 3, and 4 respectively). Onset of sensory and motor block, hemodynamic changes, regression of motor block, and incidence of complications were recorded.
Unilateral sensory block was reported in 90% and 85% of patients in Group 1 and Group 2, respectively, but not in any patient in Group 3 and Group 4. Unilateral motor block (modified Bromage scale 0) was reported in 95% of patients in Group 1, 90% in Group 2, and only 5% in Group 3, while no patient in Group 4 showed unilateral motor block. The time required for regression of motor block (Bromage scale 0) was prolonged with higher doses. The incidence of nausea, vomiting, and urine retention was similar in the study groups.
Unilateral sensory and motor block can be achieved with doses of 5 mg and 7.5 mg hyperbaric bupivacaine 0.5% with a stable hemodynamic state. However, 7.5 mg of hyperbaric bupivacaine 0.5% was the dose required for adequate unilateral spinal anesthesia.
确定诊断性膝关节镜检查期间单侧脊髓麻醉所需的0.5%高压布比卡因剂量。
本前瞻性、随机、临床研究纳入80例患者,将其分为四组,分别接受不同剂量的鞘内注射0.5%高压布比卡因(第1组、第2组、第3组和第4组分别为5mg、7.5mg、10mg和12.5mg)。记录感觉和运动阻滞的起效时间、血流动力学变化、运动阻滞的消退情况以及并发症的发生率。
第1组和第2组分别有90%和85%的患者出现单侧感觉阻滞,但第3组和第4组无患者出现。第1组95%的患者、第2组90%的患者出现单侧运动阻滞(改良Bromage分级为0级),第3组仅5%的患者出现,而第4组无患者出现单侧运动阻滞。运动阻滞(Bromage分级为0级)消退所需时间随剂量增加而延长。各研究组恶心、呕吐和尿潴留的发生率相似。
0.5%高压布比卡因5mg和7.5mg剂量可实现单侧感觉和运动阻滞,血流动力学状态稳定。然而,0.5%高压布比卡因7.5mg是充分单侧脊髓麻醉所需的剂量。